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Lisa Bastarache

Showing results (131-140 of 159) with videos related to

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Blood|August 13, 2015
Genetics of glucocorticoid-associated osteonecrosis in children with acute lymphoblastic leukemiaSeth E Karol, Wenjian Yang, Sara L Van Driest, et al.
Bioinformatics (Oxford, England)|November 6, 2023
Next-generation phenotyping: introducing phecodeX for enhanced discovery research in medical phenomicsMegan M Shuey, William W Stead, Ida Aka, et al.
Medrxiv : the Preprint Server for Health Sciences|November 24, 2025
Genome sequencing of 35,024 predominantly African ancestry persons addresses gaps in genomics and healthcareCecile Avery, Mojgan Babanejad, James Baker, et al.
Nature Communications|April 22, 2024
Clinical associations with a polygenic predisposition to benign lower white blood cell countsJonathan D Mosley, John P Shelley, Alyson L Dickson, et al.
Circulation|March 7, 2013
Genome- and phenome-wide analyses of cardiac conduction identifies markers of arrhythmia riskMarylyn D Ritchie, Joshua C Denny, Rebecca L Zuvich, et al.
Medrxiv : the Preprint Server for Health Sciences|September 4, 2023
Clinical consequences of a polygenic predisposition to benign lower white blood cell counts: Consequences of benign WBC count geneticsJonathan D Mosley, John P Shelley, Alyson L Dickson, et al.
European Journal of Human Genetics : EJHG|July 27, 2023
Heterozygous rare variants in NR2F2 cause a recognizable multiple congenital anomaly syndrome with developmental delaysMythily Ganapathi, Leticia S Matsuoka, Michael March, et al.
NPJ Genomic Medicine|February 19, 2019
A phenome-wide association study to discover pleiotropic effects of <i>PCSK9</i>, <i>APOB</i>, and <i>LDLR</i>Maya S Safarova, Benjamin A Satterfield, Xiao Fan, et al.
American Journal of Human Genetics|October 11, 2011
Variants near FOXE1 are associated with hypothyroidism and other thyroid conditions: using electronic medical records for genome- and phenome-wide studiesJoshua C Denny, Dana C Crawford, Marylyn D Ritchie, et al.
World Journal of Surgery|October 13, 2019
Association of Genetic Risk of Obesity with Postoperative Complications Using Mendelian RandomizationJamie R Robinson, Robert J Carroll, Lisa Bastarache, et al.
Pageof 16

Showing results (131-140 of 159) with videos related to

Sort By:
Pageof 16
Blood|August 13, 2015
Genetics of glucocorticoid-associated osteonecrosis in children with acute lymphoblastic leukemiaSeth E Karol, Wenjian Yang, Sara L Van Driest, et al.
Bioinformatics (Oxford, England)|November 6, 2023
Next-generation phenotyping: introducing phecodeX for enhanced discovery research in medical phenomicsMegan M Shuey, William W Stead, Ida Aka, et al.
Medrxiv : the Preprint Server for Health Sciences|November 24, 2025
Genome sequencing of 35,024 predominantly African ancestry persons addresses gaps in genomics and healthcareCecile Avery, Mojgan Babanejad, James Baker, et al.
Nature Communications|April 22, 2024
Clinical associations with a polygenic predisposition to benign lower white blood cell countsJonathan D Mosley, John P Shelley, Alyson L Dickson, et al.
Circulation|March 7, 2013
Genome- and phenome-wide analyses of cardiac conduction identifies markers of arrhythmia riskMarylyn D Ritchie, Joshua C Denny, Rebecca L Zuvich, et al.
Medrxiv : the Preprint Server for Health Sciences|September 4, 2023
Clinical consequences of a polygenic predisposition to benign lower white blood cell counts: Consequences of benign WBC count geneticsJonathan D Mosley, John P Shelley, Alyson L Dickson, et al.
European Journal of Human Genetics : EJHG|July 27, 2023
Heterozygous rare variants in NR2F2 cause a recognizable multiple congenital anomaly syndrome with developmental delaysMythily Ganapathi, Leticia S Matsuoka, Michael March, et al.
NPJ Genomic Medicine|February 19, 2019
A phenome-wide association study to discover pleiotropic effects of <i>PCSK9</i>, <i>APOB</i>, and <i>LDLR</i>Maya S Safarova, Benjamin A Satterfield, Xiao Fan, et al.
American Journal of Human Genetics|October 11, 2011
Variants near FOXE1 are associated with hypothyroidism and other thyroid conditions: using electronic medical records for genome- and phenome-wide studiesJoshua C Denny, Dana C Crawford, Marylyn D Ritchie, et al.
World Journal of Surgery|October 13, 2019
Association of Genetic Risk of Obesity with Postoperative Complications Using Mendelian RandomizationJamie R Robinson, Robert J Carroll, Lisa Bastarache, et al.
Pageof 16