Detalhe da pesquisa
1.
The shared ancestry between the C9orf72 hexanucleotide repeat expansion and intermediate-length alleles using haplotype sharing trees and HAPTK.
Am J Hum Genet
; 111(2): 383-392, 2024 Feb 01.
Artigo
Inglês
| MEDLINE | ID: mdl-38242117
2.
Genetic evaluation of dementia with Lewy bodies implicates distinct disease subgroups.
Brain
; 145(5): 1757-1762, 2022 06 03.
Artigo
Inglês
| MEDLINE | ID: mdl-35381062
3.
Primary age-related tauopathy in a Finnish population-based study of the oldest old (Vantaa 85+).
Neuropathol Appl Neurobiol
; 48(3): e12788, 2022 04.
Artigo
Inglês
| MEDLINE | ID: mdl-34927275
4.
Lewy-related pathology exhibits two anatomically and genetically distinct progression patterns: a population-based study of Finns aged 85.
Acta Neuropathol
; 138(5): 771-782, 2019 11.
Artigo
Inglês
| MEDLINE | ID: mdl-31494694
5.
Alpha-synuclein pathology of olfactory bulbs/peduncles in the Vantaa85+ cohort exhibit two divergent patterns: a population-based study.
Acta Neuropathol
; 142(4): 777-780, 2021 10.
Artigo
Inglês
| MEDLINE | ID: mdl-34468835
6.
Job-related exhaustion risk variant in UST is associated with dementia and DNA methylation.
Sci Rep
; 14(1): 13668, 2024 06 13.
Artigo
Inglês
| MEDLINE | ID: mdl-38871764
7.
Differential methylation analysis in neuropathologically confirmed dementia with Lewy bodies.
Commun Biol
; 7(1): 35, 2024 01 05.
Artigo
Inglês
| MEDLINE | ID: mdl-38182665
8.
Genome sequence analyses identify novel risk loci for multiple system atrophy.
Neuron
; 2024 Apr 24.
Artigo
Inglês
| MEDLINE | ID: mdl-38701790
9.
C9orf72 hexanucleotide repeat allele tagging SNPs: Associations with ALS risk and longevity.
Front Genet
; 14: 1087098, 2023.
Artigo
Inglês
| MEDLINE | ID: mdl-36936421
10.
Genome-wide structural variant analysis identifies risk loci for non-Alzheimer's dementias.
Cell Genom
; 3(6): 100316, 2023 Jun 14.
Artigo
Inglês
| MEDLINE | ID: mdl-37388914
11.
ALS in Finland: Major Genetic Variants and Clinical Characteristics of Patients With and Without the C9orf72 Hexanucleotide Repeat Expansion.
Neurol Genet
; 8(2): e665, 2022 Apr.
Artigo
Inglês
| MEDLINE | ID: mdl-35295181
12.
A Novel Genetic Marker for the C9orf72 Repeat Expansion in the Finnish Population.
J Alzheimers Dis
; 83(3): 1325-1332, 2021.
Artigo
Inglês
| MEDLINE | ID: mdl-34397416
13.
APOE ε4 associates with increased risk of severe COVID-19, cerebral microhaemorrhages and post-COVID mental fatigue: a Finnish biobank, autopsy and clinical study.
Acta Neuropathol Commun
; 9(1): 199, 2021 12 23.
Artigo
Inglês
| MEDLINE | ID: mdl-34949230
14.
Carriership of two copies of C9orf72 hexanucleotide repeat intermediate-length alleles is a risk factor for ALS in the Finnish population.
Acta Neuropathol Commun
; 8(1): 187, 2020 11 09.
Artigo
Inglês
| MEDLINE | ID: mdl-33168078
15.
Putative risk alleles for LATE-NC with hippocampal sclerosis in population-representative autopsy cohorts.
Brain Pathol
; 30(2): 364-372, 2020 03.
Artigo
Inglês
| MEDLINE | ID: mdl-31376286
16.
C9orf72 hexanucleotide repeat length in older population: normal variation and effects on cognition.
Neurobiol Aging
; 84: 242.e7-242.e12, 2019 12.
Artigo
Inglês
| MEDLINE | ID: mdl-30979436
17.
Oligogenic basis of sporadic ALS: The example of SOD1 p.Ala90Val mutation.
Neurol Genet
; 5(3): e335, 2019 Jun.
Artigo
Inglês
| MEDLINE | ID: mdl-31086828
18.
Alzheimer risk loci and associated neuropathology in a population-based study (Vantaa 85+).
Neurol Genet
; 4(1): e211, 2018 Feb.
Artigo
Inglês
| MEDLINE | ID: mdl-29379882
19.
Heterozygous TYROBP deletion (PLOSLFIN) is not a strong risk factor for cognitive impairment.
Neurobiol Aging
; 64: 159.e1-159.e4, 2018 04.
Artigo
Inglês
| MEDLINE | ID: mdl-29336840
20.
Melatonin receptor type 1A gene linked to Alzheimer's disease in old age.
Sleep
; 41(7)2018 07 01.
Artigo
Inglês
| MEDLINE | ID: mdl-29982836