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Kent D Taylor

Showing results (371-380 of 515) with videos related to

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Blood|June 25, 2015
Rare and low-frequency variants and their association with plasma levels of fibrinogen, FVII, FVIII, and vWFJennifer E Huffman, Paul S de Vries, Alanna C Morrison, et al.
Journal of Hepatology|September 4, 2020
rs641738C>T near MBOAT7 is associated with liver fat, ALT and fibrosis in NAFLD: A meta-analysisKevin Teo, Kushala W M Abeysekera, Leon Adams, et al.
Journal of Medical Genetics|January 1, 2017
A genome-wide interaction analysis of tricyclic/tetracyclic antidepressants and RR and QT intervals: a pharmacogenomics study from the Cohorts for Heart and Aging Research in Genomic Epidemiology (CHARGE) consortiumRaymond Noordam, Colleen M Sitlani, Christy L Avery, et al.
Diabetes|February 15, 2023
Investigating Gene-Diet Interactions Impacting the Association Between Macronutrient Intake and Glycemic TraitsKenneth E Westerman, Maura E Walker, Sheila M Gaynor, et al.
Nature Methods|October 27, 2022
A framework for detecting noncoding rare-variant associations of large-scale whole-genome sequencing studiesZilin Li, Xihao Li, Hufeng Zhou, et al.
Nature Communications|January 4, 2019
Trans-ethnic kidney function association study reveals putative causal genes and effects on kidney-specific disease aetiologiesAndrew P Morris, Thu H Le, Haojia Wu, et al.
Medrxiv : the Preprint Server for Health Sciences|May 5, 2025
Genome-wide association study and multi-ancestry meta-analysis identify common variants associated with carotid artery intima-media thicknessDevendra Meena, Jian Huang, Marjan Zare, et al.
Nature Genetics|May 23, 2017
Fifteen new risk loci for coronary artery disease highlight arterial-wall-specific mechanismsJoanna M M Howson, Wei Zhao, Daniel R Barnes, et al.
Cell Genomics|January 8, 2024
Genome-wide study investigating effector genes and polygenic prediction for kidney function in persons with ancestry from Africa and the AmericasOdessica Hughes, Amy R Bentley, Charles E Breeze, et al.
BMC Genomics|February 20, 2022
Rare coding variants in RCN3 are associated with blood pressureKaren Y He, Tanika N Kelly, Heming Wang, et al.
Pageof 52

Showing results (371-380 of 515) with videos related to

Sort By:
Pageof 52
Blood|June 25, 2015
Rare and low-frequency variants and their association with plasma levels of fibrinogen, FVII, FVIII, and vWFJennifer E Huffman, Paul S de Vries, Alanna C Morrison, et al.
Journal of Hepatology|September 4, 2020
rs641738C>T near MBOAT7 is associated with liver fat, ALT and fibrosis in NAFLD: A meta-analysisKevin Teo, Kushala W M Abeysekera, Leon Adams, et al.
Journal of Medical Genetics|January 1, 2017
A genome-wide interaction analysis of tricyclic/tetracyclic antidepressants and RR and QT intervals: a pharmacogenomics study from the Cohorts for Heart and Aging Research in Genomic Epidemiology (CHARGE) consortiumRaymond Noordam, Colleen M Sitlani, Christy L Avery, et al.
Diabetes|February 15, 2023
Investigating Gene-Diet Interactions Impacting the Association Between Macronutrient Intake and Glycemic TraitsKenneth E Westerman, Maura E Walker, Sheila M Gaynor, et al.
Nature Methods|October 27, 2022
A framework for detecting noncoding rare-variant associations of large-scale whole-genome sequencing studiesZilin Li, Xihao Li, Hufeng Zhou, et al.
Nature Communications|January 4, 2019
Trans-ethnic kidney function association study reveals putative causal genes and effects on kidney-specific disease aetiologiesAndrew P Morris, Thu H Le, Haojia Wu, et al.
Medrxiv : the Preprint Server for Health Sciences|May 5, 2025
Genome-wide association study and multi-ancestry meta-analysis identify common variants associated with carotid artery intima-media thicknessDevendra Meena, Jian Huang, Marjan Zare, et al.
Nature Genetics|May 23, 2017
Fifteen new risk loci for coronary artery disease highlight arterial-wall-specific mechanismsJoanna M M Howson, Wei Zhao, Daniel R Barnes, et al.
Cell Genomics|January 8, 2024
Genome-wide study investigating effector genes and polygenic prediction for kidney function in persons with ancestry from Africa and the AmericasOdessica Hughes, Amy R Bentley, Charles E Breeze, et al.
BMC Genomics|February 20, 2022
Rare coding variants in RCN3 are associated with blood pressureKaren Y He, Tanika N Kelly, Heming Wang, et al.
Pageof 52