Last Posted: Feb 26, 2020
- Current controversies in prenatal diagnosis 2: The 59 genes ACMG recommends reporting as secondary findings when sequencing postnatally should be reported when detected on fetal (and parental) sequencing.
Amor David J et al. Prenatal diagnosis 2020 Feb - Disclosure of Genetic Risk Revealed in a Research Study.
Castellanos Angela et al. The New England journal of medicine 2020 Feb (8) 763-765 - Why genomics researchers are sometimes morally required to hunt for secondary findings.
Koplin Julian J et al. BMC medical ethics 2020 Jan 21(1) 11 - Effectiveness of the Genomics ADvISER decision aid for the selection of secondary findings from genomic sequencing: a randomized clinical trial.
Bombard Yvonne et al. Genetics in medicine : official journal of the American College of Medical Genetics 2019 Dec - Dilemma of Reporting Incidental Findings in Newborn Screening Programs for SCID: Parents' Perspective on Ataxia Telangiectasia.
Blom Maartje et al. Frontiers in immunology 2019 102438 - Returning incidental findings in African genomics research.
Wonkam Ambroise et al. Nature genetics 2019 Nov - Machine Learning by Ultrasonography for Genetic Risk Stratification of Thyroid Nodules.
Daniels Kelly et al. JAMA otolaryngology-- head & neck surgery 2019 Oct 1-6 - Media Coverage of Ethical Issues in Predictive Genetic Testing: A Qualitative Analysis.
Zimmermann Bettina et al. AJOB empirical bioethics 2019 Oct 1-15 - Genome sequencing in healthcare: understanding the UK general public’s views and implications for clinical practice
LM Ballard et al, Eur J Humn Genetics, September 16, 2019 - Genome sequencing in healthcare: understanding the UK general public's views and implications for clinical practice.
Ballard Lisa M, et al. European journal of human genetics : EJHG 2019 9 0.
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