Lista de obras -

A 22-single nucleotide polymorphism Alzheimer's disease risk score correlates with family history, onset age, and cerebrospinal fluid Aβ42.

artículo científico publicado en 2015

A C9orf72 promoter repeat expansion in a Flanders-Belgian cohort with disorders of the frontotemporal lobar degeneration-amyotrophic lateral sclerosis spectrum: a gene identification study

artículo científico publicado en 2011

A comprehensive study of the genetic impact of rare variants in SORL1 in European early-onset Alzheimer's disease

artículo científico publicado en 2016

APP and BACE1 miRNA genetic variability has no major role in risk for Alzheimer disease.

artículo científico publicado en 2009

Both common variations and rare non-synonymous substitutions and small insertion/deletions in CLU are associated with increased Alzheimer risk

artículo científico publicado en 2012

C9orf72 G4C2 repeat expansions in Alzheimer's disease and mild cognitive impairment

artículo científico publicado en 2013

Common variants at ABCA7, MS4A6A/MS4A4E, EPHA1, CD33 and CD2AP are associated with Alzheimer's disease

artículo científico publicado en 2011

Common variation in GRB-associated Binding Protein 2 (GAB2) and increased risk for Alzheimer dementia

artículo científico publicado en 2009

Complement receptor 1 coding variant p.Ser1610Thr in Alzheimer's disease and related endophenotypes

artículo científico publicado en 2013

Contribution of TARDBP to Alzheimer's disease genetic etiology

artículo científico publicado en 2010

DNMBP is genetically associated with Alzheimer dementia in the Belgian population

artículo científico publicado en 2008

Erratum: Genome-wide association study identifies variants at CLU and PICALM associated with Alzheimer's disease

scholarly article published in Nature Genetics

Erratum: Genome-wide association study identifies variants at CLU and PICALM associated with Alzheimer's disease

article

Follow-up study of susceptibility loci for Alzheimer's disease and onset age identified by genome-wide association

artículo científico publicado en 2010

Gene-wide analysis detects two new susceptibility genes for Alzheimer's disease

artículo científico publicado en 2014

Genetic variability in SQSTM1 and risk of early-onset Alzheimer dementia: a European early-onset dementia consortium study

artículo científico publicado en 2015

Genome-wide association study identifies variants at CLU and PICALM associated with Alzheimer's disease

artículo científico publicado en 2009

Investigating the role of rare heterozygous TREM2 variants in Alzheimer's disease and frontotemporal dementia

artículo científico publicado en 2013

Meta-analysis of the association between variants in SORL1 and Alzheimer disease

artículo científico publicado en 2011

Mutations in ABCA7 in a Belgian cohort of Alzheimer's disease patients: a targeted resequencing study

artículo científico publicado en 2015

No association between CALHM1 and risk for Alzheimer dementia in a Belgian population

artículo científico publicado en 2009

Reduced secreted clusterin as a mechanism for Alzheimer-associated CLU mutations

artículo científico publicado en 2015

SORL1 is genetically associated with increased risk for late-onset Alzheimer disease in the Belgian population

artículo científico publicado en 2008

The CALHM1 P86L polymorphism is a genetic modifier of age at onset in Alzheimer's disease: a meta-analysis study

artículo científico publicado en 2010

Lista de obras de

A 22-single nucleotide polymorphism Alzheimer's disease risk score correlates with family history, onset age, and cerebrospinal fluid Aβ42.

A C9orf72 promoter repeat expansion in a Flanders-Belgian cohort with disorders of the frontotemporal lobar degeneration-amyotrophic lateral sclerosis spectrum: a gene identification study

A comprehensive study of the genetic impact of rare variants in SORL1 in European early-onset Alzheimer's disease

APP and BACE1 miRNA genetic variability has no major role in risk for Alzheimer disease.

Both common variations and rare non-synonymous substitutions and small insertion/deletions in CLU are associated with increased Alzheimer risk

C9orf72 G4C2 repeat expansions in Alzheimer's disease and mild cognitive impairment

Common variants at ABCA7, MS4A6A/MS4A4E, EPHA1, CD33 and CD2AP are associated with Alzheimer's disease

Common variation in GRB-associated Binding Protein 2 (GAB2) and increased risk for Alzheimer dementia

Complement receptor 1 coding variant p.Ser1610Thr in Alzheimer's disease and related endophenotypes

Contribution of TARDBP to Alzheimer's disease genetic etiology

DNMBP is genetically associated with Alzheimer dementia in the Belgian population

Erratum: Genome-wide association study identifies variants at CLU and PICALM associated with Alzheimer's disease

Erratum: Genome-wide association study identifies variants at CLU and PICALM associated with Alzheimer's disease

Follow-up study of susceptibility loci for Alzheimer's disease and onset age identified by genome-wide association

Gene-wide analysis detects two new susceptibility genes for Alzheimer's disease

Genetic variability in SQSTM1 and risk of early-onset Alzheimer dementia: a European early-onset dementia consortium study

Genome-wide association study identifies variants at CLU and PICALM associated with Alzheimer's disease

Investigating the role of rare heterozygous TREM2 variants in Alzheimer's disease and frontotemporal dementia

Meta-analysis of the association between variants in SORL1 and Alzheimer disease

Mutations in ABCA7 in a Belgian cohort of Alzheimer's disease patients: a targeted resequencing study

No association between CALHM1 and risk for Alzheimer dementia in a Belgian population

Reduced secreted clusterin as a mechanism for Alzheimer-associated CLU mutations

SORL1 is genetically associated with increased risk for late-onset Alzheimer disease in the Belgian population

The CALHM1 P86L polymorphism is a genetic modifier of age at onset in Alzheimer's disease: a meta-analysis study