Publications by authors named "W Carre"

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Genetic analyses using chromosomal microarray and exome sequencing in fetuses and women with Müllerian duct anomalies.
Auriane Cospain, Paul Rollier, Anna Lokchine, Erika Launay, Ludivine Dion

J Assist Reprod Genet· December 2025

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SWS1-complex in premature ovarian insufficiency: SWSAP1 as a new POI gene.
Anna Lokchine, Fang Zhang, Laurence Cluzeau, Lorrie Le Page, Marc-Antoine Belaud-Rotureau

Hum Reprod· November 2025

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The Clinical and Genetic Landscape of a French Multicenter Cohort of 2563 Epilepsy Patients Referred for Genetic Diagnosis.
Jean-Madeleine de Sainte Agathe, Pauline Monin, Florence Riccardi, Caroline Nava, Lionel Arnaud, Wilfrid Carre

Eur J Neurol· August 2025

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Expanding the TUBB3-Related Phenotypic Landscape: Fetal Diagnosis of Novel TUBB3 Variant Linked With Phenotypic Variability Within a Single Family.
Abdelhakim Bouazzaoui, Chloé Quélin, Céline Rozel, Wilfrid Carré, Christèle Dubourg

Prenat Diagn· January 2025

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DISP1 deficiency: Monoallelic and biallelic variants cause a spectrum of midline craniofacial malformations.
Alinoë Lavillaureix, Paul Rollier, Artem Kim, Veranika Panasenkava, Marie De Tayrac

Genet Med· July 2024

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