Author

Jürgen‐Christoph von Kleist-Retzow

Observed names: J. -Ch. von Kleist-Retzow, J. C. von Kleist-Retzow, J.-C. von Kleist-Retzow, J.C. von Kleist‐Retzow, JC von Kleist-Retzow, JC von Kleist‐Retzow, Jurgen-Christoph von Kleist-Retzow, Jurgen‐Christoph Von Kleist‐Retzow, JÜRGEN-CHRISTOPH VON KLEIST-RETZOW, Jürgen-Christoph Von Kleist-Retzow, Jürgen-Christoph von Kleist-Retzow, Jürgen-Christoph von Kleist-Retzow, Jürgen‐Christoph Von Kleist‐Retzow, Jürgen‐Christoph von Kleist‐Retzow, Von Kleist-Retzow, Jürgen-Christoph

Institutions: University of Cologne, University Hospital Cologne

Observed institutions: Hôpital Necker-Enfants Malades, Montreal Neurological Institute and Hospital, National Institutes of Health, Max Planck Society, Inserm, University of Cologne, The Royal Free Hospital, Centre Hospitalier Universitaire de Lille, Institut Necker Enfants Malades, Centre Hospitalier Universitaire Amiens-Picardie, Klinik und Poliklinik für Kinder- und Jugendmedizin, Hôpital Saint-Antoine, National Cancer Institute, Center for Cancer Research, University Hospital Cologne, Heinrich Heine University Düsseldorf, University College London, McGill University

ORCID: 0000-0002-1999-9673

Observed ORCID: 0000-0002-1999-9673

OpenAlex ID: A5081925177

Prohibitins control cell proliferation and apoptosis by regulating OPA1-dependent cristae morphogenesis in mitochondria

2008 · Carsten Merkwirth, Sascha Dargazanli, et al. · Genes & Development · 526

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Effect of idebenone on cardiomyopathy in Friedreich's ataxia: a preliminary study

1999 · Pierre Rustin, Jürgen-Christoph von Kleist-Retzow, et al. · The Lancet · 349

Inversion of the circadian rhythm of melatonin in the Smith-Magenis syndrome

2001 · Hélène De Leersnyder, Marie-Christine de Blois, et al. · The Journal of Pediatrics · 200

Antenatal manifestations of mitochondrial respiratory chain deficiency

2003 · Jürgen-Christoph von Kleist-Retzow, Valérie Cormier-Daire, et al. · The Journal of Pediatrics · 136

Targeted disruption of hepatic frataxin expression causes impaired mitochondrial function, decreased life span and tumor growth in mice

2005 · René Thierbach, Tim J. Schulz, et al. · Human Molecular Genetics · 127

Recessive TRAPPC11 Mutations Cause a Disease Spectrum of Limb Girdle Muscular Dystrophy and Myopathy with Movement Disorder and Intellectual Disability

2013 · Nina Bögershausen, Nassim Shahrzad, et al. · The American Journal of Human Genetics · 118

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Mosaic Deficiency in Mitochondrial Oxidative Metabolism Promotes Cardiac Arrhythmia during Aging

2015 · Olivier R. Baris, Stefan Ederer, et al. · Cell Metabolism · 87

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A High Rate (20%–30%) of Parental Consanguinity in Cytochrome-Oxidase Deficiency

1998 · Jürgen-Christoph von Kleist-Retzow, Valérie Cormier-Daire, et al. · The American Journal of Human Genetics · 82

Novel mutations in the NDUFS1 gene cause low residual activities in human complex I deficiencies

2010 · Saskia J.G. Hoefs, Ola H. Skjeldal, et al. · Molecular Genetics and Metabolism · 70

Acute liver failure with subsequent cirrhosis as the primary manifestation of TRMU mutations

2010 · Ulrike Schara, Jürgen‐Christoph von Kleist‐Retzow, et al. · Journal of Inherited Metabolic Disease · 69

Clinical pattern, mutations and in vitro residual activity in 33 patients with severe 5, 10 methylenetetrahydrofolate reductase (MTHFR) deficiency

2015 · Martina Huemer, Regina Mulder‐Bleile, et al. · Journal of Inherited Metabolic Disease · 67

Liver adapts mitochondrial function to insulin resistant and diabetic states in mice

2013 · Andras Franko, Jürgen-Christoph von Kleist-Retzow, et al. · Journal of Hepatology · 67

The neurogenic weakness, ataxia and retinitis pigmentosa (NARP) syndrome mtDNA mutation (T8993G) triggers muscle ATPase deficiency and hypocitrullinaemia

1999 · B. Parfait, P. de Lonlay, et al. · European Journal of Pediatrics · 57

Human Epidermal Keratinocytes Accumulate Superoxide Due to Low Activity of Mn-SOD, Leading to Mitochondrial Functional Impairment

2006 · Hue-Tran Hornig-Do, Jürgen-Christoph von Kleist-Retzow, et al. · Journal of Investigative Dermatology · 50

2010 · Georgia Vlahou, Marek Eliáš, et al. · European Journal of Cell Biology · 48

Integration of proteomics with genomics and transcriptomics increases the diagnostic rate of Mendelian disorders

2021 · Robert Kopajtich, Dmitrii Smirnov, et al. · medRxiv · 47

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Mutations in SURF1 are not specifically associated with Leigh syndrome

2001 · JÜRGEN-CHRISTOPH VON KLEIST-RETZOW, JIANBO YAO, et al. · Journal of Medical Genetics · 42

For debate: defective mitochondria, free radicals, cell death, aging-reality or myth-ochondria?

2000 · Pierre Rustin, Jurgen-Christoph von Kleist-Retzow, et al. · Mechanisms of Ageing and Development · 42

Cerebral white matter disease in children may be caused by mitochondrial respiratory chain deficiency

2000 · Pascale de Lonlay-Debeney, Jürgen-Christoph von Kleist-Retzow, et al. · The Journal of Pediatrics · 42

Negative regulation of mitochondrial transcription by mitochondrial topoisomerase I

2013 · Stefan Sobek, Ilaria Dalla Rosa, et al. · Nucleic Acids Research · 40

Restoration of complex V deficiency caused by a novel deletion in the human TMEM70 gene normalizes mitochondrial morphology

2011 · An I. Jonckheere, Merei Huigsloot, et al. · Mitochondrion · 40

Complete failure of insulin-transmitted signaling, but not obesity-induced insulin resistance, impairs respiratory chain function in muscle

2012 · A. Franko, J. C. von Kleist-Retzow, et al. · Journal of Molecular Medicine · 39

Whole-body high-field MRI shows no skeletal muscle degeneration in young patients with recessive myotonia congenita

2009 · C. Kornblum, G. G. Lutterbey, et al. · Acta Neurologica Scandinavica · 34

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Mitochondrial Diseases ‐ An Expanding Spectrum of Disorders and Affected Genes

2003 · Jürgen‐Christoph von Kleist‐Retzow, Ulrike Schauseil‐Zipf, et al. · Experimental Physiology · 31

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Biochemical, genetic and immunoblot analyses of 17 patients with an isolated cytochrome c oxidase deficiency

1999 · Jürgen-Christoph von Kleist-Retzow, Elodie Vial, et al. · Biochimica et Biophysica Acta (BBA) - Molecular Basis of Disease · 31

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Works count: 55

Citation count: 2,671

H-index: 27

I10-index: 35