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Lisa Bastarache

Showing results (81-90 of 159) with videos related to

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Frontiers in Genetics|May 1, 2023
Genetic predisposition may not improve prediction of cardiac surgery-associated acute kidney injuryNicholas J Douville, Daniel B Larach, Adam Lewis, et al.
Bioinformatics (Oxford, England)|March 26, 2010
PheWAS: demonstrating the feasibility of a phenome-wide scan to discover gene-disease associationsJoshua C Denny, Marylyn D Ritchie, Melissa A Basford, et al.
American Journal of Medical Genetics. Part A|March 21, 2024
Undiagnosed Disease Network collaborative approach in diagnosing rare disease in a patient with a mosaic CACNA1D variantKimberly M Ezell, Rory J Tinker, Yutaka Furuta, et al.
Medrxiv : the Preprint Server for Health Sciences|December 8, 2025
Common variant approaches to study Mendelian disease gene function identify novel phenome and pathways associated with <i>PLOD3</i>Alexandra Scalici, James T Baker, Freida Blostein, et al.
Plos One|February 17, 2017
Comparison of HLA allelic imputation programsJason H Karnes, Christian M Shaffer, Lisa Bastarache, et al.
The Journal of Clinical Investigation|October 25, 2016
Transcription factor ETV1 is essential for rapid conduction in the heartAkshay Shekhar, Xianming Lin, Fang-Yu Liu, et al.
HGG Advances|May 22, 2023
Genetic and clinical determinants of telomere lengthPatrick Allaire, Jing He, John Mayer, et al.
The Journal of Clinical Endocrinology and Metabolism|April 17, 2018
Rare Variants in the Gene ALPL That Cause Hypophosphatasia Are Strongly Associated With Ovarian and Uterine DisordersKathryn M Dahir, Daniel R Tilden, Jeremy L Warner, et al.
Journal of Biomedical Informatics|April 10, 2021
Phenotyping coronavirus disease 2019 during a global health pandemic: Lessons learned from the characterization of an early cohortSarah DeLozier, Harris T Bland, Melissa McPheeters, et al.
American Journal of Human Genetics|August 22, 2023
The phenotype-genotype reference map: Improving biobank data science through replicationLisa Bastarache, Sarah Delozier, Anita Pandit, et al.
Pageof 16

Showing results (81-90 of 159) with videos related to

Sort By:
Pageof 16
Frontiers in Genetics|May 1, 2023
Genetic predisposition may not improve prediction of cardiac surgery-associated acute kidney injuryNicholas J Douville, Daniel B Larach, Adam Lewis, et al.
Bioinformatics (Oxford, England)|March 26, 2010
PheWAS: demonstrating the feasibility of a phenome-wide scan to discover gene-disease associationsJoshua C Denny, Marylyn D Ritchie, Melissa A Basford, et al.
American Journal of Medical Genetics. Part A|March 21, 2024
Undiagnosed Disease Network collaborative approach in diagnosing rare disease in a patient with a mosaic CACNA1D variantKimberly M Ezell, Rory J Tinker, Yutaka Furuta, et al.
Medrxiv : the Preprint Server for Health Sciences|December 8, 2025
Common variant approaches to study Mendelian disease gene function identify novel phenome and pathways associated with <i>PLOD3</i>Alexandra Scalici, James T Baker, Freida Blostein, et al.
Plos One|February 17, 2017
Comparison of HLA allelic imputation programsJason H Karnes, Christian M Shaffer, Lisa Bastarache, et al.
The Journal of Clinical Investigation|October 25, 2016
Transcription factor ETV1 is essential for rapid conduction in the heartAkshay Shekhar, Xianming Lin, Fang-Yu Liu, et al.
HGG Advances|May 22, 2023
Genetic and clinical determinants of telomere lengthPatrick Allaire, Jing He, John Mayer, et al.
The Journal of Clinical Endocrinology and Metabolism|April 17, 2018
Rare Variants in the Gene ALPL That Cause Hypophosphatasia Are Strongly Associated With Ovarian and Uterine DisordersKathryn M Dahir, Daniel R Tilden, Jeremy L Warner, et al.
Journal of Biomedical Informatics|April 10, 2021
Phenotyping coronavirus disease 2019 during a global health pandemic: Lessons learned from the characterization of an early cohortSarah DeLozier, Harris T Bland, Melissa McPheeters, et al.
American Journal of Human Genetics|August 22, 2023
The phenotype-genotype reference map: Improving biobank data science through replicationLisa Bastarache, Sarah Delozier, Anita Pandit, et al.
Pageof 16