Benjamin M. Neale
Broad Institute
Public scientific profile · Unclaimed
Built from public scholarly sources. Expertise is inferred by ScienceWe from publications and has not been confirmed by the scientist.
Top expertise
Genetic Associations and Epidemiology
Strong evidence · 17 supporting papers · latest 2026
Mitochondrial Function and Pathology
Strong evidence · 1 supporting paper · latest 2026
Genomic variations and chromosomal abnormalities
Strong evidence · 3 supporting papers · latest 2026
Genomics and Rare Diseases
Strong evidence · 7 supporting papers · latest 2026
Obsessive-Compulsive Spectrum Disorders
Strong evidence · 1 supporting paper · latest 2026
Schizophrenia research and treatment
Solid evidence · 7 supporting papers · latest 2026
Autism Spectrum Disorder Research
Solid evidence · 1 supporting paper · latest 2026
Single-cell and spatial transcriptomics
Solid evidence · 2 supporting papers · latest 2026
Publications (22)
Systematic common and rare variant association testing in 392,030 whole genomes in All of Us
2026DOIPMID 42180372
A 515,579-Genome Reference Panel Improves Rare-Variant Imputation Across Multiple Underrepresented Populations
2026DOI
A unified framework for local-ancestry-aware genetic association analysis across biobanks
2026DOI
RICOPILI: Rapid Imputation for COnsortias PIpeLIne
2026DOI
Mechanism of age-related accumulation of mtDNA mutations in human blood
2026DOIPMID 42203880
The Biobank Rare Variant consortium powers the discovery of rare genetic associations through global collaboration
2026DOIPMID 42238450
Genome-wide analyses identify 30 loci associated with obsessive–compulsive disorder
2026DOI
Contribution of copy number variants to schizophrenia in East Asian populations
2026DOIPMID 42728386
A blended genome and exome sequencing method captures genetic variation in an unbiased and cost-effective manner
2026DOIPMID 42420521
Analysis of Rare Coding Variation Identifies New Genetic Contributors to Schizophrenia
2026DOI
Scalable context-dependent single-cell eQTL mapping reveals disease-relevant regulatory variation beyond static models
2026DOIPMID 42780159
Meta-analysis across six global biobanks identifies recessive coding associations with complex traits and diseases
2026DOIPMID 42068978
Rare variation illuminates the distinct and pleiotropic genetic architecture of autism across neuropsychiatric traits
2026DOI
6. GENOME-WIDE ASSOCIATION STUDIES OF PSYCHOTIC DISORDERS IN DIVERSE AFRICAN POPULATIONS REVEAL SHARED AND POPULATION-SPECIFIC GENETIC RISK
2026DOI
Identification of hub genes involved in early-onset schizophrenia: from genetic susceptibility to predicted regulated gene expression
2026DOIPMID 39975901
Organizations in sourced records
Affiliation evidence only — not confirmed current employment.
- Broad Institute
Source: OpenAlex · retrieved 2026-09-29
Source: ScienceWe Extractor · retrieved 2026-09-27