Lista de obras -

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

scientific article published on 24 October 2018

A hexanucleotide repeat expansion in C9ORF72 is the cause of chromosome 9p21-linked ALS-FTD

artículo científico publicado en 2011

APOE and AβPP gene variation in cortical and cerebrovascular amyloid-β pathology and Alzheimer's disease: a population-based analysis

artículo científico publicado en 2011

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

artículo científico publicado en 2018

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

artículo científico publicado en 2016

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

scientific article published on 29 January 2020

Chromosome 9 ALS and FTD locus is probably derived from a single founder

artículo científico publicado en 2011

Genome-wide Analyses Identify KIF5A as a Novel ALS Gene.

artículo científico publicado en 2018

Genome-wide association study of neocortical Lewy-related pathology

artículo científico publicado en 2015

Homozygosity analysis in amyotrophic lateral sclerosis

artículo científico publicado en 2013

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

artículo científico publicado en 2017

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

scientific article published on 07 September 2019

Matrix metalloproteinase–19 expressed in cerebral amyloid angiopathy ⬇️

artículo científico publicado el 25 de enero de 2011

Neurofibrillary tau pathology modulated by genetic variation of alpha-synuclein

artículo científico publicado en 2008

Neuropathologic features of four autopsied COVID-19 patients

scientific article published on 06 August 2020

Senile systemic amyloidosis affects 25% of the very aged and associates with genetic variation in alpha2-macroglobulin and tau: a population-based autopsy study

artículo científico publicado en 2008

Whole-exome sequencing of Finnish patients with vascular cognitive impairment

scientific article published on 02 December 2020

Lista de obras de

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

A hexanucleotide repeat expansion in C9ORF72 is the cause of chromosome 9p21-linked ALS-FTD

APOE and AβPP gene variation in cortical and cerebrovascular amyloid-β pathology and Alzheimer's disease: a population-based analysis

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

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

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

Chromosome 9 ALS and FTD locus is probably derived from a single founder

Genome-wide Analyses Identify KIF5A as a Novel ALS Gene.

Genome-wide association study of neocortical Lewy-related pathology

Homozygosity analysis in amyotrophic lateral sclerosis

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

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

Matrix metalloproteinase–19 expressed in cerebral amyloid angiopathy ⬇️

Neurofibrillary tau pathology modulated by genetic variation of alpha-synuclein

Neuropathologic features of four autopsied COVID-19 patients

Senile systemic amyloidosis affects 25% of the very aged and associates with genetic variation in alpha2-macroglobulin and tau: a population-based autopsy study

Whole-exome sequencing of Finnish patients with vascular cognitive impairment