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Publications by Martin Krahn
Identification of Variants in the 4q35 GeneFAT1in Patients With a Facioscapulohumeral Dystrophy-Like Phenotype
Human Mutation
Genetics
A National French Consensus on Gene Lists for the Diagnosis of Myopathies Using Next-Generation Sequencing
European Journal of Human Genetics
Genetics
Calf Hypertrophy and Gastrocnemius MRI Short Tau Inversion Recovery (STIR) Hyperintensity in a Patient With Asymptomatic hyperCKemia Caused by Caveolin-3 Gene Mutation
Neuromuscular Disorders
Child Health
Neurology
Pediatrics
Perinatology
Genetics
Muscle Cells Fix Breaches by Orchestrating a Membrane Repair Ballet
Journal of Neuromuscular Diseases
Neurology
Exon 32 Skipping of Dysferlin Rescues Membrane Repair in Patients’ Cells
Journal of Neuromuscular Diseases
Neurology
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Recent Human Adaptation: Genomic Approaches, Interpretation and Insights
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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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