Claude Férec is an expert in Genetics at Centre Hospitalier Régional Universitaire de Brest (France). As of August 2026, ScienceLeadR ranks Claude Férec in the top 1% of experts worldwide for Cystic Fibrosis, Pancreatic Diseases and Pancreatitis. Claude Férec has authored 748 publications, the most recent in 2026, and is an investigator in 1 clinical trial. SLR score: 2,066 (community average: 125). How the SLR is computed.

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2 066 ScienceLeadR Reputation 2066
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Genetics

Subspecialties: Biochemistry - Gastroenterology - Hepatology

Full career – Last 3 years

Main Topics

Publications and Clinical Studies

Publications – Clinical Studies

Profile data updated on

Organizations

Career arc: 1988 - 2026

Source: PubMed

Centre Hospitalier Régional Universitaire de Brest

Publications Synthesis

Sources: PubMed, OpenAlex

Number : 748

Citations

Citations: 23 815 1st author: 32 Last author: 273 Unique author: 5


Breakdown by type

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Latest Publications

5 most recent indexed articles

Source: Pubmed

Title Journal Year Citations
When splicing is not all or none: GT>GC 5' splice-site variants as a model for intermediate effects and challenges in variant classification.
PMID 41928472 — classification
HGG Adv20260
De novo variants in the splicing factor gene SF3B1 are associated with neurodevelopmental disorders.
PMID 41577671 — genes, neoplasms, neurodevelopmental disorders, rna splicing factors, neurodevelopment
Nat Commun20260
Genetic and Electrophysiological Characterization of Acute Recurrent Pancreatitis in Israeli Patients.
PMID 41417682 — research design, pancreas, pancreatitis, prevalence
Pancreas20250
TRPV6-related pancreatitis: natural history and the impact of the pancreas-specific deletion on pancreatitis in mice.
PMID 41247519 — diabetes mellitus, cells, genes, pancreatitis, chronic, acinar cells, natural history, ion channels, pancreas, pancreatitis, history, gastrointestinal diseases
J Gastroenterol20250
Compound Heterozygous Complete Loss-of-Function SPINK1 Variants as a Novel Cause of Severe Infantile Isolated Exocrine Pancreatic Insufficiency.
PMID 41009946 — genes, exocrine pancreatic insufficiency, genomics, maternal inheritance, trypsin inhibitor, kazal pancreatic, exons
Genes (Basel)20250

Clinical Studies 1

Sources: ClinicalTrials, EU CTIS

Synthesis

By phase:

N/A 1

By status:

Completed 1

By type:

Observational 1

By Monocentric/Multicentric:

monocentric 0
multicentric2to4 0
multicentric5to9 1
multicentricup10 0

Main Topics

Cohort/Consortium Investigators 2

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