Chad Huff

10PUBLICATIONS

108CO-AUTHORS

Gene expression (incl. microarray and other genome-wide approaches)Cancer geneticsSolid tumoursCardiology (incl. cardiovascular diseases)Predictive and prognostic markers

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Publications (10)

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|Jun 27, 2026

DRIVE v3: Command Line Application for Identity-by-Descent Haplotype Clustering in Large Biobank Scale Data.

|May 25, 2026

A high-penetrance intergenic variant at 9p21 confers melanoma susceptibility.

|May 22, 2026

Increased Risk of Sarcomas in Children With Congenital Anomalies: Findings From the Genetic Overlap Between Anomalies and Cancer in Kids (GOBACK) Registry Linkage Study.

|Mar 23, 2026

Large Impact of Genetic Data Processing Steps on Stability and Reproducibility of Set-Based Analyses in Genome-Wide Association Studies.

Naishu Kui, Yao Yu, Jaihee Choi

|Sep 04, 2025

Homologous Recombination Deficiency and Survival in Ovarian High-Grade Serous Carcinoma by Self-Reported Race.

Katherine A Lawson-Michod, Courtney E Johnson, Mollie E Barnard

|Mar 26, 2025

Co-occurrence of congenital anomalies and childhood brain tumors in 22 million live births.

Thanh T Hoang, Jeremy M Schraw, Charles Shumate

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Frequent Collaborators

Yao Yu

Lindsay J Collin

Lauren C Peres

David A Nix

Lucas A Salas

Jeffrey R Marks

Courtney E Johnson

Natalie R Davidson

Katherine A Lawson-Michod

2 joint publications

Arjun Bhattacharya

Frequent Collaborators

Yao Yu

Lindsay J Collin

Lauren C Peres

David A Nix