Incidental findings ▲ Public Health Genomics Knowledge Base (v1.2)

Public Health Genomics Knowledge Base (v1.2)






Last Updated: Sep 08, 2016

• Accuracy and clinical value of maternal incidental findings during noninvasive prenatal testing for fetal aneuploidies.
  Brison Nathalie et al. Genetics in medicine : official journal of the American College of Medical Genetics 2016 Sep
• Opportunities for community awareness platforms in personal genomics and bioinformatics education.
  Bianchi Lucia et al. Briefings in bioinformatics 2016 Aug
• Accuracy and clinical value of maternal incidental findings during noninvasive prenatal testing for fetal aneuploidies
  A Brison et al, Genetics in Medicine, September 1, 2016
• Prenatal Whole Exome Sequencing; the Views of Clinicians, Scientists, Genetic Counsellors and Patient Representatives.
  Quinlan-Jones Elizabeth et al. Prenatal diagnosis 2016 Aug
• Unsolved challenges of clinical whole-exome sequencing: a systematic literature review of end-users' views.
  Bertier Gabrielle et al. BMC medical genomics 2016 9(1) 52
• Is "incidental finding" the best term?: a study of patients' preferences.
  Tan Nina et al. Genetics in medicine : official journal of the American College of Medical Genetics 2016 Aug
• A Clinical Service to Support the Return of Secondary Genomic Findings in Human Research.
  Darnell Andrew J et al. American journal of human genetics 2016 Mar 98(3) 435-41
• A framework for analyzing the ethics of disclosing genetic research findings.
  Eckstein Lisa et al. The Journal of law, medicine & ethics : a journal of the American Society of Law, Medicine & Ethics 2014 42(2) 190-207
• Choices of Incidental Findings of Individuals Undergoing Genome Wide Sequencing, a Single Center's Experience.
  Bishop Callie L et al. Clinical genetics 2016 Jul
• Disclosure of incidental findings in cancer genomic research: investigators' perceptions on obligations and barriers.
  Kleiderman E et al. Clinical genetics 2015 Oct 88(4) 320-6
• Raising Genomic Citizens: Adolescents and the Return of Secondary Genomic Findings.
  Sabatello Maya et al. The Journal of law, medicine & ethics : a journal of the American Society of Law, Medicine & Ethics 2016 Jun 44(2) 292-308
• Personal utility in genomic testing: is there such a thing?
  Bunnik Eline M et al. Journal of medical ethics 2015 Apr 41(4) 322-6
• Pharmacogenomic incidental findings in 308 families: The NIH Undiagnosed Diseases Program experience.
  Lee Elizabeth M J et al. Genetics in medicine : official journal of the American College of Medical Genetics 2016 Jun
• DECIDE: a Decision Support Tool to Facilitate Parents' Choices Regarding Genome-Wide Sequencing.
  Birch Patricia et al. Journal of genetic counseling 2016 May
• Ethical considerations in biobanks: how a public health ethics perspective sheds new light on old controversies.
  Virani Alice Hawkins et al. Journal of genetic counseling 2015 Jun 24(3) 428-32

• CDC Information (1)
• CDC-Authored Pub (2)

• Human (45)
• Pathogen (0)

• Human (13)
• Pathogen (0)

• Human (50)
• Pathogen (1)

• Guidelines (6)
• Tier Table (0)
• Synthesis (8)

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