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Laura Kytövuori

Oulu University Hospital
University of Oulu

20

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103

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Molecular epidemiology of hereditary ataxia in Finland

2021 BMC Neurology
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Association of mitochondrial DNA haplogroups J and K with low response in exercise training among Finnish military conscripts.

2021 BMC Genomics
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Mutation Analysis of the Genes Associated with Parkinson's Disease in a Finnish Cohort of Early-Onset Dementia.

2020 Journal of Alzheimer's Disease
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Mutation Analysis of the Genes Linked to Early Onset Alzheimer’s Disease and Frontotemporal Lobar Degeneration

2019 Journal of Alzheimer's Disease
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Finnish Parkinson's disease study integrating protein-protein interaction network data with exome sequencing analysis.

2019 Scientific Reports
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Finnish Parkinson's disease study integrating protein-protein interaction network data with exome sequencing analysis

2019
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Analysis of functional variants in mitochondrial DNA of Finnish athletes

2019 BMC Genomics
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Mitochondrial DNA variation in sudden cardiac death: a population-based study

2019 International Journal of Legal Medicine
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Mutation m.15923A>G in the MT-TT gene causes mild myopathy – case report of an adult-onset phenotype

2018 BMC Neurology
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Molecular Epidemiology of Charcot-Marie-Tooth Disease in Northern Ostrobothnia, Finland: A Population-Based Study

2017 Neuroepidemiology
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