Refreshing results…
Identification of four novel associations for B-cell acute lymphoblastic leukaemia risk
Download from www.nature.comCanVar: A resource for sharing germline variation in cancer patients
Download from dx.doi.orgRare variants of large effect in BRCA2 and CHEK2 affect risk of lung cancer
Download from www.nature.comInherited genetic susceptibility to monoclonal gammopathy of unknown significance
Download from ashpublications.orgVariation at 3p24.1 and 6q23.3 influences the risk of Hodgkin’s lymphoma
Download from www.nature.comCommon variation at 3q26.2, 6p21.33, 17p11.2 and 22q13.1 influences multiple myeloma risk
Download from www.nature.comDeciphering the genetic architecture of low-penetrance susceptibility to colorectal cancer
Download from academic.oup.comGenome-Wide Association Study on Differentiated Thyroid Cancer
Download from academic.oup.comThe CCND1 c.870G>A polymorphism is a risk factor for t(11;14)(q13;q32) multiple myeloma
Download from www.nature.comDeciphering the 8q24.21 association for glioma
Download from academic.oup.comLow penetrance susceptibility to glioma is caused by the TP53 variant rs78378222.
Download from www.nature.comCommon variation at 2q22.3 (ZEB2) influences the risk of renal cancer.
Download from academic.oup.comThe TERT variant rs2736100 is associated with colorectal cancer risk
Download from www.nature.comRisk of developing chronic lymphocytic leukemia is influenced by HLA-A class I variation
Download from www.nature.comMissing publications? Search for publications with a matching author name.