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Neale, Benjamin M

Stanley Center for Psychiatric Research, Broad Institute of MIT and Harvard, Cambridge, MA, USA

TitleYearPMID
Genome-wide analyses identify 30 loci associated with obsessive-compulsive disorder. 2025 40360802
Genome-wide analyses identify 30 loci associated with obsessive-compulsive disorder. preprint 2025 38712091
Genome-wide analyses of ADHD identify 27 risk loci, refine the genetic architecture and implicate several cognitive domains. 2023 36702997
Mapping genomic loci implicates genes and synaptic biology in schizophrenia. 2022 35396580
Genome-wide association study of more than 40,000 bipolar disorder cases provides new insights into the underlying biology. 2021 34002096
Shared genetic risk between eating disorder- and substance-use-related phenotypes: Evidence from genome-wide association studies. 2021 32064741
A global overview of pleiotropy and genetic architecture in complex traits. 2019 31427789
Clinical use of current polygenic risk scores may exacerbate health disparities. 2019 30926966
Discovery of the first genome-wide significant risk loci for attention deficit/hyperactivity disorder. 2019 30478444
Genome-wide association study identifies 30 loci associated with bipolar disorder. 2019 31043756
International meta-analysis of PTSD genome-wide association studies identifies sex- and ancestry-specific genetic risk loci. 2019 31594949
Interrogating the Genetic Determinants of Tourette's Syndrome and Other Tic Disorders Through Genome-Wide Association Studies. 2019 30818990
Predicting Polygenic Risk of Psychiatric Disorders. 2019 30737014
A Genetic Investigation of Sex Bias in the Prevalence of Attention-Deficit/Hyperactivity Disorder. 2018 29325848
Heritability enrichment of specifically expressed genes identifies disease-relevant tissues and cell types. 2018 29632380
Multi-trait analysis of genome-wide association summary statistics using MTAG. 2018 29292387
Transancestral GWAS of alcohol dependence reveals common genetic underpinnings with psychiatric disorders. 2018 30482948
De Novo Coding Variants Are Strongly Associated with Tourette Disorder. 2017 28472652
Human Demographic History Impacts Genetic Risk Prediction across Diverse Populations. 2017 28366442
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 correlation analysis. 2017 27663502
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