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Amy C Sturm

Showing results (91-100 of 105) with videos related to

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Nature Reviews. Cardiology|June 15, 2023
International Atherosclerosis Society guidance for implementing best practice in the care of familial hypercholesterolaemiaGerald F Watts, Samuel S Gidding, Robert A Hegele, et al.
BMC Medical Genomics|January 7, 2021
Association between triglycerides, known risk SNVs and conserved rare variation in SLC25A40 in a multi-ancestry cohortElisabeth A Rosenthal, David R Crosslin, Adam S Gordon, et al.
American Journal of Human Genetics|May 11, 2020
Predictive Utility of Polygenic Risk Scores for Coronary Heart Disease in Three Major Racial and Ethnic GroupsOzan Dikilitas, Daniel J Schaid, Matthew L Kosel, et al.
Circulation. Genomic and Precision Medicine|April 18, 2023
Familial Hypercholesterolemia in the Electronic Medical Records and Genomics Network: Prevalence, Penetrance, Cardiovascular Risk, and Outcomes After Return of ResultsOzan Dikilitas, Alborz Sherafati, Seyedmohammad Saadatagah, et al.
American Journal of Human Genetics|August 14, 2018
A Model for Genome-First Care: Returning Secondary Genomic Findings to Participants and Their Healthcare Providers in a Large Research CohortMarci L B Schwartz, Cara Zayac McCormick, Amanda L Lazzeri, et al.
Circulation|January 30, 2015
Dysfunction in the βII spectrin-dependent cytoskeleton underlies human arrhythmiaSakima A Smith, Amy C Sturm, Jerry Curran, et al.
Circulation. Genomic and Precision Medicine|January 22, 2021
Developing and Optimizing Innovative Tools to Address Familial Hypercholesterolemia Underdiagnosis: Identification Methods, Patient Activation, and Cascade Testing for Familial HypercholesterolemiaGemme Campbell-Salome, Laney K Jones, Max F Masnick, et al.
Medrxiv : the Preprint Server for Health Sciences|April 17, 2023
Beyond gene-disease validity: capturing structured data on inheritance, allelic-requirement, disease-relevant variant classes, and disease mechanism for inherited cardiac conditionsKatherine S Josephs, Angharad M Roberts, Pantazis Theotokis, et al.
Genome Medicine|October 23, 2023
Beyond gene-disease validity: capturing structured data on inheritance, allelic requirement, disease-relevant variant classes, and disease mechanism for inherited cardiac conditionsKatherine S Josephs, Angharad M Roberts, Pantazis Theotokis, et al.
Medrxiv : the Preprint Server for Health Sciences|November 19, 2025
Cardiovascular genetic counseling is associated with improved patient-reported outcomes across clinical indications and settingsBrittney Murray, Catherine Gordon, Susan Christian, et al.
Pageof 11

Showing results (91-100 of 105) with videos related to

Sort By:
Pageof 11
Nature Reviews. Cardiology|June 15, 2023
International Atherosclerosis Society guidance for implementing best practice in the care of familial hypercholesterolaemiaGerald F Watts, Samuel S Gidding, Robert A Hegele, et al.
BMC Medical Genomics|January 7, 2021
Association between triglycerides, known risk SNVs and conserved rare variation in SLC25A40 in a multi-ancestry cohortElisabeth A Rosenthal, David R Crosslin, Adam S Gordon, et al.
American Journal of Human Genetics|May 11, 2020
Predictive Utility of Polygenic Risk Scores for Coronary Heart Disease in Three Major Racial and Ethnic GroupsOzan Dikilitas, Daniel J Schaid, Matthew L Kosel, et al.
Circulation. Genomic and Precision Medicine|April 18, 2023
Familial Hypercholesterolemia in the Electronic Medical Records and Genomics Network: Prevalence, Penetrance, Cardiovascular Risk, and Outcomes After Return of ResultsOzan Dikilitas, Alborz Sherafati, Seyedmohammad Saadatagah, et al.
American Journal of Human Genetics|August 14, 2018
A Model for Genome-First Care: Returning Secondary Genomic Findings to Participants and Their Healthcare Providers in a Large Research CohortMarci L B Schwartz, Cara Zayac McCormick, Amanda L Lazzeri, et al.
Circulation|January 30, 2015
Dysfunction in the βII spectrin-dependent cytoskeleton underlies human arrhythmiaSakima A Smith, Amy C Sturm, Jerry Curran, et al.
Circulation. Genomic and Precision Medicine|January 22, 2021
Developing and Optimizing Innovative Tools to Address Familial Hypercholesterolemia Underdiagnosis: Identification Methods, Patient Activation, and Cascade Testing for Familial HypercholesterolemiaGemme Campbell-Salome, Laney K Jones, Max F Masnick, et al.
Medrxiv : the Preprint Server for Health Sciences|April 17, 2023
Beyond gene-disease validity: capturing structured data on inheritance, allelic-requirement, disease-relevant variant classes, and disease mechanism for inherited cardiac conditionsKatherine S Josephs, Angharad M Roberts, Pantazis Theotokis, et al.
Genome Medicine|October 23, 2023
Beyond gene-disease validity: capturing structured data on inheritance, allelic requirement, disease-relevant variant classes, and disease mechanism for inherited cardiac conditionsKatherine S Josephs, Angharad M Roberts, Pantazis Theotokis, et al.
Medrxiv : the Preprint Server for Health Sciences|November 19, 2025
Cardiovascular genetic counseling is associated with improved patient-reported outcomes across clinical indications and settingsBrittney Murray, Catherine Gordon, Susan Christian, et al.
Pageof 11