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Georgia L Wiesner

Showing results (41-50 of 71) with videos related to

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Frontiers in Genetics|November 19, 2019
Genomic Information for Clinicians in the Electronic Health Record: Lessons Learned From the Clinical Genome Resource Project and the Electronic Medical Records and Genomics NetworkMarc S Williams, Casey Overby Taylor, Nephi A Walton, et al.
HGG Advances|December 7, 2025
Healthcare professionals' experiences returning monogenic, polygenic, and integrated risk results in the eMERGE studySabrina A Suckiel, Laura Golfinopoulos, Courtney L Scherr, et al.
Hereditary Cancer in Clinical Practice|January 1, 2020
Recommended care and care adherence following a diagnosis of Lynch syndrome: a mixed-methods studyKathleen F Mittendorf, Jessica Ezzell Hunter, Jennifer L Schneider, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|August 9, 2022
Pathogenic variants in arteriopathy genes detected in a targeted sequencing study: Penetrance and 1-year outcomes after return of resultsAlborz Sherafati, Omar Elsekaily, Seyedmohammad Saadatagah, et al.
JAMA Network Open|April 29, 2026
Streamlining Inherited Cancer Identification via an EMR-Integrated Risk Assessment Platform: A Nonrandomized Clinical TrialLori A Orlando, Kathleen F Mittendorf, Nathan A Bihlmeyer, et al.
Familial Cancer|February 8, 2019
Implementation of a Systematic Tumor Screening Program for Lynch Syndrome in an Integrated Health Care SettingElizabeth V Clarke, Kristin R Muessig, Jamilyn Zepp, et al.
Proceedings of the National Academy of Sciences of the United States of America|July 21, 2009
Inactivating germ-line and somatic mutations in polypeptide N-acetylgalactosaminyltransferase 12 in human colon cancersKishore Guda, Helen Moinova, Jian He, 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.
JAMA Network Open|August 4, 2021
Generalizability of Polygenic Risk Scores for Breast Cancer Among Women With European, African, and Latinx AncestryCong Liu, Nur Zeinomar, Wendy K Chung, et al.
Journal of Clinical Oncology : Official Journal of the American Society of Clinical Oncology|August 14, 2023
Germline <i>EGFR</i> Mutations and Familial Lung CancerGeoffrey R Oxnard, Ruthia Chen, Jennifer C Pharr, et al.
Pageof 8

Showing results (41-50 of 71) with videos related to

Sort By:
Pageof 8
Frontiers in Genetics|November 19, 2019
Genomic Information for Clinicians in the Electronic Health Record: Lessons Learned From the Clinical Genome Resource Project and the Electronic Medical Records and Genomics NetworkMarc S Williams, Casey Overby Taylor, Nephi A Walton, et al.
HGG Advances|December 7, 2025
Healthcare professionals' experiences returning monogenic, polygenic, and integrated risk results in the eMERGE studySabrina A Suckiel, Laura Golfinopoulos, Courtney L Scherr, et al.
Hereditary Cancer in Clinical Practice|January 1, 2020
Recommended care and care adherence following a diagnosis of Lynch syndrome: a mixed-methods studyKathleen F Mittendorf, Jessica Ezzell Hunter, Jennifer L Schneider, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|August 9, 2022
Pathogenic variants in arteriopathy genes detected in a targeted sequencing study: Penetrance and 1-year outcomes after return of resultsAlborz Sherafati, Omar Elsekaily, Seyedmohammad Saadatagah, et al.
JAMA Network Open|April 29, 2026
Streamlining Inherited Cancer Identification via an EMR-Integrated Risk Assessment Platform: A Nonrandomized Clinical TrialLori A Orlando, Kathleen F Mittendorf, Nathan A Bihlmeyer, et al.
Familial Cancer|February 8, 2019
Implementation of a Systematic Tumor Screening Program for Lynch Syndrome in an Integrated Health Care SettingElizabeth V Clarke, Kristin R Muessig, Jamilyn Zepp, et al.
Proceedings of the National Academy of Sciences of the United States of America|July 21, 2009
Inactivating germ-line and somatic mutations in polypeptide N-acetylgalactosaminyltransferase 12 in human colon cancersKishore Guda, Helen Moinova, Jian He, 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.
JAMA Network Open|August 4, 2021
Generalizability of Polygenic Risk Scores for Breast Cancer Among Women With European, African, and Latinx AncestryCong Liu, Nur Zeinomar, Wendy K Chung, et al.
Journal of Clinical Oncology : Official Journal of the American Society of Clinical Oncology|August 14, 2023
Germline <i>EGFR</i> Mutations and Familial Lung CancerGeoffrey R Oxnard, Ruthia Chen, Jennifer C Pharr, et al.
Pageof 8