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Laura Kytövuori

Observed names: Kytövuori, Laura, Laura Kytovuori
ORCID: 0000-0003-2790-5646
Observed ORCID: 0000-0003-2790-5646
OpenAlex ID: A5039512469
A novel mutation m.8561C>G in MT-ATP6/8 causing a mitochondrial syndrome with ataxia, peripheral neuropathy, diabetes mellitus, and hypergonadotropic hypogonadism
2016 · Laura Kytövuori, Joonas Lipponen, et al. · Journal of Neurology · 57
Biallelic expansion in RFC1 as a rare cause of Parkinson’s disease
2022 · Laura Kytövuori, Jussi Sipilä, et al. · npj Parkinson s Disease · 39
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Molecular Epidemiology of Charcot-Marie-Tooth Disease in Northern Ostrobothnia, Finland: A Population-Based Study
2017 · Maria Marttila, Laura Kytövuori, et al. · Neuroepidemiology · 29
Molecular epidemiology of hereditary ataxia in Finland
2021 · Joonas Lipponen, Seppo Helisalmi, et al. · BMC Neurology · 26
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Association of biallelic RFC1 expansion with early‐onset Parkinson's disease
2023 · Pauli Ylikotila, Jussi Sipilä, et al. · European Journal of Neurology · 24
Juvenile parkinsonism, hypogonadism and Leigh-like MRI changes in a patient with m.4296G>A mutation in mitochondrial DNA
2013 · Mika H. Martikainen, Laura Kytövuori, et al. · Mitochondrion · 23
Burden of Modifiable Risk Factors in Young-Onset Cryptogenic Ischemic Stroke by High-Risk Patent Foramen Ovale
2025 · Jukka Putaala, Nicolas Martinez-Majander, et al. · Stroke · 16
NDUFA1 p.Gly32Arg variant in early-onset dementia
2022 · Samuli Huttula, Henri Väyrynen, et al. · Neurobiology of Aging · 15
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A nonsynonymous mutation in the WFS1 gene in a Finnish family with age-related hearing impairment
2017 · Laura Kytövuori, Samuli Hannula, et al. · Hearing Research · 14
Finnish Parkinson’s disease study integrating protein-protein interaction network data with exome sequencing analysis
2019 · Ari Siitonen, Laura Kytövuori, et al. · Scientific Reports · 12
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Analysis of functional variants in mitochondrial DNA of Finnish athletes
2019 · Jukka Kiiskilä, Jukka S. Moilanen, et al. · BMC Genomics · 12
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Mitochondrial DNA variation in sudden cardiac death: a population-based study
2019 · Laura Kytövuori, Juhani Junttila, et al. · International Journal of Legal Medicine · 12
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WFS1 variants in Finnish patients with diabetes mellitus, sensorineural hearing impairment or optic atrophy, and in suicide victims
2013 · Laura Kytövuori, Allan Seppänen, et al. · Journal of Human Genetics · 12
Cognitive impairment is not uncommon in patients with biallelic RFC1 AAGGG repeat expansion, but the expansion is rare in patients with cognitive disease
2022 · Anita Korpioja, Johanna Krüger, et al. · Parkinsonism & Related Disorders · 11
Mutation Analysis of the Genes Linked to Early Onset Alzheimer’s Disease and Frontotemporal Lobar Degeneration
2019 · Laura Luukkainen, Seppo Helisalmi, et al. · Journal of Alzheimer s Disease · 11
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Association of mitochondrial DNA haplogroups J and K with low response in exercise training among Finnish military conscripts
2021 · Jukka Kiiskilä, Jari Jokelainen, et al. · BMC Genomics · 10
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WFS1 mutations in hearing-impaired children
2014 · Sanna Häkli, Laura Kytövuori, et al. · International Journal of Audiology · 10
Case report: a novel frameshift mutation in the mitochondrial cytochrome c oxidase II gene causing mitochondrial disorder
2017 · Laura Kytövuori, Mikko Kärppä, et al. · BMC Neurology · 9
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Mutation m.15923A>G in the MT-TT gene causes mild myopathy – case report of an adult-onset phenotype
2018 · Mikko Kärppä, Laura Kytövuori, et al. · BMC Neurology · 7
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The m.7510T>C mutation: Hearing impairment and a complex neurologic phenotype
2017 · Laura Kytövuori, Maria Gardberg, et al. · Brain and Behavior · 7
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Novel mitofusin 2 splice-site mutation causes Charcot–Marie–Tooth disease type 2 with prominent sensory dysfunction
2014 · Mika H. Martikainen, Laura Kytövuori, et al. · Neuromuscular Disorders · 6
FGF14 (GAA∙TTC) repeat expansion-related ataxia SCA27B is common in Northern Finland
2025 · Laura Kytövuori, David Pellerin, et al. · Parkinsonism & Related Disorders · 5
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Relative contribution of comorbid diseases to health-related quality of life in patients with Parkinson’s disease
2024 · Maija-Helena Keränen, Laura Kytövuori, et al. · Journal of Patient-Reported Outcomes · 5
A severe neurodegenerative disease with Lewy bodies and a mutation in the glucocerebrosidase gene
2023 · Jussi O. T. Sipilä, Laura Kytövuori, et al. · npj Parkinson s Disease · 4
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Clinical spectrum and genotype-phenotype associations in Finnish patients with Wilson's disease
2023 · Jussi O.T. Sipilä, Laura Kytövuori, et al. · Journal of the Neurological Sciences · 4
Works count: 60
Citation count: 387
H-index: 12
I10-index: 17
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