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Ebba Lohmann

Affiliation : Pitié-Salpêtrière Hospital · Inserm

• 3Publications (affiliation in France)
• 170Total publications
• 9198Citations
• 42h-index

ORCIDOpenAlex

Research profile

Ebba Lohmann 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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Research areas

• Parkinson's Disease Mechanisms and Treatments
• Neurological disorders and treatments
• Dementia and Cognitive Impairment Research
• Alzheimer's disease research and treatments
• Nuclear Receptors and Signaling

Publications (3)

• The Val158Met COMT polymorphism is a modifier of the age at onset in Parkinson's disease with a sexual dimorphism
  2013 · Journal of Neurology Neurosurgery & Psychiatry · cited 43 times
• Parkinson's disease-related LRRK2 G2019S mutation results from independent mutational events in humans
  2010 · Human Molecular Genetics · cited 63 times
• G2019S LRRK2 mutation in French and North African families with Parkinson's disease
  2005 · Annals of Neurology · cited 212 times

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 : Institut du Cerveau · Centre National de la Recherche Scientifique · Université Pierre-et-Marie-Curie · Assistance Publique – Hôpitaux de Paris · Physiopathologie des Comportements

Co-authors’ countries : Germany

Co-authors

• Pierre Pollak
• Yves Agid
• Suzanne Lesage
• Alexis Brice
• Alexandra Dürr
• François Viallet
• François Tison
• Christiane Penet
• Anne‐Louise Leutenegger
• M. Borg
• M. Martinez
• A. Destée

Bibliographic data from OpenAlex (open database).