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Germline Analysis from Tumor-Germline Sequencing Dyads to Identify Clinically Actionable Secondary Findings

Clinical cancer research, 2016-08, Vol.22 (16), p.4087-4094

2016

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Secondary findings: How did we get here, and where are we going?

Journal of genetic counseling, 2019-04, Vol.28 (2), p.326-333

2019

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Group-based medical mistrust in genomic medicine: Associations with patient and provider perceptions of a specialty clinical encounter

Genetics in medicine, 2024-09, p.101279, Article 101279

2024

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

Genetics in medicine, 2013-07, Vol.15 (7), p.565-574

2013

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P399: Increasing equitable access and uptake for hereditary cancer testing in patients with breast cancer

Genetics in Medicine Open, 2023, Vol.1 (1), p.100435, Article 100435

2023

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A semiquantitative metric for evaluating clinical actionability of incidental or secondary findings from genome-scale sequencing

Genetics in medicine, 2016-05, Vol.18 (5), p.467-475

2016

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A standardized, evidence-based protocol to assess clinical actionability of genetic disorders associated with genomic variation

Genetics in medicine, 2016-12, Vol.18 (12), p.1258-1268

2016

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Evaluating the Clinical Validity of Gene-Disease Associations: An Evidence-Based Framework Developed by the Clinical Genome Resource

American journal of human genetics, 2017-06, Vol.100 (6), p.895-906

2017

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Parents’ perceptions of personal utility of exome sequencing results

Genetics in medicine, 2020-04, Vol.22 (4), p.752-757

2020

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Effect of genetic testing for risk of type 2 diabetes mellitus on health behaviors and outcomes: study rationale, development and design

BMC health services research, 2012-01, Vol.12 (1), p.16-16, Article 16

2012

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Professional perspectives about pharmacogenetic testing and managing ancillary findings

Genetic testing and molecular biomarkers, 2012-01, Vol.16 (1), p.21-24

2012

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Parental Guidance Suggested: Engaging Parents as Partners in Research Studies of Genomic Screening for a Pediatric Population

Frontiers in genetics, 2022-03, Vol.13, p.867030-867030

2022

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P530: Point-of-care genetic testing with paired E-consult: An effective alternative service delivery model for patients with breast cancer

Genetics in Medicine Open, 2024, Vol.2, p.101429, Article 101429

2024

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Public perspectives about pharmacogenetic testing and managing ancillary findings

Genetic testing and molecular biomarkers, 2012-03, Vol.16 (3), p.193-197

2012

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Next-generation sequencing for constitutional variants in the clinical laboratory, 2021 revision: a technical standard of the American College of Medical Genetics and Genomics (ACMG)

Genetics in medicine, 2021-08, Vol.23 (8), p.1399-1415

2021

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P563: With great panels comes great responsibility: In pursuit of a well-evidenced age-based genomic screen

Genetics in Medicine Open, 2024, Vol.2, p.101462, Article 101462

2024

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Genomic Sequencing for Newborn Screening: Results of the NC NEXUS Project

American journal of human genetics, 2020-10, Vol.107 (4), p.596-611

2020

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Reflections on ‘common’ genetic medical history questions: Time to examine the what, why, and how

Patient education and counseling, 2024-05, Vol.122, p.108190, Article 108190

2024

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P376: Co-designing genetics and genomics educational modules for community engagement

Genetics in Medicine Open, 2023, Vol.1 (1), p.100412, Article 100412

2023

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The who, what, and why of research participants’ intentions to request a broad range of secondary findings in a diagnostic genomic sequencing study

Genetics in medicine, 2018-07, Vol.20 (7), p.760-769

2018

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Variant interpretation is a component of clinical practice among genetic counselors in multiple specialties

Genetics in medicine, 2020-04, Vol.22 (4), p.785-792

2020

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An Age-Based Framework for Evaluating Genome-Scale Sequencing Results in Newborn Screening

The Journal of pediatrics, 2019-06, Vol.209, p.68-76

2019

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The designated record set for clinical genetic and genomic testing: A points to consider statement of the American College of Medical Genetics and Genomics (ACMG)

Genetics in medicine, 2023-03, Vol.25 (3), p.100342-100342, Article 100342

2023

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Genomic knowledge in the context of diagnostic exome sequencing: changes over time, persistent subgroup differences, and associations with psychological sequencing outcomes

Genetics in medicine, 2020-01, Vol.22 (1), p.60-68

2020

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Actionability of commercial laboratory sequencing panels for newborn screening and the importance of transparency for parental decision-making

Genome medicine, 2021-03, Vol.13 (1), p.50-50, Article 50

2021

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Germline Analysis from Tumor-Germline Sequencing Dyads to Identify Clinically Actionable Secondary Findings

Secondary findings: How did we get here, and where are we going?

Group-based medical mistrust in genomic medicine: Associations with patient and provider perceptions of a specialty clinical encounter

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

P399: Increasing equitable access and uptake for hereditary cancer testing in patients with breast cancer

A semiquantitative metric for evaluating clinical actionability of incidental or secondary findings from genome-scale sequencing

A standardized, evidence-based protocol to assess clinical actionability of genetic disorders associated with genomic variation

Evaluating the Clinical Validity of Gene-Disease Associations: An Evidence-Based Framework Developed by the Clinical Genome Resource

Parents’ perceptions of personal utility of exome sequencing results

Effect of genetic testing for risk of type 2 diabetes mellitus on health behaviors and outcomes: study rationale, development and design

Professional perspectives about pharmacogenetic testing and managing ancillary findings

Parental Guidance Suggested: Engaging Parents as Partners in Research Studies of Genomic Screening for a Pediatric Population

P530: Point-of-care genetic testing with paired E-consult: An effective alternative service delivery model for patients with breast cancer

Public perspectives about pharmacogenetic testing and managing ancillary findings

Next-generation sequencing for constitutional variants in the clinical laboratory, 2021 revision: a technical standard of the American College of Medical Genetics and Genomics (ACMG)

P563: With great panels comes great responsibility: In pursuit of a well-evidenced age-based genomic screen

Genomic Sequencing for Newborn Screening: Results of the NC NEXUS Project

Reflections on ‘common’ genetic medical history questions: Time to examine the what, why, and how

P376: Co-designing genetics and genomics educational modules for community engagement

The who, what, and why of research participants’ intentions to request a broad range of secondary findings in a diagnostic genomic sequencing study

Variant interpretation is a component of clinical practice among genetic counselors in multiple specialties

An Age-Based Framework for Evaluating Genome-Scale Sequencing Results in Newborn Screening

The designated record set for clinical genetic and genomic testing: A points to consider statement of the American College of Medical Genetics and Genomics (ACMG)

Genomic knowledge in the context of diagnostic exome sequencing: changes over time, persistent subgroup differences, and associations with psychological sequencing outcomes

Actionability of commercial laboratory sequencing panels for newborn screening and the importance of transparency for parental decision-making

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