Juliane Müller - Concepedia

Author

Juliane Müller

Also Known As

J MULLER, J Müller, J. Muller, J. Müller, J. S. Muller, J. S. Müller, J.S. Müller, Juliane Müller, Juliane S Müller, Juliane S. Müller

Publications

1.8K

Citations

H-Index

Concepts

All Affiliations

Newcastle University Friedrich Baur Stiftung Ludwig-Maximilians-Universität München University of Cambridge Wellcome Centre for Mitochondrial Research

About

Juliane Müller is an author at Newcastle University specializing in medicine, neuromuscular pathology, and developmental biology.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	10	10	683
2	Health Sciences	2	2	129
3	Natural Sciences	2	2	73
4	Humanities	1	1	16
5	Language Studies	1	1	16

Juliane Müller

Publications

1.7K

Citations

H-Index

Page 1

	Year	Citations
Hexosamine Biosynthetic Pathway Mutations Cause Neuromuscular Transmission Defect Jan Senderek, Juliane Müller, Marina Dusl, The American Journal of Human Genetics Neuromuscular JunctionMolecular NeuroscienceMedicineMolecular BiologyDegenerative Disease	2011	171
Isolation and characterization of Staufen-containing ribonucleoprotein particles from rat brain Massimo Mallardo, Anke Deitinghoff, Juliane Müller, Proceedings of the National Academy of Sciences	2003	163
EXOSC8 mutations alter mRNA metabolism and cause hypomyelination with spinal muscular atrophy and cerebellar hypoplasia Veronika Boczonadi, Juliane Müller, Angela Pyle, Nature Communications	2014	154
Escobar Syndrome Is a Prenatal Myasthenia Caused by Disruption of the Acetylcholine Receptor Fetal γ Subunit Katrin Hoffmann, Juliane Müller, Sigmar Stricker, The American Journal of Human Genetics Developmental BiologyPhysiologyEscobar SyndromePrenatal MyastheniaMedicine	2006	151
Agrin mutations lead to a congenital myasthenic syndrome with distal muscle weakness and atrophy Sophie Nicole, Amina Chaouch, T. Torbergsen, Brain Distal Muscle WeaknessMuscle FunctionAgrin MutationsOrthopaedic SurgeryKinesiology	2014	100
Congenital myasthenic syndrome with tubular aggregates caused by GFPT1 mutations Velina Guergueltcheva, Juliane Müller, Marina Dusl, Journal of Neurology Mendelian DisorderGenetic DisorderPathologyTubular AggregatesConnective Tissue Disease	2011	96
Mutations in the Mitochondrial Citrate Carrier SLC25A1 are Associated with Impaired Neuromuscular Transmission Amina Chaouch, Vito Porcelli, Simon Edvardson, Journal of Neuromuscular Diseases	2014	90
Variants in EXOSC9 Disrupt the RNA Exosome and Result in Cerebellar Atrophy with Spinal Motor Neuronopathy D T Burns, Sandra Donkervoort, Juliane Müller, The American Journal of Human Genetics	2018	89
Ephedrine therapy in eight patients with congenital myasthenic syndrome due to DOK7 mutations Ulrike Schara, Nina Barišić, Marcus Deschauer, Neuromuscular Disorders Dok7 MutationsEphedrine TherapyPediatricsCongenital Myasthenic SyndromeMedicine	2009	57
Long-term improvement of slow-channel congenital myasthenic syndrome with fluoxetine J. Colomer, Juliane Müller, Anna Vernet, Neuromuscular Disorders ChannelopathiesPediatricsDegenerative DiseaseLong-term ImprovementMedicine	2006	47

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