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International Journal of Cancer|July 2, 2009
The CDH1-160C>A polymorphism is a risk factor for colorectal cancerAlan M Pittman, Philip Twiss, Peter Broderick, et al.Journal of Human Genetics|June 18, 2010
A genome-wide analysis of loss of heterozygosity and chromosomal copy number variation in Proteus syndrome using high-density SNP microarraysAhmet Yilmaz, Nancy Hamel, Charles E Schwartz, et al.Scientific Reports|September 10, 2015
Quantifying the heritability of testicular germ cell tumour using both population-based and genomic approachesKevin Litchfield, Hauke Thomsen, Jonathan S Mitchell, et al.Cancer Epidemiology, Biomarkers & Prevention : a Publication of the American Association for Cancer Research, Cosponsored by the American Society of Preventive Oncology|May 30, 2020
Leveraging Genome and Phenome-Wide Association Studies to Investigate Genetic Risk of Acute Lymphoblastic LeukemiaEleanor C Semmes, Jayaram Vijayakrishnan, Chenan Zhang, et al.Blood|August 10, 2007
A high-density SNP genome-wide linkage search of 206 families identifies susceptibility loci for chronic lymphocytic leukemiaGabrielle S Sellick, Lynn R Goldin, Ruth W Wild, et al.Oncogene|February 1, 2002
Breakpoints in the ataxia telangiectasia gene arise at the RGYW somatic hypermutation motifPaul S Bradshaw, Alison Condie, Estella Matutes, et al.Genes, Chromosomes & Cancer|December 4, 2002
Deletion mapping on the long arm of chromosome 7 in splenic lymphoma with villous lymphocytesAlicja M Gruszka-Westwood, Rifat Hamoudi, Lucy Osborne, et al.Nature Communications|August 11, 2019
Insight into genetic predisposition to chronic lymphocytic leukemia from integrative epigenomicsHelen E Speedy, Renée Beekman, Vicente Chapaprieta, et al.Cancer Epidemiology, Biomarkers & Prevention : a Publication of the American Association for Cancer Research, Cosponsored by the American Society of Preventive Oncology|November 15, 2005
The predicted impact of coding single nucleotide polymorphisms databaseMatthew F Rudd, Richard D Williams, Emily L Webb, et al.Annals of Human Genetics|February 16, 2019
Regions of homozygosity as risk factors for multiple myelomaMolly Went, Amit Sud, Ni Li, et al.Pageof 49