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Genetic testing for neurodegenerative diseases: Ethical and health communication challenges

Neurobiology of disease, 2020-07, Vol.141, p.104871-104871, Article 104871

2020

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Genetic susceptibility testing for neurodegenerative diseases: ethical and practice issues

Progress in neurobiology, 2013-11, Vol.110, p.89-101

2013

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Genetic counseling, virtual visits, and equity in the era of COVID‐19 and beyond

Journal of genetic counseling, 2021-08, Vol.30 (4), p.1038-1045

2021

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40 years and beyond for the National Society of Genetic Counselors: Reflections on genetic counseling practice

Journal of genetic counseling, 2020-12, Vol.29 (6), p.888-893

2020

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The persistent lack of knowledge and misunderstanding of the Genetic Information Nondiscrimination Act (GINA) more than a decade after passage

Genetics in medicine, 2021-12, Vol.23 (12), p.2324-2334

2021

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Family members' perspectives on learning cognitively unimpaired older adults' amyloid-β PET scan results

Journal of the American Geriatrics Society (JAGS), 2021-11, Vol.69 (11), p.3203-3211

2021

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Defining critical educational components of informed consent for genetic testing: views of US-based genetic counselors and medical geneticists

European journal of human genetics : EJHG, 2023-10, Vol.31 (10), p.1165-1174

2023

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Genetic Testing of HTT Modifiers for Huntington's Disease: Considerations for Clinical Guidelines

Movement disorders, 2023-12, Vol.38 (12), p.2151-2154

2023

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Direct-to-Consumer Genetic Testing: User Motivations, Decision Making, and Perceived Utility of Results

Public health genomics, 2017-01, Vol.20 (1), p.36-45

2017

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Recommendations for returning genomic incidental findings? We need to talk

Genetics in medicine, 2013-11, Vol.15 (11), p.854-859

2013

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Incorporating Genetic Testing Into the Care of Patients With Amyotrophic Lateral Sclerosis/Frontotemporal Degeneration Spectrum Disorders

Neurology. Clinical practice, 2023-10, Vol.13 (5), p.e200201

2023

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Assessment of the Needs of Nephrology Divisions to Implement Return of Clinically Significant Research Genetic Results: A Survey of Nephrotic Syndrome Study Network (NEPTUNE) Investigators

Glomerular diseases, 2023-08, Vol.3 (1), p.178-188

2023

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Response to "assessment of risk of ALS conferred by the GGGGCC hexanucleotide expansion in C9orf72 among first-degree relatives of patients with ALS carrying the repeat expansion"

Amyotrophic lateral sclerosis and frontotemporal degeneration, 2024-10, Vol.25 (7-8), p.1-799

2024

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Ehlers-Danlos syndrome, hypermobility type: A characterization of the patients' lived experience

American journal of medical genetics. Part A, 2013-12, Vol.161A (12), p.2981-2988

2013

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Disclosure of clinically actionable genetic variants to thoracic aortic dissection biobank participants

BMC medical genomics, 2021-03, Vol.14 (1), p.66-12, Article 66

2021

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

Journal of genetic counseling, 2021-02, Vol.30 (1), p.329-334

2021

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Utilization of Genetic Counseling after Direct-to-Consumer Genetic Testing: Findings from the Impact of Personal Genomics (PGen) Study

Journal of genetic counseling, 2017-12, Vol.26 (6), p.1270-1279

2017

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Development of a Streamlined Work Flow for Handling Patients’ Genetic Testing Insurance Authorizations

Journal of genetic counseling, 2017-08, Vol.26 (4), p.657-668

2017

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Primary Care Providers' Initial Evaluation of Children with Global Developmental Delay: A Clinical Vignette Study

The Journal of pediatrics, 2015-12, Vol.167 (6), p.1404-1408.e1

2015

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The Michigan Genetic Hereditary Testing (MiGHT) study's innovative approaches to promote uptake of clinical genetic testing among cancer patients: a study protocol for a 3-arm randomized controlled trial

Trials, 2023-02, Vol.24 (1), p.105-105, Article 105

2023

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Correction: The persistent lack of knowledge and misunderstanding of the Genetic Information Nondiscrimination Act (GINA) more than a decade after passage

Genetics in medicine, 2021-12, Vol.23 (12), p.2471-2471

2021

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Application of a framework to guide genetic testing communication across clinical indications

Genome medicine, 2021-04, Vol.13 (1), p.71-71, Article 71

2021

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A survey of aortic disease biorepository participants’ preferences for return of research genetic results

Journal of genetic counseling, 2021-06, Vol.30 (3), p.645-655

2021

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Health care utilization and behavior changes after workplace genetic testing at a large US health care system

Genetics in medicine, 2024-08, Vol.26 (8), p.101160, Article 101160

2024

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The goldilocks conundrum: Disclosing discrimination risks in informed consent

Journal of genetic counseling, 2022-12, Vol.31 (6), p.1383-1393

2022

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Genetic testing for neurodegenerative diseases: Ethical and health communication challenges

Genetic susceptibility testing for neurodegenerative diseases: ethical and practice issues

Genetic counseling, virtual visits, and equity in the era of COVID‐19 and beyond

40 years and beyond for the National Society of Genetic Counselors: Reflections on genetic counseling practice

The persistent lack of knowledge and misunderstanding of the Genetic Information Nondiscrimination Act (GINA) more than a decade after passage

Family members' perspectives on learning cognitively unimpaired older adults' amyloid-β PET scan results

Defining critical educational components of informed consent for genetic testing: views of US-based genetic counselors and medical geneticists

Genetic Testing of HTT Modifiers for Huntington's Disease: Considerations for Clinical Guidelines

Direct-to-Consumer Genetic Testing: User Motivations, Decision Making, and Perceived Utility of Results

Recommendations for returning genomic incidental findings? We need to talk

Incorporating Genetic Testing Into the Care of Patients With Amyotrophic Lateral Sclerosis/Frontotemporal Degeneration Spectrum Disorders

Assessment of the Needs of Nephrology Divisions to Implement Return of Clinically Significant Research Genetic Results: A Survey of Nephrotic Syndrome Study Network (NEPTUNE) Investigators

Response to "assessment of risk of ALS conferred by the GGGGCC hexanucleotide expansion in C9orf72 among first-degree relatives of patients with ALS carrying the repeat expansion"

Ehlers-Danlos syndrome, hypermobility type: A characterization of the patients' lived experience

Disclosure of clinically actionable genetic variants to thoracic aortic dissection biobank participants

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

Utilization of Genetic Counseling after Direct-to-Consumer Genetic Testing: Findings from the Impact of Personal Genomics (PGen) Study

Development of a Streamlined Work Flow for Handling Patients’ Genetic Testing Insurance Authorizations

Primary Care Providers' Initial Evaluation of Children with Global Developmental Delay: A Clinical Vignette Study

The Michigan Genetic Hereditary Testing (MiGHT) study's innovative approaches to promote uptake of clinical genetic testing among cancer patients: a study protocol for a 3-arm randomized controlled trial

Correction: The persistent lack of knowledge and misunderstanding of the Genetic Information Nondiscrimination Act (GINA) more than a decade after passage

Application of a framework to guide genetic testing communication across clinical indications

A survey of aortic disease biorepository participants’ preferences for return of research genetic results

Health care utilization and behavior changes after workplace genetic testing at a large US health care system

The goldilocks conundrum: Disclosing discrimination risks in informed consent

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