Breast and Ovarian Cancer :: Public Health Genomics Knowledge Base (v1.0)

Public Health Genomics Knowledge Base (v1.0)

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Last Updated: Feb 13, 2016

• Novel germline mutations and unclassified variants of BRCA1 and BRCA2 genes in Chinese women with familial breast/ovarian cancer.
  Cao Wen-Ming, et al. BMC cancer 2015 0 (1) 64 (From HuGE Literature Finder)
• Tracking of the origin of recurrent mutations of the BRCA1 and BRCA2 genes in the North-East of Italy and improved mutation analysis strategy.
  Cini Giulia, et al. BMC medical genetics 2016 0 (1) 11 (From HuGE Literature Finder)
• Modeling the dyadic effects of parenting, stress, and coping on parent-child communication in families tested for hereditary breast-ovarian cancer risk.
  Hamilton Jada G et al. Familial cancer 2016 Feb (From Genomics & Health Impact Scan Database)
• Genetic/Familial High-Risk Assessment: Breast and Ovarian, Version 2.2015.
  Daly Mary B et al. Journal of the National Comprehensive Cancer Network : JNCCN 2016 Feb 14(2) 153-62 (From Genomics & Health Impact Scan Database)
• Risk-reducing surgery on the uterine adnexa: timing and type of surgical treatment and pathology report.
  Mauro Signorelli, et al. Minerva ginecologica 2016 2 (From HuGE Literature Finder)
• Somatic Mosaic Mutations in PPM1D and TP53 in the Blood of Women With Ovarian Carcinoma.
  Swisher Elizabeth M, et al. JAMA oncology 2016 2 (From HuGE Literature Finder)
• Prevalence and spectrum of BRCA germline variants in mainland Chinese familial breast and ovarian cancer patients.
  Kim Yeong C, et al. Oncotarget 2016 2 (From HuGE Literature Finder)
• Recurrent mutations of BRCA1, BRCA2 and PALB2 in the population of breast and ovarian cancer patients in Southern Poland.
  Wojcik P, et al. Hereditary cancer in clinical practice 2016 0 5 (From HuGE Literature Finder)
• Ovarian cancer patients at high risk of BRCA mutation: the constitutional genetic characterization does not change prognosis.
  Sabatier Renaud, et al. Familial cancer 2016 2 (From HuGE Literature Finder)
• BRCA1/BRCA2 founder mutations and cancer risks: impact in the western Danish population.
  Nielsen Henriette Roed, et al. Familial cancer 2016 2 (From HuGE Literature Finder)
• Tools for Bidirectional Cancer Registry Reporting to Identify Individuals at Risk for Hereditary Breast and Ovarian Cancer syndrome
  Disease: Breast Cancer|Ovarian Cancer; Type: Tools; State: Multiple States (From Implementation Database)
• What is your family’s risk of hereditary breast and ovarian cancer? You have to look at the male side, too,
  WCSH6, February 2, 2016 (From Genomics & Health Impact Scan Database)
• Selecting Patients with Ovarian Cancer for Germline BRCA Mutation Testing: Findings from Guidelines and a Systematic Literature Review.
  Eccles Diana M et al. Advances in therapy 2016 Jan (From Genomics & Health Impact Scan Database)
• Mutation screening of MIR146A/B and BRCA1/2 3'-UTRs in the GENESIS study.
  Garcia Amandine I, et al. European journal of human genetics : EJHG 2016 1 (From HuGE Literature Finder)
• BRCA1 founder mutations do not contribute to increased risk of gastric cancer in the Polish population.
  ?awniczak Ma?gorzata, et al. Hereditary cancer in clinical practice 2016 0 3 (From HuGE Literature Finder)
• Investigating the effect of 28 BRCA1 and BRCA2 mutations on their related transcribed mRNA.
  Quiles Francisco, et al. Breast cancer research and treatment 2016 1 (From HuGE Literature Finder)
• Singapore Cancer Network (SCAN) Guidelines for Referral for Genetic Evaluation of Common Hereditary Cancer Syndromes.
  et al. Annals of the Academy of Medicine, Singapore 2015 Oct 44(10) 492-510 (From Genomics & Health Impact Scan Database)
• KOHBRA BRCA risk calculator (KOHCal): a model for predicting BRCA1 and BRCA2 mutations in Korean breast cancer patients.
  Kang Eunyoung et al. Journal of human genetics 2016 Jan (From Genomics & Health Impact Scan Database)
• Reach of the Montana Cancer Control Program to Women with Disabilities.
  Disease: Breast Cancer|Ovarian Cancer; Type: Data|Program; State: Montana (From Implementation Database)