Wolfram S. Kunz - Concepedia

Author

Wolfram S. Kunz

Also Known As

Albert J Becker, Ilona Krey, Ingo Helbig, Kunz, Wolfram S, Kunz, Wolfram S., Lucie Sedláčková, Maria Roberta Cilio, Norman Delanty, P KUNZ, P Kunz

419

Publications

19.3K

Citations

H-Index

216

Concepts

All Affiliations

University of Bonn Life & Brain (Germany)University Hospital Magdeburg University of Cologne Hertie Institute for Clinical Brain Research

About

Wolfram S. Kunz is an author at University of Bonn specializing in medicine, mitochondrial function, and physiology.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	48	97	9.2K
2	Natural Sciences	15	17	1.7K
3	Health Sciences	10	10	402
4	Public Health	6	6	2.2K
5	Engineering	1	1	27

Wolfram S. Kunz

179

Publications

14.5K

Citations

H-Index

Page 1

	Year	Citations
Analysis of shared heritability in common disorders of the brain Verneri Anttila, Brendan Bulik‐Sullivan, Hilary K. Finucane, Science Brain FunctionPsychiatric DisordersGeneticsGenetic EpidemiologyNeuropsychiatry	2018	2K
Analysis of mitochondrial function in situ in permeabilized muscle fibers, tissues and cells Andrey Kuznetsov, Vladimir Veksler, Frank N. Gellerich, Nature Protocols Mitochondrial MyopathyMitochondrial FunctionSkeletal MuscleBiomechanicsPhysiology	2008	780
Characterization of Superoxide-producing Sites in Isolated Brain Mitochondria Alexei P. Kudin, Nana Yaw-B. Bimpong-Buta, Stefan Vielhaber, Journal of Biological Chemistry	2004	504
Genome-wide mega-analysis identifies 16 loci and highlights diverse biological mechanisms in the common epilepsies Bassel Abou‐Khalil, Pauls Auce, Andreja Avberšek, Nature Communications Epilepsy TherapiesGeneticsGenetic EpidemiologyMolecular GeneticsMonogenic Epilepsy Genes	2018	493
Parkinson Phenotype in Aged PINK1-Deficient Mice Is Accompanied by Progressive Mitochondrial Dysfunction in Absence of Neurodegeneration Suzana Gispert, Filomena Ricciardi, Alexander Kurz, PLoS ONE	2009	369
Permeabilized cell and skinned fiber techniques in studies of mitochondrial function in vivo Valdur Saks, Vladimir Veksler, Laurence Kay, Tissue EngineeringRegenerative MedicineMitochondrial FunctionPhysiologyHuman Tissue	1998	360
Recombination of Human Mitochondrial DNA Yevgenya Kraytsberg, Marianne Schwartz, Timothy A. Brown, Science BiologyMaternal InheritanceGenome InstabilityDnaMitochondrial Biogenesis	2004	304
Ultra-Rare Genetic Variation in the Epilepsies: A Whole-Exome Sequencing Study of 17,606 Individuals Yen‐Chen Anne Feng, Daniel P. Howrigan, Liam Abbott, The American Journal of Human Genetics Allelic VariantUltra-rare Genetic VariationWhole-exome Sequencing StudyGeneticsGenetic Disorder	2019	298
Impairment of mitochondrial function in skeletal muscle of patients with amyotrophic lateral sclerosis Falk R. Wiedemann, Kirstin Winkler, Andrey V. Kuznetsov, Journal of the Neurological Sciences Mitochondrial MyopathyAmyotrophic Lateral SclerosisMotor DysfunctionMitochondrial FunctionSkeletal Muscle	1998	255
Mitochondrial complex I deficiency in the epileptic focus of patients with temporal lobe epilepsy Wolfram S. Kunz, Alexei P. Kudin, Stefan Vielhaber, Annals of Neurology NeuropsychologyMitochondrial DysfunctionNeurological DisorderTemporal Lobe EpilepsyClinical Neuroscience	2000	228

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