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| 36765432 | 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 |
| 37308598 | Defining critical educational components of informed consent for genetic testing: views of US-based genetic counselors and medical geneticists. | Eur J Hum Genet | 2023 |
| 35058451 | Voluntary workplace genomic testing: wellness benefit or Pandora's box? | NPJ Genom Med | 2022 |
| 35570496 | Searching for Answers: Information-Seeking by Young People At-Risk for Huntington's Disease. | J Huntingtons Dis | 2022 |
| 36446806 | Tools for communicating risk for Parkinson's disease. | NPJ Parkinsons Dis | 2022 |
| 35930740 | The goldilocks conundrum: Disclosing discrimination risks in informed consent. | J Genet Couns | 2022 |
| 32648332 | Genetic counseling following direct-to consumer genetic testing: Consumer perspectives. | J Genet Couns | 2021 |
| 35663290 | Genetic testing and insurance implications: Surveying the US general population about discrimination concerns and knowledge of the Genetic Information Nondiscrimination Act (GINA). | Risk Manag Insur Rev | 2021 |
| 33648514 | Disclosure of clinically actionable genetic variants to thoracic aortic dissection biobank participants. | BMC Med Genomics | 2021 |
| 33926532 | Application of a framework to guide genetic testing communication across clinical indications. | Genome Med | 2021 |
| 34945775 | Defining the Critical Components of Informed Consent for Genetic Testing. | J Pers Med | 2021 |
| 34400812 | The persistent lack of knowledge and misunderstanding of the Genetic Information Nondiscrimination Act (GINA) more than a decade after passage. | Genet Med | 2021 |
| 34446926 | Correction: The persistent lack of knowledge and misunderstanding of the Genetic Information Nondiscrimination Act (GINA) more than a decade after passage. | Genet Med | 2021 |
| 34252201 | Family members' perspectives on learning cognitively unimpaired older adults' amyloid-β PET scan results. | J Am Geriatr Soc | 2021 |
| 34291525 | Genetic counseling, virtual visits, and equity in the era of COVID-19 and beyond. | J Genet Couns | 2021 |
| 33319384 | A survey of aortic disease biorepository participants' preferences for return of research genetic results. | J Genet Couns | 2021 |
| 32302673 | Genetic testing for neurodegenerative diseases: Ethical and health communication challenges. | Neurobiol Dis | 2020 |
| 33072517 | The diagnosis of inborn errors of metabolism in previously undiagnosed adults referred for medical genetics evaluation. | Mol Genet Metab Rep | 2020 |
| 32643233 | 40 years and beyond for the National Society of Genetic Counselors: Reflections on genetic counseling practice. | J Genet Couns | 2020 |
| 32211507 | Disclosing genetic risk for Alzheimer's dementia to individuals with mild cognitive impairment. | Alzheimers Dement (N Y) | 2020 |
| 30964581 | Interpretations of the Term "Actionable" when Discussing Genetic Test Results: What you Mean Is Not What I Heard. | J Genet Couns | 2019 |
| 29976988 | Developing a conceptual, reproducible, rubric-based approach to consent and result disclosure for genetic testing by clinicians with minimal genetics background. | Genet Med | 2019 |
| 28726810 | A randomized controlled trial of disclosing genetic risk information for Alzheimer disease via telephone. | Genet Med | 2018 |
| 29034736 | Family History Collection Practices: National Survey of Pediatric Primary Care Providers. | Clin Pediatr (Phila) | 2018 |
| 29325614 | Ethical issues in neurogenetics. | Handb Clin Neurol | 2018 |
| 27307100 | Effect of Public Deliberation on Attitudes toward Return of Secondary Results in Genomic Sequencing. | J Genet Couns | 2017 |
| 28439751 | Development of a Streamlined Work Flow for Handling Patients' Genetic Testing Insurance Authorizations. | J Genet Couns | 2017 |
| 28357777 | Public's Views toward Return of Secondary Results in Genomic Sequencing: It's (Almost) All about the Choice. | J Genet Couns | 2017 |
| 28512697 | Utilization of Genetic Counseling after Direct-to-Consumer Genetic Testing: Findings from the Impact of Personal Genomics (PGen) Study. | J Genet Couns | 2017 |
| 28612151 | The Genetics Journey: A Case Report of a Genetic Diagnosis Made 30 Years Later. | J Genet Couns | 2017 |
| 27739187 | A Marfan syndrome-like phenotype caused by a neocentromeric supernumerary ring chromosome 15. | Am J Med Genet A | 2017 |
| 28068660 | Direct-to-Consumer Genetic Testing: User Motivations, Decision Making, and Perceived Utility of Results. | Public Health Genomics | 2017 |
| 25995036 | Getting personal: Head and neck cancer management in the era of genomic medicine. | Head Neck | 2016 |
| 27333894 | 2013 Review and Update of the Genetic Counseling Practice Based Competencies by a Task Force of the Accreditation Council for Genetic Counseling. | J Genet Couns | 2016 |
| 27363385 | Prenatal Testing for Adult-Onset Conditions: the Position of the National Society of Genetic Counselors. | J Genet Couns | 2016 |
| 26810768 | Disclosing Pleiotropic Effects During Genetic Risk Assessment for Alzheimer Disease: A Randomized Trial. | Ann Intern Med | 2016 |
| 25736541 | Biallelic mutations in huntington disease: A new case with just one affected parent, review of the literature and terminology. | Am J Med Genet A | 2015 |
| 26477869 | Primary Care Providers' Initial Evaluation of Children with Global Developmental Delay: A Clinical Vignette Study. | J Pediatr | 2015 |
| 26087778 | How Well Do Customers of Direct-to-Consumer Personal Genomic Testing Services Comprehend Genetic Test Results? Findings from the Impact of Personal Genomics Study. | Public Health Genomics | 2015 |
| 25957366 | Prompting Primary Care Providers about Increased Patient Risk As a Result of Family History: Does It Work? | J Am Board Fam Med | 2015 |
| 24763861 | Amyotrophic lateral sclerosis in a patient with a family history of huntington disease: genetic counseling challenges. | J Genet Couns | 2014 |
| 23583530 | Genetic susceptibility testing for neurodegenerative diseases: ethical and practice issues. | Prog Neurobiol | 2013 |
| 24254846 | Ehlers-Danlos syndrome, hypermobility type: A characterization of the patients' lived experience. | Am J Med Genet A | 2013 |
| 23907645 | Recommendations for returning genomic incidental findings? We need to talk! | Genet Med | 2013 |
| 23435755 | Genetic counseling services and training of genetic counselors in Israel: an overview. | J Genet Couns | 2013 |
| 22271376 | National Society of Genetic Counselors Natalie Weissburger Paul lifetime achievement award address: the power of connecting. | J Genet Couns | 2012 |
| 22498844 | Effectiveness of a condensed protocol for disclosing APOE genotype and providing risk education for Alzheimer disease. | Genet Med | 2012 |
| 22566244 | Report from the National Society of Genetic Counselors service delivery model task force: a proposal to define models, components, and modes of referral. | J Genet Couns | 2012 |
| 22246561 | Genetic testing integration panels (GTIPs): a novel approach for considering integration of direct-to-consumer and other new genetic tests into patient care. | J Genet Couns | 2012 |
| 21233722 | Direct-to-consumer genetic testing: an assessment of genetic counselors' knowledge and beliefs. | Genet Med | 2011 |