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Blood|September 3, 2013
Variation at 10p12.2 and 10p14 influences risk of childhood B-cell acute lymphoblastic leukemia and phenotypeGabriele Migliorini, Bettina Fiege, Fay J Hosking, et al.Nature Genetics|March 19, 2013
The CCND1 c.870G>A polymorphism is a risk factor for t(11;14)(q13;q32) multiple myelomaNiels Weinhold, David C Johnson, Daniel Chubb, et al.Nature Genetics|August 20, 2013
Common variation at 3q26.2, 6p21.33, 17p11.2 and 22q13.1 influences multiple myeloma riskDaniel Chubb, Niels Weinhold, Peter Broderick, et al.Human Molecular Genetics|February 13, 2013
Deciphering the 8q24.21 association for gliomaVictor Enciso-Mora, Fay J Hosking, Ben Kinnersley, et al.Scientific Reports|January 24, 2017
Genome-wide association analysis of chronic lymphocytic leukaemia, Hodgkin lymphoma and multiple myeloma identifies pleiotropic risk lociPhilip J Law, Amit Sud, Jonathan S Mitchell, et al.Human Molecular Genetics|May 3, 2011
Chromosome 7p11.2 (EGFR) variation influences glioma riskMarc Sanson, Fay J Hosking, Sanjay Shete, et al.Nature Genetics|April 19, 2017
Large-scale analyses of common and rare variants identify 12 new loci associated with atrial fibrillationIngrid E Christophersen, Michiel Rienstra, Carolina Roselli, et al.Diabetes|June 2, 2017
An Expanded Genome-Wide Association Study of Type 2 Diabetes in EuropeansRobert A Scott, Laura J Scott, Reedik Mägi, et al.Nature Genetics|November 10, 2015
Genetic fine mapping and genomic annotation defines causal mechanisms at type 2 diabetes susceptibility lociKyle J Gaulton, Teresa Ferreira, Yeji Lee, et al.Nature Genetics|June 23, 2014
Genetic association study of QT interval highlights role for calcium signaling pathways in myocardial repolarizationDan E Arking, Sara L Pulit, Lia Crotti, et al.Pageof 7