Kari Majamaa

Professor

Oulu University Hospital

Finland

Research Interests

Explore related searches

Professors in Finland Professors in Medical Science Medical Science professors in Finland

Contact this professor

Get a free first email built on one of their papers, ready for you to edit and send yourself.

About

Kari Majamaa is a Professor at Oulu University Hospital in Finland. His research primarily focuses on genetic factors in neurological disorders, particularly mitochondrial DNA variants, Parkinson's disease, and hereditary ataxia. His recent articles explore the cognitive impairment associated with mitochondrial mutations and the molecular epidemiology of neurodegenerative diseases. He is actively involved in advancing the understanding of genetic contributions to these conditions.

Articles (10)

Year:

2025

Year:

2024

Year:

2023

Year:

2022

Year:

2021

Year:

2021

Year:

2021

Year:

2020

Year:

2020

Year:

2020

Collaborators (8)

Valtteri Kaasinen

Professor of Neurology

University of Turku

FINLAND

View details

Jussi Sipilä

University of Eastern Finland

FINLAND

View details

Sebastian R. Schreglmann

GERMANY

View details

Hiroshi Doi

Associate professor/M.D., Ph.D.

Yokohama National University

JAPAN

View details

Luis Bonet-Ponce

National Institutes of Health

UNITED STATES

View details

Jukka Moilanen

Oulu University Hospital

FINLAND

View details

Karri Kaivola

University of Helsinki

FINLAND

View details

Laura Kytövuori

FINLAND

View details

ApplyKite TwinLearns as you apply

Make your next move.

Prepare your application

Review drafts before you send them.

Kari Majamaa

Research Interests

Explore related searches

Contact this professor

About

Articles (10)

Cognitive impairment profile in patients with the m.3243A> G variant in mitochondrial DNA

Neurological manifestations in adult patients with the m.3243A>G variant in mitochondrial DNA

A severe neurodegenerative disease with Lewy bodies and a mutation in the glucocerebrosidase gene

Biallelic expansion in RFC1 as a rare cause of Parkinson’s disease

Molecular epidemiology of hereditary ataxia in Finland

Association of mitochondrial DNA haplogroups J and K with low response in exercise training among Finnish military conscripts.

Investigation of Autosomal Genetic Sex Differences in Parkinson's Disease.

Carriership of two copies of C9orf72 hexanucleotide repeat intermediate-length alleles is a risk factor for ALS in the Finnish population

Erratum: Genetic modifiers of risk and age at onset in GBA associated Parkinson's disease and Lewy body dementia (Brain (2020) 143 (234-48) DOI: 10.1093/brain/awz350)

Genetic modifiers of risk and age at onset in GBA associated Parkinson's disease and Lewy body dementia

Collaborators (8)

Valtteri Kaasinen

Jussi Sipilä

Sebastian R. Schreglmann

Hiroshi Doi

Luis Bonet-Ponce

Jukka Moilanen

Karri Kaivola

Laura Kytövuori

Make your next move.