Jove
Visualize
Contact Us
JoVE
x logofacebook logolinkedin logoyoutube logo
ABOUT JoVE
OverviewLeadershipBlogJoVE Help Center
AUTHORS
Publishing ProcessEditorial BoardScope & PoliciesPeer ReviewFAQSubmit
LIBRARIANS
TestimonialsSubscriptionsAccessResourcesLibrary Advisory BoardFAQ
RESEARCH
JoVE JournalMethods CollectionsJoVE Encyclopedia of ExperimentsArchive
EDUCATION
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab ManualFaculty Resource CenterFaculty Site
Terms & Conditions of Use
Privacy Policy
Policies

Filters

Nathan Pankratz

Showing results (71-80 of 173) with videos related to

Pageof 18
Sort By:
Plos One|February 1, 2020
Evaluation of mitochondrial DNA copy number estimation techniquesRyan J Longchamps, Christina A Castellani, Stephanie Y Yang, et al.
JAMA Cardiology|October 20, 2017
Association of Mitochondrial DNA Copy Number With Cardiovascular DiseaseForam N Ashar, Yiyi Zhang, Ryan J Longchamps, et al.
Research Square|April 1, 2024
Extreme Phenotype Sampling and Next Generation Sequencing to Identify Genetic Variants Associated with Tacrolimus in African American Kidney Transplant RecipientsMoataz Mohamed, Bin Guo, Baolin Wu, et al.
Cancer Epidemiology, Biomarkers & Prevention : a Publication of the American Association for Cancer Research, Cosponsored by the American Society of Preventive Oncology|March 23, 2023
Associations between MICA and MICB Genetic Variants, Protein Levels, and Colorectal Cancer: Atherosclerosis Risk in Communities (ARIC)Shuo Wang, Guillaume C Onyeaghala, Nathan Pankratz, et al.
Journal of the National Cancer Institute|April 6, 2026
Overlapping genetic etiology of pediatric and adult germ cell tumorsShannon M Sullivan, John Lane, Abigail Standafer, et al.
Neuroimage|April 19, 2011
Voxelwise gene-wide association study (vGeneWAS): multivariate gene-based association testing in 731 elderly subjectsDerrek P Hibar, Jason L Stein, Omid Kohannim, et al.
European Journal of Medical Genetics|November 28, 2017
Rare copy number variants identified in prune belly syndromeNansi S Boghossian, Robert J Sicko, Andreas Giannakou, et al.
Journal of Cellular and Molecular Medicine|February 12, 2026
Plasma Proteome Signature for Leukocyte Telomere Length and Its Link to Abdominal Aortic AneurysmAixin Li, Thomas R Austin, Brian T Steffen, et al.
Genetic Epidemiology|November 30, 2007
Issues in association mapping with high-density SNP data and diverse family structuresHeike Bickeböller, Katrina A B Goddard, Robert P Igo, et al.
The Journal of Clinical Endocrinology and Metabolism|May 16, 2017
Somatic USP8 Gene Mutations Are a Common Cause of Pediatric Cushing DiseaseFabio R Faucz, Amit Tirosh, Christina Tatsi, et al.
Pageof 18

Showing results (71-80 of 173) with videos related to

Sort By:
Pageof 18
Plos One|February 1, 2020
Evaluation of mitochondrial DNA copy number estimation techniquesRyan J Longchamps, Christina A Castellani, Stephanie Y Yang, et al.
JAMA Cardiology|October 20, 2017
Association of Mitochondrial DNA Copy Number With Cardiovascular DiseaseForam N Ashar, Yiyi Zhang, Ryan J Longchamps, et al.
Research Square|April 1, 2024
Extreme Phenotype Sampling and Next Generation Sequencing to Identify Genetic Variants Associated with Tacrolimus in African American Kidney Transplant RecipientsMoataz Mohamed, Bin Guo, Baolin Wu, et al.
Cancer Epidemiology, Biomarkers & Prevention : a Publication of the American Association for Cancer Research, Cosponsored by the American Society of Preventive Oncology|March 23, 2023
Associations between MICA and MICB Genetic Variants, Protein Levels, and Colorectal Cancer: Atherosclerosis Risk in Communities (ARIC)Shuo Wang, Guillaume C Onyeaghala, Nathan Pankratz, et al.
Journal of the National Cancer Institute|April 6, 2026
Overlapping genetic etiology of pediatric and adult germ cell tumorsShannon M Sullivan, John Lane, Abigail Standafer, et al.
Neuroimage|April 19, 2011
Voxelwise gene-wide association study (vGeneWAS): multivariate gene-based association testing in 731 elderly subjectsDerrek P Hibar, Jason L Stein, Omid Kohannim, et al.
European Journal of Medical Genetics|November 28, 2017
Rare copy number variants identified in prune belly syndromeNansi S Boghossian, Robert J Sicko, Andreas Giannakou, et al.
Journal of Cellular and Molecular Medicine|February 12, 2026
Plasma Proteome Signature for Leukocyte Telomere Length and Its Link to Abdominal Aortic AneurysmAixin Li, Thomas R Austin, Brian T Steffen, et al.
Genetic Epidemiology|November 30, 2007
Issues in association mapping with high-density SNP data and diverse family structuresHeike Bickeböller, Katrina A B Goddard, Robert P Igo, et al.
The Journal of Clinical Endocrinology and Metabolism|May 16, 2017
Somatic USP8 Gene Mutations Are a Common Cause of Pediatric Cushing DiseaseFabio R Faucz, Amit Tirosh, Christina Tatsi, et al.
Pageof 18