Terkko Navigator / Myllykangas, L(iisa)*

Frequency of LATE neuropathologic change across the spectrum of Alzheimer's disease neuropathology: combined data from 13 community-based or population-based autopsy cohorts

Genetic analysis reveals novel variants for vascular cognitive impairment

APOEε4 associates with increased risk of severe COVID-19, cerebral microhaemorrhages and post-COVID mental fatigue: a Finnish biobank, autopsy and clinical study

Primary Age-Related Tauopathy (PART) in a Finnish Population-Based Study of the Oldest Old (Vantaa 85+)

Neuropathological evidence of body-first vs. brain-first Lewy body disease

<em>COL4A1</em> and <em>COL4A2</em> Duplication Causes Cerebral Small Vessel Disease With Recurrent Early Onset Ischemic Strokes

Alpha-synuclein pathology of olfactory bulbs/peduncles in the Vantaa85+ cohort exhibit two divergent patterns: a population-based study

Association of Variants in the SPTLC1 Gene With Juvenile Amyotrophic Lateral Sclerosis

PHACTR1 genetic variability is not critical in small vessel ischemic disease patients and PcomA recruitment in C57BL/6J mice

Genome sequencing analysis identifies new loci associated with Lewy body dementia and provides insights into its genetic architecture

Whole-exome sequencing of Finnish patients with vascular cognitive impairment

Neuropathologic features of four autopsied COVID-19 patients

Analysis of neurodegenerative disease-causing genes in dementia with Lewy bodies

Chorea-acanthocytosis associated with two novel heterozygous mutations in the VPS13A gene

Lewy-related pathology exhibits two anatomically and genetically distinct progression patterns: a population-based study of Finns aged 85

Putative risk alleles for LATE-NC with hippocampal sclerosis in population-representative autopsy cohorts

Causes of Death of Professional Musicians in the Classical Genre

Oligogenic basis of sporadic ALS: The example of <em>SOD1</em> p.Ala90Val mutation

C9orf72 hexanucleotide repeat length in older population: normal variation and effects on cognition

Heritability and genetic variance of dementia with Lewy bodies

Prediction models for dementia and neuropathology in the oldest old: the Vantaa 85+ cohort study

A comprehensive screening of copy number variability in dementia with Lewy bodies

Melatonin receptor type 1A gene linked to Alzheimer's disease in old age

Fatal Tick-Borne Encephalitis Virus Infections Caused by Siberian and European Subtypes, Finland, 2015

Hippocampal Sclerosis in the Oldest Old: A Finnish Population-Based Study

Genome-wide Analyses Identify KIF5A as a Novel ALS Gene

Genetics of dementia in a Finnish cohort

CAIDE Dementia Risk Score, Alzheimer and cerebrovascular pathology: a population-based autopsy study

Alzheimer risk loci and associated neuropathology in a population-based study (Vantaa 85+)

Heterozygous TYROBP deletion (PLOSL_FIN is not a strong risk factor for cognitive impairment

Investigating the genetic architecture of dementia with Lewy bodies: a two-stage genome-wide association study

"Genetic code" of brain ageing

Amygdalaα-Synuclein Pathology in the Population-Based Vantaa 85+ Study

Multi-infarct dementia of Swedish type is caused by a 3'UTR mutation of COL4A1

Population-based analysis of pathological correlates of dementia in the oldest old

SNCA mutation p.Ala53Glu is derived from a common founder in the Finnish population

A Novel Loss-of-Function GRN Mutation p.(Tyr229*): Clinical and Neuropathological Features

Primary familial brain calcification linked to deletion of 5' noncoding region of SLC20A2

Amyloid tracers binding sites in autosomal dominant and sporadic Alzheimer's disease

Analysis of C9orf72 repeat expansions in a large international cohort of dementia with Lewy bodies

A novel transthyretin Lys70Glu (p.Lys90Glu) mutation presenting with vitreous amyloidosis and carpal tunnel syndrome

Capillary amyloid-β protein deposition in a population-based study (Vantaa 85+)

Genome-wide association study of neocortical Lewy-related pathology

Intrafamilial clinical variability in individuals carrying the CHCHD10 mutation Gly66Val

CADASIL and CARASIL

Novelα-synuclein mutation A53E associated with atypical multiple system atrophy and Parkinson's disease-type pathology

Relationships between white matter hyperintensities, cerebral amyloid angiopathy and dementia in a population-based sample of the oldest old

Familial frontotemporal dementia associated with C9orf72 repeat expansion and dysplastic gangliocytoma

Plasma homocysteine, Alzheimer and cerebrovascular pathology: a population-based autopsy study

Homozygosity analysis in amyotrophic lateral sclerosis