Shilpa Iyer Data-verified
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Associate Professor
faculty
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Biography and Research Information
OverviewAI-generated summary
Shilpa Iyer is an investigator focusing on the metabolic regulation of Multiple Organ Dysfunction Syndrome (MODS) in pediatric mitochondrial disorders. Iyer serves as Principal Investigator on a federal grant from the NIH/Eunice Kennedy Shriver National Institute of Child Health and Human Development for this research, which received $613,390 in funding.
Iyer has 3 total publications, with the most recent published in 2022. Scholarship metrics include an h-index of 1 and 37 total citations. Key collaborators include Fibi Meshrkey and Raj R. Rao, both from the University of Arkansas at Fayetteville, with whom Iyer has shared one publication each.
Metrics
- h-index: 16
- Publications: 48
- Citations: 812
Selected Publications
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Impaired mitochondrial morphology and respiratory dysfunction in human induced pluripotent stem cells with mitochondrial tRNA mutations (m.3243A>G and m.14739G>A) (2026)
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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)
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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)
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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)
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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)
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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)
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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)
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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)
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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)
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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)
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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)
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Impaired mitochondrial morphology and respiratory dysfunction in human induced pluripotent stem cells with mitochondrial tRNA mutations (m.3243A>G and m.14739G>A) (2026)
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Impaired mitochondrial morphology and respiratory dysfunction in human induced pluripotent stem cells with mitochondrial tRNA mutations (m.3243A>G and m.14739G>A) (2026)
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Clinical-grade human induced pluripotent stem cell models for understanding mitochondrial structural abnormalities, bioenergetics and differentiation potential in mitochondrial diseases (2024)
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The Challenges and Prospects of Smooth Muscle Tissue Engineering (2024)
Federal Grants 1 $613,390 total
Metabolic regulation of MODS in pediatric mitochondrial disorders
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