Yasushi Okazaki is an expert in Genetics at Juntendo University (Japan). Yasushi Okazaki has authored 388 publications, the most recent in 2026. SLR score: 1,039 (community average: 125). How the SLR is computed.

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Yasushi Okazaki Juntendo University Japan
1 039 ScienceLeadR Reputation 1039
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Genetics

Subspecialties: Oncology - Neurology - Immunology

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: 1986 - 2026

Source: PubMed

RIKEN

Publications Synthesis

Sources: PubMed, OpenAlex

Number : 388

Citations

Citations: 23 484 1st author: 3 Last author: 75 Unique author: 0


Breakdown by type

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Latest Publications

5 most recent indexed articles

Source: Pubmed

Title Journal Year Citations
Genome-wide mapping of the Galleria mellonella transcription start sites during fungal infection and treatment.
PMID 42866649 — promoter regions, genetic, genome, transcription initiation site, mycoses, larva, therapeutics, enhancer elements, genetic, infections
iScience20260
MA-5 attenuates disease-associated transcriptomic aging and pathological microglial states in Gaucher disease.
PMID 42779990 — microglia, cells, galectins, aging, stress, physiological, mitochondria, galectin 3, inflammasomes, liver, dna, mitochondrial, gaucher disease
Res Sq20260
CD4 CTLs in supercentenarians: Signs of adaptive expansion in healthy aging.
PMID 42617599 — cells, biological science disciplines, aging, neoplasms, signs and symptoms, healthy aging, clone cells
Cell Rep20265
Non-invasive urinary heteroplasmy screening outperforms blood testing for certain mitochondrial DNA variants in mitochondrial disease patients.
PMID 42424991 — research design, mitochondrial diseases, muscles, blood, metabolic diseases, molecular biology, dna, mitochondrial, heteroplasmy, muscle, skeletal, tissues
Mol Genet Metab20260
A Lynch syndrome patient with multiple cancers who was found to have a novel pathogenic variant generating aberrant splicing of MLH1.
PMID 42407056 — genes, dna mismatch repair, polymerase chain reaction, neoplasms, exons
Jpn J Clin Oncol20260

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