Leigha Senter


Ontology type: schema:Person     


Person Info

NAME

Leigha

SURNAME

Senter

Publications in SciGraph latest 50 shown

  • 2018-12 Neck Ultrasound in Patients with Follicular Thyroid Carcinoma in HORMONES AND CANCER
  • 2018-10 Involvement and Influence of Healthcare Providers, Family Members, and Other Mutation Carriers in the Cancer Risk Management Decision-Making Process of BRCA1 and BRCA2 Mutation Carriers in JOURNAL OF GENETIC COUNSELING
  • 2018-09 Age at first full-term birth and breast cancer risk in BRCA1 and BRCA2 mutation carriers in BREAST CANCER RESEARCH AND TREATMENT
  • 2018-08 “Second-Class Status?” Insight into Communication Patterns and Common Concerns Among Men with Hereditary Breast and Ovarian Cancer Syndrome in JOURNAL OF GENETIC COUNSELING
  • 2018-02 National Society of Genetic Counselors Code of Ethics: Explication of 2017 Revisions in JOURNAL OF GENETIC COUNSELING
  • 2017-12 Identification of ten variants associated with risk of estrogen-receptor-negative breast cancer in NATURE GENETICS
  • 2017-09 Anti-thyroglobulin antibodies do not significantly increase the risk of finding iodine avid metastases on post-radioactive iodine ablation scan in low-risk thyroid cancer patients in JOURNAL OF ENDOCRINOLOGICAL INVESTIGATION
  • 2017-05 Identification of 12 new susceptibility loci for different histotypes of epithelial ovarian cancer in NATURE GENETICS
  • 2017-02-14 A genome-wide association study yields five novel thyroid cancer risk loci in NATURE COMMUNICATIONS
  • 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
  • 2016-05 The incidence of leukaemia in women with BRCA1 and BRCA2 mutations: an International Prospective Cohort Study in BRITISH JOURNAL OF CANCER
  • 2016-04-27 Identification of four novel susceptibility loci for oestrogen receptor negative breast cancer in NATURE COMMUNICATIONS
  • 2016-01 PMS2 monoallelic mutation carriers: the known unknown in GENETICS IN MEDICINE
  • 2016-01 Hormone replacement therapy after menopause and risk of breast cancer in BRCA1 mutation carriers: a case–control study in BREAST CANCER RESEARCH AND TREATMENT
  • 2015-06 Prospective evaluation of alcohol consumption and the risk of breast cancer in BRCA1 and BRCA2 mutation carriers in BREAST CANCER RESEARCH AND TREATMENT
  • 2014-08 Mammography screening and the risk of breast cancer in BRCA1 and BRCA2 mutation carriers: a prospective study in BREAST CANCER RESEARCH AND TREATMENT
  • 2014-07 Duration of tamoxifen use and the risk of contralateral breast cancer in BRCA1 and BRCA2 mutation carriers in BREAST CANCER RESEARCH AND TREATMENT
  • 2014-02 Timing of oral contraceptive use and the risk of breast cancer in BRCA1 mutation carriers in BREAST CANCER RESEARCH AND TREATMENT
  • 2014-01 Incidence of colorectal cancer in BRCA1 and BRCA2 mutation carriers: results from a follow-up study in BRITISH JOURNAL OF CANCER
  • 2013-11 The impact of pregnancy on breast cancer survival in women who carry a BRCA1 or BRCA2 mutation in BREAST CANCER RESEARCH AND TREATMENT
  • 2013-11 International Rates of Breast Reconstruction After Prophylactic Mastectomy in BRCA1 and BRCA2 Mutation Carriers in ANNALS OF SURGICAL ONCOLOGY
  • 2012-12 Consumer awareness and attitudes about insurance discrimination post enactment of the Genetic Information Nondiscrimination Act in FAMILIAL CANCER
  • 2012-12 The incidence of pancreatic cancer in BRCA1 and BRCA2 mutation carriers in BRITISH JOURNAL OF CANCER
  • 2012-08 Identification of Individuals at Risk for Lynch Syndrome Using Targeted Evaluations and Genetic Testing: National Society of Genetic Counselors and the Collaborative Group of the Americas on Inherited Colorectal Cancer Joint Practice Guideline in JOURNAL OF GENETIC COUNSELING
  • 2012-04 Essential Elements of Genetic Cancer Risk Assessment, Counseling, and Testing: Updated Recommendations of the National Society of Genetic Counselors in JOURNAL OF GENETIC COUNSELING
  • 2012-04 Breastfeeding and the risk of breast cancer in BRCA1 and BRCA2 mutation carriers in BREAST CANCER RESEARCH
  • 2012-01 Implementing screening for Lynch syndrome among patients with newly diagnosed colorectal cancer: summary of a public health/clinical collaborative meeting in GENETICS IN MEDICINE
  • 2011-10 Implementing screening for Lynch syndrome among patients with newly diagnosed colorectal cancer: Summary of a public health/clinical collaborative meeting in GENETICS IN MEDICINE
  • 2010-06 No evidence for a genetic modifier for renal cell cancer risk in HLRCC syndrome in FAMILIAL CANCER
  • 2010-02 Characterization of BRCA1 ring finger variants of uncertain significance in BREAST CANCER RESEARCH AND TREATMENT
  • 2009-12 Epitope-positive truncating MLH1 mutation and loss of PMS2: implications for IHC-directed genetic testing for lynch syndrome in FAMILIAL CANCER
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