Informed Consent ► Public Health Genomics Knowledge Base (v1.0)

Public Health Genomics Knowledge Base (v1.0)

What's New

Last Updated: Feb 18, 2016

• The Geisinger MyCode community health initiative: an electronic health record-linked biobank for precision medicine research.
  Carey David J et al. Genetics in medicine : official journal of the American College of Medical Genetics 2016 Feb (From Genomics & Health Impact Scan Database)
• Was it worth it? Patients' perspectives on the perceived value of genomic-based individualized medicine.
  Halverson Colin Me et al. Journal of community genetics 2016 Feb (From Genomics & Health Impact Scan Database)
• Improving the informed consent process in international collaborative rare disease research: effective consent for effective research.
  Gainotti Sabina et al. European journal of human genetics : EJHG 2016 Feb (From Genomics & Health Impact Scan Database)
• Consenting postpartum women for use of routinely collected biospecimens and/or future biospecimen collection.
  Kozinetz Claudia A et al. Journal of community genetics 2016 Feb (From Discoveries and Insights Database)
• Improving the informed consent process in international collaborative rare disease research: effective consent for effective research
  S Ginotti et al, Eur J Human Genetics, February 10, 2016 (From Discoveries and Insights Database)
• [Identification of a novel mutation of DSPP gene in a Chinese family affected with dentinogenesis imperfecta shields type II].
  Liu Yanshan, et al. Zhonghua yi xue yi chuan xue za zhi = Zhonghua yixue yichuanxue zazhi = Chinese journal of medical genetics 2016 2 (1) 34-7 (From HuGE Literature Finder)
• Influence of interleukin-1 beta gene polymorphisms on the risk of myocardial infarction and ischemic stroke at young age in vivo and in vitro.
  Yang Bo, et al. International journal of clinical and experimental pathology 2015 0 (11) 13806-13(From HuGE Literature Finder)
• Association of genetic polymorphisms of CYP2C9 and VKORC1 with bleeding following warfarin: A case-control study.
  Thatte Urmila, et al. Current clinical pharmacology 2016 1 (From HuGE Literature Finder)
• Building the Partners HealthCare Biobank at Partners Personalized Medicine: Informed Consent, Return of Research Results, Recruitment Lessons and Operational Considerations.
  Karlson Elizabeth W et al. Journal of personalized medicine 6(1) (From Genomics & Health Impact Scan Database)
• Association of N-Methyl-D-Aspartate Receptor 2B Subunit (GRIN2B) polymorphism with earlier age at onset of withdrawal symptoms in Indian alcohol dependent subjects.
  Paul Pradip, et al. Journal of addictive diseases 2016 1 0 (From HuGE Literature Finder)
• Association between CRP and TNF-? genes Variants and Cardiovascular Heart Disease in a Mexican Population: Protocol for a Case-Control Study.
  Hernández-Díaz Yazmín, et al. International journal of environmental research and public health 2016 0 (1) (From HuGE Literature Finder)
• Regulation of Biobanks in France.
  Rial-Sebbag Emmanuelle et al. The Journal of law, medicine & ethics : a journal of the American Society of Law, Medicine & Ethics 2015 Dec 43(4) 754-65 (From Genomics & Health Impact Scan Database)
• Biobank/Genomic Research in Nigeria: Examining Relevant Privacy and Confidentiality Frameworks.
  Nnamuchi Obiajulu et al. The Journal of law, medicine & ethics : a journal of the American Society of Law, Medicine & Ethics 2015 Dec 43(4) 776-86(From Genomics & Health Impact Scan Database)
• Parental Views on Expanded Newborn Screening Using Whole-Genome Sequencing.
  Joseph Galen et al. Pediatrics 2016 Jan 137 Suppl 1S36-46 (From Genomics & Health Impact Scan Database)
• Balancing Benefits and Risks of Immortal Data: Participants' Views of Open Consent in the Personal Genome Project.
  Zarate Oscar A et al. The Hastings Center report 2015 Dec (From Genomics & Health Impact Scan Database)
• Screening for germline mutations in breast/ovarian cancer susceptibility genes in high-risk families in Israel.
  Yablonski-Peretz Tamar et al. Breast cancer research and treatment 2015 Dec (From Genomics & Health Impact Scan Database)
• Hereditary Colon and Rectal Cancer Registry
  Disease: Lynch syndrome; Type: Data|Program; State: Massachusetts (From Implementation Database)