Laura Kytövuori

ORCID

Publication Activity (10 Years)

Years Active: 2017-2023
Publications (10 Years): 8

Top Venues

European journal of neurology

NPJ Parkinson's disease

BMC neurology

Scientific reports

This page only lists publications with an associated author ORCID identifier.

Publications

Pauli Ylikotila, Jussi O T Sipilä, Tiina Alapirtti, Riitta Ahmasalo, Eriko Koshimizu, Satoko Miyatake, Anri Hurme-Niiranen, Ari Siitonen, Hiroshi Doi, Fumiaki Tanaka, Naomichi Matsumoto, Kari Majamaa, Laura Kytövuori
Association of biallelic RFC1 expansion with early-onset Parkinson's disease. European journal of neurology (2023)
Jussi O T Sipilä, Laura Kytövuori, Tuomas Rauramaa, Hugo Rauhamaa, Valtteri Kaasinen, Kari Majamaa
A severe neurodegenerative disease with Lewy bodies and a mutation in the glucocerebrosidase gene. NPJ Parkinson's disease 9 (1) (2023)
Pauli Ylikotila, Jussi O T Sipilä, Tiina Alapirtti, Riitta Ahmasalo, Eriko Koshimizu, Satoko Miyatake, Anri Hurme-Niiranen, Ari Siitonen, Hiroshi Doi, Fumiaki Tanaka, Naomichi Matsumoto, Kari Majamaa, Laura Kytövuori
Association of biallelic RFC1 expansion with early-onset Parkinson's disease. European journal of neurology (2023)
Laura Kytövuori, Jussi O T Sipilä, Hiroshi Doi, Anri Hurme-Niiranen, Ari Siitonen, Eriko Koshimizu, Satoko Miyatake, Naomichi Matsumoto, Fumiaki Tanaka, Kari Majamaa
Biallelic expansion in RFC1 as a rare cause of Parkinson's disease. NPJ Parkinson's disease 8 (1) (2022)
Laura Kytövuori, Juhani Junttila, Heikki Huikuri, Sirkka Keinänen-Kiukaanniemi, Kari Majamaa, Mika H Martikainen
Mitochondrial DNA variation in sudden cardiac death: a population-based study. International journal of legal medicine 134 (1) (2019)
Ari Siitonen, Laura Kytövuori, Mike A Nalls, Raphael Gibbs, Dena G Hernandez, Pauli Ylikotila, Markku Peltonen, Andrew B Singleton, Kari Majamaa
Finnish Parkinson's disease study integrating protein-protein interaction network data with exome sequencing analysis. Scientific reports 9 (1) (2019)
Mikko Kärppä, Laura Kytövuori, Markku Saari, Kari Majamaa
Mutation m.15923A>G in the MT-TT gene causes mild myopathy - case report of an adult-onset phenotype. BMC neurology 18 (1) (2018)
Laura Kytövuori, Mikko Kärppä, Hannu Tuominen, Johanna Uusimaa, Markku Saari, Reetta Hinttala, Kari Majamaa
Case report: a novel frameshift mutation in the mitochondrial cytochrome c oxidase II gene causing mitochondrial disorder. BMC neurology 17 (1) (2017)

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Publication Activity (10 Years)

Top Topics

Top Venues

Laura Kytövuori