Saara Finnilä
Oulu University Hospital(FI)University of Oulu(FI)
Publications by Year
Research Areas
Mitochondrial Function and Pathology, Metabolism and Genetic Disorders, Genomics and Phylogenetic Studies, RNA modifications and cancer, Cerebrovascular and genetic disorders
Most-Cited Works
- → Phylogenetic Network for European mtDNA(2001)360 cited
- → Phylogenetic Network of the mtDNA Haplogroup U in Northern Finland Based on Sequence Analysis of the Complete Coding Region by Conformation-Sensitive Gel Electrophoresis(2000)107 cited
- → Evidence for mtDNA Admixture between the Finns and the Saami(2001)83 cited
- → Mitochondrial DNA haplogroup U as a risk factor for occipital stroke in migraine(1998)74 cited
- → Hydrolethalus syndrome is caused by a missense mutation in a novel gene HYLS1(2005)71 cited
- → Molecular Epidemiology of Childhood Mitochondrial Encephalomyopathies in a Finnish Population: Sequence Analysis of Entire mtDNA of 17 Children Reveals Heteroplasmic Mutations in tRNAArg, tRNAGlu, and tRNALeu(UUR) Genes(2004)58 cited
- → Phylogenetic analysis of mitochondrial DNA in patients with an occipital stroke(2001)44 cited
- → Increase of collagen synthesis and deposition in the arachnoid and the dura following subarachnoid hemorrhage in the rat(1999)41 cited
- → A novel mitochondrial DNA mutation and a mutation in the Notch3 gene in a patient with myopathy and CADASIL(2001)39 cited
- → Adult‐onset ataxia and polyneuropathy caused by mitochondrial 8993T→C mutation(2005)39 cited