Huntington Faxon Willard

Adjunct Professor in the Department of Biology

Office: 
101 Science Dr, Room 2379, Ciemas Bldg, Durham, NC 27708
Campus Box: 
3382 Med Ctr
Phone: 
(919) 668-4477
Genome biology
Genome sciences and policy

Education

  • Ph.D. 1979, Yale University

  • B.A. 1975, Harvard University

Papers Published

Genomic characterization of large heterochromatic gaps in the human genome assembly., 5, 2014
Altemose, N and Miga, KH and Maggioni, M and Willard, HF, PLoS computational biology. 10 pp. e1003628

Genomic characterization of large heterochromatic gaps in the human genome assembly., 5, 2014
Altemose, N; Miga, KH; Maggioni, M; Willard, HF, PLoS computational biology. 10 vol. (5); pp. e1003628

Centromere reference models for human chromosomes X and Y satellite arrays., 4, 2014
Miga, KH and Newton, Y and Jain, M and Altemose, N and Willard, HF and Kent, WJ, Genome research. 24 pp. 697--707

Centromere reference models for human chromosomes X and Y satellite arrays., 4, 2014
Miga, KH; Newton, Y; Jain, M; Altemose, N; Willard, HF; Kent, WJ, Genome research. 24 vol. (4); pp. 697-707

Impact of delivery models on understanding genomic risk for type 2 diabetes, 1, 2014
Haga, S; Barry, WT; Mills, RA; Svetkey, LL; Suchindran, S; Willard, HF; Ginsburg, GS, Public health genomics. 17 vol. (2); pp. 95-104

An international effort towards developing standards for best practices in analysis, interpretation and reporting of clinical genome sequencing results in the CLARITY Challenge., 0, 2014
Brownstein, CA; Beggs, AH; Homer, N; Merriman, B; Yu, TW; Flannery, KC; DeChene, ET; Towne, MC; Savage, SK; Price, EN; Holm, IA; Luquette, LJ; Lyon, E; Majzoub, J; Neupert, P; McCallie, D; Szolovits, P; Willard, HF; Mendelsohn, NJ; Temme, R; Finkel, RS; Yum, SW; Medne, L; Sunyaev, SR; Adzhubey, I; Cassa, CA; de Bakker, PI; Duzkale, H; Dworzyński, P; Fairbrother, W; Francioli, L; Funke, BH; Giovanni, MA; Handsaker, RE; Lage, K; Lebo, MS; Lek, M; Leshchiner, I; MacArthur, DG; McLaughlin, HM; Murray, MF; Pers, TH; Polak, PP; Raychaudhuri, S; Rehm, HL; Soemedi, R; Stitziel, NO; Vestecka, S; Supper, J; Gugenmus, C; Klocke, B; Hahn, A; Schubach, M; Menzel, M; Biskup, S; Freisinger, P; Deng, M; Braun, M; Perner, S; Smith, RJ; Andorf, JL; Huang, J; Ryckman, K; Sheffield, VC; Stone, EM; Bair, T; Black-Ziegelbein, EA; Braun, TA; Darbro, B; DeLuca, AP; Kolbe, DL; Scheetz, TE; Shearer, AE; Sompallae, R; Wang, K; Bassuk, AG; Edens, E; Mathews, K; Moore, SA; Shchelochkov, OA; Trapane, P; Bossler, A; Campbell, CA; Heusel, JW; Kwitek, A; Maga, T; Panzer, K; Wassink, T; Van Daele, D; Azaiez, H; Booth, K; Meyer, N; Segal, MM; Williams, MS; Tromp, G; White, P; Corsmeier, D; Fitzgerald-Butt, S; Herman, G; Lamb-Thrush, D; McBride, KL; Newsom, D; Pierson, CR; Rakowsky, AT; Maver, A; Lovrečić, L; Palandačić, A; Peterlin, B; Torkamani, A; Wedell, A; Huss, M; Alexeyenko, A; Lindvall, JM; Magnusson, M; Nilsson, D; Stranneheim, H; Taylan, F; Gilissen, C; Hoischen, A; van Bon, B; Yntema, H; Nelen, M; Zhang, W; Sager, J; Zhang, L; Blair, K; Kural, D; Cariaso, M; Lennon, GG; Javed, A; Agrawal, S; Ng, PC; Sandhu, KS; Krishna, S; Veeramachaneni, V; Isakov, O; Halperin, E; Friedman, E; Shomron, N; Glusman, G; Roach, JC; Caballero, J; Cox, HC; Mauldin, D; Ament, SA; Rowen, L; Richards, DR; San Lucas, FA; Gonzalez-Garay, ML; Caskey, CT; Bai, Y; Huang, Y; Fang, F; Zhang, Y; Wang, Z; Barrera, J; Garcia-Lobo, JM; González-Lamuño, D; Llorca, J; Rodriguez, MC; Varela, I; Reese, MG; De La Vega, FM; Kiruluta, E; Cargill, M; Hart, RK; Sorenson, JM; Lyon, GJ; Stevenson, DA; Bray, BE; Moore, BM; Eilbeck, K; Yandell, M; Zhao, H; Hou, L; Chen, X; Yan, X; Chen, M; Li, C; Yang, C; Gunel, M; Li, P; Kong, Y; Alexander, AC; Albertyn, ZI; Boycott, KM; Bulman, DE; Gordon, PM; Innes, AM; Knoppers, BM; Majewski, J; Marshall, CR; Parboosingh, JS; Sawyer, SL; Samuels, ME; Schwartzentruber, J; Kohane, IS; Margulies, DM, Genome Biology. 15 vol. (3); pp. R53

Impact of delivery models on understanding genomic risk for type 2 diabetes., 0, 2014
Haga, SB and Barry, WT and Mills, R and Svetkey, L and Suchindran, S and Willard, HF and Ginsburg, GS, Public health genomics. 17 pp. 95--104

Impact of delivery models on understanding genomic risk for type 2 diabetes., 0, 2014
Haga, SB; Barry, WT; Mills, R; Svetkey, L; Suchindran, S; Willard, HF; Ginsburg, GS, Public health genomics. 17 vol. (2); pp. 95-104

Esperanto for histones: CENP-A, not CenH3, is the centromeric histone H3 variant, 4, 2013
Earnshaw, WC and Allshire, RC and Black, BE and Bloom, K and Brinkley, BR and Brown, W and Cheeseman, IM and Choo, KHA and Copenhaver, GP and DeLuca, JG and Desai, A and Diekmann, S and Erhardt, S and Fitzgerald-Hayes, M and Foltz, D and Fukagawa, T and Gassmann, R and Gerlich, DW and Glover, DM and Gorbsky, GJ and Harrison, SC and Heun, P and Hirota, T and Jansen, LET and Karpen, G and Kops, GJPL and Lampson, MA and Lens, SM and Losada, A and Luger, K and Maiato, H and Maddox, PS and Margolis, RL and Masumoto, H and McAinsh, AD and Mellone, BG and Meraldi, P and Musacchio, A and Oegema, K and O'Neill, RJ and Salmon, ED and Scott, KC and Straight, AF and Stukenberg, PT and Sullivan, BA and Sullivan, KF and Sunkel, CE and Swedlow, JR and Walczak, CE and Warburton, PE and Westermann, S and Willard, HF and Wordeman, L and Yanagida, M and Yen, TJ and Yoda, K and Cleveland, DW, CHROMOSOME RESEARCH. 21 pp. 101--106

Public knowledge of and attitudes toward genetics and genetic testing., 4, 2013
Haga, SB and Barry, WT and Mills, R and Ginsburg, GS and Svetkey, L and Sullivan, J and Willard, HF, Genet Test Mol Biomarkers. 17 pp. 327--335

Public knowledge of and attitudes toward genetics and genetic testing., 4, 2013
Haga, SB; Barry, WT; Mills, R; Ginsburg, GS; Svetkey, L; Sullivan, J; Willard, HF, Genetic Testing and Molecular Biomarkers. 17 vol. (4); pp. 327-335

Sequences associated with centromere competency in the human genome., 2, 2013
Hayden, KE and Strome, ED and Merrett, SL and Lee, HR and Rudd, MK and Willard, HF, Mol Cell Biol. 33 pp. 763--772

Sequences associated with centromere competency in the human genome., 2, 2013
Hayden, KE; Strome, ED; Merrett, SL; Lee, HR; Rudd, MK; Willard, HF, Molecular and Cellular Biology. 33 vol. (4); pp. 763-772

Genomic and Personalized Medicine, 0, 2013
Ginsburg, G and Willard, H, Genomic and Personalized Medicine. 1-2

Preface, 0, 2013
Ginsburg, GS and Willard, HF, Genomic and Personalized Medicine. 1 pp. xi--xii

The human genome: A window on human genetics, biology, and medicine, 0, 2013
Willard, HF, Genomic and Personalized Medicine. 1 pp. 4--27

Esperanto for histones: CENP-A, not CenH3, is the centromeric histone H3 variant, 0, 2013
Earnshaw, WC and Allshire, RC and Black, BE and Bloom, K and Brinkley, BR and Brown, W and Cheeseman, IM and Choo, KHA and Copenhaver, GP and Deluca, JG and Desai, A and Diekmann, S and Erhardt, S and Fitzgerald-Hayes, M and Foltz, D and Fukagawa, T and Gassmann, R and Gerlich, DW and Glover, DM and Gorbsky, GJ and Harrison, SC and Heun, P and Hirota, T and Jansen, LET and Karpen, G and Kops, GJPL and Lampson, MA and Lens, SM and Losada, A and Luger, K and Maiato, H and Maddox, PS and Margolis, RL and Masumoto, H and McAinsh, AD and Mellone, BG and Meraldi, P and Musacchio, A and Oegema, K and O'Neill, RJ and Salmon, ED and Scott, KC and Straight, AF and Stukenberg, PT and Sullivan, BA and Sullivan, KF and Sunkel, CE and Swedlow, JR and Walczak, CE and Warburton, PE and Westermann, S and Willard, HF and Wordeman, L and Yanagida, M and Yen, TJ and Yoda, K and Cleveland, DW, Chromosome Research. 21 pp. 101--106

Effects of sequence variation on differential allelic transcription factor occupancy and gene expression., 5, 2012
Reddy, TE and Gertz, J and Pauli, F and Kucera, KS and Varley, KE and Newberry, KM and Marinov, GK and Mortazavi, A and Williams, BA and Song, L and Crawford, GE and Wold, B and Willard, HF and Myers, RM, Genome Res. 22 pp. 860--869

Effects of sequence variation on differential allelic transcription factor occupancy and gene expression., 5, 2012
Reddy, TE; Gertz, J; Pauli, F; Kucera, KS; Varley, KE; Newberry, KM; Marinov, GK; Mortazavi, A; Williams, BA; Song, L; Crawford, GE; Wold, B; Willard, HF; Myers, RM, Genome research. 22 vol. (5); pp. 860-869

Uncoupling of genomic and epigenetic signals in the maintenance and inheritance of heterochromatin domains in fission yeast., 2, 2012
Wheeler, BS and Ruderman, BT and Willard, HF and Scott, KC, Genetics. 190 pp. 549--557

Uncoupling of genomic and epigenetic signals in the maintenance and inheritance of heterochromatin domains in fission yeast., 2, 2012
Wheeler, BS; Ruderman, BT; Willard, HF; Scott, KC, Genetics. 190 vol. (2); pp. 549-557

Composition and organization of active centromere sequences in complex genomes., 0, 2012
Hayden, KE and Willard, HF, BMC Genomics. 13 pp. 324

Evidence for sequence biases associated with patterns of histone methylation., 0, 2012
Wang, Z and Willard, HF, BMC Genomics. 13 pp. 367

Nonrandom X chromosome inactivation is influenced by multiple regions on the murine X chromosome, 0, 2012
Thorvaldsen, JL and Krapp, C and Willard, HF and Bartolomei, MS, Genetics. 192 pp. 1095--1107

Composition and organization of active centromere sequences in complex genomes., 0, 2012
Hayden, KE; Willard, HF, BMC Genomics. 13 pp. 324

Evidence for sequence biases associated with patterns of histone methylation., 0, 2012
Wang, Z; Willard, HF, BMC Genomics. 13 pp. 367

Nonrandom X chromosome inactivation is influenced by multiple regions on the murine X chromosome, 0, 2012
Thorvaldsen, JL; Krapp, C; Willard, HF; Bartolomei, MS, Genetics. 192 vol. (3); pp. 1095-1107

Comparative analysis of the primate X-inactivation center region and reconstruction of the ancestral primate XIST locus., 6, 2011
Horvath, JE and Sheedy, CB and Merrett, SL and Diallo, AB and Swofford, DL and NISC Comparative Sequencing Program and Green, ED and Willard, HF, Genome Res. 21 pp. 850--862

Comparative analysis of the primate X-inactivation center region and reconstruction of the ancestral primate XIST locus., 6, 2011
Horvath, JE; Sheedy, CB; Merrett, SL; Diallo, AB; Swofford, DL; NISC Comparative Sequencing Program, ; Green, ED; Willard, HF, Genome research. 21 vol. (6); pp. 850-862

Allele-specific distribution of RNA polymerase II on female X chromosomes., 10, 2011
Kucera, KS and Reddy, TE and Pauli, F and Gertz, J and Logan, JE and Myers, RM and Willard, HF, Hum Mol Genet. 20 pp. 3964--3973

Allele-specific distribution of RNA polymerase II on female X chromosomes., 10, 2011
Kucera, KS; Reddy, TE; Pauli, F; Gertz, J; Logan, JE; Myers, RM; Willard, HF, Human Molecular Genetics. 20 vol. (20); pp. 3964-3973

Analysis of dna methylation in a three-generation family reveals widespread genetic influence on epigenetic regulation, 0, 2011
Gertz, J and Varley, KE and Reddy, TE and Bowling, KM and Pauli, F and Parker, SL and Kucera, KS and Willard, HF and Myers, RM, PLoS Genetics. 7

Organization and molecular evolution of CENP-A--associated satellite DNA families in a basal primate genome., 0, 2011
Lee, HR and Hayden, KE and Willard, HF, Genome Biol Evol. 3 pp. 1136--1149

Competencies: A cure for pre-med curriculum, 0, 2011
Anderson, WA and Amasino, RM and Jr, MA and Banerjee, U and Bartel, B and Corces, VG and Drennan, CL and Elgin, SCR and Epstein, IR and Fanning, E and Jr, LJG and Handelsman, JO and Hatfull, GF and Hoy, RR and Kelley, D and Leinwand, LA and Losick, R and Lu, Y and Lynn, DG and Neuhauser, C and O'Dowd, DK and Olivera, T and Pevzner, P and Richards-Kortum, RR and Rine, J and Sah, RL and Strobel, SA and Walker, GC and Walt, DR and Warner, IM and Wessler, S and Willard, HF and Zare, RN, Science. 334 pp. 760--761

Organization and molecular evolution of CENP-A--associated satellite DNA families in a basal primate genome., 0, 2011
Lee, HR; Hayden, KE; Willard, HF, Genome Biology and Evolution. 3 pp. 1136-1149

Analysis of dna methylation in a three-generation family reveals widespread genetic influence on epigenetic regulation, 0, 2011
Gertz, J; Varley, KE; Reddy, TE; Bowling, KM; Pauli, F; Parker, SL; Kucera, KS; Willard, HF; Myers, RM, PLoS genetics. 7 vol. (8);

Heritable individual-specific and allele-specific chromatin signatures in humans., 4, 2010
McDaniell, R and Lee, BK and Song, L and Liu, Z and Boyle, AP and Erdos, MR and Scott, LJ and Morken, MA and Kucera, KS and Battenhouse, A and Keefe, D and Collins, FS and Willard, HF and Lieb, JD and Furey, TS and Crawford, GE and Iyer, VR and Birney, E, Science. 328 pp. 235--239

ASHG Awards and Addresses. 2009 William Allan Award address: Life in the sandbox: unfinished business., 3, 2010
Willard, HF, The American Journal of Human Genetics. 86 vol. (3); pp. 318-327

The Foundations of Genomic and Personalized Medicine, 0, 2010
Ginsburg, GS and Willard, HF, Essentials of Genomic and Personalized Medicine. pp. 1--10

Preface, 0, 2010
Ginsburg, GS and Willard, HF, Essentials of Genomic and Personalized Medicine. pp. ix--ix

Organization, Variation and Expression of the Human Genome, 0, 2010
Willard, HF, Essentials of Genomic and Personalized Medicine. pp. 13--26

The impact of local genome sequence on defining heterochromatin domains., 4, 2009
Wheeler, BS and Blau, JA and Willard, HF and Scott, KC, PLoS Genet. 5 pp. e1000453

Genomic and Personalized Medicine, Two-Vol Set, 0, 2009
Ginsburg, GS and Willard, HF, Genomic and Personalized Medicine, Two-Vol Set.

A national clinical decision support infrastructure to enable the widespread and consistent practice of genomic and personalized medicine., 0, 2009
Kawamoto, K and Lobach, DF and Willard, HF and Ginsburg, GS, BMC Med Inform Decis Mak. 9 pp. 17

Organization, Variation and Expression of the Human Genome as a Foundation of Genomic and Personalized Medicine, 0, 2009
Willard, HF, Genomic and Personalized Medicine, Two-Vol Set. pp. 1--21

Preface, 0, 2009
Willard, HF and Ginsburg, GS, Genomic and Personalized Medicine, Two-Vol Set. pp. xxvii--xxviii

Development and application of a phylogenomic toolkit: resolving the evolutionary history of Madagascar's lemurs., 3, 2008
Horvath, JE and Weisrock, DW and Embry, SL and Fiorentino, I and Balhoff, JP and Kappeler, P and Wray, GA and Willard, HF and Yoder, AD, Genome Res. 18 pp. 489--499

Letting the genome out of the bottle, 0, 2008
Haga, SB and Willard, HF, New England Journal of Medicine. 358 pp. 2184-

Primate comparative genomics: lemur biology and evolution., 4, 2007
Horvath, JE and Willard, HF, Trends Genet. 23 pp. 173--182

Avoid boring people: And other lessons from a life in science, 10, 2007
Willard, HF, Nature. 449 vol. (7164); pp. 787-787

Human artificial chromosome assembly by transposon-based retrofitting of genomic BACs with synthetic alpha-satellite arrays., 1, 2007
Basu, J and Willard, HF and Stromberg, G, Curr Protoc Hum Genet. Chapter 5 pp. Unit--5.18

An RNA polymerase III-dependent heterochromatin barrier at fission yeast centromere 1., 0, 2007
Scott, KC and White, CV and Willard, HF, PLoS One. 2 pp. e1099

Evidence of influence of genomic DNA sequence on human X chromosome inactivation., 9, 2006
Wang, Z and Willard, HF and Mukherjee, S and Furey, TS, PLoS Comput Biol. 2 pp. e113

Genetic control of X chromosome inactivation in mice: definition of the Xce candidate interval., 8, 2006
Chadwick, LH and Pertz, LM and Broman, KW and Bartolomei, MS and Willard, HF, Genetics. 173 pp. 2103--2110

Chromosome-wide, allele-specific analysis of the histone code on the human X chromosome., 8, 2006
Valley, CM and Pertz, LM and Balakumaran, BS and Willard, HF, Hum Mol Genet. 15 pp. 2335--2347

Genomic and epigenomic approaches to the study of X chromosome inactivation., 6, 2006
Valley, CM and Willard, HF, Curr Opin Genet Dev. 16 pp. 240--245

Defining the spectrum of genome policy., 12, 2006
Haga, SB and Willard, HF, Nat Rev Genet. 7 pp. 966--972

Human artificial chromosomes: potential applications and clinical considerations., 10, 2006
Basu, J and Willard, HF, Pediatr Clin North Am. 53 pp. 843--viii

The evolutionary dynamics of alpha-satellite., 1, 2006
Rudd, MK and Wray, GA and Willard, HF, Genome Res. 16 pp. 88--96

A heterochromatin barrier partitions the fission yeast centromere into discrete chromatin domains., 1, 2006
Scott, KC and Merrett, SL and Willard, HF, Curr Biol. 16 pp. 119--129

Human genomics: In search of normality, 0, 2006
Shianna, KV and Willard, HF, Nature. 444 pp. 428--429

Genomic organization and function of human centromeres, 0, 2006
Willard, HE and Rudd, MK, Genomic Disorders: The Genomic Basis of Disease. pp. 115--129

X chromosome-inactivation patterns of 1,005 phenotypically unaffected females, 0, 2006
Amos-Landgraf, JM and Cottle, A and Plenge, RM and Friez, M and Schwartz, CE and Longshore, J and Willard, HF, American Journal of Human Genetics. 79 pp. 493--499

Evidence of Influence of Genomic DNA Sequence on Human X Chromosome Inactivation., 0, 2006
Wang, Z; Willard, HF; Mukherjee, S; Furey, TS, PLoS Computational Biology. 2 vol. (9);

Genetic and parent-of-origin influences on X chromosome choice in Xce heterozygous mice., 9, 2005
Chadwick, LH and Willard, HF, Mamm Genome. 16 pp. 691--699

Genomic medicine: genetic variation and its impact on the future of health care., 8, 2005
Willard, HF and Angrist, M and Ginsburg, GS, Philos Trans R Soc Lond B Biol Sci. 360 pp. 1543--1550

Artificial and engineered chromosomes: non-integrating vectors for gene therapy., 5, 2005
Basu, J and Willard, HF, Trends Mol Med. 11 pp. 251--258

The DNA sequence of the human X chromosome., 3, 2005
Ross, MT and Grafham, DV and Coffey, AJ and Scherer, S and McLay, K and Muzny, D and Platzer, M and Howell, GR and Burrows, C and Bird, CP and Frankish, A and Lovell, FL and Howe, KL and Ashurst, JL and Fulton, RS and Sudbrak, R and Wen, G and Jones, MC and Hurles, ME and Andrews, TD and Scott, CE and Searle, S and Ramser, J and Whittaker, A and Deadman, R and Carter, NP and Hunt, SE and Chen, R and Cree, A and Gunaratne, P and Havlak, P and Hodgson, A and Metzker, ML and Richards, S and Scott, G and Steffen, D and Sodergren, E and Wheeler, DA and Worley, KC and Ainscough, R and Ambrose, KD and Ansari-Lari, MA and Aradhya, S and Ashwell, RI and Babbage, AK and Bagguley, CL and Ballabio, A and Banerjee, R and Barker, GE and Barlow, KF and Barrett, IP and Bates, KN and Beare, DM and Beasley, H and Beasley, O and Beck, A and Bethel, G and Blechschmidt, K and Brady, N and Bray-Allen, S and Bridgeman, AM and Brown, AJ and Brown, MJ and Bonnin, D and Bruford, EA and Buhay, C and Burch, P and Burford, D and Burgess, J and Burrill, W and Burton, J and Bye, JM and Carder, C and Carrel, L and Chako, J and Chapman, JC and Chavez, D and Chen, E and Chen, G and Chen, Y and Chen, Z and Chinault, C and Ciccodicola, A and Clark, SY and Clarke, G and Clee, CM and Clegg, S and Clerc-Blankenburg, K and Clifford, K and Cobley, V and Cole, CG and Conquer, JS and Corby, N and Connor, RE and David, R and Davies, J and Davis, C and Davis, J and Delgado, O and Deshazo, D and Dhami, P and Ding, Y and Dinh, H and Dodsworth, S and Draper, H and Dugan-Rocha, S and Dunham, A and Dunn, M and Durbin, KJ and Dutta, I and Eades, T and Ellwood, M and Emery-Cohen, A and Errington, H and Evans, KL and Faulkner, L and Francis, F and Frankland, J and Fraser, AE and Galgoczy, P and Gilbert, J and Gill, R and Glöckner, G and Gregory, SG and Gribble, S and Griffiths, C and Grocock, R and Gu, Y and Gwilliam, R and Hamilton, C and Hart, EA and Hawes, A and Heath, PD and Heitmann, K and Hennig, S and Hernandez, J and Hinzmann, B and Ho, S and Hoffs, M and Howden, PJ and Huckle, EJ and Hume, J and Hunt, PJ and Hunt, AR and Isherwood, J and Jacob, L and Johnson, D and Jones, S and de Jong, PJ and Joseph, SS and Keenan, S and Kelly, S and Kershaw, JK and Khan, Z and Kioschis, P and Klages, S and Knights, AJ and Kosiura, A and Kovar-Smith, C and Laird, GK and Langford, C and Lawlor, S and Leversha, M and Lewis, L and Liu, W and Lloyd, C and Lloyd, DM and Loulseged, H and Loveland, JE and Lovell, JD and Lozado, R and Lu, J and Lyne, R and Ma, J and Maheshwari, M and Matthews, LH and McDowall, J and McLaren, S and McMurray, A and Meidl, P and Meitinger, T and Milne, S and Miner, G and Mistry, SL and Morgan, M and Morris, S and Müller, I and Mullikin, JC and Nguyen, N and Nordsiek, G and Nyakatura, G and O'Dell, CN and Okwuonu, G and Palmer, S and Pandian, R and Parker, D and Parrish, J and Pasternak, S and Patel, D and Pearce, AV and Pearson, DM and Pelan, SE and Perez, L and Porter, KM and Ramsey, Y and Reichwald, K and Rhodes, S and Ridler, KA and Schlessinger, D and Schueler, MG and Sehra, HK and Shaw-Smith, C and Shen, H and Sheridan, EM and Shownkeen, R and Skuce, CD and Smith, ML and Sotheran, EC and Steingruber, HE and Steward, CA and Storey, R and Swann, RM and Swarbreck, D and Tabor, PE and Taudien, S and Taylor, T and Teague, B and Thomas, K and Thorpe, A and Timms, K and Tracey, A and Trevanion, S and Tromans, AC and d'Urso, M and Verduzco, D and Villasana, D and Waldron, L and Wall, M and Wang, Q and Warren, J and Warry, GL and Wei, X and West, A and Whitehead, SL and Whiteley, MN and Wilkinson, JE and Willey, DL and Williams, G and Williams, L and Williamson, A and Williamson, H and Wilming, L and Woodmansey, RL and Wray, PW and Yen, J and Zhang, J and Zhou, J and Zoghbi, H and Zorilla, S and Buck, D and Reinhardt, R and Poustka, A and Rosenthal, A and Lehrach, H and Meindl, A and Minx, PJ and Hillier, LW and Willard, HF and Wilson, RK and Waterston, RH and Rice, CM and Vaudin, M and Coulson, A and Nelson, DL and Weinstock, G and Sulston, JE and Durbin, R and Hubbard, T and Gibbs, RA and Beck, S and Rogers, J and Bentley, DR, Nature. 434 pp. 325--337

Rapid creation of BAC-based human artificial chromosome vectors by transposition with synthetic alpha-satellite arrays., 0, 2005
J Basu, G Stromberg, G Compitello, HF Willard, G Van Bokkelen, Nucleic Acids Res. 33 vol. (2); pp. 587-96

Erratum: Rapid creation of BAC-based human artifical chromosome vectors by transposition with synthetic alpha-satellite arrays (Nucleic Acids Research (2005) vol. 33 (587-596)), 0, 2005
Basu, J and Stromberg, G and Compitello, G and Willard, HF and Bokkelen, GV, Nucleic Acids Research. 33 pp. 1421--1422

X-inactivation profile reveals extensive variability in X-linked gene expression in females, 0, 2005
Carrel, L and Willard, HF, Nature. 434 pp. 400--404

Engineered human dicentric chromosomes show centromere plasticity, 0, 2005
Higgins, AW and Gustashaw, KM and Willard, HF, Chromosome Research. 13 pp. 745--762

Efficient assembly of de novo human artificial chromosomes from large genomic loci., 0, 2005
Basu, J and Compitello, G and Stromberg, G and Willard, HF and Van Bokkelen, G, BMC Biotechnol. 5 pp. 21

Rapid creation of BAC-based human artificial chromosome vectors by transposition with synthetic alpha-satellite arrays., 0, 2005
Basu, J and Stromberg, G and Compitello, G and Willard, HF and Van Bokkelen, G, Nucleic Acids Res. 33 pp. 587--596

Progressive proximal expansion of the primate X chromosome centromere, 0, 2005
Schueler, MG and Dunn, JM and Bird, CP and Ross, MT and Viggiano, L and Rocchi, M and Willard, HF and Green, ED, Proceedings of the National Academy of Sciences of the United States of America. 102 pp. 10563--10568

Multiple spatially distinct types of facultative heterochromatin on the human inactive X chromosome., 12, 2004
Chadwick, BP and Willard, HF, Proc Natl Acad Sci U S A. 101 pp. 17450--17455

Multiple spatially distinct types of facultative heterochromatin on the human inactive X chromosome., 12, 2004
BP Chadwick, HF Willard, Proc Natl Acad Sci U S A. 101 vol. (50); pp. 17450-5

Analysis of the centromeric regions of the human genome assembly., 11, 2004
Rudd, MK and Willard, HF, Trends Genet. 20 pp. 529--533

Analysis of the centromeric regions of the human genome assembly., 11, 2004
MK Rudd, HF Willard, Trends Genet. 20 vol. (11); pp. 529-33

Assembly and characterization of heterochromatin and euchromatin on human artificial chromosomes., 0, 2004
BR Grimes, J Babcock, MK Rudd, B Chadwick, HF Willard, Genome Biol. 5 vol. (11); pp. R89

Assembly and characterization of heterochromatin and euchromatin on human artificial chromosomes., 0, 2004
Grimes, BR and Babcock, J and Rudd, MK and Chadwick, B and Willard, HF, Genome Biol. 5 pp. R89

Introductory Speech for David Page, 0, 2004
Willard, HF, American Journal of Human Genetics. 74 pp. 397--398

New Year's wishes: All I want for 2005 is..., 0, 2004
Baltimore, D and Nossal, G and Navratil, G and Daley, G and Barakat, R and Kay, M and Daley, G and Friedman, L and Buick, R and Trautmann, A and Sharav, V and Stein, J and Rahmstorf, S and Rapley, C and Collins, F and Fauci, A and Clarke, AC and Tam, P and Willard, H, Nature. 432 pp. 942--948

Chromatin of the Barr body: histone and non-histone proteins associated with or excluded from the inactive X chromosome., 9, 2003
BP Chadwick, HF Willard, Hum Mol Genet. 12 vol. (17); pp. 2167-78

Chromatin of the Barr body: histone and non-histone proteins associated with or excluded from the inactive X chromosome., 9, 2003
Chadwick, BP and Willard, HF, Hum Mol Genet. 12 pp. 2167--2178

An N-ethyl-N-nitrosourea mutagenesis screen for epigenetic mutations in the mouse., 8, 2003
I Percec, JL Thorvaldsen, RM Plenge, CJ Krapp, JH Nadeau, HF Willard, MS Bartolomei, Genetics. 164 vol. (4); pp. 1481-94

An N-ethyl-N-nitrosourea mutagenesis screen for epigenetic mutations in the mouse., 8, 2003
Percec, I and Thorvaldsen, JL and Plenge, RM and Krapp, CJ and Nadeau, JH and Willard, HF and Bartolomei, MS, Genetics. 164 pp. 1481--1494

Tales of the Y chromosome., 6, 2003
Willard, HF, Nature. 423 pp. 810--813

Tales of the Y chromosome., 6, 2003
HF Willard, Nature. 423 vol. (6942); pp. 810-1, 813

SETting the stage. Eed-Enx1 leaves an epigenetic signature on the inactive X chromosome., 4, 2003
BP Chadwick, HF Willard, Dev Cell. 4 vol. (4); pp. 445-7

Personalized health planning., 4, 2003
RS Williams, HF Willard, R Snyderman, Science. 300 vol. (5619); pp. 549

SETting the stage. Eed-Enx1 leaves an epigenetic signature on the inactive X chromosome., 4, 2003
Chadwick, BP and Willard, HF, Dev Cell. 4 pp. 445--447

Personalized health planning., 4, 2003
Williams, RS and Willard, HF and Snyderman, R, Science. 300 pp. 549

Barring gene expression after XIST: maintaining facultative heterochromatin on the inactive X., 12, 2003
BP Chadwick, HF Willard, Semin Cell Dev Biol. 14 vol. (6); pp. 359-67

Barring gene expression after XIST: maintaining facultative heterochromatin on the inactive X., 12, 2003
Chadwick, BP and Willard, HF, Semin Cell Dev Biol. 14 pp. 359--367

Human artificial chromosomes with alpha satellite-based de novo centromeres show increased frequency of nondisjunction and anaphase lag., 11, 2003
MK Rudd, RW Mays, S Schwartz, HF Willard, Mol Cell Biol. 23 vol. (21); pp. 7689-97

Human artificial chromosomes with alpha satellite-based de novo centromeres show increased frequency of nondisjunction and anaphase lag., 11, 2003
Rudd, MK and Mays, RW and Schwartz, S and Willard, HF, Mol Cell Biol. 23 pp. 7689--7697

A comprehensive X inactivation profile of the human X chromosome., 11, 2003
Carrel, L; Nickel, G; Trevarthen, K; Dunn, J; Willard, HF, The American Journal of Human Genetics. 73 vol. (5); pp. 180-180

Functional and evolutionary annotation of the chromosome 17 centromere., 11, 2003
Rudd, K; Dunn, J; Willard, HF, The American Journal of Human Genetics. 73 vol. (5); pp. 217-217

Sequence organization and functional annotation of human centromeres., 0, 2003
MK Rudd, MG Schueler, HF Willard, Cold Spring Harb Symp Quant Biol. 68 pp. 141-9

Sequence organization and functional annotation of human centromeres., 0, 2003
Rudd, MK and Schueler, MG and Willard, HF, Cold Spring Harb Symp Quant Biol. 68 pp. 141--149

Editorial, 0, 2003
Davies, K and Willard, H, Human Molecular Genetics. 12 pp. 699-

Klinefelter syndrome: Expanding the phenotype and identifying new research directions, 0, 2003
Simpson, JL and Cruz, FDL and Swerdloff, RS and Samango-Sprouse, C and Skakkebaek, NE and Jr, JMG and Hassold, T and Aylstock, M and Meyer-Bahlburg, HFL and Willard, HF and Hall, JG and Salameh, W and Boone, K and Staessen, C and Geschwind, D and Giedd, J and Dobs, AS and Rogol, A and Brinton, B and Paulsen, CA, Genetics in Medicine. 5 pp. 460--468

Skewed X-chromosome inactivation is a common feature of X-linked mental retardation disorders., 7, 2002
RM Plenge, RA Stevenson, HA Lubs, CE Schwartz, HF Willard, Am J Hum Genet. 71 vol. (1); pp. 168-73

Skewed X-chromosome inactivation is a common feature of X-linked mental retardation disorders., 7, 2002
Plenge, RM and Stevenson, RA and Lubs, HA and Schwartz, CE and Willard, HF, Am J Hum Genet. 71 pp. 168--173

Alpha-satellite DNA and vector composition influence rates of human artificial chromosome formation., 6, 2002
BR Grimes, AA Rhoades, HF Willard, Mol Ther. 5 vol. (6); pp. 798-805

An ectopic human XIST gene can induce chromosome inactivation in postdifferentiation human HT-1080 cells., 6, 2002
LL Hall, M Byron, K Sakai, L Carrel, HF Willard, JB Lawrence, Proc Natl Acad Sci U S A. 99 vol. (13); pp. 8677-82

Cell cycle-dependent localization of macroH2A in chromatin of the inactive X chromosome., 6, 2002
Chadwick, BP and Willard, HF, J Cell Biol. 157 pp. 1113--1123

Alpha-satellite DNA and vector composition influence rates of human artificial chromosome formation., 6, 2002
Grimes, BR and Rhoades, AA and Willard, HF, Mol Ther. 5 pp. 798--805

An ectopic human XIST gene can induce chromosome inactivation in postdifferentiation human HT-1080 cells., 6, 2002
Hall, LL and Byron, M and Sakai, K and Carrel, L and Willard, HF and Lawrence, JB, Proc Natl Acad Sci U S A. 99 pp. 8677--8682

Cell cycle-dependent localization of macroH2A in chromatin of the inactive X chromosome., 6, 2002
BP Chadwick, HF Willard, J Cell Biol. 157 vol. (7); pp. 1113-23

Autosomal dominant mutations affecting X inactivation choice in the mouse., 5, 2002
I Percec, RM Plenge, JH Nadeau, MS Bartolomei, HF Willard, Science. 296 vol. (5570); pp. 1136-9

Autosomal dominant mutations affecting X inactivation choice in the mouse., 5, 2002
Percec, I and Plenge, RM and Nadeau, JH and Bartolomei, MS and Willard, HF, Science. 296 pp. 1136--1139

2001 ASHG Presidential Address. On black boxes and storytellers: lessons learned in human genetics., 2, 2002
HF Willard, Am J Hum Genet. 70 vol. (2); pp. 285-96

2001 ASHG Presidential Address. On black boxes and storytellers: lessons learned in human genetics., 2, 2002
Willard, HF, Am J Hum Genet. 70 pp. 285--296

Making sense (and antisense) of the X inactivation center., 8, 2001
HF Willard, L Carrel, Proc Natl Acad Sci U S A. 98 vol. (18); pp. 10025-7

Making sense (and antisense) of the X inactivation center., 8, 2001
Willard, HF and Carrel, L, Proc Natl Acad Sci U S A. 98 pp. 10025--10027

Histone variant macroH2A contains two distinct macrochromatin domains capable of directing macroH2A to the inactive X chromosome., 7, 2001
BP Chadwick, CM Valley, HF Willard, Nucleic Acids Res. 29 vol. (13); pp. 2699-705

Histone variant macroH2A contains two distinct macrochromatin domains capable of directing macroH2A to the inactive X chromosome., 7, 2001
Chadwick, BP and Valley, CM and Willard, HF, Nucleic Acids Res. 29 pp. 2699--2705

Histone H2A variants and the inactive X chromosome: identification of a second macroH2A variant., 5, 2001
BP Chadwick, HF Willard, Hum Mol Genet. 10 vol. (10); pp. 1101-13

Neocentromeres and human artificial chromosomes: an unnatural act., 5, 2001
HF Willard, Proc Natl Acad Sci U S A. 98 vol. (10); pp. 5374-6

Neocentromeres and human artificial chromosomes: an unnatural act., 5, 2001
Willard, HF, Proc Natl Acad Sci U S A. 98 pp. 5374--5376

Histone H2A variants and the inactive X chromosome: identification of a second macroH2A variant., 5, 2001
Chadwick, BP and Willard, HF, Hum Mol Genet. 10 pp. 1101--1113

Clinical objectives in medical genetics for undergraduate medical students. Association of Professors of Human Genetics, Clinical Objectives Task Force., 4, 2001
JM Friedman, M Blitzer, LJ Elsas, U Francke, HF Willard, Genet Med. 1 vol. (1); pp. 54-5

You say tomato and I say tomahto: human genetics and gene therapy., 12, 2001
HF Willard, Mol Ther. 4 vol. (6); pp. 514

You say tomato and I say tomahto: human genetics and gene therapy., 12, 2001
Willard, HF, Mol Ther. 4 pp. 514

Genomic and genetic definition of a functional human centromere., 10, 2001
Schueler, MG and Higgins, AW and Rudd, MK and Gustashaw, K and Willard, HF, Science. 294 pp. 109--115

Genomic and genetic definition of a functional human centromere., 10, 2001
MG Schueler, AW Higgins, MK Rudd, K Gustashaw, HF Willard, Science. 294 vol. (5540); pp. 109-15

A novel chromatin protein, distantly related to histone H2A, is largely excluded from the inactive X chromosome., 1, 2001
BP Chadwick, HF Willard, J Cell Biol. 152 vol. (2); pp. 375-84

A novel chromatin protein, distantly related to histone H2A, is largely excluded from the inactive X chromosome., 1, 2001
Chadwick, BP and Willard, HF, J Cell Biol. 152 pp. 375--384

Evolution and function of alpha satellite DNA, 0, 2001
Willard, HF, Pathologie Biologie. 49 pp. 390-

Expression-based assay of an X-linked gene to examine effects of the X-controlling element (Xce) locus., 5, 2000
RM Plenge, I Percec, JH Nadeau, HF Willard, Mamm Genome. 11 vol. (5); pp. 405-8

Large-insert clone/STS contigs in Xq11-q12, spanning deletions in patients with androgen insensitivity and mental retardation., 5, 2000
MG Schueler, AW Higgins, R Nagaraja, D Tentler, N Dahl, K Gustashaw, HF Willard, Genomics. 66 vol. (1); pp. 104-9

Large-insert clone/STS contigs in Xq11-q12, spanning deletions in patients with androgen insensitivity and mental retardation., 5, 2000
Schueler, MG and Higgins, AW and Nagaraja, R and Tentler, D and Dahl, N and Gustashaw, K and Willard, HF, Genomics. 66 pp. 104--109

Expression-based assay of an X-linked gene to examine effects of the X-controlling element (Xce) locus., 5, 2000
Plenge, RM and Percec, I and Nadeau, JH and Willard, HF, Mamm Genome. 11 pp. 405--408

Study of V(1)-vascular vasopressin receptor gene microsatellite polymorphisms in human essential hypertension., 4, 2000
M Thibonnier, MK Graves, MS Wagner, N Chatelain, F Soubrier, P Corvol, HF Willard, X Jeunemaitre, J Mol Cell Cardiol. 32 vol. (4); pp. 557-64

Study of V(1)-vascular vasopressin receptor gene microsatellite polymorphisms in human essential hypertension., 4, 2000
Thibonnier, M and Graves, MK and Wagner, MS and Chatelain, N and Soubrier, F and Corvol, P and Willard, HF and Jeunemaitre, X, J Mol Cell Cardiol. 32 pp. 557--564

Genomics and gene therapy. Artificial chromosomes coming to life., 11, 2000
Willard, HF, Science. 290 pp. 1308--1309

Genomics and gene therapy. Artificial chromosomes coming to life., 11, 2000
HF Willard, Science. 290 vol. (5495); pp. 1308-9

Chromosomal domains and escape from X inactivation: comparative X inactivation analysis in mouse and human., 10, 2000
KD Tsuchiya, HF Willard, Mamm Genome. 11 vol. (10); pp. 849-54

Artificial chromosomes coming to life, 0, 2000
Willard, HF, Science. 290 pp. 1308--1309

Chromosome engineering: generation of mono- and dicentric isochromosomes in a somatic cell hybrid system., 8, 1999
AW Higgins, MG Schueler, HF Willard, Chromosoma. 108 vol. (4); pp. 256-65

Deletion including the oligophrenin-1 gene associated with enlarged cerebral ventricles, cerebellar hypoplasia, seizures and ataxia., 7, 1999
D Tentler, P Gustavsson, J Leisti, M Schueler, J Chelly, E Timonen, G Annerén, HF Willard, N Dahl, Eur J Hum Genet. 7 vol. (5); pp. 541-8

Deletion including the oligophrenin-1 gene associated with enlarged cerebral ventricles, cerebellar hypoplasia, seizures and ataxia., 7, 1999
Tentler, D and Gustavsson, P and Leisti, J and Schueler, M and Chelly, J and Timonen, E and Annerén, G and Willard, HF and Dahl, N, Eur J Hum Genet. 7 pp. 541--548

Heterogeneous gene expression from the inactive X chromosome: an X-linked gene that escapes X inactivation in some human cell lines but is inactivated in others., 6, 1999
L Carrel, HF Willard, Proc Natl Acad Sci U S A. 96 vol. (13); pp. 7364-9

Evidence that mutations in the X-linked DDP gene cause incompletely penetrant and variable skewed X inactivation., 3, 1999
RM Plenge, L Tranebjaerg, PK Jensen, C Schwartz, HF Willard, Am J Hum Genet. 64 vol. (3); pp. 759-67

Evidence that mutations in the X-linked DDP gene cause incompletely penetrant and variable skewed X inactivation., 3, 1999
Plenge, RM and Tranebjaerg, L and Jensen, PK and Schwartz, C and Willard, HF, Am J Hum Genet. 64 pp. 759--767

A first-generation X-inactivation profile of the human X chromosome., 12, 1999
L Carrel, AA Cottle, KC Goglin, HF Willard, Proc Natl Acad Sci U S A. 96 vol. (25); pp. 14440-4

Breaking the silence in Rett syndrome., 10, 1999
HF Willard, BD Hendrich, Nat Genet. 23 vol. (2); pp. 127-8

Breaking the silence in Rett syndrome., 10, 1999
Willard, HF and Hendrich, BD, Nat Genet. 23 pp. 127--128

Counting on Xist., 7, 1998
L Carrel, HF Willard, Nat Genet. 19 vol. (3); pp. 211-2

Chromosomal basis of X chromosome inactivation: identification of a multigene domain in Xp11.21-p11.22 that escapes X inactivation., 7, 1998
AP Miller, HF Willard, Proc Natl Acad Sci U S A. 95 vol. (15); pp. 8709-14

The spreading of X inactivation into autosomal material of an x;autosome translocation: evidence for a difference between autosomal and X-chromosomal DNA., 7, 1998
WM White, HF Willard, DL Van Dyke, DJ Wolff, Am J Hum Genet. 63 vol. (1); pp. 20-8

Chromosomal basis of X chromosome inactivation: identification of a multigene domain in Xp11.21-p11.22 that escapes X inactivation., 7, 1998
Miller, AP and Willard, HF, Proc Natl Acad Sci U S A. 95 pp. 8709--8714

Counting on Xist., 7, 1998
Carrel, L and Willard, HF, Nat Genet. 19 pp. 211--212

Genetics of disease Complex genetics, complex diseases, 6, 1998
HF Willard, KE Davies, Curr Opin Genet Dev. 8 vol. (3); pp. 271-3

Orangutan alpha-satellite monomers are closely related to the human consensus sequence., 6, 1998
T Haaf, HF Willard, Mamm Genome. 9 vol. (6); pp. 440-7

Orangutan alpha-satellite monomers are closely related to the human consensus sequence., 6, 1998
Haaf, T and Willard, HF, Mamm Genome. 9 pp. 440--447

Genetics of disease Complex genetics, complex diseases, 6, 1998
Willard, HF and Davies, KE, Curr Opin Genet Dev. 8 pp. 271--273

Human artificial chromosomes coming into focus., 5, 1998
HF Willard, Nat Biotechnol. 16 vol. (5); pp. 415-6

Human artificial chromosomes coming into focus., 5, 1998
Willard, HF, Nat Biotechnol. 16 pp. 415--416

Centromeres: the missing link in the development of human artificial chromosomes., 4, 1998
HF Willard, Curr Opin Genet Dev. 8 vol. (2); pp. 219-25

The UTX gene escapes X inactivation in mice and humans., 4, 1998
A Greenfield, L Carrel, D Pennisi, C Philippe, N Quaderi, P Siggers, K Steiner, PP Tam, AP Monaco, HF Willard, P Koopman, Hum Mol Genet. 7 vol. (4); pp. 737-42

The UTX gene escapes X inactivation in mice and humans., 4, 1998
Greenfield, A and Carrel, L and Pennisi, D and Philippe, C and Quaderi, N and Siggers, P and Steiner, K and Tam, PP and Monaco, AP and Willard, HF and Koopman, P, Hum Mol Genet. 7 pp. 737--742

Centromeres: the missing link in the development of human artificial chromosomes., 4, 1998
Willard, HF, Curr Opin Genet Dev. 8 pp. 219--225

The mouse Mid1 gene: implications for the pathogenesis of Opitz syndrome and the evolution of the mammalian pseudoautosomal region., 3, 1998
L Dal Zotto, NA Quaderi, R Elliott, PA Lingerfelter, L Carrel, V Valsecchi, E Montini, CH Yen, V Chapman, I Kalcheva, G Arrigo, O Zuffardi, S Thomas, HF Willard, A Ballabio, CM Disteche, EI Rugarli, Hum Mol Genet. 7 vol. (3); pp. 489-99

The mouse Mid1 gene: implications for the pathogenesis of Opitz syndrome and the evolution of the mammalian pseudoautosomal region., 3, 1998
Dal Zotto, L and Quaderi, NA and Elliott, R and Lingerfelter, PA and Carrel, L and Valsecchi, V and Montini, E and Yen, CH and Chapman, V and Kalcheva, I and Arrigo, G and Zuffardi, O and Thomas, S and Willard, HF and Ballabio, A and Disteche, CM and Rugarli, EI, Hum Mol Genet. 7 pp. 489--499

Physical and genetic mapping of the human X chromosome centromere: repression of recombination., 2, 1998
MM Mahtani, HF Willard, Genome Res. 8 vol. (2); pp. 100-10

Physical and genetic mapping of the human X chromosome centromere: repression of recombination., 2, 1998
Mahtani, MM and Willard, HF, Genome Res. 8 pp. 100--110

Stable dicentric X chromosomes with two functional centromeres., 11, 1998
BA Sullivan, HF Willard, Nat Genet. 20 vol. (3); pp. 227-8

Stable dicentric X chromosomes with two functional centromeres., 11, 1998
Sullivan, BA and Willard, HF, Nat Genet. 20 pp. 227--228

Clinical objectives in medical genetics for undergraduate medical students. Association of Professors of Human Genetics, Clinical Objectives Task Force., 11, 1998
Friedman, JM and Blitzer, M and Elsas, LJ and Francke, U and Willard, HF, Genet Med. 1 pp. 54--55

X inactivation in females with X-linked disease., 1, 1998
JM Puck, HF Willard, N Engl J Med. 338 vol. (5); pp. 325-8

X inactivation in females with X-linked disease., 1, 1998
Puck, JM and Willard, HF, N Engl J Med. 338 pp. 325--328

Complex genetics, complex diseases: Editorial overview, 0, 1998
Willard, HF and Davies, KE, Current Opinion in Genetics and Development. 8 pp. 271--273

Chromosome-specific alpha-satellite DNA from the centromere of chimpanzee chromosome 4., 9, 1997
T Haaf, HF Willard, Chromosoma. 106 vol. (4); pp. 226-32

Chromosome-specific alpha-satellite DNA from the centromere of chimpanzee chromosome 4., 9, 1997
Haaf, T and Willard, HF, Chromosoma. 106 pp. 226--232

Autism and multiple exostoses associated with an X;8 translocation occurring within the GRPR gene and 3' to the SDC2 gene., 8, 1997
Y Ishikawa-Brush, JF Powell, P Bolton, AP Miller, F Francis, HF Willard, H Lehrach, AP Monaco, Hum Mol Genet. 6 vol. (8); pp. 1241-50

Deletions in Xq26.3-q27.3 including FMR1 result in a severe phenotype in a male and variable phenotypes in females depending upon the X inactivation pattern., 8, 1997
DJ Wolff, KM Gustashaw, V Zurcher, L Ko, W White, L Weiss, DL Van Dyke, S Schwartz, HF Willard, Hum Genet. 100 vol. (2); pp. 256-61

Characterization of neo-centromeres in marker chromosomes lacking detectable alpha-satellite DNA., 8, 1997
TW Depinet, JL Zackowski, WC Earnshaw, S Kaffe, GS Sekhon, R Stallard, BA Sullivan, GH Vance, DL Van Dyke, HF Willard, AB Zinn, S Schwartz, Hum Mol Genet. 6 vol. (8); pp. 1195-204

Deletions in Xq26.3-q27.3 including FMR1 result in a severe phenotype in a male and variable phenotypes in females depending upon the X inactivation pattern., 8, 1997
Wolff, DJ and Gustashaw, KM and Zurcher, V and Ko, L and White, W and Weiss, L and Van Dyke, DL and Schwartz, S and Willard, HF, Hum Genet. 100 pp. 256--261

Autism and multiple exostoses associated with an X;8 translocation occurring within the GRPR gene and 3' to the SDC2 gene., 8, 1997
Ishikawa-Brush, Y and Powell, JF and Bolton, P and Miller, AP and Francis, F and Willard, HF and Lehrach, H and Monaco, AP, Hum Mol Genet. 6 pp. 1241--1250

Characterization of neo-centromeres in marker chromosomes lacking detectable alpha-satellite DNA., 8, 1997
Depinet, TW and Zackowski, JL and Earnshaw, WC and Kaffe, S and Sekhon, GS and Stallard, R and Sullivan, BA and Vance, GH and Van Dyke, DL and Willard, HF and Zinn, AB and Schwartz, S, Hum Mol Genet. 6 pp. 1195--1204

Identification and characterization of the human XIST gene promoter: implications for models of X chromosome inactivation., 7, 1997
BD Hendrich, RM Plenge, HF Willard, Nucleic Acids Res. 25 vol. (13); pp. 2661-71

Identification and characterization of the human XIST gene promoter: implications for models of X chromosome inactivation., 7, 1997
Hendrich, BD and Plenge, RM and Willard, HF, Nucleic Acids Res. 25 pp. 2661--2671

Expression of genes from the human active and inactive X chromosomes., 6, 1997
CJ Brown, L Carrel, HF Willard, Am J Hum Genet. 60 vol. (6); pp. 1333-43

Expression of genes from the human active and inactive X chromosomes., 6, 1997
Brown, CJ and Carrel, L and Willard, HF, Am J Hum Genet. 60 pp. 1333--1343

Formation of de novo centromeres and construction of first-generation human artificial microchromosomes., 4, 1997
JJ Harrington, G Van Bokkelen, RW Mays, K Gustashaw, HF Willard, Nat Genet. 15 vol. (4); pp. 345-55

Formation of de novo centromeres and construction of first-generation human artificial microchromosomes., 4, 1997
Harrington, JJ and Van Bokkelen, G and Mays, RW and Gustashaw, K and Willard, HF, Nat Genet. 15 pp. 345--355

Remodelling chromatin with RNA., 3, 1997
HF Willard, HK Salz, Nature. 386 vol. (6622); pp. 228-9

Remodelling chromatin with RNA., 3, 1997
Willard, HF and Salz, HK, Nature. 386 pp. 228--229

Molecular characterization of isochromosomes of Xq., 11, 1997
James, RS and Dalton, P and Gustashaw, K and Wolff, DJ and Willard, HF and Mitchell, C and Jacobs, PA, Ann Hum Genet. 61 pp. 485--490

A promoter mutation in the XIST gene in two unrelated families with skewed X-chromosome inactivation., 11, 1997
RM Plenge, BD Hendrich, C Schwartz, JF Arena, A Naumova, C Sapienza, RM Winter, HF Willard, Nat Genet. 17 vol. (3); pp. 353-6

Molecular characterization of isochromosomes of Xq., 11, 1997
RS James, P Dalton, K Gustashaw, DJ Wolff, HF Willard, C Mitchell, PA Jacobs, Ann Hum Genet. 61 vol. (Pt 6); pp. 485-90

A promoter mutation in the XIST gene in two unrelated families with skewed X-chromosome inactivation., 11, 1997
Plenge, RM and Hendrich, BD and Schwartz, C and Arena, JF and Naumova, A and Sapienza, C and Winter, RM and Willard, HF, Nat Genet. 17 pp. 353--356

Molecular characterization of isochromosomes of xq, 0, 1997
James, RS and Dalton, P and Gustashaw, K and Wolff, DJ and Willard, HF and Mitchell, C and Jacobs, PA, Annals of Human Genetics. 61 pp. 485--490

Tissue and lineage-specific variation in inactive X chromosome expression of the murine Smcx gene., 9, 1996
L Carrel, PA Hunt, HF Willard, Hum Mol Genet. 5 vol. (9); pp. 1361-6

Tissue and lineage-specific variation in inactive X chromosome expression of the murine Smcx gene., 9, 1996
Carrel, L and Hunt, PA and Willard, HF, Hum Mol Genet. 5 pp. 1361--1366

Chromosome manipulation: a systematic approach toward understanding human chromosome structure and function., 7, 1996
HF Willard, Proc Natl Acad Sci U S A. 93 vol. (14); pp. 6847-50

X chromosome inactivation and X-linked mental retardation., 7, 1996
HF Willard, Am J Med Genet. 64 vol. (1); pp. 21-6

An assay for X inactivation based on differential methylation at the fragile X locus, FMR1., 7, 1996
L Carrel, HF Willard, Am J Med Genet. 64 vol. (1); pp. 27-30

X chromosome inactivation, XIST, and pursuit of the X-inactivation center., 7, 1996
HF Willard, Cell. 86 vol. (1); pp. 5-7

Chromosome manipulation: a systematic approach toward understanding human chromosome structure and function., 7, 1996
Willard, HF, Proc Natl Acad Sci U S A. 93 pp. 6847--6850

X chromosome inactivation, XIST, and pursuit of the X-inactivation center., 7, 1996
Willard, HF, Cell. 86 pp. 5--7

An assay for X inactivation based on differential methylation at the fragile X locus, FMR1., 7, 1996
Carrel, L and Willard, HF, Am J Med Genet. 64 pp. 27--30

Heritability of X chromosome--inactivation phenotype in a large family., 6, 1996
AK Naumova, RM Plenge, LM Bird, M Leppert, K Morgan, HF Willard, C Sapienza, Am J Hum Genet. 58 vol. (6); pp. 1111-9

Heritability of X chromosome--inactivation phenotype in a large family., 6, 1996
Naumova, AK and Plenge, RM and Bird, LM and Leppert, M and Morgan, K and Willard, HF and Sapienza, C, Am J Hum Genet. 58 pp. 1111--1119

Characterization of a chromosome-specific chimpanzee alpha satellite subset: evolutionary relationship to subsets on human chromosomes., 4, 1996
Warburton, PE and Haaf, T and Gosden, J and Lawson, D and Willard, HF, Genomics. 33 pp. 220--228

Characterization of a chromosome-specific chimpanzee alpha satellite subset: evolutionary relationship to subsets on human chromosomes., 4, 1996
PE Warburton, T Haaf, J Gosden, D Lawson, HF Willard, Genomics. 33 vol. (2); pp. 220-8

X inactivation analysis and DNA methylation studies of the ubiquitin activating enzyme E1 and PCTAIRE-1 genes in human and mouse., 3, 1996
L Carrel, CM Clemson, JM Dunn, AP Miller, PA Hunt, JB Lawrence, HF Willard, Hum Mol Genet. 5 vol. (3); pp. 391-401

X inactivation analysis and DNA methylation studies of the ubiquitin activating enzyme E1 and PCTAIRE-1 genes in human and mouse., 3, 1996
Carrel, L and Clemson, CM and Dunn, JM and Miller, AP and Hunt, PA and Lawrence, JB and Willard, HF, Hum Mol Genet. 5 pp. 391--401

XIST RNA paints the inactive X chromosome at interphase: evidence for a novel RNA involved in nuclear/chromosome structure., 2, 1996
CM Clemson, JA McNeil, HF Willard, JB Lawrence, J Cell Biol. 132 vol. (3); pp. 259-75

Structure, sequence, expression, and chromosomal localization of the human V1a vasopressin receptor gene., 2, 1996
M Thibonnier, MK Graves, MS Wagner, C Auzan, E Clauser, HF Willard, Genomics. 31 vol. (3); pp. 327-34

XIST RNA paints the inactive X chromosome at interphase: evidence for a novel RNA involved in nuclear/chromosome structure., 2, 1996
Clemson, CM and McNeil, JA and Willard, HF and Lawrence, JB, J Cell Biol. 132 pp. 259--275

Structure, sequence, expression, and chromosomal localization of the human V1a vasopressin receptor gene., 2, 1996
Thibonnier, M and Graves, MK and Wagner, MS and Auzan, C and Clauser, E and Willard, HF, Genomics. 31 pp. 327--334

A novel gene, DXS8237E, lies within 20 kb upstream of UBE1 in Xp11.23 and has a different X inactivation status., 1, 1996
MP Coleman, HJ Ambrose, L Carrel, AH Németh, HF Willard, KE Davies, Genomics. 31 vol. (1); pp. 135-8

Molecular definition of breakpoints associated with human Xq isochromosomes: implications for mechanisms of formation., 1, 1996
DJ Wolff, AP Miller, DL Van Dyke, S Schwartz, HF Willard, Am J Hum Genet. 58 vol. (1); pp. 154-60

A novel gene, DXS8237E, lies within 20 kb upstream of UBE1 in Xp11.23 and has a different X inactivation status., 1, 1996
Coleman, MP and Ambrose, HJ and Carrel, L and Németh, AH and Willard, HF and Davies, KE, Genomics. 31 pp. 135--138

Molecular definition of breakpoints associated with human Xq isochromosomes: implications for mechanisms of formation., 1, 1996
Wolff, DJ and Miller, AP and Van Dyke, DL and Schwartz, S and Willard, HF, Am J Hum Genet. 58 pp. 154--160

Centromeres of human chromosomes., 0, 1996
BA Sullivan, S Schwartz, HF Willard, Environ Mol Mutagen. 28 vol. (3); pp. 182-91

Seventh International Workshop on the Fragile X and X-linked mental retardation, 0, 1996
Tranebjaerg, L and Lubs, HA and Borghgraef, M and Brown, WT and Fisch, G and J-, PF and Hagerman, R and Jacobs, PA and Mandel, JL and Mulley, J and Oostra, B and Schwartz, C and Sherman, S and Willard, H and Willems, P, American Journal of Medical Genetics. 64 pp. 1--14

Centromeres of human chromosomes., 0, 1996
Sullivan, BA and Schwartz, S and Willard, HF, Environ Mol Mutagen. 28 pp. 182--191

The mouse Sb1.8 gene located at the distal end of the X chromosome is subject to X inactivation., 2, 1995
R Sultana, DA Adler, S Edelhoff, L Carrel, KH Lee, VC Chapman, HF Willard, CM Disteche, Hum Mol Genet. 4 vol. (2); pp. 257-63

A 6-Mb YAC contig in Xp22.1-p22.2 spanning the DXS69E, XE59, GLRA2, PIGA, GRPR, CALB3, and PHKA2 genes., 2, 1995
T Alitalo, F Francis, J Kere, H Lehrach, D Schlessinger, HF Willard, Genomics. 25 vol. (3); pp. 691-700

The DXS423E gene in Xp11.21 escapes X chromosome inactivation., 2, 1995
CJ Brown, AP Miller, L Carrel, JL Rupert, KE Davies, HF Willard, Hum Mol Genet. 4 vol. (2); pp. 251-5

The mouse Sb1.8 gene located at the distal end of the X chromosome is subject to X inactivation., 2, 1995
Sultana, R and Adler, DA and Edelhoff, S and Carrel, L and Lee, KH and Chapman, VC and Willard, HF and Disteche, CM, Hum Mol Genet. 4 pp. 257--263

The DXS423E gene in Xp11.21 escapes X chromosome inactivation., 2, 1995
Brown, CJ and Miller, AP and Carrel, L and Rupert, JL and Davies, KE and Willard, HF, Hum Mol Genet. 4 pp. 251--255

A 6-Mb YAC contig in Xp22.1-p22.2 spanning the DXS69E, XE59, GLRA2, PIGA, GRPR, CALB3, and PHKA2 genes., 2, 1995
Alitalo, T and Francis, F and Kere, J and Lehrach, H and Schlessinger, D and Willard, HF, Genomics. 25 pp. 691--700

X inactivation of the FMR1 fragile X mental retardation gene., 12, 1995
CU Kirchgessner, ST Warren, HF Willard, J Med Genet. 32 vol. (12); pp. 925-9

Interhomologue sequence variation of alpha satellite DNA from human chromosome 17: evidence for concerted evolution along haplotypic lineages., 12, 1995
PE Warburton, HF Willard, J Mol Evol. 41 vol. (6); pp. 1006-15

X inactivation of the FMR1 fragile X mental retardation gene., 12, 1995
Kirchgessner, CU and Warren, ST and Willard, HF, J Med Genet. 32 pp. 925--929

Interhomologue sequence variation of alpha satellite DNA from human chromosome 17: evidence for concerted evolution along haplotypic lineages., 12, 1995
Warburton, PE and Willard, HF, J Mol Evol. 41 pp. 1006--1015

Epigenetic regulation of gene expression: the effect of altered chromatin structure from yeast to mammals., 0, 1995
BD Hendrich, HF Willard, Hum Mol Genet. 4 Spec No pp. 1765-77

Direct detection of non-random X chromosome inactivation by use of a transcribed polymorphism in the XIST gene., 0, 1995
JL Rupert, CJ Brown, HF Willard, Eur J Hum Genet. 3 vol. (6); pp. 333-43

Editorial overview, 0, 1995
Davies, KE and Willard, HF, Current Opinion in Genetics and Development. 5 pp. 295--297

Direct detection of non-random X chromosome inactivation by use of a transcribed polymorphism in the XIST gene., 0, 1995
Rupert, JL and Brown, CJ and Willard, HF, Eur J Hum Genet. 3 pp. 333--343

Three genes that escape X chromosome inactivation are clustered within a 6 mb YAC contig and STS map in Xp11.21-p11.22, 0, 1995
Miller, AP and Gustashaw, K and Wolff, DJ and Rider, SH and Monaco, AP and Eble, B and Schlessinger, D and Gorski, JL and Ommen, GJV and Weissenbach, J and Willard, HF, Human Molecular Genetics. 4 pp. 731--739

Epigenetic regulation of gene expression: the effect of altered chromatin structure from yeast to mammals., 0, 1995
Hendrich, BD and Willard, HF, Hum Mol Genet. 4 Spec No pp. 1765--1777

A novel transmembrane transporter encoded by the XPCT gene in Xq13.2., 7, 1994
RG Lafrenière, L Carrel, HF Willard, Hum Mol Genet. 3 vol. (7); pp. 1133-9

Absence of the XIST gene from late-replicating isodicentric X chromosomes in leukaemia., 7, 1994
KA Rack, J Chelly, RJ Gibbons, S Rider, D Benjamin, RG Lafreniére, D Oscier, RW Hendriks, IW Craig, HF Willard, Hum Mol Genet. 3 vol. (7); pp. 1053-9

Small marker X chromosomes lack the X inactivation center: implications for karyotype/phenotype correlations., 7, 1994
DJ Wolff, CJ Brown, S Schwartz, AM Duncan, U Surti, HF Willard, Am J Hum Genet. 55 vol. (1); pp. 87-95

Small marker X chromosomes lack the X inactivation center: implications for karyotype/phenotype correlations., 7, 1994
Wolff, DJ and Brown, CJ and Schwartz, S and Duncan, AM and Surti, U and Willard, HF, Am J Hum Genet. 55 pp. 87--95

Absence of the XIST gene from late-replicating isodicentric X chromosomes in leukaemia., 7, 1994
Rack, KA and Chelly, J and Gibbons, RJ and Rider, S and Benjamin, D and Lafreniére, RG and Oscier, D and Hendriks, RW and Craig, IW and Willard, HF, Hum Mol Genet. 3 pp. 1053--1059

A novel transmembrane transporter encoded by the XPCT gene in Xq13.2., 7, 1994
Lafrenière, RG and Carrel, L and Willard, HF, Hum Mol Genet. 3 pp. 1133--1139

Mapping of loci and translocation breakpoints in Xq13: isolation of a conserved locus that maps close to CCG1 in human and mouse., 4, 1994
V Reed, SH Laval, V McCabe, HF Willard, Y Boyd, Mamm Genome. 5 vol. (4); pp. 237-40

Mapping of loci and translocation breakpoints in Xq13: isolation of a conserved locus that maps close to CCG1 in human and mouse., 4, 1994
Reed, V and Laval, SH and McCabe, V and Willard, HF and Boyd, Y, Mamm Genome. 5 pp. 237--240

The human X-inactivation centre is not required for maintenance of X-chromosome inactivation., 3, 1994
CJ Brown, HF Willard, Nature. 368 vol. (6467); pp. 154-6

The human X-inactivation centre is not required for maintenance of X-chromosome inactivation., 3, 1994
Brown, CJ and Willard, HF, Nature. 368 pp. 154--156

Partial X chromosome trisomy with functional disomy of Xp due to failure of X inactivation., 10, 1994
KM Gustashaw, V Zurcher, LH Dickerman, R Stallard, HF Willard, Am J Med Genet. 53 vol. (1); pp. 39-45

Partial X chromosome trisomy with functional disomy of Xp due to failure of X inactivation., 10, 1994
Gustashaw, KM and Zurcher, V and Dickerman, LH and Stallard, R and Willard, HF, Am J Med Genet. 53 pp. 39--45

Report and abstracts of the Fifth International Workshop on Human X Chromosome Mapping 1994. Heidelberg, Germany, April 24-27, 1994., 0, 1994
HF Willard, F Cremers, JL Mandel, AP Monaco, DL Nelson, D Schlessinger, Cytogenet Cell Genet. 67 vol. (4); pp. 295-358

Report and abstracts of the Fifth International Workshop on Human X Chromosome Mapping 1994. Heidelberg, Germany, April 24-27, 1994., 0, 1994
Willard, HF and Cremers, F and Mandel, JL and Monaco, AP and Nelson, DL and Schlessinger, D, Cytogenet Cell Genet. 67 pp. 295--358

Report of the Fifth International Workshop on Human X Chromosome Mapping 1994, 0, 1994
Willard, HF and Cremers, F and Mandel, JL and Monaco, AP and Nelson, DL and Schlessinger, D, Cytogenetics and Cell Genetics. 67 pp. 295--328

Editorial, 0, 1994
Willard, HF and Davies, KE, Human Molecular Genetics. 3 pp. I+

Pulsed-field map of Xq13 in the region of the human X inactivation center., 8, 1993
RG Lafrenière, HF Willard, Genomics. 17 vol. (2); pp. 502-6

The interleukin-2 receptor gamma chain maps to Xq13.1 and is mutated in X-linked severe combined immunodeficiency, SCIDX1., 8, 1993
JM Puck, SM Deschênes, JC Porter, AS Dutra, CJ Brown, HF Willard, PS Henthorn, Hum Mol Genet. 2 vol. (8); pp. 1099-104

2.6 Mb YAC contig of the human X inactivation center region in Xq13: physical linkage of the RPS4X, PHKA1, XIST and DXS128E genes., 8, 1993
RG Lafrenière, CJ Brown, S Rider, J Chelly, P Taillon-Miller, AC Chinault, AP Monaco, HF Willard, Hum Mol Genet. 2 vol. (8); pp. 1105-15

Pulsed-field map of Xq13 in the region of the human X inactivation center., 8, 1993
Lafrenière, RG and Willard, HF, Genomics. 17 pp. 502--506

2.6 Mb YAC contig of the human X inactivation center region in Xq13: physical linkage of the RPS4X, PHKA1, XIST and DXS128E genes., 8, 1993
Lafrenière, RG and Brown, CJ and Rider, S and Chelly, J and Taillon-Miller, P and Chinault, AC and Monaco, AP and Willard, HF, Hum Mol Genet. 2 pp. 1105--1115

The interleukin-2 receptor gamma chain maps to Xq13.1 and is mutated in X-linked severe combined immunodeficiency, SCIDX1., 8, 1993
Puck, JM and Deschênes, SM and Porter, JC and Dutra, AS and Brown, CJ and Willard, HF and Henthorn, PS, Hum Mol Genet. 2 pp. 1099--1104

Mapping of the distal boundary of the X-inactivation center in a rearranged X chromosome from a female expressing XIST., 7, 1993
KA Leppig, CJ Brown, SL Bressler, K Gustashaw, RA Pagon, HF Willard, CM Disteche, Hum Mol Genet. 2 vol. (7); pp. 883-7

Mapping of the distal boundary of the X-inactivation center in a rearranged X chromosome from a female expressing XIST., 7, 1993
Leppig, KA and Brown, CJ and Bressler, SL and Gustashaw, K and Pagon, RA and Willard, HF and Disteche, CM, Hum Mol Genet. 2 pp. 883--887

Evolutionary conservation of possible functional domains of the human and murine XIST genes., 6, 1993
BD Hendrich, CJ Brown, HF Willard, Hum Mol Genet. 2 vol. (6); pp. 663-72

Mammalian chromosome structure., 6, 1993
C Tyler-Smith, HF Willard, Curr Opin Genet Dev. 3 vol. (3); pp. 390-7

Mammalian chromosome structure., 6, 1993
Tyler-Smith, C and Willard, HF, Curr Opin Genet Dev. 3 pp. 390--397

Evolutionary conservation of possible functional domains of the human and murine XIST genes., 6, 1993
Hendrich, BD and Brown, CJ and Willard, HF, Hum Mol Genet. 2 pp. 663--672

Organization and molecular cytogenetics of a satellite DNA family from Hoplias malabaricus (Pisces, Erythrinidae)., 5, 1993
T Haaf, M Schmid, C Steinlein, PM Galetti, HF Willard, Chromosome Res. 1 vol. (1); pp. 77-86

The needle found!!! Trinucleotide repeat expansion in the Huntington's disease gene., 5, 1993
HF Willard, Hum Mol Genet. 2 vol. (5); pp. 497-8

The needle found!!! Trinucleotide repeat expansion in the Huntington's disease gene., 5, 1993
Willard, HF, Hum Mol Genet. 2 pp. 497--498

Organization and molecular cytogenetics of a satellite DNA family from Hoplias malabaricus (Pisces, Erythrinidae)., 5, 1993
Haaf, T and Schmid, M and Steinlein, C and Galetti, PM and Willard, HF, Chromosome Res. 1 pp. 77--86

A polymorphic X-linked tetranucleotide repeat locus displaying a high rate of new mutation: implications for mechanisms of mutation at short tandem repeat loci., 4, 1993
MM Mahtani, HF Willard, Hum Mol Genet. 2 vol. (4); pp. 431-7

A polymorphic X-linked tetranucleotide repeat locus displaying a high rate of new mutation: implications for mechanisms of mutation at short tandem repeat loci., 4, 1993
Mahtani, MM and Willard, HF, Hum Mol Genet. 2 pp. 431--437

Cloning of the X-linked glycerol kinase gene., 2, 1993
HF Willard, Hum Mol Genet. 2 vol. (2); pp. 95-6

Cloning of the X-linked glycerol kinase gene., 2, 1993
Willard, HF, Hum Mol Genet. 2 pp. 95--96

Characterization of a small supernumerary ring X chromosome by fluorescence in situ hybridization., 12, 1993
AM Duncan, A Macdonald, CJ Brown, D Wolff, HF Willard, B Sutton, Am J Med Genet. 47 vol. (8); pp. 1153-6

Characterization of a small supernumerary ring X chromosome by fluorescence in situ hybridization., 12, 1993
Duncan, AM and Macdonald, A and Brown, CJ and Wolff, D and Willard, HF and Sutton, B, Am J Med Genet. 47 pp. 1153--1156

Organization and evolution of an alpha satellite DNA subset shared by human chromosomes 13 and 21., 11, 1993
GM Greig, PE Warburton, HF Willard, J Mol Evol. 37 vol. (5); pp. 464-75

Organization and evolution of an alpha satellite DNA subset shared by human chromosomes 13 and 21., 11, 1993
Greig, GM and Warburton, PE and Willard, HF, J Mol Evol. 37 pp. 464--475

Duplicated zinc finger protein genes on the proximal short arm of the human X chromosome: isolation, characterization and X-inactivation studies., 10, 1993
GM Greig, CB Sharp, L Carrel, HF Willard, Hum Mol Genet. 2 vol. (10); pp. 1611-8

Nonrandom localization of recombination events in human alpha satellite repeat unit variants: implications for higher-order structural characteristics within centromeric heterochromatin., 10, 1993
PE Warburton, JS Waye, HF Willard, Mol Cell Biol. 13 vol. (10); pp. 6520-9

The inv(16) in acute nonlymphocytic leukemia: a turnabout for myosin heavy chain., 10, 1993
HF Willard, Hum Mol Genet. 2 vol. (10); pp. 1525-6

The inv(16) in acute nonlymphocytic leukemia: a turnabout for myosin heavy chain., 10, 1993
Willard, HF, Hum Mol Genet. 2 pp. 1525--1526

Duplicated zinc finger protein genes on the proximal short arm of the human X chromosome: isolation, characterization and X-inactivation studies., 10, 1993
Greig, GM and Sharp, CB and Carrel, L and Willard, HF, Hum Mol Genet. 2 pp. 1611--1618

Nonrandom localization of recombination events in human alpha satellite repeat unit variants: implications for higher-order structural characteristics within centromeric heterochromatin., 10, 1993
Warburton, PE and Waye, JS and Willard, HF, Mol Cell Biol. 13 pp. 6520--6529

Epigenetic and chromosomal control of gene expression: molecular and genetic analysis of X chromosome inactivation., 0, 1993
HF Willard, CJ Brown, L Carrel, B Hendrich, AP Miller, Cold Spring Harb Symp Quant Biol. 58 pp. 315-22

Report and abstracts of the Fourth International Workshop on Human X Chromosome Mapping 1993. St. Louis, Missouri, May 9-12, 1993., 0, 1993
D Schlessinger, JL Mandel, AP Monaco, DL Nelson, HF Willard, Cytogenet Cell Genet. 64 vol. (3-4); pp. 147-94

Molecular and genetic studies of human X chromosome in activation, 0, 1993
Brown, CJ and Willard, HF, Advances in Developmental Biology (1992). 2 pp. 37--72

Organization and molecular cytogenetics of a satellite DNA family from Hoplias malabaricus (Pisces, Erythrinidae)., 0, 1993
Haaf, T and Schmid, M and Steinlein, C and Jr, PMG and Willard, HF, Chromosome research : an international journal on the molecular, supramolecular and evolutionary aspects of chromosome biology. 1 pp. 77--86

Epigenetic and chromosomal control of gene expression: molecular and genetic analysis of X chromosome inactivation., 0, 1993
Willard, HF and Brown, CJ and Carrel, L and Hendrich, B and Miller, AP, Cold Spring Harb Symp Quant Biol. 58 pp. 315--322

Report of the Fourth International Workshop on Human X Chromosome mapping 1993, 0, 1993
Schlessinger, D and Mandel, JL and Monaco, AP and Nelson, DL and Willard, HF, Cytogenetics and Cell Genetics. 64 pp. 148--170

Report and abstracts of the Fourth International Workshop on Human X Chromosome Mapping 1993. St. Louis, Missouri, May 9-12, 1993., 0, 1993
Schlessinger, D and Mandel, JL and Monaco, AP and Nelson, DL and Willard, HF, Cytogenet Cell Genet. 64 pp. 147--194

A sampler of current opinion, 0, 1993
Willard, HF and Davies, KE, Current Opinion in Genetics and Development. 3 pp. 387--389

Integration of human alpha-satellite DNA into simian chromosomes: centromere protein binding and disruption of normal chromosome segregation., 8, 1992
T Haaf, PE Warburton, HF Willard, Cell. 70 vol. (4); pp. 681-96

Integration of human alpha-satellite DNA into simian chromosomes: centromere protein binding and disruption of normal chromosome segregation., 8, 1992
Haaf, T and Warburton, PE and Willard, HF, Cell. 70 pp. 681--696

Refined localization of human connexin32 gene locus, GJB1, to Xq13.1., 6, 1992
IA Corcos, RG Lafrenière, CR Begy, R Loch-Caruso, HF Willard, TW Glover, Genomics. 13 vol. (2); pp. 479-80

Mammalian X-chromosome inactivation and the XIST gene., 6, 1992
A Ballabio, HF Willard, Curr Opin Genet Dev. 2 vol. (3); pp. 439-47

Refined localization of human connexin32 gene locus, GJB1, to Xq13.1., 6, 1992
Corcos, IA and Lafrenière, RG and Begy, CR and Loch-Caruso, R and Willard, HF and Glover, TW, Genomics. 13 pp. 479--480

Mammalian X-chromosome inactivation and the XIST gene., 6, 1992
Ballabio, A and Willard, HF, Curr Opin Genet Dev. 2 pp. 439--447

Organization, polymorphism, and molecular cytogenetics of chromosome-specific alpha-satellite DNA from the centromere of chromosome 2., 5, 1992
T Haaf, HF Willard, Genomics. 13 vol. (1); pp. 122-8

Assignment of human erythroid delta-aminolevulinate synthase (ALAS2) to a distal subregion of band Xp11.21 by PCR analysis of somatic cell hybrids containing X; autosome translocations., 5, 1992
PD Cotter, HF Willard, JL Gorski, DF Bishop, Genomics. 13 vol. (1); pp. 211-2

Assignment of human erythroid delta-aminolevulinate synthase (ALAS2) to a distal subregion of band Xp11.21 by PCR analysis of somatic cell hybrids containing X; autosome translocations., 5, 1992
Cotter, PD and Willard, HF and Gorski, JL and Bishop, DF, Genomics. 13 pp. 211--212

Organization, polymorphism, and molecular cytogenetics of chromosome-specific alpha-satellite DNA from the centromere of chromosome 2., 5, 1992
Haaf, T and Willard, HF, Genomics. 13 pp. 122--128

Complete deletion of the androgen receptor gene: definition of the null phenotype of the androgen insensitivity syndrome and determination of carrier status., 4, 1992
CA Quigley, KJ Friedman, A Johnson, RG Lafreniere, LM Silverman, DB Lubahn, TR Brown, EM Wilson, HF Willard, FS French, J Clin Endocrinol Metab. 74 vol. (4); pp. 927-33

Complete deletion of the androgen receptor gene: definition of the null phenotype of the androgen insensitivity syndrome and determination of carrier status., 4, 1992
Quigley, CA and Friedman, KJ and Johnson, A and Lafreniere, RG and Silverman, LM and Lubahn, DB and Brown, TR and Wilson, EM and Willard, HF and French, FS, J Clin Endocrinol Metab. 74 pp. 927--933

Beta satellite DNA: characterization and localization of two subfamilies from the distal and proximal short arms of the human acrocentric chromosomes., 3, 1992
GM Greig, HF Willard, Genomics. 12 vol. (3); pp. 573-80

Beta satellite DNA: characterization and localization of two subfamilies from the distal and proximal short arms of the human acrocentric chromosomes., 3, 1992
Greig, GM and Willard, HF, Genomics. 12 pp. 573--580

Structure of DNA near long tandem arrays of alpha satellite DNA at the centromere of human chromosome 7., 12, 1992
R Wevrick, VP Willard, HF Willard, Genomics. 14 vol. (4); pp. 912-23

Nondisjunction of chromosome 21: comparisons of cytogenetic and molecular studies of the meiotic stage and parent of origin., 12, 1992
BJ Lorber, M Grantham, J Peters, HF Willard, TJ Hassold, Am J Hum Genet. 51 vol. (6); pp. 1265-76

Centromeres--primary constrictions are primarily complicated., 12, 1992
HF Willard, Hum Mol Genet. 1 vol. (9); pp. 667-8

Nondisjunction of chromosome 21: comparisons of cytogenetic and molecular studies of the meiotic stage and parent of origin., 12, 1992
Lorber, BJ and Grantham, M and Peters, J and Willard, HF and Hassold, TJ, Am J Hum Genet. 51 pp. 1265--1276

Centromeres--primary constrictions are primarily complicated., 12, 1992
Willard, HF, Hum Mol Genet. 1 pp. 667--668

Structure of DNA near long tandem arrays of alpha satellite DNA at the centromere of human chromosome 7., 12, 1992
Wevrick, R and Willard, VP and Willard, HF, Genomics. 14 pp. 912--923

PCR amplification of tandemly repeated DNA: analysis of intra- and interchromosomal sequence variation and homologous unequal crossing-over in human alpha satellite DNA., 11, 1992
PE Warburton, HF Willard, Nucleic Acids Res. 20 vol. (22); pp. 6033-42

Localization of the photoreceptor gene ROM1 to human chromosome 11 and mouse chromosome 19: sublocalization to human 11q13 between PGA and PYGM., 11, 1992
RA Bascom, J García-Heras, CL Hsieh, DS Gerhard, C Jones, U Francke, HF Willard, DH Ledbetter, RR McInnes, Am J Hum Genet. 51 vol. (5); pp. 1028-35

Localization of the photoreceptor gene ROM1 to human chromosome 11 and mouse chromosome 19: sublocalization to human 11q13 between PGA and PYGM., 11, 1992
Bascom, RA and García-Heras, J and Hsieh, CL and Gerhard, DS and Jones, C and Francke, U and Willard, HF and Ledbetter, DH and McInnes, RR, Am J Hum Genet. 51 pp. 1028--1035

PCR amplification of tandemly repeated DNA: analysis of intra- and interchromosomal sequence variation and homologous unequal crossing-over in human alpha satellite DNA., 11, 1992
Warburton, PE and Willard, HF, Nucleic Acids Res. 20 pp. 6033--6042

The human XIST gene: analysis of a 17 kb inactive X-specific RNA that contains conserved repeats and is highly localized within the nucleus., 10, 1992
Brown, CJ and Hendrich, BD and Rupert, JL and Lafrenière, RG and Xing, Y and Lawrence, J and Willard, HF, Cell. 71 pp. 527--542

Genome maps III. 1992. Wall Chart., 10, 1992
Mandel, JL and Monaco, AP and Nelson, DL and Schlessinger, D and Willard, HF and Chipperfield, M and Pearson, P and Gilna, P and Cinkosky, M, Science. 258 pp. 87--102

The human XIST gene: analysis of a 17 kb inactive X-specific RNA that contains conserved repeats and is highly localized within the nucleus., 10, 1992
CJ Brown, BD Hendrich, JL Rupert, RG Lafrenière, Y Xing, J Lawrence, HF Willard, Cell. 71 vol. (3); pp. 527-42

Genome maps III. 1992. Wall Chart., 10, 1992
JL Mandel, AP Monaco, DL Nelson, D Schlessinger, HF Willard, M Chipperfield, P Pearson, P Gilna, M Cinkosky, Science. 258 vol. (5079); pp. 87-102

A microchromosome derived from chromosome 11 in a patient with the CREST syndrome of scleroderma., 0, 1992
T Haaf, AT Sumner, J Köhler, HF Willard, M Schmid, AT Summer, Cytogenet Cell Genet. 60 vol. (1); pp. 12-7

A microchromosome derived from chromosome 11 in a patient with the CREST syndrome of scleroderma., 0, 1992
Haaf, T and Sumner, AT and Köhler, J and Willard, HF and Schmid, M, Cytogenet Cell Genet. 60 pp. 12--17

Genome maps III, 0, 1992
Mandel, JL and Monaco, AP and Nelson, DL and Schlessinger, D and Willard, HF and Chipperfield, M and Pearson, P and Gilna, P and Cinkosky, M, Science. 258 pp. 87--88

Genome analysis and the human X chromosome, 0, 1992
Mandel, JL and Monaco, AP and Nelson, DL and Schlessinger, D and Willard, H, Science. 258 pp. 103--109

β satellite DNA: Characterization and localization of two subfamilies from the distal and proximal short arms of the human acrocentric chromosomes, 0, 1992
Greig, GM and Willard, HF, Genomics. 12 pp. 573--580

A comprehensive genetic linkage map of the human genome, 0, 1992
Dracopoli, NC and O'Connell, P and Elsner, TI and Lalouel, JM and White, RL and Buetow, KH and Nishimura, DY and Murray, JC and Helms, C and Mishra, SK and al, E, Science. 258 pp. 67--86

Erratum: A microchromosome derived from chromosome 11 in a patient with the CREST syndrome of scleroderma (Cytogenet Cell Genet 60:12-17 (1992)), 0, 1992
Haaf, T and Sumner, AT and Kohler, J and Willard, HF and Schmid, M, Cytogenetics and Cell Genetics. 61 pp. 224-

Editorial, 0, 1992
Davies, KE and Willard, HF, Human Molecular Genetics. 1 pp. 3-

Trisomy 12 in chronic lymphocytic leukemia: an interphase cytogenetic study., 8, 1991
AP Losada, M Wessman, M Tiainen, AH Hopman, HF Willard, F Solé, MR Caballín, S Woessner, S Knuutila, Blood. 78 vol. (3); pp. 775-9

An 18-locus linkage map of the pericentromeric region of the human X chromosome: genetic framework for mapping X-linked disorders., 8, 1991
MM Mahtani, RG Lafrenière, TA Kruse, HF Willard, Genomics. 10 vol. (4); pp. 849-57

Trisomy 12 in chronic lymphocytic leukemia: an interphase cytogenetic study., 8, 1991
Losada, AP and Wessman, M and Tiainen, M and Hopman, AH and Willard, HF and Solé, F and Caballín, MR and Woessner, S and Knuutila, S, Blood. 78 pp. 775--779

An 18-locus linkage map of the pericentromeric region of the human X chromosome: genetic framework for mapping X-linked disorders., 8, 1991
Mahtani, MM and Lafrenière, RG and Kruse, TA and Willard, HF, Genomics. 10 pp. 849--857

A highly polymorphic dinucleotide repeat on the proximal short arm of the human X chromosome: linkage mapping of the synapsin I/A-raf-1 genes., 7, 1991
CU Kirchgessner, JA Trofatter, MM Mahtani, HF Willard, LJ DeGennaro, Am J Hum Genet. 49 vol. (1); pp. 184-91

A highly polymorphic dinucleotide repeat on the proximal short arm of the human X chromosome: linkage mapping of the synapsin I/A-raf-1 genes., 7, 1991
Kirchgessner, CU and Trofatter, JA and Mahtani, MM and Willard, HF and DeGennaro, LJ, Am J Hum Genet. 49 pp. 184--191

Structure of the rabbit phospholamban gene, cloning of the human cDNA, and assignment of the gene to human chromosome 6., 6, 1991
J Fujii, A Zarain-Herzberg, HF Willard, M Tada, DH MacLennan, J Biol Chem. 266 vol. (18); pp. 11669-75

Structure of the rabbit phospholamban gene, cloning of the human cDNA, and assignment of the gene to human chromosome 6., 6, 1991
Fujii, J and Zarain-Herzberg, A and Willard, HF and Tada, M and MacLennan, DH, J Biol Chem. 266 pp. 11669--11675

Ornithine aminotransferase-related sequences map to two nonadjacent intervals on the human X chromosome short arm., 5, 1991
RG Lafreniere, MT Geraghty, D Valle, TB Shows, HF Willard, Genomics. 10 vol. (1); pp. 276-9

Physical map of the centromeric region of human chromosome 7: relationship between two distinct alpha satellite arrays., 5, 1991
R Wevrick, HF Willard, Nucleic Acids Res. 19 vol. (9); pp. 2295-301

Physical map of the centromeric region of human chromosome 7: relationship between two distinct alpha satellite arrays., 5, 1991
Wevrick, R and Willard, HF, Nucleic Acids Res. 19 pp. 2295--2301

Genetic and physical mapping around the properdin P gene., 12, 1991
MP Coleman, JC Murray, HF Willard, KF Nolan, KB Reid, DJ Blake, S Lindsay, SS Bhattacharya, A Wright, KE Davies, Genomics. 11 vol. (4); pp. 991-6

Evolution of alpha satellite., 12, 1991
HF Willard, Curr Opin Genet Dev. 1 vol. (4); pp. 509-14

Evolution of alpha satellite., 12, 1991
Willard, HF, Curr Opin Genet Dev. 1 pp. 509--514

Genetic and physical mapping around the properdin P gene., 12, 1991
Coleman, MP and Murray, JC and Willard, HF and Nolan, KF and Reid, KB and Blake, DJ and Lindsay, S and Bhattacharya, SS and Wright, A and Davies, KE, Genomics. 11 pp. 991--996

PCR amplification of chromosome-specific alpha satellite DNA: definition of centromeric STS markers and polymorphic analysis., 10, 1991
PE Warburton, GM Greig, T Haaf, HF Willard, Genomics. 11 vol. (2); pp. 324-33

Physical mapping of 60 DNA markers in the p21.1----q21.3 region of the human X chromosome., 10, 1991
RG Lafrenière, CJ Brown, VE Powers, L Carrel, KE Davies, DF Barker, HF Willard, Genomics. 11 vol. (2); pp. 352-63

Physical mapping of 60 DNA markers in the p21.1----q21.3 region of the human X chromosome., 10, 1991
Lafrenière, RG and Brown, CJ and Powers, VE and Carrel, L and Davies, KE and Barker, DF and Willard, HF, Genomics. 11 pp. 352--363

PCR amplification of chromosome-specific alpha satellite DNA: definition of centromeric STS markers and polymorphic analysis., 10, 1991
Warburton, PE and Greig, GM and Haaf, T and Willard, HF, Genomics. 11 pp. 324--333

The 56/58 kDa androgen-binding protein in male genital skin fibroblasts with a deleted androgen receptor gene., 1, 1991
M Trifiro, B Gottlieb, L Pinsky, M Kaufman, L Prior, DD Belsham, K Wrogemann, CJ Brown, HF Willard, J Trapman, Mol Cell Endocrinol. 75 vol. (1); pp. 37-47

Localization of the X inactivation centre on the human X chromosome in Xq13., 1, 1991
CJ Brown, RG Lafreniere, VE Powers, G Sebastio, A Ballabio, AL Pettigrew, DH Ledbetter, E Levy, IW Craig, HF Willard, Nature. 349 vol. (6304); pp. 82-4

A gene from the region of the human X inactivation centre is expressed exclusively from the inactive X chromosome., 1, 1991
CJ Brown, A Ballabio, JL Rupert, RG Lafreniere, M Grompe, R Tonlorenzi, HF Willard, Nature. 349 vol. (6304); pp. 38-44

The 56/58 kDa androgen-binding protein in male genital skin fibroblasts with a deleted androgen receptor gene., 1, 1991
Trifiro, M and Gottlieb, B and Pinsky, L and Kaufman, M and Prior, L and Belsham, DD and Wrogemann, K and Brown, CJ and Willard, HF and Trapman, J, Mol Cell Endocrinol. 75 pp. 37--47

Localization of the X inactivation centre on the human X chromosome in Xq13., 1, 1991
Brown, CJ and Lafreniere, RG and Powers, VE and Sebastio, G and Ballabio, A and Pettigrew, AL and Ledbetter, DH and Levy, E and Craig, IW and Willard, HF, Nature. 349 pp. 82--84

A gene from the region of the human X inactivation centre is expressed exclusively from the inactive X chromosome., 1, 1991
Brown, CJ and Ballabio, A and Rupert, JL and Lafreniere, RG and Grompe, M and Tonlorenzi, R and Willard, HF, Nature. 349 pp. 38--44

Molecular cytogenetics of alpha satellite DNA from chromosome 12: fluorescence in situ hybridization and description of DNA and array length polymorphisms., 0, 1991
GM Greig, S Parikh, J George, VE Powers, HF Willard, Cytogenet Cell Genet. 56 vol. (3-4); pp. 144-8

Localization of histidase to human chromosome region 12q22----q24.1 and mouse chromosome region 10C2----D1., 0, 1991
RG Taylor, J García-Heras, SJ Sadler, RG Lafreniere, HF Willard, DH Ledbetter, RR McInnes, Cytogenet Cell Genet. 56 vol. (3-4); pp. 178-81

Report of the committee on the genetic constitution of the X chromosome, 0, 1991
Davies, KE and Mandel, JL and Monaco, AP and Nussbaum, RL and Willard, HF, Cytogenetics and Cell Genetics. 58 pp. 853--966

Localization of histidase to human chromosome region 12q22----q24.1 and mouse chromosome region 10C2----D1., 0, 1991
Taylor, RG and García-Heras, J and Sadler, SJ and Lafreniere, RG and Willard, HF and Ledbetter, DH and McInnes, RR, Cytogenet Cell Genet. 56 pp. 178--181

Molecular cytogenetics of alpha satellite DNA from chromosome 12: fluorescence in situ hybridization and description of DNA and array length polymorphisms., 0, 1991
Greig, GM and Parikh, S and George, J and Powers, VE and Willard, HF, Cytogenet Cell Genet. 56 pp. 144--148

Characterization of a murine gene expressed from the inactive X chromosome, 0, 1991
Borsani, G and Tonlorenzi, R and Simmler, MC and Dandolo, L and Arnaud, D and Capra, V and Grompe, M and Pizzuti, A and Muzny, D and Lawrence, C and Willard, HF and Avner, P and Ballabio, A, Nature. 351 pp. 325--329

A gene deleted in Kallmann's syndrome shares homology with neural cell adhesion and axonal path-finding molecules, 0, 1991
Franco, B and Guioli, S and Pragliola, A and Incerti, B and Bardoni, B and Tonlorenzi, R and Carrozzo, R and Maestrini, E and Pieretti, M and Taillon-Miller, P and Brown, CJ and Willard, HF and Lawrence, C and Persico, MG and Camerino, G and Ballabio, A, Nature. 353 pp. 529--536

The CEPH consortium linkage map of human chromosome 1, 0, 1991
Dracopoli, NC and O'Connell, P and Elsner, TI and Lalouel, JM and White, RL and Buetow, KH and Nishimura, DY and Murray, JC and Helms, C and Mishra, SK and Donis-Keller, H and Hall, JM and Lee, MK and King, MC and Attwood, J and Morton, NE and Robson, EB and Mahtani, M and Willard, HF and Royle, NJ and Patel, I and Jeffreys, AJ and Verga, V and Jenkins, T and Weber, JL and Mitchell, AL and Bale, AE, Genomics. 9 pp. 686--700

Synaptophysin: structure of the human gene and assignment to the X chromosome in man and mouse., 9, 1990
T Ozçelik, RG Lafreniere, BT Archer, PA Johnston, HF Willard, U Francke, TC Südhof, Am J Hum Genet. 47 vol. (3); pp. 551-61

Synaptophysin: structure of the human gene and assignment to the X chromosome in man and mouse., 9, 1990
Ozçelik, T and Lafreniere, RG and Archer, BT and Johnston, PA and Willard, HF and Francke, U and Südhof, TC, Am J Hum Genet. 47 pp. 551--561

Pulsed-field gel analysis of alpha-satellite DNA at the human X chromosome centromere: high-frequency polymorphisms and array size estimate., 8, 1990
MM Mahtani, HF Willard, Genomics. 7 vol. (4); pp. 607-13

Pericentromeric structure of human X "isochromosomes": evidence for molecular heterogeneity., 8, 1990
CB Sharp, HM Bedford, HF Willard, Hum Genet. 85 vol. (3); pp. 330-6

Molecular cloning of cDNA encoding the Ca2+ release channel (ryanodine receptor) of rabbit cardiac muscle sarcoplasmic reticulum., 8, 1990
K Otsu, HF Willard, VK Khanna, F Zorzato, NM Green, DH MacLennan, J Biol Chem. 265 vol. (23); pp. 13472-83

Pulsed-field gel analysis of alpha-satellite DNA at the human X chromosome centromere: high-frequency polymorphisms and array size estimate., 8, 1990
Mahtani, MM and Willard, HF, Genomics. 7 pp. 607--613

Molecular cloning of cDNA encoding the Ca2+ release channel (ryanodine receptor) of rabbit cardiac muscle sarcoplasmic reticulum., 8, 1990
Otsu, K and Willard, HF and Khanna, VK and Zorzato, F and Green, NM and MacLennan, DH, J Biol Chem. 265 pp. 13472--13483

X chromosome inactivation of the human TIMP gene., 7, 1990
CJ Brown, AM Flenniken, BR Williams, HF Willard, Nucleic Acids Res. 18 vol. (14); pp. 4191-5

X chromosome inactivation of the human TIMP gene., 7, 1990
Brown, CJ and Flenniken, AM and Williams, BR and Willard, HF, Nucleic Acids Res. 18 pp. 4191--4195

A BstE II RFLP at the DXS153 locus., 6, 1990
RG Lafreniere, HF Willard, Nucleic Acids Res. 18 vol. (12); pp. 3673

A Rsal RFLP at the DXS467 locus., 6, 1990
RG Lafreniere, HF Willard, Nucleic Acids Res. 18 vol. (12); pp. 3673

The human ryanodine receptor gene: its mapping to 19q13.1, placement in a chromosome 19 linkage group, and exclusion as the gene causing myotonic dystrophy., 6, 1990
AE MacKenzie, RG Korneluk, F Zorzato, J Fujii, M Phillips, D Iles, B Wieringa, S Leblond, J Bailly, HF Willard, Am J Hum Genet. 46 vol. (6); pp. 1082-9

A Rsal RFLP at the DXS467 locus., 6, 1990
Lafreniere, RG and Willard, HF, Nucleic Acids Res. 18 pp. 3673

A BstE II RFLP at the DXS153 locus., 6, 1990
Lafreniere, RG and Willard, HF, Nucleic Acids Res. 18 pp. 3673

The human ryanodine receptor gene: its mapping to 19q13.1, placement in a chromosome 19 linkage group, and exclusion as the gene causing myotonic dystrophy., 6, 1990
MacKenzie, AE and Korneluk, RG and Zorzato, F and Fujii, J and Phillips, M and Iles, D and Wieringa, B and Leblond, S and Bailly, J and Willard, HF, Am J Hum Genet. 46 pp. 1082--1089

Hunter disease (mucopolysaccharidosis type II) in a karyotypically normal girl., 5, 1990
JT Clarke, HF Willard, I Teshima, PL Chang, MA Skomorowski, Clin Genet. 37 vol. (5); pp. 355-62

Hunter disease (mucopolysaccharidosis type II) in a karyotypically normal girl., 5, 1990
Clarke, JT and Willard, HF and Teshima, I and Chang, PL and Skomorowski, MA, Clin Genet. 37 pp. 355--362

Five polymorphic microsatellite VNTRs on the human X chromosome., 4, 1990
JA Luty, Z Guo, HF Willard, DH Ledbetter, S Ledbetter, M Litt, Am J Hum Genet. 46 vol. (4); pp. 776-83

A case of 46,XX,r(X) (p1q1) diagnosed by in situ hybridization., 3, 1990
J Koch, S Kølvraa, N Hobolt, GB Petersen, HF Willard, JS Waye, N Gregersen, L Bolund, Clin Genet. 37 vol. (3); pp. 216-20

Characterization and localization to human chromosome 1 of human fast-twitch skeletal muscle calsequestrin gene., 3, 1990
Fujii, J and Willard, HF and MacLennan, DH, Somat Cell Mol Genet. 16 pp. 185--189

A case of 46,XX,r(X) (p1q1) diagnosed by in situ hybridization., 3, 1990
Koch, J and Kølvraa, S and Hobolt, N and Petersen, GB and Willard, HF and Waye, JS and Gregersen, N and Bolund, L, Clin Genet. 37 pp. 216--220

Characterization and localization to human chromosome 1 of human fast-twitch skeletal muscle calsequestrin gene., 3, 1990
J Fujii, HF Willard, DH MacLennan, Somat Cell Mol Genet. 16 vol. (2); pp. 185-9

Localization of a gene that escapes inactivation to the X chromosome proximal short arm: implications for X inactivation., 2, 1990
CJ Brown, HF Willard, Am J Hum Genet. 46 vol. (2); pp. 273-9

Concerted evolution of primate alpha satellite DNA. Evidence for an ancestral sequence shared by gorilla and human X chromosome alpha satellite., 12, 1990
SJ Durfy, HF Willard, J Mol Biol. 216 vol. (3); pp. 555-66

Replication timing of DNA sequences associated with human centromeres and telomeres., 12, 1990
Ten Hagen, KG and Gilbert, DM and Willard, HF and Cohen, SN, Mol Cell Biol. 10 pp. 6348--6355

Partial deletion of alpha satellite DNA associated with reduced amounts of the centromere protein CENP-B in a mitotically stable human chromosome rearrangement., 12, 1990
Wevrick, R and Earnshaw, WC and Howard-Peebles, PN and Willard, HF, Mol Cell Biol. 10 pp. 6374--6380

Isolation, characterization and chromosomal localization of cDNA clones for the E1 beta subunit of the pyruvate dehydrogenase complex., 12, 1990
Chun, K and Mackay, N and Willard, HF and Robinson, BH, Eur J Biochem. 194 pp. 587--592

Homologous ribosomal protein genes on the human X and Y chromosomes: escape from X inactivation and possible implications for Turner syndrome., 12, 1990
Fisher, EM and Beer-Romero, P and Brown, LG and Ridley, A and McNeil, JA and Lawrence, JB and Willard, HF and Bieber, FR and Page, DC, Cell. 63 pp. 1205--1218

Concerted evolution of primate alpha satellite DNA. Evidence for an ancestral sequence shared by gorilla and human X chromosome alpha satellite., 12, 1990
Durfy, SJ and Willard, HF, J Mol Biol. 216 pp. 555--566

Centromeres of mammalian chromosomes., 12, 1990
Willard, HF, Trends Genet. 6 pp. 410--416

Replication timing of DNA sequences associated with human centromeres and telomeres., 12, 1990
KG Ten Hagen, DM Gilbert, HF Willard, SN Cohen, Mol Cell Biol. 10 vol. (12); pp. 6348-55

Centromeres of mammalian chromosomes., 12, 1990
HF Willard, Trends Genet. 6 vol. (12); pp. 410-6

Partial deletion of alpha satellite DNA associated with reduced amounts of the centromere protein CENP-B in a mitotically stable human chromosome rearrangement., 12, 1990
R Wevrick, WC Earnshaw, PN Howard-Peebles, HF Willard, Mol Cell Biol. 10 vol. (12); pp. 6374-80

Homologous ribosomal protein genes on the human X and Y chromosomes: escape from X inactivation and possible implications for Turner syndrome., 12, 1990
EM Fisher, P Beer-Romero, LG Brown, A Ridley, JA McNeil, JB Lawrence, HF Willard, FR Bieber, DC Page, Cell. 63 vol. (6); pp. 1205-18

Isolation, characterization and chromosomal localization of cDNA clones for the E1 beta subunit of the pyruvate dehydrogenase complex., 12, 1990
K Chun, N Mackay, HF Willard, BH Robinson, Eur J Biochem. 194 vol. (2); pp. 587-92

Genomic analysis of sequence variation in tandemly repeated DNA. Evidence for localized homogeneous sequence domains within arrays of alpha-satellite DNA., 11, 1990
PE Warburton, HF Willard, J Mol Biol. 216 vol. (1); pp. 3-16

Genomic analysis of sequence variation in tandemly repeated DNA. Evidence for localized homogeneous sequence domains within arrays of alpha-satellite DNA., 11, 1990
Warburton, PE and Willard, HF, J Mol Biol. 216 pp. 3--16

The human aminopeptidase N gene: isolation, chromosome localization, and DNA polymorphism analysis., 10, 1990
VM Watt, HF Willard, Hum Genet. 85 vol. (6); pp. 651-4

Linkage of the multiple endocrine neoplasia type 2B gene (MEN2B) to chromosome 10 markers linked to MEN2A., 10, 1990
RA Norum, RG Lafreniere, LW O'Neal, TF Nikolai, JP Delaney, JC Sisson, H Sobol, GM Lenoir, BA Ponder, HF Willard, Genomics. 8 vol. (2); pp. 313-7

The human aminopeptidase N gene: isolation, chromosome localization, and DNA polymorphism analysis., 10, 1990
Watt, VM and Willard, HF, Hum Genet. 85 pp. 651--654

Linkage of the multiple endocrine neoplasia type 2B gene (MEN2B) to chromosome 10 markers linked to MEN2A., 10, 1990
Norum, RA and Lafreniere, RG and O'Neal, LW and Nikolai, TF and Delaney, JP and Sisson, JC and Sobol, H and Lenoir, GM and Ponder, BA and Willard, HF, Genomics. 8 pp. 313--317

Report of the committee on the genetic constitution of the X chromosome., 0, 1990
KE Davies, JL Mandel, AP Monaco, RL Nussbaum, HF Willard, Cytogenet Cell Genet. 55 vol. (1-4); pp. 254-313

Alpha and beta satellite sequences on chromosome 21: the possible role of centromere and chromosome structure in nondisjunction., 0, 1990
HF Willard, Prog Clin Biol Res. 360 pp. 39-52

Localization of the insulin receptor-related receptor gene to human chromosome 1., 0, 1990
P Shier, HF Willard, VM Watt, Cytogenet Cell Genet. 54 vol. (1-2); pp. 80-1

Isolation, characterization, and physical localization of 33 human X-chromosome RFLP markers., 0, 1990
JN Dietz-Band, AE Turco, HF Willard, A Vincent, MH Skolnick, DF Barker, Cytogenet Cell Genet. 54 vol. (3-4); pp. 137-41

Localization of the insulin receptor-related receptor gene to human chromosome 1., 0, 1990
Shier, P and Willard, HF and Watt, VM, Cytogenet Cell Genet. 54 pp. 80--81

Alpha and beta satellite sequences on chromosome 21: the possible role of centromere and chromosome structure in nondisjunction., 0, 1990
Willard, HF, Prog Clin Biol Res. 360 pp. 39--52

A RsaI RFLP at the DXS467 locus, 0, 1990
Lafreniere, RG and Willard, HF, Nucleic Acids Research. 18 pp. 3673-

Report of the committee on the genetic constitution of the X chromosome., 0, 1990
Davies, KE and Mandel, JL and Monaco, AP and Nussbaum, RL and Willard, HF, Cytogenet Cell Genet. 55 pp. 254--313

An X-linked DraI RFLP recognized by cpX23 [DXS132], 8, 1989
RG Lafreniere, MM Mahtani, HF Willard, Nucleic Acids Res. 17 vol. (16); pp. 6754

Human beta satellite DNA: genomic organization and sequence definition of a class of highly repetitive tandem DNA., 8, 1989
JS Waye, HF Willard, Proc Natl Acad Sci U S A. 86 vol. (16); pp. 6250-4

An X-linked DraI RFLP recognized by cpX23 [DXS132]., 8, 1989
Lafreniere, RG and Mahtani, MM and Willard, HF, Nucleic Acids Res. 17 pp. 6754

Human beta satellite DNA: genomic organization and sequence definition of a class of highly repetitive tandem DNA., 8, 1989
Waye, JS and Willard, HF, Proc Natl Acad Sci U S A. 86 pp. 6250--6254

Chromosome specificity of satellite DNAs: short- and long-range organization of a diverged dimeric subset of human alpha satellite from chromosome 3., 5, 1989
JS Waye, HF Willard, Chromosoma. 97 vol. (6); pp. 475-80

Chromosome specificity of satellite DNAs: short- and long-range organization of a diverged dimeric subset of human alpha satellite from chromosome 3., 5, 1989
Waye, JS and Willard, HF, Chromosoma. 97 pp. 475--480

Gene on short arm of human X chromosome complements murine tsA1S9 DNA synthesis mutation., 3, 1989
CJ Brown, VE Powers, DL Munroe, R Sheinin, HF Willard, Somat Cell Mol Genet. 15 vol. (2); pp. 173-8

Gene on short arm of human X chromosome complements murine tsA1S9 DNA synthesis mutation., 3, 1989
Brown, CJ and Powers, VE and Munroe, DL and Sheinin, R and Willard, HF, Somat Cell Mol Genet. 15 pp. 173--178

Regional localization of the TIMP gene on the human X chromosome. Extension of a conserved synteny and linkage group on proximal Xp., 2, 1989
HF Willard, SJ Durfy, MM Mahtani, H Dorkins, KE Davies, BR Williams, Hum Genet. 81 vol. (3); pp. 234-8

Chromosomal localization of the human homeo box-containing genes, EN1 and EN2., 2, 1989
C Logan, HF Willard, JM Rommens, AL Joyner, Genomics. 4 vol. (2); pp. 206-9

Androgen receptor locus on the human X chromosome: regional localization to Xq11-12 and description of a DNA polymorphism., 2, 1989
CJ Brown, SJ Goss, DB Lubahn, DR Joseph, EM Wilson, FS French, HF Willard, Am J Hum Genet. 44 vol. (2); pp. 264-9

Chromosomal localization of the human homeo box-containing genes, EN1 and EN2., 2, 1989
Logan, C and Willard, HF and Rommens, JM and Joyner, AL, Genomics. 4 pp. 206--209

Androgen receptor locus on the human X chromosome: regional localization to Xq11-12 and description of a DNA polymorphism., 2, 1989
Brown, CJ and Goss, SJ and Lubahn, DB and Joseph, DR and Wilson, EM and French, FS and Willard, HF, Am J Hum Genet. 44 pp. 264--269

Regional localization of the TIMP gene on the human X chromosome. Extension of a conserved synteny and linkage group on proximal Xp., 2, 1989
Willard, HF and Durfy, SJ and Mahtani, MM and Dorkins, H and Davies, KE and Williams, BR, Hum Genet. 81 pp. 234--238

Long-range organization of tandem arrays of alpha satellite DNA at the centromeres of human chromosomes: high-frequency array-length polymorphism and meiotic stability., 12, 1989
R Wevrick, HF Willard, Proc Natl Acad Sci U S A. 86 vol. (23); pp. 9394-8

Chromosome-specific alpha satellite DNA from the centromere of human chromosome 16., 12, 1989
GM Greig, SB England, HM Bedford, HF Willard, Am J Hum Genet. 45 vol. (6); pp. 862-72

Long-range organization of tandem arrays of alpha satellite DNA at the centromeres of human chromosomes: high-frequency array-length polymorphism and meiotic stability., 12, 1989
Wevrick, R and Willard, HF, Proc Natl Acad Sci U S A. 86 pp. 9394--9398

Chromosome-specific alpha satellite DNA from the centromere of human chromosome 16., 12, 1989
Greig, GM and England, SB and Bedford, HM and Willard, HF, Am J Hum Genet. 45 pp. 862--872

Patterns of intra- and interarray sequence variation in alpha satellite from the human X chromosome: evidence for short-range homogenization of tandemly repeated DNA sequences., 11, 1989
SJ Durfy, HF Willard, Genomics. 5 vol. (4); pp. 810-21

Patterns of intra- and interarray sequence variation in alpha satellite from the human X chromosome: evidence for short-range homogenization of tandemly repeated DNA sequences., 11, 1989
Durfy, SJ and Willard, HF, Genomics. 5 pp. 810--821

Linkage studies of the Wiskott-Aldrich syndrome: polymorphisms at TIMP and the X chromosome centromere are informative markers for genetic prediction., 10, 1989
WL Greer, MM Mahtani, PC Kwong, LA Rubin, M Peacocke, HF Willard, KA Siminovitch, Hum Genet. 83 vol. (3); pp. 227-30

The common acute lymphoblastic leukemia antigen (neutral endopeptidase-3.4.24.11) gene is located on human chromosome 3., 10, 1989
R Tran-Paterson, HF Willard, M Letarte, Cancer Genet Cytogenet. 42 vol. (1); pp. 129-34

Concerted evolution of alpha satellite DNA: evidence for species specificity and a general lack of sequence conservation among alphoid sequences of higher primates., 10, 1989
JS Waye, HF Willard, Chromosoma. 98 vol. (4); pp. 273-9

Noninactivation of a selectable human X-linked gene that complements a murine temperature-sensitive cell cycle defect., 10, 1989
CJ Brown, HF Willard, Am J Hum Genet. 45 vol. (4); pp. 592-8

Linkage studies of the Wiskott-Aldrich syndrome: polymorphisms at TIMP and the X chromosome centromere are informative markers for genetic prediction., 10, 1989
Greer, WL and Mahtani, MM and Kwong, PC and Rubin, LA and Peacocke, M and Willard, HF and Siminovitch, KA, Hum Genet. 83 pp. 227--230

The common acute lymphoblastic leukemia antigen (neutral endopeptidase-3.4.24.11) gene is located on human chromosome 3., 10, 1989
Tran-Paterson, R and Willard, HF and Letarte, M, Cancer Genet Cytogenet. 42 pp. 129--134

Concerted evolution of alpha satellite DNA: evidence for species specificity and a general lack of sequence conservation among alphoid sequences of higher primates., 10, 1989
Waye, JS and Willard, HF, Chromosoma. 98 pp. 273--279

Noninactivation of a selectable human X-linked gene that complements a murine temperature-sensitive cell cycle defect., 10, 1989
Brown, CJ and Willard, HF, Am J Hum Genet. 45 pp. 592--598

Regional localization of CCG1 gene which complements hamster cell cycle mutation BN462 to Xq11-Xq13., 1, 1989
CJ Brown, T Sekiguchi, T Nishimoto, HF Willard, Somat Cell Mol Genet. 15 vol. (1); pp. 93-6

The order of loci in the pericentric region of chromosome 17, based on evidence from physical and genetic breakpoints., 1, 1989
PR Fain, E Wright, HF Willard, K Stephens, DF Barker, Am J Hum Genet. 44 vol. (1); pp. 68-72

Genetic analysis of eight loci tightly linked to neurofibromatosis 1., 1, 1989
K Stephens, P Green, VM Riccardi, S Ng, M Rising, D Barker, JK Darby, KM Falls, FS Collins, HF Willard, Am J Hum Genet. 44 vol. (1); pp. 13-9

Genetic analysis of eight loci tightly linked to neurofibromatosis 1., 1, 1989
Stephens, K and Green, P and Riccardi, VM and Ng, S and Rising, M and Barker, D and Darby, JK and Falls, KM and Collins, FS and Willard, HF, Am J Hum Genet. 44 pp. 13--19

The order of loci in the pericentric region of chromosome 17, based on evidence from physical and genetic breakpoints., 1, 1989
Fain, PR and Wright, E and Willard, HF and Stephens, K and Barker, DF, Am J Hum Genet. 44 pp. 68--72

Regional localization of CCG1 gene which complements hamster cell cycle mutation BN462 to Xq11-Xq13., 1, 1989
Brown, CJ and Sekiguchi, T and Nishimoto, T and Willard, HF, Somat Cell Mol Genet. 15 pp. 93--96

Report of the DNA committee and catalogs of cloned and mapped genes and DNA polymorphisms., 0, 1989
KK Kidd, AM Bowcock, J Schmidtke, RK Track, F Ricciuti, G Hutchings, A Bale, P Pearson, HF Willard, J Gelernter, Cytogenet Cell Genet. 51 vol. (1-4); pp. 622-947

Human centromere structure: organization and potential role of alpha satellite DNA., 0, 1989
HF Willard, R Wevrick, PE Warburton, Prog Clin Biol Res. 318 pp. 9-18

Determination of the breakpoints of 1;7 translocations in myelodysplastic syndrome by in situ hybridization using chromosome-specific alpha satellite DNA from human chromosomes 1 and 7., 0, 1989
T Alitalo, HF Willard, A de la Chapelle, Cytogenet Cell Genet. 50 vol. (1); pp. 49-53

The genomics of long tandem arrays of satellite DNA in the human genome., 0, 1989
HF Willard, Genome. 31 vol. (2); pp. 737-44

Report of the committee on the genetic constitution of the X chromosome., 0, 1989
JL Mandel, HF Willard, RL Nussbaum, G Romeo, JM Puck, KE Davies, Cytogenet Cell Genet. 51 vol. (1-4); pp. 384-437

Isolated and combined deficiencies of the α-keto acid dehydrogenase complexes, 0, 1989
Robinson, BH and Chun, K and Mackay, N and Otulakowski, G and Petrova-Benedict, R and Willard, H, Annals of the New York Academy of Sciences. 573 pp. 337--346

Determination of the breakpoints of 1;7 translocations in myelodysplastic syndrome by in situ hybridization using chromosome-specific alpha satellite DNA from human chromosomes 1 and 7., 0, 1989
Alitalo, T and Willard, HF and de la Chapelle, A, Cytogenet Cell Genet. 50 pp. 49--53

Human centromere structure: organization and potential role of alpha satellite DNA., 0, 1989
Willard, HF and Wevrick, R and Warburton, PE, Prog Clin Biol Res. 318 pp. 9--18

Protein kinase C: A new linkage marker for growth hormone and for COL1A1, 0, 1989
Summar, ML and III, JAP and Krishnamani, MRS and Keefer, J and Trofatter, J and Schwartz, RC and Tsipouras, P and Willard, H and Ullrich, A, Genomics. 5 pp. 163--165

Report of the committee on the genetic constitution of the X chromosome., 0, 1989
Mandel, JL and Willard, HF and Nussbaum, RL and Romeo, G and Puck, JM and Davies, KE, Cytogenet Cell Genet. 51 pp. 384--437

Report of the DNA committee and catalogs of cloned and mapped genes and DNA polymorphisms., 0, 1989
Kidd, KK and Bowcock, AM and Schmidtke, J and Track, RK and Ricciuti, F and Hutchings, G and Bale, A and Pearson, P and Willard, HF and Gelernter, J, Cytogenet Cell Genet. 51 pp. 622--947

Chromosome-specific alpha satellite DNA: isolation and mapping of a polymorphic alphoid repeat from human chromosome 10., 7, 1988
P Devilee, T Kievits, JS Waye, PL Pearson, HF Willard, Genomics. 3 vol. (1); pp. 1-7

Chromosome-specific alpha satellite DNA: isolation and mapping of a polymorphic alphoid repeat from human chromosome 10., 7, 1988
Devilee, P and Kievits, T and Waye, JS and Pearson, PL and Willard, HF, Genomics. 3 pp. 1--7

Gene for lipoamide dehydrogenase maps to human chromosome 7., 7, 1988
Otulakowski, G and Robinson, BH and Willard, HF, Somat Cell Mol Genet. 14 pp. 411--414

Gene for lipoamide dehydrogenase maps to human chromosome 7., 7, 1988
G Otulakowski, BH Robinson, HF Willard, Somat Cell Mol Genet. 14 vol. (4); pp. 411-4

A primary genetic map of the pericentromeric region of the human X chromosome., 5, 1988
MM Mahtani, HF Willard, Genomics. 2 vol. (4); pp. 294-301

A primary genetic map of the pericentromeric region of the human X chromosome., 5, 1988
Mahtani, MM and Willard, HF, Genomics. 2 pp. 294--301

Cloning of human androgen receptor complementary DNA and localization to the X chromosome., 4, 1988
DB Lubahn, DR Joseph, PM Sullivan, HF Willard, FS French, EM Wilson, Science. 240 vol. (4850); pp. 327-30

Cloning of human androgen receptor complementary DNA and localization to the X chromosome., 4, 1988
Lubahn, DB and Joseph, DR and Sullivan, PM and Willard, HF and French, FS and Wilson, EM, Science. 240 pp. 327--330

Gene encoding the beta subunit of S100 protein is on chromosome 21: implications for Down syndrome., 3, 1988
R Allore, D O'Hanlon, R Price, K Neilson, HF Willard, DR Cox, A Marks, RJ Dunn, Science. 239 vol. (4845); pp. 1311-3

Two PstI RFLPs in the PCCB gene on the long arm of chromosome 3., 3, 1988
JS Waye, RA Gravel, HF Willard, Nucleic Acids Res. 16 vol. (5); pp. 2362

Gene encoding the beta subunit of S100 protein is on chromosome 21: implications for Down syndrome., 3, 1988
Allore, R and O'Hanlon, D and Price, R and Neilson, K and Willard, HF and Cox, DR and Marks, A and Dunn, RJ, Science. 239 pp. 1311--1313

Two PstI RFLPs in the PCCB gene on the long arm of chromosome 3., 3, 1988
Waye, JS and Gravel, RA and Willard, HF, Nucleic Acids Res. 16 pp. 2362

Uniparental disomy as a mechanism for human genetic disease., 2, 1988
JE Spence, RG Perciaccante, GM Greig, HF Willard, DH Ledbetter, JF Hejtmancik, MS Pollack, WE O'Brien, AL Beaudet, Am J Hum Genet. 42 vol. (2); pp. 217-26

Uniparental disomy as a mechanism for human genetic disease., 2, 1988
Spence, JE and Perciaccante, RG and Greig, GM and Willard, HF and Ledbetter, DH and Hejtmancik, JF and Pollack, MS and O'Brien, WE and Beaudet, AL, Am J Hum Genet. 42 pp. 217--226

Genetic mapping of four DNA markers (DXS16, DXS43, DXS85, and DXS143) from the p22 region of the human X chromosome., 11, 1988
CJ Brown, MM Mahtani, HF Willard, Hum Genet. 80 vol. (3); pp. 296-8

Genetic mapping of four DNA markers (DXS16, DXS43, DXS85, and DXS143) from the p22 region of the human X chromosome., 11, 1988
Brown, CJ and Mahtani, MM and Willard, HF, Hum Genet. 80 pp. 296--298

Detection of chromosome aneuploidy in interphase nuclei from human primary breast tumors using chromosome-specific repetitive DNA probes., 10, 1988
P Devilee, RF Thierry, T Kievits, R Kolluri, AH Hopman, HF Willard, PL Pearson, CJ Cornelisse, Cancer Res. 48 vol. (20); pp. 5825-30

Human ornithine-delta-aminotransferase. cDNA cloning and analysis of the structural gene., 10, 1988
GA Mitchell, JE Looney, LC Brody, G Steel, M Suchanek, JF Engelhardt, HF Willard, D Valle, J Biol Chem. 263 vol. (28); pp. 14288-95

Human ornithine-delta-aminotransferase. cDNA cloning and analysis of the structural gene., 10, 1988
Mitchell, GA and Looney, JE and Brody, LC and Steel, G and Suchanek, M and Engelhardt, JF and Willard, HF and Valle, D, J Biol Chem. 263 pp. 14288--14295

Detection of chromosome aneuploidy in interphase nuclei from human primary breast tumors using chromosome-specific repetitive DNA probes., 10, 1988
Devilee, P and Thierry, RF and Kievits, T and Kolluri, R and Hopman, AH and Willard, HF and Pearson, PL and Cornelisse, CJ, Cancer Res. 48 pp. 5825--5830

Organization and genomic distribution of "82H" alpha satellite DNA. Evidence for a low-copy or single-copy alphoid domain located on human chromosome 14., 1, 1988
JS Waye, AR Mitchell, HF Willard, Hum Genet. 78 vol. (1); pp. 27-32

Human ribosomal RNA genes: orientation of the tandem array and conservation of the 5' end., 1, 1988
RG Worton, J Sutherland, JE Sylvester, HF Willard, S Bodrug, I Dubé, C Duff, V Kean, PN Ray, RD Schmickel, Science. 239 vol. (4835); pp. 64-8

Human ribosomal RNA genes: orientation of the tandem array and conservation of the 5' end., 1, 1988
Worton, RG and Sutherland, J and Sylvester, JE and Willard, HF and Bodrug, S and Dubé, I and Duff, C and Kean, V and Ray, PN and Schmickel, RD, Science. 239 pp. 64--68

Report of the committee on the genetic constitution of the X chromosome., 0, 1988
JL Mandel, HF Willard, RL Nussbaum, KE Davies, G Romeo, Cytogenet Cell Genet. 49 vol. (1-3); pp. 107-28

Report of the committee on human gene mapping by recombinant DNA techniques., 0, 1988
KK Kidd, AM Bowcock, PL Pearson, J Schmidtke, HF Willard, RK Track, F Ricciuti, Cytogenet Cell Genet. 49 vol. (1-3); pp. 132-218

A centromere-based linkage group on the long arm of human chromosome 17., 0, 1988
P Tsipouras, RC Schwartz, JA Phillips, HF Willard, Cytogenet Cell Genet. 47 vol. (1-2); pp. 109-10

Report of the committee on the genetic constitution of the X chromosome., 0, 1988
Mandel, JL and Willard, HF and Nussbaum, RL and Davies, KE and Romeo, G, Cytogenet Cell Genet. 49 pp. 107--128

Fast-twitch and slow-twitch/cardiac Ca<sup>2+</sup> ATPase genes map to human chromosomes 16 and 12, 0, 1988
MacLennan, DH and Brandi, CJ and Champaneria, S and Holland, PC and Powers, VE and Willard, HF, Somatic Cell and Molecular Genetics. 14 pp. 645-

Report of the committee on human gene mapping by recombinant DNA techniques., 0, 1988
Kidd, KK and Bowcock, AM and Pearson, PL and Schmidtke, J and Willard, HF and Track, RK and Ricciuti, F, Cytogenet Cell Genet. 49 pp. 132--218

A centromere-based linkage group on the long arm of human chromosome 17., 0, 1988
Tsipouras, P and Schwartz, RC and Phillips, JA and Willard, HF, Cytogenet Cell Genet. 47 pp. 109--110

Chromosome-specific alpha satellite DNA from human chromosome 1: hierarchical structure and genomic organization of a polymorphic domain spanning several hundred kilobase pairs of centromeric DNA., 9, 1987
JS Waye, SJ Durfy, D Pinkel, S Kenwrick, M Patterson, KE Davies, HF Willard, Genomics. 1 vol. (1); pp. 43-51

Clonal analysis using recombinant DNA probes from the X-chromosome., 9, 1987
B Vogelstein, ER Fearon, SR Hamilton, AC Preisinger, HF Willard, AM Michelson, AD Riggs, SH Orkin, Cancer Res. 47 vol. (18); pp. 4806-13

Molecular analysis of a polymorphic domain of alpha satellite from the human X chromosome., 9, 1987
Durfy, SJ and Willard, HF, Am J Hum Genet. 41 pp. 391--401

Nucleotide sequence heterogeneity of alpha satellite repetitive DNA: a survey of alphoid sequences from different human chromosomes., 9, 1987
Waye, JS and Willard, HF, Nucleic Acids Res. 15 pp. 7549--7569

Chromosome-specific alpha satellite DNA from human chromosome 1: hierarchical structure and genomic organization of a polymorphic domain spanning several hundred kilobase pairs of centromeric DNA., 9, 1987
Waye, JS and Durfy, SJ and Pinkel, D and Kenwrick, S and Patterson, M and Davies, KE and Willard, HF, Genomics. 1 pp. 43--51

Clonal analysis using recombinant DNA probes from the X-chromosome., 9, 1987
Vogelstein, B and Fearon, ER and Hamilton, SR and Preisinger, AC and Willard, HF and Michelson, AM and Riggs, AD and Orkin, SH, Cancer Res. 47 pp. 4806--4813

Molecular analysis of a polymorphic domain of alpha satellite from the human X chromosome., 9, 1987
SJ Durfy, HF Willard, Am J Hum Genet. 41 vol. (3); pp. 391-401

Nucleotide sequence heterogeneity of alpha satellite repetitive DNA: a survey of alphoid sequences from different human chromosomes., 9, 1987
JS Waye, HF Willard, Nucleic Acids Res. 15 vol. (18); pp. 7549-69

Human T-cell tumours containing chromosome 14 inversion or translocation with breakpoints proximal to immunoglobulin joining regions at 14q32., 8, 1987
L Mengle-Gaw, HF Willard, CI Smith, L Hammarström, P Fischer, P Sherrington, G Lucas, PW Thompson, R Baer, TH Rabbitts, EMBO J. 6 vol. (8); pp. 2273-80

Human T-cell tumours containing chromosome 14 inversion or translocation with breakpoints proximal to immunoglobulin joining regions at 14q32., 8, 1987
Mengle-Gaw, L and Willard, HF and Smith, CI and Hammarström, L and Fischer, P and Sherrington, P and Lucas, G and Thompson, PW and Baer, R and Rabbitts, TH, EMBO J. 6 pp. 2273--2280

Fast-twitch and slow-twitch/cardiac Ca2+ ATPase genes map to human chromosomes 16 and 12., 7, 1987
DH MacLennan, CJ Brandl, S Champaneria, PC Holland, VE Powers, HF Willard, Somat Cell Mol Genet. 13 vol. (4); pp. 341-6

Fast-twitch and slow-twitch/cardiac Ca2+ ATPase genes map to human chromosomes 16 and 12., 7, 1987
MacLennan, DH and Brandl, CJ and Champaneria, S and Holland, PC and Powers, VE and Willard, HF, Somat Cell Mol Genet. 13 pp. 341--346

PstI RFLP in the human hexosaminidase (HEXB) gene on chromosome 5., 4, 1987
BF O'Dowd, K Neote, DL Munroe, RA Gravel, D Mahuran, HF Willard, Nucleic Acids Res. 15 vol. (7); pp. 3194

PstI RFLP in the human hexosaminidase (HEXB) gene on chromosome 5., 4, 1987
O'Dowd, BF and Neote, K and Munroe, DL and Gravel, RA and Mahuran, D and Willard, HF, Nucleic Acids Res. 15 pp. 3194

Chromosomal location of human P-glycoprotein gene sequences., 3, 1987
DR Bell, JM Trent, HF Willard, JR Riordan, V Ling, Cancer Genet Cytogenet. 25 vol. (1); pp. 141-8

Chromosomal location of human P-glycoprotein gene sequences., 3, 1987
Bell, DR and Trent, JM and Willard, HF and Riordan, JR and Ling, V, Cancer Genet Cytogenet. 25 pp. 141--148

MSP RFLP for X-linked proteolipid protein gene (PLP) identified with either rat or human PLP cDNA clone., 2, 1987
JS Wu, JR Riordan, HF Willard, R Milner, KK Kidd, Nucleic Acids Res. 15 vol. (4); pp. 1882

MSP RFLP for X-linked proteolipid protein gene (PLP) identified with either rat or human PLP cDNA clone., 2, 1987
Wu, JS and Riordan, JR and Willard, HF and Milner, R and Kidd, KK, Nucleic Acids Res. 15 pp. 1882

Molecular organization and haplotype analysis of centromeric DNA from human chromosome 17: implications for linkage in neurofibromatosis., 12, 1987
HF Willard, GM Greig, VE Powers, JS Waye, Genomics. 1 vol. (4); pp. 368-73

MspI RFLP detected with chromosome-walk clone pXUT23-SE3.2L from DXS16 in Xp22.1-22.3., 11, 1987
CJ Brown, HF Willard, Nucleic Acids Res. 15 vol. (22); pp. 9614

MspI RFLP detected with chromosome-walk clone pXUT23-SE3.2L from DXS16 in Xp22.1-22.3., 11, 1987
Brown, CJ and Willard, HF, Nucleic Acids Res. 15 pp. 9614

Detection of novel centromeric polymorphisms associated with alpha satellite DNA from human chromosome 11., 10, 1987
JS Waye, GM Greig, HF Willard, Hum Genet. 77 vol. (2); pp. 151-6

Detection of novel centromeric polymorphisms associated with alpha satellite DNA from human chromosome 11., 10, 1987
Waye, JS and Greig, GM and Willard, HF, Hum Genet. 77 pp. 151--156

Genomic organization of alpha satellite DNA on human chromosome 7: evidence for two distinct alphoid domains on a single chromosome., 1, 1987
JS Waye, SB England, HF Willard, Mol Cell Biol. 7 vol. (1); pp. 349-56

Genomic organization of alpha satellite DNA on human chromosome 7: evidence for two distinct alphoid domains on a single chromosome., 1, 1987
Waye, JS and England, SB and Willard, HF, Mol Cell Biol. 7 pp. 349--356

Chromosome-specific subsets of human alpha satellite DNA: analysis of sequence divergence within and between chromosomal subsets and evidence for an ancestral pentameric repeat., 0, 1987
HF Willard, JS Waye, J Mol Evol. 25 vol. (3); pp. 207-14

Report of the committee on human gene mapping by recombinant DNA techniques., 0, 1987
PL Pearson, KK Kidd, HF Willard, Cytogenet Cell Genet. 46 vol. (1-4); pp. 390-566

Organization and evolution of alpha satellite DNA from human chromosome 11., 0, 1987
JS Waye, LA Creeper, HF Willard, Chromosoma. 95 vol. (3); pp. 182-8

A genomic search for linkage of neurofibromatosis to RFLPs, 0, 1987
Barker, D and Wright, E and Nguyen, K and Cannon, L and Fain, P and Goldgar, D and Bishop, DT and Carey, J and Kivlin, J and Willard, H and Nakamura, Y and O'Connell, P and Leppert, M and White, R and Skolnick, M, Journal of Medical Genetics. 24 pp. 536--538

Genetic linkage map of human chromosome 7 with 63 DNA markers, 0, 1987
Barker, D and Green, P and Knowlton, R and Schumm, J and Lander, E and Oliphant, A and Willard, H and Akots, G and Brown, V and Gravius, T and Helms, C and Nelson, C and Parker, C and Rediker, K and Rising, M and Watt, D and Weiffenbach, B and Donis-Keller, H, Proceedings of the National Academy of Sciences of the United States of America. 84 pp. 8006--8010

Human gene mapping by recombinant DNA techniques, 0, 1987
Pearson, PL and Kidd, KK and Willard, HF, Cytogenetics and Cell Genetics. 46 pp. 390--566

Genetic analysis of NF1: Identification of close flanking markers on chromosome 17, 0, 1987
Fain, PR and Barker, DF and Goldgar, DE and Wright, E and Nguyen, K and Carey, J and Johnson, J and Kivlin, J and Willard, H and Mathew, C and Ponder, B and Skolnick, M, Genomics. 1 pp. 340--345

Chromosome-specific subsets of human alpha satellite DNA: analysis of sequence divergence within and between chromosomal subsets and evidence for an ancestral pentameric repeat., 0, 1987
Willard, HF and Waye, JS, J Mol Evol. 25 pp. 207--214

Hierarchical order in chromosome-specific human alpha satellite DNA, 0, 1987
Willard, HF and Waye, JS, Trends in Genetics. 3 pp. 192--198

Report of the committee on human gene mapping by recombinant DNA techniques., 0, 1987
Pearson, PL and Kidd, KK and Willard, HF, Cytogenet Cell Genet. 46 pp. 390--566

Organization and evolution of alpha satellite DNA from human chromosome 11., 0, 1987
Waye, JS and Creeper, LA and Willard, HF, Chromosoma. 95 pp. 182--188

Cloning of the esterase D gene: a polymorphic gene probe closely linked to the retinoblastoma locus on chromosome 13., 9, 1986
J Squire, TP Dryja, J Dunn, A Goddard, T Hofmann, M Musarella, HF Willard, AJ Becker, BL Gallie, RA Phillips, Proc Natl Acad Sci U S A. 83 vol. (17); pp. 6573-7

Molecular heterogeneity in the infantile and juvenile forms of Sandhoff disease (O-variant GM2 gangliosidosis)., 9, 1986
O'Dowd, BF and Klavins, MH and Willard, HF and Gravel, R and Lowden, JA and Mahuran, DJ, J Biol Chem. 261 pp. 12680--12685

Molecular analysis of a deletion polymorphism in alpha satellite of human chromosome 17: evidence for homologous unequal crossing-over and subsequent fixation., 9, 1986
Waye, JS and Willard, HF, Nucleic Acids Res. 14 pp. 6915--6927

Structure, organization, and sequence of alpha satellite DNA from human chromosome 17: evidence for evolution by unequal crossing-over and an ancestral pentamer repeat shared with the human X chromosome., 9, 1986
Waye, JS and Willard, HF, Mol Cell Biol. 6 pp. 3156--3165

Cloning of the esterase D gene: a polymorphic gene probe closely linked to the retinoblastoma locus on chromosome 13., 9, 1986
Squire, J and Dryja, TP and Dunn, J and Goddard, A and Hofmann, T and Musarella, M and Willard, HF and Becker, AJ and Gallie, BL and Phillips, RA, Proc Natl Acad Sci U S A. 83 pp. 6573--6577

Molecular heterogeneity in the infantile and juvenile forms of Sandhoff disease (O-variant GM2 gangliosidosis)., 9, 1986
BF O'Dowd, MH Klavins, HF Willard, R Gravel, JA Lowden, DJ Mahuran, J Biol Chem. 261 vol. (27); pp. 12680-5

Molecular analysis of a deletion polymorphism in alpha satellite of human chromosome 17: evidence for homologous unequal crossing-over and subsequent fixation., 9, 1986
JS Waye, HF Willard, Nucleic Acids Res. 14 vol. (17); pp. 6915-27

Structure, organization, and sequence of alpha satellite DNA from human chromosome 17: evidence for evolution by unequal crossing-over and an ancestral pentamer repeat shared with the human X chromosome., 9, 1986
JS Waye, HF Willard, Mol Cell Biol. 6 vol. (9); pp. 3156-65

The beta-subunit of follicle-stimulating hormone is deleted in patients with aniridia and Wilms' tumour, allowing a further definition of the WAGR locus., 8, 1986
T Glaser, WH Lewis, GA Bruns, PC Watkins, CE Rogler, TB Shows, VE Powers, HF Willard, JM Goguen, KO Simola, Nature. 321 vol. (6073); pp. 882-7

Detection of restriction fragment length polymorphisms at the centromeres of human chromosomes by using chromosome-specific alpha satellite DNA probes: implications for development of centromere-based genetic linkage maps., 8, 1986
HF Willard, JS Waye, MH Skolnick, CE Schwartz, VE Powers, SB England, Proc Natl Acad Sci U S A. 83 vol. (15); pp. 5611-5

Detection of restriction fragment length polymorphisms at the centromeres of human chromosomes by using chromosome-specific alpha satellite DNA probes: implications for development of centromere-based genetic linkage maps., 8, 1986
Willard, HF and Waye, JS and Skolnick, MH and Schwartz, CE and Powers, VE and England, SB, Proc Natl Acad Sci U S A. 83 pp. 5611--5615

Direct regional assignment of the gene for vitamin D binding protein (Gc-globulin) to human chromosome 4q11-q13 and identification of an associated DNA polymorphism., 7, 1986
NE Cooke, HF Willard, EV David, DL George, Hum Genet. 73 vol. (3); pp. 225-9

Isolation of cDNA clones coding for the alpha and beta chains of human propionyl-CoA carboxylase: chromosomal assignments and DNA polymorphisms associated with PCCA and PCCB genes., 7, 1986
AM Lamhonwah, TJ Barankiewicz, HF Willard, DJ Mahuran, F Quan, RA Gravel, Proc Natl Acad Sci U S A. 83 vol. (13); pp. 4864-8

Interferon-regulated human 2-5A synthetase gene maps to chromosome 12., 7, 1986
BR Williams, ME Saunders, HF Willard, Somat Cell Mol Genet. 12 vol. (4); pp. 403-8

Interferon-regulated human 2-5A synthetase gene maps to chromosome 12., 7, 1986
Williams, BR and Saunders, ME and Willard, HF, Somat Cell Mol Genet. 12 pp. 403--408

Isolation of cDNA clones coding for the alpha and beta chains of human propionyl-CoA carboxylase: chromosomal assignments and DNA polymorphisms associated with PCCA and PCCB genes., 7, 1986
Lamhonwah, AM and Barankiewicz, TJ and Willard, HF and Mahuran, DJ and Quan, F and Gravel, RA, Proc Natl Acad Sci U S A. 83 pp. 4864--4868

Direct regional assignment of the gene for vitamin D binding protein (Gc-globulin) to human chromosome 4q11-q13 and identification of an associated DNA polymorphism., 7, 1986
Cooke, NE and Willard, HF and David, EV and George, DL, Hum Genet. 73 pp. 225--229

Isolation of cDNA clones coding for the alpha-subunit of human beta-hexosaminidase. Extensive homology between the alpha- and beta-subunits and studies on Tay-Sachs disease., 6, 1986
RG Korneluk, DJ Mahuran, K Neote, MH Klavins, BF O'Dowd, M Tropak, HF Willard, MJ Anderson, JA Lowden, RA Gravel, J Biol Chem. 261 vol. (18); pp. 8407-13

Isolation of cDNA clones coding for the alpha-subunit of human beta-hexosaminidase. Extensive homology between the alpha- and beta-subunits and studies on Tay-Sachs disease., 6, 1986
Korneluk, RG and Mahuran, DJ and Neote, K and Klavins, MH and O'Dowd, BF and Tropak, M and Willard, HF and Anderson, MJ and Lowden, JA and Gravel, RA, J Biol Chem. 261 pp. 8407--8413

The beta-subunit of follicle-stimulating hormone is deleted in patients with aniridia and Wilms' tumour, allowing a further definition of the WAGR locus., 6, 1986
Glaser, T and Lewis, WH and Bruns, GA and Watkins, PC and Rogler, CE and Shows, TB and Powers, VE and Willard, HF and Goguen, JM and Simola, KO, Nature. 321 pp. 882--887

RFLP detected by an X-linked cDNA encoding erythroid-potentiating activity/tissue inhibitor of metalloproteinase (EPA/TIMP)., 11, 1986
SJ Durfy, SC Clark, BR Williams, HF Willard, Nucleic Acids Res. 14 vol. (22); pp. 9226

RFLP detected by an X-linked cDNA encoding erythroid-potentiating activity/tissue inhibitor of metalloproteinase (EPA/TIMP)., 11, 1986
Durfy, SJ and Clark, SC and Williams, BR and Willard, HF, Nucleic Acids Res. 14 pp. 9226

Mapping of the cystic fibrosis locus on chromosome 7., 0, 1986
LC Tsui, S Zengerling, HF Willard, M Buchwald, Cold Spring Harb Symp Quant Biol. 51 Pt 1 pp. 325-35

Linkage of cystic fibrosis to the pro alpha 2(I) collagen gene, COL1A2, on chromosome 7., 0, 1986
M Buchwald, M Zsiga, D Markiewicz, N Plavsic, D Kennedy, S Zengerling, HF Willard, P Tsipouras, K Schmiegelow, M Schwartz, Cytogenet Cell Genet. 41 vol. (4); pp. 234-9

Linkage of cystic fibrosis to the pro alpha 2(I) collagen gene, COL1A2, on chromosome 7., 0, 1986
Buchwald, M and Zsiga, M and Markiewicz, D and Plavsic, N and Kennedy, D and Zengerling, S and Willard, HF and Tsipouras, P and Schmiegelow, K and Schwartz, M, Cytogenet Cell Genet. 41 pp. 234--239

Mapping of the cystic fibrosis locus on chromosome 7., 0, 1986
Tsui, LC and Zengerling, S and Willard, HF and Buchwald, M, Cold Spring Harb Symp Quant Biol. 51 Pt 1 pp. 325--335

The β-subunit of follicle-stimulating hormone is deleted in patients with aniridia and Wilms' tumour, allowing a further definition of the WAGR locus, 0, 1986
Glaser, T and Lewis, WH and Bruns, GAP and Watkins, PC and Rogler, CE and Shows, TB and Powers, VE and Willard, HF and Goguen, JM and Simola, KO, Nature. 321 pp. 882--887

Assignment of human gamma crystallin multigene family to chromosome 2., 9, 1985
HF Willard, SO Meakin, LC Tsui, ML Breitman, Somat Cell Mol Genet. 11 vol. (5); pp. 511-6

Assignment of human gamma crystallin multigene family to chromosome 2., 9, 1985
Willard, HF and Meakin, SO and Tsui, LC and Breitman, ML, Somat Cell Mol Genet. 11 pp. 511--516

An anonymous single-copy X-chromosome RFLP for DXS72 from Xq13-Xq22 [HGM8 provisional no. DXS72]., 8, 1985
BJ Schmeckpeper, J Davis, HF Willard, KD Smith, Nucleic Acids Res. 13 vol. (15); pp. 5724

An anonymous single-copy X-chromosome RFLP for DXS72 from Xq13-Xq22 [HGM8 provisional no. DXS72]., 8, 1985
Schmeckpeper, BJ and Davis, J and Willard, HF and Smith, KD, Nucleic Acids Res. 13 pp. 5724

Chromosome-specific organization of human alpha satellite DNA., 5, 1985
HF Willard, Am J Hum Genet. 37 vol. (3); pp. 524-32

Mapping DNA sequences in a human X-chromosome deletion which extends across the region of the Duchenne muscular dystrophy mutation., 5, 1985
C Ingle, R Williamson, A de la Chapelle, RR Herva, K Haapala, G Bates, HF Willard, P Pearson, KE Davies, Am J Hum Genet. 37 vol. (3); pp. 451-62

Chromosome-specific organization of human alpha satellite DNA., 5, 1985
Willard, HF, Am J Hum Genet. 37 pp. 524--532

Mapping DNA sequences in a human X-chromosome deletion which extends across the region of the Duchenne muscular dystrophy mutation., 5, 1985
Ingle, C and Williamson, R and de la Chapelle, A and Herva, RR and Haapala, K and Bates, G and Willard, HF and Pearson, P and Davies, KE, Am J Hum Genet. 37 pp. 451--462

Chromosome-specific alpha satellite DNA: nucleotide sequence analysis of the 2.0 kilobasepair repeat from the human X chromosome., 4, 1985
Waye, JS and Willard, HF, Nucleic Acids Res. 13 pp. 2731--2743

Isolation and characterization of an alphoid centromeric repeat family from the human Y chromosome., 4, 1985
Wolfe, J and Darling, SM and Erickson, RP and Craig, IW and Buckle, VJ and Rigby, PW and Willard, HF and Goodfellow, PN, J Mol Biol. 182 pp. 477--485

Isolation and characterization of an alphoid centromeric repeat family from the human Y chromosome., 4, 1985
J Wolfe, SM Darling, RP Erickson, IW Craig, VJ Buckle, PW Rigby, HF Willard, PN Goodfellow, J Mol Biol. 182 vol. (4); pp. 477-85

Chromosome-specific alpha satellite DNA: nucleotide sequence analysis of the 2.0 kilobasepair repeat from the human X chromosome., 4, 1985
JS Waye, HF Willard, Nucleic Acids Res. 13 vol. (8); pp. 2731-43

Prenatal diagnosis and carrier detection of Duchenne muscular dystrophy with closely linked RFLPs., 3, 1985
E Bakker, MH Hofker, N Goor, JL Mandel, K Wrogemann, KE Davies, LM Kunkel, HF Willard, WA Fenton, L Sandkuyl, Lancet. 1 vol. (8430); pp. 655-8

Prenatal diagnosis and carrier detection of Duchenne muscular dystrophy with closely linked RFLPs., 3, 1985
Bakker, E and Hofker, MH and Goor, N and Mandel, JL and Wrogemann, K and Davies, KE and Kunkel, LM and Willard, HF and Fenton, WA and Sandkuyl, L, Lancet. 1 pp. 655--658

Molecular cloning and chromosomal localization of DNA sequences associated with a human DNA repair gene., 2, 1985
JS Rubin, VR Prideaux, HF Willard, AM Dulhanty, GF Whitmore, A Bernstein, Mol Cell Biol. 5 vol. (2); pp. 398-405

Isolation of cDNA clones coding for the beta subunit of human beta-hexosaminidase., 2, 1985
BF O'Dowd, F Quan, HF Willard, AM Lamhonwah, RG Korneluk, JA Lowden, RA Gravel, DJ Mahuran, Proc Natl Acad Sci U S A. 82 vol. (4); pp. 1184-8

Molecular cloning and chromosomal localization of DNA sequences associated with a human DNA repair gene., 2, 1985
Rubin, JS and Prideaux, VR and Willard, HF and Dulhanty, AM and Whitmore, GF and Bernstein, A, Mol Cell Biol. 5 pp. 398--405

Isolation of cDNA clones coding for the beta subunit of human beta-hexosaminidase., 2, 1985
O'Dowd, BF and Quan, F and Willard, HF and Lamhonwah, AM and Korneluk, RG and Lowden, JA and Gravel, RA and Mahuran, DJ, Proc Natl Acad Sci U S A. 82 pp. 1184--1188

Assignment of the gene for myelin proteolipid protein to the X chromosome: implications for X-linked myelin disorders., 11, 1985
HF Willard, JR Riordan, Science. 230 vol. (4728); pp. 940-2

Assignment of the gene for myelin proteolipid protein to the X chromosome: implications for X-linked myelin disorders., 11, 1985
Willard, HF and Riordan, JR, Science. 230 pp. 940--942

Molecular analysis of gene deletion in aniridia--Wilms tumor association., 0, 1985
EE Michalopoulos, PJ Bevilacqua, N Stokoe, VE Powers, HF Willard, WH Lewis, Hum Genet. 70 vol. (2); pp. 157-62

Gene order on the short arm of human chromosome 11: regional assignment of the LDH A gene distal to catalase in two translocations., 0, 1985
WH Lewis, JM Goguen, VE Powers, HF Willard, EE Michalopoulos, Hum Genet. 71 vol. (3); pp. 249-53

Regional localization of the phosphoglycerate kinase gene and pseudogene on the human X chromosome and assignment of a related DNA sequence to chromosome 19., 0, 1985
HF Willard, SJ Goss, MT Holmes, DL Munroe, Hum Genet. 71 vol. (2); pp. 138-43

Report of the Committee on Human Gene Mapping by Recombinant DNA Techniques., 0, 1985
HF Willard, MH Skolnick, PL Pearson, JL Mandel, Cytogenet Cell Genet. 40 vol. (1-4); pp. 360-489

Gene order on the short arm of human chromosome 11: regional assignment of the LDH A gene distal to catalase in two translocations., 0, 1985
Lewis, WH and Goguen, JM and Powers, VE and Willard, HF and Michalopoulos, EE, Hum Genet. 71 pp. 249--253

Report of the committee on human gene mapping by recombinant DNA techniques, 0, 1985
Willard, HF and Skolnick, MH and Pearson, PL and Mandel, JL, Birth Defects: Original Article Series. 21 pp. 360--489

Regional localization of the phosphoglycerate kinase gene and pseudogene on the human X chromosome and assignment of a related DNA sequence to chromosome 19., 0, 1985
Willard, HF and Goss, SJ and Holmes, MT and Munroe, DL, Hum Genet. 71 pp. 138--143

Report of the Committee on Human Gene Mapping by Recombinant DNA Techniques., 0, 1985
Willard, HF and Skolnick, MH and Pearson, PL and Mandel, JL, Cytogenet Cell Genet. 40 pp. 360--489

Characterization of the small 2-5A synthetase gene in human and mouse cells., 0, 1985
Saunders, M and Gewert, D and Castelino, M and Rutherford, M and Flenniken, A and Willard, H and Williams, BR, Progress in clinical and biological research. 202 pp. 163--174

Molecular analysis of gene deletion in aniridia--Wilms tumor association., 0, 1985
Michalopoulos, EE and Bevilacqua, PJ and Stokoe, N and Powers, VE and Willard, HF and Lewis, WH, Hum Genet. 70 pp. 157--162

Duchenne muscular dystrophy involving translocation of the dmd gene next to ribosomal RNA genes., 6, 1984
RG Worton, C Duff, JE Sylvester, RD Schmickel, HF Willard, Science. 224 vol. (4656); pp. 1447-9

Duchenne muscular dystrophy involving translocation of the dmd gene next to ribosomal RNA genes., 6, 1984
Worton, RG and Duff, C and Sylvester, JE and Schmickel, RD and Willard, HF, Science. 224 pp. 1447--1449

Isolation of human fibroblast catalase cDNA clones. Sequence of clones derived from spliced and unspliced mRNA., 11, 1984
RG Korneluk, F Quan, WH Lewis, KS Guise, HF Willard, MT Holmes, RA Gravel, J Biol Chem. 259 vol. (22); pp. 13819-23

Isolation of human fibroblast catalase cDNA clones. Sequence of clones derived from spliced and unspliced mRNA., 11, 1984
Korneluk, RG and Quan, F and Lewis, WH and Guise, KS and Willard, HF and Holmes, MT and Gravel, RA, J Biol Chem. 259 pp. 13819--13823

Report of the Committee on Human Gene Mapping by Recombinant DNA Techniques., 0, 1984
MH Skolnick, HF Willard, LA Menlove, Cytogenet Cell Genet. 37 vol. (1-4); pp. 210-73

A sensitive and dependable assay for distinguishing hamster and human X-linked steroid sulfatase activity in somatic cell hybrids., 0, 1984
HF Willard, MT Holmes, Hum Genet. 66 vol. (2-3); pp. 272-5

The T cell receptor β chain genes are located on chromosome 6 in mice and chromosome 7 in humans, 0, 1984
Caccia, N and Kronenberg, M and Saxe, D and Haars, R and Bruns, GAP and Goverman, J and Malissen, M and Willard, H and Yoshikai, Y and Simon, M and Hood, L and Mak, TW, Cell. 37 pp. 1091--1099

A sensitive and dependable assay for distinguishing hamster and human X-linked steroid sulfatase activity in somatic cell hybrids., 0, 1984
Willard, HF and Holmes, MT, Hum Genet. 66 pp. 272--275

Report of the Committee on Human Gene Mapping by Recombinant DNA Techniques., 0, 1984
Skolnick, MH and Willard, HF and Menlove, LA, Cytogenet Cell Genet. 37 pp. 210--273

Isolation and characterization of a major tandem repeat family from the human X chromosome., 4, 1983
HF Willard, KD Smith, J Sutherland, Nucleic Acids Res. 11 vol. (7); pp. 2017-33

Isolation and characterization of a major tandem repeat family from the human X chromosome., 4, 1983
Willard, HF and Smith, KD and Sutherland, J, Nucleic Acids Res. 11 pp. 2017--2033

Purification and properties of methylmalonyl coenzyme A mutase from human liver., 4, 1982
WA Fenton, AM Hack, HF Willard, A Gertler, LE Rosenberg, Arch Biochem Biophys. 214 vol. (2); pp. 815-23

Purification and properties of methylmalonyl coenzyme A mutase from human liver., 4, 1982
Fenton, WA and Hack, AM and Willard, HF and Gertler, A and Rosenberg, LE, Arch Biochem Biophys. 214 pp. 815--823

Isolation and characterization of cloned human DNA fragments carrying reiterated sequences common to both autosomes and the X chromosome., 4, 1981
Schmeckpeper, BJ and Willard, HF and Smith, KD, Nucleic Acids Res. 9 pp. 1853--1872

Isolation and characterization of cloned human DNA fragments carrying reiterated sequences common to both autosomes and the X chromosome., 4, 1981
BJ Schmeckpeper, HF Willard, KD Smith, Nucleic Acids Res. 9 vol. (8); pp. 1853-72

Human X chromosomes: synchrony of DNA replication in diploid and triploid fibroblasts with multiple active or inactive X chromosomes., 3, 1980
HF Willard, WR Breg, Somatic Cell Genet. 6 vol. (2); pp. 187-98

Interactions of methylmalonyl CoA mutase from normal human fibroblasts with adenosylcobalamin and methylmalonyl CoA: evidence for non-equivalent active sites., 3, 1980
HF Willard, LE Rosenberg, Arch Biochem Biophys. 200 vol. (1); pp. 130-9

Inherited methylmalonyl CoA mutase apoenzyme deficiency in human fibroblasts: evidence for allelic heterogeneity, genetic compounds, and codominant expression., 3, 1980
HF Willard, LE Rosenberg, J Clin Invest. 65 vol. (3); pp. 690-8

Interactions of methylmalonyl CoA mutase from normal human fibroblasts with adenosylcobalamin and methylmalonyl CoA: evidence for non-equivalent active sites., 3, 1980
Willard, HF and Rosenberg, LE, Arch Biochem Biophys. 200 pp. 130--139

Inherited methylmalonyl CoA mutase apoenzyme deficiency in human fibroblasts: evidence for allelic heterogeneity, genetic compounds, and codominant expression., 3, 1980
Willard, HF and Rosenberg, LE, J Clin Invest. 65 pp. 690--698

Human X chromosomes: synchrony of DNA replication in diploid and triploid fibroblasts with multiple active or inactive X chromosomes., 3, 1980
Willard, HF and Breg, WR, Somatic Cell Genet. 6 pp. 187--198

Kinetic analysis of genetic complementation in heterokaryons of propionyl CoA carboxylase-deficient human fibroblasts., 1, 1980
B Wolf, HF Willard, LE Rosenberg, Am J Hum Genet. 32 vol. (1); pp. 16-25

Kinetic analysis of genetic complementation in heterokaryons of propionyl CoA carboxylase-deficient human fibroblasts., 1, 1980
Wolf, B and Willard, HF and Rosenberg, LE, Am J Hum Genet. 32 pp. 16--25

Inborn errors of cobalamin metabolism: effect of cobalamin supplementation in culture on methylmalonyl CoA mutase activity in normal and mutant human fibroblasts., 2, 1979
HF Willard, LE Rosenberg, Biochem Genet. 17 vol. (1-2); pp. 57-75

Inborn errors of cobalamin metabolism: effect of cobalamin supplementation in culture on methylmalonyl CoA mutase activity in normal and mutant human fibroblasts., 2, 1979
Willard, HF and Rosenberg, LE, Biochem Genet. 17 pp. 57--75

Cobalamin coenzyme synthesis in normal and mutant human fibroblasts. Evidence for a processing enzyme activity deficient in cblC cells., 12, 1979
I Mellman, HF Willard, P Youngdahl-Turner, LE Rosenberg, J Biol Chem. 254 vol. (23); pp. 11847-53

Cobalamin coenzyme synthesis in normal and mutant human fibroblasts. Evidence for a processing enzyme activity deficient in cblC cells., 12, 1979
Mellman, I and Willard, HF and Youngdahl-Turner, P and Rosenberg, LE, J Biol Chem. 254 pp. 11847--11853

Irreversible enzyme inhibition by hydroxocobalamin: Possible mechanism of water-soluble vitamin toxicity, 0, 1979
Willard, HF and Rosenberg, LE, Clinical Research. 27 pp. 508A

Cobalamin binding and cobalamin-dependent enzyme activity in normal and mutant human fibroblasts., 11, 1978
I Mellman, HF Willard, LE Rosenberg, J Clin Invest. 62 vol. (5); pp. 952-60

Cobalamin binding and cobalamin-dependent enzyme activity in normal and mutant human fibroblasts., 11, 1978
Mellman, I and Willard, HF and Rosenberg, LE, J Clin Invest. 62 pp. 952--960

Genetic complementation among inherited deficiencies of methylmalonyl-CoA mutase activity: evidence for a new class of human cobalamin mutant., 1, 1978
HF Willard, IS Mellman, LE Rosenberg, Am J Hum Genet. 30 vol. (1); pp. 1-13

Genetic complementation among inherited deficiencies of methylmalonyl-CoA mutase activity: evidence for a new class of human cobalamin mutant., 1, 1978
Willard, HF and Mellman, IS and Rosenberg, LE, Am J Hum Genet. 30 pp. 1--13

Tissue-specific heterogeneity in DNA replication patterns of human X chromosomes., 4, 1977
HF Willard, Chromosoma. 61 vol. (1); pp. 61-73

Tissue-specific heterogeneity in DNA replication patterns of human X chromosomes., 4, 1977
Willard, HF, Chromosoma. 61 pp. 61--73

Intracellular binding of radioactive hydroxocobalamin to cobalamin-dependent apoenzymes in rat liver., 3, 1977
IS Mellman, P Youngdahl-Turner, HF Willard, LE Rosenberg, Proc Natl Acad Sci U S A. 74 vol. (3); pp. 916-20

Inherited deficiencies of human methylmalonyl CaA mutase activity: reduced affinity of mutant apoenzyme for adenosylcobalamin., 10, 1977
HF Willard, LE Rosenberg, Biochem Biophys Res Commun. 78 vol. (3); pp. 927-34

Inherited deficiencies of human methylmalonyl CaA mutase activity: reduced affinity of mutant apoenzyme for adenosylcobalamin., 10, 1977
Willard, HF and Rosenberg, LE, Biochem Biophys Res Commun. 78 pp. 927--934

Biochemical heterogeneity within a class of human mutants deficient in cobalamin coenzyme synthesis International symposium on inborn errors of metabolism in man, Tel Aviv, June 19-25, 1977, 0, 1977
Willard, H and Mellman, I and Rosenberg, L, Human Heredity. 27 pp. 221-

BrdU-33258 Hoechst analysis of DNA replication in human lymphocytes with supernumerary or structurally abnormal X chromosomes., 8, 1976
SA Latt, HF Willard, PS Gerald, Chromosoma. 57 vol. (2); pp. 135-53

BrdU-33258 Hoechst analysis of DNA replication in human lymphocytes with supernumerary or structurally abnormal X chromosomes., 8, 1976
Latt, SA and Willard, HF and Gerald, PS, Chromosoma. 57 pp. 135--153

Analysis of deoxyribonucleic acid replication in human X chromosomes by fluorescence microscopy., 5, 1976
HF Willard, SA Latt, Am J Hum Genet. 28 vol. (3); pp. 213-27

Analysis of deoxyribonucleic acid replication in human X chromosomes by fluorescence microscopy., 5, 1976
Willard, HF and Latt, SA, Am J Hum Genet. 28 pp. 213--227

Rapid prenatal and postnatal detection of inborn errors of propionate, methylmalonate, and cobalamin metabolism: a sensitive assay using cultured cells., 12, 1976
HF Willard, LM Ambani, AC Hart, MJ Mahoney, LE Rosenberg, Hum Genet. 34 vol. (3); pp. 277-83

Rapid prenatal and postnatal detection of inborn errors of propionate, methylmalonate, and cobalamin metabolism: a sensitive assay using cultured cells., 12, 1976
Willard, HF and Ambani, LM and Hart, AC and Mahoney, MJ and Rosenberg, LE, Hum Genet. 34 pp. 277--283

Human X chromosomes: DNA replication sequence heterogeneity in different tissues, 0, 1976
Willard, HF and Mahoney, MJ, EXCERPTA MED.,AMSTERDAM,I.C.S.. No. 397 pp. No.444

Detection and characterization of propionate methylmalonate disorders in cell culture: a simple method, 0, 1976
Willard, HF and Ambani, LM and Mahoney, MJ and Rosenberg, LE, Pediatric Research. 10 pp. No.431

Recent developments in the detection of deoxyribonucleic acid synthesis by 33258 Hoechst fluorescence., 7, 1975
SA Latt, G Stetten, LA Juergens, HF Willard, CD Scher, J Histochem Cytochem. 23 vol. (7); pp. 493-505

Recent developments in the detection of deoxyribonucleic acid synthesis by 33258 Hoechst fluorescence., 7, 1975
Latt, SA and Stetten, G and Juergens, LA and Willard, HF and Scher, CD, J Histochem Cytochem. 23 pp. 493--505

Awards

  • 2013 Members/ Foreign Associates, National Academy of Science

  • 2009 WILLIAM ALLAN AWARD, American Society of Human Genetics

  • 2008 Fellows, American Academy of Arts and Sciences