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Gastroenterology|February 16, 2019
Systems Biology Analyses Show Hyperactivation of Transforming Growth Factor-β and JNK Signaling Pathways in Esophageal CancerAndrew E Blum, Srividya Venkitachalam, Durgadevi Ravillah, et al.Cancer Research|August 10, 2016
RNA Sequencing Identifies Transcriptionally Viable Gene Fusions in Esophageal AdenocarcinomasAndrew E Blum, Srividya Venkitachalam, Yan Guo, 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.Clinical Gastroenterology and Hepatology : the Official Clinical Practice Journal of the American Gastroenterological Association|September 16, 2023
Prevalence and Predictors of Barrett's Esophagus After Negative Initial Endoscopy: Analysis From Two National DatabasesLovekirat Dhaliwal, Amrit K Kamboj, J Lucas Williams, 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 One|October 27, 2017
Genomic regions associated with susceptibility to Barrett's esophagus and esophageal adenocarcinoma in African Americans: The cross BETRNet admixture studyXiangqing Sun, Apoorva K Chandar, Marcia I Canto, 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 5