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Verneri Anttila
Verneri Anttila
Post-doctoral Fellow, Broad Institute / Harvard Medical School
Verified email at atgu.mgh.harvard.edu
Title
Cited by
Cited by
Year
An atlas of genetic correlations across human diseases and traits
B Bulik-Sullivan, HK Finucane, V Anttila, A Gusev, FR Day, PR Loh, ...
Nature genetics 47 (11), 1236-1241, 2015
33582015
Integrating common and rare genetic variation in diverse human populations
International HapMap 3 Consortium
Nature 467 (7311), 52, 2010
31382010
Genetic relationship between five psychiatric disorders estimated from genome-wide SNPs
SH Lee, S Ripke, BM Neale, SV Faraone, SM Purcell, RH Perlis, ...
Nature genetics 45 (9), 984-994, 2013
23292013
Partitioning heritability by functional annotation using genome-wide association summary statistics
HK Finucane, B Bulik-Sullivan, A Gusev, G Trynka, Y Reshef, PR Loh, ...
Nature genetics 47 (11), 1228-1235, 2015
21372015
Analysis of shared heritability in common disorders of the brain
Brainstorm Consortium, V Anttila, B Bulik-Sullivan, HK Finucane, ...
Science 360 (6395), eaap8757, 2018
13632018
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
10162019
LD Hub: a centralized database and web interface to perform LD score regression that maximizes the potential of summary level GWAS data for SNP heritability and genetic …
J Zheng, AM Erzurumluoglu, BL Elsworth, JP Kemp, L Howe, PC Haycock, ...
Bioinformatics 33 (2), 272-279, 2017
9122017
Heritability enrichment of specifically expressed genes identifies disease-relevant tissues and cell types
HK Finucane, YA Reshef, V Anttila, K Slowikowski, A Gusev, A Byrnes, ...
Nature genetics 50 (4), 621-629, 2018
8522018
IFITM3 restricts the morbidity and mortality associated with influenza
AR Everitt, S Clare, T Pertel, SP John, RS Wash, SE Smith, CR Chin, ...
Nature 484 (7395), 519-523, 2012
8172012
Meta-analysis of 375,000 individuals identifies 38 susceptibility loci for migraine
P Gormley, V Anttila, BS Winsvold, P Palta, T Esko, TH Pers, KH Farh, ...
Nature genetics 48 (8), 856-866, 2016
7222016
Psychiatric genome-wide association study analyses implicate neuronal, immune and histone pathways
B Devlin, JR Kelsoe, P Sklar, MJ Daly, MC O'Donovan, N Craddock, ...
Nature neuroscience 18 (2), 199-209, 2015
5172015
Genome-wide association study reveals three susceptibility loci for common migraine in the general population
DI Chasman, M Schürks, V Anttila, B de Vries, U Schminke, LJ Launer, ...
Nature genetics 43 (7), 695-698, 2011
4932011
Genome-wide association study of migraine implicates a common susceptibility variant on 8q22. 1
Nature genetics 42 (10), 869-873, 2010
4882010
Significant locus and metabolic genetic correlations revealed in genome-wide association study of anorexia nervosa
L Duncan, Z Yilmaz, H Gaspar, R Walters, J Goldstein, V Anttila, ...
American journal of psychiatry 174 (9), 850-858, 2017
4632017
Genome-wide meta-analysis identifies new susceptibility loci for migraine
V Anttila, BS Winsvold, P Gormley, T Kurth, F Bettella, G McMahon, ...
Nature genetics 45 (8), 912-917, 2013
4572013
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
4282018
Genetic risk for autism spectrum disorders and neuropsychiatric variation in the general population
EB Robinson, B St Pourcain, V Anttila, JA Kosmicki, B Bulik-Sullivan, ...
Nature genetics 48 (5), 552-555, 2016
4272016
Genome-wide association analysis identifies susceptibility loci for migraine without aura
T Freilinger, V Anttila, B De Vries, R Malik, M Kallela, GM Terwindt, ...
Nature genetics 44 (7), 777-782, 2012
4042012
Genetic Consortium for Anorexia Nervosa of the Wellcome Trust Case Control Consortium 3. An atlas of genetic correlations across human diseases and traits
B Bulik-Sullivan, HK Finucane, V Anttila
Nat Genet 47 (11), 1236-1241, 2015
3812015
Meta-analysis of GWAS of over 16,000 individuals with autism spectrum disorder highlights a novel locus at 10q24. 32 and a significant overlap with schizophrenia
Molecular autism 8, 1-17, 2017
3272017
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