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Gastroenterology|January 20, 2024
Genomic Landscape of Lynch Syndrome Colorectal Neoplasia Identifies Shared Mutated Neoantigens for ImmunopreventionAna M Bolivar, Fahriye Duzagac, Nan Deng, et al.European Journal of Human Genetics : EJHG|March 28, 2013
Population structure, migration, and diversifying selection in the NetherlandsAbdel Abdellaoui, Jouke-Jan Hottenga, Peter de Knijff, et al.HGG Advances|January 20, 2022
A whole-exome case-control association study to characterize the contribution of rare coding variation to pancreatic cancer riskYao Yu, Kyle Chang, Jiun-Sheng Chen, et al.Twin Research and Human Genetics : the Official Journal of the International Society for Twin Studies|October 2, 2012
Twins, tissue, and time: an assessment of SNPs and CNVsPaul Scheet, Erik A Ehli, Xiangjun Xiao, et al.JAMA Oncology|May 1, 2018
Immune Profiling of Premalignant Lesions in Patients With Lynch SyndromeKyle Chang, Melissa W Taggart, Laura Reyes-Uribe, et al.Blood|November 22, 2015
Genetic risk factors for the development of osteonecrosis in children under age 10 treated for acute lymphoblastic leukemiaSeth E Karol, Leonard A Mattano, Wenjian Yang, et al.Blood|September 26, 2012
Genome-wide association study identifies germline polymorphisms associated with relapse of childhood acute lymphoblastic leukemiaJun J Yang, Cheng Cheng, Meenakshi Devidas, et al.Cancer|July 16, 2024
Association of clonal hematopoiesis and mosaic chromosomal alterations with solid malignancy incidence and mortalityPinkal Desai, Ying Zhou, Justin Grenet, et al.Nature Biotechnology|May 20, 2014
A unified test of linkage analysis and rare-variant association for analysis of pedigree sequence dataHao Hu, Jared C Roach, Hilary Coon, et al.American Journal of Respiratory and Critical Care Medicine|March 22, 2019
Driver Mutations in Normal Airway Epithelium Elucidate Spatiotemporal Resolution of Lung CancerHumam Kadara, Smruthy Sivakumar, Yasminka Jakubek, et al.Pageof 14