Alinoë Lavillaureix

5PUBLICATIONS
38CO-AUTHORS
NeurogeneticsGene expression (incl. microarray and other genome-wide approaches)Numerical modelling and mechanical characterisationDevelopmental genetics (incl. sex determination)
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Publications (5)

|Oct 23, 2023
Episignatures in practice: independent evaluation of published episignatures for the molecular diagnostics of ten neurodevelopmental disorders.

Thomas Husson, François Lecoquierre, Gaël Nicolas

|Jan 28, 2021
Skraban-Deardorff syndrome: Six new cases of WDR26-related disease and expansion of the clinical phenotype.

Auriane Cospain, Elise Schaefer, Marie Faoucher

|Aug 02, 2017
Mosaic intragenic deletion of FBN2 and severe congenital contractural arachnodactyly.

A Lavillaureix, S Heide, S Chantot-Bastaraud

|Jan 12, 2017
Reverse Pathway Genetic Approach Identifies Epistasis in Autism Spectrum Disorders.

Ileena Mitra, Alinoë Lavillaureix, Erika Yeh

|Nov 16, 2016
Pleiotropic Mechanisms Indicated for Sex Differences in Autism.

Ileena Mitra, Kathryn Tsang, Christine Ladd-Acosta

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