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APP duplication is sufficient to cause early onset Alzheimer's dementia with cerebral amyloid angiopathy

Brain (London, England : 1878), 2006-11, Vol.129 (11), p.2977-2983

2006

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Genetic risk and transcriptional variability of amyloid precursor protein in Alzheimer's disease

Brain (London, England : 1878), 2006-11, Vol.129 (11), p.2984-2991

2006

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Mutation of POLG is associated with progressive external ophthalmoplegia characterized by mtDNA deletions

Nature genetics, 2001-07, Vol.28 (3), p.211-212

2001

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Hot-spot residue in small heat-shock protein 22 causes distal motor neuropathy

Nature genetics, 2004-06, Vol.36 (6), p.597-601

2004

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Promoter Mutations That Increase Amyloid Precursor-Protein Expression Are Associated with Alzheimer Disease

American journal of human genetics, 2006-06, Vol.78 (6), p.936-946

2006

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Alzheimer-associated C allele of the promoter polymorphism −22C>T causes a critical neuron-specific decrease of presenilin 1 expression

Human molecular genetics, 2003-04, Vol.12 (8), p.869-877

2003

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α-Synuclein promoter confers susceptibility to Parkinson's disease

Annals of neurology, 2004-10, Vol.56 (4), p.591-595

2004

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Glucocorticoid Receptor Gene-Based SNP Analysis in Patients with Recurrent Major Depression

Neuropsychopharmacology (New York, N.Y.), 2006-03, Vol.31 (3), p.620-627

2006

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Mutations in SEPT9 cause hereditary neuralgic amyotrophy

Nature genetics, 2005-10, Vol.37 (10), p.1044-1046

2005

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The dopamine D4 receptor gene 48-base-pair-repeat polymorphism and mood disorders: A meta-analysis

Biological psychiatry (1969), 2005-05, Vol.57 (9), p.999-1003

2005

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GIGYF2 has no major role in Parkinson genetic etiology in a Belgian population

Neurobiology of aging, 2011-02, Vol.32 (2), p.308-312

2011

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Transcriptional regulation of Alzheimer's disease genes : implications for susceptibility

Human molecular genetics, 2000-10, Vol.9 (16), p.2383-2394

2000

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Linkage and Association Studies Identify a Novel Locus for Alzheimer Disease at 7q36 in a Dutch Population-Based Sample

American journal of human genetics, 2005-10, Vol.77 (4), p.643-652

2005

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Molecular genetics of Alzheimer's disease: An update

Annals of medicine (Helsinki), 2008, Vol.40 (8), p.562-583

2008

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Genetic variability in the regulatory region of presenilin 1 associated with risk for Alzheimer's disease and variable expression

Human molecular genetics, 2000-02, Vol.9 (3), p.325-331

2000

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Mutational analysis of the MPZ, PMP22 and Cx32 genes in patients of Spanish ancestry with Charcot-Marie-Tooth disease and hereditary neuropathy with liability to pressure palsies

Human genetics, 1997-06, Vol.99 (6), p.746-754

1997

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Genome-wide linkage of febrile seizures and epilepsy to the FEB4 locus at 5q14.3-q23.1 and no MASS1 mutation

Human genetics, 2006, Vol.118 (5), p.618-625

2006

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The pursuit of susceptibility genes for Alzheimer's disease: progress and prospects

Trends in genetics, 2010-02, Vol.26 (2), p.84-93

2010

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Cellular ageing, increased mortality and FTLD-TDP-associated neuropathology in progranulin knockout mice

The Journal of pathology, 2012-09, Vol.228 (1), p.67-76

2012

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The Gene Encoding Nicastrin, a Major γ-Secretase Component, Modifies Risk for Familial Early-Onset Alzheimer Disease in a Dutch Population-Based Sample

American journal of human genetics, 2002-06, Vol.70 (6), p.1568-1574

2002

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Diagnostic accuracy of the Preclinical AD Scale (PAS) in cognitively mildly impaired subjects

Journal of neurology, 2002-03, Vol.249 (3), p.312-319

2002

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Parametric and nonparametric genome scan analyses for human handedness

European journal of human genetics : EJHG, 2003-10, Vol.11 (10), p.779-783

2003

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Belgian Fabry Study: Prevalence of Fabry Disease in a Cohort of 1000 Young Patients With Cerebrovascular Disease

Stroke (1970), 2010-05, Vol.41 (5), p.863-868

2010

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Disruption of endocytic trafficking in frontotemporal dementia with CHMP2B mutations

Human molecular genetics, 2010-06, Vol.19 (11), p.2228-2238

2010

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APP duplication is sufficient to cause early onset Alzheimer's dementia with cerebral amyloid angiopathy

Genetic risk and transcriptional variability of amyloid precursor protein in Alzheimer's disease

Mutation of POLG is associated with progressive external ophthalmoplegia characterized by mtDNA deletions

Hot-spot residue in small heat-shock protein 22 causes distal motor neuropathy

Promoter Mutations That Increase Amyloid Precursor-Protein Expression Are Associated with Alzheimer Disease

Alzheimer-associated C allele of the promoter polymorphism −22C>T causes a critical neuron-specific decrease of presenilin 1 expression

α-Synuclein promoter confers susceptibility to Parkinson's disease

Glucocorticoid Receptor Gene-Based SNP Analysis in Patients with Recurrent Major Depression

Mutations in SEPT9 cause hereditary neuralgic amyotrophy

The dopamine D4 receptor gene 48-base-pair-repeat polymorphism and mood disorders: A meta-analysis

GIGYF2 has no major role in Parkinson genetic etiology in a Belgian population

Transcriptional regulation of Alzheimer's disease genes : implications for susceptibility

Linkage and Association Studies Identify a Novel Locus for Alzheimer Disease at 7q36 in a Dutch Population-Based Sample

Molecular genetics of Alzheimer's disease: An update

Genetic variability in the regulatory region of presenilin 1 associated with risk for Alzheimer's disease and variable expression

Null mutations in progranulin cause ubiquitin-positive frontotemporal dementia linked to chromosome 17q21

Mutational analysis of the MPZ, PMP22 and Cx32 genes in patients of Spanish ancestry with Charcot-Marie-Tooth disease and hereditary neuropathy with liability to pressure palsies

Genome-wide linkage of febrile seizures and epilepsy to the FEB4 locus at 5q14.3-q23.1 and no MASS1 mutation

The pursuit of susceptibility genes for Alzheimer's disease: progress and prospects

Cellular ageing, increased mortality and FTLD-TDP-associated neuropathology in progranulin knockout mice

The Gene Encoding Nicastrin, a Major γ-Secretase Component, Modifies Risk for Familial Early-Onset Alzheimer Disease in a Dutch Population-Based Sample

Diagnostic accuracy of the Preclinical AD Scale (PAS) in cognitively mildly impaired subjects

Parametric and nonparametric genome scan analyses for human handedness

Belgian Fabry Study: Prevalence of Fabry Disease in a Cohort of 1000 Young Patients With Cerebrovascular Disease

Disruption of endocytic trafficking in frontotemporal dementia with CHMP2B mutations

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