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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)

Genetics in medicine, 2021-08, Vol.23 (8), p.1381-1390

2021

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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)

Genetics in medicine, 2022-07, Vol.24 (7), p.1407-1414

2022

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Next-Generation Sequencing Panels for the Diagnosis of Colorectal Cancer and Polyposis Syndromes: A Cost-Effectiveness Analysis

Journal of clinical oncology, 2015-06, Vol.33 (18), p.2084-2091

2015

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Clinical providers' experiences with returning results from genomic sequencing: an interview study

BMC medical genomics, 2018-05, Vol.11 (1), p.45-45, Article 45

2018

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Preconception Carrier Screening by Genome Sequencing: Results from the Clinical Laboratory

American journal of human genetics, 2018-06, Vol.102 (6), p.1078-1089

2018

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Processes and preliminary outputs for identification of actionable genes as incidental findings in genomic sequence data in the Clinical Sequencing Exploratory Research Consortium

Genetics in medicine, 2013-11, Vol.15 (11), p.860-867

2013

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ShareDNA: a smartphone app to facilitate family communication of genetic results

BMC medical genomics, 2021-01, Vol.14 (1), p.10-10, Article 10

2021

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Primary Care Physician Experiences with Integrated Population-Scale Genetic Testing: A Mixed-Methods Assessment

Journal of personalized medicine, 2020-10, Vol.10 (4), p.165

2020

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Family Studies for Classification of Variants of Uncertain Classification: Current Laboratory Clinical Practice and a New Web-Based Educational Tool

Journal of genetic counseling, 2016-12, Vol.25 (6), p.1146-1156

2016

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Scaling Genetic Counseling in the Genomics Era

Annual review of genomics and human genetics, 2021-01, Vol.22 (1), p.339-355

2021

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Lessons learned and recommendations for data coordination in collaborative research: The CSER consortium experience

HGG advances, 2022-07, Vol.3 (3), p.100120-100120, Article 100120

2022

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Reactive gene curation to support interpretation and reporting of a clinical genome test for rare disease: Experience from over 1,000 cases

Cell genomics, 2023-02, Vol.3 (2), p.100258-100258, Article 100258

2023

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Genomic Sequencing Results Disclosure in Diverse and Medically Underserved Populations: Themes, Challenges, and Strategies from the CSER Consortium

Journal of personalized medicine, 2021-03, Vol.11 (3), p.202

2021

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Actionable exomic incidental findings in 6503 participants: challenges of variant classification

Genome research, 2015-03, Vol.25 (3), p.305

2015

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ACMG SF v3.2 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)

Genetics in medicine, 2023-08, Vol.25 (8), p.100866-100866, Article 100866

2023

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The Clinical Sequencing Evidence-Generating Research Consortium: Integrating Genomic Sequencing in Diverse and Medically Underserved Populations

American journal of human genetics, 2018-09, Vol.103 (3), p.319-327

2018

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Actionable, Pathogenic Incidental Findings in 1,000 Participants’ Exomes

American journal of human genetics, 2013-10, Vol.93 (4), p.631-640

2013

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A framework for the evaluation and reporting of incidental findings in clinical genomic testing

European journal of human genetics : EJHG, 2024-04

2024

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Management of individuals with germline pathogenic/likely pathogenic variants in CHEK2: A clinical practice resource of the American College of Medical Genetics and Genomics (ACMG)

Genetics in medicine, 2023-10, Vol.25 (10), p.100870-100870, Article 100870

2023

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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)

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)

Performance of ACMG-AMP Variant-Interpretation Guidelines among Nine Laboratories in the Clinical Sequencing Exploratory Research Consortium

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)

Next-Generation Sequencing Panels for the Diagnosis of Colorectal Cancer and Polyposis Syndromes: A Cost-Effectiveness Analysis

Clinical providers' experiences with returning results from genomic sequencing: an interview study

Preconception Carrier Screening by Genome Sequencing: Results from the Clinical Laboratory

Processes and preliminary outputs for identification of actionable genes as incidental findings in genomic sequence data in the Clinical Sequencing Exploratory Research Consortium

ShareDNA: a smartphone app to facilitate family communication of genetic results

Primary Care Physician Experiences with Integrated Population-Scale Genetic Testing: A Mixed-Methods Assessment

Family Studies for Classification of Variants of Uncertain Classification: Current Laboratory Clinical Practice and a New Web-Based Educational Tool

Scaling Genetic Counseling in the Genomics Era

Lessons learned and recommendations for data coordination in collaborative research: The CSER consortium experience

Reactive gene curation to support interpretation and reporting of a clinical genome test for rare disease: Experience from over 1,000 cases

Genomic Sequencing Results Disclosure in Diverse and Medically Underserved Populations: Themes, Challenges, and Strategies from the CSER Consortium

Actionable exomic incidental findings in 6503 participants: challenges of variant classification

ACMG SF v3.2 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)

The Clinical Sequencing Evidence-Generating Research Consortium: Integrating Genomic Sequencing in Diverse and Medically Underserved Populations

Actionable, Pathogenic Incidental Findings in 1,000 Participants’ Exomes

Performance of ACMG-AMP Variant-Interpretation Guidelines among Nine Laboratories in the Clinical Sequencing Exploratory Research Consortium

Frequency of genomic secondary findings among 21,915 eMERGE network participants

Variant Classification Concordance using the ACMG-AMP Variant Interpretation Guidelines across Nine Genomic Implementation Research Studies

A framework for the evaluation and reporting of incidental findings in clinical genomic testing

ADCY5-related dyskinesia: Broader spectrum and genotype-phenotype correlations

Management of individuals with germline pathogenic/likely pathogenic variants in CHEK2: A clinical practice resource of the American College of Medical Genetics and Genomics (ACMG)

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