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Environmental and Molecular Mutagenesis|July 31, 2021
Elevated urinary mutagenicity among those exposed to bituminous coal combustion emissions or diesel engine exhaustJason Y Y Wong, Roel Vermeulen, Yufei Dai, et al.Nature Communications|June 3, 2020
Massively parallel reporter assays of melanoma risk variants identify MX2 as a gene promoting melanomaJiyeon Choi, Tongwu Zhang, Andrew Vu, et al.American Journal of Human Genetics|August 3, 2021
A UVB-responsive common variant at chromosome band 7p21.1 confers tanning response and melanoma risk via regulation of the aryl hydrocarbon receptor, AHRMai Xu, Lindsey Mehl, Tongwu Zhang, et al.BMC Genetics|July 19, 2019
Meta-analysis of GWA studies provides new insights on the genetic architecture of skin pigmentation in recently admixed populationsFrida Lona-Durazo, Natalia Hernandez-Pacheco, Shaohua Fan, et al.Biorxiv : the Preprint Server for Biology|April 27, 2026
Single-cell full-length transcriptome of human lung reveals genetic effects on isoform regulation beyond gene-level expressionBolun Li, Thong Luong, Elelta Sisay, et al.Biorxiv : the Preprint Server for Biology|May 8, 2026
Functional characterization of the 9q34.13 locus identifies <i>RAPGEF1</i> as modulating risk for melanoma and nevi via RAS activationRohit Thakur, Mai Xu, Alexandra M Thornock, et al.Nature Genetics|April 2, 2014
POT1 loss-of-function variants predispose to familial melanomaCarla Daniela Robles-Espinoza, Mark Harland, Andrew J Ramsay, et al.Journal of Thoracic Oncology : Official Publication of the International Association for the Study of Lung Cancer|December 13, 2025
High-Penetrance Rare Variants Underlying Familial Lung Cancer Risk: Insights From Genetic Epidemiology of Lung Cancer ConsortiumYanhong Liu, Yafang Li, Jinyoung Byun, et al.Nature Communications|April 4, 2026
Targeting IP<sub>6</sub> signaling to destabilize homologous recombination proteins to overcome PARP inhibitor resistanceSeon-Gyeong Lee, Yuri Seo, Seula Jeong, et al.Medrxiv : the Preprint Server for Health Sciences|June 12, 2026
Disruption of CTCF binding by germline non-coding variants in <i>CDKN2B</i> suppress <i>CDKN2A</i> expression and predispose to melanomaJessica L Scales, Jayne A Barbour, Alisa M Goldstein, et al.Pageof 21