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Vladimir Vacic
Vladimir Vacic
23andMe, Inc.
在 23andme.com 的电子邮件经过验证 - 首页
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引用次数
年份
The impact on clinical success from the 23andMe cohort
X Wang, S Karagounis, SS Shringarpure, R Srivas, QJ Su, ...
medRxiv, 2024.06. 17.24309059, 2024
2024
GWAS of cataract in Puerto Ricans identifies a novel large-effect variant in ITGA6
J Shi, J O’Connell, B Hicks, W Wang, K Bryc, JJ Brady, V Vacic, ...
medRxiv, 2023.07. 25.23293173, 2023
2023
Author Correction: Protein interaction network of alternatively spliced isoforms from brain links genetic risk factors for autism
R Corominas, X Yang, GN Lin, S Kang, Y Shen, L Ghamsari, M Broly, ...
Nature communications 14, 2023
2023
Genetic overlap analysis of endometriosis and asthma identifies shared loci implicating sex hormones and thyroid signalling pathways
EO Adewuyi, D Mehta, DR Nyholt
Human Reproduction 37 (2), 366-383, 2022
212022
Genome-wide analysis of 53,400 people with irritable bowel syndrome highlights shared genetic pathways with mood and anxiety disorders
C Eijsbouts, T Zheng, NA Kennedy, F Bonfiglio, CA Anderson, ...
Nature genetics 53 (11), 1543-1552, 2021
1542021
Genome-wide analysis of 944 133 individuals provides insights into the etiology of haemorrhoidal disease
T Zheng, D Ellinghaus, S Juzenas, F Cossais, G Burmeister, G Mayr, ...
Gut 70 (8), 1538-1549, 2021
332021
pH and proton sensor GPR65 determine susceptibility to atopic dermatitis
L Xie, CI McKenzie, X Qu, Y Mu, Q Wang, N Bing, K Naidoo, MJ Alam, ...
The Journal of Immunology 207 (1), 101-109, 2021
192021
Advancing drug discovery using the power of the human genome
K Heilbron, SV Mozaffari, V Vacic, P Yue, W Wang, J Shi, AM Jubb, ...
The Journal of Pathology 254 (4), 418-429, 2021
202021
The effect of LRRK2 loss-of-function variants in humans (vol 26, pg 869, 2020)
N Whiffin, IM Armean, A Kleinman, JL Marshall, EV Minikel, JK Goodrich, ...
NATURE MEDICINE 27 (2), 355-355, 2021
2021
Inherited myeloproliferative neoplasm risk affects haematopoietic stem cells
EL Bao, SK Nandakumar, X Liao, AG Bick, J Karjalainen, M Tabaka, ...
Nature 586 (7831), 769-775, 2020
1122020
Genome-wide study identifies association between HLA-B∗ 55: 01 and self-reported penicillin allergy
K Krebs, J Bovijn, N Zheng, M Lepamets, JC Censin, T Jürgenson, D Särg, ...
The American Journal of Human Genetics 107 (4), 612-621, 2020
482020
Genetic consequences of the transatlantic slave trade in the Americas
SJ Micheletti, K Bryc, SGA Esselmann, WA Freyman, ME Moreno, ...
The American Journal of Human Genetics 107 (2), 265-277, 2020
1342020
Genomic analysis of male puberty timing highlights shared genetic basis with hair colour and lifespan
B Hollis, FR Day, AS Busch, DJ Thompson, ALG Soares, PRHJ Timmers, ...
Nature communications 11 (1), 1536, 2020
542020
Identification of novel risk loci, causal insights, and heritable risk for Parkinson's disease: a meta-analysis of genome-wide association studies
MA Nalls, C Blauwendraat, CL Vallerga, K Heilbron, S Bandres-Ciga, ...
The Lancet Neurology 18 (12), 1091-1102, 2019
16872019
Sequencing and curation strategies for identifying candidate glioblastoma treatments
MO Frank, T Koyama, K Rhrissorrakrai, N Robine, F Utro, AK Emde, ...
BMC medical genomics 12, 1-16, 2019
112019
Characterization of prevalence and health consequences of uniparental disomy in four million individuals from the general population
P Nakka, SP Smith, AH O’Donnell-Luria, KF McManus, M Agee, A Auton, ...
The American Journal of Human Genetics 105 (5), 921-932, 2019
972019
Genome-wide analysis of insomnia in 1,331,010 individuals identifies new risk loci and functional pathways
PR Jansen, K Watanabe, S Stringer, N Skene, J Bryois, ...
Nature genetics 51 (3), 394-403, 2019
7292019
Association studies of up to 1.2 million individuals yield new insights into the genetic etiology of tobacco and alcohol use
M Liu, Y Jiang, R Wedow, Y Li, DM Brazel, F Chen, G Datta, ...
Nature genetics 51 (2), 237-244, 2019
15912019
Genome-wide association analyses of risk tolerance and risky behaviors in over 1 million individuals identify hundreds of loci and shared genetic influences
R Karlsson Linnér, P Biroli, E Kong, SFW Meddens, R Wedow, ...
Nature genetics 51 (2), 245-257, 2019
6262019
An atlas of genetic influences on osteoporosis in humans and mice
JA Morris, JP Kemp, SE Youlten, L Laurent, JG Logan, RC Chai, ...
Nature genetics 51 (2), 258-266, 2019
6532019
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