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HGG Advances|August 6, 2021
Large-scale cross-cancer fine-mapping of the 5p15.33 region reveals multiple independent signalsHongjie Chen, Arunabha Majumdar, Lu Wang, et al.
Nature Genetics|May 29, 2012
Common variation near CDKN1A, POLD3 and SHROOM2 influences colorectal cancer riskMalcolm G Dunlop, Sara E Dobbins, Susan Mary Farrington, et al.
Journal of the National Cancer Institute|March 17, 2023
Genome-wide analyses characterize shared heritability among cancers and identify novel cancer susceptibility regionsSara Lindström, Lu Wang, Helian Feng, et al.
Journal of Thoracic Oncology : Official Publication of the International Association for the Study of Lung Cancer|April 23, 2019
Lung Cancer Risk in Never-Smokers of European Descent is Associated With Genetic Variation in the 5p15.33 TERT-CLPTM1Ll RegionRayjean J Hung, Margaret R Spitz, Richard S Houlston, et al.
Human Molecular Genetics|August 30, 2008
Refinement of the basis and impact of common 11q23.1 variation to the risk of developing colorectal cancerAlan M Pittman, Emily Webb, Luis Carvajal-Carmona, et al.
Medrxiv : the Preprint Server for Health Sciences|January 10, 2024
Rare disease gene association discovery from burden analysis of the 100,000 Genomes Project dataValentina Cipriani, Letizia Vestito, Emma F Magavern, et al.
Nature Communications|September 15, 2018
Identification of multiple risk loci and regulatory mechanisms influencing susceptibility to multiple myelomaMolly Went, Amit Sud, Asta Försti, et al.
Nature|February 26, 2025
Rare disease gene association discovery in the 100,000 Genomes ProjectValentina Cipriani, Letizia Vestito, Emma F Magavern, et al.
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