Peter White

Chief Data Sciences Officer

Nationwide Children's Hospital

United States

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About

Dr. Peter White serves as the Chief Data Sciences Officer at Nationwide Children's Hospital in the United States. His research focuses on genomic characterization of congenital and infantile cancers, with an emphasis on identifying medically relevant findings from genomic data. Recent publications highlight his work in RNA sequencing, genomic variants in disease, and algorithm development for genetic analysis. Dr. White's contributions significantly enhance understanding of genetic variations and their implications in pediatric health.

Articles (14)

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2025

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2025

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2025

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2024

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2024

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2024

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2023

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2023

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2023

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2023

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2022

Collaborators (4)

Emmi Helle

University of Helsinki

FINLAND

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Stephanie Ware

Indiana University Bloomington

UNITED STATES

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Jessica Chong

University of Washington

UNITED STATES

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Elizabeth Blue

Associate Professor

University of Washington

UNITED STATES

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Peter White

Research Interests

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Articles (14)

Identification of Long Noncoding RNA Candidate Disease Genes Associated With Clinically Reported Copy Number Variants in Congenital Heart Disease

Comprehensive Genomic Characterization of Congenital and Infantile Cancers Reveals High Yield of Medically Meaningful Findings.

Variant calling from RNA-Seq data reveals allele-specific differential expression of pathogenic cancer variants

CAVaLRi: An Algorithm for Rapid Identification of Diagnostic Germline Variation

Increase in Full-Length Dystrophin by Exon Skipping in Duchenne Muscular Dystrophy Patients with Single Exon Duplications: An Open-label Study.

SNVstory: inferring genetic ancestry from genome sequencing data.

Full-length isoform concatenation sequencing to resolve cancer transcriptome complexity.

Biallelic variants in HTRA2 cause 3-methylglutaconic aciduria mitochondrial disorder: case report and literature review.

Identification of Long Non-coding RNA Candidate Disease Genes Associated with Clinically Reported CNVs in Congenital Heart Disease

Rare variants in CAPN2 increase risk for isolated hypoplastic left heart syndrome

Glucocorticoid- and pioglitazone-induced proteinuria reduction in experimental NS both correlate with glomerular ECM modulation.

Novel pathogenic GATA6 variant associated with congenital heart disease, diabetes mellitus and necrotizing enterocolitis.

CRISPR-Cas9 homology-independent targeted integration of exons 1-19 restores full-length dystrophin in mice.

Pacific Biosciences Fusion and Long Isoform Pipeline for Cancer Transcriptome-Based Resolution of Isoform Complexity.

Collaborators (4)

Emmi Helle

Stephanie Ware

Jessica Chong

Elizabeth Blue

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