CDC, PerkinElmer Readying Molecular SMA Tests as Stakeholders Push for Nationwide Newborn Screening
Parents’ Experiences 12 Years after Newborn Screening for Genetic Susceptibility to Type 1 Diabetes and Their Attitudes to Whole-Genome Sequencing in Newborns
Development of a Tiered and Binned Genetic Counseling Model for Informed Consent in the Era of Multiplex Testing for Cancer Susceptibility
The FDA and 23andMe: Overreaching and overreacting?
Prenatal Identification of Increased Risk for Schizophrenia
Genetic Information Not Always Benign
Columbia University to Explore Impact of Genetic Information about Autism on Families, Individuals
Post-Doctoral Fellowship in Ethical, Legal and Social Implications of Genetics
Conducting Potentially “Sensitive” Research Using Biobank Data Collected Under Broad or Blanket Consent: Participant Perspectives and Responsible Communication
Moral Trajectories in Genomic Medicine: From Personalized Medicine to Precision Prevention and Wellness Genomics?
Case Studies in the Return of Individual Research Results
Genes, Race, and Ancestry: The Meanderings of Two Sociologists in the Weeds of Genetic Methods