FIND

researchers

DISCOVER

relevant articles

PROMOTE

your research

now for free

Huntington Willard

Research Profile

Anatomy

Chemicals & Drugs

Procedures

Concepts & Ideas

Co-author Network

Publications

TOP 3
Susanne B Haga; Rachel Mills; Jennifer Sullivan; Laura Svetkey; William T Barry; Geoffrey S Ginsburg; Huntington F Willard
Public knowledge of and attitudes toward genetics and genetic testing.
Karen E Hayden; Hye-Ran Lee; Stephanie L Merrett; M Katharine Rudd; Erin D Strome; Huntington F Willard
Sequences associated with centromere competency in the human genome.
Joanne L Thorvaldsen; Huntington F Willard; Christopher Krapp; Marisa S Bartolomei
Nonrandom X chromosome inactivation is influenced by multiple regions on the murine X chromosome.

Register for free to view:

Visualized networks:

See your personal network in
sophisticated graphical views

GeoTargeted Searches:

Locate experts around the world
and connect with global collaborators

Research Profiles:

See the research activity
of experts around the globe

Geonetwork of Huntington Willard (preview)

Cities where this author has publications
Cities where co-authors of this author have publications

Flash Player Required

All Publications

2013: Susanne B Haga; Rachel Mills; Jennifer Sullivan; Laura Svetkey; William T Barry; Geoffrey S Ginsburg; Huntington F Willard
Public knowledge of and attitudes toward genetics and genetic testing.
Genetic testing and molecular biomarkers 2013;17(4):327-35.
2013: Karen E Hayden; Hye-Ran Lee; Stephanie L Merrett; M Katharine Rudd; Erin D Strome; Huntington F Willard
Sequences associated with centromere competency in the human genome.
Molecular and cellular biology 2013;33(4):763-72.
2012: Joanne L Thorvaldsen; Huntington F Willard; Christopher Krapp; Marisa S Bartolomei
Nonrandom X chromosome inactivation is influenced by multiple regions on the murine X chromosome.
Genetics 2012;192(3):1095-107.
2012: Timothy E Reddy; Lingyun Song; Katherine E Varley; Huntington F Willard; Brian A Williams; Barbara Wold; Gregory E Crawford; Jason Gertz; Katerina S Kucera; Georgi K Marinov; Ali Mortazavi; Kimberly M Newberry; Florencia Pauli; Richard M Myers
Effects of sequence variation on differential allelic transcription factor occupancy and gene expression.
Genome research 2012;22(5):860-9.
2012: Bayly S Wheeler; Huntington F Willard; Brandon T Ruderman; Kristin C Scott
Uncoupling of genomic and epigenetic signals in the maintenance and inheritance of heterochromatin domains in fission yeast.
Genetics 2012;190(2):549-57.
2012: Zhong Wang; Huntington F Willard
Evidence for sequence biases associated with patterns of histone methylation.
BMC genomics 2012;13():367.
2012: Karen E Hayden; Huntington F Willard
Composition and organization of active centromere sequences in complex genomes.
BMC genomics 2012;13():324.
2011: Katerina S Kucera; Jenae E Logan; Richard M Myers; Florencia Pauli; Timothy E Reddy; Jason Gertz; Huntington F Willard
Allele-specific distribution of RNA polymerase II on female X chromosomes.
Human molecular genetics 2011;20(20):3964-73.
2011: Jason Gertz; Katerina S Kucera; Kevin M Bowling; Stephanie L Parker; Florencia Pauli; Timothy E Reddy; Katherine E Varley; Huntington F Willard; Richard M Myers
Analysis of DNA methylation in a three-generation family reveals widespread genetic influence on epigenetic regulation.
PLoS genetics 2011;7(8):e1002228.
2011: Julie E Horvath; Christina B Sheedy; Stephanie L Merrett; Abdoulaye Banire Diallo; David L Swofford; Eric D Green; Huntington F Willard
Comparative analysis of the primate X-inactivation center region and reconstruction of the ancestral primate XIST locus.
Genome research 2011;21(6):850-62.
2011: Hye-Ran Lee; Karen E Hayden; Huntington F Willard
Organization and molecular evolution of CENP-A--associated satellite DNA families in a basal primate genome.
Genome biology and evolution 2011;3():1136-49.
2010: Julianne M O'Daniel; Susanne B Haga; Huntington F Willard
Considerations for the impact of personal genome information: a study of genomic profiling among genetics and genomics professionals.
Journal of genetic counseling 2010;19(4):387-401.
2010: Ryan McDaniell; Bum-Kyu Lee; Lingyun Song; Zheng Liu; Alan P Boyle; Michael R Erdos; Laura J Scott; Mario A Morken; Katerina S Kucera; Anna Battenhouse; Damian Keefe; Francis S Collins; Huntington F Willard; Jason Dillon Lieb; Terrence S Furey; Gregory E Crawford; Vishwanath R Iyer; Ewan Birney
Heritable individual-specific and allele-specific chromatin signatures in humans.
Science (New York, N.Y.) 2010;328(5975):235-9.
2010: Huntington F Willard
ASHG Awards and Addresses. 2009 William Allan Award address: Life in the sandbox: unfinished business.
American journal of human genetics 2010;86(3):318-27.
2009: Geoffrey S Ginsburg; Huntington F Willard
Genomic and personalized medicine: foundations and applications.
Translational research : the journal of laboratory and clinical medicine 2009;154(6):277-87.
2009: Bayly S Wheeler; Jared A Blau; Huntington F Willard; Kristin C Scott
The impact of local genome sequence on defining heterochromatin domains.
PLoS genetics 2009;5(4):e1000453.
2009: Kensaku Kawamoto; David F Lobach; Huntington F Willard; Geoffrey S Ginsburg
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: Reed V Tuckson; Huntington F Willard
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: Susanne B Haga; Huntington F Willard
Letting the genome out of the bottle.
The New England journal of medicine 2008;358(20):2184; author reply 2185.
2008: Julie E Horvath; David W Weisrock; Stephanie L Embry; Isabella Fiorentino; James P Balhoff; Peter Kappeler; Gregory A Wray; Huntington F Willard; Anne D Yoder
Development and application of a phylogenomic toolkit: resolving the evolutionary history of Madagascar's lemurs.
Genome research 2008;18(3):489-99.
2007: Julie E Horvath; Huntington F Willard
Primate comparative genomics: lemur biology and evolution.
Trends in genetics : TIG 2007;23(4):173-82.
2007: Joydeep Basu; Huntington F Willard; Gregory Stromberg
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: Kristin C Scott; Caroline V White; Huntington F Willard
An RNA polymerase III-dependent heterochromatin barrier at fission yeast centromere 1.
PloS one 2007;2(10):e1099.
2006: Susanne B Haga; Huntington F Willard
Defining the spectrum of genome policy.
Nature reviews. Genetics 2006;7(12):966-72.
2006: Kevin V Shianna; Huntington F Willard
Human genomics: in search of normality.
Nature 2006;444(7118):428-9.
2006: Joydeep Basu; Huntington F Willard
Human artificial chromosomes: potential applications and clinical considerations.
Pediatric clinics of North America 2006;53(5):843-53, viii.
2006: Zhong Wang; Huntington F Willard; Sayan Mukherjee; Terrence S Furey
Evidence of influence of genomic DNA sequence on human X chromosome inactivation.
PLoS computational biology 2006;2(9):e113.
2006: James M Amos-Landgraf; Amy Cottle; Robert M Plenge; Mike Friez; Charles E Schwartz; John Longshore; Huntington F Willard
X chromosome-inactivation patterns of 1,005 phenotypically unaffected females.
American journal of human genetics 2006;79(3):493-9.
2006: Cory M Valley; Lisa M Pertz; Bala S Balakumaran; Huntington F Willard
Chromosome-wide, allele-specific analysis of the histone code on the human X chromosome.
Human molecular genetics 2006;15(15):2335-47.
2006: Lisa Helbling Chadwick; Lisa M Pertz; Karl W Broman; Marisa S Bartolomei; Huntington F Willard
Genetic control of X chromosome inactivation in mice: definition of the Xce candidate interval.
Genetics 2006;173(4):2103-10.
2006: Cory M Valley; Huntington F Willard
Genomic and epigenomic approaches to the study of X chromosome inactivation.
Current opinion in genetics & development 2006;16(3):240-5.
2006: Kristin C Scott; Stephanie L Merrett; Huntington F Willard
A heterochromatin barrier partitions the fission yeast centromere into discrete chromatin domains.
Current biology : CB 2006;16(2):119-29.
2006: M Katharine Rudd; Gregory A Wray; Huntington F Willard
The evolutionary dynamics of alpha-satellite.
Genome research 2006;16(1):88-96.
2005: Lisa Helbling Chadwick; Huntington F Willard
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: Huntington F Willard; Misha Angrist; Geoffrey S Ginsburg
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: Mary G Schueler; John M Dunn; Christine P Bird; Mark T Ross; Luigi Viggiano; Mariano Rocchi; Huntington F Willard; Eric Green
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: Joydeep Basu; Huntington F Willard
Artificial and engineered chromosomes: non-integrating vectors for gene therapy.
Trends in molecular medicine 2005;11(5):251-8.
2005: Laura Carrel; Huntington F Willard
X-inactivation profile reveals extensive variability in X-linked gene expression in females.
Nature 2005;434(7031):400-4.
2005: Anne W Higgins; Karen M Gustashaw; Huntington F Willard
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: Joydeep Basu; George A Compitello; Gregory Stromberg; Huntington F Willard; Gil Van Bokkelen
Efficient assembly of de novo human artificial chromosomes from large genomic loci.
BMC biotechnology 2005;5():21.
2005: Joydeep Basu; Gregory Stromberg; George A Compitello; Huntington F Willard; Gil Van Bokkelen
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: Brian P Chadwick; Huntington F Willard
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: M Katharine Rudd; Huntington F Willard
Analysis of the centromeric regions of the human genome assembly.
Trends in genetics : TIG 2004;20(11):529-33.
2004: Brenda R Grimes; Jennifer Babcock; M Katharine Rudd; Brian P Chadwick; Huntington F Willard
Assembly and characterization of heterochromatin and euchromatin on human artificial chromosomes.
Genome biology 2004;5(11):R89.
2003: Brian P Chadwick; Huntington F Willard
Barring gene expression after XIST: maintaining facultative heterochromatin on the inactive X.
Seminars in cell & developmental biology 2003;14(6):359-67.
2003: Joe Simpson; Felix de la Cruz; Ronald S Swerdloff; Carole Samango-Sprouse; Niels E Skakkebaek; John M Graham; Terry J Hassold; Melissa Aylstock; Heino F L Meyer-Bahlburg; Huntington F Willard; Judith G Hall; Wael Salameh; Kyle Boone; Catherine Staessen; Daniel Geschwind; Jay Giedd; Adrian S Dobs; Alan D Rogol; Bonnie Brinton; C Alvin Paulsen
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: M Katharine Rudd; Robert Mays; Stuart Schwartz; Huntington F Willard
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: Brian P Chadwick; Huntington F Willard
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: Ivona Percec; Joanne L Thorvaldsen; Robert M Plenge; Christopher J Krapp; Joseph H Nadeau; Huntington F Willard; Marisa S Bartolomei
An N-ethyl-N-nitrosourea mutagenesis screen for epigenetic mutations in the mouse.
Genetics 2003;164(4):1481-94.
2003: Huntington F Willard
Tales of the Y chromosome.
Nature 2003;423(6942):810-1, 813.
2003: R Sanders Williams; Huntington F Willard; Ralph Snyderman
Personalized health planning.
Science (New York, N.Y.) 2003;300(5619):549.
2003: Brian P Chadwick; Huntington F Willard
SETting the stage. Eed-Enx1 leaves an epigenetic signature on the inactive X chromosome.
Developmental cell 2003;4(4):445-7.
2003: M Katharine Rudd; Mary G Schueler; Huntington F Willard
Sequence organization and functional annotation of human centromeres.
Cold Spring Harbor symposia on quantitative biology 2003;68():141-9.
2002: Robert M Plenge; Roger A Stevenson; Herbert A Lubs; Charles E Schwartz; Huntington F Willard
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: Lisa L Hall; Meg Byron; Kosuke Sakai; Laura Carrel; Huntington F Willard; Jeanne B Lawrence
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: Brian P Chadwick; Huntington F Willard
Cell cycle-dependent localization of macroH2A in chromatin of the inactive X chromosome.
The Journal of cell biology 2002;157(7):1113-23.
2002: Brenda R Grimes; Angela A Rhoades; Huntington F Willard
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: Ivona Percec; Robert M Plenge; Joseph H Nadeau; Marisa S Bartolomei; Huntington F Willard
Autosomal dominant mutations affecting X inactivation choice in the mouse.
Science (New York, N.Y.) 2002;296(5570):1136-9.
2002: Huntington F Willard
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: Mary G Schueler; Anne W Higgins; M Katharine Rudd; Karen M Gustashaw; Huntington F Willard
Genomic and genetic definition of a functional human centromere.
Science (New York, N.Y.) 2001;294(5540):109-15.
2001: Huntington F Willard; Laura Carrel
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: Brian P Chadwick; Cory M Valley; Huntington F Willard
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: Huntington F Willard
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: Brian P Chadwick; Huntington F Willard
Histone H2A variants and the inactive X chromosome: identification of a second macroH2A variant.
Human molecular genetics 2001;10(10):1101-13.
2001: Brian P Chadwick; Huntington F Willard
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: Huntington F Willard
Genomics and gene therapy. Artificial chromosomes coming to life.
Science (New York, N.Y.) 2000;290(5495):1308-9.
2000: K D Tsuchiya; Huntington F Willard
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: Mary G Schueler; Anne W Higgins; R Nagaraja; Dmitry Tentler; Niklas Dahl; Karen M Gustashaw; Huntington F Willard
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: Robert M Plenge; Ivona Percec; Joseph H Nadeau; Huntington F Willard
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: Laura Carrel; A A Cottle; K C Goglin; Huntington F Willard
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: Huntington F Willard; BD Hendrich
Breaking the silence in Rett syndrome.
Nature genetics 1999;23(2):127-8.
1999: Anne W Higgins; Mary G Schueler; Huntington F Willard
Chromosome engineering: generation of mono- and dicentric isochromosomes in a somatic cell hybrid system.
Chromosoma 1999;108(4):256-65.
1999: Dmitry Tentler; Peter Gustavsson; J Leisti; Mary G Schueler; J Chelly; E Timonen; Göran Annerén; Huntington F Willard; Niklas Dahl
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: Laura Carrel; Huntington F Willard
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: Robert M Plenge; L Tranebjaerg; P K Jensen; C Schwartz; Huntington F Willard
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: BA Sullivan; Huntington F Willard
Stable dicentric X chromosomes with two functional centromeres.
Nature genetics 1998;20(3):227-8.
1998: A P Miller; Huntington F Willard
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: Laura Carrel; Huntington F Willard
Counting on Xist.
Nature genetics 1998;19(3):211-2.
1998: W M White; Huntington F Willard; Daniel L Van Dyke; Daynna J Wolff
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: Huntington F Willard
Centromeres: the missing link in the development of human artificial chromosomes.
Current opinion in genetics & development 1998;8(2):219-25.
1998: Andy Greenfield; Laura Carrel; David J Pennisi; C Philippe; NA Quaderi; Pam Siggers; K Steiner; P P Tam; Anthony P Monaco; Huntington F Willard; Peter Koopman
The UTX gene escapes X inactivation in mice and humans.
Human molecular genetics 1998;7(4):737-42.
1998: L Dal Zotto; NA Quaderi; R Elliott; P A Lingerfelter; Laura Carrel; V Valsecchi; Eugenio Montini; C H Yen; Verne M Chapman; I Kalcheva; Giulia Arrigo; Orsetta Zuffardi; S Thomas; Huntington F Willard; Andrea Ballabio; Christine M Disteche; Elena I Rugarli
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: M M Mahtani; Huntington F Willard
Physical and genetic mapping of the human X chromosome centromere: repression of recombination.
Genome research 1998;8(2):100-10.
1997: RS James; P Dalton; Karen M Gustashaw; Daynna J Wolff; Huntington F Willard; C Mitchell; Patricia A Jacobs
Molecular characterization of isochromosomes of Xq.
Annals of human genetics 1997;61(Pt 6):485-90.
1997: Robert M Plenge; BD Hendrich; C Schwartz; J F Arena; Anna K Naumova; C Sapienza; R M Winter; Huntington F Willard
A promoter mutation in the XIST gene in two unrelated families with skewed X-chromosome inactivation.
Nature genetics 1997;17(3):353-6.
1997: Yumiko Ishikawa-Brush; J F Powell; Patrick Bolton; A P Miller; F Francis; Huntington F Willard; H Lehrach; Anthony P Monaco
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: TW Depinet; JL Zackowski; W C Earnshaw; S Kaffe; G S Sekhon; R Stallard; BA Sullivan; Gail H Vance; Daniel L Van Dyke; Huntington F Willard; A B Zinn; Stuart Schwartz
Characterization of neo-centromeres in marker chromosomes lacking detectable alpha-satellite DNA.
Human molecular genetics 1997;6(8):1195-204.
1997: Daynna J Wolff; Karen M Gustashaw; VL Zurcher; L Ko; W White; L Weiss; Daniel L Van Dyke; Stuart Schwartz; Huntington F Willard
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: BD Hendrich; Robert M Plenge; Huntington F Willard
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: C J Brown; Laura Carrel; Huntington F Willard
Expression of genes from the human active and inactive X chromosomes.
American journal of human genetics 1997;60(6):1333-43.
1997: John J Harrington; Gil Van Bokkelen; Robert Mays; Karen M Gustashaw; Huntington F Willard
Formation of de novo centromeres and construction of first-generation human artificial microchromosomes.
Nature genetics 1997;15(4):345-55.
1996: Laura Carrel; Patricia A Hunt; Huntington F Willard
Tissue and lineage-specific variation in inactive X chromosome expression of the murine Smcx gene.
Human molecular genetics 1996;5(9):1361-6.
1996: Laura Carrel; Huntington F Willard
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: Huntington F Willard
X chromosome inactivation and X-linked mental retardation.
American journal of medical genetics 1996;64(1):21-6.
1996: Huntington F Willard
X chromosome inactivation, XIST, and pursuit of the X-inactivation center.
Cell 1996;86(1):5-7.
1996: Huntington F Willard
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: Anna K Naumova; Robert M Plenge; L M Bird; Mark Leppert; Kenneth Morgan; Huntington F Willard; Carmen Sapienza
Heritability of X chromosome--inactivation phenotype in a large family.
American journal of human genetics 1996;58(6):1111-9.
1996: Laura Carrel; C M Clemson; J M Dunn; A P Miller; Patricia A Hunt; Jeanne B Lawrence; Huntington F Willard
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: C M Clemson; J A McNeil; Huntington F Willard; Jeanne B Lawrence
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: B A Sullivan; Stuart Schwartz; Huntington F Willard
Centromeres of human chromosomes.
Environmental and molecular mutagenesis 1996;28(3):182-91.
1996: Daynna J Wolff; A P Miller; Daniel L Van Dyke; Stuart Schwartz; Huntington F Willard
Molecular definition of breakpoints associated with human Xq isochromosomes: implications for mechanisms of formation.
American journal of human genetics 1996;58(1):154-60.
1995: C U Kirchgessner; Stephen Warren; Huntington F Willard
X inactivation of the FMR1 fragile X mental retardation gene.
Journal of medical genetics 1995;32(12):925-9.
1995: P E Warburton; Huntington F Willard
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: T Alitalo; F Francis; J Kere; H Lehrach; David Schlessinger; Huntington F Willard
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: Carolyn J Brown; A P Miller; Laura Carrel; J L Rupert; Kay E Davies; Huntington F Willard
The DXS423E gene in Xp11.21 escapes X chromosome inactivation.
Human molecular genetics 1995;4(2):251-5.
1995: J L Rupert; Carolyn J Brown; Huntington F Willard
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: B D Hendrich; Huntington F Willard
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: Karen M Gustashaw; V Zurcher; L H Dickerman; R Stallard; Huntington F Willard
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: Daynna J Wolff; Carolyn J Brown; Stuart Schwartz; A M Duncan; U Surti; Huntington F Willard
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: R G Lafrenière; Laura Carrel; Huntington F Willard
A novel transmembrane transporter encoded by the XPCT gene in Xq13.2.
Human molecular genetics 1994;3(7):1133-9.
1994: Carolyn J Brown; Huntington F Willard
The human X-inactivation centre is not required for maintenance of X-chromosome inactivation.
Nature 1994;368(6467):154-6.
1993: G M Greig; P E Warburton; Huntington F Willard
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: P E Warburton; J S Waye; Huntington F Willard
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: G M Greig; C B Sharp; Laura Carrel; Huntington F Willard
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: Huntington F Willard
The inv(16) in acute nonlymphocytic leukemia: a turnabout for myosin heavy chain.
Human molecular genetics 1993;2(10):1525-6.
1993: R G Lafrenière; Huntington F Willard
Pulsed-field map of Xq13 in the region of the human X inactivation center.
Genomics 1993;17(2):502-6.
1993: R G Lafrenière; Carolyn J Brown; S Rider; J Chelly; P Taillon-Miller; A C Chinault; Anthony P Monaco; Huntington F Willard
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: B D Hendrich; Carolyn J Brown; Huntington F Willard
Evolutionary conservation of possible functional domains of the human and murine XIST genes.
Human molecular genetics 1993;2(6):663-72.
1993: Huntington F Willard
The needle found!!! Trinucleotide repeat expansion in the Huntington's disease gene.
Human molecular genetics 1993;2(5):497-8.
1993: Thomas Haaf; Michael Schmid; Claus Steinlein; Pedro Galetti; Huntington F Willard
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: M M Mahtani; Huntington F Willard
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: Huntington F Willard
Cloning of the X-linked glycerol kinase gene.
Human molecular genetics 1993;2(2):95-6.
1993: Huntington F Willard; Carolyn J Brown; Laura Carrel; B Hendrich; A P Miller
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: R Wevrick; V P Willard; Huntington F Willard
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: Huntington F Willard
Centromeres--primary constrictions are primarily complicated.
Human molecular genetics 1992;1(9):667-8.
1992: P E Warburton; Huntington F Willard
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: Carolyn J Brown; B D Hendrich; J L Rupert; R G Lafrenière; Y Xing; J Lawrence; Huntington F Willard
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: Thomas Haaf; P E Warburton; Huntington F Willard
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: Thomas Haaf; Huntington F Willard
Organization, polymorphism, and molecular cytogenetics of chromosome-specific alpha-satellite DNA from the centromere of chromosome 2.
Genomics 1992;13(1):122-8.
1992: G M Greig; Huntington F Willard
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: P E Warburton; Rachel Wevrick; M M Mahtani; Huntington F Willard
Pulsed-field and two-dimensional gel electrophoresis of long arrays of tandemly repeated DNA : analysis of human centromeric alpha satellite.
Methods in molecular biology (Clifton, N.J.) 1992;12():299-317.
1992: Thomas Haaf; A T Sumner; J Köhler; Huntington F Willard; Michael Schmid; A T Summer
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: Huntington F Willard
Evolution of alpha satellite.
Current opinion in genetics & development 1991;1(4):509-14.
1991: R G Lafrenière; Carolyn J Brown; V E Powers; Laura Carrel; Kay E Davies; David Barker; Huntington F Willard
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: P E Warburton; G M Greig; Thomas Haaf; Huntington F Willard
PCR amplification of chromosome-specific alpha satellite DNA: definition of centromeric STS markers and polymorphic analysis.
Genomics 1991;11(2):324-33.
1991: M M Mahtani; R G Lafrenière; T A Kruse; Huntington F Willard
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: A P Losada; Maija Wessman; Marjaana Tiainen; Anton H N Hopman; Huntington F Willard; Francesc Solé; Maria Rosa Caballín; S Woessner; Sakari Knuutila
Trisomy 12 in chronic lymphocytic leukemia: an interphase cytogenetic study.
Blood 1991;78(3):775-9.
1991: J Fujii; A Zarain-Herzberg; Huntington F Willard; Michihiko Tada; David H MacLennan
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: R Wevrick; Huntington F Willard
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: R G Lafreniere; M T Geraghty; David Valle; T B Shows; Huntington F Willard
Ornithine aminotransferase-related sequences map to two nonadjacent intervals on the human X chromosome short arm.
Genomics 1991;10(1):276-9.
1991: Carolyn J Brown; R G Lafreniere; V E Powers; G Sebastio; A Ballabio; A L Pettigrew; David Ledbetter; E Levy; I W Craig; Huntington F Willard
Localization of the X inactivation centre on the human X chromosome in Xq13.
Nature 1991;349(6304):82-4.
1991: Carolyn J Brown; A Ballabio; J L Rupert; R G Lafreniere; Markus Grompe; R Tonlorenzi; Huntington F Willard
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: G M Greig; S Parikh; J George; V E Powers; Huntington F Willard
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: Elizabeth M C Fisher; P Beer-Romero; Laura G Brown; A Ridley; J A McNeil; Jeanne B Lawrence; Huntington F Willard; F R Bieber; David C Page
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: S J Durfy; Huntington F Willard
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: Rachel Wevrick; W C Earnshaw; P N Howard-Peebles; Huntington F Willard
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: K G Ten Hagen; David M Gilbert; Huntington F Willard; Stanley N Cohen
Replication timing of DNA sequences associated with human centromeres and telomeres.
Molecular and cellular biology 1990;10(12):6348-55.
1990: Huntington F Willard
Centromeres of mammalian chromosomes.
Trends in genetics : TIG 1990;6(12):410-6.
1990: P E Warburton; Huntington F Willard
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: V M Watt; Huntington F Willard
The human aminopeptidase N gene: isolation, chromosome localization, and DNA polymorphism analysis.
Human genetics 1990;85(6):651-4.
1990: K Otsu; Huntington F Willard; Vijay K Khanna; F Zorzato; N Michael Green; David H MacLennan
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: C B Sharp; H M Bedford; Huntington F Willard
Pericentromeric structure of human X "isochromosomes": evidence for molecular heterogeneity.
Human genetics 1990;85(3):330-6.
1990: M M Mahtani; Huntington F Willard
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: Carolyn J Brown; A M Flenniken; B R Williams; Huntington F Willard
X chromosome inactivation of the human TIMP gene.
Nucleic acids research 1990;18(14):4191-5.
1990: R G Lafreniere; Huntington F Willard
A Rsal RFLP at the DXS467 locus.
Nucleic acids research 1990;18(12):3673.
1990: R G Lafreniere; Huntington F Willard
A BstE II RFLP at the DXS153 locus.
Nucleic acids research 1990;18(12):3673.
1990: Alex E MacKenzie; Robert G Korneluk; F Zorzato; J Fujii; M Phillips; D Iles; B Wieringa; S Leblond; J Bailly; Huntington F Willard
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: J Fujii; Huntington F Willard; David H MacLennan
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: Carolyn J Brown; Huntington F Willard
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: P Shier; Huntington F Willard; V M Watt
Localization of the insulin receptor-related receptor gene to human chromosome 1.
Cytogenetics and cell genetics 1990;54(1-2):80-1.
1990: Huntington F Willard
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: Rachel Wevrick; Huntington F Willard
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: G M Greig; S B England; H M Bedford; Huntington F Willard
Chromosome-specific alpha satellite DNA from the centromere of human chromosome 16.
American journal of human genetics 1989;45(6):862-72.
1989: S J Durfy; Huntington F Willard
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: Carolyn J Brown; Huntington F Willard
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: R G Lafreniere; M M Mahtani; Huntington F Willard
An X-linked DraI RFLP recognized by cpX23 [DXS132].
Nucleic acids research 1989;17(16):6754.
1989: J S Waye; Huntington F Willard
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: J S Waye; Huntington F Willard
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: Carolyn J Brown; V E Powers; D L Munroe; R Sheinin; Huntington F Willard
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: Huntington F Willard; S J Durfy; M M Mahtani; H Dorkins; K E Davies; Bryan R G Williams
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: Carolyn J Brown; S J Goss; D B Lubahn; David R Joseph; Elizabeth M Wilson; Frank S French; Huntington F Willard
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: Carolyn J Brown; T Sekiguchi; T Nishimoto; Huntington F Willard
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: Tiina Alitalo; Huntington F Willard; Albert de La Chapelle
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: Huntington F Willard
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: Huntington F Willard; Rachel Wevrick; P E Warburton
Human centromere structure: organization and potential role of alpha satellite DNA.
Progress in clinical and biological research 1989;318():9-18.
1989: Brian H Robinson; K Chun; Neviana Mackay; Gail Otulakowski; R Petrova-Benedict; Huntington F Willard
Isolated and combined deficiencies of the alpha-keto acid dehydrogenase complexes.
Annals of the New York Academy of Sciences 1989;573():337-46.
1988: C J Brown; M M Mahtani; Huntington F Willard
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: M M Mahtani; Huntington F Willard
A primary genetic map of the pericentromeric region of the human X chromosome.
Genomics 1988;2(4):294-301.
1988: J S Waye; Roy A Gravel; Huntington F Willard
Two PstI RFLPs in the PCCB gene on the long arm of chromosome 3.
Nucleic acids research 1988;16(5):2362.
1988: R Allore; David O'Hanlon; R Price; K Neilson; Huntington F Willard; D R Cox; Alexander Marks; Robert J Dunn
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: J S Waye; A R Mitchell; Huntington F Willard
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: Huntington F Willard; G M Greig; V E Powers; J S Waye
Molecular organization and haplotype analysis of centromeric DNA from human chromosome 17: implications for linkage in neurofibromatosis.
Genomics 1987;1(4):368-73.
1987: Carolyn J Brown; Huntington F Willard
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: J S Waye; G M Greig; Huntington F Willard
Detection of novel centromeric polymorphisms associated with alpha satellite DNA from human chromosome 11.
Human genetics 1987;77(2):151-6.
1987: J S Waye; Huntington F Willard
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: J S Waye; S J Durfy; D Pinkel; S Kenwrick; M Patterson; K E Davies; Huntington F Willard
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: David H MacLennan; C J Brandl; S Champaneria; P C Holland; V E Powers; Huntington F Willard
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: Huntington F Willard; J S Waye
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: Huntington F Willard; J S Waye; M H Skolnick; C E Schwartz; V E Powers; S B England
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.