Jason M. Tennessen
Neuroscience · Indiana University
Publications
117
Citations
3,391
Est. group size
~8
Recurring co-author estimate
Active years
24
Publishing since 2003
Jason M. Tennessen studies how metabolism controls animal growth, development, and aging, using the fruit fly Drosophila melanogaster as a model organism. His work examines how cells generate and use energy, focusing on mitochondria (the cell's energy factories) and molecules like NAD+, and how disruptions in these processes relate to development, neuroinflammation, and disease states such as cancer. His lab also investigates how environmental chemicals and symbiotic bacteria affect metabolism.
Publication activity has grown over the last decade, rising notably from around 8 per year in the late 2010s to a peak in 2023 and remaining high since, averaging about 12.6 per year over the last five years.
Generated by claude-opus-4-8 from public bibliographic data · Jul 9, 2026
Current awards run through July 2029 — about 3 years of funding on record from today. Awards are often renewed, so this is what is currently public, not a forecast.
Bloomington Drosophila Stock Center at Indiana University
Investigating metabolic responses to high sugar diets and the onset of diabetic phenotypes
2 earlier awards
- NIH R35GM119557Jul 2016 – Jul 2026 · $442k awarded
A Drosophila Model for the Regulation of Aerobic Glycolysis
- NIH R00GM101341Dec 2013 – Dec 2016 · $246k awarded
A Drosophila Model for the regulation of Aerobic Glycolysis
Matched to public NIH RePORTER and NSF records by name and institution. Awards from other agencies are not shown, and a match is not always found — this list may be incomplete.
Typically publishes in teams of ~8 · 25% small-team papers (≤3 authors) · across 30 venues
- Exposure to perfluorooctanoic acid accelerates Drosophila melanogaster juvenile development and disrupts mitochondrial metabolism
Zenodo (CERN European Organization for Nuclear Research) · 2026
- Comparative Lipidomics Identifies Conserved Glycerophospholipid Disruption Across Evolutionarily Distant Models of PFOA Exposure
Zenodo (CERN European Organization for Nuclear Research) · 2026
- Exposure to perfluorooctanoic acid accelerates Drosophila melanogaster juvenile development and disrupts mitochondrial metabolism
Zenodo (CERN European Organization for Nuclear Research) · 2026
- Comparative Lipidomics Identifies Conserved Glycerophospholipid Disruption Across Evolutionarily Distant Models of PFOA Exposure
Zenodo (CERN European Organization for Nuclear Research) · 2026
- Structural modeling supports an interaction between the Drosophila Estrogen-Related Receptor and Sima/HIF1α
bioRxiv (Cold Spring Harbor Laboratory) · 2026
- Exposure to perfluorooctanoic acid accelerates Drosophila melanogaster juvenile development and disrupts mitochondrial metabolism
bioRxiv (Cold Spring Harbor Laboratory) · 2026
- Comparative metabolomics identifies recurrent age-associated pathway remodeling across species
bioRxiv (Cold Spring Harbor Laboratory) · 2026
- New alleles of D-2-hydroxyglutarate dehydrogenase enable studies of oncometabolite function in Drosophila melanogaster
G3 Genes Genomes Genetics · 2025
- New alleles of D-2-hydroxyglutarate dehydrogenase enable studies of oncometabolite function in Drosophila melanogaster
bioRxiv (Cold Spring Harbor Laboratory) · 2025
- The alternative oxidase reconfigures the larval mitochondrial electron transport system to accelerate growth and development in Drosophila melanogaster
eLife · 2025
- The alternative oxidase reconfigures the larval mitochondrial electron transport system to accelerate growth and development in Drosophila melanogaster
eLife · 2025
- The alternative oxidase reconfigures the larval mitochondrial electron transport system to accelerate growth and development in Drosophila melanogaster
bioRxiv (Cold Spring Harbor Laboratory) · 2025
- NAD + reduction in glutamatergic neurons triggers fatty acid catabolism and neuroinflammation in the brain, mitigated by SARM1 deletion
bioRxiv (Cold Spring Harbor Laboratory) · 2025
- Author response: The alternative oxidase reconfigures the larval mitochondrial electron transport system to accelerate growth and development in Drosophila melanogaster
2025
- Abstract 1496: Understanding a novel interaction between HSF1 and ERRα in breast cancer
Cancer Research · 2025
- bioRxiv (Cold Spring Harbor Laboratory)×28
- eLife×9
- G3 Genes Genomes Genetics×5
- Development×4
- Zenodo (CERN European Organization for Nuclear Research)×4
- Elizabeth J. Rideout
Neuroscience · Indiana University
- Peter M. Piermarini
Neuroscience · The Ohio State University
- Molly Duman-Scheel
Neuroscience · Indiana University
- Hana Hall
Neuroscience · Purdue University West Lafayette
- Megan E. Meuti
Neuroscience · The Ohio State University
This profile was generated automatically from public scholarly data (OpenAlex). Group size and activity levels are estimates derived from co-authorship patterns.
Last updated Sep 1, 2026.
Claim or correct this profile