Publications by authors named "Chad D Huff"

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Early history of Neanderthals and Denisovans.
Alan R Rogers, Ryan J Bohlender, Chad D Huff

September 2017

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Structural birth defects and leukemia risk in children with Down syndrome.
Ching-Ju Hsu, Jeremy M Schraw, Sonja A Rasmussen, Tiffany M Chambers, Tania A Desrosiers, Chad D Huff

Sci Rep· December 2025

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Evaluating the Genetic Overlap Between Congenital Heart Disease and Neuroblastoma Risk.
Ji Yun Tark, Alexander Renwick, Yao Yu, Aniko Sabo, Andrew F Olshan, Chad D Huff

Pediatr Blood Cancer· December 2025

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A Population-Based Assessment of Cancer Risk in Children With VACTERL.
Ji Yun Tark, Alexander Renwick, Giorgio Tettamanti, Rachel D Harris, Tania A Desrosiers, Chad D Huff

Am J Med Genet A· December 2025

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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, Natalie R Davidson, Lindsay J Collin, Chad D Huff

Cancer Epidemiol Biomarkers Prev· November 2025

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COMPADRE: Combined pedigree-aware distant relatedness estimation for improved pedigree reconstruction.
Grahame F Evans, James T Baker, Lauren E Petty, Alexander S Petty, Hannah G Polikowsky, Chad D Huff

Am J Hum Genet· November 2025

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Integrating Pathogenic Variants, Polygenic Risk Score, and Family History for Prostate Cancer Risk Estimation in Men of African Ancestry.
Fei Chen, Xin Sheng, Anqi Wang, Yili Xu, Raymond Hughley, Chad D Huff

Eur Urol· November 2025

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Genome-wide association study of 398,238 women unveils seven loci associated with high-grade serous ovarian cancer.
Daniel R Barnes, Jonathan P Tyrer, Joe Dennis, Goska Leslie, Manjeet K Bolla, Chad D Huff

NPJ Genom Med· November 2025

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Isoform-level analyses of 6 cancers uncover extensive genetic risk mechanisms undetected at the gene-level.
Yung-Han Chang, Sean T Bresnahan, S Taylor Head, Tabitha A Harrison, Yao Yu, Chad D Huff

Br J Cancer· October 2025

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Body composition as a determinant of the therapeutic index with androgen signaling inhibition.
Andrew W Hahn, Rebecca S Tidwell, Patrick G Pilie, Yao Yu, Jingjing Liu, Chad D Huff

Prostate Cancer Prostatic Dis· September 2025

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Co-occurrence of congenital anomalies and childhood brain tumors in 22 million live births.
Thanh T Hoang, Jeremy M Schraw, Charles Shumate, Tania A Desrosiers, Wendy N Nembhard, Chad D Huff

Neuro Oncol· September 2025

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Large-scale genome-wide analyses of stuttering.
Hannah G Polikowsky, Alyssa C Scartozzi, Douglas M Shaw, Dillon G Pruett, Hung-Hsin Chen, Chad D Huff

Nat Genet· August 2025

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Targeted sequencing for hereditary breast and ovarian cancer in BRCA1/2-negative families reveals complex genetic architecture and phenocopies.
Jocelyn N Plowman, Evanjalina J Matoy, Lavanya V Uppala, Samantha B Draves, Cynthia J Watson, Chad D Huff

HGG Adv· July 2025

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The impact of genetic ancestry on survival outcomes in pediatric rhabdomyosarcoma: A report from the Children's Oncology Group.
Ekene A Onwuka, Christina L Magyar, Bailey A Martin-Giacalone, Michael E Scheurer, Deborah A Marquez-Do, Chad D Huff

HGG Adv· July 2025

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Isoform-level analyses of 6 cancers uncover extensive genetic risk mechanisms undetected at the gene-level.
Yung-Han Chang, Sean T Bresnahan, S Taylor Head, Tabitha Harrison, Yao Yu, Chad D Huff

medRxiv· May 2025

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Genomic Characterization of High-Grade Serous Ovarian Carcinoma Reveals Distinct Somatic Features in Black Individuals.
Katherine A Lawson-Michod, Jeffrey R Marks, Lindsay J Collin, David A Nix, Natalie R Davidson, Chad D Huff

Cancer Res· May 2025

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Risk of carcinomas among children and adolescents with birth defects.
Jeremy M Schraw, Ji Yun Tark, Tania A Desrosiers, Tiffany M Chambers, Charles J Shumate, Chad D Huff

Cancer Epidemiol· April 2025

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A phase II trial of apalutamide for intermediate-risk prostate cancer and molecular correlates.
Andrew W Hahn, Ganiraju C Manyam, Brian F Chapin, Miao Zhang, Yao Yu, Chad D Huff

BJU Int· September 2024

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Detection of distant relatedness in biobanks to identify undiagnosed cases of Mendelian disease as applied to Long QT syndrome.
Megan C Lancaster, Hung-Hsin Chen, M Benjamin Shoemaker, Matthew R Fleming, Teresa L Strickland, Chad D Huff

Nat Commun· August 2024

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In vitro data suggest a role for PMS2 Kozak sequence mutations in Lynch syndrome risk.
Evanjalina J Matoy, Jocelyn N Plowman, Cynthia J Watson, Michael A Belshan, Elizabeth E Blue, Chad D Huff

HGG Adv· July 2024

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Targeted sequencing for hereditary breast and ovarian cancer in BRCA1/2-negative families reveals complex genetic architecture and phenocopies.
Jocelyn N Plowman, Evanjalina J Matoy, Lavanya V Uppala, Samantha B Draves, Cynthia J Watson, Chad D Huff

HGG Adv· July 2024

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Large-scale genome-wide association study of 398,238 women unveils seven novel loci associated with high-grade serous epithelial ovarian cancer risk.
Daniel R Barnes, Jonathan P Tyrer, Joe Dennis, Goska Leslie, Manjeet K Bolla, Chad D Huff

medRxiv· March 2024

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Functional / missense variant is associated with hematocrit in Andean highlanders.
Elijah S Lawrence, Wanjun Gu, Ryan J Bohlender, Cecilia Anza-Ramirez, Amy M Cole, Chad D Huff

Sci Adv· February 2024

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Characterizing prostate cancer risk through multi-ancestry genome-wide discovery of 187 novel risk variants.
Anqi Wang, Jiayi Shen, Alex A Rodriguez, Edward J Saunders, Fei Chen, Chad D Huff

Nat Genet· December 2023

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Detection of distant relatedness in biobanks for identification of undiagnosed carriers of a Mendelian disease variant: application to Long QT Syndrome.
Megan C Lancaster, Hung-Hsin Chen, M Benjamin Shoemaker, Matthew R Fleming, James T Baker, Chad D Huff

Res Sq· September 2023

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Detection of distant familial relatedness in biobanks for identification of undiagnosed carriers of a Mendelian disease variant: application to Long QT syndrome.
Megan C Lancaster, Hung-Hsin Chen, M Benjamin Shoemaker, Matthew R Fleming, James T Baker, Chad D Huff

medRxiv· April 2023

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