Wolfram S. Kunz

University of Bonn

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Articles (15)

Collaborators (5)

Souvik Kar

Senior Scientist, Head Biobank

Andrea Perrelli

Postdoctoral fellowship

University of Rochester

UNITED STATES

Gábor Zsurka

University of Bonn

Saverio Francesco Retta

Full Professor of Applied Biology

University of Turin

Kerstin Becker

University of Cologne

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Wolfram S. Kunz

Research Interests

Explore related searches

Contact this professor

Articles (15)

Collaborators (5)

Souvik Kar

Andrea Perrelli

Gábor Zsurka

Saverio Francesco Retta

Kerstin Becker

Make your next move.

Wolfram S. Kunz

Research Interests

Explore related searches

Contact this professor

Articles (15)

Identification of galectin-3 as a novel potential prognostic/predictive biomarker and therapeutic target for cerebral cavernous malformation disease

The Fate of Oxidative Strand Breaks in Mitochondrial DNA

Loss of the Immunomodulatory Transcription Factor BATF2 in Humans Is Associated with a Neurological Phenotype

De Novo Variants in RAB11B Cause Various Degrees of Global Developmental Delay and Intellectual Disability in Children

Genome-wide identification and phenotypic characterization of seizure-associated copy number variations in 741,075 individuals

Secondary structure of the human mitochondrial genome affects formation of deletions

Selenium Ameliorated Oxidized Fish Oil-Induced Lipotoxicity <i>via</i> the Inhibition of Mitochondrial Oxidative Stress, Remodeling of Usp4-Mediated Deubiquitination, and Stabilization of Pparα

Testing for pharmacogenomic predictors of ppRNFL thinning in individuals exposed to vigabatrin

Novel Pathogenic Sequence Variation m.5789T>C Causes NARP Syndrome and Promotes Formation of Deletions of the Mitochondrial Genome

Lysine Reduction and Cognitive Outcomes in Pyridoxine-Dependent Epilepsy

Large Phenotypic Variation of Individuals from a Family with a Novel <i>ASPM</i> Mutation Associated with Microcephaly, Epilepsy, and Behavioral and Cognitive Deficits

A pharmacogenomic assessment of psychiatric adverse drug reactions to levetiracetam

Defective lipid signalling caused by mutations in PIK3C2B underlies focal epilepsy

Genetic causes of rare and common epilepsies: What should the epileptologist know?

Genetic testing before epilepsy surgery-An exploratory survey and case collection from German epilepsy centers

Collaborators (5)

Souvik Kar

Andrea Perrelli

Gábor Zsurka

Saverio Francesco Retta

Kerstin Becker

Make your next move.