A. Destée

Affiliation : Centre Hospitalier Universitaire de Lille

3Publications (affiliation in France)
523Total publications
19324Citations
68h-index

Research profile

A. Destée has 3 indexed publications (2010–2016). Their work appears mainly in “The American Journal of Human Genetics” and “Human Molecular 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.

Is this you? Get your research seen

Create your free DzCademia profile and add your articles: they will show up more easily on Google and in AI assistants like ChatGPT, so more people can read and cite your work.

Create my free profile Add my publications

Research areas

Parkinson's Disease Mechanisms and Treatments
Neurological disorders and treatments
Dementia and Cognitive Impairment Research
Genetic Neurodegenerative Diseases
Balance, Gait, and Falls Prevention

Publications (3)

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
Translation Initiator EIF4G1 Mutations in Familial Parkinson Disease
2011 · The American Journal of Human Genetics · cited 298 times
Parkinson's disease-related LRRK2 G2019S mutation results from independent mutational events in humans
2010 · Human Molecular Genetics · cited 63 times

Publication venues

The American Journal of Human Genetics × 2
Human Molecular Genetics × 1

Publications per year

20161
20111
20101

Collaborations

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

Co-authors

Bibliographic data from OpenAlex (open database).