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JCO Precision Oncology|July 12, 2021
Prevalence and Characterization of Biallelic and Monoallelic NTHL1 and MSH3 Variant Carriers From a Pan-Cancer Patient PopulationErin E Salo-Mullen, Anna Maio, Semanti Mukherjee, et al.
Journal of Clinical Oncology : Official Journal of the American Society of Clinical Oncology|December 4, 2019
Cancer Susceptibility Mutations in Patients With Urothelial MalignanciesMaria I Carlo, Vignesh Ravichandran, Preethi Srinavasan, et al.
Cancer Epidemiology, Biomarkers & Prevention : a Publication of the American Association for Cancer Research, Cosponsored by the American Society of Preventive Oncology|April 27, 2022
Germline Pathogenic Variants Impact Clinicopathology of Advanced Lung CancerSemanti Mukherjee, Chaitanya Bandlamudi, Matthew D Hellmann, et al.
Nature Genetics|July 15, 2025
Germline genetic variation impacts clonal hematopoiesis landscape and progression to malignancyJie Liu, Duc Tran, Liying Xue, et al.
Journal of Clinical Oncology : Official Journal of the American Society of Clinical Oncology|October 31, 2018
Microsatellite Instability Is Associated With the Presence of Lynch Syndrome Pan-CancerAlicia Latham, Preethi Srinivasan, Yelena Kemel, et al.
Cancer Discovery|August 26, 2024
Chromothripsis-Mediated Small Cell Lung CarcinomaNatasha Rekhtman, Sam E Tischfield, Christopher A Febres-Aldana, et al.
JAMA|September 6, 2017
Mutation Detection in Patients With Advanced Cancer by Universal Sequencing of Cancer-Related Genes in Tumor and Normal DNA vs Guideline-Based Germline TestingDiana Mandelker, Liying Zhang, Yelena Kemel, et al.
The New England Journal of Medicine|March 22, 2018
A Protein-Truncating HSD17B13 Variant and Protection from Chronic Liver DiseaseNoura S Abul-Husn, Xiping Cheng, Alexander H Li, et al.
American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics|May 9, 2015
Independent evidence for an association between general cognitive ability and a genetic locus for educational attainmentJoey W Trampush, Todd Lencz, Emma Knowles, et al.
Science (New York, N.Y.)|December 24, 2016
Distribution and clinical impact of functional variants in 50,726 whole-exome sequences from the DiscovEHR studyFrederick E Dewey, Michael F Murray, John D Overton, et al.
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