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Scientific Reports|November 11, 2015
Recurrent Coding Sequence Variation Explains Only A Small Fraction of the Genetic Architecture of Colorectal CancerMaria N Timofeeva, Ben Kinnersley, Susan M Farrington, et al.Nature Genetics|May 29, 2012
Common variation near CDKN1A, POLD3 and SHROOM2 influences colorectal cancer riskMalcolm G Dunlop, Sara E Dobbins, Susan Mary Farrington, et al.BMJ Open Respiratory Research|December 6, 2014
Regional variations in the prevalence and misdiagnosis of air flow obstruction in China: baseline results from a prospective cohort of the China Kadoorie Biobank (CKB)Om P Kurmi, Liming Li, Margaret Smith, et al.Human Molecular Genetics|February 11, 2012
Genotypic variants at 2q33 and risk of esophageal squamous cell carcinoma in China: a meta-analysis of genome-wide association studiesChristian C Abnet, Zhaoming Wang, Xin Song, et al.Nature Genetics|December 20, 2022
Deciphering colorectal cancer genetics through multi-omic analysis of 100,204 cases and 154,587 controls of European and east Asian ancestriesCeres Fernandez-Rozadilla, Maria Timofeeva, Zhishan Chen, et al.Nature Communications|April 26, 2024
Fine-mapping analysis including over 254,000 East Asian and European descendants identifies 136 putative colorectal cancer susceptibility genesZhishan Chen, Xingyi Guo, Ran Tao, et al.Pageof 151