| Year |
Citation |
Score |
| 2014 |
Kertai MD, Li YW, Li YJ, Shah SH, Kraus WE, Fontes ML, Stafford-Smith M, Newman MF, Podgoreanu MV, Mathew JP. G protein-coupled receptor kinase 5 gene polymorphisms are associated with postoperative atrial fibrillation after coronary artery bypass grafting in patients receiving β-blockers. Circulation. Cardiovascular Genetics. 7: 625-33. PMID 25049040 DOI: 10.1161/CIRCGENETICS.113.000451 |
1 |
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| 2014 |
Altemose N, Miga KH, Maggioni M, Willard HF. Genomic Characterization of Large Heterochromatic Gaps in the Human Genome Assembly Plos Computational Biology. 10. PMID 24831296 DOI: 10.1371/journal.pcbi.1003628 |
1 |
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| 2014 |
Haga SB, Barry WT, Mills R, Svetkey L, Suchindran S, Willard HF, Ginsburg GS. Impact of delivery models on understanding genomic risk for type 2 diabetes Public Health Genomics. 17: 95-104. PMID 24577154 DOI: 10.1159/000358413 |
1 |
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| 2014 |
Miga KH, Newton Y, Jain M, Altemose N, Willard HF, Kent EJ. Centromere reference models for human chromosomes X and y satellite arrays Genome Research. 24: 697-707. PMID 24501022 DOI: 10.1101/gr.159624.113 |
1 |
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| 2013 |
Earnshaw WC, Allshire RC, Black BE, Bloom K, Brinkley BR, Brown W, Cheeseman IM, Choo KH, Copenhaver GP, Deluca JG, Desai A, Diekmann S, Erhardt S, Fitzgerald-Hayes M, Foltz D, ... ... Willard HF, et al. Esperanto for histones: CENP-A, not CenH3, is the centromeric histone H3 variant. Chromosome Research : An International Journal On the Molecular, Supramolecular and Evolutionary Aspects of Chromosome Biology. 21: 101-6. PMID 23580138 DOI: 10.1007/s10577-013-9347-y |
1 |
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| 2013 |
Haga SB, Barry WT, Mills R, Ginsburg GS, Svetkey L, Sullivan J, Willard HF. Public knowledge of and attitudes toward genetics and genetic testing Genetic Testing and Molecular Biomarkers. 17: 327-335. PMID 23406207 DOI: 10.1089/gtmb.2012.0350 |
1 |
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| 2013 |
Hayden KE, Strome ED, Merrett SL, Lee HR, Rudd MK, Willard HF. Sequences associated with centromere competency in the human genome. Molecular and Cellular Biology. 33: 763-72. PMID 23230266 DOI: 10.1128/MCB.01198-12 |
1 |
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| 2013 |
Ginsburg GS, Willard HF. Preface Genomic and Personalized Medicine. 1: xi-xii. DOI: 10.1016/B978-0-12-382227-7.00125-7 |
1 |
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| 2013 |
Willard HF. The human genome: A window on human genetics, biology, and medicine Genomic and Personalized Medicine. 1: 4-27. DOI: 10.1016/B978-0-12-382227-7.00001-X |
1 |
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| 2012 |
Thorvaldsen JL, Krapp C, Willard HF, Bartolomei MS. Nonrandom X chromosome inactivation is influenced by multiple regions on the murine X chromosome Genetics. 192: 1095-1107. PMID 22887817 DOI: 10.1534/genetics.112.144477 |
1 |
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| 2012 |
Wang Z, Willard HF. Evidence for sequence biases associated with patterns of histone methylation Bmc Genomics. 13. PMID 22857523 DOI: 10.1186/1471-2164-13-367 |
1 |
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| 2012 |
Hayden KE, Willard HF. Composition and organization of active centromere sequences in complex genomes. Bmc Genomics. 13: 324. PMID 22817545 DOI: 10.1186/1471-2164-13-324 |
1 |
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| 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. Effects of sequence variation on differential allelic transcription factor occupancy and gene expression. Genome Research. 22: 860-9. PMID 22300769 DOI: 10.1101/gr.131201.111 |
1 |
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| 2012 |
Wheeler BS, Ruderman BT, Willard HF, Scott KC. Uncoupling of genomic and epigenetic signals in the maintenance and inheritance of heterochromatin domains in fission yeast. Genetics. 190: 549-57. PMID 22143918 DOI: 10.1534/genetics.111.137083 |
1 |
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| 2011 |
Anderson WA, Amasino RM, Ares M, Banerjee U, Bartel B, Corces VG, Drennan CL, Elgin SC, Epstein IR, Fanning E, Guillette LJ, Handelsman J, Hatfull GF, Hoy RR, Kelley D, ... ... Willard HF, et al. Competencies: a cure for pre-med curriculum. Science (New York, N.Y.). 334: 760-1. PMID 22076362 DOI: 10.1126/science.334.6057.760-b |
1 |
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| 2011 |
Gertz J, Varley KE, Reddy TE, Bowling KM, Pauli F, Parker SL, Kucera KS, Willard HF, Myers RM. Analysis of DNA methylation in a three-generation family reveals widespread genetic influence on epigenetic regulation. Plos Genetics. 7: e1002228. PMID 21852959 DOI: 10.1371/journal.pgen.1002228 |
1 |
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| 2011 |
Lee HR, Hayden KE, Willard HF. Organization and molecular evolution of CENP-A--associated satellite DNA families in a basal primate genome. Genome Biology and Evolution. 3: 1136-49. PMID 21828373 DOI: 10.1093/gbe/evr083 |
1 |
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| 2011 |
Kucera KS, Reddy TE, Pauli F, Gertz J, Logan JE, Myers RM, Willard HF. Allele-specific distribution of RNA polymerase II on female X chromosomes. Human Molecular Genetics. 20: 3964-73. PMID 21791549 DOI: 10.1093/hmg/ddr315 |
1 |
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| 2011 |
Horvath JE, Sheedy CB, Merrett SL, Diallo AB, Swofford DL, NISC Comparative Sequencing Program, Green ED, Willard HF. Comparative analysis of the primate X-inactivation center region and reconstruction of the ancestral primate XIST locus. Genome Research. 21: 850-62. PMID 21518738 DOI: 10.1101/gr.111849.110 |
1 |
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| 2010 |
O'Daniel JM, Haga SB, Willard HF. Considerations for the impact of personal genome information: A study of genomic profiling among genetics and genomics professionals Journal of Genetic Counseling. 19: 387-401. PMID 20352309 DOI: 10.1007/s10897-010-9297-x |
1 |
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| 2010 |
McDaniell R, Lee BK, Song L, Liu Z, Boyle AP, Erdos MR, Scott LJ, Morken MA, Kucera KS, Battenhouse A, Keefe D, Collins FS, Willard HF, Lieb JD, Furey TS, et al. Heritable individual-specific and allele-specific chromatin signatures in humans. Science (New York, N.Y.). 328: 235-9. PMID 20299549 DOI: 10.1126/science.1184655 |
1 |
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| 2010 |
Willard HF. Organization, Variation and Expression of the Human Genome Essentials of Genomic and Personalized Medicine. 13-26. DOI: 10.1016/B978-0-12-374934-5.00002-7 |
1 |
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| 2010 |
Ginsburg GS, Willard HF. The Foundations of Genomic and Personalized Medicine Essentials of Genomic and Personalized Medicine. 1-10. DOI: 10.1016/B978-0-12-374934-5.00001-5 |
1 |
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| 2009 |
Ginsburg GS, Willard HF. Genomic and personalized medicine: foundations and applications Translational Research. 154: 277-287. PMID 19931193 DOI: 10.1016/j.trsl.2009.09.005 |
1 |
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| 2009 |
Wheeler BS, Blau JA, Willard HF, Scott KC. The impact of local genome sequence on defining heterochromatin domains. Plos Genetics. 5: e1000453. PMID 19360117 DOI: 10.1371/journal.pgen.1000453 |
1 |
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| 2009 |
Kawamoto K, Lobach DF, Willard HF, Ginsburg GS. A national clinical decision support infrastructure to enable the widespread and consistent practice of genomic and personalized medicine. Bmc Medical Informatics and Decision Making. 9: 17. PMID 19309514 DOI: 10.1186/1472-6947-9-17 |
1 |
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| 2009 |
Willard HF. Organization, Variation and Expression of the Human Genome as a Foundation of Genomic and Personalized Medicine Genomic and Personalized Medicine, Two-Vol Set. 1-21. DOI: 10.1016/B978-0-12-369420-1.00001-9 |
1 |
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| 2009 |
Ginsburg GS, Willard HF. Genomic and Personalized Medicine, Two-Vol Set Genomic and Personalized Medicine, Two-Vol Set. |
1 |
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| 2008 |
Tuckson RV, Willard HF. A letter response to Chaufan's "How much can a large population study on genes, environments, their interactions and common diseases contribute to the health of the American people?" (65:8, 2007, 1730-1741) Social Science and Medicine. 67: 673-674. PMID 18534733 DOI: 10.1016/j.socscimed.2008.04.011 |
1 |
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| 2008 |
Haga SB, Willard HF. Letting the genome out of the bottle New England Journal of Medicine. 358: 2184. PMID 18480218 DOI: 10.1056/NEJMc086053 |
1 |
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| 2008 |
Horvath JE, Weisrock DW, Embry SL, Fiorentino I, Balhoff JP, Kappeler P, Wray GA, Willard HF, Yoder AD. Development and application of a phylogenomic toolkit: resolving the evolutionary history of Madagascar's lemurs. Genome Research. 18: 489-99. PMID 18245770 DOI: 10.1101/gr.7265208 |
1 |
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| 2007 |
Basu J, Willard HF, Stromberg G. Human artificial chromosome assembly by transposon-based retrofitting of genomic BACs with synthetic alpha-satellite arrays. Current Protocols in Human Genetics / Editorial Board, Jonathan L. Haines ... [Et Al.]. Unit 5.18. PMID 18428412 DOI: 10.1002/0471142905.hg0518s52 |
1 |
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| 2007 |
Scott KC, White CV, Willard HF. An RNA polymerase III-dependent heterochromatin barrier at fission yeast centromere 1. Plos One. 2: e1099. PMID 17971862 DOI: 10.1371/journal.pone.0001099 |
1 |
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| 2007 |
Horvath JE, Willard HF. Primate comparative genomics: lemur biology and evolution Trends in Genetics. 23: 173-182. PMID 17331617 DOI: 10.1016/j.tig.2007.02.007 |
1 |
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| 2006 |
Haga SB, Willard HF. Defining the spectrum of genome policy Nature Reviews Genetics. 7: 966-972. PMID 17139328 DOI: 10.1038/nrg2003 |
1 |
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| 2006 |
Shianna KV, Willard HF. Human genomics: In search of normality Nature. 444: 428-429. PMID 17122840 DOI: 10.1038/444428a |
1 |
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| 2006 |
Basu J, Willard HF. Human artificial chromosomes: potential applications and clinical considerations. Pediatric Clinics of North America. 53: 843-53, viii. PMID 17027613 DOI: 10.1016/j.pcl.2006.08.013 |
1 |
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| 2006 |
Wang Z, Willard HF, Mukherjee S, Furey TS. Evidence of influence of genomic DNA sequence on human X chromosome inactivation Plos Computational Biology. 2: 0979-0988. PMID 16948528 DOI: 10.1371/journal.pcbi.0020113 |
1 |
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| 2006 |
Amos-Landgraf JM, Cottle A, Plenge RM, Friez M, Schwartz CE, Longshore J, Willard HF. X chromosome-inactivation patterns of 1,005 phenotypically unaffected females American Journal of Human Genetics. 79: 493-499. PMID 16909387 DOI: 10.1086/507565 |
1 |
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| 2006 |
Valley CM, Pertz LM, Balakumaran BS, Willard HF. Chromosome-wide, allele-specific analysis of the histone code on the human X chromosome Human Molecular Genetics. 15: 2335-2347. PMID 16787966 DOI: 10.1093/hmg/ddl159 |
1 |
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| 2006 |
Valley CM, Willard HF. Genomic and epigenomic approaches to the study of X chromosome inactivation Current Opinion in Genetics and Development. 16: 240-245. PMID 16647845 DOI: 10.1016/j.gde.2006.04.008 |
1 |
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| 2006 |
Chadwick LH, Pertz LM, Broman KW, Bartolomei MS, Willard HF. Genetic control of X chromosome inactivation in mice: Definition of the Xce candidate interval Genetics. 173: 2103-2110. PMID 16582439 DOI: 10.1534/genetics.105.054882 |
1 |
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| 2006 |
Scott KC, Merrett SL, Willard HF. A heterochromatin barrier partitions the fission yeast centromere into discrete chromatin domains. Current Biology : Cb. 16: 119-29. PMID 16431364 DOI: 10.1016/j.cub.2005.11.065 |
1 |
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| 2006 |
Rudd MK, Wray GA, Willard HF. The evolutionary dynamics of alpha-satellite. Genome Research. 16: 88-96. PMID 16344556 DOI: 10.1101/gr.3810906 |
1 |
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| 2005 |
Higgins AW, Gustashaw KM, Willard HF. Engineered human dicentric chromosomes show centromere plasticity Chromosome Research. 13: 745-762. PMID 16331407 DOI: 10.1007/s10577-005-1009-2 |
1 |
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| 2005 |
Chadwick LH, Willard HF. Genetic and parent-of-origin influences on X chromosome choice in Xce heterozygous mice Mammalian Genome. 16: 691-699. PMID 16245026 DOI: 10.1007/s00335-005-0059-2 |
1 |
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| 2005 |
Willard HF, Angrist M, Ginsburg GS. Genomic medicine: Genetic variation and its impact on the future of health care Philosophical Transactions of the Royal Society B: Biological Sciences. 360: 1543-1550. PMID 16096102 DOI: 10.1098/rstb.2005.1683 |
1 |
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| 2005 |
Schueler MG, Dunn JM, Bird CP, Ross MT, Viggiano L, Rocchi M, Willard HF, Green ED. Progressive proximal expansion of the primate X chromosome centromere Proceedings of the National Academy of Sciences of the United States of America. 102: 10563-10568. PMID 16030148 DOI: 10.1073/pnas.0503346102 |
1 |
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| 2005 |
Basu J, Compitello G, Stromberg G, Willard HF, Van Bokkelen G. Efficient assembly of de novo human artificial chromosomes from large genomic loci. Bmc Biotechnology. 5: 21. PMID 15998466 DOI: 10.1186/1472-6750-5-21 |
1 |
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| 2005 |
Basu J, Willard HF. Artificial and engineered chromosomes: non-integrating vectors for gene therapy. Trends in Molecular Medicine. 11: 251-8. PMID 15882613 DOI: 10.1016/j.molmed.2005.03.006 |
1 |
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| 2005 |
Carrel L, Willard HF. X-inactivation profile reveals extensive variability in X-linked gene expression in females Nature. 434: 400-404. PMID 15772666 DOI: 10.1038/nature03479 |
1 |
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| 2005 |
Basu J, Stromberg G, Compitello G, Willard HF, Van Bokkelen G. Rapid creation of BAC-based human artificial chromosome vectors by transposition with synthetic alpha-satellite arrays. Nucleic Acids Research. 33: 587-96. PMID 15673719 DOI: 10.1093/nar/gki207 |
1 |
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| 2004 |
Chadwick BP, Willard HF. Multiple spatially distinct types of facultative heterochromatin on the human inactive X chromosome. Proceedings of the National Academy of Sciences of the United States of America. 101: 17450-5. PMID 15574503 DOI: 10.1073/pnas.0408021101 |
1 |
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| 2004 |
Grimes BR, Babcock J, Rudd MK, Chadwick B, Willard HF. Assembly and characterization of heterochromatin and euchromatin on human artificial chromosomes. Genome Biology. 5: R89. PMID 15535865 DOI: 10.1186/gb-2004-5-11-r89 |
1 |
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| 2004 |
Rudd MK, Willard HF. Analysis of the centromeric regions of the human genome assembly Trends in Genetics. 20: 529-533. PMID 15475110 DOI: 10.1016/j.tig.2004.08.008 |
1 |
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| 2004 |
Watt VM, Willard HF. The human aminopeptidase N gene: isolation, chromosome localization, and DNA polymorphism analysis Human Genetics. 85: 651-654. PMID 1977688 DOI: 10.1007/BF00193592 |
1 |
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| 2004 |
Willard HF. Introductory Speech for David Page American Journal of Human Genetics. 74: 397-398. DOI: 10.1086/381769 |
1 |
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| 2003 |
Rudd MK, Schueler MG, Willard HF. Sequence organization and functional annotation of human centromeres Cold Spring Harbor Symposia On Quantitative Biology. 68: 141-149. PMID 15338612 |
1 |
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| 2003 |
Chadwick BP, Willard HF. Barring gene expression after XIST: maintaining facultative heterochromatin on the inactive X. Seminars in Cell & Developmental Biology. 14: 359-67. PMID 15015743 DOI: 10.1016/j.semcdb.2003.09.016 |
1 |
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| 2003 |
Simpson JL, de la Cruz F, Swerdloff RS, Samango-Sprouse C, Skakkebaek NE, Graham JM, Hassold T, Aylstock M, Meyer-Bahlburg HF, Willard HF, Hall JG, Salameh W, Boone K, Staessen C, Geschwind D, et al. Klinefelter syndrome: expanding the phenotype and identifying new research directions. Genetics in Medicine : Official Journal of the American College of Medical Genetics. 5: 460-8. PMID 14614399 DOI: 10.1097/01.GIM.0000095626.54201.D0 |
1 |
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| 2003 |
Rudd MK, Mays RW, Schwartz S, Willard HF. Human Artificial Chromosomes with Alpha Satellite-Based De Novo Centromeres Show Increased Frequency of Nondisjunction and Anaphase Lag Molecular and Cellular Biology. 23: 7689-7697. PMID 14560014 DOI: 10.1128/MCB.23.21.7689-7697.2003 |
1 |
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| 2003 |
Percec I, Thorvaldsen JL, Plenge RM, Krapp CJ, Nadeau JH, Willard HF, Bartolomei MS. An N-ethyl-N-nitrosourea mutagenesis screen for epigenetic mutations in the mouse Genetics. 164: 1481-1494. PMID 12930754 |
1 |
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| 2003 |
Chadwick BP, Willard HF. Chromatin of the Barr body: histone and non-histone proteins associated with or excluded from the inactive X chromosome. Human Molecular Genetics. 12: 2167-78. PMID 12915472 DOI: 10.1093/hmg/ddg229 |
1 |
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| 2003 |
Willard HF. Tales of the Y chromosome Nature. 423: 810-813. PMID 12815408 DOI: 10.1038/423810a |
1 |
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| 2003 |
Williams RS, Willard HF, Snyderman R. Personalized health planning Science. 300: 549. PMID 12714710 DOI: 10.1126/science.300.5619.549 |
1 |
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| 2003 |
Chadwick BP, Willard HF. SETting the stage. Eed-Enx1 leaves an epigenetic signature on the inactive X chromosome. Developmental Cell. 4: 445-7. PMID 12689584 DOI: 10.1016/S1534-5807(03)00097-2 |
1 |
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| 2002 |
Chadwick BP, Willard HF. Cell cycle-dependent localization of macroH2A in chromatin of the inactive X chromosome. The Journal of Cell Biology. 157: 1113-23. PMID 12082075 DOI: 10.1083/jcb.200112074 |
1 |
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| 2002 |
Hall LL, Byron M, Sakai K, Carrel L, Willard HF, Lawrence JB. An ectopic human XIST gene can induce chromosome inactivation in postdifferentiation human HT-1080 cells Proceedings of the National Academy of Sciences of the United States of America. 99: 8677-8682. PMID 12072569 DOI: 10.1073/pnas.132468999 |
1 |
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| 2002 |
Plenge RM, Stevenson RA, Lubs HA, Schwartz CE, Willard HF. Skewed X-chromosome inactivation is a common feature of X-linked mental retardation disorders. American Journal of Human Genetics. 71: 168-73. PMID 12068376 DOI: 10.1086/341123 |
1 |
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| 2002 |
Grimes BR, Rhoades AA, Willard HF. Alpha-satellite DNA and vector composition influence rates of human artificial chromosome formation. Molecular Therapy : the Journal of the American Society of Gene Therapy. 5: 798-805. PMID 12027565 DOI: 10.1006/mthe.2002.0612 |
1 |
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| 2002 |
Percec I, Plenge RM, Nadeau JH, Bartolomei MS, Willard HF. Autosomal dominant mutations affecting X inactivation choice in the mouse Science. 296: 1136-1139. PMID 12004136 DOI: 10.1126/science.1070087 |
1 |
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| 2002 |
Willard HF. 2001 ASHG Presidential Address. On black boxes and storytellers: lessons learned in human genetics. American Journal of Human Genetics. 70: 285-96. PMID 11781874 DOI: 10.1086/338917 |
1 |
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| 2001 |
Willard HF. You say tomato and i say tomahto: Human genetics and gene therapy Molecular Therapy. 4: 514. PMID 11735334 DOI: 10.1006/mthe.2001.0488 |
1 |
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| 2001 |
Schueler MG, Higgins AW, Rudd MK, Gustashaw K, Willard HF. Genomic and genetic definition of a functional human centromere Science. 294: 109-115. PMID 11588252 DOI: 10.1126/science.1065042 |
1 |
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| 2001 |
Willard HF, Carrel L. Making sense (and antisense) of the X inactivation center Proceedings of the National Academy of Sciences of the United States of America. 98: 10025-10027. PMID 11526224 DOI: 10.1073/pnas.191380198 |
1 |
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| 2001 |
Chadwick BP, Valley CM, Willard HF. Histone variant macroH2A contains two distinct macrochromatin domains capable of directing macroH2A to the inactive X chromosome. Nucleic Acids Research. 29: 2699-705. PMID 11433014 |
1 |
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| 2001 |
Willard HF. Neocentromeres and human artificial chromosomes: An unnatural act Proceedings of the National Academy of Sciences of the United States of America. 98: 5374-5376. PMID 11344277 DOI: 10.1073/pnas.111167398 |
1 |
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| 2001 |
Chadwick BP, Willard HF. Histone H2A variants and the inactive X chromosome: identification of a second macroH2A variant. Human Molecular Genetics. 10: 1101-13. PMID 11331621 |
1 |
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| 2001 |
Chadwick BP, Willard HF. A novel chromatin protein, distantly related to histone H2A, is largely excluded from the inactive X chromosome. The Journal of Cell Biology. 152: 375-84. PMID 11266453 DOI: 10.1083/jcb.152.2.375 |
1 |
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| 2001 |
Willard HF. Evolution and function of alpha satellite DNA Pathologie Biologie. 49: 390. DOI: 10.1016/S0369-8114(01)00183-3 |
1 |
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| 2000 |
Willard HF. Artificial chromosomes coming to life Science. 290: 1308-1309. PMID 11185406 DOI: 10.1126/science.290.5495.1308 |
1 |
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| 2000 |
Tsuchiya KD, Willard HF. Chromosomal domains and escape from X inactivation: Comparative X inactivation analysis in mouse and human Mammalian Genome. 11: 849-854. PMID 11003698 |
1 |
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| 2000 |
Schueler MG, Higgins AW, Nagaraja R, Tentler D, Dahl N, Gustashaw K, Willard HF. Large-insert clone/STS contigs in Xq11-q12, spanning deletions in patients with androgen insensitivity and mental retardation Genomics. 66: 104-109. PMID 10843811 DOI: 10.1006/geno.2000.6180 |
1 |
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| 2000 |
Plenge RM, Percec I, Nadeau JH, Willard HF. Expression-based assay of an X-linked gene to examine effects of the X- controlling element (Xce) locus Mammalian Genome. 11: 405-408. PMID 10790543 DOI: 10.1007/s003350010077 |
1 |
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| 2000 |
Thibonnier M, Graves MK, Wagner MS, Chatelain N, Soubrier F, Corvol P, Willard HF, Jeunemaitre X. Study of V1-vascular vasopressin receptor gene microsatellite polymorphisms in human essential hypertension Journal of Molecular and Cellular Cardiology. 32: 557-564. PMID 10756113 DOI: 10.1006/jmcc.2000.1108 |
1 |
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| 1999 |
Carrel L, Cottle AA, Goglin KC, Willard HF. A first-generation X-inactivation profile of the human X chromosome Proceedings of the National Academy of Sciences of the United States of America. 96: 14440-14444. PMID 10588724 DOI: 10.1073/pnas.96.25.14440 |
1 |
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| 1999 |
Willard HF, Hendrich BD. Breaking the silence in Rett syndrome Nature Genetics. 23: 127-128. PMID 10508498 DOI: 10.1038/13751 |
1 |
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| 1999 |
Higgins AW, Schueler MG, Willard HF. Chromosome engineering: Generation of mono- and dicentric isochromosomes in a somatic cell hybrid system Chromosoma. 108: 256-265. PMID 10460414 DOI: 10.1007/s004120050376 |
1 |
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| 1999 |
Tentler D, Gustavsson P, Leisti J, Schueler M, Chelly J, Timonen E, Annerén G, Willard HF, Dahl N. Deletion including the oligophrenin-1 gene associated with enlarged cerebral ventricles, cerebellar hypoplasia, seizures and ataxia European Journal of Human Genetics. 7: 541-548. PMID 10439959 DOI: 10.1038/sj.ejhg.5200320 |
1 |
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| 1999 |
Carrel L, Willard HF. 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 Proceedings of the National Academy of Sciences of the United States of America. 96: 7364-7369. PMID 10377420 DOI: 10.1073/pnas.96.13.7364 |
1 |
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| 1999 |
Plenge RM, Tranebjaerg L, Jensen PKA, Schwartz C, Willard HF. Evidence that mutations in the X-linked DDP gene cause incompletely penetrant and variable skewed X inactivation American Journal of Human Genetics. 64: 759-767. PMID 10053010 DOI: 10.1086/302286 |
1 |
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| 1998 |
Friedman JM, Blitzer M, Elsas LJ, Francke U, Willard HF. Clinical objectives in medical genetics for undergraduate medical students. Association of Professors of Human Genetics, Clinical Objectives Task Force. Genetics in Medicine : Official Journal of the American College of Medical Genetics. 1: 54-5. PMID 11261431 DOI: 10.1097/00125817-199811000-00013 |
1 |
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| 1998 |
Sullivan BA, Willard HF. Stable dicentric X chromosomes with two functional centromeres [1] Nature Genetics. 20: 227-228. PMID 9806536 DOI: 10.1038/3024 |
1 |
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| 1998 |
Miller AP, Willard HF. Chromosomal basis of X chromosome inactivation: identification of a multigene domain in Xp11.21-p11.22 that escapes X inactivation. Proceedings of the National Academy of Sciences of the United States of America. 95: 8709-14. PMID 9671743 DOI: 10.1073/pnas.95.15.8709 |
1 |
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| 1998 |
Carrel L, Willard HF. Counting on Xist Nature Genetics. 19: 211-212. PMID 9662385 DOI: 10.1038/878 |
1 |
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| 1998 |
White WM, Willard HF, Van Dyke DL, Wolff DJ. The spreading of X inactivation into autosomal material of an x;autosome translocation: evidence for a difference between autosomal and X-chromosomal DNA. American Journal of Human Genetics. 63: 20-8. PMID 9634520 DOI: 10.1086/301922 |
1 |
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| 1998 |
Willard HF. Centromeres: The missing link in the development of human artificial chromosomes Current Opinion in Genetics and Development. 8: 219-225. PMID 9610413 DOI: 10.1016/S0959-437X(98)80144-5 |
1 |
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| 1998 |
Willard HF. Human artificial chromosomes coming into focus Nature Biotechnology. 16: 415-417. PMID 9592384 |
1 |
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| 1998 |
Haaf T, Willard HF. Orangutan α-satellite monomers are closely related to the human consensus sequence Mammalian Genome. 9: 440-447. PMID 9585431 DOI: 10.1007/s003359900793 |
1 |
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| 1998 |
Greenfield A, Carrel L, Pennisi D, Philippe C, Quaderi N, Siggers P, Steiner K, Tam PP, Monaco AP, Willard HF, Koopman P. The UTX gene escapes X inactivation in mice and humans. Human Molecular Genetics. 7: 737-42. PMID 9499428 DOI: 10.1093/hmg/7.4.737 |
1 |
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| 1998 |
Mahtani MM, Willard HF. Physical and genetic mapping of the human X chromosome centromere: Repression of recombination Genome Research. 8: 100-110. PMID 9477338 |
1 |
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| 1998 |
Dal Zotto L, Quaderi NA, Elliott R, Lingerfelter PA, Carrel L, Valsecchi V, Montini E, Yen CH, Chapman V, Kalcheva I, Arrigo G, Zuffardi O, Thomas S, Willard HF, Ballabio A, et al. The mouse Mid1 gene: implications for the pathogenesis of Opitz syndrome and the evolution of the mammalian pseudoautosomal region. Human Molecular Genetics. 7: 489-99. PMID 9467009 DOI: 10.1093/hmg/7.3.489 |
1 |
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| 1998 |
Puck JM, Willard HF. X inactivation in females with X-linked disease New England Journal of Medicine. 338: 325-328. PMID 9445416 DOI: 10.1056/NEJM199801293380511 |
1 |
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| 1998 |
Willard HF, Davies KE. Complex genetics, complex diseases: Editorial overview Current Opinion in Genetics and Development. 8: 271-273. DOI: 10.1016/S0959-437X(98)80080-4 |
1 |
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| 1997 |
James RS, Dalton P, Gustashaw K, Wolff DJ, Willard HF, Mitchell C, Jacobs PA. Molecular characterization of isochromosomes of Xq. Annals of Human Genetics. 61: 485-90. PMID 9543548 DOI: 10.1046/j.1469-1809.1997.6160485.x |
1 |
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| 1997 |
Plenge RM, Hendrich BD, Schwartz C, Arena JF, Naumova A, Sapienza C, Winter RM, Willard HF. A promoter mutation in the XIST gene in two unrelated families with skewed X-chromosome inactivation Nature Genetics. 17: 353-356. PMID 9354806 DOI: 10.1038/ng1197-353 |
1 |
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| 1997 |
Ishikawa-Brush Y, Powell JF, Bolton P, Miller AP, Francis F, Willard HF, Lehrach H, Monaco AP. Autism and multiple exostoses associated with an X;8 translocation occurring within the GRPR gene and 3' to the SDC2 gene. Human Molecular Genetics. 6: 1241-50. PMID 9259269 DOI: 10.1093/hmg/6.8.1241 |
1 |
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| 1997 |
Depinet TW, Zackowski JL, Earnshaw WC, Kaffe S, Sekhon GS, Stallard R, Sullivan BA, Vance GH, Van Dyke DL, Willard HF, Zinn AB, Schwartz S. Characterization of neo-centromeres in marker chromosomes lacking detectable alpha-satellite DNA. Human Molecular Genetics. 6: 1195-204. PMID 9259264 DOI: 10.1093/hmg/6.8.1195 |
1 |
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| 1997 |
Wolff DJ, Gustashaw KM, Zurcher V, Ko L, White W, Weiss L, Van Dyke DL, Schwartz S, Willard HF. 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. Human Genetics. 100: 256-61. PMID 9254860 DOI: 10.1007/s004390050501 |
1 |
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| 1997 |
Haaf T, Willard HF. Chromosome-specific α-satellite DNA from the centromere of chimpanzee chromosome 4 Chromosoma. 106: 226-232. PMID 9254724 DOI: 10.1007/s004120050243 |
1 |
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| 1997 |
Brown CJ, Carrel L, Willard HF. Expression of genes from the human active and inactive X chromosomes American Journal of Human Genetics. 60: 1333-1343. PMID 9199554 |
1 |
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| 1997 |
Hendrich BD, Plenge RM, Willard HF. Identification and characterization of the human XIST gene promoter: Implications for models of X chromosome inactivation Nucleic Acids Research. 25: 2661-2671. PMID 9185579 DOI: 10.1093/nar/25.13.2661 |
1 |
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| 1997 |
Harrington JJ, Van Bokkelen G, Mays RW, Gustashaw K, Willard HF. Formation of de novo centromeres and construction of first-generation human artificial microchromosomes Nature Genetics. 15: 345-355. PMID 9090378 DOI: 10.1038/ng0497-345 |
1 |
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| 1997 |
Willard HF, Salz HK. Remodelling chromatin with RNA. Nature. 386: 228-9. PMID 9069277 DOI: 10.1038/386228a0 |
1 |
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| 1996 |
Sullivan BA, Schwartz S, Willard HF. Centromeres of the human chromosomes Environmental and Molecular Mutagenesis. 28: 182-191. PMID 8908179 DOI: 10.1002/(SICI)1098-2280(1996)28:3<182::AID-EM4>3.0.CO;2-G |
1 |
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| 1996 |
Carrel L, Hunt PA, Willard HF. Tissue and lineage-specific variation in inactive X chromosome expression of the murine Smcx gene Human Molecular Genetics. 5: 1361-1366. PMID 8872478 DOI: 10.1093/hmg/5.9.1361 |
1 |
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| 1996 |
Carrel L, Clemson CM, Dunn JM, Miller AP, Hunt PA, Lawrence JB, Willard HF. X inactivation analysis and DNA methylation studies of the ubiquitin activating enzyme E1 and PCTAIRE-1 genes in human and mouse. Human Molecular Genetics. 5: 391-401. PMID 8852665 DOI: 10.1093/hmg/5.3.391 |
1 |
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| 1996 |
Thibonnier M, Graves MK, Wagner MS, Auzan C, Clauser E, Willard HF. Structure, sequence, expression, and chromosomal localization of the human V1a vasopressin receptor gene Genomics. 31: 327-334. PMID 8838314 DOI: 10.1006/geno.1996.0055 |
1 |
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| 1996 |
Carrel L, Willard HF. An assay for X inactivation based on differential methylation at the fragile X locus, FMR1 American Journal of Medical Genetics. 64: 27-30. PMID 8826444 DOI: 10.1002/(SICI)1096-8628(19960712)64:1<27::AID-AJMG3>3.0.CO;2-O |
1 |
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| 1996 |
Willard HF. X chromosome inactivation and X-linked mental retardation American Journal of Medical Genetics. 64: 21-26. PMID 8826443 DOI: 10.1002/(SICI)1096-8628(19960712)64:1<21::AID-AJMG2>3.0.CO;2-U |
1 |
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| 1996 |
Coleman MP, Ambrose HJ, Carrel L, Németh AH, Willard HF, Davies KE. A novel gene, DXS8237E, lies within 20 kb upstream of UBE1 in Xp11.23 and has a different X inactivation status. Genomics. 31: 135-8. PMID 8808293 DOI: 10.1006/geno.1996.0022 |
1 |
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| 1996 |
Willard HF. Chromosome manipulation: A systematic approach toward understanding human chromosome structure and function Proceedings of the National Academy of Sciences of the United States of America. 93: 6847-6850. PMID 8692907 DOI: 10.1073/pnas.93.14.6847 |
1 |
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| 1996 |
Willard HF. X chromosome inactivation, XIST, and pursuit of the X-inactivation center Cell. 86: 5-7. PMID 8689687 DOI: 10.1016/S0092-8674(00)80071-9 |
1 |
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| 1996 |
Warburton PE, Haaf T, Gosden J, Lawson D, Willard HF. Characterization of a chromosome-specific chimpanzee alpha satellite subset: Evolutionary relationship to subsets on human chromosomes Genomics. 33: 220-228. PMID 8660971 DOI: 10.1006/geno.1996.0187 |
1 |
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| 1996 |
Naumova AK, Plenge RM, Bird LM, Leppert M, Morgan K, Willard HF, Sapienza C. Heritability of X chromosome - Inactivation phenotype in a large family American Journal of Human Genetics. 58: 1111-1119. PMID 8651287 |
1 |
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| 1996 |
Clemson CM, McNeil JA, Willard HF, Lawrence JB. XIST RNA paints the inactive X chromosome at interphase: evidence for a novel RNA involved in nuclear/chromosome structure. The Journal of Cell Biology. 132: 259-75. PMID 8636206 DOI: 10.1083/jcb.132.3.259 |
1 |
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| 1996 |
Wolff DJ, Miller AP, Van Dyke DL, Schwartz S, Willard HF. Molecular definition of breakpoints associated with human Xq isochromosomes: implications for mechanisms of formation. American Journal of Human Genetics. 58: 154-60. PMID 8554051 |
1 |
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| 1995 |
Kirchgessner CU, Warren ST, Willard HF. X inactivation of the FMR1 fragile X mental retardation gene Journal of Medical Genetics. 32: 925-929. PMID 8825916 DOI: 10.1136/jmg.32.12.925 |
1 |
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| 1995 |
Rupert JL, Brown CJ, Willard HF. Direct detection of non-random X chromosome inactivation by use of a transcribed polymorphism in the XIST gene European Journal of Human Genetics. 3: 333-343. PMID 8825575 |
1 |
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| 1995 |
Warburton PE, Willard HF. Interhomologue sequence variation of alpha satellite DNA from human chromosome 17: Evidence for concerted evolution along haplotypic lineages Journal of Molecular Evolution. 41: 1006-1015. PMID 8587099 DOI: 10.1007/BF00173182 |
1 |
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| 1995 |
Hendrich BD, Willard HF. Epigenetic regulation of gene expression: The effect of altered chromatin structure from yeast to mammals Human Molecular Genetics. 4: 1765-1777. PMID 8541877 |
1 |
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| 1995 |
Alitalo T, Francis F, Kere J, Lehrach H, Schlessinger D, Willard HF. A 6-Mb YAC contig in Xp22.1-p22.2 spanning the DXS69E, XE59, GLRA2, PIGA, GRPR, CALB3, and PHKA2 genes. Genomics. 25: 691-700. PMID 7759104 DOI: 10.1016/0888-7543(95)80012-B |
1 |
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| 1995 |
Sultana R, Adler DA, Edelhoff S, Carrel L, Lee KH, Chapman VC, Willard HF, Disteche CM. The mouse Sb1.8 gene located at the distal end of the X chromosome is subject to X inactivation. Human Molecular Genetics. 4: 257-63. PMID 7757076 DOI: 10.1093/hmg/4.2.257 |
1 |
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| 1995 |
Brown CJ, Miller AP, Carrel L, Rupert JL, Davies KE, Willard HF. The DXS423E gene in Xp11.21 escapes X chromosome inactivation. Human Molecular Genetics. 4: 251-5. PMID 7757075 DOI: 10.1093/hmg/4.2.251 |
1 |
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| 1995 |
Litt M, Kramer P, Kort E, Fain P, Cox S, Root D, White R, Weissenbach J, Donis-Keller H, Gatti R, Weber J, Nakamura Y, Julier C, Hayashi K, Spurr N, ... ... Willard HF, et al. The CEPH Consortium Linkage Map of Human Chromosome 11 Genomics. 27: 101-112. PMID 7665156 DOI: 10.1006/geno.1995.1011 |
1 |
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| 1995 |
Miller AP, Gustashaw K, Wolff DJ, Rider SH, Monaco AP, Eble B, Schlessinger D, Gorski JL, van Ommen GJ, Weissenbach J. Three genes that escape X chromosome inactivation are clustered within a 6 Mb YAC contig and STS map in Xp11.21-p11.22. Human Molecular Genetics. 4: 731-9. PMID 7633424 DOI: 10.1093/hmg/4.4.731 |
1 |
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| 1995 |
Davies KE, Willard HF. Genetics of disease Current Opinion in Genetics and Development. 5: 295-297. |
1 |
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| 1994 |
Brown CJ, Willard HF. The human X-inactivation centre is not required for maintenance of X-chromosome inactivation Nature. 368: 154-156. PMID 8139659 |
1 |
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| 1994 |
Wolff DJ, Brown CJ, Schwartz S, Duncan AM, Surti U, Willard HF. Small marker X chromosomes lack the X inactivation center: implications for karyotype/phenotype correlations. American Journal of Human Genetics. 55: 87-95. PMID 8023855 |
1 |
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| 1994 |
Reed V, Laval SH, McCabe V, Willard HF, Boyd Y. Mapping of loci and translocation breakpoints in Xq13: isolation of a conserved locus that maps close to CCG1 in human and mouse Mammalian Genome. 5: 237-240. PMID 8012115 DOI: 10.1007/BF00360553 |
1 |
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| 1994 |
Lafrenière RG, Carrel L, Willard HF. A novel transmembrane transporter encoded by the XPCT gene in xq13.2 Human Molecular Genetics. 3: 1133-1139. PMID 7981683 DOI: 10.1093/hmg/3.7.1133 |
1 |
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| 1994 |
Rack KA, Chelly J, Gibbons RJ, Rider S, Benjamin D, Lafreniére RG, Oscier D, Hendriks RW, Craig IW, Willard HF. Absence of the XIST gene from late-replicating isodicentric X chromosomes in leukaemia. Human Molecular Genetics. 3: 1053-9. PMID 7981672 DOI: 10.1093/hmg/3.7.1053 |
1 |
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| 1994 |
Willard HF, Cremers F, Mandel JL, Monaco AP, Nelson DL, Schlessinger D. Report and abstracts of the Fifth International Workshop on Human X Chromosome Mapping 1994. Heidelberg, Germany, April 24-27, 1994. Cytogenetics and Cell Genetics. 67: 295-358. PMID 7924455 |
1 |
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| 1994 |
Gustashaw KM, Zurcher V, Dickerman LH, Stallard R, Willard HF. Partial X chromosome trisomy with functional disomy of Xp due to failure of X inactivation American Journal of Medical Genetics. 53: 39-45. PMID 7802034 DOI: 10.1002/ajmg.1320530109 |
1 |
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| 1994 |
Willard HF, Davies KE. Editorial Human Molecular Genetics. 3. |
1 |
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| 1993 |
Willard HF. The needle found!!! trinucleotide repeat expansion in the huntington's disease gene Human Molecular Genetics. 2: 497-498. PMID 8518785 DOI: 10.1093/hmg/2.5.497 |
1 |
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| 1993 |
Mahtani MM, Willard HF. A polymorphic X-linked tetranucleotide repeat locus displaying a high rate of new mutation: Implications for mechanisms of mutation at short tandem repeat loci Human Molecular Genetics. 2: 431-437. PMID 8504304 DOI: 10.1093/hmg/2.4.431 |
1 |
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| 1993 |
Willard HF. Cloning of the X-linked glycerol kinase gene Human Molecular Genetics. 2: 95-96. PMID 8499911 DOI: 10.1093/hmg/2.2.95 |
1 |
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| 1993 |
Warburton PE, Waye JS, Willard HF. Nonrandom localization of recombination events in human alpha satellite repeat unit variants: Implications for higher-order structural characteristics within centromeric heterochromatin Molecular and Cellular Biology. 13: 6520-6529. PMID 8413251 |
1 |
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| 1993 |
Lafrenière RG, Willard HF. Pulsed-Field Map of Xq13 in the Region of the Human X Inactivation Center Genomics. 17: 502-506. PMID 8406503 DOI: 10.1006/geno.1993.1356 |
1 |
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| 1993 |
Schlessinger D, Mandel JL, Monaco AP, Nelson DL, Willard HF. Report and abstracts of the Fourth International Workshop on Human X Chromosome Mapping 1993. St. Louis, Missouri, May 9-12, 1993. Cytogenetics and Cell Genetics. 64: 147-94. PMID 8404034 |
1 |
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| 1993 |
Lafrenlère RG, Brown CJ, Rider S, Chelly J, Taillon-miller P, Chinault AC, Monaco AP, Willard HF. 2.6 mb YAC contig of the human X inactivation center region in Xq13: Physical linkage of the RPS4X, PHKA1, XIST and DXS128E genes Human Molecular Genetics. 2: 1105-1115. PMID 8401491 DOI: 10.1093/hmg/2.8.1105 |
1 |
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| 1993 |
Puck JM, Deschenes SM, Porter JC, Dutra AS, Brown CJ, Willard HF, Henthorn PS. The interleukin-2 receptor γ chain maps to Xq13.1 and is mutated in X-linked severe combined immunodeficiency, SCIDX1 Human Molecular Genetics. 2: 1099-1104. PMID 8401490 DOI: 10.1093/hmg/2.8.1099 |
1 |
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| 1993 |
Leppig KA, Brown CJ, Bressler SL, Gustashaw K, Pagon RA, Willard HF, Disteche CM. Mapping of the distal boundary of the X-inactivation center in a rearranged X chromosome from a female expressing XIST. Human Molecular Genetics. 2: 883-7. PMID 8364571 DOI: 10.1093/hmg/2.7.883 |
1 |
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| 1993 |
Hendrich BD, Brown CJ, Willard HF. Evolutionary conservation of possible functional domains of the human and murine Xist genes Human Molecular Genetics. 2: 663-672. PMID 8353487 DOI: 10.1093/hmg/2.6.663 |
1 |
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| 1993 |
Tyler-Smith C, Willard HF. Mammalian chromosome structure Current Opinion in Genetics and Development. 3: 390-397. PMID 8353411 DOI: 10.1016/0959-437X(93)90110-B |
1 |
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| 1993 |
Duncan AMV, Macdonald A, Brown CJ, Wolff D, Willard HF, Sutton B. Characterization of a small supernumerary ring X chromosome by fluorescence in situ hybridization American Journal of Medical Genetics. 47: 1153-1156. PMID 8291547 DOI: 10.1002/ajmg.1320470804 |
1 |
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| 1993 |
Greig GM, Warburton PE, Willard HF. Organization and evolution of an alpha satellite DNA subset shared by human chromosomes 13 and 21 Journal of Molecular Evolution. 37: 464-475. PMID 8283478 DOI: 10.1007/BF00160427 |
1 |
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| 1993 |
Greig GM, Sharp CB, Carrel L, Willard HF. Duplicated zinc finger protein genes on the proximal short arm of the human X chromosome: isolation, characterization and X-inactivation studies. Human Molecular Genetics. 2: 1611-8. PMID 8268913 DOI: 10.1093/hmg/2.10.1611 |
1 |
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| 1993 |
Willard HF. The inv(16) in acute nonlymphocytic leukemia: A turnabout for myosin heavy chain Human Molecular Genetics. 2: 1525-1526. PMID 8268904 DOI: 10.1093/hmg/2.10.1525 |
1 |
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| 1993 |
Willard HF, Brown CJ, Carrel L, Hendrich B, Miller AP. Epigenetic and chromosomal control of gene expression: molecular and genetic analysis of X chromosome inactivation. Cold Spring Harbor Symposia On Quantitative Biology. 58: 315-22. PMID 7956044 |
1 |
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| 1993 |
Haff T, Schmid M, Steinlein C, Galetti PM, Willard HF. Organization and molecular cytogenetics of a satellite DNA family from Hoplias malabaricus (Pisces, Erythrinidae) Chromosome Research. 1: 77-86. DOI: 10.1007/BF00710610 |
1 |
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| 1993 |
Brown CJ, Willard HF. Molecular and genetic studies of human X chromosome in activation Advances in Developmental Biology (1992). 2: 37-72. |
1 |
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| 1993 |
Willard HF, Davies KE. Mammalian genetics Editorial overview: a sampler of current opinion Current Opinion in Genetics and Development. 3: 387-389. |
1 |
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| 1993 |
Schlessinger D, Mandel JL, Monaco AP, Nelson DL, Willard HF. Report of the Fourth International Workshop on Human X Chromosome mapping 1993 Cytogenetics and Cell Genetics. 64: 148-170. |
1 |
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| 1992 |
Haaf T, Summer AT, Köhler J, Willard HF, Schmid M. A microchromosome derived from chromosome 11 in a patient with the CREST syndrome of scleroderma Cytogenetic and Genome Research. 60: 12-17. PMID 1582251 DOI: 10.1159/000133284 |
1 |
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| 1992 |
Cotter PD, Willard HF, Gorski JL, Bishop DF. Assignment of human erythroid δ-aminolevulinate synthase (ALAS2) to a distal subregion of band Xp11.21 by PCR analysis of somatic cell hybrids containing X;Autosome translocations Genomics. 13: 211-212. PMID 1577484 DOI: 10.1016/0888-7543(92)90223-F |
1 |
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| 1992 |
Haaf T, Willard HF. Organization, polymorphism, and molecular cytogenetics of chromosome-specific α-satellite DNA from the centromere of chromosome 2 Genomics. 13: 122-128. PMID 1577477 DOI: 10.1016/0888-7543(92)90211-A |
1 |
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| 1992 |
Greig GM, Willard HF. β satellite DNA: Characterization and localization of two subfamilies from the distal and proximal short arms of the human acrocentric chromosomes Genomics. 12: 573-580. PMID 1559708 DOI: 10.1016/0888-7543(92)90450-7 |
1 |
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| 1992 |
Haaf T, Warburton PE, Willard HF. Integration of human α-satellite DNA into simian chromosomes: Centromere protein binding and disruption of normal chromosome segregation Cell. 70: 681-696. PMID 1505032 DOI: 10.1016/0092-8674(92)90436-G |
1 |
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| 1992 |
Ballabio A, Willard HF. Mammalian X-chromosome inactivation and the XIST gene Current Opinion in Genetics and Development. 2: 439-447. PMID 1504619 DOI: 10.1016/S0959-437X(05)80155-8 |
1 |
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| 1992 |
Wevrick R, Willard VP, Willard HF. Structure of DNA near long tandem arrays of alpha satellite DNA at the centromere of human chromosome 7 Genomics. 14: 912-923. PMID 1478672 DOI: 10.1016/S0888-7543(05)80112-0 |
1 |
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| 1992 |
Lorber BJ, Grantham M, Peters J, Willard HF, Hassold TJ. Nondisjunction of chromosome 21: comparisons of cytogenetic and molecular studies of the meiotic stage and parent of origin. American Journal of Human Genetics. 51: 1265-76. PMID 1463010 |
1 |
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| 1992 |
Warburton PE, Willard HF. PCR amplification of tandemly repeated DNA: Analysis of intra- and interchromosomal sequence variation and homologous unequal crossing-over in human alpha satellite DNA Nucleic Acids Research. 20: 6033-6042. PMID 1461735 DOI: 10.1093/nar/20.22.6033 |
1 |
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| 1992 |
Mandel JL, Monaco AP, Nelson DL, Schlessinger D, Willard HF, Chipperfield M, Pearson P, Gilna P, Cinkosky M. Genome maps III. 1992. Wall Chart. Science (New York, N.Y.). 258: 87-102. PMID 1439771 DOI: 10.1126/science.1439771 |
1 |
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| 1992 |
Brown CJ, Hendrich BD, Rupert JL, Lafrenière RG, Xing Y, Lawrence J, Willard HF. The human XIST gene: Analysis of a 17 kb inactive X-specific RNA that contains conserved repeats and is highly localized within the nucleus Cell. 71: 527-542. PMID 1423611 DOI: 10.1016/0092-8674(92)90520-M |
1 |
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| 1992 |
Bascom RA, García-Heras J, Hsieh CL, Gerhard DS, Jones C, Francke U, Willard HF, Ledbetter DH, Mclnnes RR. Localization of the photoreceptor gene ROM1 to human chromosome 11 and mouse chromosome 19: Sublocalization to human 11q13 between PGA and PYCM American Journal of Human Genetics. 51: 1028-1035. PMID 1415249 |
1 |
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| 1992 |
Quigley CA, Friedman KJ, Johnson A, Lafreniere RG, Silverman LM, Lubahn DB, Brown TR, Wilson EM, Willard HF, French FS. Complete deletion of the androgen receptor gene: definition of the null phenotype of the androgen insensitivity syndrome and determination of carrier status. The Journal of Clinical Endocrinology and Metabolism. 74: 927-33. PMID 1347772 DOI: 10.1210/jcem.74.4.1347772 |
1 |
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| 1992 |
Corcos IA, Lafrenière RG, Begy CR, Loch-Caruso R, Willard HF, Glover TW. Refined localization of human connexin32 gene locus, GJB1, to Xq13.1 Genomics. 13: 479-480. PMID 1319395 DOI: 10.1016/0888-7543(92)90278-Z |
1 |
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| 1992 |
Willard HF. Centromeres-primary constrictions are primarily complicated Human Molecular Genetics. 1: 667-668. PMID 1302604 DOI: 10.1093/hmg/1.9.667 |
1 |
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| 1992 |
Mandel JL, Monaco AP, Nelson DL, Schlessinger D, Willard HF, Chipperfield M, Pearson P, Gilna P, Cinkosky M. Genome maps III Science. 258: 87-88. |
1 |
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| 1991 |
Wevrick R, Willard HF. Physical map of the centromeric region of human chromosome 7: Relationship between two distinct alpha satellite arrays Nucleic Acids Research. 19: 2295-2301. PMID 2041770 DOI: 10.1093/nar/19.9.2295 |
1 |
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| 1991 |
Borsani G, Tonlorenzi R, Simmler MC, Dandolo L, Arnaud D, Capra V, Grompe M, Pizzuti A, Muzny D, Lawrence C, Willard HF, Avner P, Ballabio A. Characterization of a murine gene expressed from the inactive X chromosome Nature. 351: 325-329. PMID 2034278 |
1 |
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| 1991 |
Brown CJ, Lafreniere RG, Powers VE, Sebastio G, Ballabio A, Pettigrew AL, Ledbetter DH, Levy E, Craig IW, Willard HF. Localization of the X inactivation centre on the human X chromosome in Xq13 Nature. 349: 82-84. PMID 1985270 |
1 |
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| 1991 |
Brown CJ, Ballabio A, Rupert JL, Lafreniere RG, Grompe M, Tonlorenzi R, Willard HF. A gene from the region of the human X inactivation centre is expressed exclusively from the inactive X chromosome Nature. 349: 38-44. PMID 1985261 |
1 |
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| 1991 |
Franco B, Guioli S, Pragliola A, Incerti B, Bardoni B, Tonlorenzi R, Carrozzo R, Maestrini E, Pieretti M, Taillon-Miller P, Brown CJ, Willard HF, Lawrence C, Graziella Persico M, Camerino G, et al. A gene deleted in Kallmann's syndrome shares homology with neural cell adhesion and axonal path-finding molecules. Nature. 353: 529-36. PMID 1922361 DOI: 10.1038/353529a0 |
1 |
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| 1991 |
Kirchgessner CU, Trofatter JA, Mahtani MM, Willard HF, DeGennaro LJ. A highly polymorphic dinucleotide repeat on the proximal short arm of the human X chromosome: Linkage mapping of the synapsin I/A-raf-I genes American Journal of Human Genetics. 49: 184-191. PMID 1905878 |
1 |
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| 1991 |
Losada AP, Wessman M, Tiainen M, Hopman AHN, Willard HF, Sole F, Caballín MR, Woessner S, Knuutila S. Trisomy 12 in chronic lymphocytic leukemia: An interphase cytogenetic study Blood. 78: 775-779. PMID 1859890 |
1 |
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| 1991 |
Fujii J, Zarain-Herzberg A, Willard HF, Tada M, MacLennan DH. Structure of the rabbit phospholamban gene, cloning of the human cDNA, and assignment of the gene to human chromosome 6. The Journal of Biological Chemistry. 266: 11669-75. PMID 1828805 |
1 |
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| 1991 |
Greig GM, Parikh S, George J, Powers VE, Willard HF. Molecular cytogenetics of α satellite DNA from chromosome 12: Fluorescence in situ hybridization and description of DNA and array length polymorphisms Cytogenetics and Cell Genetics. 56: 144-148. PMID 1675980 |
1 |
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| 1991 |
Davies KE, Mandel JL, Monaco AP, Nussbaum RL, Willard HF. Report of the committee on the genetic constitution of the X chromosome Cytogenetics and Cell Genetics. 58: 853-966. |
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