Dalil Hamroun

The 2019 version of the gene table of neuromuscular disorders (nuclear genome)

Gisèle Bonne, F. Rivier, D. Hamroun, 2018, Neuromuscular Disorders.

UMD‐predictor, a new prediction tool for nucleotide substitution pathogenicity—application to four genes: FBN1, FBN2, TGFBR1, and TGFBR2

Christophe Béroud, Catherine Boileau, Mireille Claustres, 2009, Human mutation.

UMD‐DYSF, a novel locus specific database for the compilation and interactive analysis of mutations in the dysferlin gene

Nilah Monnier, Pierre Cau, Nicolas Lévy, 2012, Human mutation.

Genotype–phenotype analysis in 2,405 patients with a dystrophinopathy using the UMD–DMD database: a model of nationwide knowledgebase

Christophe Béroud, Jamel Chelly, Mireille Claustres, 2009, Human mutation.

Rasch analysis of the motor function measure in patients with congenital muscle dystrophy and congenital myopathy

Allan M. Glanzman, Jean Iwaz, Carole Vuillerot, 2014 .

Multiexon skipping leading to an artificial DMD protein lacking amino acids from exons 45 through 55 could rescue up to 63% of patients with Duchenne muscular dystrophy

Christophe Béroud, Olivier Danos, Mireille Claustres, 2007, Human mutation.

UMD (Universal Mutation Database): 2005 update

Thierry Soussi, Christophe Béroud, Catherine Boileau, 2005, Human mutation.

Bioinformatics identification of splice site signals and prediction of mutation effects

Christophe Béroud, Mireille Claustres, C. Béroud, 2010 .