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Edor Kabashi

Affiliation : Inserm

2Publications (affiliation in France)
120Total publications
7445Citations
41h-index

Research profile

Edor Kabashi has 2 indexed publications (2013–2016). Their work appears in “The American Journal of Human Genetics”. Their most cited article, “Loss of VPS13C Function in Autosomal-Recessive Parkinsonism Causes Mitochondrial Dysfunction and Increases PINK1/Parkin-Dependent Mitophagy” (2016), has been cited 438 times. Their work is co-authored with at least 12 researchers.

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Research areas

Amyotrophic Lateral Sclerosis Research
Hereditary Neurological Disorders
Alzheimer's disease research and treatments
Genetic Neurodegenerative Diseases
Muscle Physiology and Disorders

Publications (2)

Loss of VPS13C Function in Autosomal-Recessive Parkinsonism Causes Mitochondrial Dysfunction and Increases PINK1/Parkin-Dependent Mitophagy
2016 · The American Journal of Human Genetics · cited 438 times
Loss of Function of Glucocerebrosidase GBA2 Is Responsible for Motor Neuron Defects in Hereditary Spastic Paraplegia
2013 · The American Journal of Human Genetics · cited 179 times

Publications per year

20161
20131

Collaborations

Partner institutions : Centre National de la Recherche Scientifique · Institut du Cerveau · Université Pierre-et-Marie-Curie · Sorbonne Université · Pitié-Salpêtrière Hospital

Co-authors

Bibliographic data from OpenAlex (open database).