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Genetic variations underlying Alzheimer's disease: evidence from genome-wide association studies and beyond

Lancet neurology, 2016-07, Vol.15 (8), p.857-868

2016

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Expression of ABCA7 in Alzheimer’s disease

Acta neuropathologica, 2020-05, Vol.139 (5), p.941-942

Sleegers, Kristel

2020

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Genetic insights in Alzheimer's disease

Lancet neurology, 2013, Vol.12 (1), p.92-104

2013

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Mutations in ABCA7 in a Belgian cohort of Alzheimer's disease patients: a targeted resequencing study

Lancet neurology, 2015-08, Vol.14 (8), p.814-822

2015

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Analysis of the Cerebrospinal Fluid Proteome in Alzheimer's Disease

PloS one, 2016-03, Vol.11 (3), p.e0150672-e0150672

2016

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Picalm reduction exacerbates tau pathology in a murine tauopathy model

Acta neuropathologica, 2020-04, Vol.139 (4), p.773-789

2020

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Mixed evidence for the relationship between periodontitis and Alzheimer's disease: A bidirectional Mendelian randomization study

PloS one, 2020-01, Vol.15 (1), p.e0228206-e0228206

2020

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Understanding Alzheimer Disease at the Interface between Genetics and Transcriptomics

Trends in genetics, 2018-06, Vol.34 (6), p.434-447

2018

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The Pareidolia Test: A Simple Neuropsychological Test Measuring Visual Hallucination-Like Illusions

PloS one, 2016-05, Vol.11 (5), p.e0154713-e0154713

2016

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Impact of high risk drug use on hospitalization and mortality in older people with and without Alzheimer's disease: a national population cohort study

PloS one, 2014-01, Vol.9 (1), p.e83224

2014

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C-terminal neurogranin is increased in cerebrospinal fluid but unchanged in plasma in Alzheimer's disease

Alzheimer's & dementia, 2015-12, Vol.11 (12), p.1461-1469

2015

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Non-melanoma skin cancer and risk of Alzheimer's disease and all-cause dementia

PloS one, 2017-02, Vol.12 (2), p.e0171527-e0171527

2017

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Serum proteins mediate depression's association with dementia

PloS one, 2017-06, Vol.12 (6), p.e0175790

2017

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Definition of a Threshold for the Plasma Aβ42/Aβ40 Ratio Measured by Single-Molecule Array to Predict the Amyloid Status of Individuals without Dementia

International journal of molecular sciences, 2024-01, Vol.25 (2), p.1173

2024

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Whole exome sequence-based association analyses of plasma amyloid-β in African and European Americans; the Atherosclerosis Risk in Communities-Neurocognitive Study

PloS one, 2017-07, Vol.12 (7), p.e0180046

2017

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Association of a body mass index genetic risk score with growth throughout childhood and adolescence

PloS one, 2013-11, Vol.8 (11), p.e79547-e79547

2013

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The impact of spinal cord nerve roots and denticulate ligaments on cerebrospinal fluid dynamics in the cervical spine

PloS one, 2014-04, Vol.9 (4), p.e91888-e91888

2014

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Few serum proteins mediate APOE's association with dementia

PloS one, 2017-03, Vol.12 (3), p.e0172268-e0172268

2017

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IPSC-Derived Neuronal Cultures Carrying the Alzheimer's Disease Associated TREM2 R47H Variant Enables the Construction of an Aβ-Induced Gene Regulatory Network

International journal of molecular sciences, 2020-06, Vol.21 (12), p.4516

2020

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Plasma Proteomic Biomarkers Relating to Alzheimer’s Disease: A Meta-Analysis Based on Our Own Studies

Frontiers in aging neuroscience, 2021-07, Vol.13, p.712545-712545

2021

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Integration of Alzheimer’s Disease GWAS with Molecular QTLs Reveals Prioritized Risk Genes and Disease‐associated Molecular Alterations

Alzheimer's & dementia, 2023-12, Vol.19 (S12), p.n/a

2023

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Predicting AT(N) pathologies in Alzheimer's disease from blood-based proteomic data using neural networks

Frontiers in aging neuroscience, 2022-11, Vol.14, p.1040001-1040001

2022

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Functional Interpretation of Alzheimer’s Disease Genetic Risk and Systematic Gene Prioritization

Alzheimer's & dementia, 2022-12, Vol.18 (S4), p.n/a

2022

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CMT-associated mutations in glycyl- and tyrosyl-tRNA synthetases exhibit similar pattern of toxicity and share common genetic modifiers in Drosophila

Neurobiology of disease, 2014-08, Vol.68, p.180-189

2014

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Genetic variations underlying Alzheimer's disease: evidence from genome-wide association studies and beyond

Expression of ABCA7 in Alzheimer’s disease

Genetic insights in Alzheimer's disease

Mutations in ABCA7 in a Belgian cohort of Alzheimer's disease patients: a targeted resequencing study

Analysis of the Cerebrospinal Fluid Proteome in Alzheimer's Disease

Picalm reduction exacerbates tau pathology in a murine tauopathy model

Mixed evidence for the relationship between periodontitis and Alzheimer's disease: A bidirectional Mendelian randomization study

Understanding Alzheimer Disease at the Interface between Genetics and Transcriptomics

The Pareidolia Test: A Simple Neuropsychological Test Measuring Visual Hallucination-Like Illusions

Impact of high risk drug use on hospitalization and mortality in older people with and without Alzheimer's disease: a national population cohort study

C-terminal neurogranin is increased in cerebrospinal fluid but unchanged in plasma in Alzheimer's disease

Non-melanoma skin cancer and risk of Alzheimer's disease and all-cause dementia

Serum proteins mediate depression's association with dementia

Definition of a Threshold for the Plasma Aβ42/Aβ40 Ratio Measured by Single-Molecule Array to Predict the Amyloid Status of Individuals without Dementia

Whole exome sequence-based association analyses of plasma amyloid-β in African and European Americans; the Atherosclerosis Risk in Communities-Neurocognitive Study

Association of a body mass index genetic risk score with growth throughout childhood and adolescence

The impact of spinal cord nerve roots and denticulate ligaments on cerebrospinal fluid dynamics in the cervical spine

Few serum proteins mediate APOE's association with dementia

ITPR2 as a susceptibility gene in sporadic amyotrophic lateral sclerosis: a genome-wide association study

IPSC-Derived Neuronal Cultures Carrying the Alzheimer's Disease Associated TREM2 R47H Variant Enables the Construction of an Aβ-Induced Gene Regulatory Network

Plasma Proteomic Biomarkers Relating to Alzheimer’s Disease: A Meta-Analysis Based on Our Own Studies

Integration of Alzheimer’s Disease GWAS with Molecular QTLs Reveals Prioritized Risk Genes and Disease‐associated Molecular Alterations

Predicting AT(N) pathologies in Alzheimer's disease from blood-based proteomic data using neural networks

Functional Interpretation of Alzheimer’s Disease Genetic Risk and Systematic Gene Prioritization

CMT-associated mutations in glycyl- and tyrosyl-tRNA synthetases exhibit similar pattern of toxicity and share common genetic modifiers in Drosophila

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