A. Buchanan

发表

Randomized Trial of Telegenetics vs. In-Person Cancer Genetic Counseling: Cost, Patient Satisfaction and Attendance

Martha B. Adams, Henry F. Beresford, S. Datta, 2015, Journal of Genetic Counseling.

Developing patient-friendly genetic and genomic test reports: formats to promote patient engagement and understanding

I. Lipkus, M. Datto, C. Rehder, 2014, Genome Medicine.

The reckoning: The return of genomic results to 1444 participants across the eMERGE3 Network.

Marc S. Williams, W. Chung, H. Hakonarson, 2022, Genetics in medicine : official journal of the American College of Medical Genetics.

Evaluating the clinical validity of gene-disease associations: an evidence-based framework developed by the Clinical Genome Resource

J. Michael Cherry, Heidi L. Rehm, Erin Rooney Riggs, 2017, bioRxiv.

Evaluating the clinical validity of gene-disease associations: an evidence-based framework developed by the Clinical Genome Resource

J. Michael Cherry, Avni Santani, Heidi L. Rehm, 2017, bioRxiv.

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.

Quality of family history collection with use of a patient facing family history assessment tool

Geoffrey S Ginsburg, Lori A Orlando, Elizabeth R Hauser, 2014, BMC Family Practice.

A framework for integrated clinical risk assessment using population sequencing data

C. Cassa, D. Carey, R. Metpally, 2021, medRxiv.

Providing patient education: impact on quantity and quality of family health history collection

G. Ginsburg, E. Hauser, V. Henrich, 2014, Familial Cancer.

Effect of Sociodemographic Factors on Uptake of a Patient-Facing Information Technology Family Health History Risk Assessment Platform

Melissa L. Harry, G. Ginsburg, C. Voils, 2019, Applied Clinical Informatics.

Implementing family health history risk stratification in primary care: Impact of guideline criteria on populations and resource demand

Geoffrey S Ginsburg, Lori A Orlando, Elizabeth R Hauser, 2014, American journal of medical genetics. Part C, Seminars in medical genetics.

Implementation, Adoption, and Utility of Family Health History Risk Assessment in Diverse Care Settings: evaluating implementation processes and impact with an implementation framework

Melissa L. Harry, G. Ginsburg, C. Voils, 2018, Genetics in Medicine.

A RE-AIM Framework Analysis of DNA-Based Population Screening: Using Implementation Science to Translate Research Into Practice in a Healthcare System

Laney K. Jones, Marc S. Williams, R. Glasgow, 2022, Frontiers in Genetics.

Design and Reporting Considerations for Genetic Screening Tests.

K. Jacobs, M. Hegde, B. Funke, 2020, The Journal of molecular diagnostics : JMD.

Clinical outcomes of a genomic screening program for actionable genetic conditions

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

Healthcare Utilization and Costs after Receiving a Positive BRCA1/2 Result from a Genomic Screening Program

Dustin N. Hartzel, Marc S. Williams, M. Murray, 2020, Journal of personalized medicine.

Observational study of population genomic screening for variants associated with endocrine tumor syndromes in a large, healthcare-based cohort

A. Sturm, A. Buchanan, M. Kelly, 2022, BMC Medicine.

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.

Understanding the Return of Genomic Sequencing Results Process: Content Review of Participant Summary Letters in the eMERGE Research Network

John A. Lynch, David C. Kochan, Marc S. Williams, 2020, Journal of personalized medicine.

Cancer genetic counseling in rural north carolina oncology clinics: Program establishment and patient characteristics

C. Skinner, P. Marcom, J. Schildkraut, 2009 .

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.

Developing a conceptual, reproducible, rubric-based approach to consent and result disclosure for genetic testing by clinicians with minimal genetics background

Seema M Jamal, K. Ormond, L. Hudgins, 2018, Genetics in Medicine.

Defining the Critical Components of Informed Consent for Genetic Testing

K. Ormond, Maureen E. Smith, W. Faucett, 2021, medRxiv.

Understanding the Patient Experience of Receiving Clinically Actionable Genetic Results from the MyCode Community Health Initiative, a Population-Based Genomic Screening Initiative

Laney K. Jones, Cassandra J. Pisieczko, A. Sturm, 2022, Journal of personalized medicine.

Cost Comparison of Genetic Testing Strategies in Women With Epithelial Ovarian Cancer.

A. Secord, E. Myers, L. Havrilesky, 2017, Journal of oncology practice.

Balancing External Validity and Concern for Psychosocial Harms in Translational Genetic Research.

M. Meyer, A. Rahm, A. Buchanan, 2021, Ethics & human research.

Investigating Psychological Impact after Receiving Genetic Risk Results—A Survey of Participants in a Population Genomic Screening Program

A. Sturm, A. Buchanan, C. McCormick, 2022, Journal of personalized medicine.

Prospective multicenter cohort study of estrogen and insulin-like growth factor system in BRCA mutation carriers

C. Gracia, C. Skrzynia, A. Buchanan, 2015, Cancer Causes & Control.

Cancer Genetic Counseling and Testing in an Era of Rapid Change

R. Nagy, P. Summerour, J. Quillin, 2017, Journal of Genetic Counseling.

Implementation-effectiveness trial of systematic family health history based risk assessment and impact on clinical disease prevention and surveillance activities

Melissa L. Harry, D. Dimmock, R. Myers, 2022, BMC Health Services Research.

Preferences of women with epithelial ovarian cancer for aspects of genetic testing

L. Havrilesky, B. Davidson, S. Reed, 2019, Gynecologic Oncology Research and Practice.

Prevalence of BRCA Mutations Among Women with Triple-Negative Breast Cancer (TNBC) in a Genetic Counseling Cohort

P. Marcom, W. Lorizio, R. Greenup, 2013, Annals of Surgical Oncology.

Feasibility of blood testing combined with PET-CT to screen for cancer and guide intervention

D. Ledbetter, K. Kinzler, C. Bettegowda, 2020, Science.

Underestimation of risk of a BRCA1 or BRCA2 mutation in women with high-grade serous ovarian cancer by BRCAPRO: a multi-institution study.

Christopher I Amos, C. Amos, D. Mutch, 2014, Journal of clinical oncology : official journal of the American Society of Clinical Oncology.

Gene-level analysis of rare variants in 379,066 whole exome sequences identifies an association of GIGYF1 loss of function with type 2 diabetes

Alexander E. Lopez, Dustin N. Hartzel, Andrew L Blumenfeld, 2021, Scientific Reports.

Developing and Optimizing Innovative Tools to Address Familial Hypercholesterolemia Underdiagnosis

Laney K. Jones, Ilene G. Ladd, Nephi A. Walton, 2021, Circulation. Genomic and precision medicine.

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.

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

Sheri D Schully, Katrina A B Goddard, Alan F Scott, 2016, Genetics in Medicine.

Penetrance of Breast Cancer Susceptibility Genes From the eMERGE III Network

Marc S. Williams, W. Chung, Yufeng Shen, 2021, JNCI cancer spectrum.

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.

A practice guideline from the American College of Medical Genetics and Genomics and the National Society of Genetic Counselors: referral indications for cancer predisposition assessment

R. Bennett, G. Wiesner, H. Hampel, 2014, Genetics in Medicine.

Alternate Service Delivery Models in Cancer Genetic Counseling: A Mini-Review

A. Rahm, A. Buchanan, Janet L. Williams, 2016, Front. Oncol..

Design and Reporting Considerations for Genetic Screening Tests.

Matthew S. Lebo, K. Jacobs, M. Hegde, 2019, The Journal of molecular diagnostics : JMD.

Evidence‐based assessments of clinical actionability in the context of secondary findings: Updates from ClinGen's Actionability Working Group

Elizabeth M Webber, Elizabeth M. Webber, Meredith A. Weaver, 2018, Human mutation.

Multi-disciplinary summit on genetics services for women with gynecologic cancers: A Society of Gynecologic Oncology White Paper.

M. Robson, E. Swisher, R. Coleman, 2017, Gynecologic oncology.

Historical review of Lynch syndrome

A. Buchanan, L. Farkas, Andrew I. Wolf, 2013 .

ClinGen's Pediatric Actionability Working Group: Clinical actionability of secondary findings from genome-scale sequencing in children and adolescents.

Elizabeth M Webber, Elizabeth M. Webber, Charisma L. Jenkins, 2022, Genetics in medicine : official journal of the American College of Medical Genetics.

Use of a Patient-Entered Family Health History Tool with Decision Support in Primary Care: Impact of Identification of Increased Risk Patients on Genetic Counseling Attendance

G. Ginsburg, V. Henrich, A. Buchanan, 2015, Journal of Genetic Counseling.

Pediatric reporting of genomic results study (PROGRESS): a mixed-methods, longitudinal, observational cohort study protocol to explore disclosure of actionable adult- and pediatric-onset genomic variants to minors and their parents

Marc S. Williams, Marc S. Williams, M. Meyer, 2020, BMC Pediatrics.

Adherence to Recommended Risk Management among Unaffected Women with a BRCA Mutation

C. Voils, C. Skinner, P. Marcom, 2017, 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.

Parental attitudes and expectations towards receiving genomic test results in healthy children.

Audrey L. Fan, Marc S. Williams, M. Murray, 2018, Translational behavioral medicine.

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

K. Ormond, Julianne M. O’Daniel, Maureen E. Smith, 2021, Genome Medicine.

Evidence synthesis and guideline development in genomic medicine: current status and future prospects

Marc S. Williams, M. Relling, T. Klein, 2014, Genetics in Medicine.

Hereditary hemochromatosis: gene discovery and its implications for population-based screening.

F. Collins, E. Thomson, E. Clayton, 1998, JAMA.

Patient and primary care provider experience using a family health history collection, risk stratification, and clinical decision support tool: a type 2 hybrid controlled implementation-effectiveness trial

G. Ginsburg, E. Hauser, V. Henrich, 2013, BMC Family Practice.

Protocol for implementation of family health history collection and decision support into primary care using a computerized family health history system

Lori A Orlando, Elizabeth R Hauser, G. Ginsburg, 2011, BMC health services research.

Clinical utility of a Web-enabled risk-assessment and clinical decision support program

G. Ginsburg, E. Hauser, R. Myers, 2016, Genetics in Medicine.

Development and validation of a primary care-based family health history and decision support program (MeTree).

Celette Sugg Skinner, Geoffrey S Ginsburg, Lori A Orlando, 2013, North Carolina medical journal.

Penetrance of breast cancer genes from the eMERGE III Network

W. Chung, S. Hebbring, J. Wynn, 2021, medRxiv.

Patients' interest in discussing cancer risk and risk management with primary care physicians.

Linda L. Scott, C. Skinner, V. Champion, 2005, Patient education and counseling.

Randomized trial of DVD, telephone, and usual care for increasing mammography adherence

Lisa G. Smith, C. Skinner, V. Champion, 2016, Journal of health psychology.

Process outcomes from a randomized controlled trial comparing tailored mammography interventions delivered via telephone vs. DVD.

Jeffrey K. Springston, C. Skinner, V. Champion, 2011, Patient education and counseling.

Uncertainty management for individuals with Lynch Syndrome: Identifying and responding to healthcare barriers.

A. Sturm, A. Rahm, A. Buchanan, 2020, Patient education and counseling.

At the intersection of precision medicine and population health: an implementation-effectiveness study of family health history based systematic risk assessment in primary care

Melissa L. Harry, G. Ginsburg, D. Dimmock, 2020, BMC Health Services Research.

Identifying Patients at Increased Disease Risk: Comparing Clinical Judgment and a Clinical Risk Assessment

E. Hauser, A. Buchanan, R. R. Wu, 2014 .

Telemedicine vs in-person cancer genetic counseling: measuring satisfaction and conducting economic analysis

Martha B. Adams, Henry F. Beresford, S. Datta, 2011 .

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

K. Ormond, Maureen E. Smith, W. Faucett, 2023, European Journal of Human Genetics.

Impact of the cancer risk intake system on patient-clinician discussions of tamoxifen, genetic counseling, and colonoscopy

Shelly J. Clark, Linda L. Scott, G. Parmigiani, 2005, Journal of General Internal Medicine.

Establishing the Medical Actionability of Genomic Variants

K. Goddard, Kristy Lee, J. Hunter, 2022, Annual review of genomics and human genetics.

Thyroidectomy Outcomes in Patients Identified With RET Pathogenic Variants Through a Population Genomic Screening Program.

A. Buchanan, J. Savatt, P. Pellitteri, 2023, JAMA otolaryngology-- head & neck surgery.

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.

Adapting tailored intervention message libraries for new populations

Celette Sugg Skinner, Cheryl L. Holt, Matthew W. Kreuter, 2003 .

Developing a Conceptual, Reproducible, Rubric-Based Approach to Consent and Result Disclosure for Genetic Testing by Clinicians with Minimal Genetics Background

K. Ormond, L. Hudgins, M. Cho, 2018, 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.

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.

Randomized trial of DVD, telephone, and usual care for increasing mammography adherence

Lisa G. Smith, C. Skinner, V. Champion, 2016, Journal of health psychology.