Huntington  F Willard
Huntington F Willard
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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, 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
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
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
Formation of de novo centromeres and construction of first-generation human artificial microchromosomes
JJ Harrington, G Van Bokkelen, RW Mays, K Gustashaw, HF Willard
Nature genetics 15 (4), 345-355, 1997
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
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 personalized medicine: foundations and applications
GS Ginsburg, HF Willard
Translational research 154 (6), 277-287, 2009
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
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
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
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
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
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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