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Johanna K. DiStefano

Researcher at Translational Genomics Research Institute

Publications -  35
Citations -  799

Johanna K. DiStefano is an academic researcher from Translational Genomics Research Institute. The author has contributed to research in topics: Diabetes mellitus & Nonalcoholic fatty liver disease. The author has an hindex of 17, co-authored 34 publications receiving 664 citations.

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Journal ArticleDOI

High-throughput sequencing reveals altered expression of hepatic microRNAs in nonalcoholic fatty liver disease-related fibrosis.

TL;DR: A role for hepatic miRNAs in the pathogenesis of NAFLD-related fibrosis is supported and possible new insight is yielded into the molecular mechanisms underlying the initiation and progression of liver fibrosis and cirrhosis.
Journal ArticleDOI

Long Noncoding RNAs as Diagnostic and Therapeutic Targets in Type 2 Diabetes and Related Complications.

Fatjon Leti, +1 more
- 22 Aug 2017 - 
TL;DR: The role of lncRNAs in the pathogenesis of type 2 diabetes mellitus and related complications has only recently been recognized, but there is already evidence for their involvement in many of the pathophysiological mechanisms underlying the disease.
Book ChapterDOI

Targeted SNP Genotyping Using the TaqMan® Assay

TL;DR: This commonly used technique to genotype a moderate number of markers in this kind of study is introduced and described and protocols that can be directly used in laboratories aiming to perform moderate- to large-scale genotyping studies are included.
Journal ArticleDOI

Long noncoding RNAs in the initiation, progression, and metastasis of hepatocellular carcinoma.

TL;DR: This review summarizes select lncRNAs that have been shown to wield functional relevance in the initiation, progression, or metastasis of HCC, focusing on the specific mechanisms by which lncRNA effects might be linked to clinical manifestations of the disease.
Journal ArticleDOI

Transcriptomic Profiling of Obesity-Related Nonalcoholic Steatohepatitis Reveals a Core Set of Fibrosis-Specific Genes.

TL;DR: Se sequencing-based mRNA profiling analysis of liver samples from individuals with normal histology found evidence for differential levels of 3820 and 2980 transcripts in lobular inflammation and advanced fibrosis, respectively, compared withnormal histology, including 176 genes specific to fibrosis.