Points to Consider: Ethical, Legal, and Psychosocial Implications of Genetic Testing in Children and Adolescents
Top Cited Papers
Open Access
- 1 July 2015
- journal article
- review article
- Published by Elsevier BV in American Journal of Human Genetics
- Vol. 97 (1), 6-21
- https://doi.org/10.1016/j.ajhg.2015.05.022
Abstract
No abstract availableKeywords
This publication has 100 references indexed in Scilit:
- Primary care patients’ views and decisions about, experience of and reactions to direct-to-consumer genetic testing: a longitudinal studyJournal of Community Genetics, 2013
- Dealing with the unexpected: consumer responses to direct-accessBRCAmutation testingPeerJ, 2013
- Genomic Patterns of Homozygosity in Worldwide Human PopulationsAmerican Journal of Human Genetics, 2012
- Health-care providers’ views on pursuing reproductive benefit through newborn screening: the case of sickle cell disordersEuropean Journal of Human Genetics, 2011
- Genomics really gets personal: How exome and whole genome sequencing challenge the ethical framework of human genetics researchAmerican Journal of Medical Genetics Part A, 2011
- Influence of Genetic Risk Information on Parental Role Identity in Adolescent Girls and Young Women from Families with Fragile X SyndromeJournal of Genetic Counseling, 2011
- Are the kids really all right? Direct-to-consumer genetic testing in children: are company policies clashing with professional norms?European Journal of Human Genetics, 2011
- Where are you going, where have you been: a recent history of the direct-to-consumer genetic testing marketJournal of Community Genetics, 2010
- Consensus Statement: Chromosomal Microarray Is a First-Tier Clinical Diagnostic Test for Individuals with Developmental Disabilities or Congenital AnomaliesAmerican Journal of Human Genetics, 2010
- Living with genetic risk: Effect on adolescent self‐conceptSeminars in Medical Genetics, Part C of the American Journal of Medical Genetics, 2008