Seppo Helisalmi
P.O.Box 100, KYS
Kuopio, 70029, Finland
Kuopio, 70029, Finland
Last Updated: 09/26/2026
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Found 69 publications
Functional polymorphisms in pigmentation-related genes MC1R and DCT display population-specific association with wet age-related macular degeneration.
Journal: Biochemistry and biophysics reports
Published: April 17, 2025
Low prevalence of CWH43 variants among Finnish and Norwegian idiopathic normal pressure hydrocephalus patients: a cohort-based observational study.
Journal: Fluids and barriers of the CNS
Published: October 24, 2024
Author Correction: Common variants in Alzheimer's disease and risk stratification by polygenic risk scores.
Journal: Nature communications
Published: February 09, 2023
Late-onset and classic phenotypes of Fabry disease in males with the GLA-Thr410Ala mutation.
Journal: Open heart
Published: January 04, 2023
Serum total TDP-43 levels are decreased in frontotemporal dementia patients with C9orf72 repeat expansion or concomitant motoneuron disease phenotype.
Journal: Alzheimer's research & therapy
Published: June 10, 2022
Genome-wide meta-analysis for Alzheimer's disease cerebrospinal fluid biomarkers.
Journal: Acta neuropathologica
Published: February 16, 2022
New insights into the genetic etiology of Alzheimer's disease and related dementias.
Journal: Nature genetics
Published: June 16, 2021
Novel Rare SORL1 Variants in Early-Onset Dementia.
Journal: Journal of Alzheimer's disease : JAD
Published: June 07, 2021
NDUFA1 p.Gly32Arg variant in early-onset dementia.
Journal: Neurobiology of aging
Published: April 22, 2021
Molecular epidemiology of hereditary ataxia in Finland.
Journal: BMC neurology
Published: March 17, 2021
Last Updated: 09/26/2026