Christophe Arnoult, PhD is an expert in Genetics at Centre Hospitalier Universitaire de Grenoble (France). As of October 2026, ScienceLeadR ranks Christophe Arnoult in the top 1% of experts worldwide for Infertility. Christophe Arnoult has authored 178 publications, the most recent in 2026. SLR score: 721 (community average: 125). How the SLR is computed.

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Christophe Arnoult, PhD Centre Hospitalier Universitaire de Grenoble France
721 ScienceLeadR Reputation 721
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Genetics

Subspecialties: Pharmacy - Biochemistry - Dermatology

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: 1994 - 2026

Source: PubMed

CNRS

Publications Synthesis

Sources: PubMed, OpenAlex

Number : 178

Citations

Citations: 8 475 1st author: 14 Last author: 30 Unique author: 1


Best Journals

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Latest Publications

5 most recent indexed articles

Source: Pubmed

Title Journal Year Citations
Exploring the spatial distribution of biomolecules in Pseudomonas aeruginosa biofilms formed on PDMS and lung explants by mass spectrometry imaging.
PMID 42787713 — lung, pseudomonas, pseudomonas aeruginosa, biofilms, bacteria, infections
Biofilm20260
Biallelic Truncating Variant in LRGUK Is Associated With Severe Multiple Morphological Abnormalities of the Sperm Flagella and Sperm Nuclear Defects in Humans.
PMID 42493466 — genes, flagella, infertility, teratozoospermia, exome, infertility, male, spermatozoa
Clin Genet20260
Cellular and Cytokine Responses of Corneal Fibroblasts Exposed to Keratopigmentation Inks in Vitro.
PMID 42480955 — cytokines, vascular endothelial growth factor a, solvents, ophthalmology, macrophages, corneal neovascularization, phagocytosis, fibroblasts, ink
Exp Eye Res20260
ARMC2 loss impairs cilia structure and leads to primary ciliary dyskinesia symptoms in mouse organs.
PMID 42272638 — dyskinesias, flagella, ciliary motility disorders, axoneme, cilia, signs and symptoms, kartagener syndrome, trachea
Front Cell Dev Biol20260
Single-cell proteomics reveals cytoplasmic defects in Patl2-deficient oocytes rescued by spindle transfer.
PMID 42062216 — cells, reproduction, carrier proteins, embryonic development, infertility, rna-binding proteins, oocytes, cytoplasm, calcium, proteomics, therapeutics, rna
Hum Reprod20260

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