Michel Longy is an expert in Genetics at INSERM (France). Michel Longy has authored 303 publications, the most recent in 2026. SLR score: 624 (community average: 125). How the SLR is computed.

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Michel Longy INSERM France
624 ScienceLeadR Reputation 624
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Genetics

Subspecialties:

Full career – Last 3 years

Main Topics

Publications and Clinical Studies

Publications – Clinical Studies

Profile data updated on

Organizations

Career arc: 1996 - 2026

Source: PubMed

University of Bordeaux

Publications Synthesis

Sources: PubMed, OpenAlex

Number : 303

Citations

Citations: 15 164 1st author: 20 Last author: 41 Unique author: 5


Breakdown by type

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Latest Publications

5 most recent indexed articles

Source: Pubmed

Title Journal Year Citations
High-resolution 3D chromatin maps reveal PTEN enhancer hubs bridged to the promoter through flanking anchors.
PMID 42350754 — genes, promoter regions, genetic, biological science disciplines, neoplasms, multiple chronic conditions, chromatin, enhancer elements, genetic
Commun Biol20260
Screening Mammography and Breast Cancer: Variation in Risk with Rare Deleterious or Predicted Deleterious Variants in DNA Repair Genes.
PMID 40227588 — genes, dna repair, breast neoplasms, neoplasms, mammography, breast, dna
Cancers (Basel)20250
Classification of germline non-truncating variants: a new approach to interpretation.
PMID 39358013 — molecular biology, classification, phosphoric monoester hydrolases
J Med Genet20240
Impaired social cognition and fine dexterity in patients with Cowden syndrome associated with germline variants.
PMID 34937768 — psychology, genetics, molecular biology, hamartoma syndrome, multiple, germ-line mutation, social cognition, neurology, cognition
J Med Genet20213
Increased incidence of pathogenic variants in ATM in the context of testing for breast and ovarian cancer predisposition.
PMID 35017683 — incidence, research design, genetic testing, ovarian neoplasms, genes, hereditary breast and ovarian cancer syndrome, high-throughput nucleotide sequencing
J Hum Genet20223

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