Match tier Confirmed
Presence Current · Arkansas
Last published 2022
Sources OpenAlex · ORCID
Refreshed 2026-08-20

Shilpa Iyer

Affiliation confirmed via AI analysis of OpenAlex, ORCID, and web sources.

Federal Grant PI

Associate Professor

Also affiliated: University of Pennsylvania (2016)

Faculty Researcher

1 h-index 3 pubs 37 cited

  • Humans
  • Mutation
  • Mitochondria
  • Genes, Mitochondrial
  • Fibroblasts
  • Induced Pluripotent Stem Cells
  • DNA-Binding Proteins
  • DNA, Mitochondrial
  • Transcription Factors
  • Mitochondrial Proteins
  • Leigh Disease
  • Recombination, Genetic
  • Telomere
  • Animals
  • Genetic Therapy

Biography and Research Information

OverviewAI-generated summary

Shilpa Iyer investigates the role of mitochondrial function in human disease, particularly focusing on pediatric mitochondrial disorders and their impact on development. Her research utilizes induced pluripotent stem cells (iPSCs) derived from patients to study cellular phenotypes and disease mechanisms. A significant area of her work involves quantifying mitochondrial morphology and bioenergetics in patient-derived cells, including fibroblasts and iPSCs, to understand disease severity and potential therapeutic targets.

Iyer is the Principal Investigator on a $606,257 grant from the NIH/Eunice Kennedy Shriver National Institute of Child Health and Human Development. This funding supports research into the metabolic regulation of Multiple Organ Dysfunction Syndrome (MODS) in pediatric mitochondrial disorders. Her recent publications explore quantitative analysis of mitochondrial dynamics, bioenergetics health index ratios, and the effects of cell-permeable succinate on mitochondrial function in the context of Leigh syndrome, a severe neurological disorder.

Her work also involves developing and applying computational tools, such as MitoCellPhe, for analyzing mitochondrial morphologies in single cells and cell clusters. Iyer collaborates with several researchers at the University of Arkansas at Fayetteville, including Raj R. Rao, Fibi Meshrkey, Bibhuti Ballav Saikia, and Joshua Stabach, with whom she has multiple shared publications, indicating a collaborative research environment.

Metrics

  • h-index: 1
  • Publications: 3
  • Citations: 37

Selected Publications

  • Evaluation of Human Stem Cell Conditioned Medium and Culture Conditions on Alleviating Elastase-Compromised Human Aortic Smooth Muscle Cell Function (2026)
    Cardiovascular Engineering and Technology DOI OpenAlex
  • Mitochondrial morphology in human fibroblasts and induced pluripotent stem cells in Leigh syndrome: A comparative analysis (2026)
    Physiological Reports DOI OpenAlex
  • Impaired mitochondrial morphology and respiratory dysfunction in human induced pluripotent stem cells with mitochondrial tRNA mutations (m.3243A>G and m.14739G>A) (2026)
    Figshare DOI OpenAlex
  • Additional file 4 of Impaired mitochondrial morphology and respiratory dysfunction in human induced pluripotent stem cells with mitochondrial tRNA mutations (m.3243A>G and m.14739G>A) (2026)
    Figshare DOI OpenAlex
  • Additional file 3 of Impaired mitochondrial morphology and respiratory dysfunction in human induced pluripotent stem cells with mitochondrial tRNA mutations (m.3243A>G and m.14739G>A) (2026)
    Figshare DOI OpenAlex
  • Additional file 4 of Impaired mitochondrial morphology and respiratory dysfunction in human induced pluripotent stem cells with mitochondrial tRNA mutations (m.3243A>G and m.14739G>A) (2026)
    Figshare DOI OpenAlex
  • Additional file 5 of Impaired mitochondrial morphology and respiratory dysfunction in human induced pluripotent stem cells with mitochondrial tRNA mutations (m.3243A>G and m.14739G>A) (2026)
    Figshare DOI OpenAlex
  • Additional file 1 of Impaired mitochondrial morphology and respiratory dysfunction in human induced pluripotent stem cells with mitochondrial tRNA mutations (m.3243A>G and m.14739G>A) (2026)
    Figshare DOI OpenAlex
  • Additional file 2 of Impaired mitochondrial morphology and respiratory dysfunction in human induced pluripotent stem cells with mitochondrial tRNA mutations (m.3243A>G and m.14739G>A) (2026)
    Figshare DOI OpenAlex
  • Additional file 3 of Impaired mitochondrial morphology and respiratory dysfunction in human induced pluripotent stem cells with mitochondrial tRNA mutations (m.3243A>G and m.14739G>A) (2026)
    Figshare DOI OpenAlex
  • Additional file 1 of Impaired mitochondrial morphology and respiratory dysfunction in human induced pluripotent stem cells with mitochondrial tRNA mutations (m.3243A>G and m.14739G>A) (2026)
    Figshare DOI OpenAlex
  • Additional file 5 of Impaired mitochondrial morphology and respiratory dysfunction in human induced pluripotent stem cells with mitochondrial tRNA mutations (m.3243A>G and m.14739G>A) (2026)
    Figshare DOI OpenAlex
  • Additional file 2 of Impaired mitochondrial morphology and respiratory dysfunction in human induced pluripotent stem cells with mitochondrial tRNA mutations (m.3243A>G and m.14739G>A) (2026)
    Figshare DOI OpenAlex
  • Impaired mitochondrial morphology and respiratory dysfunction in human induced pluripotent stem cells with mitochondrial tRNA mutations (m.3243A>G and m.14739G>A) (2026)
    Open MIND DOI OpenAlex
  • Impaired mitochondrial morphology and respiratory dysfunction in human induced pluripotent stem cells with mitochondrial tRNA mutations (m.3243A>G and m.14739G>A) (2026)
    Orphanet Journal of Rare Diseases DOI OpenAlex

View all publications on OpenAlex →

Federal Grants 1 $606,257 total

NIH Contact PI Aug 2023 - May 2028

Metabolic regulation of MODS in pediatric mitochondrial disorders

Eunice Kennedy Shriver National Institute of Child Health and Human Development $606,257 R01

Collaboration Network

60 Collaborators 31 Institutions 6 Countries

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