Robert E. Handsaker

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 Neurodegenerative Diseases

    Strong evidence · 5 supporting papers · latest 2026

  • Genomics and Rare Diseases

    Strong evidence · 4 supporting papers · latest 2024

  • Mitochondrial Function and Pathology

    Strong evidence · 4 supporting papers · latest 2026

  • Genetic Associations and Epidemiology

    Strong evidence · 4 supporting papers · latest 2026

  • RNA Research and Splicing

    Strong evidence · 2 supporting papers · latest 2025

  • Single-cell and spatial transcriptomics

    Strong evidence · 2 supporting papers · latest 2024

  • Genomic variations and chromosomal abnormalities

    Strong evidence · 2 supporting papers · latest 2024

  • Receptor Mechanisms and Signaling

    Strong evidence · 1 supporting paper · latest 2024

Publications (15)

  • Protein-altering variants at copy number-variable regions influence diverse human phenotypes

    2024DOIPMID 38548989

  • Whole genome sequence-based association analysis of African American individuals with bipolar disorder and schizophrenia

    2024DOIPMID 39763555

  • Antisense oligonucleotide–mediated MSH3 suppression reduces somatic CAG repeat expansion in Huntington’s disease iPSC–derived striatal neurons

    2025DOIPMID 39937881

  • Long somatic DNA-repeat expansion drives neurodegeneration in Huntington’s disease

    2025DOIPMID 39824182

  • Concerted neuron-astrocyte gene expression declines in aging and schizophrenia

    2024DOIPMID 38260461

  • Long somatic DNA-repeat expansion drives neurodegeneration in Huntington disease

    2024DOI

  • A concerted neuron–astrocyte program declines in ageing and schizophrenia

    2024DOIPMID 38448582

  • A shared DNA-repeat toxicity threshold, reached somatically at cell-type-specific rates, unites cortical and striatal neurodegeneration in Huntington’s disease

    2025DOIPMID 41427302

  • Utility of long-read sequencing for All of Us

    2024DOIPMID 38281971

  • Insights into the causes and consequences of DNA repeat expansions from 700,000 biobank participants

    2024DOIPMID 39651202

  • Whole-genome sequence-based association analysis of African American individuals with bipolar disorder and schizophrenia

    2025DOIPMID 40886051

  • Insights into DNA repeat expansions among 900,000 biobank participants

    2026DOIPMID 41501457

  • Human and bacterial genetic variation shape oral microbiomes and health

    2026DOIPMID 41606319

  • Human and bacterial genetic variation shape oral microbiomes and health

    2025DOIPMID 40236410

  • Common α-globin variants modify hematologic and other clinical phenotypes in sickle cell trait and disease

    2024DOI

Organizations in sourced records

Affiliation evidence only — not confirmed current employment.

  • Broad Institute

Source: OpenAlex · retrieved 2026-09-29

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