Marie Vincent

25PUBLICATIONS

322CO-AUTHORS

Predictive and prognostic markersMolecular targetsEpigenetics (incl. genome methylation and epigenomics)Epidemiological methodsNeurology and neuromuscular diseases

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Publications (25)

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|Jun 12, 2026

A progeria syndrome links DNA hypermethylation to age-related pathology.

|May 18, 2026

Trametinib for multiple non-ossifying fibromas due to KRAS mosaic mutations: two case reports.

|Nov 21, 2025

9q34.11 Microduplications Encompassing SET Gene Are Associated With Neurodevelopmental Disorder and Recurrent Dysmorphisms.

Alessandro De Falco, Marie Vincent, Gaëlle Vieville

|Jul 23, 2025

The Arrival of Exome Sequencing in French Prenatal Diagnosis: An Exploratory Qualitative Study Among Professionals in Prenatal Diagnosis Centers: Prenatome-SHS.

Charlène Daval, Nicolas Meunier-Beillard, Eléonore Viora-Dupont

|May 16, 2025

Dominant variants in major spliceosome U4 and U5 small nuclear RNA genes cause neurodevelopmental disorders through splicing disruption.

Caroline Nava, Benjamin Cogne, Amandine Santini

|Apr 04, 2025

Reanalysis of unsolved prenatal exome sequencing for structural defects: diagnostic yield and contribution of postnatal/postmortem features.

Christel Thauvin-Robinet, Aurore Garde, Maud Favier

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Frequent Collaborators

7 joint publications

Anne-Sophie Denommé-Pichon

David Geneviève

Laurence Faivre

Smaïl Hadj-Rabia

Frédéric Tran-Mau-Them

Benjamin Cogne

Laurent Pasquier

Mathilde Nizon

Caroline Racine

Ange-Line Bruel

Frequent Collaborators

7 joint publications

Anne-Sophie Denommé-Pichon

6 joint publications

David Geneviève

6 joint publications

Laurence Faivre

5 joint publications

Smaïl Hadj-Rabia