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Publications by Dalil Hamroun
The 2017 Version of the Gene Table of Monogenic Neuromuscular Disorders (Nuclear Genome)
Neuromuscular Disorders
Child Health
Neurology
Pediatrics
Perinatology
Genetics
Progrès Dans La Classification Clinique De La Dystrophie Myotonique De Type 1
Les Cahiers de Myologie
TheFBN2gene: New Mutations, Locus-Specific Database (Universal Mutation DatabaseFBN2), and Genotype-Phenotype Correlations
Human Mutation
Genetics
UMD-predictor, a New Prediction Tool for Nucleotide Substitution Pathogenicity-Application to Four Genes:FBN1,FBN2,TGFBR1, andTGFBR2
Human Mutation
Genetics
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ChIP–seq and Beyond: New and Improved Methodologies to Detect and Characterize Protein–DNA Interactions
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Sex and the Singular DM Domain: Insights Into Sexual Regulation, Evolution and Plasticity
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Putting Gene Essentiality Into Context
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Promoter-Proximal Pausing of RNA Polymerase II: Emerging Roles in Metazoans
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Stress and the Epigenetic Landscape: A Link to the Pathobiology of Human Diseases?
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Autoimmune Diseases — Connecting Risk Alleles With Molecular Traits of the Immune System
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Bayesian Molecular Clock Dating of Species Divergences in the Genomics Era
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