| 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 | 1401 | 2005 |
| 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 | 610 | 2001 |
| HNF-1 alpha and HNF-1 beta (vHNF-1) share dimerization and homeo domains, but not activation domains, and form heterodimers in vitro. DB Mendel, LP Hansen, MK Graves, PB Conley, GR Crabtree Genes & development 5 (6), 1042-1056, 1991 | 376 | 1991 |
| HNF-1 shares three sequence motifs with the POU domain proteins and is identical to LF-B1 and APF. S Baumhueter, DB Mendel, PB Conley, CJ Kuo, C Turk, MK Graves, ... Genes & development 4 (3), 372-379, 1990 | 338 | 1990 |
| Characterization of a cofactor that regulates dimerization of a mammalian homeodomain protein DB Mendel, PA Khavari, PB Conley, MK Graves, LP Hansen, A Admon, ... Science 254 (5039), 1762-1767, 1991 | 272 | 1991 |
| Structural and functional dynamics of human centromeric chromatin MG Schueler, BA Sullivan Annu. Rev. Genomics Hum. Genet. 7 (1), 301-313, 2006 | 228 | 2006 |
| DNA sequence and analysis of human chromosome 8 C Nusbaum, TS Mikkelsen, MC Zody, S Asakawa, S Taudien, M Garber, ... Nature 439 (7074), 331-335, 2006 | 146 | 2006 |
| Progressive proximal expansion of the primate X chromosome centromere MG Schueler, JM Dunn, CP Bird, MT Ross, L Viggiano, ... Proceedings of the National Academy of Sciences 102 (30), 10563-10568, 2005 | 98 | 2005 |
| Structure, sequence, expression, and chromosomal localization of the human v1avasopressin receptor gene M Thibonnier, MK Graves, MS Wagner, C Auzan, E Clauser, HF Willard Genomics 31 (3), 327-334, 1996 | 97 | 1996 |
| Study of V1-vascular vasopressin receptor gene microsatellite polymorphisms in human essential hypertension M Thibonnier, MK Graves, MS Wagner, N Chatelain, F Soubrier, P Corvol, ... Journal of Molecular and Cellular Cardiology 32 (4), 557-564, 2000 | 88 | 2000 |
| Adaptive evolution of foundation kinetochore proteins in primates MG Schueler, W Swanson, PJ Thomas, NCS Program, ED Green Molecular biology and evolution 27 (7), 1585-1597, 2010 | 79* | 2010 |
| Deletion including the oligophrenin-1 gene associated with enlarged cerebral ventricles, cerebellar hypoplasia, seizures and ataxia D Tentler, P Gustavsson, J Leisti, M Schueler, J Chelly, E Timonen, ... European Journal of Human Genetics 7 (5), 541-548, 1999 | 64 | 1999 |
| Sequence organization and functional annotation of human centromeres MK Rudd, MG Schueler, HF Willard Cold Spring Harbor symposia on quantitative biology 68, 141-150, 2003 | 56 | 2003 |
| Pericentromeric duplications in the laboratory mouse JW Thomas, MG Schueler, TJ Summers, RW Blakesley, JC McDowell, ... Genome research 13 (1), 55-63, 2003 | 47 | 2003 |
| Histone modifications within the human X centromere region B Mravinac, LL Sullivan, JW Reeves, CM Yan, KS Kopf, CJ Farr, ... PloS one 4 (8), e6602, 2009 | 39 | 2009 |
| Comparative sequence analyses reveal sites of ancestral chromosomal fusions in the Indian muntjac genome V Tsipouri, MG Schueler, S Hu, ... Genome Biology 9, 1-16, 2008 | 39 | 2008 |
| Chromosome engineering: generation of mono-and dicentric isochromosomes in a somatic cell hybrid system AW Higgins, MG Schueler, HF Willard Chromosoma 108 (4), 256-265, 1999 | 27 | 1999 |
| Large-insert clone/STS contigs in Xq11–q12, spanning deletions in patients with androgen insensitivity and mental retardation MG Schueler, AW Higgins, R Nagaraja, D Tentler, N Dahl, K Gustashaw, ... Genomics 66 (1), 104-109, 2000 | 19 | 2000 |
| Familial X centromere variant resulting in false‐positive prenatal diagnosis of monosomy X by interphase FISH K Tsuchiya, MG Schueler, VG Dev Prenatal Diagnosis: Published in Affiliation With the International Society …, 2001 | 11 | 2001 |
| Xp and Xq isochromosomes: mapping the functional centromere and testing Darlington's model of centromere misdivision. HF Willard, AW Higgins, MG Schueler, K Gustashaw AMERICAN JOURNAL OF HUMAN GENETICS 67 (4), 44-44, 2000 | 2 | 2000 |
Gerald R Crabtreestanford universityVerified email at stanford.edu