Tim M. Strom
Helmholtz Zentrum München(DE)Technical University of Munich(DE)
Publications by Year
Research Areas
Mitochondrial Function and Pathology, Metabolism and Genetic Disorders, ATP Synthase and ATPases Research, Genetic Neurodegenerative Diseases, Ubiquitin and proteasome pathways
Most-Cited Works
- → A Mutation in VPS35, Encoding a Subunit of the Retromer Complex, Causes Late-Onset Parkinson Disease(2011)898 cited
- → Exome Sequence Reveals Mutations in CoA Synthase as a Cause of Neurodegeneration with Brain Iron Accumulation(2013)200 cited
- → Mutations in FBXL4, Encoding a Mitochondrial Protein, Cause Early-Onset Mitochondrial Encephalomyopathy(2013)177 cited
- → Haploinsufficiency of KMT2B, Encoding the Lysine-Specific Histone Methyltransferase 2B, Results in Early-Onset Generalized Dystonia(2016)169 cited
- → Mutations in GTPBP3 Cause a Mitochondrial Translation Defect Associated with Hypertrophic Cardiomyopathy, Lactic Acidosis, and Encephalopathy(2014)152 cited
- → CLPB Mutations Cause 3-Methylglutaconic Aciduria, Progressive Brain Atrophy, Intellectual Disability, Congenital Neutropenia, Cataracts, Movement Disorder(2015)135 cited
- → Biallelic Mutations in NBAS Cause Recurrent Acute Liver Failure with Onset in Infancy(2015)129 cited
- → Biallelic Mutations of Methionyl-tRNA Synthetase Cause a Specific Type of Pulmonary Alveolar Proteinosis Prevalent on Réunion Island(2015)124 cited
- → Absence of BiP Co-chaperone DNAJC3 Causes Diabetes Mellitus and Multisystemic Neurodegeneration(2014)112 cited
- → DHTKD1 Mutations Cause 2-Aminoadipic and 2-Oxoadipic Aciduria(2012)111 cited