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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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CXCR4 involvement in neurodegenerative diseases

Translational psychiatry, 2018-04, Vol.8 (1), p.73-10, Article 73

2018

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Genetic variation in the CHRNA5 gene affects mRNA levels and is associated with risk for alcohol dependence

Molecular psychiatry, 2009-05, Vol.14 (5), p.501-510

2009

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Suggestive synergy between genetic variants in TF and HFE as risk factors for Alzheimer's disease

American journal of medical genetics. Part B, Neuropsychiatric genetics, 2010-06, Vol.153B (4), p.955-959

2010

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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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Whole exome sequencing study identifies novel rare and common Alzheimer's-Associated variants involved in immune response and transcriptional regulation

Molecular psychiatry, 2020-08, Vol.25 (8), p.1859-1875

2020

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A novel Alzheimer disease locus located near the gene encoding tau protein

Molecular psychiatry, 2016-01, Vol.21 (1), p.108-117

2016

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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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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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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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Genetic architecture of sporadic frontotemporal dementia and overlap with Alzheimer's and Parkinson's diseases

Journal of neurology, neurosurgery and psychiatry, 2017-02, Vol.88 (2), p.152

2017

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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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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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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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Association of TMEM106B gene polymorphism with age at onset in granulin mutation carriers and plasma granulin protein levels

Archives of neurology (Chicago), 2011-05, Vol.68 (5), p.581

2011

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Protein network analysis reveals selectively vulnerable regions and biological processes in FTD

Neurology. Genetics, 2018-10, Vol.4 (5), p.e266-e266

2018

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Non-nucleoside Inhibitors of HIV-1 Reverse Transcriptase Inhibit Phosphorolysis and Resensitize the 3′-Azido-3′-deoxythymidine (AZT)-resistant Polymerase to AZT-5′-triphosphate

The Journal of biological chemistry, 2003-10, Vol.278 (43), p.42710-42716

2003

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Genomic atlas of the proteome from brain, CSF and plasma prioritizes proteins implicated in neurological disorders

Nature neuroscience, 2021-09, Vol.24 (9), p.1302

2021

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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

CXCR4 involvement in neurodegenerative diseases

Genetic variation in the CHRNA5 gene affects mRNA levels and is associated with risk for alcohol dependence

Suggestive synergy between genetic variants in TF and HFE as risk factors for Alzheimer's disease

The MS4A gene cluster is a key modulator of soluble TREM2 and Alzheimer's disease risk

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

Whole exome sequencing study identifies novel rare and common Alzheimer's-Associated variants involved in immune response and transcriptional regulation

A novel Alzheimer disease locus located near the gene encoding tau protein

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

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

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

Genetic architecture of sporadic frontotemporal dementia and overlap with Alzheimer's and Parkinson's diseases

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

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

Genetic Complexities of Cerebral Small Vessel Disease, Blood Pressure, and Dementia

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

Association of TMEM106B gene polymorphism with age at onset in granulin mutation carriers and plasma granulin protein levels

Single-subject grey matter network trajectories over the disease course of autosomal dominant Alzheimer’s disease

Protein network analysis reveals selectively vulnerable regions and biological processes in FTD

Non-nucleoside Inhibitors of HIV-1 Reverse Transcriptase Inhibit Phosphorolysis and Resensitize the 3′-Azido-3′-deoxythymidine (AZT)-resistant Polymerase to AZT-5′-triphosphate

Genomic atlas of the proteome from brain, CSF and plasma prioritizes proteins implicated in neurological disorders

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