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Uwe Ahting

The Tom Core Complex
1999 · Uwe Ahting, Clemens Thun, et al. · The Journal of Cell Biology · 226
Regulatory myeloid cells paralyze T cells through cell–cell transfer of the metabolite methylglyoxal
2020 · Tobias Baumann, Andreas Dunkel, et al. · Nature Immunology · 225
Molecular diagnosis in mitochondrial complex I deficiency using exome sequencing
2012 · Tobias B Haack, Birgit Haberberger, et al. · Journal of Medical Genetics · 187
Tom40, the Pore-Forming Component of the Protein-Conducting Tom Channel in the Outer Membrane of Mitochondria
2001 · Uwe Ahting, Michel Thieffry, et al. · The Journal of Cell Biology · 181
Thiamine Pyrophosphokinase Deficiency in Encephalopathic Children with Defects in the Pyruvate Oxidation Pathway
2011 · Johannes A. Mayr, Peter Freisinger, et al. · The American Journal of Human Genetics · 124
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Spectrum of combined respiratory chain defects
2015 · Johannes A. Mayr, Tobias B. Haack, et al. · Journal of Inherited Metabolic Disease · 110
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COQ4 Mutations Cause a Broad Spectrum of Mitochondrial Disorders Associated with CoQ10 Deficiency
2015 · Gloria Brea-Calvo, Tobias B. Haack, et al. · The American Journal of Human Genetics · 110
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Sengers syndrome: six novel AGK mutations in seven new families and review of the phenotypic and mutational spectrum of 29 patients
2014 · Alireza Haghighi, Tobias B Haack, et al. · Orphanet Journal of Rare Diseases · 101
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Clinical, biochemical, and genetic spectrum of seven patients with NFU1 deficiency
2015 · Uwe Ahting, Johannes A. Mayr, et al. · Frontiers in Genetics · 97
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Impaired riboflavin transport due to missense mutations in SLC52A2 causes Brown‐Vialetto‐Van Laere syndrome
2012 · Tobias B. Haack, Christine Makowski, et al. · Journal of Inherited Metabolic Disease · 96
Clinical, biochemical and genetic spectrum of 70 patients with ACAD9 deficiency: is riboflavin supplementation effective?
2018 · Birgit M. Repp, Elisa Mastantuono, et al. · Orphanet Journal of Rare Diseases · 93
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Mutation screening of 75 candidate genes in 152 complex I deficiency cases identifies pathogenic variants in 16 genes including NDUFB9
2011 · Tobias B Haack, Florence Madignier, et al. · Journal of Medical Genetics · 93
Proteome analysis of mitochondrial outer membrane from Neurospora crassa
2005 · Simone Schmitt, Holger Prokisch, et al. · PROTEOMICS · 87
DJ‐1‐deficient mice show less TH‐positive neurons in the ventral tegmental area and exhibit non‐motoric behavioural impairments
2009 · T. T. Pham, F. Giesert, et al. · Genes Brain & Behavior · 85
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Signal-anchored Proteins Follow a Unique Insertion Pathway into the Outer Membrane of Mitochondria
2004 · Uwe Ahting, Thomas Waizenegger, et al. · Journal of Biological Chemistry · 85
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Dynamics of the TOM Complex of Mitochondria during Binding and Translocation of Preproteins
1998 · Doron Rapaport, Klaus-Peter Künkele, et al. · Molecular and Cellular Biology · 82
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Reconstituted TOM Core Complex and Tim9/Tim10 Complex of Mitochondria Are Sufficient for Translocation of the ADP/ATP Carrier across Membranes
2003 · Andreja Vasiljev, Uwe Ahting, et al. · Molecular Biology of the Cell · 80
Mitochondrial DNA mutation analysis from exome sequencing—A more holistic approach in diagnostics of suspected mitochondrial disease
2019 · Matias Wagner, Riccardo Berutti, et al. · Journal of Inherited Metabolic Disease · 78
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NAD(P)HX dehydratase (NAXD) deficiency: a novel neurodegenerative disorder exacerbated by febrile illnesses
2018 · Nicole J Van Bergen, Yiran Guo, et al. · Brain · 78
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Assessing Systems Properties of Yeast Mitochondria through an Interaction Map of the Organelle
2006 · Fabiana Perocchi, Lars J Jensen, et al. · PLoS Genetics · 76
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MitoP2: An Integrative Tool for the Analysis of the Mitochondrial Proteome
2008 · Matthias Elstner, Christophe Andreoli, et al. · Molecular Biotechnology · 69
Phenotypic spectrum of eleven patients and five novel MTFMT mutations identified by exome sequencing and candidate gene screening
2013 · Tobias B. Haack, Matteo Gorza, et al. · Molecular Genetics and Metabolism · 67
Role of Tom5 in Maintaining the Structural Stability of the TOM Complex of Mitochondria
2005 · Simone Schmitt, Uwe Ahting, et al. · Journal of Biological Chemistry · 65
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Biallelic variants in the transcription factor PAX7 are a new genetic cause of myopathy
2019 · René G. Feichtinger, Bettina E. Mucha, et al. · Genetics in Medicine · 40
Mutations in TTC19: expanding the molecular, clinical and biochemical phenotype
2015 · Johannes Koch, Peter Freisinger, et al. · Orphanet Journal of Rare Diseases · 37
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Works count: 83
Citation count: 2,937
H-index: 29
I10-index: 40
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