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 | 3884 | 2015 |
Integrating common and rare genetic variation in diverse human populations International HapMap 3 Consortium Nature 467 (7311), 52, 2010 | 3283 | 2010 |
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 | 2475 | 2015 |
Genetic relationship between five psychiatric disorders estimated from genome-wide SNPs B Devlin, JR Kelsoe, P Sklar, MJ Daly, MC O'Donovan, N Craddock, ... Nature genetics 45 (9), 984-994, 2013 | 2432 | 2013 |
Analysis of shared heritability in common disorders of the brain Brainstorm Consortium, V Anttila, B Bulik-Sullivan, HK Finucane, ... Science 360 (6395), eaap8757, 2018 | 1490 | 2018 |
Detection and interpretation of shared genetic influences on 42 human traits JK Pickrell, T Berisa, JZ Liu, L Ségurel, JY Tung, DA Hinds Nature genetics 48 (7), 709-717, 2016 | 1244 | 2016 |
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 | 1191 | 2019 |
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 | 981 | 2018 |
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 | 973 | 2017 |
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 | 862 | 2012 |
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 | 799 | 2016 |
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 | 556 | 2018 |
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 | 540 | 2015 |
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 | 523 | 2017 |
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 | 522 | 2011 |
Genome-wide association study of migraine implicates a common susceptibility variant on 8q22. 1 Nature genetics 42 (10), 869-873, 2010 | 502 | 2010 |
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 | 487 | 2013 |
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 | 453 | 2016 |
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 | 432 | 2012 |
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 | 422 | 2015 |