Vedrana Milić Rašić

The TREAT-NMD DMD Global Database: Analysis of More than 7,000 Duchenne Muscular Dystrophy Mutations

Catherine L. Bladen, David Salgado, Soledad Monges et al. · Human Mutation · 2015 · 744 citations · Full text

Life Sciences, Genetics, Molecular Genetics +15

Clinical Outcomes in Duchenne Muscular Dystrophy: A Study of 5345 Patients from the TREAT-NMD DMD Global Database

Zaïda Koeks, Catherine L. Bladen, David Salgado et al. · Journal of Neuromuscular Diseases · 2017 · 182 citations · Full text

Medicine, Neurology, Clinical Epidemiology +4

Clinical and molecular genetic findings in COLQ-mutant congenital myasthenic syndromes

Violeta Mihaylova, Juliane S. Müller, Juan J. Vílchez et al. · Brain · 2008 · 160 citations · Full text

Life Sciences, Genetics, Molecular Genetics +17

Loss-of-function mutations in HINT1 cause axonal neuropathy with neuromyotonia

Jonathan Baets, Le­onardo Almeida-Souza, Els De Vriendt et al. · Nature Genetics · 2012 · 129 citations

Life Sciences, Neurology, Neuroscience +12

Truncating and Missense Mutations in IGHMBP2 Cause Charcot-Marie Tooth Disease Type 2

Ellen Cottenie, Andrzej Kochański, Albena Jordanova et al. · The American Journal of Human Genetics · 2014 · 110 citations · Full text

Life Sciences, Genetics, Molecular Genetics +14