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Nathan Pankratz

Showing results (91-100 of 173) with videos related to

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Neuroimage|February 23, 2010
Voxelwise genome-wide association study (vGWAS)Jason L Stein, Xue Hua, Suh Lee, et al.
Human Molecular Genetics|January 18, 2025
Functional variants in the cystic fibrosis transmembrane conductance regulator (CFTR) gene are associated with increased risk of colorectal cancerAnna Prizment, Abby Standafer, Conghui Qu, et al.
American Journal of Medical Genetics. Part A|August 6, 2021
Exome sequencing of child-parent trios with bladder exstrophy: Findings in 26 childrenGeorgia Pitsava, Marcia L Feldkamp, Nathan Pankratz, et al.
Frontiers in Endocrinology|July 28, 2020
Rare Germline <i>DICER1</i> Variants in Pediatric Patients With Cushing's Disease: What Is Their Role?Idoia Martínez de LaPiscina, Laura C Hernández-Ramírez, Nancy Portillo, et al.
BMC Proceedings|March 1, 2012
Identifying rare variants from exome scans: the GAW17 experienceSaurabh Ghosh, Heike Bickeböller, Julia Bailey, et al.
Genome Medicine|September 29, 2020
Mitochondrial DNA copy number can influence mortality and cardiovascular disease via methylation of nuclear DNA CpGsChristina A Castellani, Ryan J Longchamps, Jason A Sumpter, et al.
JAMA|May 27, 2015
Copy number variations and cognitive phenotypes in unselected populationsKatrin Männik, Reedik Mägi, Aurélien Macé, et al.
Circulation|February 16, 2026
Novel Plasma Proteomic Markers and Risk of Venous ThromboembolismWeihong Tang, Aixin Li, Thomas R Austin, et al.
Human Molecular Genetics|October 12, 2018
Whole genome sequence association with E-selectin levels reveals loss-of-function variant in African AmericansLinda M Polfus, Laura M Raffield, Marsha M Wheeler, et al.
Nature Communications|September 30, 2023
Deleterious heteroplasmic mitochondrial mutations are associated with an increased risk of overall and cancer-specific mortalityYun Soo Hong, Stephanie L Battle, Wen Shi, et al.
Pageof 18

Showing results (91-100 of 173) with videos related to

Sort By:
Pageof 18
Neuroimage|February 23, 2010
Voxelwise genome-wide association study (vGWAS)Jason L Stein, Xue Hua, Suh Lee, et al.
Human Molecular Genetics|January 18, 2025
Functional variants in the cystic fibrosis transmembrane conductance regulator (CFTR) gene are associated with increased risk of colorectal cancerAnna Prizment, Abby Standafer, Conghui Qu, et al.
American Journal of Medical Genetics. Part A|August 6, 2021
Exome sequencing of child-parent trios with bladder exstrophy: Findings in 26 childrenGeorgia Pitsava, Marcia L Feldkamp, Nathan Pankratz, et al.
Frontiers in Endocrinology|July 28, 2020
Rare Germline <i>DICER1</i> Variants in Pediatric Patients With Cushing's Disease: What Is Their Role?Idoia Martínez de LaPiscina, Laura C Hernández-Ramírez, Nancy Portillo, et al.
BMC Proceedings|March 1, 2012
Identifying rare variants from exome scans: the GAW17 experienceSaurabh Ghosh, Heike Bickeböller, Julia Bailey, et al.
Genome Medicine|September 29, 2020
Mitochondrial DNA copy number can influence mortality and cardiovascular disease via methylation of nuclear DNA CpGsChristina A Castellani, Ryan J Longchamps, Jason A Sumpter, et al.
JAMA|May 27, 2015
Copy number variations and cognitive phenotypes in unselected populationsKatrin Männik, Reedik Mägi, Aurélien Macé, et al.
Circulation|February 16, 2026
Novel Plasma Proteomic Markers and Risk of Venous ThromboembolismWeihong Tang, Aixin Li, Thomas R Austin, et al.
Human Molecular Genetics|October 12, 2018
Whole genome sequence association with E-selectin levels reveals loss-of-function variant in African AmericansLinda M Polfus, Laura M Raffield, Marsha M Wheeler, et al.
Nature Communications|September 30, 2023
Deleterious heteroplasmic mitochondrial mutations are associated with an increased risk of overall and cancer-specific mortalityYun Soo Hong, Stephanie L Battle, Wen Shi, et al.
Pageof 18