Search research articles
Contact Us
Filters
Showing results (1-10 of 12) with videos related to
Page
of 2
Sort By:
Cerebral Cortex (New York, N.Y. : 1991)
|
September 1, 2016
Interaction of Intrinsic and Synaptic Currents Mediate Network Resonance Driven by Layer V Pyramidal Cells
Stephen L Schmidt, Christopher R Dorsett, Apoorva K Iyengar, et al.
Brain Stimulation
|
August 18, 2014
Endogenous cortical oscillations constrain neuromodulation by weak electric fields
Stephen 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 locus
James 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 traits
Sarah 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 IX
Apoorva 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 IX
Apoorva K Iyengar, Xue Zou, Jian Dai, et al.
Plos Genetics
|
September 11, 2020
Adiponectin GWAS loci harboring extensive allelic heterogeneity exhibit distinct molecular consequences
Cassandra 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 Dyskinesia
M 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 T2D
Ana 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 variation
Danny E Miller, Arvis Sulovari, Tianyun Wang, et al.
Page
of 2
Search research articles
Search
Showing results (1-10 of 12) with videos related to
Sort By:
Page
of 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 Cells
Stephen L Schmidt, Christopher R Dorsett, Apoorva K Iyengar, et al.
Brain Stimulation
|
August 18, 2014
Endogenous cortical oscillations constrain neuromodulation by weak electric fields
Stephen 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 locus
James 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 traits
Sarah 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 IX
Apoorva 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 IX
Apoorva K Iyengar, Xue Zou, Jian Dai, et al.
Plos Genetics
|
September 11, 2020
Adiponectin GWAS loci harboring extensive allelic heterogeneity exhibit distinct molecular consequences
Cassandra 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 Dyskinesia
M 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 T2D
Ana 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 variation
Danny E Miller, Arvis Sulovari, Tianyun Wang, et al.
Page
of 2