Michael P. Epstein

Career Trajectory

Research Cluster Map

Direct collaborators. Node size = influence, colour = community, dashed = past collaboration.

• Haploinsufficiency of <i>GRHL2</i> is associated with orofacial clefting in humans

  Human Molecular Genetics · 2025-10-21

• Distinguishing syndromic and nonsyndromic cleft palate through analysis of protein-altering de novo variants in 818 trios

  The American Journal of Human Genetics · 2025-10-06 · 3 citations

• Supplementary Table S1 from An Analytic Pipeline to Obtain Reliable Genetic Ancestry Estimates from Tumor-Derived RNA Sequencing Data

  2025-09-02

• Supplementary Table S2 from An Analytic Pipeline to Obtain Reliable Genetic Ancestry Estimates from Tumor-Derived RNA Sequencing Data

  2025-09-02

• Supplementary Figure S1 from An Analytic Pipeline to Obtain Reliable Genetic Ancestry Estimates from Tumor-Derived RNA Sequencing Data

  2025-09-02

• Rare variants in PRKCI cause Van der Woude syndrome and other features of peridermopathy

  The American Journal of Human Genetics · 2025-09-02 · 3 citations

• Data from An Analytic Pipeline to Obtain Reliable Genetic Ancestry Estimates from Tumor-Derived RNA Sequencing Data

  2025-09-02

• Multiancestry brain pQTL fine-mapping and integration with genome-wide association studies of 21 neurologic and psychiatric conditions

  Nature Genetics · 2025-09-01 · 13 citations

• Expectations for papers performing Mendelian randomization analyses

  PLoS Genetics · 2025-07-17 · 4 citations

• An Analytic Pipeline to Obtain Reliable Genetic Ancestry Estimates from Tumor-Derived RNA Sequencing Data

  Cancer Epidemiology Biomarkers & Prevention · 2025-07-07

• Bridging cell morphological behaviors and molecular dynamics in multi-modal spatial omics with MorphLink

  Nature Communications · 2025-07-01 · 8 citations

• Proteome-wide association studies using summary pQTL data of brain, CSF, and plasma identify 30 risk genes of Alzheimer’s disease dementia

  Alzheimer s Research & Therapy · 2025-06-18 · 5 citations

• Distinguishing syndromic and nonsyndromic cleft palate through analysis of protein-altering de novo variants in 816 triosPreprint

  medRxiv · 2025-03-04

• Rare variants in PRKCI cause Van der Woude syndrome and other features of peridermopathyPreprint

  medRxiv · 2025-01-17 · 1 citations

• Genome-wide study of gene-by-sex interactions identifies risks for cleft palate

  Human Genetics · 2024-10-03 · 4 citations

• SCAMPI: A scalable statistical framework for genome-wide interaction testing harnessing cross-trait correlationsPreprint

  bioRxiv (Cold Spring Harbor Laboratory) · 2024-09-14 · 2 citations

• MorphLink: Bridging Cell Morphological Behaviors and Molecular Dynamics in Multi-modal Spatial OmicsPreprint

  bioRxiv (Cold Spring Harbor Laboratory) · 2024-08-27 · 1 citations

• SR-TWAS: leveraging multiple reference panels to improve transcriptome-wide association study power by ensemble machine learning

  Nature Communications · 2024-08-05 · 13 citations

• Omnibus proteome-wide association study identifies 43 risk genes for Alzheimer disease dementia

  The American Journal of Human Genetics · 2024-07-29 · 13 citations