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Author Details

Chad D Huff
University of Texas M.D. Anderson Cancer Center
2007
94
34
PMIDPaper TitleJournal TitlePublished Year
36018819Clonal hematopoiesis and risk of prostate cancer in large samples of European ancestry men.Hum Mol Genet2023
37292833Evaluating Approaches for Constructing Polygenic Risk Scores for Prostate Cancer in Men of African and European Ancestry.medRxiv2023
36951526Germline genetic variants and pediatric rhabdomyosarcoma outcomes: a report from the Children's Oncology Group.J Natl Cancer Inst2023
37311464Evaluating approaches for constructing polygenic risk scores for prostate cancer in men of African and European ancestry.Am J Hum Genet2023
36973285Rewired m<sup>6</sup>A epitranscriptomic networks link mutant p53 to neoplastic transformation.Nat Commun2023
37163006Detection of distant familial relatedness in biobanks for identification of undiagnosed carriers of a Mendelian disease variant: application to Long QT syndrome.medRxiv2023
36872133Evidence of Novel Susceptibility Variants for Prostate Cancer and a Multiancestry Polygenic Risk Score Associated with Aggressive Disease in Men of African Ancestry.Eur Urol2023
35031163A Rare Germline HOXB13 Variant Contributes to Risk of Prostate Cancer in Men of African Ancestry.Eur Urol2022
35412907Hereditary retinoblastoma iPSC model reveals aberrant spliceosome function driving bone malignancies.Proc Natl Acad Sci U S A2022
36210504Copy Number Variants Are Ovarian Cancer Risk Alleles at Known and Novel Risk Loci.J Natl Cancer Inst2022
36127509Impact of conditioning chemotherapy on lymphocyte kinetics and outcomes in LBCL patients treated with CAR T-cell therapy.Leukemia2022
35152271Prostate cancer risk stratification improvement across multiple ancestries with new polygenic hazard score.Prostate Cancer Prostatic Dis2022
35147171Polygenic risk impacts PDGFRA mutation penetrance in non-syndromic cleft lip and palate.Hum Mol Genet2022
32546565Population-based targeted sequencing of 54 candidate genes identifies <i>PALB2</i> as a susceptibility gene for high-grade serous ovarian cancer.J Med Genet2021
33713608Discovery and fine-mapping of height loci via high-density imputation of GWASs in individuals of African ancestry.Am J Hum Genet2021
33623038Polygenic hazard score is associated with prostate cancer in multi-ethnic populations.Nat Commun2021
34077726Inhibiting an RBM39/MLL1 epigenomic regulatory complex with dominant-negative peptides disrupts cancer cell transcription and proliferation.Cell Rep2021
33436325Rare Germline Variants in ATM Predispose to Prostate Cancer: A PRACTICAL Consortium Study.Eur Urol Oncol2021
33398198Trans-ancestry genome-wide association meta-analysis of prostate cancer identifies new susceptibility loci and informs genetic risk prediction.Nat Genet2021
33473200Publisher Correction: Trans-ancestry genome-wide association meta-analysis of prostate cancer identifies new susceptibility loci and informs genetic risk prediction.Nat Genet2021
33357513Host genetic effects in pneumonia.Am J Hum Genet2021
33386679Pedigree reconstruction and distant pairwise relatedness estimation from genome sequence data: A demonstration in a population of rhesus macaques (Macaca mulatta).Mol Ecol Resour2021
32447321Integrated case-control and somatic-germline interaction analyses of soft-tissue sarcoma.J Med Genet2021
31226226A genome-wide association study of prostate cancer in Latinos.Int J Cancer2020
31685958Large-scale analysis of acquired chromosomal alterations in non-tumor samples from patients with cancer.Nat Biotechnol2020
32409115A Germline Variant at 8q24 Contributes to Familial Clustering of Prostate Cancer in Men of African Ancestry.Eur Urol2020
32424863A novel ribosomal protein S20 variant in a family with unexplained colorectal cancer and polyposis.Clin Genet2020
32251345Author Correction: Personalized Risk Assessment in Never, Light, and Heavy Smokers in a prospective cohort in Taiwan.Sci Rep2020
30624610Functionally oriented analysis of cardiometabolic traits in a trans-ethnic sample.Hum Mol Genet2019
31241222Assessing the performance of in silico methods for predicting the pathogenicity of variants in the gene CHEK2, among Hispanic females with breast cancer.Hum Mutat2019
31372681Tbx3-Mediated Regulation of Cardiac Conduction System Development and Function: Potential Contributions of Alternative RNA Processing.Pediatr Cardiol2019
31219523Association Between Birth Defects and Cancer Risk Among Children and Adolescents in a Population-Based Assessment of 10 Million Live Births.JAMA Oncol2019
30352910DNA Sequencing of Small Bowel Adenocarcinomas Identifies Targetable Recurrent Mutations in the ERBB2 Signaling Pathway.Clin Cancer Res2019
28607096The somatic mutation landscape of premalignant colorectal adenoma.Gut2018
30166421Targeted Gene Sequencing in Children with Crohn's Disease and Their Parents: Implications for Missing Heritability.G3 (Bethesda)2018
30014848Introgression of regulatory alleles and a missense coding mutation drive plumage pattern diversity in the rock pigeon.Elife2018
30503519DNA Polymerase Epsilon Deficiency Causes IMAGe Syndrome with Variable Immunodeficiency.Am J Hum Genet2018
29463208The VAAST Variant Prioritizer (VVP): ultrafast, easy to use whole genome variant prioritization tool.BMC Bioinformatics2018
29659923A Nonsynonymous Variant in the GOLM1 Gene in Cutaneous Malignant Melanoma.J Natl Cancer Inst2018
29317335Integrated case-control and somatic-germline interaction analyses of melanoma susceptibility genes.Biochim Biophys Acta Mol Basis Dis2018
29294048XPAT: a toolkit to conduct cross-platform association studies with heterogeneous sequencing datasets.Nucleic Acids Res2018
28036300Evolutionary selected Tibetan variants of HIF pathway and risk of lung cancer.Oncotarget2017
28233034Gain-of-function EGLN1 prolyl hydroxylase (PHD2 D4E:C127S) in combination with EPAS1 (HIF-2α) polymorphism lowers hemoglobin concentration in Tibetan highlanders.J Mol Med (Berl)2017
28430825Discovery and fine-mapping of adiposity loci using high density imputation of genome-wide association studies in individuals of African ancestry: African Ancestry Anthropometry Genetics Consortium.PLoS Genet2017
28448578Evolutionary history of Tibetans inferred from whole-genome sequencing.PLoS Genet2017
29117387Two Novel Susceptibility Loci for Prostate Cancer in Men of African Ancestry.J Natl Cancer Inst2017
29138325Reply to Mafessoni and Prüfer: Inferences with and without singleton site patterns.Proc Natl Acad Sci U S A2017
28784789Early history of Neanderthals and Denisovans.Proc Natl Acad Sci U S A2017
28006848Global methylation of blood leukocyte DNA and risk of melanoma.Int J Cancer2017
26988264Mitochondrial DNA 4977-base pair common deletion in blood leukocytes and melanoma risk.Pigment Cell Melanoma Res2016
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Cezary Cybulski
International Hereditary Cancer Center, Pomeranian Medical University
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Demetrius Albanes
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David E Neal
University of Oxford, John Radcliffe Hospital
Co-authored papers 7
Stephen K Van Den Eeden
Kaiser Permanente Northern California, University of California san francisco
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