Laurent Castera is an expert in Genetics at Centre François Baclesse (France). Laurent Castera has authored 73 publications, the most recent in 2026, and is an investigator in 3 clinical trials, 2 of them ongoing. SLR score: 237 (community average: 125). How the SLR is computed.

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Laurent Castera Centre François Baclesse France
237 ScienceLeadR Reputation 237
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Genetics

Subspecialties: Hepatology - Oncology - Gastroenterology

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: 2010 - 2026

Source: PubMed

Hôpital Charles-Nicolle (France)

Publications Synthesis

Sources: PubMed, OpenAlex

Number : 73

Citations

Citations: 1 945 1st author: 6 Last author: 2 Unique author: 2


Breakdown by type

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Latest Publications

5 most recent indexed articles

Source: Pubmed

Title Journal Year Citations
Cancer risks for ATM variant heterozygotes.
PMID 42052916 — heterozygote, pancreatic neoplasms, breast neoplasms, neoplasms, penetrance, breast, genetics, medical
Genet Med20260
Comparative performance of a targeted next-generation sequencing assay against multiplexed digital PCR assays in detecting ERBB2, ESR1, and PIK3CA mutations in plasma circulating cell-free DNA from liquid biopsies.
PMID 41072730 — cells, genes, high-throughput nucleotide sequencing, breast neoplasms, polymerase chain reaction, neoplasms, multiple chronic conditions, biopsy, cell-free nucleic acids, solutions, breast, dna, liquid biopsy, mutation, plasma
J Mol Diagn20250
Long-term patient-derived ovarian cancer organoids closely recapitulate tumor of origin and clinical response.
PMID 41057919 — pharmaceutical preparations, ovary, neoplasms, drug therapy, organoids, ovarian neoplasms, genomic instability, medical oncology, chemotherapy
J Exp Clin Cancer Res20256
Decipher RNA isoform combinations from minigene splicing assays and massive parallel sequencing with MAGIC.
PMID 40973179 — magic, protein isoforms, rna
Bioinformatics20250
Bridging the Diagnostic Gap in Hereditary Cancers with Simple, Cost-Effective, High-Throughput RNA Splicing Analysis.
PMID 40712994 — genes, neoplasms, ligation, rna splicing, rna
J Mol Diagn20251

Clinical Studies 3

Sources: ClinicalTrials, EU CTIS

Synthesis

By phase:

N/A 1
Phase 1/Phase 2 1
Phase 2 1

By status:

Recruiting 2
Active not recruiting 1

By type:

Interventional 2
Observational 1

By Monocentric/Multicentric:

monocentric 1
multicentric2to4 1
multicentric5to9 0
multicentricup10 1

Main Topics

Ongoing Clinical Trials

2 ongoing trials started since 2021, where this expert is an investigator

Source: ClinicalTrials

Study Phase Status Start
Collection of Endometrial Cancer derived Organoids to Evaluate the Efficacy of PARP Inhibitors PENDOR Pilot Study
NCT06603506 — pilot projects, pilots, poly(adp-ribose) polymerase inhibitors, blood, neoplasms, organoids, endometrial neoplasms
N/ARecruiting2024
HRD Tests for Ovarian cancER
NCT06152731 — recombination, genetic, poly(adp-ribose) polymerase inhibitors, homologous recombination, ovary, neoplasms, drug therapy, ovarian neoplasms, therapeutics, chemotherapy, carcinoma
Phase 2Recruiting2024

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