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Claire Palles
Claire Palles
Verified email at bham.ac.uk
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Year
COVID-19 mortality in patients with cancer on chemotherapy or other anticancer treatments: a prospective cohort study
LYW Lee, JB Cazier, V Angelis, R Arnold, V Bisht, NA Campton, ...
The Lancet 395 (10241), 1919-1926, 2020
11992020
Germline mutations affecting the proofreading domains of POLE and POLD1 predispose to colorectal adenomas and carcinomas
C Palles, JB Cazier, KM Howarth, E Domingo, AM Jones, P Broderick, ...
Nature genetics 45 (2), 136-144, 2013
10792013
COVID-19 prevalence and mortality in patients with cancer and the effect of primary tumour subtype and patient demographics: a prospective cohort study
LYW Lee, JB Cazier, T Starkey, SEW Briggs, R Arnold, V Bisht, S Booth, ...
The Lancet Oncology 21 (10), 1309-1316, 2020
6142020
DNA polymerase ɛ and δ exonuclease domain mutations in endometrial cancer
DN Church, SEW Briggs, C Palles, E Domingo, SJ Kearsey, JM Grimes, ...
Human molecular genetics 22 (14), 2820-2828, 2013
3912013
Clinical relevance of DPYD variants c. 1679T> G, c. 1236G> A/HapB3, and c. 1601G> A as predictors of severe fluoropyrimidine-associated toxicity: a systematic review and meta …
D Meulendijks, LM Henricks, GS Sonke, MJ Deenen, TK Froehlich, ...
The Lancet Oncology 16 (16), 1639-1650, 2015
3692015
A panoply of errors: polymerase proofreading domain mutations in cancer
E Rayner, IC Van Gool, C Palles, SE Kearsey, T Bosse, I Tomlinson, ...
Nature Reviews Cancer 16 (2), 71-81, 2016
3392016
POLE proofreading mutations elicit an antitumor immune response in endometrial cancer
IC van Gool, FA Eggink, L Freeman-Mills, E Stelloo, E Marchi, M de Bruyn, ...
Clinical Cancer Research 21 (14), 3347-3355, 2015
2992015
Novel breast cancer susceptibility locus at 9q31. 2: results of a genome-wide association study
O Fletcher, N Johnson, N Orr, FJ Hosking, LJ Gibson, K Walker, ...
Journal of the National Cancer Institute 103 (5), 425-435, 2011
2962011
Common variation near CDKN1A, POLD3 and SHROOM2 influences colorectal cancer risk
MG Dunlop, SE Dobbins, SM Farrington, AM Jones, C Palles, N Whiffin, ...
Nature genetics 44 (7), 770-776, 2012
2792012
Genetic markers of toxicity from capecitabine and other fluorouracil-based regimens: investigation in the QUASAR2 study, systematic review, and meta-analysis
D Rosmarin, C Palles, D Church, E Domingo, A Jones, E Johnstone, ...
Journal of Clinical Oncology 32 (10), 1031, 2014
2602014
Multiple Common Susceptibility Variants near BMP Pathway Loci GREM1, BMP4, and BMP2 Explain Part of the Missing Heritability of Colorectal Cancer
IPM Tomlinson, LG Carvajal-Carmona, SE Dobbins, A Tenesa, AM Jones, ...
PLoS genetics 7 (6), e1002105, 2011
2402011
Common variants at the MHC locus and at chromosome 16q24. 1 predispose to Barrett's esophagus
Esophageal Adenocarcinoma Genetics Consortium, ...
Nature genetics 44 (10), 1131-1136, 2012
2062012
Association analyses identify 31 new risk loci for colorectal cancer susceptibility
PJ Law, M Timofeeva, C Fernandez-Rozadilla, P Broderick, J Studd, ...
Nature communications 10 (1), 2154, 2019
2032019
Identification of nine new susceptibility loci for endometrial cancer
TA O’mara, DM Glubb, F Amant, D Annibali, K Ashton, J Attia, PL Auer, ...
Nature communications 9 (1), 3166, 2018
2012018
Genome-wide association studies in oesophageal adenocarcinoma and Barrett's oesophagus: a large-scale meta-analysis
P Gharahkhani, RC Fitzgerald, TL Vaughan, C Palles, I Gockel, ...
The lancet oncology 17 (10), 1363-1373, 2016
1762016
Identification of susceptibility loci for colorectal cancer in a genome-wide meta-analysis
N Whiffin, FJ Hosking, SM Farrington, C Palles, SE Dobbins, L Zgaga, ...
Human molecular genetics 23 (17), 4729-4737, 2014
1642014
Mutational signature analysis reveals NTHL1 deficiency to cause a multi-tumor phenotype
JE Grolleman, RM De Voer, FA Elsayed, M Nielsen, RDA Weren, C Palles, ...
Cancer cell 35 (2), 256-266. e5, 2019
1572019
Counting potentially functional variants in BRCA1, BRCA2 and ATM predicts breast cancer susceptibility
N Johnson, O Fletcher, C Palles, M Rudd, E Webb, G Sellick, ...
Human molecular genetics 16 (9), 1051-1057, 2007
1542007
Rare disruptive mutations and their contribution to the heritable risk of colorectal cancer
D Chubb, P Broderick, SE Dobbins, M Frampton, B Kinnersley, S Penegar, ...
Nature communications 7 (1), 11883, 2016
1532016
A new GWAS and meta-analysis with 1000Genomes imputation identifies novel risk variants for colorectal cancer
NA Al-Tassan, N Whiffin, FJ Hosking, C Palles, SM Farrington, ...
Scientific reports 5 (1), 10442, 2015
1412015
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