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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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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)

Genetics in medicine, 2021-08, Vol.23 (8), p.1391-1398

2021

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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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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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Delayed administration of recombinant human parathyroid hormone improves early biomechanical strength in a rat rotator cuff repair model

Journal of shoulder and elbow surgery, 2016-08, Vol.25 (8), p.1280-1287

2016

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

BMC medical genomics, 2021-01, Vol.14 (1), p.10-8, 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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The role of interventional radiology in venous blood sampling revisited

Journal of vascular and interventional radiology, 2016-03, Vol.27 (3), p.S291-S292

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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Immunoglobulin replacement therapy for yellow nail syndrome

Scandinavian journal of immunology, 2018-03, Vol.87 (3), p.n/a

2018

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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

Volltextzugriff (PDF)

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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Harnack Inequalities and ABP Estimates for Nonlinear Second-Order Elliptic Equations in Unbounded Domains

Abstract and Applied Analysis, 2008-01, Vol.2008 (1)

2008

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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)

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)

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

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)

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

Delayed administration of recombinant human parathyroid hormone improves early biomechanical strength in a rat rotator cuff repair model

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

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

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

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

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

The role of interventional radiology in venous blood sampling revisited

Scaling Genetic Counseling in the Genomics Era

Immunoglobulin replacement therapy for yellow nail syndrome

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

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

Harnack Inequalities and ABP Estimates for Nonlinear Second-Order Elliptic Equations in Unbounded Domains

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

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