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Pathogenesis of polyglutamine disorders: aggregation revisited

Human molecular genetics, 2003-10, Vol.12 (suppl-2), p.R173-R186

2003

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The role of tau (MAPT) in frontotemporal dementia and related tauopathies

Human mutation, 2004-10, Vol.24 (4), p.277-295

2004

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Progranulin genetic variability contributes to amyotrophic lateral sclerosis

Neurology, 2008-07, Vol.71 (4), p.253

2008

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Pathological mechanisms underlying TDP-43 driven neurodegeneration in FTLD-ALS spectrum disorders

Human molecular genetics, 2013-10, Vol.22 (R1), p.R77-R87

2013

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Genetics of personality: are we making progress?

Molecular psychiatry, 2003-10, Vol.8 (10), p.840-852

2003

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Lrrk2 R1441C parkinsonism is clinically similar to sporadic Parkinson disease

Neurology, 2008-04, Vol.70 (16 Pt 2), p.1456

2008

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The C9orf72 repeat size correlates with onset age of disease, DNA methylation and transcriptional downregulation of the promoter

Molecular psychiatry, 2016-08, Vol.21 (8), p.1112-1124

2016

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A major SNP haplotype of the arginine vasopressin 1B receptor protects against recurrent major depression

Molecular psychiatry, 2004-03, Vol.9 (3), p.287-292

2004

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EFNS guidelines for the molecular diagnosis of neurogenetic disorders: motoneuron, peripheral nerve and muscle disorders

European journal of neurology, 2011-02, Vol.18 (2), p.207-217

2011

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Granulin mutations associated with frontotemporal lobar degeneration and related disorders: An update

Human mutation, 2008-12, Vol.29 (12), p.1373-1386

2008

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Estimation of the Genetic Contribution of Presenilin-1 and -2 Mutations in a Population-Based Study of Presenile Alzheimer Disease

Human molecular genetics, 1998-01, Vol.7 (1), p.43-51

1998

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Variability of 5-HT2C receptor cys23ser polymorphism among European populations and vulnerability to affective disorder

Molecular psychiatry, 2001-09, Vol.6 (5), p.579-585

2001

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The association between APOE genotype and memory dysfunction in subjects with mild cognitive impairment is related to age and Alzheimer pathology

Dementia and geriatric cognitive disorders, 2008-01, Vol.26 (2), p.101

2008

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Alzheimer dementia caused by a novel mutation located in the APP C‐terminal intracytosolic fragment

Human mutation, 2006-09, Vol.27 (9), p.888-896

2006

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Tau (MAPT) mutation Arg406Trp presenting clinically with Alzheimer disease does not share a common founder in Western Europe

Human mutation, 2003-11, Vol.22 (5), p.409-411

2003

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Tau negative frontal lobe dementia at 17q21: significant finemapping of the candidate region to a 4.8 cM interval

Molecular psychiatry, 2002-01, Vol.7 (10), p.1064-1074

2002

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Genetic contribution of FUS to frontotemporal lobar degeneration

Neurology, 2010-02, Vol.74 (5), p.366

2010

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Alzheimer risk associated with a copy number variation in the complement receptor 1 increasing C3b C4b binding sites

Molecular psychiatry, 2012-02, Vol.17 (2), p.223-233

2012

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Chromosome 10q harbors a susceptibility locus for bipolar disorder in Ashkenazi Jewish families

Molecular psychiatry, 2008-04, Vol.13 (4), p.442-450

2008

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HTR2C (cys23ser) polymorphism influences early onset in bipolar patients in a large European multicenter association study

Molecular psychiatry, 2007-09, Vol.12 (9), p.797-798

2007

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Familial clustering and genetic risk for dementia in a genetically isolated Dutch population

Brain (London, England : 1878), 2004-07, Vol.127 (7), p.1641-1649

2004

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Degeneration of ingestion-related brainstem nuclei in spinocerebellar ataxia type 2, 3, 6 and 7

Neuropathology and applied neurobiology, 2006-12, Vol.32 (6), p.635-649

2006

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Progranulin variability has no major role in Parkinson disease genetic etiology

Neurology, 2008-10, Vol.71 (15), p.1147

2008

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De novo KCNQ2 mutations in patients with benign neonatal seizures

Neurology, 2004-12, Vol.63 (11), p.2155

2004

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Fatigue before and after mild traumatic brain injury: pre-post-injury comparisons in relation to Apolipoprotein E

Brain injury, 2007-01, Vol.21 (10), p.1049-1054

2007

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Pathogenesis of polyglutamine disorders: aggregation revisited

The role of tau (MAPT) in frontotemporal dementia and related tauopathies

Progranulin genetic variability contributes to amyotrophic lateral sclerosis

Pathological mechanisms underlying TDP-43 driven neurodegeneration in FTLD-ALS spectrum disorders

Genetics of personality: are we making progress?

Lrrk2 R1441C parkinsonism is clinically similar to sporadic Parkinson disease

The C9orf72 repeat size correlates with onset age of disease, DNA methylation and transcriptional downregulation of the promoter

A major SNP haplotype of the arginine vasopressin 1B receptor protects against recurrent major depression

EFNS guidelines for the molecular diagnosis of neurogenetic disorders: motoneuron, peripheral nerve and muscle disorders

Granulin mutations associated with frontotemporal lobar degeneration and related disorders: An update

Estimation of the Genetic Contribution of Presenilin-1 and -2 Mutations in a Population-Based Study of Presenile Alzheimer Disease

Variability of 5-HT2C receptor cys23ser polymorphism among European populations and vulnerability to affective disorder

The association between APOE genotype and memory dysfunction in subjects with mild cognitive impairment is related to age and Alzheimer pathology

Alzheimer dementia caused by a novel mutation located in the APP C‐terminal intracytosolic fragment

Tau (MAPT) mutation Arg406Trp presenting clinically with Alzheimer disease does not share a common founder in Western Europe

Tau negative frontal lobe dementia at 17q21: significant finemapping of the candidate region to a 4.8 cM interval

Genetic contribution of FUS to frontotemporal lobar degeneration

Alzheimer risk associated with a copy number variation in the complement receptor 1 increasing C3b C4b binding sites

Chromosome 10q harbors a susceptibility locus for bipolar disorder in Ashkenazi Jewish families

HTR2C (cys23ser) polymorphism influences early onset in bipolar patients in a large European multicenter association study

Familial clustering and genetic risk for dementia in a genetically isolated Dutch population

Degeneration of ingestion-related brainstem nuclei in spinocerebellar ataxia type 2, 3, 6 and 7

Progranulin variability has no major role in Parkinson disease genetic etiology

De novo KCNQ2 mutations in patients with benign neonatal seizures

Fatigue before and after mild traumatic brain injury: pre-post-injury comparisons in relation to Apolipoprotein E

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