Marci L. B. Schwartz

发表

A Model for Genome-First Care: Returning Secondary Genomic Findings to Participants and Their Healthcare Providers in a Large Research Cohort.

Marc S. Williams, D. Ledbetter, M. Murray, 2018, American journal of human genetics.

The impact of the number of tests presented and a provider recommendation on decisions about genetic testing for cancer risk.

W. Klein, D. Roter, Marci L. B. Schwartz, 2020, Patient education and counseling.

Managing Secondary Genomic Findings Associated With Arrhythmogenic Right Ventricular Cardiomyopathy: Case Studies and Proposal for Clinical Surveillance

Brandon K. Fornwalt, H. Calkins, D. Judge, 2018, Circulation. Genomic and precision medicine.

Patient assessment of chatbots for the scalable delivery of genetic counseling

H. Kirchner, A. Sturm, Marci L. B. Schwartz, 2019, Journal of genetic counseling.

Clinical outcomes of a genomic screening program for actionable genetic conditions

Laney K. Jones, Marc S. Williams, D. Ledbetter, 2020, Genetics in Medicine.

Adding Protective Genetic Variants to Clinical Reporting of Genomic Screening Results: Restoring Balance

Marc S. Williams, M. Murray, Marci L. B. Schwartz, 2017, JAMA.

Patient-Centered Precision Health In A Learning Health Care System: Geisinger's Genomic Medicine Experience.

Marc S. Williams, D. Ledbetter, H. Willard, 2018, Health affairs.

1 TITLE : A Model for Genome-First Care : Returning Secondary Genomic Findings to Participants 1 and Their Healthcare Providers in a Large Research Cohort . 2 RUNNING TITLE : A Model for Genome-First Care

Matthew S. Lebo, Marc S. Williams, M. Murray, 2017 .

A Model for Genome-First Care: Returning Secondary Genomic Findings to Participants and Their Healthcare Providers in a Large Research Cohort

Matthew S. Lebo, Marc S. Williams, D. Ledbetter, 2017, bioRxiv.

Genetic counseling for patients with positive genomic screening results: Considerations for when the genetic test comes first

A. Sturm, C. Haggerty, A. Buchanan, 2021, Journal of genetic counseling.

Motivating cascade testing for familial hypercholesterolemia: applying the extended parallel process model for clinician communication

Ilene G. Ladd, Carla L. Fisher, A. Sturm, 2022, Translational behavioral medicine.

Electronic Health Record Phenotype in Subjects with Genetic Variants Associated with Arrhythmogenic Right Ventricular Cardiomyopathy: A Study in 30,716 Subjects with Exome Sequencing: Genotype-Phenotype Association in Incidental ARVC Genetic Findings

Matthew S. Lebo, Alexander E. Lopez, Christopher D. Nevius, 2017 .

Clinical Findings and Diagnostic Yield of Arrhythmogenic Cardiomyopathy Through Genomic Screening of Pathogenic or Likely Pathogenic Desmosome Gene Variants

Brandon K. Fornwalt, Christopher D. Nevius, Eric D. Carruth, 2021, Circulation. Genomic and precision medicine.

Exome Sequencing–Based Screening for BRCA1/2 Expected Pathogenic Variants Among Adult Biobank Participants

Matthew S. Lebo, Daniel R. Lavage, Dustin N. Hartzel, 2018, JAMA network open.

Elective genomic testing: Practice resource of the National Society of Genetic Counselors

Matthew S. Lebo, E. Orlova, D. Bick, 2023, Journal of genetic counseling.

Early cancer diagnoses through BRCA1/2 screening of unselected adult biobank participants

Matthew S. Lebo, Audrey L. Fan, Marc S. Williams, 2017, Genetics in Medicine.

Electronic Health Record Phenotype in Subjects with Genetic Variants Associated with Arrhythmogenic Right Ventricular Cardiomyopathy: A Study in 30,716 Subjects with Exome Sequencing

Matthew S. Lebo, Alexander E. Lopez, Brandon K. Fornwalt, 2017, Genetics in Medicine.

A Model for the Integration of Genome Sequencing into a Paediatric Cardiology Clinic.

R. Jobling, Eriskay Liston, R. Hayeems, 2022, The Canadian journal of cardiology.

Adopted individuals’ interest in elective genomic testing

Marci L. B. Schwartz, S. Spencer, T. Maga, 2020, Journal of medical genetics.

Positive impact of genetic counseling assistants on genetic counseling efficiency, patient volume, and cost in a cancer genetics clinic

Marc S. Williams, M. Hallquist, H. Kirchner, 2020, Genetics in Medicine.

Exome Sequencing–Based Screening for BRCA1/2 Expected Pathogenic Variants Among Adult Biobank Participants

Matthew S. Lebo, Daniel R. Lavage, Dustin N. Hartzel, 2018, JAMA network open.

Patient-Centered Precision Health In A Learning Health Care System: Geisinger's Genomic Medicine Experience.

F. D. Davis, W. Faucett, A. Rahm, 2018, Health affairs.

Testing and Management of Iron Overload After Genetic Screening–Identified Hemochromatosis

A. Buchanan, J. Savatt, Marci L. B. Schwartz, 2023, JAMA network open.

Optimizing communication strategies and designing a comprehensive program to facilitate cascade testing for familial hypercholesterolemia

A. Sturm, A. Rahm, Emilie Simmons, 2023, BMC Health Services Research.

Using whole genome sequence findings to assess gene-disease causality in cardiomyopathy and arrhythmia patients.

Marci L. B. Schwartz, C. Somerville, Raymond H Kim, 2023, Future cardiology.

Genetics Visit Uptake Among Individuals Receiving Clinically Actionable Genomic Screening Results

A. Buchanan, Marci L. B. Schwartz, C. McCormick, 2024, JAMA network open.

Proceedings from the 9th annual conference on the science of dissemination and implementation

Caitlin N. Dorsey, Robert D. Lieberthal, Julie E. Reed, 2017, Implementation Science.