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Neuro-Oncology|May 19, 2019
A genome-wide association study identifies susceptibility loci for primary central nervous system lymphoma at 6p25.3 and 3p22.1: a LOC Network studyKarim Labreche, Mailys Daniau, Amit Sud, et al.Journal of the National Cancer Institute|April 5, 2012
CYP3A variation, premenopausal estrone levels, and breast cancer riskNichola Johnson, Kate Walker, Lorna J Gibson, et al.Blood|January 23, 2014
Inherited genetic susceptibility to monoclonal gammopathy of unknown significanceNiels Weinhold, David C Johnson, Andrew C Rawstron, et al.Nature Communications|October 24, 2013
Variation at 3p24.1 and 6q23.3 influences the risk of Hodgkin's lymphomaMatthew Frampton, Miguel Inacio da Silva Filho, Peter Broderick, et al.Nature Genetics|August 2, 2011
Common variation at 10p12.31 near MLLT10 influences meningioma riskSara E Dobbins, Peter Broderick, Beatrice Melin, et al.Blood Cancer Journal|January 4, 2019
Genetic correlation between multiple myeloma and chronic lymphocytic leukaemia provides evidence for shared aetiologyMolly Went, Amit Sud, Helen Speedy, et al.Nature Communications|November 27, 2019
Identification of four novel associations for B-cell acute lymphoblastic leukaemia riskJayaram Vijayakrishnan, Maoxiang Qian, James B Studd, et al.Nature Communications|October 27, 2024
Genomic landscape of adult testicular germ cell tumours in the 100,000 Genomes ProjectMáire Ní Leathlobhair, Anna Frangou, Ben Kinnersley, et al.Journal of Neurology|April 25, 2018
Glioma-related seizures in relation to histopathological subtypes: a report from the glioma international case-control studyShala G Berntsson, Ryan T Merrell, E Susan Amirian, et al.Scientific Reports|October 15, 2015
The 9p21.3 risk of childhood acute lymphoblastic leukaemia is explained by a rare high-impact variant in CDKN2AJayaram Vijayakrishnan, Marc Henrion, Anthony V Moorman, et al.Pageof 49