Nangel M Lindberg - JoVE Visualize

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The Permanente Journal|August 7, 2022

Engaging Patient Advisory Committees to Inform a Genomic Cancer Risk Study: Lessons for Future EffortsNangel M Lindberg, Kathleen F Mittendorf, Devan M Duenas, et al.

Journal of Genetic Counseling|March 20, 2023

Medical interpreter-mediated genetic counseling for Spanish preferring adults at risk for a hereditary cancer syndromeGalen Joseph, Nangel M Lindberg, Claudia Guerra, et al.

Journal of Racial and Ethnic Health Disparities|June 5, 2020

Dietary Patterns with Healthy and Unhealthy Traits Among Overweight/Obese Hispanic Women with or at High Risk for Type 2 DiabetesMayra Arias-Gastélum, Nangel M Lindberg, Michael C Leo, et al.

BMC Proceedings|November 18, 2017

Personalized medicine and Hispanic health: improving health outcomes and reducing health disparities - a National Heart, Lung, and Blood Institute workshop reportM Larissa Avilés-Santa, John Heintzman, Nangel M Lindberg, et al.

Genetics in Medicine : Official Journal of the American College of Medical Genetics|February 25, 2020

Integrating stakeholder feedback in translational genomics research: an ethnographic analysis of a study protocol's evolutionStephanie A Kraft, Carmit McMullen, Nangel M Lindberg, et al.

Genetics in Medicine Open|December 13, 2024

Feasibility of an electronic patient-facing cancer family history tool in medically underserved populationsHeather Spencer Feigelson, Kathleen F Mittendorf, Sonia Okuyama, et al.

Hereditary Cancer in Clinical Practice|June 10, 2022

Literacy-adapted, electronic family history assessment for genetics referral in primary care: patient user insights from qualitative interviewsKathleen F Mittendorf, Hannah S Lewis, Devan M Duenas, et al.

Genetics in Medicine : Official Journal of the American College of Medical Genetics|March 1, 2022

Integration of stakeholder engagement from development to dissemination in genomic medicine research: Approaches and outcomes from the CSER ConsortiumJulianne M O'Daniel, Sara Ackerman, Lauren R Desrosiers, et al.

Familial Cancer|March 23, 2021

Adaptation and early implementation of the PREdiction model for gene mutations (PREMM<sub>5</sub>™) for lynch syndrome risk assessment in a diverse populationKathleen F Mittendorf, Chinedu Ukaegbu, Marian J Gilmore, et al.

Psychiatric Services (Washington, D.C.)|April 16, 2016

Racial-Ethnic Differences in Psychiatric Diagnoses and Treatment Across 11 Health Care Systems in the Mental Health Research NetworkKaren J Coleman, Christine Stewart, Beth E Waitzfelder, et al.

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Showing results (21-30 of 33) with videos related to

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The Permanente Journal|August 7, 2022

Engaging Patient Advisory Committees to Inform a Genomic Cancer Risk Study: Lessons for Future EffortsNangel M Lindberg, Kathleen F Mittendorf, Devan M Duenas, et al.

Journal of Genetic Counseling|March 20, 2023

Medical interpreter-mediated genetic counseling for Spanish preferring adults at risk for a hereditary cancer syndromeGalen Joseph, Nangel M Lindberg, Claudia Guerra, et al.

Journal of Racial and Ethnic Health Disparities|June 5, 2020

Dietary Patterns with Healthy and Unhealthy Traits Among Overweight/Obese Hispanic Women with or at High Risk for Type 2 DiabetesMayra Arias-Gastélum, Nangel M Lindberg, Michael C Leo, et al.

BMC Proceedings|November 18, 2017

Personalized medicine and Hispanic health: improving health outcomes and reducing health disparities - a National Heart, Lung, and Blood Institute workshop reportM Larissa Avilés-Santa, John Heintzman, Nangel M Lindberg, et al.

Genetics in Medicine : Official Journal of the American College of Medical Genetics|February 25, 2020

Integrating stakeholder feedback in translational genomics research: an ethnographic analysis of a study protocol's evolutionStephanie A Kraft, Carmit McMullen, Nangel M Lindberg, et al.

Genetics in Medicine Open|December 13, 2024

Feasibility of an electronic patient-facing cancer family history tool in medically underserved populationsHeather Spencer Feigelson, Kathleen F Mittendorf, Sonia Okuyama, et al.

Hereditary Cancer in Clinical Practice|June 10, 2022

Literacy-adapted, electronic family history assessment for genetics referral in primary care: patient user insights from qualitative interviewsKathleen F Mittendorf, Hannah S Lewis, Devan M Duenas, et al.

Genetics in Medicine : Official Journal of the American College of Medical Genetics|March 1, 2022

Integration of stakeholder engagement from development to dissemination in genomic medicine research: Approaches and outcomes from the CSER ConsortiumJulianne M O'Daniel, Sara Ackerman, Lauren R Desrosiers, et al.

Familial Cancer|March 23, 2021

Adaptation and early implementation of the PREdiction model for gene mutations (PREMM<sub>5</sub>™) for lynch syndrome risk assessment in a diverse populationKathleen F Mittendorf, Chinedu Ukaegbu, Marian J Gilmore, et al.

Psychiatric Services (Washington, D.C.)|April 16, 2016

Racial-Ethnic Differences in Psychiatric Diagnoses and Treatment Across 11 Health Care Systems in the Mental Health Research NetworkKaren J Coleman, Christine Stewart, Beth E Waitzfelder, et al.

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