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Utility of a virtual counselor (VICKY) to collect family health histories among vulnerable patient populations: A randomized controlled trial

Patient education and counseling, 2021-05, Vol.104 (5), p.979-988

2021

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Barriers, interventions, and recommendations: Improving the genetic testing landscape

Frontiers in digital health, 2022-11, Vol.4, p.961128-961128

2022

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Reducing the Influence of Anecdotal Reasoning on People’s Health Care Decisions: Is a Picture Worth a Thousand Statistics?

Medical decision making, 2005-07, Vol.25 (4), p.398-405

2005

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P412: Ensuring equity in the delivery of cancer genetic services: Identifying disparities along the care delivery continuum

Genetics in Medicine Open, 2023, Vol.1 (1), p.100448, Article 100448

2023

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Delivering Genetic Testing for Patients with Prostate Cancer: Moving Beyond Provider Knowledge as a Barrier to Care

Cancer control, 2023-03, Vol.30, p.10732748221143884-10732748221143884

2023

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Personal Genomic Testing for Cancer Risk: Results From the Impact of Personal Genomics Study

Journal of clinical oncology, 2017-02, Vol.35 (6), p.636-644

2017

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P388: Use of genetic services among patients with prostate cancer at a safety-net hospital: A mixed methods study

Genetics in Medicine Open, 2023, Vol.1 (1), p.100424, Article 100424

2023

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Causal beliefs about obesity and associated health behaviors: results from a population-based survey

The international journal of behavioral nutrition and physical activity, 2010-03, Vol.7 (1), p.19-19

2010

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P413: Engaging primary care patients in population-based risk assessment for hereditary cancer genetic testing: Preliminary outcomes of point-of-care engagement efforts

Genetics in Medicine Open, 2023, Vol.1 (1), p.100449, Article 100449

2023

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Diet and exercise changes following direct-to-consumer personal genomic testing

BMC medical genomics, 2017-05, Vol.10 (1), p.24-24, Article 24

2017

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Effect of Preventive Messages Tailored to Family History on Health Behaviors: The Family Healthware Impact Trial

Annals of family medicine, 2011, Vol.9 (1), p.3-11

2011

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Comparison of risk perceptions and beliefs across common chronic diseases

Preventive medicine, 2009-02, Vol.48 (2), p.197-202

2009

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Socioeconomic Status and Interest in Genetic Testing in a US-Based Sample

Healthcare (Basel), 2022-05, Vol.10 (5), p.880

2022

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Awareness, Interest, and Preferences of Primary Care Providers in Using Point-of-Care Cancer Screening Technology

PloS one, 2016-01, Vol.11 (1), p.e0145215-e0145215

2016

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Family history and perceptions about risk and prevention for chronic diseases in primary care: A report from the Family Healthware™ Impact Trial

Genetics in medicine, 2010-04, Vol.12 (4), p.212-218

2010

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Insurance and geographic variations in non‐invasive prenatal testing

Prenatal diagnosis, 2022-07, Vol.42 (8), p.1004-1007

2022

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Racial Disparities in Accessing Care along the Continuum of Cancer Genetic Service Delivery

Cancer epidemiology, biomarkers & prevention, 2024-01, Vol.33 (1), p.55-62

2024

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Counseling in a different language: An analysis of experiences and resources in multilingual genetic counseling

Journal of genetic counseling, 2024-04

2024

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Celebrity disclosures and information seeking: the case of Angelina Jolie

Genetics in medicine, 2015-07, Vol.17 (7), p.545-553

2015

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Breast cancer polygenic risk scores in the clinical cancer genetic counseling setting: Current practices and impact on patient management

Journal of genetic counseling, 2021-04, Vol.30 (2), p.588-597

2021

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Implementing digital systems to facilitate genetic testing for hereditary cancer syndromes: An observational study of 4 clinical workflows

Genetics in medicine, 2023-05, Vol.25 (5), p.100802-100802, Article 100802

2023

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Family History Assessment

American journal of preventive medicine, 2012-10, Vol.43 (4), p.392-398

2012

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Population screening to identify women at risk for hereditary breast cancer syndromes: The path forward or the road not taken?

Cancer, 2022-01, Vol.128 (1), p.30-33

2022

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Abstract PO-050: Characterizing access to genetics referrals for prostate cancer in a safety net hospital

Cancer epidemiology, biomarkers & prevention, 2022-01, Vol.31 (1_Supplement), p.PO-050-PO-050

2022

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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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Utility of a virtual counselor (VICKY) to collect family health histories among vulnerable patient populations: A randomized controlled trial

Barriers, interventions, and recommendations: Improving the genetic testing landscape

Reducing the Influence of Anecdotal Reasoning on People’s Health Care Decisions: Is a Picture Worth a Thousand Statistics?

P412: Ensuring equity in the delivery of cancer genetic services: Identifying disparities along the care delivery continuum

Delivering Genetic Testing for Patients with Prostate Cancer: Moving Beyond Provider Knowledge as a Barrier to Care

Personal Genomic Testing for Cancer Risk: Results From the Impact of Personal Genomics Study

P388: Use of genetic services among patients with prostate cancer at a safety-net hospital: A mixed methods study

Causal beliefs about obesity and associated health behaviors: results from a population-based survey

P413: Engaging primary care patients in population-based risk assessment for hereditary cancer genetic testing: Preliminary outcomes of point-of-care engagement efforts

Diet and exercise changes following direct-to-consumer personal genomic testing

Effect of Preventive Messages Tailored to Family History on Health Behaviors: The Family Healthware Impact Trial

Comparison of risk perceptions and beliefs across common chronic diseases

Socioeconomic Status and Interest in Genetic Testing in a US-Based Sample

Awareness, Interest, and Preferences of Primary Care Providers in Using Point-of-Care Cancer Screening Technology

Family history and perceptions about risk and prevention for chronic diseases in primary care: A report from the Family Healthware™ Impact Trial

Insurance and geographic variations in non‐invasive prenatal testing

Racial Disparities in Accessing Care along the Continuum of Cancer Genetic Service Delivery

Counseling in a different language: An analysis of experiences and resources in multilingual genetic counseling

Celebrity disclosures and information seeking: the case of Angelina Jolie

Breast cancer polygenic risk scores in the clinical cancer genetic counseling setting: Current practices and impact on patient management

Implementing digital systems to facilitate genetic testing for hereditary cancer syndromes: An observational study of 4 clinical workflows

Family History Assessment

Population screening to identify women at risk for hereditary breast cancer syndromes: The path forward or the road not taken?

Abstract PO-050: Characterizing access to genetics referrals for prostate cancer in a safety net hospital

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

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