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Aaron Kleinman
Aaron Kleinman
Computational Biologist, 23andMe
Verified email at 23andme.com
Title
Cited by
Cited by
Year
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
20982018
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
15582019
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
6212019
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
6052019
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
5372015
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
2952017
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
2192017
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
1792018
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
972018
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
932020
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
852019
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
472017
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
462017
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
402019
Ehrhart functions and symplectic embeddings of ellipsoids
D Cristofaro‐Gardiner, A Kleinman
Journal of the London Mathematical Society 101 (3), 1090-1111, 2020
292020
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
282019
Genome-wide association analyses of risk tolerance and risky behaviors in over one million individuals identify hundreds of loci and shared genetic influences
RK Linnér, P Biroli, E Kong, SFW Meddens, R Wedow, MA Fontana, ...
Human Capital and Economic Opportunity Working Group Working Papers, 2018
152018
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
142019
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
142018
Affine and projective tree metric theorems
A Kleinman, M Harel, L Pachter
Annals of Combinatorics 17 (1), 205-228, 2013
112013
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Articles 1–20