Next generation of free? Points to consider when navigating sponsored genetic testing

Racial disparities in cascade testing for cancer predisposition genes

(2023) Nawal M. Kassem et al.   Preventive Medicine

Value of genetic testing for pediatric epilepsy: Driving earlier diagnosis of ceroid lipofuscinosis type 2 Batten disease

(2022) Fernanda Leal‐Pardinas et al.   EPILEPSIA

Genetic testing and hospital length of stay in neonates with epilepsy

(2022) Heba Akbari et al.   PEDIATRIC NEUROLOGY

Variants in genes coding for collagen type IV α-chains are frequent causes of persistent, isolated hematuria during childhood

(2022) Joseph L. Alge et al.   PEDIATRIC NEPHROLOGY

Assessment of the Diagnostic Yield of Combined Cardiomyopathy and Arrhythmia Genetic Testing

(2022) Lisa M. Dellefave-Castillo et al.   JAMA Cardiology

Association of No-Cost Genetic Testing Program Implementation and Patient Characteristics With Access to Genetic Testing for Inherited Retinal Degenerations

(2021) Peter Y. Zhao et al.   JAMA Ophthalmology

Patient-reported anticipated barriers and benefits to sharing cancer genetic risk information with family members

(2021) Kelsey Stuttgen Finn et al.   EUROPEAN JOURNAL OF HUMAN GENETICS

Laboratory business models and practices: implications for availability and access to germline genetic testing

(2021) Maren T. Scheuner et al.   GENETICS IN MEDICINE

SMA Identified: Clinical and Molecular Findings From a Sponsored Testing Program for Spinal Muscular Atrophy in More Than 2,000 Individuals

(2021) B. Monica Bowen et al.   Frontiers in Neurology

Presence of the V122I Variant of Hereditary Transthyretin-Mediated Amyloidosis Among Self-Reported White Individuals in a Sponsored Genetic Testing Program

(2021) Barry H. Trachtenberg et al.   Circulation-Genomic and Precision Medicine

Stewardship of patient genomic data: A policy statement of the American College of Medical Genetics and Genomics (ACMG)

(2021) Robert G. Best et al.   GENETICS IN MEDICINE

Novel PHEX gene locus‐specific database: Comprehensive characterization of vast number of variants associated with X‐linked hypophosphatemia (XLH)

(2021) Soodabeh Sarafrazi et al.   HUMAN MUTATION

Molecular Diagnoses of X‐Linked and Other Genetic Hypophosphatemias: Results From a Sponsored Genetic Testing Program

(2021) Eric T. Rush et al.   JOURNAL OF BONE AND MINERAL RESEARCH

Direct-to-consumer genetic testing: Prospective users’ attitudes toward information about ancestry and biological relationships

(2021) James W. Hazel et al.   PLoS One

Genetic counseling following direct‐to consumer genetic testing: Consumer perspectives

(2020) Tessa Marzulla et al.   Journal of Genetic Counseling

Genetic testing, insurance discrimination and medical research: what the United States can learn from peer countries

(2019) Jean-Christophe Bélisle-Pipon et al.   NATURE MEDICINE

Conflicts of interest in genetic counseling: acknowledging and accepting

(2017) Katie A. Stoll et al.   GENETICS IN MEDICINE

Points to Consider: Ethical, Legal, and Psychosocial Implications of Genetic Testing in Children and Adolescents

(2015) Jeffrey R. Botkin et al.   AMERICAN JOURNAL OF HUMAN GENETICS

Standards and guidelines for the interpretation of sequence variants: a joint consensus recommendation of the American College of Medical Genetics and Genomics and the Association for Molecular Pathology

(2015) Sue Richards et al.   GENETICS IN MEDICINE

Routes for breaching and protecting genetic privacy

(2014) Yaniv Erlich et al.   NATURE REVIEWS GENETICS