| LD Score regression distinguishes confounding from polygenicity in genome-wide association studies BK Bulik-Sullivan, PR Loh, HK Finucane, S Ripke, J Yang, N Patterson, ... Nature genetics 47 (3), 291-295, 2015 | 2078 | 2015 |
| Biological insights from 108 schizophrenia-associated genetic loci S Ripke, BM Neale, A Corvin, JTR Walters, KH Farh, PA Holmans, P Lee, ... Nature 511 (7510), 421, 2014 | 1599 | 2014 |
| Schizophrenia risk from complex variation of complement component 4 A Sekar, AR Bialas, H De Rivera, A Davis, TR Hammond, N Kamitaki, ... Nature 530 (7589), 177-183, 2016 | 1454 | 2016 |
| Genome-wide association analyses identify 44 risk variants and refine the genetic architecture of major depression NR Wray, S Ripke, M Mattheisen, M Trzaskowski, EM Byrne, A Abdellaoui, ... Nature genetics 50 (5), 668-681, 2018 | 1204 | 2018 |
| Genetic variation in the 6p22. 3 gene DTNBP1, the human ortholog of the mouse dysbindin gene, is associated with schizophrenia RE Straub, Y Jiang, CJ MacLean, Y Ma, BT Webb, MV Myakishev, ... The American Journal of Human Genetics 71 (2), 337-348, 2002 | 999 | 2002 |
| Analysis of shared heritability in common disorders of the brain V Anttila, B Bulik-Sullivan, HK Finucane, RK Walters, J Bras, L Duncan, ... Science 360 (6395), 2018 | 670 | 2018 |
| Modeling linkage disequilibrium increases accuracy of polygenic risk scores BJ Vilhjálmsson, J Yang, HK Finucane, A Gusev, S Lindström, S Ripke, ... The american journal of human genetics 97 (4), 576-592, 2015 | 628 | 2015 |
| Identification of common genetic risk variants for autism spectrum disorder J Grove, S Ripke, TD Als, M Mattheisen, RK Walters, H Won, J Pallesen, ... Nature genetics 51 (3), 431-444, 2019 | 572 | 2019 |
| A potential vulnerability locus for schizophrenia on chromosome 6p24–22: evidence for genetic heterogeneity RE Straub, CJ MacLean, FA O'Neill, J Burke, B Murphy, F Duke, ... Nature genetics 11 (3), 287-293, 1995 | 568 | 1995 |
| Partitioning heritability of regulatory and cell-type-specific variants across 11 common diseases A Gusev, SH Lee, G Trynka, H Finucane, BJ Vilhjálmsson, H Xu, C Zang, ... The American Journal of Human Genetics 95 (5), 535-552, 2014 | 483 | 2014 |
| Genome-wide association meta-analysis in 269,867 individuals identifies new genetic and functional links to intelligence JE Savage, PR Jansen, S Stringer, K Watanabe, J Bryois, CA De Leeuw, ... Nature genetics 50 (7), 912-919, 2018 | 452 | 2018 |
| Contribution of copy number variants to schizophrenia from a genome-wide study of 41,321 subjects CR Marshall, DP Howrigan, D Merico, B Thiruvahindrapuram, W Wu, ... Nature genetics 49 (1), 27-35, 2017 | 440 | 2017 |
| Sparse whole-genome sequencing identifies two loci for major depressive disorder N Cai, TB Bigdeli, W Kretzschmar, Y Li, J Liang, L Song, J Hu, Q Li, W Jin, ... Nature 523 (7562), 588, 2015 | 413 | 2015 |
| Contrasting genetic architectures of schizophrenia and other complex diseases using fast variance-components analysis PR Loh, G Bhatia, A Gusev, HK Finucane, BK Bulik-Sullivan, SJ Pollack, ... Nature genetics 47 (12), 1385, 2015 | 316 | 2015 |
| Genome‐wide association study of alcohol dependence implicates a region on chromosome 11 HJ Edenberg, DL Koller, X Xuei, L Wetherill, JN McClintick, L Almasy, ... Alcoholism: Clinical and Experimental Research 34 (5), 840-852, 2010 | 296 | 2010 |
| Transancestral GWAS of alcohol dependence reveals common genetic underpinnings with psychiatric disorders RK Walters, R Polimanti, EC Johnson, JN McClintick, MJ Adams, ... Nature neuroscience 21 (12), 1656-1669, 2018 | 239 | 2018 |
| Prestin, a cochlear motor protein, is defective in non-syndromic hearing loss XZ Liu, XM Ouyang, XJ Xia, J Zheng, A Pandya, F Li, LL Du, KO Welch, ... Human molecular genetics 12 (10), 1155-1162, 2003 | 218 | 2003 |
| A genome-wide analysis of liberal and conservative political attitudes PK Hatemi, NA Gillespie, LJ Eaves, BS Maher, BT Webb, AC Heath, ... The Journal of Politics 73 (1), 271-285, 2011 | 217 | 2011 |
| Genomic dissection of bipolar disorder and schizophrenia, including 28 subphenotypes DM Ruderfer, S Ripke, A McQuillin, J Boocock, EA Stahl, JMW Pavlides, ... Cell 173 (7), 1705-1715. e16, 2018 | 216 | 2018 |
| Susceptibility genes for nicotine dependence: a genome scan and followup in an independent sample suggest that regions on chromosomes 2, 4, 10, 16, 17 and 18 merit further study RE Straub, PF Sullivan, Y Ma, MV Myakishev, C Harris-Kerr, B Wormley, ... Molecular psychiatry 4 (2), 129-144, 1999 | 194 | 1999 |
Kenneth KendlerProfessor and Eminent Scholar, Virginia Commonwealth UniversityVerified email at vcuhealth.org
