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The Journal of Pathology|July 15, 2015
Integrated genomic and transcriptomic analysis of human brain metastases identifies alterations of potential clinical significanceJodi M Saunus, Michael C J Quinn, Ann-Marie Patch, et al.Genome Medicine|September 18, 2023
The clinical utility and costs of whole-genome sequencing to detect cancer susceptibility variants-a multi-site prospective cohort studyAimee L Davidson, Uwe Dressel, Sarah Norris, et al.Medrxiv : the Preprint Server for Health Sciences|February 20, 2025
Multi-ancestral genome-wide association study of clinically defined nicotine dependence reveals strong genetic correlations with other substance use disorders and health-related traitsEmma C Johnson, Dongbing Lai, Alex P Miller, et al.American Journal of Human Genetics|November 4, 2022
Shariant platform: Enabling evidence sharing across Australian clinical genetic-testing laboratories to support variant interpretationEmma Tudini, James Andrews, David M Lawrence, et al.Nature|August 16, 2013
Signatures of mutational processes in human cancerLudmil B Alexandrov, Serena Nik-Zainal, David C Wedge, et al.Nature|May 29, 2015
Whole-genome characterization of chemoresistant ovarian cancerAnn-Marie Patch, Elizabeth L Christie, Dariush Etemadmoghadam, et al.Nature Communications|December 10, 2015
A comprehensive assessment of somatic mutation detection in cancer using whole-genome sequencingTyler S Alioto, Ivo Buchhalter, Sophia Derdak, et al.Nature|February 27, 2015
Whole genomes redefine the mutational landscape of pancreatic cancerNicola Waddell, Marina Pajic, Ann-Marie Patch, et al.Gastroenterology|November 19, 2016
Hypermutation In Pancreatic CancerJeremy L Humphris, Ann-Marie Patch, Katia Nones, et al.Nature|February 16, 2017
Whole-genome landscape of pancreatic neuroendocrine tumoursAldo Scarpa, David K Chang, Katia Nones, et al.Pageof 23