Breast and ovarian cancer WEEKLY UPDATE: August 4-11, 2016 || Public Health Genomics Knowledge Base (v1.2)

Public Health Genomics Knowledge Base (v1.2)



August 4-11, 2016


Last Updated: Aug 04, 2016

• Genetic testing and personalized ovarian cancer screening: a survey of public attitudes.
  Meisel Susanne F et al. BMC women's health 2016 16(1) 46
• Identifying Needs: a Qualitative Study of women's Experiences Regarding Rapid Genetic Testing for Hereditary Breast and Ovarian Cancer in the DNA BONus Study.
  Augestad Mirjam Tonheim et al. Journal of genetic counseling 2016 Jul
• Cardiovascular risk of BRCA1/2 mutation carriers: A review.
  van Westerop L L M, et al. Maturitas 2016 9 135-9
• The effect of referral for genetic counseling on genetic testing and surgical prevention in women at high risk for ovarian cancer: Results from a randomized controlled trial.
  Drescher Charles W et al. Cancer 2016 Jul
• First application of next-generation sequencing in Moroccan breast/ovarian cancer families and report of a novel frameshift mutation of the BRCA1 gene.
  Jouali Farah, et al. Oncology letters 2016 8 (2) 1192-1196
• JAX Genomic Education: Categorizing Cancer Risk
  Disease: Lynch syndrome|Ovarian Cancer|Breast Cancer; Type: Education; State: Multiple States
• The Activities and Impact of State Programs to Address Hereditary Breast and Ovarian Cancer, 2011–2014
  Disease: Breast Cancer|Ovarian Cancer; Type: Multipe Types; State: Georgia|Michigan|Oregon
• Expert and Advocacy Group Consensus Findings on the Horizon of Public Health Genetic Testing.
  Modell Stephen M et al. Healthcare (Basel, Switzerland) 2016 4(1)
• Public Health Approaches and Barriers to Educating Providers about Hereditary Breast and Ovarian Cancer Syndrome.
  Trepanier Angela M et al. Healthcare (Basel, Switzerland) 2016 4(1)
• Understanding the Needs of Young Women Regarding Breast Cancer Risk Assessment and Genetic Testing: Convergence and Divergence among Patient-Counselor Perceptions and the Promise of Peer Support.
  Evans Chalanda et al. Healthcare (Basel, Switzerland) 2016 4(3)
• BRCA1 and BRCA2 sequence variations detected with next-generation sequencing in patients with premature ovarian insufficiency.
  Y?lmaz Nafiye Karaka?, et al. Journal of the Turkish German Gynecological Association 2016 0 (2) 77-82
• Changes of Socio-demographic data of clients seeking genetic counseling for hereditary breast and ovarian cancer due to the "Angelina Jolie Effect".
  Staudigl Christine et al. BMC cancer 2016 16436
• The Role of Knowledge on Genetic Counseling and Testing in Black Cancer Survivors at Increased Risk of Carrying a BRCA1/2 Mutation.
  Hurtado-de-Mendoza Alejandra et al. Journal of genetic counseling 2016 Jul
• Clinical Next-Generation Sequencing Pipeline Outperforms a Combined Approach Using Sanger Sequencing and Multiplex Ligation-Dependent Probe Amplification in Targeted Gene Panel Analysis.
  Schenkel Laila C, et al. The Journal of molecular diagnostics : JMD 2016 7
• Design and validation of a next generation sequencing assay for hereditary BRCA1 and BRCA2 mutation testing.
  Kang Hyunseok P, et al. PeerJ 2016 0 e2162

• CDC Information (7)
• CDC-Authored Pub (1)

• Human (22)
• Pathogen (0)

• Human (689)
• Pathogen (0)

• Human (149)
• Pathogen (0)

• Guidelines (8)
• Tier Table (3)
• Synthesis (8)

• Huamn (83)
• Pathogen (0)

Relevant Resources

• Cancer Genomics and Epidemiology Navigator (CGEN)
• Genetics and Genomics Competencies Center (G2C2)
• NIH Genetic Testing Registry
• NIH MedGen Database
• Online Mendelian Inheritance in Man (OMIM)
• PharmGKB