Wolfram S. Kunz

University of Bonn

Germany

This profile is automatically generated from trusted academic sources.

Google Scholar

.

ORCID

.

LinkedIn

Social connections

How do I reach out?

Sign in for free to see their profile details and contact information.

Meet Kite AI

Contact this professor

LinkedIn

Google Scholar

Research Interests

Biochemistry

30%

Neurology

80%

Medical Science

60%

Molecular Biology

20%

Neuropathology

20%

Mitochondrial Biology

20%

Pharmacometrics

20%

Ask ApplyKite AI

Start chatting

How can you help me contact this professor?

What are this professor's research interests?

How should I write an email to this professor?

Articles15

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

Year:

2024

The Fate of Oxidative Strand Breaks in Mitochondrial DNA

Year:

2023

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

Year:

2023

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

Year:

2023

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

Year:

2023

Secondary structure of the human mitochondrial genome affects formation of deletions

Year:

2023

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

Year:

2023

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

Year:

2023

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

Year:

2022

Lysine Reduction and Cognitive Outcomes in Pyridoxine-Dependent Epilepsy

Year:

2022

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

Year:

2022

A pharmacogenomic assessment of psychiatric adverse drug reactions to levetiracetam

Year:

2022

Defective lipid signalling caused by mutations in PIK3C2B underlies focal epilepsy

Year:

2022

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

Year:

2022

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

Year:

2022

Collaborators4

Souvik Kar

Senior Scientist, Head Biobank

-

GERMANY

Andrea Perrelli

Postdoctoral fellowship

University of Rochester

UNITED STATES

Gábor Zsurka

University of Bonn

GERMANY

Saverio Francesco Retta

Full Professor of Applied Biology

University of Turin

ITALY

Social connections

How do I reach out?

Sign in for free to see their profile details and contact information.

Meet Kite AI