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Lea K Davis
Lea K Davis
Icahn School of Medicine at Mount Sinai
Geverifieerd e-mailadres voor vumc.org
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Genome-wide meta-analysis identifies new loci and functional pathways influencing Alzheimer’s disease risk
IE Jansen, JE Savage, K Watanabe, J Bryois, DM Williams, S Steinberg, ...
Nature genetics 51 (3), 404-413, 2019
22162019
Autism genome-wide copy number variation reveals ubiquitin and neuronal genes
JT Glessner, K Wang, G Cai, O Korvatska, CE Kim, S Wood, H Zhang, ...
Nature 459 (7246), 569-573, 2009
16472009
Multiple recurrent de novo CNVs, including duplications of the 7q11. 23 Williams syndrome region, are strongly associated with autism
SJ Sanders, AG Ercan-Sencicek, V Hus, R Luo, MT Murtha, ...
Neuron 70 (5), 863-885, 2011
15372011
Genomic relationships, novel loci, and pleiotropic mechanisms across eight psychiatric disorders
PH Lee, V Anttila, H Won, YCA Feng, J Rosenthal, Z Zhu, EM Tucker-Drob, ...
Cell 179 (7), 1469-1482. e11, 2019
12012019
A genome-wide association study with 1,126,563 individuals identifies new risk loci for Alzheimer’s disease
DP Wightman, IE Jansen, JE Savage, AA Shadrin, S Bahrami, D Holland, ...
Nature genetics 53 (9), 1276-1282, 2021
7462021
Large-scale genome-wide meta-analysis of polycystic ovary syndrome suggests shared genetic architecture for different diagnosis criteria
F Day, T Karaderi, MR Jones, C Meun, C He, A Drong, P Kraft, N Lin, ...
PLoS genetics 14 (12), e1007813, 2018
5272018
GWAS of lifetime cannabis use reveals new risk loci, genetic overlap with psychiatric traits, and a causal effect of schizophrenia liability
JA Pasman, KJH Verweij, Z Gerring, S Stringer, S Sanchez-Roige, ...
Nature neuroscience 21 (9), 1161-1170, 2018
4842018
Revealing the complex genetic architecture of obsessive-compulsive disorder using meta-analysis
D Posthuma
Molecular psychiatry 23 (5), 1181-1188, 2018
4322018
Genome-wide association study of obsessive-compulsive disorder
SE Stewart, D Yu, JM Scharf, BM Neale, JA Fagerness, CA Mathews, ...
Molecular psychiatry 18 (7), 788-798, 2013
4222013
Partitioning the heritability of Tourette syndrome and obsessive compulsive disorder reveals differences in genetic architecture
LK Davis, D Yu, CL Keenan, ER Gamazon, AI Konkashbaev, EM Derks, ...
PLoS genetics 9 (10), e1003864, 2013
3422013
Interrogating the genetic determinants of Tourette’s syndrome and other tic disorders through genome-wide association studies
D Yu, JH Sul, F Tsetsos, MS Nawaz, AY Huang, I Zelaya, C Illmann, ...
American Journal of Psychiatry 176 (3), 217-227, 2019
3382019
Genome-wide meta-analysis of problematic alcohol use in 435,563 individuals yields insights into biology and relationships with other traits
H Zhou, JM Sealock, S Sanchez-Roige, TK Clarke, DF Levey, Z Cheng, ...
Nature neuroscience 23 (7), 809-818, 2020
3272020
The role of sex in the genomics of human complex traits
EA Khramtsova, LK Davis, BE Stranger
Nature Reviews Genetics 20 (3), 173-190, 2019
3042019
A large-scale genome-wide association study meta-analysis of cannabis use disorder
EC Johnson, D Demontis, TE Thorgeirsson, RK Walters, R Polimanti, ...
The Lancet Psychiatry 7 (12), 1032-1045, 2020
2982020
Copy number variations on chromosome 12q14 in patients with normal tension glaucoma
JH Fingert, AL Robin, JL Stone, BR Roos, LK Davis, TE Scheetz, ...
Human molecular genetics 20 (12), 2482-2494, 2011
2372011
The biological contributions to gender identity and gender diversity: bringing data to the table
TJC Polderman, BPC Kreukels, MS Irwig, L Beach, YM Chan, EM Derks, ...
Behavior genetics 48, 95-108, 2018
2342018
Genome-wide association study of Tourette's syndrome
JM Scharf, D Yu, CA Mathews, BM Neale, SE Stewart, JA Fagerness, ...
Molecular psychiatry 18 (6), 721-728, 2013
2342013
Penetrance and pleiotropy of polygenic risk scores for schizophrenia in 106,160 patients across four health care systems
AB Zheutlin, J Dennis, R Karlsson Linnér, A Moscati, N Restrepo, ...
American Journal of Psychiatry 176 (10), 846-855, 2019
2222019
Genetic influences on eight psychiatric disorders based on family data of 4 408 646 full and half-siblings, and genetic data of 333 748 cases and controls
E Pettersson, P Lichtenstein, H Larsson, J Song, A Deficit, A Agrawal, ...
Psychological medicine 49 (7), 1166-1173, 2019
2012019
Rare copy number variants in NRXN1 and CNTN6 increase risk for Tourette syndrome
AY Huang, D Yu, LK Davis, JH Sul, F Tsetsos, V Ramensky, I Zelaya, ...
Neuron 94 (6), 1101-1111. e7, 2017
1972017
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Artikelen 1–20