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Najaf Amin

Showing results (71-80 of 263) with videos related to

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Frontiers in Genetics|May 20, 2020
Exome Sequencing Analysis Identifies Rare Variants in <i>ATM</i> and <i>RPL8</i> That Are Associated With Shorter Telomere LengthAshley van der Spek, Sophie C Warner, Linda Broer, et al.
Neurology|December 3, 2020
Association of Circulating Metabolites in Plasma or Serum and Risk of Stroke: Meta-analysis From 7 Prospective CohortsDina Vojinovic, Marita Kalaoja, Stella Trompet, et al.
Human Molecular Genetics|December 7, 2021
Fat metabolism is associated with telomere length in six population-based studiesAshley van der Spek, Hata Karamujić-Čomić, René Pool, et al.
Human Molecular Genetics|December 18, 2009
European lactase persistence genotype shows evidence of association with increase in body mass indexJohannes Kettunen, Kaisa Silander, Olli Saarela, et al.
BMC Medical Genetics|January 25, 2013
Assessment of the 9p21.3 locus in severity of coronary artery disease in the presence and absence of type 2 diabetesNatalia V Rivera, Robert Carreras-Torres, Roberta Roncarati, et al.
Ophthalmology|August 30, 2011
Clinical implications of old and new genes for open-angle glaucomaWishal D Ramdas, Leonieke M E van Koolwijk, Angela J Cree, et al.
Journal of Medical Genetics|November 8, 2011
Linkage and association analyses of glaucoma related traits in a large pedigree from a Dutch genetically isolated populationTatiana Axenovich, Irina Zorkoltseva, Nadezhda Belonogova, et al.
Human Molecular Genetics|November 2, 2017
COPD GWAS variant at 19q13.2 in relation with DNA methylation and gene expressionIvana Nedeljkovic, Lies Lahousse, Elena Carnero-Montoro, et al.
Ophthalmology|May 1, 2018
Whole-Exome Sequencing in Age-Related Macular Degeneration Identifies Rare Variants in COL8A1, a Component of Bruch's MembraneJordi Corominas, Johanna M Colijn, Maartje J Geerlings, et al.
European Journal of Human Genetics : EJHG|February 10, 2018
Understanding the role of the chromosome 15q25.1 in COPD through epigenetics and transcriptomicsIvana Nedeljkovic, Elena Carnero-Montoro, Lies Lahousse, et al.
Pageof 27

Showing results (71-80 of 263) with videos related to

Sort By:
Pageof 27
Frontiers in Genetics|May 20, 2020
Exome Sequencing Analysis Identifies Rare Variants in <i>ATM</i> and <i>RPL8</i> That Are Associated With Shorter Telomere LengthAshley van der Spek, Sophie C Warner, Linda Broer, et al.
Neurology|December 3, 2020
Association of Circulating Metabolites in Plasma or Serum and Risk of Stroke: Meta-analysis From 7 Prospective CohortsDina Vojinovic, Marita Kalaoja, Stella Trompet, et al.
Human Molecular Genetics|December 7, 2021
Fat metabolism is associated with telomere length in six population-based studiesAshley van der Spek, Hata Karamujić-Čomić, René Pool, et al.
Human Molecular Genetics|December 18, 2009
European lactase persistence genotype shows evidence of association with increase in body mass indexJohannes Kettunen, Kaisa Silander, Olli Saarela, et al.
BMC Medical Genetics|January 25, 2013
Assessment of the 9p21.3 locus in severity of coronary artery disease in the presence and absence of type 2 diabetesNatalia V Rivera, Robert Carreras-Torres, Roberta Roncarati, et al.
Ophthalmology|August 30, 2011
Clinical implications of old and new genes for open-angle glaucomaWishal D Ramdas, Leonieke M E van Koolwijk, Angela J Cree, et al.
Journal of Medical Genetics|November 8, 2011
Linkage and association analyses of glaucoma related traits in a large pedigree from a Dutch genetically isolated populationTatiana Axenovich, Irina Zorkoltseva, Nadezhda Belonogova, et al.
Human Molecular Genetics|November 2, 2017
COPD GWAS variant at 19q13.2 in relation with DNA methylation and gene expressionIvana Nedeljkovic, Lies Lahousse, Elena Carnero-Montoro, et al.
Ophthalmology|May 1, 2018
Whole-Exome Sequencing in Age-Related Macular Degeneration Identifies Rare Variants in COL8A1, a Component of Bruch's MembraneJordi Corominas, Johanna M Colijn, Maartje J Geerlings, et al.
European Journal of Human Genetics : EJHG|February 10, 2018
Understanding the role of the chromosome 15q25.1 in COPD through epigenetics and transcriptomicsIvana Nedeljkovic, Elena Carnero-Montoro, Lies Lahousse, et al.
Pageof 27