Martin Krahn

Phenotypic Study in 40 Patients With Dysferlin Gene Mutations

Karine Nguyen, Guillaume Bassez, Martin Krahn et al. · Archives of Neurology · 2007 · 265 citations

Medicine, Genetics, Molecular Genetics +15

Constitutive Activation of the Calcium Sensor STIM1 Causes Tubular-Aggregate Myopathy

Johann Böhm, Frédéric Chevessier, Catherine Koch et al. · The American Journal of Human Genetics · 2013 · 213 citations · Full text

Medicine, Biophysics, Neurology +12

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

Jean‐Pierre Desvignes, Marc Bartoli, Valérie Delague et al. · Nucleic Acids Research · 2018 · 196 citations · Full text

Life Sciences, Bioinformatics, Genetics +17

<i>CAPN3</i> mutations in patients with idiopathic eosinophilic myositis

Martin Krahn, Adolfo López de Munaín, Nathalie Streichenberger et al. · Annals of Neurology · 2006 · 121 citations

Life Sciences, Genetics, Pathology +15

Dysferlin mutations in LGMD2B, Miyoshi myopathy, and atypical dysferlinopathies

Karine Nguyen, Guillaume Bassez, Rafaëlle Bernard et al. · Human Mutation · 2005 · 118 citations · Full text

Medicine, Genetics, Molecular Genetics +17