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Nathan Pankratz

Showing results (81-90 of 173) with videos related to

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Plos One|October 18, 2019
Genetic analysis of hsCRP in American Indians: The Strong Heart Family StudyLyle G Best, Poojitha Balakrishnan, Shelley A Cole, et al.
JCI Insight|October 27, 2020
Requirement of FAT and DCHS protocadherins during hypothalamic-pituitary developmentEmily J Lodge, Paraskevi Xekouki, Tatiane S Silva, et al.
BMC Medicine|September 16, 2020
Mitochondrial DNA copy number and incident atrial fibrillationDi Zhao, Traci M Bartz, Nona Sotoodehnia, et al.
Neuroimage|January 27, 2010
Whole genome association study of brain-wide imaging phenotypes for identifying quantitative trait loci in MCI and AD: A study of the ADNI cohortLi Shen, Sungeun Kim, Shannon L Risacher, et al.
American Journal of Medical Genetics. Part A|December 15, 2015
Rare copy number variants implicated in posterior urethral valvesNansi S Boghossian, Robert J Sicko, Denise M Kay, et al.
Cancer Epidemiology, Biomarkers & Prevention : a Publication of the American Association for Cancer Research, Cosponsored by the American Society of Preventive Oncology|June 4, 2025
Multiancestry Transcriptome-Wide Association Study Identifies Candidate Genes Associated with HepatoblastomaTiankai Xie, Josey C Sorenson, Logan G Spector, et al.
The Pharmacogenomics Journal|August 23, 2024
Extreme phenotype sampling and next generation sequencing to identify genetic variants associated with tacrolimus in African American kidney transplant recipientsMoataz E Mohamed, Bin Guo, Baolin Wu, et al.
Blood|December 28, 2020
A Mendelian randomization of γ' and total fibrinogen levels in relation to venous thromboembolism and ischemic strokeJillian Maners, Dipender Gill, Nathan Pankratz, et al.
Endocrine-Related Cancer|May 24, 2017
Loss-of-function mutations in the <i>CABLES1</i> gene are a novel cause of Cushing's diseaseLaura C Hernández-Ramírez, Ryhem Gam, Nuria Valdés, et al.
Journal of Human Genetics|January 12, 2018
Genome-wide association study of homocysteine in African Americans from the Jackson Heart Study, the Multi-Ethnic Study of Atherosclerosis, and the Coronary Artery Risk in Young Adults studyLaura M Raffield, Jaclyn Ellis, Nels C Olson, et al.
Pageof 18

Showing results (81-90 of 173) with videos related to

Sort By:
Pageof 18
Plos One|October 18, 2019
Genetic analysis of hsCRP in American Indians: The Strong Heart Family StudyLyle G Best, Poojitha Balakrishnan, Shelley A Cole, et al.
JCI Insight|October 27, 2020
Requirement of FAT and DCHS protocadherins during hypothalamic-pituitary developmentEmily J Lodge, Paraskevi Xekouki, Tatiane S Silva, et al.
BMC Medicine|September 16, 2020
Mitochondrial DNA copy number and incident atrial fibrillationDi Zhao, Traci M Bartz, Nona Sotoodehnia, et al.
Neuroimage|January 27, 2010
Whole genome association study of brain-wide imaging phenotypes for identifying quantitative trait loci in MCI and AD: A study of the ADNI cohortLi Shen, Sungeun Kim, Shannon L Risacher, et al.
American Journal of Medical Genetics. Part A|December 15, 2015
Rare copy number variants implicated in posterior urethral valvesNansi S Boghossian, Robert J Sicko, Denise M Kay, et al.
Cancer Epidemiology, Biomarkers & Prevention : a Publication of the American Association for Cancer Research, Cosponsored by the American Society of Preventive Oncology|June 4, 2025
Multiancestry Transcriptome-Wide Association Study Identifies Candidate Genes Associated with HepatoblastomaTiankai Xie, Josey C Sorenson, Logan G Spector, et al.
The Pharmacogenomics Journal|August 23, 2024
Extreme phenotype sampling and next generation sequencing to identify genetic variants associated with tacrolimus in African American kidney transplant recipientsMoataz E Mohamed, Bin Guo, Baolin Wu, et al.
Blood|December 28, 2020
A Mendelian randomization of γ' and total fibrinogen levels in relation to venous thromboembolism and ischemic strokeJillian Maners, Dipender Gill, Nathan Pankratz, et al.
Endocrine-Related Cancer|May 24, 2017
Loss-of-function mutations in the <i>CABLES1</i> gene are a novel cause of Cushing's diseaseLaura C Hernández-Ramírez, Ryhem Gam, Nuria Valdés, et al.
Journal of Human Genetics|January 12, 2018
Genome-wide association study of homocysteine in African Americans from the Jackson Heart Study, the Multi-Ethnic Study of Atherosclerosis, and the Coronary Artery Risk in Young Adults studyLaura M Raffield, Jaclyn Ellis, Nels C Olson, et al.
Pageof 18