Thompson & Thompson genetics in medicine HF Willard Saunders, 2001 | 2493* | 2001 |
X-inactivation profile reveals extensive variability in X-linked gene expression in females L Carrel, HF Willard Nature 434 (7031), 400-404, 2005 | 2325 | 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 | 1799 | 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 | 1577 | 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 | 1392 | 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 | 1223 | 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 | 1017 | 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 | 982 | 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 | 918 | 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 | 839 | 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 | 784 | 1997 |
Genomic and personalized medicine: foundations and applications GS Ginsburg, HF Willard Translational research 154 (6), 277-287, 2009 | 757 | 2009 |
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 | 669 | 1991 |
Hierarchical order in chromosome-specific human alpha satellite DNA HF Willard, JS Waye Trends in Genetics 3, 192-198, 1987 | 668 | 1987 |
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 | 609 | 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 | 566 | 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 | 532 | 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 | 527 | 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 | 489 | 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 | 469 | 1991 |