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Nature Genetics|January 12, 2010
Common variants at 2q37.3, 8q24.21, 15q21.3 and 16q24.1 influence chronic lymphocytic leukemia riskDalemari Crowther-Swanepoel, Peter Broderick, Maria Chiara Di Bernardo, et al.
British Journal of Haematology|April 7, 2009
Long-term follow-up of 233 patients with hairy cell leukaemia, treated initially with pentostatin or cladribine, at a median of 16 years from diagnosisMonica Else, Claire E Dearden, Estella Matutes, et al.
Human Molecular Genetics|April 20, 2022
Frequency of pathogenic germline variants in cancer susceptibility genes in 1336 renal cell carcinoma casesBryndis Yngvadottir, Avgi Andreou, Laia Bassaganyas, et al.
American Journal of Epidemiology|May 14, 2010
Interaction between 5 genetic variants and allergy in glioma riskMinouk J Schoemaker, Lindsay Robertson, Annette Wigertz, et al.
Blood|November 10, 2010
MHC variation and risk of childhood B-cell precursor acute lymphoblastic leukemiaFay J Hosking, Stephen Leslie, Alexander Dilthey, et al.
Nature Communications|July 15, 2024
Whole genome sequencing refines stratification and therapy of patients with clear cell renal cell carcinomaRichard Culliford, Samuel E D Lawrence, Charlie Mills, et al.
Oncotarget|March 22, 2018
Validation of loci at 2q14.2 and 15q21.3 as risk factors for testicular cancerChey Loveday, Kevin Litchfield, Max Levy, et al.
British Journal of Haematology|June 26, 2009
Drug cross-resistance and therapy-induced resistance in chronic lymphocytic leukaemia by an enhanced method of individualised tumour response testingAndrew G Bosanquet, Sue M Richards, Rachel Wade, et al.
Journal of Clinical Medicine|November 13, 2021
Genetic Variation in ABCC4 and CFTR and Acute Pancreatitis during Treatment of Pediatric Acute Lymphoblastic LeukemiaThies Bartram, Peter Schütte, Anja Möricke, et al.
European Journal of Human Genetics : EJHG|August 13, 2015
Search for new loci and low-frequency variants influencing glioma risk by exome-array analysisBen Kinnersley, Yoichiro Kamatani, Marianne Labussière, et al.
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