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Journal of Clinical Oncology : Official Journal of the American Society of Clinical Oncology|January 7, 2015
Genetic diagnosis of high-penetrance susceptibility for colorectal cancer (CRC) is achievable for a high proportion of familial CRC by exome sequencingDaniel Chubb, Peter Broderick, Matthew Frampton, et al.Plos Genetics|September 28, 2011
Genetic variants at chromosomes 2q35, 5p12, 6q25.1, 10q26.13, and 16q12.1 influence the risk of breast cancer in menNick Orr, Rosie Cooke, Michael Jones, et al.European Urology|February 14, 2018
Large-scale Sequencing of Testicular Germ Cell Tumour (TGCT) Cases Excludes Major TGCT Predisposition GeneKevin Litchfield, Chey Loveday, Max Levy, et al.European Urology Open Science|March 4, 2025
Meta-analysis of Germline Whole-exome Sequencing in 1435 Cases of Testicular Germ Cell Tumour to Evaluate Disruptive Mutations Under Dominant, Recessive, and X-linked Inheritance ModelsZeid Kuzbari, Charlie F Rowlands, Isaac Wade, et al.Blood|May 21, 2011
Multiple Hodgkin lymphoma-associated loci within the HLA region at chromosome 6p21.3Loukas Moutsianas, Victor Enciso-Mora, Yussanne P Ma, et al.Scientific Reports|July 25, 2015
Implementation of genome-wide complex trait analysis to quantify the heritability in multiple myelomaJonathan S Mitchell, David C Johnson, Kevin Litchfield, et al.Nature Genetics|September 19, 2018
Promoter capture Hi-C-based identification of recurrent noncoding mutations in colorectal cancerGiulia Orlando, Philip J Law, Alex J Cornish, et al.Blood|August 17, 2016
Germ line mutations in shelterin complex genes are associated with familial chronic lymphocytic leukemiaHelen E Speedy, Ben Kinnersley, Daniel Chubb, et al.Nature Genetics|November 4, 2008
Common 5p15.33 and 6p21.33 variants influence lung cancer riskYufei Wang, Peter Broderick, Emily Webb, et al.Blood|December 7, 2011
FGFR2 genotype and risk of radiation-associated breast cancer in Hodgkin lymphomaYussanne P Ma, Flora E van Leeuwen, Rosie Cooke, et al.Pageof 11