Ethical Implications of Clinical Genomic Information, Records Research, and Informed Consent.

Main|Search|PHGKB


Last Posted: Oct 06, 2018

---

• Opening the "black box" of informed consent appointments for genome sequencing: a multisite observational study.
  Sanderson Saskia C et al. Genetics in medicine : official journal of the American College of Medical Genetics 2018 Oct
• Ethical Implications of Clinical Genomic Information, Records Research, and Informed Consent.
  Lee Susannah W et al. The Ochsner journal 2018 18(3) 196-198
• The importance of genetic counselling in genome-wide sequencing
  AM Elliot et al, October 3, 2018
• [The Roles of Designated Core Hospitals and Cooperative Hospitals for Cancer Genomic Medicine in Japan].
  Nishida Toshirou et al. Gan to kagaku ryoho. Cancer & chemotherapy 2018 Sep 45(9) 1223-1227
• Regulation of Non-consensual Genetic Testing in Australia: Use of Samples from Deceased Persons.
  McWhirter Rebekah E et al. Journal of law and medicine 24(1) 150-65
• Screening for Fabry Disease in Kidney Disease: a Cross-Sectional Study in Males and Females.
  Sodré Luciana Senra de Souza et al. Kidney & blood pressure research 2017 42(6) 1258-1265
• Ethical Issues in Contemporary Clinical Genetics.
  Braverman Genna et al. Mayo Clinic proceedings. Innovations, quality & outcomes 2018 Jun 2(2) 81-90
• Clinical practice guidance for next-generation sequencing in cancer diagnosis and treatment (Edition 1.0).
  Sunami Kuniko et al. Cancer science 2018 Sep 109(9) 2980-2985
• Ethical and Counseling Challenges in Prenatal Exome Sequencing.
  Harris Sarah et al. Prenatal diagnosis 2018 Sep
• Secondary findings from whole-exome/genome sequencing evaluating stakeholder perspectives. A review of the literature.
  Delanne J et al. European journal of medical genetics 2018 Aug

more