Center-Authored Papers

Filters: Author is Palles, Claire  [Clear All Filters]
Journal Article
Su Z, Gay LJ, Strange A, Palles C, Band G, Whiteman DC, Lescai F, Langford C, Nanji M, Edkins S et al..  2012.  Common variants at the MHC locus and at chromosome 16q24.1 predispose to Barrett's esophagus.. Nature genetics. 44(10):1131-1136. Abstract
Dunlop MG, Dobbins SE, Farrington SM, Jones AM, Palles C, Whiffin N, Tenesa A, Spain S, Broderick P, Ooi L-Y et al..  2012.  Common variation near CDKN1A, POLD3 and SHROOM2 influences colorectal cancer risk.. Nature genetics. 44(7):770-6. Abstract
Whiffin N, Dobbins SE, Hosking FJ, Palles C, Tenesa A, Wang Y, Farrington SM, Jones AM, Broderick P, Campbell H et al..  2013.  Deciphering the genetic architecture of low-penetrance susceptibility to colorectal cancer.. Human molecular genetics. 22(24):5075-82. Abstract
Gharahkhani P, Fitzgerald RC, Vaughan TL, Palles C, Gockel I, Tomlinson I, Buas MF, May A, Gerges C, Anders M et al..  2016.  Genome-wide association studies in oesophageal adenocarcinoma and Barrett's oesophagus: a large-scale meta-analysis.. The Lancet. Oncology. Abstract
Buas MF, He Q, Johnson LG, Onstad L, Levine DM, Thrift AP, Gharahkhani P, Palles C, Lagergren J, Fitzgerald RC et al..  2016.  Germline variation in inflammation-related pathways and risk of Barrett's oesophagus and oesophageal adenocarcinoma.. Gut. Abstract
Whiffin N, Hosking F, Farrington SM, Palles C, Dobbins S, Zgaga L, Lloyd A, Kinnersley B, Gorman M, Tenesa A et al..  2014.  Identification of susceptibility loci for colorectal cancer in a genome-wide meta-analysis.. Human molecular genetics. Abstract
Jarvis D, Mitchell JS, Law PJ, Palin K, Tuupanen S, Gylfe A, Hänninen UA, Cajuso T, Tanskanen T, Kondelin J et al..  2016.  Mendelian randomisation analysis strongly implicates adiposity with risk of developing colorectal cancer.. British journal of cancer. Abstract
Rodriguez-Broadbent H, Law PJ, Sud A, Palin K, Tuupanen S, Gylfe A, Hänninen UA, Cajuso T, Tanskanen T, Kondelin J et al..  2017.  Mendelian randomisation implicates hyperlipidaemia as a risk factor for colorectal cancer.. International journal of cancer. Abstract
Cheng TH, Thompson D, Painter J, O'Mara T, Gorman M, Martin L, Palles C, Jones A, Buchanan DD, Win AK et al..  2015.  Meta-analysis of genome-wide association studies identifies common susceptibility polymorphisms for colorectal and endometrial cancer near SH2B3 and TSHZ1.. Scientific reports. 5:17369. Abstract
Tomlinson IPM, Carvajal-Carmona LG, Dobbins SE, Tenesa A, Jones AM, Howarth K, Palles C, Broderick P, Jaeger EEM, Farrington S et al..  2011.  Multiple common susceptibility variants near BMP pathway loci GREM1, BMP4, and BMP2 explain part of the missing heritability of colorectal cancer.. PLoS genetics. 7(6):e1002105. Abstract
Al-Tassan NA, Whiffin N, Hosking FJ, Palles C, Farrington SM, Dobbins SE, Harris R, Gorman M, Tenesa A, Meyer BF et al..  2015.  A new GWAS and meta-analysis with 1000Genomes imputation identifies novel risk variants for colorectal cancer.. Scientific reports. 5:10442. Abstract
Palles C, Chegwidden L, Li X, Findlay JM, Farnham G, Castro Giner F, Peppelenbosch MP, Kovac M, Adams CL, Prenen H et al..  2015.  Polymorphisms near TBX5 and GDF7 are associated with increased risk for Barrett's esophagus.. Gastroenterology. 148(2):367-78. Abstract
May-Wilson S, Sud A, Law PJ, Palin K, Tuupanen S, Gylfe A, Hänninen UA, Cajuso T, Tanskanen T, Kondelin J et al..  2017.  Pro-inflammatory fatty acid profile and colorectal cancer risk: A Mendelian randomisation analysis.. European journal of cancer (Oxford, England : 1990). 84:228-238. Abstract
Orlando G, Law PJ, Palin K, Tuupanen S, Gylfe A, Hänninen U, Cajuso T, Tanskanen T, Kondelin J, Kaasinen E et al..  2016.  Variation at 2q35 (PNKD and TMBIM1) influences colorectal cancer risk and identifies a pleiotropic effect with inflammatory bowel disease.. Human molecular genetics. Abstract