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Pierre Pollak
Affiliation : Centre Hospitalier Universitaire de Grenoble
- 3Publications (affiliation in France)
- 460Total publications
- 44594Citations
- 97h-index
Research profile
Pierre Pollak has 3 indexed publications (2005–2013). Their work appears mainly in “Journal of Neurology Neurosurgery & Psychiatry”, “Human Molecular Genetics” and “Annals of Neurology”. Their most cited article, “G2019S LRRK2 mutation in French and North African families with Parkinson's disease” (2005), has been cited 212 times. Their work is co-authored with at least 12 researchers, including institutions in Germany.
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Create my free profile Add my publicationsResearch areas
- Neurological disorders and treatments
- Obsessive-Compulsive Spectrum Disorders
- Parkinson's Disease Mechanisms and Treatments
- Transcranial Magnetic Stimulation Studies
- Botulinum Toxin and Related Neurological Disorders
Publications (3)
- The Val158Met COMT polymorphism is a modifier of the age at onset in Parkinson's disease with a sexual dimorphism
- Parkinson's disease-related LRRK2 G2019S mutation results from independent mutational events in humans
- G2019S LRRK2 mutation in French and North African families with Parkinson's disease
Publication venues
- Journal of Neurology Neurosurgery & Psychiatry × 1
- Human Molecular Genetics × 1
- Annals of Neurology × 1
Publications per year
- 20131
- 20101
- 20051
Collaborations
Partner institutions : Pitié-Salpêtrière Hospital · Inserm · Institut du Cerveau · Centre National de la Recherche Scientifique · Université Pierre-et-Marie-Curie
Co-authors’ countries : Germany
Co-authors
- Yves Agid
- Suzanne Lesage
- Alexis Brice
- Alexandra Dürr
- Ebba Lohmann
- François Viallet
- François Tison
- Christiane Penet
- Anne‐Louise Leutenegger
- M. Borg
- M. Martinez
- A. Destée
Bibliographic data from OpenAlex (open database).
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