Family Health History || Public Health Genomics Knowledge Base (v1.2)

Public Health Genomics Knowledge Base (v1.2)










Last Updated: Sep 01, 2016

• Breast cancer risk prediction using a clinical risk model and polygenic risk score.
  Shieh Yiwey et al. Breast cancer research and treatment 2016 Aug
• Exploring Gaps of Family History Documentation in EHR for Precision Medicine -A Case Study of Familial Hypercholesterolemia Ascertainment.
  Mehrabi Saeed et al. AMIA Joint Summits on Translational Science proceedings. AMIA Summit on Translational Science 2016 2016160-6
• Genetic variants of the MAVS, MITA and MFN2 genes are not associated with leprosy in Han Chinese from Southwest China.
  Wang Dong, et al. Infection, genetics and evolution : journal of molecular epidemiology and evolutionary genetics in infectious diseases 2016 8
• High prevalence and predominance of BRCA1 germline mutations in Pakistani triple-negative breast cancer patients.
  Rashid Muhammad Usman, et al. BMC cancer 2016 0 (1) 673
• Psychosocial Adjustment and Perceived Risk Among Adolescent Girls From Families With BRCA1/2 or Breast Cancer History.
  Bradbury Angela R, et al. Journal of clinical oncology : official journal of the American Society of Clinical Oncology 2016 8
• Colonoscopy uptake for high-risk individuals with a family history of colorectal neoplasia: A multicenter, randomized trial of tailored counseling versus standard information.
  Ingrand Isabelle et al. Medicine 2016 Aug 95(33) e4303
• Effective Referral of Low-Income Women at Risk for Hereditary Breast and Ovarian Cancer to Genetic Counseling: A Randomized Delayed Intervention Control Trial.
  Pasick Rena J et al. American journal of public health 2016 Aug e1-e7
• Familial colorectal cancer: Patient assessment, surveillance and surgical management.
  Kennelly R P et al. European journal of surgical oncology : the journal of the European Society of Surgical Oncology and the British Association of Surgical Oncology 2016 Jul
• Primary care professionals' perceptions of using a short family history questionnaire.
  Ahmed Shenaz et al. Family practice 2016 Aug
• The Three-Generation Pedigree: A Critical Tool in Cancer Genetics Care.
  Mahon Suzanne M et al. Oncology nursing forum 2016 Sep 43(5) 655-60
• Analysis of Cyclin-Dependent Kinase Inhibitor-2B rs1063192 Polymorphism in Saudi Patients with Primary Open-Angle Glaucoma.
  Abu-Amero Khaled K, et al. Genetic testing and molecular biomarkers 2016 8
• The Clinical Spectrum of Female Epilepsy Patients with PCDH19 Mutations in a Chinese Population.
  Liu Aijie, et al. Clinical genetics 2016 8
• Lack of Association Between Polymorphism rs4986791 in TLR4 and Primary Open-Angle Glaucoma in a Saudi Cohort.
  Mousa Ahmed, et al. Genetic testing and molecular biomarkers 2016 8
• Multiple primary tumors in a family with Li-Fraumeni syndrome with a TP53 germline mutation identified by next-generation sequencing.
  Zampiga Valentina, et al. The International journal of biological markers 2016 8 0
• A state-wide population-based program for detection of lynch syndrome based upon immunohistochemical and molecular testing of colorectal tumours.
  Schofield Lyn et al. Familial cancer 2012 Mar 11(1) 1-6

• CDC Information (11)
• CDC-Authored Pub (8)

• Human (56)
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• Guidelines (14)
• Tier Table (1)
• Synthesis (39)

• Huamn (82)
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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

Public Health Genomics Knowledge Base (v1.2)