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Benjamin Neale
Benjamin Neale
Massachusetts General Hospital; Broad Institute; Harvard Medical School
在 broadinstitute.org 的电子邮件经过验证
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引用次数
引用次数
年份
PLINK: a tool set for whole-genome association and population-based linkage analyses
S Purcell, B Neale, K Todd-Brown, L Thomas, MAR Ferreira, D Bender, ...
The American journal of human genetics 81 (3), 559-575, 2007
323082007
Analysis of protein-coding genetic variation in 60,706 humans
M Lek, KJ Karczewski, EV Minikel, KE Samocha, E Banks, T Fennell, ...
Nature 536 (7616), 285-291, 2016
102742016
Biological insights from 108 schizophrenia-associated genetic loci
C Pantelis, GN Papadimitriou, S Papiol, E Parkhomenko, MT Pato, ...
Nature 511 (7510), 421-427, 2014
74232014
The mutational constraint spectrum quantified from variation in 141,456 humans
KJ Karczewski, LC Francioli, G Tiao, BB Cummings, J Alföldi, Q Wang, ...
Nature 581 (7809), 434-443, 2020
72772020
Detection of widespread horizontal pleiotropy in causal relationships inferred from Mendelian randomization between complex traits and diseases
M Verbanck, CY Chen, B Neale, R Do
Nature genetics 50 (5), 693-698, 2018
45992018
LD Score regression distinguishes confounding from polygenicity in genome-wide association studies
BK Bulik-Sullivan, PR Loh, HK Finucane, S Ripke, J Yang, ...
Nature genetics 47 (3), 291-295, 2015
44352015
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
35032015
Clonal hematopoiesis and blood-cancer risk inferred from blood DNA sequence
G Genovese, AK Kähler, RE Handsaker, J Lindberg, SA Rose, ...
New England Journal of Medicine 371 (26), 2477-2487, 2014
33752014
Identification of risk loci with shared effects on five major psychiatric disorders: a genome-wide analysis
Cross-Disorder Group of the Psychiatric Genomics Consortium
The Lancet 381 (9875), 1371-1379, 2013
30062013
Synaptic, transcriptional and chromatin genes disrupted in autism
S De Rubeis, X He, AP Goldberg, CS Poultney, K Samocha, ...
Nature 515 (7526), 209-215, 2014
27822014
Common genetic determinants of schizophrenia and bipolar disorder in Swedish families: a population-based study
P Lichtenstein, BH Yip, C Björk, Y Pawitan, TD Cannon, PF Sullivan, ...
The Lancet 373 (9659), 234-239, 2009
24362009
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
23462013
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
22282015
Discovery of the first genome-wide significant risk loci for attention deficit/hyperactivity disorder
D Demontis, RK Walters, J Martin, M Mattheisen, TD Als, E Agerbo, ...
Nature genetics 51 (1), 63-75, 2019
21212019
Patterns and rates of exonic de novo mutations in autism spectrum disorders
BM Neale, Y Kou, L Liu, A Ma’Ayan, KE Samocha, A Sabo, CF Lin, ...
Nature 485 (7397), 242-245, 2012
20302012
Clinical use of current polygenic risk scores may exacerbate health disparities
AR Martin, M Kanai, Y Kamatani, Y Okada, BM Neale, MJ Daly
Nature genetics 51 (4), 584-591, 2019
20132019
Genome-wide association study identifies five new schizophrenia loci
Nature genetics 43 (10), 969-976, 2011
20092011
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
19002019
Large-scale exome sequencing study implicates both developmental and functional changes in the neurobiology of autism
FK Satterstrom, JA Kosmicki, J Wang, MS Breen, S De Rubeis, JY An, ...
Cell 180 (3), 568-584. e23, 2020
17552020
Genome-wide association analysis identifies 13 new risk loci for schizophrenia
S Ripke, C O'dushlaine, K Chambert, JL Moran, AK Kähler, S Akterin, ...
Nature genetics 45 (10), 1150-1159, 2013
17452013
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