Claude Houdayer

Rouen, 76000, France

Last Updated: 09/26/2026

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Found 93 publications

Simultaneous Study of Circular RNAs and Messenger RNAs in Colorectal Cancer: The Unbalanced Fate of a Couple?

Simultaneous Study of Circular RNAs and Messenger RNAs in Colorectal Cancer: The Unbalanced Fate of a Couple?

Journal: Cancers
Published: December 29, 2025

Hereditary cancer: Germline testing practices across ERN GENTURIS member countries.

Hereditary cancer: Germline testing practices across ERN GENTURIS member countries.

Journal: European journal of human genetics : EJHG
Published: October 31, 2025

Optimising rare tumour risk syndromes care: clinical insights and the PREVENTABLE socioeconomic framework.

Optimising rare tumour risk syndromes care: clinical insights and the PREVENTABLE socioeconomic framework.

Journal: European journal of human genetics : EJHG
Published: June 23, 2025

Cancer prognosis and treatment results in patients with PTEN Hamartoma Tumour Syndrome (PHTS)-a European cohort study.

Cancer prognosis and treatment results in patients with PTEN Hamartoma Tumour Syndrome (PHTS)-a European cohort study.

Journal: BJC reports
Published: February 13, 2025

A functional assay to classify RB1 variants of uncertain significance.

A functional assay to classify RB1 variants of uncertain significance.

Journal: Genetics in medicine : official journal of the American College of Medical Genetics
Published: January 17, 2025

New RPS20 gene variant in colorectal cancer diagnosis: insight from a large series of patients.

New RPS20 gene variant in colorectal cancer diagnosis: insight from a large series of patients.

Journal: Familial cancer
Published: November 28, 2024

RNA-based diagnostic studies in genetics: Review and guidance from a multidisciplinary French network.

RNA-based diagnostic studies in genetics: Review and guidance from a multidisciplinary French network.

Journal: European journal of human genetics : EJHG
Published: November 27, 2024

Bridging the Diagnostic Gap in Hereditary Cancers with Simple, Cost-Effective, High-Throughput RNA Splicing Analysis.

Bridging the Diagnostic Gap in Hereditary Cancers with Simple, Cost-Effective, High-Throughput RNA Splicing Analysis.

Journal: The Journal of molecular diagnostics : JMD
Published: November 15, 2024

Li-Fraumeni syndrome: a germline TP53 splice variant reveals a novel physiological alternative transcript.

Li-Fraumeni syndrome: a germline TP53 splice variant reveals a novel physiological alternative transcript.

Journal: Journal of medical genetics
Published: October 21, 2024

First prenatal case of jumping-like translocations: unraveling complex chromosomal rearrangements.

First prenatal case of jumping-like translocations: unraveling complex chromosomal rearrangements.

Journal: Chromosome research : an international journal on the molecular, supramolecular and evolutionary aspects of chromosome biology
Published: October 02, 2024

Deciphering dual clinical entities associated with TP53 pathogenic variants: Insights from 53,085 HBOC panel analyses in French laboratories.

Deciphering dual clinical entities associated with TP53 pathogenic variants: Insights from 53,085 HBOC panel analyses in French laboratories.

Journal: International journal of cancer
Published: September 26, 2024

The risk of a second primary cancer in PTEN Hamartoma Tumor Syndrome (PHTS).

The risk of a second primary cancer in PTEN Hamartoma Tumor Syndrome (PHTS).

Journal: Genetics in medicine : official journal of the American College of Medical Genetics
Published: August 12, 2024
Showing 1-12 of 93

Last Updated: 09/26/2026