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Severe acute neurotoxicity reflects absolute intra-carotid 1-methyl-4-phenyl-1,2,3,6-tetrahydropyridine dose in non-human primates

Journal of neuroscience methods, 2022-01, Vol.366, p.109406, Article 109406

2022

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Susceptible genes and disease mechanisms identified in frontotemporal dementia and frontotemporal dementia with Amyotrophic Lateral Sclerosis by DNA-methylation and GWAS

Scientific reports, 2017-08, Vol.7 (1), p.8899-16, Article 8899

2017

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Author Correction: Susceptible genes and disease mechanisms identified in frontotemporal dementia and frontotemporal dementia with Amyotrophic Lateral Sclerosis by DNA-methylation and GWAS

Scientific reports, 2018-05, Vol.8 (1), p.7789-5, Article 7789

2018

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EMF-3 Genetic Architecture of Human Ischemic Stroke

Annals of emergency medicine, 2014-10, Vol.64 (4), p.S143-S143

2014

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Multiancestry genome-wide association study of 520,000 subjects identifies 32 loci associated with stroke and stroke subtypes

Nature genetics, 2018-04, Vol.50 (4), p.524-537

2018

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Large‐scale proteome and metabolome analysis of CSF implicates altered glucose and carbon metabolism and succinylcarnitine in Alzheimer's disease

Alzheimer's & dementia, 2023-12, Vol.19 (12), p.5447-5470

2023

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Caspase-8, association with Alzheimer's Disease and functional analysis of rare variants

PloS one, 2017-10, Vol.12 (10), p.e0185777

2017

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Early Neurological Change After Ischemic Stroke Is Associated With 90-Day Outcome

Stroke (1970), 2021-01, Vol.52 (1), p.132-141

2021

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Genome-wide meta-analysis for Alzheimer’s disease cerebrospinal fluid biomarkers

Acta neuropathologica, 2022-11, Vol.144 (5), p.821-842

2022

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Potential genetic modifiers of disease risk and age at onset in patients with frontotemporal lobar degeneration and GRN mutations: a genome-wide association study

Lancet neurology, 2018-06, Vol.17 (6), p.548-558

2018

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Post‐GWAS multiomic functional investigation of the TNIP1 locus in Alzheimer's disease highlights a potential role for GPX3

Alzheimer's & dementia, 2024-07, Vol.20 (7), p.5044-5053

2024

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Genome-wide analyses as part of the international FTLD-TDP whole-genome sequencing consortium reveals novel disease risk factors and increases support for immune dysfunction in FTLD

Acta neuropathologica, 2019-06, Vol.137 (6), p.879-899

2019

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Single nucleotide variations in ZBTB46 are associated with post-thrombolytic parenchymal haematoma

Brain (London, England : 1878), 2021-09, Vol.144 (8), p.2416-2426

2021

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Contribution of Common Genetic Variants to Risk of Early-Onset Ischemic Stroke

Neurology, 2022-10, Vol.99 (16), p.e1738

2022

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Overlapping genetic architecture between Parkinson disease and melanoma

Acta neuropathologica, 2020-02, Vol.139 (2), p.347-364

2020

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Gene-based association studies report genetic links for clinical subtypes of frontotemporal dementia

Brain (London, England : 1878), 2017-05, Vol.140 (5), p.1437-1446

2017

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C9orf72 , age at onset, and ancestry help discriminate behavioral from language variants in FTLD cohorts

Neurology, 2020-12, Vol.95 (24), p.e3288

2020

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Genome-wide association study of rate of cognitive decline in Alzheimer's disease patients identifies novel genes and pathways: Alzheimers Dement

Alzheimer's & dementia, 2020, Vol.16 (8), p.1134-1145

2020

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Genetic variation across RNA metabolism and cell death gene networks is implicated in the semantic variant of primary progressive aphasia

Scientific reports, 2019-07, Vol.9 (1), p.10854-10, Article 10854

2019

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Correction to: A nonsynonymous mutation in PLCG2 reduces the risk of Alzheimer’s disease, dementia with Lewy bodies and frontotemporal dementia, and increases the likelihood of longevity

Acta neuropathologica, 2020-05, Vol.139 (5), p.959-962

2020

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Multiancestry genome-wide association study of 520,000 subjects identifies 32 loci associated with stroke and stroke subtypes: Nat Genet

Nature genetics, 2018, Vol.50 (4), p.524-537

2018

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RP11-362K2.2:RP11-767I20.1 Genetic Variation Is Associated with Post-Reperfusion Therapy Parenchymal Hematoma. A GWAS Meta-Analysis

Journal of clinical medicine, 2021-07, Vol.10 (14), p.3137

2021

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A rare mutation in UNC5C predisposes to Alzheimer’s disease and increases neuronal cell death

Nature medicine, 2014-11, Vol.20 (12), p.1452-1457

2014

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Numerical study of bifurcation blood flows using three different non-Newtonian constitutive models

Applied Mathematical Modelling, 2020-12, Vol.88, p.529-549

2020

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Severe acute neurotoxicity reflects absolute intra-carotid 1-methyl-4-phenyl-1,2,3,6-tetrahydropyridine dose in non-human primates

Susceptible genes and disease mechanisms identified in frontotemporal dementia and frontotemporal dementia with Amyotrophic Lateral Sclerosis by DNA-methylation and GWAS

Author Correction: Susceptible genes and disease mechanisms identified in frontotemporal dementia and frontotemporal dementia with Amyotrophic Lateral Sclerosis by DNA-methylation and GWAS

EMF-3 Genetic Architecture of Human Ischemic Stroke

Multiancestry genome-wide association study of 520,000 subjects identifies 32 loci associated with stroke and stroke subtypes

Large‐scale proteome and metabolome analysis of CSF implicates altered glucose and carbon metabolism and succinylcarnitine in Alzheimer's disease

Caspase-8, association with Alzheimer's Disease and functional analysis of rare variants

Early Neurological Change After Ischemic Stroke Is Associated With 90-Day Outcome

Genome-wide meta-analysis for Alzheimer’s disease cerebrospinal fluid biomarkers

Potential genetic modifiers of disease risk and age at onset in patients with frontotemporal lobar degeneration and GRN mutations: a genome-wide association study

Post‐GWAS multiomic functional investigation of the TNIP1 locus in Alzheimer's disease highlights a potential role for GPX3

Genome-wide analyses as part of the international FTLD-TDP whole-genome sequencing consortium reveals novel disease risk factors and increases support for immune dysfunction in FTLD

CSF proteomic profiles of neurodegeneration biomarkers in Alzheimer's disease

Single nucleotide variations in ZBTB46 are associated with post-thrombolytic parenchymal haematoma

Contribution of Common Genetic Variants to Risk of Early-Onset Ischemic Stroke

Overlapping genetic architecture between Parkinson disease and melanoma

Gene-based association studies report genetic links for clinical subtypes of frontotemporal dementia

C9orf72 , age at onset, and ancestry help discriminate behavioral from language variants in FTLD cohorts

Genome-wide association study of rate of cognitive decline in Alzheimer's disease patients identifies novel genes and pathways: Alzheimers Dement

Genetic variation across RNA metabolism and cell death gene networks is implicated in the semantic variant of primary progressive aphasia

Correction to: A nonsynonymous mutation in PLCG2 reduces the risk of Alzheimer’s disease, dementia with Lewy bodies and frontotemporal dementia, and increases the likelihood of longevity

Multiancestry genome-wide association study of 520,000 subjects identifies 32 loci associated with stroke and stroke subtypes: Nat Genet

RP11-362K2.2:RP11-767I20.1 Genetic Variation Is Associated with Post-Reperfusion Therapy Parenchymal Hematoma. A GWAS Meta-Analysis

A rare mutation in UNC5C predisposes to Alzheimer’s disease and increases neuronal cell death

Numerical study of bifurcation blood flows using three different non-Newtonian constitutive models

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