Peter De Jonghe

Analysis of shared heritability in common disorders of the brain

Verneri Anttila, Brendan Bulik‐Sullivan, Hilary K. Finucane et al. · Science · 2018 · 2K citations · Full text

Brain Function, Psychiatric Disorders, Genetics +23

Mutations in the mitochondrial GTPase mitofusin 2 cause Charcot-Marie-Tooth neuropathy type 2A

Stephan Züchner, Irina Mersiyanova, M. Muglia et al. · Nature Genetics · 2004 · 1.5K citations · Full text

Neurodegenerative Diseases, Molecular Neuroscience, Mitochondrial Function +9

De Novo Mutations in the Sodium-Channel Gene SCN1A Cause Severe Myoclonic Epilepsy of Infancy

Lieve Claes, Jurgen Del‐Favero, Berten Ceulemans et al. · The American Journal of Human Genetics · 2001 · 1.3K citations · Full text

Neurophysiology, Genetic Disorder, Genetics +8

DNA/RNA Helicase Gene Mutations in a Form of Juvenile Amyotrophic Lateral Sclerosis (ALS4)

Ying-Zhang Chen, Craig L. Bennett, Huy M. Huynh et al. · The American Journal of Human Genetics · 2004 · 810 citations · Full text

Neurodegenerative Diseases, Amyotrophic Lateral Sclerosis, Genetic Disorder +8

A C9orf72 promoter repeat expansion in a Flanders-Belgian cohort with disorders of the frontotemporal lobar degeneration-amyotrophic lateral sclerosis spectrum: a gene identification study

Ilse Gijselinck, Tim Van Langenhove, Julie van der Zee et al. · The Lancet Neurology · 2011 · 625 citations

Neurodegenerative Diseases, Amyotrophic Lateral Sclerosis, Genetic Disorder +12