Fergus J Couch


Ontology type: schema:Person     


Person Info

NAME

Fergus J

SURNAME

Couch

Publications in SciGraph latest 50 shown

  • 2019-04 Current Approaches to Cancer Genetic Counseling Services for Spanish-Speaking Patients in JOURNAL OF IMMIGRANT AND MINORITY HEALTH
  • 2019-02 Molecular mechanisms linking high body mass index to breast cancer etiology in post-menopausal breast tumor and tumor-adjacent tissues in BREAST CANCER RESEARCH AND TREATMENT
  • 2019-01 Comprehensive annotation of BRCA1 and BRCA2 missense variants by functionally validated sequence-based computational prediction models in GENETICS IN MEDICINE
  • 2019-01 Correction: Evaluation of copy-number variants as modifiers of breast and ovarian cancer risk for BRCA1 pathogenic variant carriers in EUROPEAN JOURNAL OF HUMAN GENETICS
  • 2018-12-03 Clinical validity assessment of genes frequently tested on hereditary breast and ovarian cancer susceptibility sequencing panels in GENETICS IN MEDICINE
  • 2018-12 Identification of nine new susceptibility loci for endometrial cancer in NATURE COMMUNICATIONS
  • 2018-12 A contemporary review of male breast cancer: current evidence and unanswered questions in CANCER AND METASTASIS REVIEWS
  • 2018-12 E-cadherin breast tumor expression, risk factors and survival: Pooled analysis of 5,933 cases from 12 studies in the Breast Cancer Association Consortium in SCIENTIFIC REPORTS
  • 2018-12 Clinical testing of BRCA1 and BRCA2: a worldwide snapshot of technological practices in NPJ GENOMIC MEDICINE
  • 2018-07 From the laboratory to the clinic: sharing BRCA VUS reclassification tools with practicing genetics professionals in JOURNAL OF COMMUNITY GENETICS
  • 2018-07 A transcriptome-wide association study of 229,000 women identifies new candidate susceptibility genes for breast cancer in NATURE GENETICS
  • 2018-07 Does mammographic density mediate risk factor associations with breast cancer? An analysis by tumor characteristics in BREAST CANCER RESEARCH AND TREATMENT
  • 2018-02 Cardiovascular Concerns in BRCA1 and BRCA2 Mutation Carriers in CURRENT TREATMENT OPTIONS IN CARDIOVASCULAR MEDICINE
  • 2018-01 Impact of histopathology, tumor-infiltrating lymphocytes, and adjuvant chemotherapy on prognosis of triple-negative breast cancer in BREAST CANCER RESEARCH AND TREATMENT
  • 2017-12 Reproductive profiles and risk of breast cancer subtypes: a multi-center case-only study in BREAST CANCER RESEARCH
  • 2017-12 Alcohol consumption and breast tumor gene expression in BREAST CANCER RESEARCH
  • 2017-12 The contribution of pathogenic variants in breast cancer susceptibility genes to familial breast cancer risk in NPJ BREAST CANCER
  • 2017-12 Erratum to: Mammographic texture and risk of breast cancer by tumor type and estrogen receptor status in BREAST CANCER RESEARCH
  • 2017-12 Author Correction: The contribution of pathogenic variants in breast cancer susceptibility genes to familial breast cancer risk in NPJ BREAST CANCER
  • 2017-12 Identification of ten variants associated with risk of estrogen-receptor-negative breast cancer in NATURE GENETICS
  • 2017-12 Germline variation in ADAMTSL1 is associated with prognosis following breast cancer treatment in young women in NATURE COMMUNICATIONS
  • 2017-11 Association analysis identifies 65 new breast cancer risk loci in NATURE
  • 2017-10 Management of Breast Cancer Risk in Women with Ovarian Cancer and Deleterious BRCA1 or BRCA2 Mutations in ANNALS OF SURGICAL ONCOLOGY
  • 2017-10 Clinical Decision-Making in Patients with Variant of Uncertain Significance in BRCA1 or BRCA2 Genes in ANNALS OF SURGICAL ONCOLOGY
  • 2017-09 Interaction of mammographic breast density with menopausal status and postmenopausal hormone use in relation to the risk of aggressive breast cancer subtypes in BREAST CANCER RESEARCH AND TREATMENT
  • 2017-06 Genomic analyses identify hundreds of variants associated with age at menarche and support a role for puberty timing in cancer risk in NATURE GENETICS
  • 2017-05 Identification of 12 new susceptibility loci for different histotypes of epithelial ovarian cancer in NATURE GENETICS
  • 2017-05 Genetic modifiers of CHEK2*1100delC-associated breast cancer risk in GENETICS IN MEDICINE
  • 2017-04 Evaluation of copy-number variants as modifiers of breast and ovarian cancer risk for BRCA1 pathogenic variant carriers in EUROPEAN JOURNAL OF HUMAN GENETICS
  • 2017-02 Male breast cancer in a multi-gene panel testing cohort: insights and unexpected results in BREAST CANCER RESEARCH AND TREATMENT
  • 2017-01 Association of breast cancer risk in BRCA1 and BRCA2 mutation carriers with genetic variants showing differential allelic expression: identification of a modifier of breast cancer risk at locus 11q22.3 in BREAST CANCER RESEARCH AND TREATMENT
  • 2016-12 The PALB2 p.Leu939Trp mutation is not associated with breast cancer risk in BREAST CANCER RESEARCH
  • 2016-12 Inheritance of deleterious mutations at both BRCA1 and BRCA2 in an international sample of 32,295 women in BREAST CANCER RESEARCH
  • 2016-12 Patient survival and tumor characteristics associated with CHEK2:p.I157T – findings from the Breast Cancer Association Consortium in BREAST CANCER RESEARCH
  • 2016-12 Mammographic texture and risk of breast cancer by tumor type and estrogen receptor status in BREAST CANCER RESEARCH
  • 2016-12 Male breast cancer in BRCA1 and BRCA2 mutation carriers: pathology data from the Consortium of Investigators of Modifiers of BRCA1/2 in BREAST CANCER RESEARCH
  • 2016-12 Novel patient-derived xenograft mouse model for pancreatic acinar cell carcinoma demonstrates single agent activity of oxaliplatin in JOURNAL OF TRANSLATIONAL MEDICINE
  • 2016-12 Genetic predisposition to ductal carcinoma in situ of the breast in BREAST CANCER RESEARCH
  • 2016-12 rs2735383, located at a microRNA binding site in the 3’UTR of NBS1, is not associated with breast cancer risk in SCIENTIFIC REPORTS
  • 2016-12 Prognostic value of automated KI67 scoring in breast cancer: a centralised evaluation of 8088 patients from 10 study groups in BREAST CANCER RESEARCH
  • 2016-12 Identification of independent association signals and putative functional variants for breast cancer risk through fine-scale mapping of the 12p11 locus in BREAST CANCER RESEARCH
  • 2016-11 Functional assays provide a robust tool for the clinical annotation of genetic variants of uncertain significance in NPJ GENOMIC MEDICINE
  • 2016-10 Fine scale mapping of the 17q22 breast cancer locus using dense SNPs, genotyped within the Collaborative Oncological Gene-Environment Study (COGs) in SCIENTIFIC REPORTS
  • 2016-10 Impact that Timing of Genetic Mutation Diagnosis has on Surgical Decision Making and Outcome for BRCA1/BRCA2 Mutation Carriers with Breast Cancer in ANNALS OF SURGICAL ONCOLOGY
  • 2016-09-07 Functional mechanisms underlying pleiotropic risk alleles at the 19p13.1 breast–ovarian cancer susceptibility locus in NATURE COMMUNICATIONS
  • 2016-09 Counselling framework for moderate-penetrance cancer-susceptibility mutations in NATURE REVIEWS CLINICAL ONCOLOGY
  • 2016-06 Five endometrial cancer risk loci identified through genome-wide association analysis in NATURE GENETICS
  • 2016-05 Genes associated with histopathologic features of triple negative breast tumors predict molecular subtypes in BREAST CANCER RESEARCH AND TREATMENT
  • 2016-05 Association of genetic susceptibility variants for type 2 diabetes with breast cancer risk in women of European ancestry in CANCER CAUSES & CONTROL
  • 2016-04-27 Identification of four novel susceptibility loci for oestrogen receptor negative breast cancer in NATURE COMMUNICATIONS
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