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Olga Gorlova
Olga Gorlova
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Genome-wide association study of systemic sclerosis identifies CD247 as a new susceptibility locus
TRDJ Radstake, O Gorlova, B Rueda, JE Martin, BZ Alizadeh, ...
Nature genetics 42 (5), 426-429, 2010
4502010
Shifting paradigm of association studies: value of rare single-nucleotide polymorphisms
IP Gorlov, OY Gorlova, SR Sunyaev, MR Spitz, CI Amos
The American Journal of Human Genetics 82 (1), 100-112, 2008
4172008
Identification of novel genetic markers associated with clinical phenotypes of systemic sclerosis through a genome-wide association strategy
O Gorlova, JE Martin, B Rueda, BPC Koeleman, J Ying, M Teruel, ...
PLoS genetics 7 (7), e1002178, 2011
2602011
Immunochip analysis identifies multiple susceptibility loci for systemic sclerosis
MD Mayes, L Bossini-Castillo, O Gorlova, JE Martin, X Zhou, WV Chen, ...
The American Journal of Human Genetics 94 (1), 47-61, 2014
2482014
Impact of reduced tobacco smoking on lung cancer mortality in the United States during 1975–2000
SH Moolgavkar, TR Holford, DT Levy, CY Kong, M Foy, L Clarke, J Jeon, ...
Journal of the National Cancer Institute 104 (7), 541-548, 2012
1942012
Never smokers and lung cancer risk: a case‐control study of epidemiological factors
OY Gorlova, Y Zhang, MB Schabath, L Lei, Q Zhang, CI Amos, MR Spitz
International journal of cancer 118 (7), 1798-1804, 2006
1492006
Possible genomic imprinting of three human obesity–related genetic loci
C Dong, WD Li, F Geller, L Lei, D Li, OY Gorlova, J Hebebrand, CI Amos, ...
The American Journal of Human Genetics 76 (3), 427-437, 2005
1372005
Aggregation of cancer among relatives of never‐smoking lung cancer patients
OY Gorlova, SF Weng, Y Zhang, CI Amos, MR Spitz
International journal of cancer 121 (1), 111-118, 2007
1272007
A systemic sclerosis and systemic lupus erythematosus pan-meta-GWAS reveals new shared susceptibility loci
JE Martin, S Assassi, LM Diaz-Gallo, JC Broen, CP Simeon, I Castellvi, ...
Human molecular genetics 22 (19), 4021-4029, 2013
1212013
Evolutionary evidence of the effect of rare variants on disease etiology
IP Gorlov, OY Gorlova, ML Frazier, MR Spitz, CI Amos
Clinical genetics 79 (3), 199-206, 2011
1162011
Genetic linkage and imprinting effects on body mass index in children and young adults
OY Gorlova, CI Amos, NW Wang, S Shete, ST Turner, E Boerwinkle
European Journal of Human Genetics 11 (6), 425-432, 2003
982003
IRF5 polymorphism predicts prognosis in patients with systemic sclerosis
R Sharif, MD Mayes, FK Tan, OY Gorlova, LK Hummers, AA Shah, ...
Annals of the rheumatic diseases 71 (7), 1197-1202, 2012
912012
A GWAS follow-up study reveals the association of the IL12RB2 gene with systemic sclerosis in Caucasian populations
L Bossini-Castillo, JE Martin, J Broen, O Gorlova, CP Simeón, L Beretta, ...
Human molecular genetics 21 (4), 926-933, 2012
912012
Assessment of lung-cancer mortality reduction from CT Screening
CI Henschke, P Boffetta, O Gorlova, R Yip, JO DeLancey, M Foy
Lung Cancer 71 (3), 328-332, 2011
912011
The IRF5TNPO3 association with systemic lupus erythematosus has two components that other autoimmune disorders variably share
LC Kottyan, EE Zoller, J Bene, X Lu, JA Kelly, AM Rupert, CJ Lessard, ...
Human molecular genetics 24 (2), 582-596, 2015
872015
Genes with a large intronic burden show greater evolutionary conservation on the protein level
O Gorlova, A Fedorov, C Logothetis, C Amos, I Gorlov
BMC evolutionary biology 14, 1-7, 2014
762014
Identification of susceptibility pathways for the role of chromosome 15q25. 1 in modifying lung cancer risk
X Ji, Y Bossé, MT Landi, J Gui, X Xiao, D Qian, P Joubert, M Lamontagne, ...
Nature Communications 9 (1), 3221, 2018
712018
Confirmation of TNIP1 but not RHOB and PSORS1C1 as systemic sclerosis risk factors in a large independent replication study
L Bossini-Castillo, JE Martin, J Broen, CP Simeon, L Beretta, OY Gorlova, ...
Annals of the rheumatic diseases 72 (4), 602-607, 2013
692013
Candidate pathways and genes for prostate cancer: a meta-analysis of gene expression data
IP Gorlov, J Byun, OY Gorlova, AM Aparicio, E Efstathiou, CJ Logothetis
BMC medical genomics 2, 1-11, 2009
692009
Missense mutations in hMLH1 and hMSH2 are associated with exonic splicing enhancers
IP Gorlov, OY Gorlova, ML Frazier, CI Amos
The American Journal of Human Genetics 73 (5), 1157-1161, 2003
642003
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Artikelen 1–20