Wei Zhou

Broad Institute — United States

Biochemistry, Genetics and Molecular Biology · Life Sciences

73h-index31.3kcitations371works11.92yr avg
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Research Topics

Genetic Associations and Epidemiology(113), Genomics and Rare Diseases(27), Cardiac electrophysiology and arrhythmias(26), Bioinformatics and Genomic Networks(19), Genetic Mapping and Diversity in Plants and Animals(19)

Publications334 total

OpenGround: Active Cognition-based Reasoning for Open-World 3D Visual Grounding
ArXiv.org·2025Open Access
OpenGround: Active Cognition-based Reasoning for Open-World 3D Visual Grounding
arXiv (Cornell University)·2025Open Access
Effect of sensory integration training combined with Schroth therapy on adolescents with mild idiopathic scoliosis: a 12-week randomized controlled trial
European journal of medical research·2025Open Access
Expanding the genetic landscape of endometriosis: Integrative -omics analyses implicate key genes and pathways in a multi-ancestry study of over one million women
2025Open Access
Scalable and accurate rare variant meta-analysis with Meta-SAIGE
Nature Genetics·2025· 1 citedOpen Access
Genomic loci and molecular genetic mechanisms for hidradenitis suppurativa
UNC Libraries·2025Open Access
Abstract 4366183: Development of a High-Throughput Drug Screening Platform to Identify Novel Therapeutics for Long QT Syndrome
Circulation·2025
SPAmix: a scalable, accurate, and universal analysis framework for large-scale genetic association studies in admixed populations
Genome biology·2025· 1 citedOpen Access
X-ray crystallography reveals insulin lisargine structure and mechanisms of glucose regulation
Scientific Reports·2025Open Access
Pan-UK Biobank genome-wide association analyses enhance discovery and resolution of ancestry-enriched effects
Nature Genetics·2025· 33 cited
186eP A random forest model to predict the type of pulmonary nodule based on DNA methylation sequencing data
Annals of Oncology·2025
AAV9-mediated <i>KCNH2</i> suppression-replacement gene therapy in a transgenic rabbit model of type 1 short QT syndrome
European Heart Journal·2025· 2 citedOpen Access
GRAB: Genome-Wide Robust Analysis for Biobank Data (GRAB)
2025Open Access
0098 Identification of novel druggable targets for rosacea: Triangulating evidence from multi-omics mendelian randomization, transcriptomic, and animal experiments
Journal of Investigative Dermatology·2025Open Access
Genomic loci and molecular genetic mechanisms for hidradenitis suppurativa
British Journal of Dermatology·2025· 2 citedOpen Access
No significant association between anesthetics administered during delivery and autism spectrum disorder: a Mendelian randomization study
Minerva Anestesiologica·2025· 1 cited
A comprehensive splicing characterization of COL4A5 mutations and prognostic significance in a single cohort with X-linked alport syndrome
Frontiers in Genetics·2025Open Access
Extending Genome-Wide Association Studies to admixed cohorts with high degrees of relatedness
2025Open Access
Mechanism of age-related accumulation of mitochondrial DNA mutations in human blood
2025· 2 citedOpen Access
A Grid-Based Hierarchical Representation Method for Large-Scale Scenes Based on Three-Dimensional Gaussian Splatting
Remote Sensing·2025· 1 citedOpen Access
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Frequent Co-authors

Cristen J. Willer(24), Lars G. Fritsche(21), Jonas B. Nielsen(19), Kristian Hveem(18), Brooke N. Wolford(15), Gonçalo R. Abecasis(14), Maiken E. Gabrielsen(13), Masahiro Kanai(12), Ben Brumpton(12), Ida Surakka(11), Anne Heidi Skogholt(10), Benjamin M. Neale(10), Mark J. Daly(10), Juha Karjalainen(8), Seunggeun Lee(8), Sarah E. Graham(8), Whitney Hornsby(8), Mitja Kurki(7), Hilary K. Finucane(7), Andrea Ganna(7)