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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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Structural variants identified by Oxford Nanopore PromethION sequencing of the human genome

Genome research, 2019-07, Vol.29 (7), p.1178-1187

2019

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NanoSatellite: accurate characterization of expanded tandem repeat length and sequence through whole genome long-read sequencing on PromethION

Genome Biology, 2019-11, Vol.20 (1), p.239-239, Article 239

2019

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CSF biomarker analysis of ABCA7 mutation carriers suggests altered APP processing and reduced inflammatory response

Alzheimer's research & therapy, 2023-11, Vol.15 (1), p.195-195, Article 195

2023

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Interactive medical and safety monitoring in clinical trials with clinDataReview: a validated and open-source reporting tool

Frontiers in medicine, 2024-07, Vol.11, p.1356323

2024

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Phenotypic characteristics of Alzheimer patients carrying an ABCA7 mutation

Neurology, 2016-06, Vol.86 (23), p.2126-2133

2016

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Amyloid-β1–43 cerebrospinal fluid levels and the interpretation of APP, PSEN1 and PSEN2 mutations

Alzheimer's research & therapy, 2020-09, Vol.12 (1), p.1-14, Article 108

2020

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[O2–13–05]: DELETERIOUS ABCA7 MUTATIONS CONTRIBUTE TO EARLY‐ONSET ALZHEIMER's DISEASE AND ARE SUBJECT TO TRANSCRIPT RESCUE MECHANISMS

Alzheimer's & dementia, 2017-07, Vol.13 (7S_Part_11), p.P589-P590

2017

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The role of ABCA7 in Alzheimer’s disease: evidence from genomics, transcriptomics and methylomics

Acta neuropathologica, 2019-08, Vol.138 (2), p.201-220

2019

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TOWARDS AN IMPROVED UNDERSTANDING AND ASSESSMENT OF ABCA7 RISK ON ALZHEIMER’S DISEASE

Alzheimer's & dementia, 2019-07, Vol.15 (7), p.P1310-P1310

2019

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P4‐093: TOWARDS AN IMPROVED UNDERSTANDING AND ASSESSMENT OF ABCA7 RISK ON ALZHEIMER'S DISEASE

Alzheimer's & dementia, 2019-07, Vol.15 (7S_Part_25), p.P1310-P1310

2019

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A 22-single nucleotide polymorphism Alzheimer's disease risk score correlates with family history, onset age, and cerebrospinal fluid Aβ42

Alzheimer's & dementia, 2015-12, Vol.11 (12), p.1452-1460

2015

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An intronic VNTR affects splicing of ABCA7 and increases risk of Alzheimer’s disease

Acta neuropathologica, 2018-06, Vol.135 (6), p.827-837

2018

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Deleterious ABCA7 mutations and transcript rescue mechanisms in early onset Alzheimer’s disease

Acta neuropathologica, 2017-09, Vol.134 (3), p.475-487

2017

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ABCA7 mutations are major contributors to Alzheimer’s disease in Belgian patients: Genetics/genetic factors of Alzheimer's disease

Alzheimer's & dementia, 2020-12, Vol.16 (S3)

2020

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ABCA7 mutations are major contributors to Alzheimer’s disease in Belgian patients

Alzheimer's & dementia, 2020-12, Vol.16, p.n/a

2020

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Transcript analysis using long‐read sequencing reveals the complex splicing profile of AD‐associated gene ABCA7: Genetics: Genetics and omics of AD I

Alzheimer's & dementia, 2020-12, Vol.16 (S3)

2020

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Transcript analysis using long‐read sequencing reveals the complex splicing profile of AD‐associated gene ABCA7

Alzheimer's & dementia, 2020-12, Vol.16, p.n/a

2020

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TRANSCRIPTOME ANALYSIS IN BLOOD AND BRAIN IDENTIFIES GENE EXPRESSION REGULATION AND CORRESPONDING QUANTITATIVE TRAIT LOCI IN ALZHEIMER’S DISEASE

Alzheimer's & dementia, 2017-07, Vol.13 (7), p.P651-P651

2017

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IN-DEPTH ANALYSIS OF AN ABCA7 VNTR IN ALZHEIMER’S DISEASE

Alzheimer's & dementia, 2018-07, Vol.14 (7), p.P1400-P1400

2018

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O4‐01‐01: IN‐DEPTH ANALYSIS OF AN ABCA7 VNTR IN ALZHEIMER'S DISEASE

Alzheimer's & dementia, 2018-07, Vol.14 (7S_Part_26), p.P1400-P1400

2018

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Amyloid-[beta]1-43 cerebrospinal fluid levels and the interpretation of APP, PSEN1 and PSEN2 mutations

Alzheimer's research & therapy, 2020-09, Vol.12 (1)

2020

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CONTRIBUTION OF RARE DELETERIOUS ABCA7 MUTATIONS TO A BELGIAN EARLY-ONSET ALZHEIMER’S DISEASE COHORT

Alzheimer's & dementia, 2017-07, Vol.13 (7), p.P573-P574

2017

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

Structural variants identified by Oxford Nanopore PromethION sequencing of the human genome

NanoSatellite: accurate characterization of expanded tandem repeat length and sequence through whole genome long-read sequencing on PromethION

CSF biomarker analysis of ABCA7 mutation carriers suggests altered APP processing and reduced inflammatory response

Interactive medical and safety monitoring in clinical trials with clinDataReview: a validated and open-source reporting tool

Phenotypic characteristics of Alzheimer patients carrying an ABCA7 mutation

Amyloid-β1–43 cerebrospinal fluid levels and the interpretation of APP, PSEN1 and PSEN2 mutations

[O2–13–05]: DELETERIOUS ABCA7 MUTATIONS CONTRIBUTE TO EARLY‐ONSET ALZHEIMER's DISEASE AND ARE SUBJECT TO TRANSCRIPT RESCUE MECHANISMS

The role of ABCA7 in Alzheimer’s disease: evidence from genomics, transcriptomics and methylomics

TOWARDS AN IMPROVED UNDERSTANDING AND ASSESSMENT OF ABCA7 RISK ON ALZHEIMER’S DISEASE

P4‐093: TOWARDS AN IMPROVED UNDERSTANDING AND ASSESSMENT OF ABCA7 RISK ON ALZHEIMER'S DISEASE

A 22-single nucleotide polymorphism Alzheimer's disease risk score correlates with family history, onset age, and cerebrospinal fluid Aβ42

An intronic VNTR affects splicing of ABCA7 and increases risk of Alzheimer’s disease

Loss of DPP6 in neurodegenerative dementia: a genetic player in the dysfunction of neuronal excitability

Deleterious ABCA7 mutations and transcript rescue mechanisms in early onset Alzheimer’s disease

ABCA7 mutations are major contributors to Alzheimer’s disease in Belgian patients: Genetics/genetic factors of Alzheimer's disease

ABCA7 mutations are major contributors to Alzheimer’s disease in Belgian patients

Transcript analysis using long‐read sequencing reveals the complex splicing profile of AD‐associated gene ABCA7: Genetics: Genetics and omics of AD I

Transcript analysis using long‐read sequencing reveals the complex splicing profile of AD‐associated gene ABCA7

TRANSCRIPTOME ANALYSIS IN BLOOD AND BRAIN IDENTIFIES GENE EXPRESSION REGULATION AND CORRESPONDING QUANTITATIVE TRAIT LOCI IN ALZHEIMER’S DISEASE

IN-DEPTH ANALYSIS OF AN ABCA7 VNTR IN ALZHEIMER’S DISEASE

O4‐01‐01: IN‐DEPTH ANALYSIS OF AN ABCA7 VNTR IN ALZHEIMER'S DISEASE

Clinicopathological contribution of rare deleterious ABCA7 mutations to early-onset Alzheimer disease (P6.101)

Amyloid-[beta]1-43 cerebrospinal fluid levels and the interpretation of APP, PSEN1 and PSEN2 mutations

CONTRIBUTION OF RARE DELETERIOUS ABCA7 MUTATIONS TO A BELGIAN EARLY-ONSET ALZHEIMER’S DISEASE COHORT

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