Jeffrey J Brault is an expert in Biochemistry at Indiana University School of Medicine (United States). Jeffrey J Brault has authored 80 publications, the most recent in 2026. SLR score: 306 (community average: 125). How the SLR is computed.

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Jeffrey J Brault Indiana University School of Medicine United States
306 ScienceLeadR Reputation 306
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Biochemistry

Subspecialties: Genetics - Endocrinology - Rheumatology

Full career – Last 3 years

Main Topics

Publications and Clinical Studies

Publications – Clinical Studies

Profile data updated on

Expert Rankings

Top experts on the MeSH terms this expert works on

Organizations

Career arc: 2001 - 2026

Source: PubMed

Indiana University School of Medicine

Publications Synthesis

Sources: PubMed, OpenAlex

Number : 80

Citations

Citations: 3 950 1st author: 9 Last author: 19 Unique author: 0


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Latest Publications

5 most recent indexed articles

Source: Pubmed

Title Journal Year Citations
Deficient Cardiolipin Remodelling Alters Muscle Fibre Composition and Neuromuscular Connectivity in Barth Syndrome.
PMID 41841200 — blotting, western, electrophysiology, adenine nucleotides, muscles, cardiolipins, stress, physiological, mitochondria, barth syndrome, neuromuscular junction, muscle, skeletal, mutation, cachexia, sarcopenia, integrated stress response
J Cachexia Sarcopenia Muscle20260
Intestinal Barrier Loss Enables Microbiota-Mediated Purinergic Suppression During Malaria.
PMID 41648313 — malaria, adenosine, parasites, immunosuppression therapy, microbiota, child
bioRxiv20260
Deficient Cardiolipin Remodeling Alters Muscle Fiber Composition and Neuromuscular Connectivity in Barth Syndrome.
PMID 41278990 — blotting, western, muscles, cardiolipins, stress, physiological, barth syndrome, muscle, skeletal, mutation
bioRxiv20250
Loss of adenylosuccinate synthetase 1 in mice recapitulates features of ADSS1 myopathy.
PMID 41263703 — muscular diseases, ligases, genes, adenine nucleotides, muscles, phenotype, adenylosuccinate synthase, therapeutics, mutation, adenine
Hum Mol Genet20250
Loss of adenylosuccinate synthetase 1 in mice recapitulates features of ADSS1 myopathy.
PMID 41256550 — muscular diseases, ligases, genes, adenine nucleotides, muscles, phenotype, adenylosuccinate synthase, therapeutics, mutation, adenine
bioRxiv20250

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