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Simon Gregory
Simon Gregory
Professor, Duke University
Adresă de e-mail confirmată pe duke.edu - Pagina de pornire
Titlu
Citat de
Citat de
Anul
Initial sequencing and analysis of the human genome
US DOE Joint Genome Institute: Hawkins Trevor 4 Branscomb Elbert 4 Predki ...
nature 409 (6822), 860-921, 2001
302842001
Initial sequencing and comparative analysis of the mouse genome
European Bioinformatics Institute: Birney Ewan 3 Goldman Nick 3 Kasprzyk ...
Nature 420 (6915), 520-562, 2002
85532002
Identification of the breast cancer susceptibility gene BRCA2
R Wooster, G Bignell, J Lancaster, S Swift, S Seal, J Mangion, N Collins, ...
Nature 378 (6559), 789-792, 1995
49071995
Association of the T-cell regulatory gene CTLA4 with susceptibility to autoimmune disease
H Ueda, JMM Howson, L Esposito, J Heward, Snook, G Chamberlain, ...
Nature 423 (6939), 506-511, 2003
26802003
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
13892005
A physical map of the human genome.
JD McPherson, M Marra, LD Hillier, RH Waterston, A Chinwalla, J Wallis, ...
Nature 409 (6822), 934-942, 2001
1244*2001
A high-resolution HLA and SNP haplotype map for disease association studies in the extended human MHC
PIW De Bakker, G McVean, PC Sabeti, MM Miretti, T Green, J Marchini, ...
Nature genetics 38 (10), 1166-1172, 2006
9242006
Interleukin 7 receptor α chain ( IL7R ) shows allelic and functional association with multiple sclerosis
SG Gregory, S Schmidt, P Seth, JR Oksenberg, J Hart, A Prokop, ...
Nature genetics 39 (9), 1083-1091, 2007
8312007
LMNA, encoding lamin A/C, is mutated in partial lipodystrophy
S Shackleton, DJ Lloyd, SNJ Jackson, R Evans, MF Niermeijer, BM Singh, ...
Nature genetics 24 (2), 153-156, 2000
8262000
Genomic and epigenetic evidence for oxytocin receptor deficiency in autism
SG Gregory, JJ Connelly, AJ Towers, J Johnson, D Biscocho, ...
BMC medicine 7, 1-13, 2009
6622009
A stress response pathway regulates DNA damage through β2-adrenoreceptors and β-arrestin-1
MR Hara, JJ Kovacs, EJ Whalen, S Rajagopal, RT Strachan, W Grant, ...
Nature 477 (7364), 349-353, 2011
4802011
Interleukin-2 gene variation impairs regulatory T cell function and causes autoimmunity
J Yamanouchi, D Rainbow, P Serra, S Howlett, K Hunter, VES Garner, ...
Nature genetics 39 (3), 329-337, 2007
4722007
The DNA sequence and biological annotation of human chromosome 1
SG Gregory, KF Barlow, KE McLay, R Kaul, D Swarbreck, A Dunham, ...
Nature 441 (7091), 315-321, 2006
4622006
A physical map of the mouse genome
SG Gregory, M Sekhon, J Schein, S Zhao, K Osoegawa, CE Scott, ...
Nature 418 (6899), 743-750, 2002
4322002
A high-density screen for linkage in multiple sclerosis
International Multiple Sclerosis Genetics Consortium
The American Journal of Human Genetics 77 (3), 454-467, 2005
3632005
Prospective multicenter validation of androgen receptor splice variant 7 and hormone therapy resistance in high-risk castration-resistant prostate cancer: the PROPHECY study
AJ Armstrong, S Halabi, J Luo, DM Nanus, P Giannakakou, ...
Journal of Clinical Oncology 37 (13), 1120, 2019
3092019
Mutations in SLC19A2 cause thiamine-responsive megaloblastic anaemia associated with diabetes mellitus and deafness
V Labay, T Raz, D Baron, H Mandel, H Williams, T Barrett, R Szargel, ...
nature genetics 22 (3), 300-304, 1999
3081999
Erratum: Initial sequencing and analysis of the human genome: international human genome sequencing consortium (Nature (2001) 409 (860-921))
ES Lander, LM Linton, B Birren, C Nusbaum, MC Zody, J Baldwin, ...
Nature 412 (6846), 565-566, 2001
2752001
Mutation of TBCE causes hypoparathyroidism–retardation–dysmorphism and autosomal recessive Kenny–Caffey syndrome.
R Parvari, E Hershkovitz, N Grossman, R Gorodischer, B Loeys, A Zecic, ...
Nature genetics 32 (3), 2002
2462002
A second major histocompatibility complex susceptibility locus for multiple sclerosis
TW Yeo, PL De Jager, SG Gregory, LF Barcellos, A Walton, A Goris, ...
Annals of Neurology: Official Journal of the American Neurological …, 2007
2402007
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