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The association between human blood clot analogue computed tomography imaging, composition, contraction, and mechanical characteristics

PloS one, 2023-11, Vol.18 (11), p.e0293456-e0293456

2023

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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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Contribution of Red Blood Cells and Platelets to Blood Clot Computed Tomography Imaging and Compressive Mechanical Characteristics

Annals of biomedical engineering, 2024-08, Vol.52 (8), p.2151-2161

2024

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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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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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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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Genetic contribution of FUS to frontotemporal lobar degeneration

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

2010

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Genetic variability in progranulin contributes to risk for clinically diagnosed Alzheimer disease

Neurology, 2008-08, Vol.71 (9), p.656

2008

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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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Clinical heterogeneity in 3 unrelated families linked to VCP p.Arg159His

Neurology, 2009-08, Vol.73 (8), p.626

2009

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Progranulin locus deletion in frontotemporal dementia

Human mutation, 2008, Vol.29 (1), p.53-58

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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APOE influences on neuropsychological function after mild head injury: within-person comparisons

Neurology, 2004-06, Vol.62 (11), p.1963

2004

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Prospective Belgian study of neurodegenerative and vascular dementia: APOE genotype effects

Journal of neurology, neurosurgery and psychiatry, 2003-08, Vol.74 (8), p.1148-1151

2003

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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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Loss of progranulin function in frontotemporal lobar degeneration

Trends in genetics, 2008-04, Vol.24 (4), p.186-194

2008

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Increased risk of dementia following mild head injury for carriers but not for non-carriers of the APOE ε4 allele

International psychogeriatrics, 2007-02, Vol.19 (1), p.159-165

2007

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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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Octapeptide repeat insertions in the prion protein gene and early onset dementia

Journal of neurology, neurosurgery and psychiatry, 2004-08, Vol.75 (8), p.1166-1170

2004

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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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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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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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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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novoSNP, a novel computational tool for sequence variation discovery

Genome research, 2005-03, Vol.15 (3), p.436

2005

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Cerebral amyloid angiopathy is a pathogenic lesion in Alzheimer's disease due to a novel presenilin 1 mutation

Brain (London, England : 1878), 2001-12, Vol.124 (12), p.2383-2392

2001

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The association between human blood clot analogue computed tomography imaging, composition, contraction, and mechanical characteristics

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

Contribution of Red Blood Cells and Platelets to Blood Clot Computed Tomography Imaging and Compressive Mechanical Characteristics

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

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

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

Genetic contribution of FUS to frontotemporal lobar degeneration

Genetic variability in progranulin contributes to risk for clinically diagnosed Alzheimer disease

Progranulin genetic variability contributes to amyotrophic lateral sclerosis

Clinical heterogeneity in 3 unrelated families linked to VCP p.Arg159His

Progranulin locus deletion in frontotemporal dementia

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

APOE influences on neuropsychological function after mild head injury: within-person comparisons

Prospective Belgian study of neurodegenerative and vascular dementia: APOE genotype effects

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

Loss of progranulin function in frontotemporal lobar degeneration

Increased risk of dementia following mild head injury for carriers but not for non-carriers of the APOE ε4 allele

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

Octapeptide repeat insertions in the prion protein gene and early onset dementia

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

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

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

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

novoSNP, a novel computational tool for sequence variation discovery

Cerebral amyloid angiopathy is a pathogenic lesion in Alzheimer's disease due to a novel presenilin 1 mutation

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