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Gang Wu

Associate Member

St. Jude Children's Research Hospital

United States

Research Interests

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Articles (20)

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2026

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Collaborators (18)

Robert Autry

Group Leader- Clinical Bioinformatics -Translational Genomics

Deutsches Krebsforschungszentrum

GERMANY

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Kathrin Bernt

Children's Hospital of Philadelphia

UNITED STATES

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Mignon L. Loh

Professor

University of Washington

UNITED STATES

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Motomi Mori

Member and Chair

St. Jude Children's Research Hospital

UNITED STATES

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Karen Rabin

Professor

Baylor College of Medicine

UNITED STATES

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Stella T. Chou

Associate Professor of Pediatrics

University of Pennsylvania School of Medicine

UNITED STATES

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Kai Tan

Professor

University of Pennsylvania

UNITED STATES

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Kim Erika Nichols

Full Member

St. Jude Children's Research Hospital

UNITED STATES

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Charles Gawad

Stanford University School of Medicine

UNITED STATES

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Nickhill Bhakta

St. Jude Children's Research Hospital

UNITED STATES

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Timothy Shaw

Assistant Member/Professor

Moffitt Cancer Center

UNITED STATES

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Beisi Xu

Principal Bioinformatics Research Scientist

St. Jude Children's Research Hospital

UNITED STATES

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Catherine E Welsh

Associate Professor

Hope College

UNITED STATES

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Jiyang Yu

Interim Chair

St. Jude Children's Research Hospital

UNITED STATES

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Xueyuan Cao

Associate Professor

University of Tennessee

UNITED STATES

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Richard Webby

St. Jude Children's Research Hospital

UNITED STATES

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Taosheng Chen

Full Member

St. Jude Children's Research Hospital

UNITED STATES

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Meritxell B. Cutrona

Head of Platform | Patient-derived organoids for Precision Medicine

Institut Gustave Roussy

FRANCE

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Gang Wu

Research Interests

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Articles (20)

Reply to: Beyond Parametric Assumptions: Unsupervised Methods Enhance DNA Repair Gene Discovery in SMARCAL1 Identification

Bridging Genomics and Clinical Medicine: RSVrecon Enhances RSV Surveillance With Automated Genotyping and Clinically Important Mutation Reporting

Inferring germline pharmacogenomics from tumor transcriptome

nf-core/pacsomatic: a scalable somatic analytic pipeline using PacBio HiFi data

CoCoRV-nf: a powerful and cost-effective tool for rare variant analysis leveraging external biobank sequence data identified new candidate predisposition genes in amyotrophic lateral sclerosis and neuroblastoma

Genetic landscape of pediatric acute myeloid leukemia in Taiwan.

Somatic mtDNA mutations at intermediate levels of heteroplasmy are a source of functional heterogeneity among primary leukemic cells

Inferring chromosome segregation error stage and crossover in trisomic disorders with application to Down syndrome

Direct targeting and regulation of RNA polymerase II by cell signaling kinases

Comprehensive genomic analysis reveals molecular heterogeneity in pediatric ALK-positive anaplastic large cell lymphoma

Author Response: Genetic Associations With an Amyotrophic Lateral Sclerosis Reversal Phenotype

Shared burden of ultra-rare genetic variants across a spectrum of motor neuron diseases

MitoEdit: A pipeline for optimizing mtDNA base editing and predicting bystander effects

Genomic Determinants of Outcome in Acute Lymphoblastic Leukemia

Machine learning to optimize automated RH genotyping using whole-exome sequencing data

The genomic basis of childhood T-lineage acute lymphoblastic leukaemia.

PHF6 cooperates with SWI/SNF complexes to facilitate transcriptional progression.

Genetic Associations With an Amyotrophic Lateral Sclerosis Reversal Phenotype

Blinatumomab for MRD-Negative Acute Lymphoblastic Leukemia in Adults.

Germ line genetic NBN variation and predisposition to B-cell acute lymphoblastic leukemia in children.

Collaborators (18)

Robert Autry

Kathrin Bernt

Mignon L. Loh

Motomi Mori

Karen Rabin

Stella T. Chou

Kai Tan

Kim Erika Nichols

Charles Gawad

Nickhill Bhakta

Timothy Shaw

Beisi Xu

Catherine E Welsh

Jiyang Yu

Xueyuan Cao

Richard Webby

Taosheng Chen

Meritxell B. Cutrona

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