Rebecca Sutphen

Ontology type: schema:Person     

Person Info





Publications in SciGraph latest 50 shown

  • 2019-12 Shared heritability and functional enrichment across six solid cancers in NATURE COMMUNICATIONS
  • 2017-05 Identification of 12 new susceptibility loci for different histotypes of epithelial ovarian cancer in NATURE GENETICS
  • 2015-09 Obesity and survival among women with ovarian cancer: results from the Ovarian Cancer Association Consortium in BRITISH JOURNAL OF CANCER
  • 2015-02 American BRCA Outcomes and Utilization of Testing (ABOUT) Study: A Pragmatic Research Model that Incorporates Personalized Medicine/Patient-Centered Outcomes in a Real World Setting in JOURNAL OF GENETIC COUNSELING
  • 2014-01 Kernel canonical correlation analysis for assessing gene–gene interactions and application to ovarian cancer in EUROPEAN JOURNAL OF HUMAN GENETICS
  • 2013-12 Identification and molecular characterization of a new ovarian cancer susceptibility locus at 17q21.31 in NATURE COMMUNICATIONS
  • 2013-05 Cigarette smoking and risk of ovarian cancer: a pooled analysis of 21 case–control studies in CANCER CAUSES & CONTROL
  • 2012-11 ABO blood group and risk of epithelial ovarian cancer within the Ovarian Cancer Association Consortium in CANCER CAUSES & CONTROL
  • 2010-12 Real world experience with cancer genetic counseling via telephone in FAMILIAL CANCER
  • 2010-11 Evaluation of established breast cancer risk factors as modifiers of BRCA1 or BRCA2: a multi-center case-only analysis in BREAST CANCER RESEARCH AND TREATMENT
  • 2010-10 A genome-wide association study identifies susceptibility loci for ovarian cancer at 2q31 and 8q24 in NATURE GENETICS
  • 2007-03 Improved survival in BRCA2 carriers with ovarian cancer in FAMILIAL CANCER
  • 2005-11 Surface-enhanced Raman scattering detection of lysophosphatidic acid in ANALYTICAL AND BIOANALYTICAL CHEMISTRY
  • 1999-10 Mutations in the skeletal muscle α-actin gene in patients with actin myopathy and nemaline myopathy in NATURE GENETICS
  • 1999-02 platformpresentations in moleculargenetics in GENETICS IN MEDICINE
  • 1998-04 The genetic basis of Cowden’s syndrome: three novel mutations in PTEN/MMAC1/TEP1 in HUMAN GENETICS
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