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Peter De Jonghe
Researcher Next ID · RN-007778
Researcher · Neuroscience
Antwerp, Belgium
Not currently recruitingFunding unknown
- Works count
- 619
- Citation count
- 37,449
- H-index
- 102
- i10-index
- 312
Research interests
Neuroscience
Biochemistry, Genetics and Molecular Biology
Medicine
Hereditary Neurological Disorders
Genetic Neurodegenerative Diseases
Neurological diseases and metabolism
Genomics and Rare Diseases
Epilepsy research and treatment
Publications
Mutations in the mitochondrial GTPase mitofusin 2 cause Charcot-Marie-Tooth neuropathy type 2A
Nature Genetics · 2004 · https://doi.org/10.1038/ng1341
DNA/RNA Helicase Gene Mutations in a Form of Juvenile Amyotrophic Lateral Sclerosis (ALS4)
The American Journal of Human Genetics · 2004 · https://doi.org/10.1086/421054
De Novo Mutations in the Sodium-Channel Gene SCN1A Cause Severe Myoclonic Epilepsy of Infancy
The American Journal of Human Genetics · 2001 · https://doi.org/10.1086/320609
Current projects
No projects listed.