Morgane Miltgen

VarAFT: a variant annotation and filtration system for human next generation sequencing data

David Salgado, Christophe Béroud, Marc Bartoli, 2018, Nucleic Acids Res..

Novel heterozygous mutation in ANO3 responsible for craniocervical dystonia

Christophe Béroud, Arnaud Blanchard, Morgane Miltgen, 2016, Movement disorders : official journal of the Movement Disorder Society.

UMD‐Predictor: A High‐Throughput Sequencing Compliant System for Pathogenicity Prediction of any Human cDNA Substitution

Christophe Béroud, Arnaud Blanchard, Nicolas Lévy, 2016, Human mutation.