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Apoorva K Iyengar

Showing results (1-10 of 12) with videos related to

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Cerebral Cortex (New York, N.Y. : 1991)|September 1, 2016
Interaction of Intrinsic and Synaptic Currents Mediate Network Resonance Driven by Layer V Pyramidal CellsStephen L Schmidt, Christopher R Dorsett, Apoorva K Iyengar, et al.
Brain Stimulation|August 18, 2014
Endogenous cortical oscillations constrain neuromodulation by weak electric fieldsStephen L Schmidt, Apoorva K Iyengar, A Alban Foulser, et al.
Human Molecular Genetics|November 17, 2018
Enhancer deletion and allelic effects define a regulatory molecular mechanism at the VLDLR cholesterol GWAS locusJames P Davis, Swarooparani Vadlamudi, Tamara S Roman, et al.
American Journal of Human Genetics|January 7, 2022
Subcutaneous adipose tissue splice quantitative trait loci reveal differences in isoform usage associated with cardiometabolic traitsSarah M Brotman, Chelsea K Raulerson, Swarooparani Vadlamudi, et al.
Biorxiv : the Preprint Server for Biology|June 4, 2025
Cell Modeling and Rescue of a Novel Non-coding Genetic Cause of Glycogen Storage Disease IXApoorva K Iyengar, Xue Zou, Jian Dai, et al.
Genetics in Medicine Open|February 20, 2026
Cell modeling and rescue of a novel noncoding genetic cause of glycogen storage disease IXApoorva K Iyengar, Xue Zou, Jian Dai, et al.
Plos Genetics|September 11, 2020
Adiponectin GWAS loci harboring extensive allelic heterogeneity exhibit distinct molecular consequencesCassandra N Spracklen, Apoorva K Iyengar, Swarooparani Vadlamudi, et al.
American Journal of Medical Genetics. Part A|October 4, 2024
Promoter Deletion Leading to Allele Specific Expression in a Genetically Unsolved Case of Primary Ciliary DyskinesiaM Makenzie Beaman, Weining Yin, Amanda J Smith, et al.
Nature Communications|October 1, 2020
Genetic variant effects on gene expression in human pancreatic islets and their implications for T2DAna Viñuela, Arushi Varshney, Martijn van de Bunt, et al.
American Journal of Human Genetics|July 3, 2021
Targeted long-read sequencing identifies missing disease-causing variationDanny E Miller, Arvis Sulovari, Tianyun Wang, et al.
Pageof 2

Showing results (1-10 of 12) with videos related to

Sort By:
Pageof 2
Cerebral Cortex (New York, N.Y. : 1991)|September 1, 2016
Interaction of Intrinsic and Synaptic Currents Mediate Network Resonance Driven by Layer V Pyramidal CellsStephen L Schmidt, Christopher R Dorsett, Apoorva K Iyengar, et al.
Brain Stimulation|August 18, 2014
Endogenous cortical oscillations constrain neuromodulation by weak electric fieldsStephen L Schmidt, Apoorva K Iyengar, A Alban Foulser, et al.
Human Molecular Genetics|November 17, 2018
Enhancer deletion and allelic effects define a regulatory molecular mechanism at the VLDLR cholesterol GWAS locusJames P Davis, Swarooparani Vadlamudi, Tamara S Roman, et al.
American Journal of Human Genetics|January 7, 2022
Subcutaneous adipose tissue splice quantitative trait loci reveal differences in isoform usage associated with cardiometabolic traitsSarah M Brotman, Chelsea K Raulerson, Swarooparani Vadlamudi, et al.
Biorxiv : the Preprint Server for Biology|June 4, 2025
Cell Modeling and Rescue of a Novel Non-coding Genetic Cause of Glycogen Storage Disease IXApoorva K Iyengar, Xue Zou, Jian Dai, et al.
Genetics in Medicine Open|February 20, 2026
Cell modeling and rescue of a novel noncoding genetic cause of glycogen storage disease IXApoorva K Iyengar, Xue Zou, Jian Dai, et al.
Plos Genetics|September 11, 2020
Adiponectin GWAS loci harboring extensive allelic heterogeneity exhibit distinct molecular consequencesCassandra N Spracklen, Apoorva K Iyengar, Swarooparani Vadlamudi, et al.
American Journal of Medical Genetics. Part A|October 4, 2024
Promoter Deletion Leading to Allele Specific Expression in a Genetically Unsolved Case of Primary Ciliary DyskinesiaM Makenzie Beaman, Weining Yin, Amanda J Smith, et al.
Nature Communications|October 1, 2020
Genetic variant effects on gene expression in human pancreatic islets and their implications for T2DAna Viñuela, Arushi Varshney, Martijn van de Bunt, et al.
American Journal of Human Genetics|July 3, 2021
Targeted long-read sequencing identifies missing disease-causing variationDanny E Miller, Arvis Sulovari, Tianyun Wang, et al.
Pageof 2