Stephen N Thibodeau


Ontology type: schema:Person     


Person Info

NAME

Stephen N

SURNAME

Thibodeau

Publications in SciGraph latest 50 shown

  • 2019-12 Author Correction: Germline variation at 8q24 and prostate cancer risk in men of European ancestry in NATURE COMMUNICATIONS
  • 2019-12 Shared heritability and functional enrichment across six solid cancers in NATURE COMMUNICATIONS
  • 2019-02 Author Correction: Association analyses of more than 140,000 men identify 63 new prostate cancer susceptibility loci in NATURE GENETICS
  • 2019-01 Discovery of common and rare genetic risk variants for colorectal cancer in NATURE GENETICS
  • 2018-12 Germline variation at 8q24 and prostate cancer risk in men of European ancestry in NATURE COMMUNICATIONS
  • 2018-12 Fine-mapping of prostate cancer susceptibility loci in a large meta-analysis identifies candidate causal variants in NATURE COMMUNICATIONS
  • 2018-12 Distinct microbes, metabolites, and ecologies define the microbiome in deficient and proficient mismatch repair colorectal cancers in GENOME MEDICINE
  • 2018-12 High-throughput screening of prostate cancer risk loci by single nucleotide polymorphisms sequencing in NATURE COMMUNICATIONS
  • 2018-10 DNA mismatch repair protein deficient non-neoplastic colonic crypts: a novel indicator of Lynch syndrome in MODERN PATHOLOGY
  • 2018-07 Association analyses of more than 140,000 men identify 63 new prostate cancer susceptibility loci in NATURE GENETICS
  • 2016-09 Chromatin interactions and candidate genes at ten prostate cancer risk loci in SCIENTIFIC REPORTS
  • 2016-08 Polyunsaturated fatty acids and prostate cancer risk: a Mendelian randomisation analysis from the PRACTICAL consortium in BRITISH JOURNAL OF CANCER
  • 2016-08 Cholecystectomy and the risk of colorectal cancer by tumor mismatch repair deficiency status in INTERNATIONAL JOURNAL OF COLORECTAL DISEASE
  • 2016-08 Genome-wide association of familial prostate cancer cases identifies evidence for a rare segregating haplotype at 8q24.21 in HUMAN GENETICS
  • 2016-05 Tumor eosinophil infiltration and improved survival of colorectal cancer patients: Iowa Women’s Health Study in MODERN PATHOLOGY
  • 2016-04-07 Atlas of prostate cancer heritability in European and African-American men pinpoints tissue-specific regulation in NATURE COMMUNICATIONS
  • 2016-04 Gene and pathway level analyses of germline DNA-repair gene variants and prostate cancer susceptibility using the iCOGS-genotyping array in BRITISH JOURNAL OF CANCER
  • 2016-01 PMS2 monoallelic mutation carriers: the known unknown in GENETICS IN MEDICINE
  • 2015-12 Risk of colorectal cancer for people with a mutation in both a MUTYH and a DNA mismatch repair gene in FAMILIAL CANCER
  • 2015-12 Childhood cancers in families with and without Lynch syndrome in FAMILIAL CANCER
  • 2015-04 Associations of prostate cancer risk variants with disease aggressiveness: results of the NCI-SPORE Genetics Working Group analysis of 18,343 cases in HUMAN GENETICS
  • 2014-12 eRNA: a graphic user interface-based tool optimized for large data analysis from high-throughput RNA sequencing in BMC GENOMICS
  • 2014-12 Colorectal cancer and self-reported tooth agenesis in HEREDITARY CANCER IN CLINICAL PRACTICE
  • 2014-12 High prevalence of mismatch repair deficiency in prostate cancers diagnosed in mismatch repair gene mutation carriers from the colon cancer family registry in FAMILIAL CANCER
  • 2014-12 Trans-ethnic genome-wide association study of colorectal cancer identifies a new susceptibility locus in VTI1A in NATURE COMMUNICATIONS
  • 2014-10 A meta-analysis of 87,040 individuals identifies 23 new susceptibility loci for prostate cancer in NATURE GENETICS
  • 2014-06 Large-scale genetic study in East Asians identifies six new loci associated with colorectal cancer risk in NATURE GENETICS
  • 2014-03 The Association of Telomere Length with Colorectal Cancer Differs by the Age of Cancer Onset in CLINICAL AND TRANSLATIONAL GASTROENTEROLOGY
  • 2014-03 Association analysis of 9,560 prostate cancer cases from the International Consortium of Prostate Cancer Genetics confirms the role of reported prostate cancer associated SNPs for familial disease in HUMAN GENETICS
  • 2013-12 Characterization of human plasma-derived exosomal RNAs by deep sequencing in BMC GENOMICS
  • 2013-12 Efficient recovery of proteins from multiple source samples after trizol® or trizol®LS RNA extraction and long-term storage in BMC GENOMICS
  • 2013-11 Detecting genomic clustering of risk variants from sequence data: cases versus controls in HUMAN GENETICS
  • 2013-09 Detection of large scale 3′ deletions in the PMS2 gene amongst Colon-CFR participants: have we been missing anything? in FAMILIAL CANCER
  • 2013-04 Identification of 23 new prostate cancer susceptibility loci using the iCOGS custom genotyping array in NATURE GENETICS
  • 2013-02 Genome-wide association analyses in east Asians identify new susceptibility loci for colorectal cancer in NATURE GENETICS
  • 2013-01 HOXB13 is a susceptibility gene for prostate cancer: results from the International Consortium for Prostate Cancer Genetics (ICPCG) in HUMAN GENETICS
  • 2012-12 Multiple jejunal cancers resulting from combination of germline APC and MLH1 mutations in FAMILIAL CANCER
  • 2012-12 Analysis of Xq27-28 linkage in the international consortium for prostate cancer genetics (ICPCG) families in BMC MEDICAL GENETICS
  • 2012-07 Validation of prostate cancer risk-related loci identified from genome-wide association studies using family-based association analysis: evidence from the International Consortium for Prostate Cancer Genetics (ICPCG) in HUMAN GENETICS
  • 2012-05 Cigarette Smoking and Colorectal Cancer Risk by KRAS Mutation Status Among Older Women in THE AMERICAN JOURNAL OF GASTROENTEROLOGY
  • 2012-05 Immunohistochemical testing of conventional adenomas for loss of expression of mismatch repair proteins in Lynch syndrome mutation carriers: a case series from the Australasian site of the colon cancer family registry in MODERN PATHOLOGY
  • 2011-10 Lynch Syndrome-Associated Extracolonic Tumors Are Rare in Two Extended Families With the Same EPCAM Deletion in THE AMERICAN JOURNAL OF GASTROENTEROLOGY
  • 2011-08 Seven prostate cancer susceptibility loci identified by a multi-stage genome-wide association study in NATURE GENETICS
  • 2011-06 Body mass index in early adulthood and colorectal cancer risk for carriers and non-carriers of germline mutations in DNA mismatch repair genes in BRITISH JOURNAL OF CANCER
  • 2011-06 HEF1, a novel target of Wnt signaling, promotes colonic cell migration and cancer progression in ONCOGENE
  • 2011-03 Germline PKHD1 mutations are protective against colorectal cancer in HUMAN GENETICS
  • 2010-12 Heritable epigenetic mutation of MLHI in a mother and daughter with Lynch syndrome in HEREDITARY CANCER IN CLINICAL PRACTICE
  • 2009-12 Human colon cancer profiles show differential microRNA expression depending on mismatch repair status and are characteristic of undifferentiated proliferative states in BMC CANCER
  • 2009-12 Epitope-positive truncating MLH1 mutation and loss of PMS2: implications for IHC-directed genetic testing for lynch syndrome in FAMILIAL CANCER
  • 2009-12 Evaluation of a new high-dimensional miRNA profiling platform in BMC MEDICAL GENOMICS
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