Author details

Full Name

Gilles Thomas

Affiliation

ORCID

Career Start Year

2003

Papers

H Index

Expertise

CM4AI Collaborator

PMID	Paper Title	Journal Title	Published Year
30988298	Partially methylated domains are hypervariable in breast cancer and fuel widespread CpG island hypermethylation.	Nat Commun	2019
28649644	Constitutional variants are not associated with HER2-positive breast cancer: results from the SIGNAL/PHARE clinical cohort.	NPJ Breast Cancer	2017
28830573	Assessment of the prognostic role of a 94-single nucleotide polymorphisms risk score in early breast cancer in the SIGNAL/PHARE prospective cohort: no correlation with clinico-pathological characteristics and outcomes.	Breast Cancer Research	2017
27666519	Breast cancer genome and transcriptome integration implicates specific mutational signatures with immune cell infiltration.	Nat Commun	2016
27197245	Corrigendum: Frequent somatic transfer of mitochondrial DNA into the nuclear genome of human cancer cells.	Genome Res	2016
27136393	The topography of mutational processes in breast cancer genomes.	Nat Commun	2016
27135926	Landscape of somatic mutations in 560 breast cancer whole-genome sequences.	Nature	2016
27406316	A whole-genome sequence and transcriptome perspective on HER2-positive breast cancers.	Nat Commun	2016
27764800	GWAS in the SIGNAL/PHARE clinical cohort restricts the association between the FGFR2 locus and estrogen receptor status to HER2-negative breast cancer patients.	Oncotarget	2016
27498871	Direct Transcriptional Consequences of Somatic Mutation in Breast Cancer.	Cell Rep	2016
26406445	Targeted Sequencing of the Mitochondrial Genome of Women at High Risk of Breast Cancer without Detectable Mutations in BRCA1/2.	PLoS ONE	2015
25925750	An original phylogenetic approach identified mitochondrial haplogroup T1a1 as inversely associated with breast cancer risk in BRCA2 mutation carriers.	Breast Cancer Res	2015
25963125	Frequent somatic transfer of mitochondrial DNA into the nuclear genome of human cancer cells.	Genome Res	2015
25082706	Mobile DNA in cancer. Extensive transduction of nonrepetitive DNA mediated by L1 retrotransposition in cancer genomes.	Science	2014
21959381	Fine mapping of 14q24.1 breast cancer susceptibility locus.	Hum Genet	2012
22722201	The landscape of cancer genes and mutational processes in breast cancer.	Nature	2012
22327514	Common variants near TARDBP and EGR2 are associated with susceptibility to Ewing sarcoma.	Nat Genet	2012
22561519	Detectable clonal mosaicism and its relationship to aging and cancer.	Nat Genet	2012
22271044	Y chromosome haplogroups and prostate cancer in populations of European and Ashkenazi Jewish ancestry.	Hum Genet	2012
22608084	Mutational processes molding the genomes of 21 breast cancers.	Cell	2012
22608083	The life history of 21 breast cancers.	Cell	2012
22086326	Application of a novel score test for genetic association incorporating gene-gene interaction suggests functionality for prostate cancer susceptibility regions.	Hum Hered	2011
21372204	Large-scale exploration of gene-gene interactions in prostate cancer using a multistage genome-wide association study.	Cancer Res	2011
21318478	Fine mapping the KLK3 locus on chromosome 19q13.33 associated with prostate cancer susceptibility and PSA levels.	Hum Genet	2011
21531787	Fine mapping of a region of chromosome 11q13 reveals multiple independent loci associated with risk of prostate cancer.	Hum Mol Genet	2011
21177793	Comprehensive analysis of hormone and genetic variation in 36 genes related to steroid hormone metabolism in pre- and postmenopausal women from the breast and prostate cancer cohort consortium (BPC3).	J Clin Endocrinol Metab	2011
21131975	Genome-wide association study of renal cell carcinoma identifies two susceptibility loci on 2p21 and 11q13.3.	Nat Genet	2011
21576123	Large-scale fine mapping of the HNF1B locus and prostate cancer risk.	Hum Mol Genet	2011
22033276	Evaluation of variation in the phosphoinositide-3-kinase catalytic subunit alpha oncogene and breast cancer risk.	Br J Cancer	2011
21795498	Confirmation of 5p12 as a susceptibility locus for progesterone-receptor-positive, lower grade breast cancer.	Cancer Epidemiol Biomarkers Prev	2011
20049842	Family history of cancer and risk of pancreatic cancer: a pooled analysis from the Pancreatic Cancer Cohort Consortium (PanScan).	Int J Cancer	2010
20810604	Eighteen insulin-like growth factor pathway genes, circulating levels of IGF-I and its binding protein, and risk of prostate and breast cancer.	Cancer Epidemiol Biomarkers Prev	2010
20967209	Genetic admixture and population substructure in Guanacaste Costa Rica.	PLoS One	2010
20332263	A genome-wide association study of prognosis in breast cancer.	Cancer Epidemiol Biomarkers Prev	2010
19965896	PTGS2 and IL6 genetic variation and risk of breast and prostate cancer: results from the Breast and Prostate Cancer Cohort Consortium (BPC3).	Carcinogenesis	2010
19823874	A comprehensive resequence analysis of the KLK15-KLK3-KLK2 locus on chromosome 19q13.33.	Hum Genet	2010
20598279	Mosaic uniparental disomies and aneuploidies as large structural variants of the human genome.	Am J Hum Genet	2010
20418484	Common variants associated with breast cancer in genome-wide association studies are modifiers of breast cancer risk in BRCA1 and BRCA2 mutation carriers.	Hum Mol Genet	2010
20373013	Alcohol intake and pancreatic cancer: a pooled analysis from the pancreatic cancer cohort consortium (PanScan).	Cancer Causes Control	2010
20458087	Anthropometric measures, body mass index, and pancreatic cancer: a pooled analysis from the Pancreatic Cancer Cohort Consortium (PanScan).	Arch Intern Med	2010
20197460	Pooled analysis of phosphatidylinositol 3-kinase pathway variants and risk of prostate cancer.	Cancer Res	2010
20103627	Pancreatic cancer risk and ABO blood group alleles: results from the pancreatic cancer cohort consortium.	Cancer Res	2010
20101243	A genome-wide association study identifies pancreatic cancer susceptibility loci on chromosomes 13q22.1, 1q32.1 and 5p15.33.	Nat Genet	2010
20237344	Performance of common genetic variants in breast-cancer risk models.	N Engl J Med	2010
20406964	Risk of meningioma and common variation in genes related to innate immunity.	Cancer Epidemiol Biomarkers Prev	2010
20406958	Refining the prostate cancer genetic association within the JAZF1 gene on chromosome 7p15.2.	Cancer Epidemiol Biomarkers Prev	2010
20095854	Novel breast cancer risk alleles and interaction with ionizing radiation among U.S. radiologic technologists.	Radiat Res	2010
20634197	Comprehensive analysis of common genetic variation in 61 genes related to steroid hormone and insulin-like growth factor-I metabolism and breast cancer risk in the NCI breast and prostate cancer cohort consortium.	Hum Mol Genet	2010
19801980	A new statistic and its power to infer membership in a genome-wide association study using genotype frequencies.	Nat Genet	2009
19648918	Genome-wide association study identifies variants in the ABO locus associated with susceptibility to pancreatic cancer.	Nat Genet	2009