Gene discovery and polygenic prediction from a genome-wide association study of educational attainment in 1.1 million individuals JJ Lee, R Wedow, A Okbay, E Kong, O Maghzian, M Zacher, ... Nature genetics 50 (8), 1112-1121, 2018 | 2419 | 2018 |
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 | 1976 | 2019 |
Genome-wide association analyses of risk tolerance and risky behaviors in over 1 million individuals identify hundreds of loci and shared genetic influences RK Linnér, P Biroli, E Kong, SFW Meddens, R Wedow, MA Fontana, ... Nature genetics 51 (2), 245-257, 2019 | 714 | 2019 |
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 | 704 | 2019 |
Whole‐genome sequencing identifies EN1 as a determinant of bone density and fracture HF Zheng, V Forgetta, YH Hsu, K Estrada, A Rosello‐Diez, PJ Leo, ... Nature 526 (7571), 112-117, 2015 | 585 | 2015 |
Genetic evidence of assortative mating in humans MR Robinson, A Kleinman, M Graff, AAE Vinkhuyzen, D Couper, ... Nature Human Behaviour 1 (1), 1-13, 2017 | 353 | 2017 |
Identification of novel risk loci for restless legs syndrome in genome-wide association studies in individuals of European ancestry: a meta-analysis B Schormair, C Zhao, S Bell, E Tilch, AV Salminen, B Pütz, Y Dauvilliers, ... The Lancet Neurology 16 (11), 898-907, 2017 | 233 | 2017 |
A genetic investigation of sex bias in the prevalence of attention-deficit/hyperactivity disorder J Martin, RK Walters, D Demontis, M Mattheisen, SH Lee, E Robinson, ... Biological psychiatry 83 (12), 1044-1053, 2018 | 200 | 2018 |
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 | 107 | 2019 |
Common Variant Burden Contributes to the Familial Aggregation of Migraine in 1,589 Families P Gormley, MI Kurki, ME Hiekkala, K Veerapen, P Häppölä, AA Mitchell, ... Neuron 98 (4), 743-753. e4, 2018 | 106 | 2018 |
The effect of LRRK2 loss-of-function variants in humans N Whiffin, IM Armean, A Kleinman, JL Marshall, EV Minikel, JK Goodrich, ... Nature Medicine, 1-9, 2020 | 104 | 2020 |
Multiethnic GWAS reveals polygenic architecture of earlobe attachment JR Shaffer, J Li, MK Lee, J Roosenboom, E Orlova, K Adhikari, M Agee, ... The American Journal of Human Genetics 101 (6), 913-924, 2017 | 51 | 2017 |
Replication and characterization of CADM2 and MSRA genes on human behavior B Boutwell, D Hinds, M Agee, B Alipanahi, A Auton, RK Bell, K Bryc, ... Heliyon 3 (7), e00349, 2017 | 48 | 2017 |
Anti-IL-13Rα2 therapy promotes recovery in a murine model of inflammatory bowel disease EP Karmele, TS Pasricha, TR Ramalingam, RW Thompson, RL Gieseck, ... Mucosal immunology 12 (5), 1174-1186, 2019 | 44 | 2019 |
Ehrhart functions and symplectic embeddings of ellipsoids D Cristofaro‐Gardiner, A Kleinman Journal of the London Mathematical Society 101 (3), 1090-1111, 2020 | 31 | 2020 |
Association of whole-genome and NETRIN1 signaling pathway–derived polygenic risk scores for major depressive disorder and white matter microstructure in the UK Biobank MC Barbu, Y Zeng, X Shen, SR Cox, TK Clarke, J Gibson, MJ Adams, ... Biological Psychiatry: Cognitive Neuroscience and Neuroimaging 4 (1), 91-100, 2019 | 28 | 2019 |
Human loss-of-function variants suggest that partial LRRK2 inhibition is a safe therapeutic strategy for Parkinson’s disease N Whiffin, IM Armean, A Kleinman, JL Marshall, EV Minikel, JK Goodrich, ... BioRxiv, 561472, 2019 | 15 | 2019 |
An atlas of human and murine genetic influences on osteoporosis JA Morris, JP Kemp, SE Youlten, L Laurent, JG Logan, R Chai, ... bioRxiv, 338863, 2018 | 15 | 2018 |
Affine and projective tree metric theorems A Kleinman, M Harel, L Pachter Annals of Combinatorics 17 (1), 205-228, 2013 | 12 | 2013 |
Author Correction: 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 (5), 920-920, 2019 | 9 | 2019 |