Huntington Willard

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Wheeler Bayly S; Blau Jared A; Willard Huntington F; Scott Kristin C
The impact of local genome sequence on defining heterochromatin domains.
Kawamoto Kensaku; Lobach David F; Willard Huntington F; Ginsburg Geoffrey S
A national clinical decision support infrastructure to enable the widespread and consistent practice of genomic and personalized medicine.
Tuckson Reed V; Willard Huntington F
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).

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All Publications

2009: Wheeler Bayly S; Blau Jared A; Willard Huntington F; Scott Kristin C
The impact of local genome sequence on defining heterochromatin domains.
PLoS genetics 2009;5(4):e1000453.
2009: Kawamoto Kensaku; Lobach David F; Willard Huntington F; Ginsburg Geoffrey S
A national clinical decision support infrastructure to enable the widespread and consistent practice of genomic and personalized medicine.
BMC medical informatics and decision making 2009;9():17.
2008: Tuckson Reed V; Willard Huntington F
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 & medicine (1982) 2008;67(4):673-4; author reply 675-83.
2008: Haga Susanne B; Willard Huntington F
Letting the genome out of the bottle.
The New England journal of medicine 2008;358(20):2184; author reply 2185.
2008: Horvath Julie E; Weisrock David W; Embry Stephanie L; Fiorentino Isabella; Balhoff James P; Kappeler Peter; Wray Gregory A; Willard Huntington F; Yoder Anne D
Development and application of a phylogenomic toolkit: resolving the evolutionary history of Madagascar's lemurs.
Genome research 2008;18(3):489-99.
2007: Horvath Julie E; Willard Huntington F
Primate comparative genomics: lemur biology and evolution.
Trends in genetics : TIG 2007;23(4):173-82.
2007: Basu Joydeep; Willard Huntington F; Stromberg Gregory
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.] 2007;Chapter 5():Unit 5.18.
2007: Scott Kristin C; White Caroline V; Willard Huntington F
An RNA polymerase III-dependent heterochromatin barrier at fission yeast centromere 1.
PloS one 2007;2(10):e1099.
2006: Haga Susanne B; Willard Huntington F
Defining the spectrum of genome policy.
Nature reviews. Genetics 2006;7(12):966-72.
2006: Shianna Kevin V; Willard Huntington F
Human genomics: in search of normality.
Nature 2006;444(7118):428-9.
2006: Basu Joydeep; Willard Huntington F
Human artificial chromosomes: potential applications and clinical considerations.
Pediatric clinics of North America 2006;53(5):843-53, viii.
2006: Wang Zhong; Willard Huntington F; Mukherjee Sayan; Furey Terrence S
Evidence of influence of genomic DNA sequence on human X chromosome inactivation.
PLoS computational biology 2006;2(9):e113.
2006: Amos-Landgraf James M; Cottle Amy; Plenge Robert M; Friez Mike; Schwartz Charles E; Longshore John; Willard Huntington F
X chromosome-inactivation patterns of 1,005 phenotypically unaffected females.
American journal of human genetics 2006;79(3):493-9.
2006: Valley Cory M; Pertz Lisa M; Balakumaran Bala S; Willard Huntington F
Chromosome-wide, allele-specific analysis of the histone code on the human X chromosome.
Human molecular genetics 2006;15(15):2335-47.
2006: Chadwick Lisa Helbling; Pertz Lisa M; Broman Karl W; Bartolomei Marisa S; Willard Huntington F
Genetic control of X chromosome inactivation in mice: definition of the Xce candidate interval.
Genetics 2006;173(4):2103-10.
2006: Valley Cory M; Willard Huntington F
Genomic and epigenomic approaches to the study of X chromosome inactivation.
Current opinion in genetics & development 2006;16(3):240-5.
2006: Scott Kristin C; Merrett Stephanie L; Willard Huntington F
A heterochromatin barrier partitions the fission yeast centromere into discrete chromatin domains.
Current biology : CB 2006;16(2):119-29.
2006: Rudd M Katharine; Wray Gregory A; Willard Huntington F
The evolutionary dynamics of alpha-satellite.
Genome research 2006;16(1):88-96.
2005: Chadwick Lisa Helbling; Willard Huntington F
Genetic and parent-of-origin influences on X chromosome choice in Xce heterozygous mice.
Mammalian genome : official journal of the International Mammalian Genome Society 2005;16(9):691-9.
2005: Willard Huntington F; Angrist Misha; Ginsburg Geoffrey S
Genomic medicine: genetic variation and its impact on the future of health care.
Philosophical transactions of the Royal Society of London. Series B, Biological sciences 2005;360(1460):1543-50.
2005: Schueler Mary G; Dunn John M; Bird Christine P; Ross Mark T; Viggiano Luigi; Rocchi Mariano; Willard Huntington F; Green Eric D
Progressive proximal expansion of the primate X chromosome centromere.
Proceedings of the National Academy of Sciences of the United States of America 2005;102(30):10563-8.
2005: Basu Joydeep; Willard Huntington F
Artificial and engineered chromosomes: non-integrating vectors for gene therapy.
Trends in molecular medicine 2005;11(5):251-8.
2005: Carrel Laura; Willard Huntington F
X-inactivation profile reveals extensive variability in X-linked gene expression in females.
Nature 2005;434(7031):400-4.
2005: Higgins Anne W; Gustashaw Karen M; Willard Huntington F
Engineered human dicentric chromosomes show centromere plasticity.
Chromosome research : an international journal on the molecular, supramolecular and evolutionary aspects of chromosome biology 2005;13(8):745-62.
2005: Basu Joydeep; Compitello George; Stromberg Gregory; Willard Huntington F; Van Bokkelen Gil
Efficient assembly of de novo human artificial chromosomes from large genomic loci.
BMC biotechnology 2005;5():21.
2005: Basu Joydeep; Stromberg Gregory; Compitello George; Willard Huntington F; Van Bokkelen Gil
Rapid creation of BAC-based human artificial chromosome vectors by transposition with synthetic alpha-satellite arrays.
Nucleic acids research 2005;33(2):587-96.
2004: Chadwick Brian P; Willard Huntington F
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 2004;101(50):17450-5.
2004: Rudd M Katharine; Willard Huntington F
Analysis of the centromeric regions of the human genome assembly.
Trends in genetics : TIG 2004;20(11):529-33.
2004: Grimes Brenda R; Babcock Jennifer; Rudd M Katharine; Chadwick Brian; Willard Huntington F
Assembly and characterization of heterochromatin and euchromatin on human artificial chromosomes.
Genome biology 2004;5(11):R89.
2003: Chadwick Brian P; Willard Huntington F
Barring gene expression after XIST: maintaining facultative heterochromatin on the inactive X.
Seminars in cell & developmental biology 2003;14(6):359-67.
2003: Simpson Joe Leigh; de la Cruz Felix; Swerdloff Ronald S; Samango-Sprouse Carole; Skakkebaek Niels E; Graham John M; Hassold Terry; Aylstock Melissa; Meyer-Bahlburg Heino F L; Willard Huntington F; Hall Judith G; Salameh Wael; Boone Kyle; Staessen Catherine; Geschwind Dan; Giedd Jay; Dobs Adrian S; Rogol Alan; Brinton Bonnie; Paulsen C Alvin
Klinefelter syndrome: expanding the phenotype and identifying new research directions.
Genetics in medicine : official journal of the American College of Medical Genetics 2003;5(6):460-8.
2003: Rudd M Katharine; Mays Robert W; Schwartz Stuart; Willard Huntington F
Human artificial chromosomes with alpha satellite-based de novo centromeres show increased frequency of nondisjunction and anaphase lag.
Molecular and cellular biology 2003;23(21):7689-97.
2003: Chadwick Brian P; Willard Huntington F
Chromatin of the Barr body: histone and non-histone proteins associated with or excluded from the inactive X chromosome.
Human molecular genetics 2003;12(17):2167-78.
2003: Percec Ivona; Thorvaldsen Joanne L; Plenge Robert M; Krapp Christopher J; Nadeau Joseph H; Willard Huntington F; Bartolomei Marisa S
An N-ethyl-N-nitrosourea mutagenesis screen for epigenetic mutations in the mouse.
Genetics 2003;164(4):1481-94.
2003: Willard Huntington F
Tales of the Y chromosome.
Nature 2003;423(6942):810-1, 813.
2003: Williams R Sanders; Willard Huntington F; Snyderman Ralph
Personalized health planning.
Science (New York, N.Y.) 2003;300(5619):549.
2003: Chadwick Brian P; Willard Huntington F
SETting the stage. Eed-Enx1 leaves an epigenetic signature on the inactive X chromosome.
Developmental cell 2003;4(4):445-7.
2003: Rudd M K; Schueler M G; Willard H F
Sequence organization and functional annotation of human centromeres.
Cold Spring Harbor symposia on quantitative biology 2003;68():141-9.
2002: Plenge Robert M; Stevenson Roger A; Lubs Herbert A; Schwartz Charles E; Willard Huntington F
Skewed X-chromosome inactivation is a common feature of X-linked mental retardation disorders.
American journal of human genetics 2002;71(1):168-73.
2002: Chadwick Brian P; Willard Huntington F
Cell cycle-dependent localization of macroH2A in chromatin of the inactive X chromosome.
The Journal of cell biology 2002;157(7):1113-23.
2002: Hall Lisa L; Byron Meg; Sakai Kosuke; Carrel Laura; Willard Huntington F; Lawrence Jeanne B
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 2002;99(13):8677-82.
2002: Grimes Brenda R; Rhoades Angela A; Willard Huntington F
Alpha-satellite DNA and vector composition influence rates of human artificial chromosome formation.
Molecular therapy : the journal of the American Society of Gene Therapy 2002;5(6):798-805.
2002: Percec Ivona; Plenge Robert M; Nadeau Joseph H; Bartolomei Marisa S; Willard Huntington F
Autosomal dominant mutations affecting X inactivation choice in the mouse.
Science (New York, N.Y.) 2002;296(5570):1136-9.
2002: Willard Huntington F
2001 ASHG Presidential Address. On black boxes and storytellers: lessons learned in human genetics.
American journal of human genetics 2002;70(2):285-96.
2001: Schueler M G; Higgins A W; Rudd M K; Gustashaw K; Willard H F
Genomic and genetic definition of a functional human centromere.
Science (New York, N.Y.) 2001;294(5540):109-15.
2001: Willard H F; Carrel L
Making sense (and antisense) of the X inactivation center.
Proceedings of the National Academy of Sciences of the United States of America 2001;98(18):10025-7.
2001: Chadwick B P; Valley C M; Willard H F
Histone variant macroH2A contains two distinct macrochromatin domains capable of directing macroH2A to the inactive X chromosome.
Nucleic acids research 2001;29(13):2699-705.
2001: Willard H F
Neocentromeres and human artificial chromosomes: an unnatural act.
Proceedings of the National Academy of Sciences of the United States of America 2001;98(10):5374-6.
2001: Chadwick B P; Willard H F
Histone H2A variants and the inactive X chromosome: identification of a second macroH2A variant.
Human molecular genetics 2001;10(10):1101-13.
2001: Chadwick B P; Willard H F
A novel chromatin protein, distantly related to histone H2A, is largely excluded from the inactive X chromosome.
The Journal of cell biology 2001;152(2):375-84.
2000: Willard H F
Genomics and gene therapy. Artificial chromosomes coming to life.
Science (New York, N.Y.) 2000;290(5495):1308-9.
2000: Tsuchiya K D; Willard H F
Chromosomal domains and escape from X inactivation: comparative X inactivation analysis in mouse and human.
Mammalian genome : official journal of the International Mammalian Genome Society 2000;11(10):849-54.
2000: Schueler M G; Higgins A W; Nagaraja R; Tentler D; Dahl N; Gustashaw K; Willard H F
Large-insert clone/STS contigs in Xq11-q12, spanning deletions in patients with androgen insensitivity and mental retardation.
Genomics 2000;66(1):104-9.
2000: Plenge R M; Percec I; Nadeau J H; Willard H F
Expression-based assay of an X-linked gene to examine effects of the X-controlling element (Xce) locus.
Mammalian genome : official journal of the International Mammalian Genome Society 2000;11(5):405-8.
1999: Carrel L; Cottle A A; Goglin K C; Willard H F
A first-generation X-inactivation profile of the human X chromosome.
Proceedings of the National Academy of Sciences of the United States of America 1999;96(25):14440-4.
1999: Willard H F; Hendrich B D
Breaking the silence in Rett syndrome.
Nature genetics 1999;23(2):127-8.
1999: Higgins A W; Schueler M G; Willard H F
Chromosome engineering: generation of mono- and dicentric isochromosomes in a somatic cell hybrid system.
Chromosoma 1999;108(4):256-65.
1999: Tentler D; Gustavsson P; Leisti J; Schueler M; Chelly J; Timonen E; Annerén G; Willard H F; Dahl N
Deletion including the oligophrenin-1 gene associated with enlarged cerebral ventricles, cerebellar hypoplasia, seizures and ataxia.
European journal of human genetics : EJHG 1999;7(5):541-8.
1999: Carrel L; Willard H F
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 1999;96(13):7364-9.
1999: Plenge R M; Tranebjaerg L; Jensen P K; Schwartz C; Willard H F
Evidence that mutations in the X-linked DDP gene cause incompletely penetrant and variable skewed X inactivation.
American journal of human genetics 1999;64(3):759-67.
1998: Sullivan B A; Willard H F
Stable dicentric X chromosomes with two functional centromeres.
Nature genetics 1998;20(3):227-8.
1998: Miller A P; Willard H F
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 1998;95(15):8709-14.
1998: Carrel L; Willard H F
Counting on Xist.
Nature genetics 1998;19(3):211-2.
1998: White W M; Willard H F; Van Dyke D L; Wolff D J
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 1998;63(1):20-8.
1998: Willard H F
Centromeres: the missing link in the development of human artificial chromosomes.
Current opinion in genetics & development 1998;8(2):219-25.
1998: Greenfield A; Carrel L; Pennisi D; Philippe C; Quaderi N; Siggers P; Steiner K; Tam P P; Monaco A P; Willard H F; Koopman P
The UTX gene escapes X inactivation in mice and humans.
Human molecular genetics 1998;7(4):737-42.
1998: Dal Zotto L; Quaderi N A; Elliott R; Lingerfelter P A; Carrel L; Valsecchi V; Montini E; Yen C H; Chapman V; Kalcheva I; Arrigo G; Zuffardi O; Thomas S; Willard H F; Ballabio A; Disteche C M; Rugarli E I
The mouse Mid1 gene: implications for the pathogenesis of Opitz syndrome and the evolution of the mammalian pseudoautosomal region.
Human molecular genetics 1998;7(3):489-99.
1998: Mahtani M M; Willard H F
Physical and genetic mapping of the human X chromosome centromere: repression of recombination.
Genome research 1998;8(2):100-10.
1997: James R S; Dalton P; Gustashaw K; Wolff D J; Willard H F; Mitchell C; Jacobs P A
Molecular characterization of isochromosomes of Xq.
Annals of human genetics 1997;61(Pt 6):485-90.
1997: Plenge R M; Hendrich B D; Schwartz C; Arena J F; Naumova A; Sapienza C; Winter R M; Willard H F
A promoter mutation in the XIST gene in two unrelated families with skewed X-chromosome inactivation.
Nature genetics 1997;17(3):353-6.
1997: Ishikawa-Brush Y; Powell J F; Bolton P; Miller A P; Francis F; Willard H F; Lehrach H; Monaco A P
Autism and multiple exostoses associated with an X;8 translocation occurring within the GRPR gene and 3' to the SDC2 gene.
Human molecular genetics 1997;6(8):1241-50.
1997: Depinet T W; Zackowski J L; Earnshaw W C; Kaffe S; Sekhon G S; Stallard R; Sullivan B A; Vance G H; Van Dyke D L; Willard H F; Zinn A B; Schwartz S
Characterization of neo-centromeres in marker chromosomes lacking detectable alpha-satellite DNA.
Human molecular genetics 1997;6(8):1195-204.
1997: Wolff D J; Gustashaw K M; Zurcher V; Ko L; White W; Weiss L; Van Dyke D L; Schwartz S; Willard H F
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 1997;100(2):256-61.
1997: Hendrich B D; Plenge R M; Willard H F
Identification and characterization of the human XIST gene promoter: implications for models of X chromosome inactivation.
Nucleic acids research 1997;25(13):2661-71.
1997: Brown C J; Carrel L; Willard H F
Expression of genes from the human active and inactive X chromosomes.
American journal of human genetics 1997;60(6):1333-43.
1997: Harrington J J; Van Bokkelen G; Mays R W; Gustashaw K; Willard H F
Formation of de novo centromeres and construction of first-generation human artificial microchromosomes.
Nature genetics 1997;15(4):345-55.
1996: Carrel L; Hunt P A; Willard H F
Tissue and lineage-specific variation in inactive X chromosome expression of the murine Smcx gene.
Human molecular genetics 1996;5(9):1361-6.
1996: Carrel L; Willard H F
An assay for X inactivation based on differential methylation at the fragile X locus, FMR1.
American journal of medical genetics 1996;64(1):27-30.
1996: Willard H F
X chromosome inactivation and X-linked mental retardation.
American journal of medical genetics 1996;64(1):21-6.
1996: Willard H F
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 1996;93(14):6847-50.
1996: Willard H F
X chromosome inactivation, XIST, and pursuit of the X-inactivation center.
Cell 1996;86(1):5-7.
1996: Naumova A K; Plenge R M; Bird L M; Leppert M; Morgan K; Willard H F; Sapienza C
Heritability of X chromosome--inactivation phenotype in a large family.
American journal of human genetics 1996;58(6):1111-9.
1996: Carrel L; Clemson C M; Dunn J M; Miller A P; Hunt P A; Lawrence J B; Willard H F
X inactivation analysis and DNA methylation studies of the ubiquitin activating enzyme E1 and PCTAIRE-1 genes in human and mouse.
Human molecular genetics 1996;5(3):391-401.
1996: Clemson C M; McNeil J A; Willard H F; Lawrence J B
XIST RNA paints the inactive X chromosome at interphase: evidence for a novel RNA involved in nuclear/chromosome structure.
The Journal of cell biology 1996;132(3):259-75.
1996: Wolff D J; Miller A P; Van Dyke D L; Schwartz S; Willard H F
Molecular definition of breakpoints associated with human Xq isochromosomes: implications for mechanisms of formation.
American journal of human genetics 1996;58(1):154-60.
1996: Sullivan B A; Schwartz S; Willard H F
Centromeres of human chromosomes.
Environmental and molecular mutagenesis 1996;28(3):182-91.
1995: Kirchgessner C U; Warren S T; Willard H F
X inactivation of the FMR1 fragile X mental retardation gene.
Journal of medical genetics 1995;32(12):925-9.
1995: Warburton P E; Willard H F
Interhomologue sequence variation of alpha satellite DNA from human chromosome 17: evidence for concerted evolution along haplotypic lineages.
Journal of molecular evolution 1995;41(6):1006-15.
1995: Alitalo T; Francis F; Kere J; Lehrach H; Schlessinger D; Willard H F
A 6-Mb YAC contig in Xp22.1-p22.2 spanning the DXS69E, XE59, GLRA2, PIGA, GRPR, CALB3, and PHKA2 genes.
Genomics 1995;25(3):691-700.
1995: Brown C J; Miller A P; Carrel L; Rupert J L; Davies K E; Willard H F
The DXS423E gene in Xp11.21 escapes X chromosome inactivation.
Human molecular genetics 1995;4(2):251-5.
1995: Rupert J L; Brown C J; Willard H F
Direct detection of non-random X chromosome inactivation by use of a transcribed polymorphism in the XIST gene.
European journal of human genetics : EJHG 1995;3(6):333-43.
1995: Hendrich B D; Willard H F
Epigenetic regulation of gene expression: the effect of altered chromatin structure from yeast to mammals.
Human molecular genetics 1995;4 Spec No():1765-77.
1994: Gustashaw K M; Zurcher V; Dickerman L H; Stallard R; Willard H F
Partial X chromosome trisomy with functional disomy of Xp due to failure of X inactivation.
American journal of medical genetics 1994;53(1):39-45.
1994: Wolff D J; Brown C J; Schwartz S; Duncan A M; Surti U; Willard H F
Small marker X chromosomes lack the X inactivation center: implications for karyotype/phenotype correlations.
American journal of human genetics 1994;55(1):87-95.
1994: Lafrenière R G; Carrel L; Willard H F
A novel transmembrane transporter encoded by the XPCT gene in Xq13.2.
Human molecular genetics 1994;3(7):1133-9.
1994: Brown C J; Willard H F
The human X-inactivation centre is not required for maintenance of X-chromosome inactivation.
Nature 1994;368(6467):154-6.
1993: Greig G M; Warburton P E; Willard H F
Organization and evolution of an alpha satellite DNA subset shared by human chromosomes 13 and 21.
Journal of molecular evolution 1993;37(5):464-75.
1993: Warburton P E; Waye J S; Willard H F
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 1993;13(10):6520-9.
1993: Greig G M; Sharp C B; Carrel L; Willard H F
Duplicated zinc finger protein genes on the proximal short arm of the human X chromosome: isolation, characterization and X-inactivation studies.
Human molecular genetics 1993;2(10):1611-8.
1993: Willard H F
The inv(16) in acute nonlymphocytic leukemia: a turnabout for myosin heavy chain.
Human molecular genetics 1993;2(10):1525-6.
1993: Lafrenière R G; Willard H F
Pulsed-field map of Xq13 in the region of the human X inactivation center.
Genomics 1993;17(2):502-6.
1993: Lafrenière R G; Brown C J; Rider S; Chelly J; Taillon-Miller P; Chinault A C; Monaco A P; Willard H F
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 1993;2(8):1105-15.
1993: Hendrich B D; Brown C J; Willard H F
Evolutionary conservation of possible functional domains of the human and murine XIST genes.
Human molecular genetics 1993;2(6):663-72.
1993: Willard H F
The needle found!!! Trinucleotide repeat expansion in the Huntington's disease gene.
Human molecular genetics 1993;2(5):497-8.
1993: Haaf T; Schmid M; Steinlein C; Galetti P M; Willard H F
Organization and molecular cytogenetics of a satellite DNA family from Hoplias malabaricus (Pisces, Erythrinidae).
Chromosome research : an international journal on the molecular, supramolecular and evolutionary aspects of chromosome biology 1993;1(1):77-86.
1993: Mahtani M M; Willard H F
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 1993;2(4):431-7.
1993: Willard H F
Cloning of the X-linked glycerol kinase gene.
Human molecular genetics 1993;2(2):95-6.
1993: Willard H F; Brown C J; Carrel L; Hendrich B; Miller A P
Epigenetic and chromosomal control of gene expression: molecular and genetic analysis of X chromosome inactivation.
Cold Spring Harbor symposia on quantitative biology 1993;58():315-22.
1992: Wevrick R; Willard V P; Willard H F
Structure of DNA near long tandem arrays of alpha satellite DNA at the centromere of human chromosome 7.
Genomics 1992;14(4):912-23.
1992: Willard H F
Centromeres--primary constrictions are primarily complicated.
Human molecular genetics 1992;1(9):667-8.
1992: Warburton P E; Willard H F
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 1992;20(22):6033-42.
1992: Brown C J; Hendrich B D; Rupert J L; Lafrenière R G; Xing Y; Lawrence J; Willard H F
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 1992;71(3):527-42.
1992: Haaf T; Warburton P E; Willard H F
Integration of human alpha-satellite DNA into simian chromosomes: centromere protein binding and disruption of normal chromosome segregation.
Cell 1992;70(4):681-96.
1992: Haaf T; Willard H F
Organization, polymorphism, and molecular cytogenetics of chromosome-specific alpha-satellite DNA from the centromere of chromosome 2.
Genomics 1992;13(1):122-8.
1992: Greig G M; Willard H F
Beta satellite DNA: characterization and localization of two subfamilies from the distal and proximal short arms of the human acrocentric chromosomes.
Genomics 1992;12(3):573-80.
1992: Haaf T; Sumner A T; Köhler J; Willard H F; Schmid M;
A microchromosome derived from chromosome 11 in a patient with the CREST syndrome of scleroderma.
Cytogenetics and cell genetics 1992;60(1):12-7.
1991: Willard H F
Evolution of alpha satellite.
Current opinion in genetics & development 1991;1(4):509-14.
1991: Lafrenière R G; Brown C J; Powers V E; Carrel L; Davies K E; Barker D F; Willard H F
Physical mapping of 60 DNA markers in the p21.1----q21.3 region of the human X chromosome.
Genomics 1991;11(2):352-63.
1991: Warburton P E; Greig G M; Haaf T; Willard H F
PCR amplification of chromosome-specific alpha satellite DNA: definition of centromeric STS markers and polymorphic analysis.
Genomics 1991;11(2):324-33.
1991: Mahtani M M; Lafrenière R G; Kruse T A; Willard H F
An 18-locus linkage map of the pericentromeric region of the human X chromosome: genetic framework for mapping X-linked disorders.
Genomics 1991;10(4):849-57.
1991: Losada A P; Wessman M; Tiainen M; Hopman A H; Willard H F; Solé F; Caballín M R; Woessner S; Knuutila S
Trisomy 12 in chronic lymphocytic leukemia: an interphase cytogenetic study.
Blood 1991;78(3):775-9.
1991: Fujii J; Zarain-Herzberg A; Willard H F; Tada M; MacLennan D H
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 1991;266(18):11669-75.
1991: Wevrick R; Willard H F
Physical map of the centromeric region of human chromosome 7: relationship between two distinct alpha satellite arrays.
Nucleic acids research 1991;19(9):2295-301.
1991: Lafreniere R G; Geraghty M T; Valle D; Shows T B; Willard H F
Ornithine aminotransferase-related sequences map to two nonadjacent intervals on the human X chromosome short arm.
Genomics 1991;10(1):276-9.
1991: Brown C J; Lafreniere R G; Powers V E; Sebastio G; Ballabio A; Pettigrew A L; Ledbetter D H; Levy E; Craig I W; Willard H F
Localization of the X inactivation centre on the human X chromosome in Xq13.
Nature 1991;349(6304):82-4.
1991: Brown C J; Ballabio A; Rupert J L; Lafreniere R G; Grompe M; Tonlorenzi R; Willard H F
A gene from the region of the human X inactivation centre is expressed exclusively from the inactive X chromosome.
Nature 1991;349(6304):38-44.
1991: Greig G M; Parikh S; George J; Powers V E; Willard H F
Molecular cytogenetics of alpha satellite DNA from chromosome 12: fluorescence in situ hybridization and description of DNA and array length polymorphisms.
Cytogenetics and cell genetics 1991;56(3-4):144-8.
1990: Durfy S J; Willard H F
Concerted evolution of primate alpha satellite DNA. Evidence for an ancestral sequence shared by gorilla and human X chromosome alpha satellite.
Journal of molecular biology 1990;216(3):555-66.
1990: Wevrick R; Earnshaw W C; Howard-Peebles P N; Willard H F
Partial deletion of alpha satellite DNA associated with reduced amounts of the centromere protein CENP-B in a mitotically stable human chromosome rearrangement.
Molecular and cellular biology 1990;10(12):6374-80.
1990: Ten Hagen K G; Gilbert D M; Willard H F; Cohen S N
Replication timing of DNA sequences associated with human centromeres and telomeres.
Molecular and cellular biology 1990;10(12):6348-55.
1990: Fisher E M; Beer-Romero P; Brown L G; Ridley A; McNeil J A; Lawrence J B; Willard H F; Bieber F R; Page D C
Homologous ribosomal protein genes on the human X and Y chromosomes: escape from X inactivation and possible implications for Turner syndrome.
Cell 1990;63(6):1205-18.
1990: Willard H F
Centromeres of mammalian chromosomes.
Trends in genetics : TIG 1990;6(12):410-6.
1990: Warburton P E; Willard H F
Genomic analysis of sequence variation in tandemly repeated DNA. Evidence for localized homogeneous sequence domains within arrays of alpha-satellite DNA.
Journal of molecular biology 1990;216(1):3-16.
1990: Watt V M; Willard H F
The human aminopeptidase N gene: isolation, chromosome localization, and DNA polymorphism analysis.
Human genetics 1990;85(6):651-4.
1990: Sharp C B; Bedford H M; Willard H F
Pericentromeric structure of human X "isochromosomes": evidence for molecular heterogeneity.
Human genetics 1990;85(3):330-6.
1990: Otsu K; Willard H F; Khanna V K; Zorzato F; Green N M; MacLennan D H
Molecular cloning of cDNA encoding the Ca2+ release channel (ryanodine receptor) of rabbit cardiac muscle sarcoplasmic reticulum.
The Journal of biological chemistry 1990;265(23):13472-83.
1990: Mahtani M M; Willard H F
Pulsed-field gel analysis of alpha-satellite DNA at the human X chromosome centromere: high-frequency polymorphisms and array size estimate.
Genomics 1990;7(4):607-13.
1990: Brown C J; Flenniken A M; Williams B R; Willard H F
X chromosome inactivation of the human TIMP gene.
Nucleic acids research 1990;18(14):4191-5.
1990: Lafreniere R G; Willard H F
A Rsal RFLP at the DXS467 locus.
Nucleic acids research 1990;18(12):3673.
1990: Lafreniere R G; Willard H F
A BstE II RFLP at the DXS153 locus.
Nucleic acids research 1990;18(12):3673.
1990: MacKenzie A E; Korneluk R G; Zorzato F; Fujii J; Phillips M; Iles D; Wieringa B; Leblond S; Bailly J; Willard H F
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.
American journal of human genetics 1990;46(6):1082-9.
1990: Fujii J; Willard H F; MacLennan D H
Characterization and localization to human chromosome 1 of human fast-twitch skeletal muscle calsequestrin gene.
Somatic cell and molecular genetics 1990;16(2):185-9.
1990: Brown C J; Willard H F
Localization of a gene that escapes inactivation to the X chromosome proximal short arm: implications for X inactivation.
American journal of human genetics 1990;46(2):273-9.
1990: Shier P; Willard H F; Watt V M
Localization of the insulin receptor-related receptor gene to human chromosome 1.
Cytogenetics and cell genetics 1990;54(1-2):80-1.
1990: Willard H F
Alpha and beta satellite sequences on chromosome 21: the possible role of centromere and chromosome structure in nondisjunction.
Progress in clinical and biological research 1990;360():39-52.
1989: Wevrick R; Willard H F
Long-range organization of tandem arrays of alpha satellite DNA at the centromeres of human chromosomes: high-frequency array-length polymorphism and meiotic stability.
Proceedings of the National Academy of Sciences of the United States of America 1989;86(23):9394-8.
1989: Greig G M; England S B; Bedford H M; Willard H F
Chromosome-specific alpha satellite DNA from the centromere of human chromosome 16.
American journal of human genetics 1989;45(6):862-72.
1989: Durfy S J; Willard H F
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.
Genomics 1989;5(4):810-21.
1989: Brown C J; Willard H F
Noninactivation of a selectable human X-linked gene that complements a murine temperature-sensitive cell cycle defect.
American journal of human genetics 1989;45(4):592-8.
1989: Waye J S; Willard H F
Human beta satellite DNA: genomic organization and sequence definition of a class of highly repetitive tandem DNA.
Proceedings of the National Academy of Sciences of the United States of America 1989;86(16):6250-4.
1989: Lafreniere R G; Mahtani M M; Willard H F
An X-linked DraI RFLP recognized by cpX23 [DXS132]
Nucleic acids research 1989;17(16):6754.
1989: Waye J S; Willard H F
Chromosome specificity of satellite DNAs: short- and long-range organization of a diverged dimeric subset of human alpha satellite from chromosome 3.
Chromosoma 1989;97(6):475-80.
1989: Brown C J; Powers V E; Munroe D L; Sheinin R; Willard H F
Gene on short arm of human X chromosome complements murine tsA1S9 DNA synthesis mutation.
Somatic cell and molecular genetics 1989;15(2):173-8.
1989: Willard H F; Durfy S J; Mahtani M M; Dorkins H; Davies K E; Williams B R
Regional localization of the TIMP gene on the human X chromosome. Extension of a conserved synteny and linkage group on proximal Xp.
Human genetics 1989;81(3):234-8.
1989: Brown C J; Goss S J; Lubahn D B; Joseph D R; Wilson E M; French F S; Willard H F
Androgen receptor locus on the human X chromosome: regional localization to Xq11-12 and description of a DNA polymorphism.
American journal of human genetics 1989;44(2):264-9.
1989: Brown C J; Sekiguchi T; Nishimoto T; Willard H F
Regional localization of CCG1 gene which complements hamster cell cycle mutation BN462 to Xq11-Xq13.
Somatic cell and molecular genetics 1989;15(1):93-6.
1989: Alitalo T; Willard H F; de la Chapelle A
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.
Cytogenetics and cell genetics 1989;50(1):49-53.
1989: Willard H F
The genomics of long tandem arrays of satellite DNA in the human genome.
Genome / National Research Council Canada = Génome / Conseil national de recherches Canada 1989;31(2):737-44.
1989: Willard H F; Wevrick R; Warburton P E
Human centromere structure: organization and potential role of alpha satellite DNA.
Progress in clinical and biological research 1989;318():9-18.
1989: Robinson B H; Chun K; Mackay N; Otulakowski G; Petrova-Benedict R; Willard H
Isolated and combined deficiencies of the alpha-keto acid dehydrogenase complexes.
Annals of the New York Academy of Sciences 1989;573():337-46.
1988: Brown C J; Mahtani M M; Willard H F
Genetic mapping of four DNA markers (DXS16, DXS43, DXS85, and DXS143) from the p22 region of the human X chromosome.
Human genetics 1988;80(3):296-8.
1988: Mahtani M M; Willard H F
A primary genetic map of the pericentromeric region of the human X chromosome.
Genomics 1988;2(4):294-301.
1988: Allore R; O'Hanlon D; Price R; Neilson K; Willard H F; Cox D R; Marks A; Dunn R J
Gene encoding the beta subunit of S100 protein is on chromosome 21: implications for Down syndrome.
Science (New York, N.Y.) 1988;239(4845):1311-3.
1988: Waye J S; Gravel R A; Willard H F
Two PstI RFLPs in the PCCB gene on the long arm of chromosome 3.
Nucleic acids research 1988;16(5):2362.
1988: Waye J S; Mitchell A R; Willard H F
Organization and genomic distribution of "82H" alpha satellite DNA. Evidence for a low-copy or single-copy alphoid domain located on human chromosome 14.
Human genetics 1988;78(1):27-32.
1987: Willard H F; Greig G M; Powers V E; Waye J S
Molecular organization and haplotype analysis of centromeric DNA from human chromosome 17: implications for linkage in neurofibromatosis.
Genomics 1987;1(4):368-73.
1987: Brown C J; Willard H F
MspI RFLP detected with chromosome-walk clone pXUT23-SE3.2L from DXS16 in Xp22.1-22.3.
Nucleic acids research 1987;15(22):9614.
1987: Waye J S; Greig G M; Willard H F
Detection of novel centromeric polymorphisms associated with alpha satellite DNA from human chromosome 11.
Human genetics 1987;77(2):151-6.
1987: Waye J S; Willard H F
Nucleotide sequence heterogeneity of alpha satellite repetitive DNA: a survey of alphoid sequences from different human chromosomes.
Nucleic acids research 1987;15(18):7549-69.
1987: Waye J S; Durfy S J; Pinkel D; Kenwrick S; Patterson M; Davies K E; Willard H F
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.
Genomics 1987;1(1):43-51.
1987: MacLennan D H; Brandl C J; Champaneria S; Holland P C; Powers V E; Willard H F
Fast-twitch and slow-twitch/cardiac Ca2+ ATPase genes map to human chromosomes 16 and 12.
Somatic cell and molecular genetics 1987;13(4):341-6.
1987: Willard H F; Waye J S
Chromosome-specific subsets of human alpha satellite DNA: analysis of sequence divergence within and between chromosomal subsets and evidence for an ancestral pentameric repeat.
Journal of molecular evolution 1987;25(3):207-14.
1986: Willard H F; Waye J S; Skolnick M H; Schwartz C E; Powers V E; England S B
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.
Proceedings of the National Academy of Sciences of the United States of America 1986;83(15):5611-5.

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