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Journal of the National Cancer Institute|January 26, 2011
Novel breast cancer susceptibility locus at 9q31.2: results of a genome-wide association studyOlivia Fletcher, Nichola Johnson, Nick Orr, et al.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.Human Molecular Genetics|April 17, 2014
Identification of susceptibility loci for colorectal cancer in a genome-wide meta-analysisNicola Whiffin, Fay J Hosking, Susan M Farrington, et al.Cancer Research|November 1, 2011
Genome-wide high-density SNP linkage search for glioma susceptibility loci: results from the Gliogene ConsortiumSanjay Shete, Ching C Lau, Richard S Houlston, et al.British Journal of Cancer|April 11, 2013
Low penetrance susceptibility to glioma is caused by the TP53 variant rs78378222V Enciso-Mora, F J Hosking, A L Di Stefano, et al.Carcinogenesis|July 30, 2010
Inherited variation in immune genes and pathways and glioblastoma riskJudith A Schwartzbaum, Yuanyuan Xiao, Yanhong Liu, et al.Nature Genetics|July 7, 2009
Genome-wide association study identifies five susceptibility loci for gliomaSanjay Shete, Fay J Hosking, Lindsay B Robertson, et al.Human Genetics|June 13, 2012
Insight in glioma susceptibility through an analysis of 6p22.3, 12p13.33-12.1, 17q22-23.2 and 18q23 SNP genotypes in familial and non-familial gliomaYanhong Liu, Beatrice S Melin, Preetha Rajaraman, et al.Human Molecular Genetics|February 13, 2013
Deciphering the 8q24.21 association for gliomaVictor Enciso-Mora, Fay J Hosking, Ben Kinnersley, et al.Pageof 20