Juliane Müller

Hexosamine Biosynthetic Pathway Mutations Cause Neuromuscular Transmission Defect

Jan Senderek, Juliane Müller, Marina Dusl et al. · The American Journal of Human Genetics · 2011 · 173 citations · Full text

Medicine, Genetics, Neuroscience +10

Isolation and characterization of Staufen-containing ribonucleoprotein particles from rat brain

Massimo Mallardo, Anke Deitinghoff, Juliane Müller et al. · Proceedings of the National Academy of Sciences · 2003 · 165 citations

Life Sciences, Biochemistry, Molecular Biology +9

EXOSC8 mutations alter mRNA metabolism and cause hypomyelination with spinal muscular atrophy and cerebellar hypoplasia

Veronika Boczonadi, Juliane Müller, Angela Pyle et al. · Nature Communications · 2014 · 158 citations · Full text

Life Sciences, Genetics, Neuroscience +17

Escobar Syndrome Is a Prenatal Myasthenia Caused by Disruption of the Acetylcholine Receptor Fetal γ Subunit

Katrin Hoffmann, Juliane Müller, Sigmar Stricker et al. · The American Journal of Human Genetics · 2006 · 154 citations · Full text

Life Sciences, Genetics, Neuroscience +9

Agrin mutations lead to a congenital myasthenic syndrome with distal muscle weakness and atrophy

Sophie Nicole, Amina Chaouch, T. Torbergsen et al. · Brain · 2014 · 102 citations · Full text

Medicine, Genetics, Neurology +15