Huntington F Willard
Huntington F Willard
Genome National Group
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Cited by
Cited by
Thompson & Thompson genetics in medicine
HF Willard
Saunders, 2001
X-inactivation profile reveals extensive variability in X-linked gene expression in females
L Carrel, HF Willard
Nature 434 (7031), 400-404, 2005
A gene from the region of the human X inactivation centre is expressed exclusively from the inactive X chromosome
CJ Brown, A Ballabio, JL Rupert, RG Lafreniere, M Grompe, R Tonlorenzi, ...
Nature 349 (6304), 38-44, 1991
The human XIST gene: analysis of a 17 kb inactive X-specific RNA that contains conserved repeats and is highly localized within the nucleus
CJ Brown, BD Hendrich, JL Rupert, RG Lafreniere, Y Xing, J Lawrence, ...
Cell 71 (3), 527-542, 1992
The DNA sequence of the human X chromosome
MT Ross, DV Grafham, AJ Coffey, S Scherer, K McLay, D Muzny, ...
Nature 434 (7031), 325-337, 2005
Cloning of human androgen receptor complementary DNA and localization to the X chromosome
DB Lubahn, DR Joseph, PM Sullivan, HF Willard, FS French, EM Wilson
Science 240 (4850), 327-330, 1988
XIST RNA paints the inactive X chromosome at interphase: evidence for a novel RNA involved in nuclear/chromosome structure.
CM Clemson, JA McNeil, HF Willard, JB Lawrence
The Journal of cell biology 132 (3), 259-275, 1996
A gene deleted in Kallmann's syndrome shares homology with neural cell adhesion and axonal path-finding molecules
B Franco, S Guioli, A Pragliola, B Incerti, B Bardoni, R Tonlorenzi, ...
Nature 353 (6344), 529-536, 1991
Gene for von Recklinghausen neurofibromatosis is in the pericentromeric region of chromosome 17
D Barker, E Wright, K Nguyen, L Cannon, P Fain, D Goldgar, DT Bishop, ...
Science 236 (4805), 1100-1102, 1987
Molecular cloning of cDNA encoding the Ca2+ release channel (ryanodine receptor) of rabbit cardiac muscle sarcoplasmic reticulum.
K Otsu, HF Willard, VK Khanna, F Zorzato, NM Green, DH MacLennan
Journal of Biological Chemistry 265 (23), 13472-13483, 1990
Formation of de novo centromeres and construction of first-generation human artificial microchromosomes
JJ Harrington, GV Bokkelen, RW Mays, K Gustashaw, HF Willard
Nature genetics 15 (4), 345-355, 1997
Genomic and personalized medicine: foundations and applications
GS Ginsburg, HF Willard
Translational research 154 (6), 277-287, 2009
Hierarchical order in chromosome-specific human alpha satellite DNA
HF Willard, JS Waye
Trends in Genetics 3, 192-198, 1987
Characterization of a murine gene expressed from the inactive X chromosome
G Borsani, R Tonlorenzi, MC Simmler, L Dandolo, D Arnaud, V Capra, ...
Nature 351 (6324), 325-329, 1991
Genomic and genetic definition of a functional human centromere
MG Schueler, AW Higgins, MK Rudd, K Gustashaw, HF Willard
Science 294 (5540), 109-115, 2001
Uniparental disomy as a mechanism for human genetic disease.
JE Spence, RG Perciaccante, GM Greig, HF Willard, DH Ledbetter, ...
American journal of human genetics 42 (2), 217, 1988
Clonal analysis using recombinant DNA probes from the X-chromosome
B Vogelstein, ER Fearon, SR Hamilton, AC Preisinger, HF Willard, ...
Cancer research 47 (18), 4806-4813, 1987
Androgen receptor locus on the human X chromosome: regional localization to Xq11-12 and description of a DNA polymorphism.
CJ Brown, SJ Goss, DB Lubahn, DR Joseph, EM Wilson, FS French, ...
American journal of human genetics 44 (2), 264, 1989
Homologous ribosomal protein genes on the human X and Y chromosomes: escape from X inactivation and possible implications for Turner syndrome
EMC Fisher, P Beer-Romero, LG Brown, A Ridley, JA McNeil, ...
Cell 63 (6), 1205-1218, 1990
Localization of the X inactivation centre on the human X chromosome in Xq13
CJ Brown, RG Lafreniere, VE Powers, G Sebastio, A Ballabio, ...
Nature 349 (6304), 82-84, 1991
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