Works by Lepage, Mathis

Results: 9

Feedback of extended panel sequencing in 1530 patients referred for suspicion of hereditary predisposition to adult cancers.

Published in:

Clinical Genetics, 2021, v. 99, n. 1, p. 166, doi. 10.1111/cge.13864

By:

Cavaillé, Mathias;
Uhrhammer, Nancy;
Privat, Maud;
Ponelle‐Chachuat, Flora;
Gay‐Bellile, Mathilde;
Lepage, Mathis;
Viala, Sandrine;
Bidet, Yannick;
Bignon, Yves‐Jean

Publication type:

Article

Identification of new candidate genes for the hereditary predisposition to uveal melanoma: IGCMU trial.

Published in:

Frontiers in Oncology, 2025, p. 1, doi. 10.3389/fonc.2025.1538924

By:

Godiveau, Mélanie;
Ginzac, Angeline;
Bidet, Yannick;
Ponelle-Chachuat, Flora;
Privat, Maud;
Durando, Xavier;
Cavaillé, Mathias;
Lepage, Mathis

Publication type:

Article

Diagnosis of PTEN mosaicism: the relevance of additional tumor DNA sequencing. A case report and review of the literature.

Published in:

2023

By:

Cavaillé, Mathias;
Crampon, Delphine;
Achim, Viorel;
Bubien, Virginie;
Uhrhammer, Nancy;
Privat, Maud;
Ponelle-Chachuat, Flora;
Gay-Bellile, Mathilde;
Lepage, Mathis;
Ouedraogo, Zangbéwendé Guy;
Jones, Natalie;
Bidet, Yannick;
Sevenet, Nicolas;
Bignon, Yves-Jean

Publication type:

Case Study

Analysis of 11 candidate genes in 849 adult patients with suspected hereditary cancer predisposition.

Published in:

Genes, Chromosomes & Cancer, 2021, v. 60, n. 2, p. 73, doi. 10.1002/gcc.22911

By:

Cavaillé, Mathias;
Uhrhammer, Nancy;
Privat, Maud;
Ponelle‐Chachuat, Flora;
Gay‐Bellile, Mathilde;
Lepage, Mathis;
Molnar, Ioana;
Viala, Sandrine;
Bidet, Yannick;
Bignon, Yves‐Jean

Publication type:

Article

Relevance of Extending FGFR3 Gene Analysis in Osteochondrodysplasia to Non-Coding Sequences: A Case Report.

Published in:

Genes, 2024, v. 15, n. 2, p. 225, doi. 10.3390/genes15020225

By:

Ouedraogo, Zangbéwendé Guy;
Janel, Caroline;
Janin, Alexandre;
Millat, Gilles;
Langlais, Sarah;
Pontier, Bénédicte;
Biard, Marie;
Lepage, Mathis;
Francannet, Christine;
Laffargue, Fanny;
Creveaux, Isabelle

Publication type:

Article

Detection Rate and Spectrum of Pathogenic Variations in a Cohort of 83 Patients with Suspected Hereditary Risk of Kidney Cancer.

Published in:

Genes, 2023, v. 14, n. 11, p. 1991, doi. 10.3390/genes14111991

By:

Ouedraogo, Zangbéwendé Guy;
Ceruti, Florian;
Lepage, Mathis;
Gay-Bellile, Mathilde;
Uhrhammer, Nancy;
Ponelle-Chachuat, Flora;
Bidet, Yannick;
Privat, Maud;
Cavaillé, Mathias

Publication type:

Article

Case Series of 11 CDH1 Families (47 Carriers) Including Incidental Findings, Signet Ring Cell Colon Cancer and Review of the Literature.

Published in:

Genes, 2023, v. 14, n. 9, p. 1677, doi. 10.3390/genes14091677

By:

Lepage, Mathis;
Uhrhammer, Nancy;
Privat, Maud;
Ponelle-Chachuat, Flora;
Kossai, Myriam;
Scanzi, Julien;
Ouedraogo, Zangbéwendé Guy;
Gay-Bellile, Mathilde;
Bidet, Yannick;
Cavaillé, Mathias

Publication type:

Article

RNA Panel Sequencing Is an Effective Tool to Help Classify Splice Variants for Clinical Oncogenetic Diagnosis.

Published in:

Human Mutation, 2024, v. 2024, p. 1, doi. 10.1155/2024/4830045

By:

Privat, Maud;
Ponelle-Chachuat, Flora;
Viala, Sandrine;
Uhrhammer, Nancy;
Lepage, Mathis;
Cayre, Anne;
Bidet, Yannick;
Bignon, Yves-Jean;
Gay-Bellile, Mathilde;
Cavaillé, Mathias

Publication type:

Article

Prevalence of Constitutional Pathogenic Variant in a Cohort of 348 Patients With Multiple Primary Cancer Addressed in Oncogenetic Consultation.

Published in:

Molecular Genetics & Genomic Medicine, 2025, v. 13, n. 3, p. 1, doi. 10.1002/mgg3.70086

By:

Lepage, Mathis;
Uhrhammer, Nancy;
Molnar, Ioana;
Privat, Maud;
Ponelle‐Chachuat, Flora;
Gay‐Bellile, Mathilde;
Bidet, Yannick;
Cavaillé, Mathias

Publication type:

Article