ACMG SF v3.1 list for reporting of secondary findings in clinical exome and genome sequencing: A policy statement of the American College of Medical Genetics and Genomics (ACMG)

A Population-Based Study of Genes Previously Implicated in Breast Cancer

(2021) Chunling Hu et al.   NEW ENGLAND JOURNAL OF MEDICINE

Breast Cancer Risk Genes — Association Analysis in More than 113,000 Women

(2021) et al.   NEW ENGLAND JOURNAL OF MEDICINE

An Evidence-Based Assessment of Genes in Dilated Cardiomyopathy

(2021) Elizabeth Jordan et al.   CIRCULATION

Recommendations for reporting of secondary findings in clinical exome and genome sequencing, 2021 update: a policy statement of the American College of Medical Genetics and Genomics (ACMG)

(2021) David T. Miller et al.   GENETICS IN MEDICINE

ACMG SF v3.0 list for reporting of secondary findings in clinical exome and genome sequencing: a policy statement of the American College of Medical Genetics and Genomics (ACMG)

(2021) David T. Miller et al.   GENETICS IN MEDICINE

Ovarian and breast cancer risks associated with pathogenic variants in RAD51C and RAD51D

(2020) Xin Yang et al.   JNCI-Journal of the National Cancer Institute

Genomics of disease risk in globally diverse populations

(2019) Deepti Gurdasani et al.   NATURE REVIEWS GENETICS

Association of the V122I Hereditary Transthyretin Amyloidosis Genetic Variant With Heart Failure Among Individuals of African or Hispanic/Latino Ancestry

(2019) Scott M. Damrauer et al.   JAMA-JOURNAL OF THE AMERICAN MEDICAL ASSOCIATION

Genetic Evaluation of Cardiomyopathy—A Heart Failure Society of America Practice Guideline

(2018) Ray E. Hershberger et al.   JOURNAL OF CARDIAC FAILURE

Association of Variants in BAG3 With Cardiomyopathy Outcomes in African American Individuals

(2018) Valerie D. Myers et al.   JAMA Cardiology

The 2016 revision to the World Health Organization classification of myeloid neoplasms and acute leukemia

(2016) D. A. Arber et al.   BLOOD

Recommendations for reporting of secondary findings in clinical exome and genome sequencing, 2016 update (ACMG SF v2.0): a policy statement of the American College of Medical Genetics and Genomics

(2016) Sarah S. Kalia et al.   GENETICS IN MEDICINE

Using Genetic Technologies To Reduce, Rather Than Widen, Health Disparities

(2016) Caren E. Smith et al.   HEALTH AFFAIRS

The prevalence and distribution of the amyloidogenic transthyretin (TTR) V122I allele in Africa

(2016) Daniel R. Jacobson et al.   Molecular Genetics & Genomic Medicine

Identification of nuclear retention domains in the RBM20 protein

(2013) Agnese Filippello et al.   FEBS LETTERS

ACMG recommendations for reporting of incidental findings in clinical exome and genome sequencing

(2013) Robert C. Green et al.   GENETICS IN MEDICINE

Mutations in Ribonucleic Acid Binding Protein Gene Cause Familial Dilated Cardiomyopathy

(2009) Katharine M. Brauch et al.   JOURNAL OF THE AMERICAN COLLEGE OF CARDIOLOGY