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The CALHM1 P86L Polymorphism is a Genetic Modifier of Age at Onset in Alzheimer's Disease: a Meta-Analysis Study.
- Published in:
- Journal of Alzheimer's Disease, 2010, v. 22, n. 1, p. 247, doi. 10.3233/JAD-2010-100933
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- Article
Contribution of TARDBP to Alzheimer's Disease Genetic Etiology.
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- Journal of Alzheimer's Disease, 2010, v. 21, n. 2, p. 423, doi. 10.3233/JAD-2010-100198
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- Publication type:
- Article
Follow-Up Study of Susceptibility Loci for Alzheimer's Disease and Onset Age Identified by Genome-Wide Association.
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- Journal of Alzheimer's Disease, 2010, v. 19, n. 4, p. 1169, doi. 10.3233/JAD-2010-1310
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- Article
A Study of the SORL1 Gene in Alzheimer's Disease and Cognitive Function.
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- Journal of Alzheimer's Disease, 2009, v. 18, n. 1, p. 51, doi. 10.3233/JAD-2009-1137
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- Article
Plasma Proteomic Biomarkers Relating to Alzheimer's Disease: A Meta-Analysis Based on Our Own Studies.
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- Frontiers in Aging Neuroscience, 2021, v. 13, p. 1, doi. 10.3389/fnagi.2021.712545
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- Publication type:
- Article
sTREM2 cerebrospinal fluid levels are a potential biomarker for microglia activity in early-stage Alzheimer's disease and associate with neuronal injury markers.
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- EMBO Molecular Medicine, 2016, v. 8, n. 5, p. 466, doi. 10.15252/emmm.201506123
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- Article
Amyloid precursor protein mutation E682K at the alternative β-secretase cleavage β′-site increases Aβ generation.
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- EMBO Molecular Medicine, 2011, v. 3, n. 5, p. 291, doi. 10.1002/emmm.201100138
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- Article
The ABC's of Alzheimer risk gene ABCA7.
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- Alzheimer's & Dementia: The Journal of the Alzheimer's Association, 2024, v. 20, n. 5, p. 3629, doi. 10.1002/alz.13805
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- Article
Association of MGMT and BIN1 genes with Alzheimer's disease risk across sex and APOE ε4 status.
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- Alzheimer's & Dementia: The Journal of the Alzheimer's Association, 2024, v. 20, n. 3, p. 2282, doi. 10.1002/alz.13550
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- Article
Path integration deficits related to Alzheimer's disease pathology in clinically normal older adults.
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- Alzheimer's & Dementia: The Journal of the Alzheimer's Association, 2023, v. 19, p. 1, doi. 10.1002/alz.078924
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- Article
Single nucleotide polymorphisms linked to Alzheimer's disease are associated with distinct neuropathological phenotypes.
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- Alzheimer's & Dementia: The Journal of the Alzheimer's Association, 2023, v. 19, p. 1, doi. 10.1002/alz.078165
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- Article
Integration of Alzheimer's Disease GWAS with Molecular QTLs Reveals Prioritized Risk Genes and Disease‐associated Molecular Alterations.
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- Alzheimer's & Dementia: The Journal of the Alzheimer's Association, 2023, v. 19, p. 1, doi. 10.1002/alz.077870
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- Publication type:
- Article
Integration of Alzheimer's Disease GWAS with Molecular QTLs Reveals Prioritized Risk Genes and Disease‐associated Molecular Alterations.
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- Alzheimer's & Dementia: The Journal of the Alzheimer's Association, 2023, v. 19, p. 1, doi. 10.1002/alz.077870
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- Publication type:
- Article
Single nucleotide polymorphisms linked to Alzheimer's disease are associated with distinct neuropathological phenotypes.
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- Alzheimer's & Dementia: The Journal of the Alzheimer's Association, 2023, v. 19, p. 1, doi. 10.1002/alz.078165
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- Publication type:
- Article
Multiomics profiling of human plasma and cerebrospinal fluid reveals ATN‐derived networks and highlights causal links in Alzheimer's disease.
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- Alzheimer's & Dementia: The Journal of the Alzheimer's Association, 2023, v. 19, n. 8, p. 3350, doi. 10.1002/alz.12961
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- Article
IC‐P‐068: A POLYGENIC AD RISK SCORE PREDICTS AMYLOID ACCUMULATION OVER A 6‐YEAR INTERVAL IN COGNITIVELY INTACT OLDER ADULTS.
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- Alzheimer's & Dementia: The Journal of the Alzheimer's Association, 2023, v. 14, p. P61, doi. 10.1016/j.jalz.2018.06.2133
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- Publication type:
- Article
Functional Interpretation of Alzheimer's Disease Genetic Risk and Systematic Gene Prioritization.
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- Alzheimer's & Dementia: The Journal of the Alzheimer's Association, 2022, v. 18, n. 4, p. 1, doi. 10.1002/alz.069298
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- Publication type:
- Article
Genome‐wide association study on Alzheimer's disease CSF profiles in the EMIF‐AD MBD and ADNI datasets.
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- Alzheimer's & Dementia: The Journal of the Alzheimer's Association, 2022, v. 18, n. 4, p. 1, doi. 10.1002/alz.062091
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- Article
ABCA7‐reducing mutation carriers have reduced CSF amyloid biomarker levels, suggestive of increased amyloid deposition.
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- Alzheimer's & Dementia: The Journal of the Alzheimer's Association, 2022, v. 18, n. 3, p. 1, doi. 10.1002/alz.065722
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- Publication type:
- Article
Exome‐wide rare variant analysis of Alzheimer's disease biomarkers: The EMIF‐AD multimodal biomarker discovery study.
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- Alzheimer's & Dementia: The Journal of the Alzheimer's Association, 2021, v. 17, n. 3, p. 1, doi. 10.1002/alz.050410
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- Article
Replication study of plasma proteins relating to Alzheimer's pathology.
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- Alzheimer's & Dementia: The Journal of the Alzheimer's Association, 2021, v. 17, n. 9, p. 1452, doi. 10.1002/alz.12322
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- Article
Transcript analysis using long‐read sequencing reveals the complex splicing profile of AD‐associated gene ABCA7: Genetics: Genetics and omics of AD I.
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- Alzheimer's & Dementia: The Journal of the Alzheimer's Association, 2020, v. 16, n. 11, p. 1, doi. 10.1002/alz.042815
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- Article
ABCA7 mutations are major contributors to Alzheimer's disease in Belgian patients: Genetics/genetic factors of Alzheimer's disease.
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- Alzheimer's & Dementia: The Journal of the Alzheimer's Association, 2020, v. 16, n. 11, p. 1, doi. 10.1002/alz.040227
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- Article
O5‐07‐02: APOLIPOPROTEIN E AND BIN1 POLYMORPHISMS DIFFERENTIALLY AFFECT CORTICAL AMYLOID AND TAU LOAD IN HEALTHY OLDER ADULTS.
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- Alzheimer's & Dementia: The Journal of the Alzheimer's Association, 2019, v. 15, p. P1631, doi. 10.1016/j.jalz.2019.06.4871
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- Article
O5‐02‐03: ONSET AGE MODIFIER FOR GRN‐ASSOCIATED FRONTOTEMPORAL LOBAR DEGENERATION.
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- Alzheimer's & Dementia: The Journal of the Alzheimer's Association, 2019, v. 15, p. P1616, doi. 10.1016/j.jalz.2019.06.4842
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- Article
P4‐093: TOWARDS AN IMPROVED UNDERSTANDING AND ASSESSMENT OF ABCA7 RISK ON ALZHEIMER'S DISEASE.
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- Alzheimer's & Dementia: The Journal of the Alzheimer's Association, 2019, v. 15, p. P1310, doi. 10.1016/j.jalz.2019.06.3753
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- Article
O3‐13‐03: THE ROLE OF ZCWPW1 SUSCEPTIBILITY LOCUS RARE VARIANTS IN ALZHEIMER'S DISEASE.
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- Alzheimer's & Dementia: The Journal of the Alzheimer's Association, 2019, v. 15, p. P920, doi. 10.1016/j.jalz.2019.06.4698
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- Article
Cerebrospinal fluid biomarkers of neurodegeneration, synaptic integrity, and astroglial activation across the clinical Alzheimer's disease spectrum.
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- Alzheimer's & Dementia: The Journal of the Alzheimer's Association, 2019, v. 15, n. 5, p. 644, doi. 10.1016/j.jalz.2019.01.004
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- Publication type:
- Article
O4‐01‐01: IN‐DEPTH ANALYSIS OF AN ABCA7 VNTR IN ALZHEIMER'S DISEASE.
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- Alzheimer's & Dementia: The Journal of the Alzheimer's Association, 2018, v. 14, p. P1400, doi. 10.1016/j.jalz.2018.06.2909
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- Article
P3‐128: EXPLORING THE MOLECULAR MECHANISM OF NEURONAL HYPEREXCITABILITY IN DEMENTIA.
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- Alzheimer's & Dementia: The Journal of the Alzheimer's Association, 2018, v. 14, p. P1116, doi. 10.1016/j.jalz.2018.06.1485
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- Article
P3‐121: RARE FRAMESHIFT AND DIGENIC MUTATIONS CONTRIBUTE TO DISEASE ETIOLOGY IN BELGIAN ALZHEIMER AND FRONTOTEMPORAL DEMENTIA PATIENTS.
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- Alzheimer's & Dementia: The Journal of the Alzheimer's Association, 2018, v. 14, p. P1113, doi. 10.1016/j.jalz.2018.06.1478
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- Article
O3‐10‐03: A POLYGENIC AD RISK SCORE PREDICTS AMYLOID ACCUMULATION OVER A 6‐YEAR INTERVAL IN COGNITIVELY INTACT OLDER ADULTS.
- Published in:
- Alzheimer's & Dementia: The Journal of the Alzheimer's Association, 2018, v. 14, p. P1041, doi. 10.1016/j.jalz.2018.06.2827
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- Publication type:
- Article
S1‐02‐04: COMPLEX MUTATIONS IN ABCA7 MODIFY DISEASE PENETRANCE BY DOSAGE REDUCTION.
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- Alzheimer's & Dementia: The Journal of the Alzheimer's Association, 2018, v. 14, p. P199, doi. 10.1016/j.jalz.2018.06.2301
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- Publication type:
- Article
IC‐P‐068: A POLYGENIC AD RISK SCORE PREDICTS AMYLOID ACCUMULATION OVER A 6‐YEAR INTERVAL IN COGNITIVELY INTACT OLDER ADULTS.
- Published in:
- Alzheimer's & Dementia: The Journal of the Alzheimer's Association, 2018, v. 14, p. P61, doi. 10.1016/j.jalz.2018.06.2133
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- Publication type:
- Article
IPSC-Derived Neuronal Cultures Carrying the Alzheimer's Disease Associated TREM2 R47H Variant Enables the Construction of an Aβ-Induced Gene Regulatory Network.
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- International Journal of Molecular Sciences, 2020, v. 21, n. 12, p. 4516, doi. 10.3390/ijms21124516
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- Article
Amyloid-β<sub>1–43</sub> cerebrospinal fluid levels and the interpretation of APP, PSEN1 and PSEN2 mutations.
- Published in:
- Alzheimer's Research & Therapy, 2020, v. 12, n. 1, p. N.PAG, doi. 10.1186/s13195-020-00676-5
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- Publication type:
- Article
The EMIF-AD Multimodal Biomarker Discovery study: design, methods and cohort characteristics.
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- Alzheimer's Research & Therapy, 2018, v. 10, n. 1, p. N.PAG, doi. 10.1186/s13195-018-0396-5
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- Publication type:
- Article
TRANSCRIPTOME ANALYSIS IN BLOOD AND BRAIN IDENTIFIES GENE EXPRESSION REGULATION AND CORRESPONDING QUANTITATIVE TRAIT LOCI IN ALZHEIMER’S DISEASE.
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- Alzheimer's & Dementia: The Journal of the Alzheimer's Association, 2017, v. 13, p. P651, doi. 10.1016/j.jalz.2017.06.766
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- Publication type:
- Article
CONTRIBUTION OF RARE DELETERIOUS ABCA7 MUTATIONS TO A BELGIAN EARLY-ONSET ALZHEIMER’S DISEASE COHORT.
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- Alzheimer's & Dementia: The Journal of the Alzheimer's Association, 2017, v. 13, p. P573, doi. 10.1016/j.jalz.2017.07.191
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- Publication type:
- Article
DELETERIOUS ABCA7 MUTATIONS CONTRIBUTE TO EARLY-ONSET ALZHEIMER’S DISEASE AND ARE SUBJECT TO TRANSCRIPT RESCUE MECHANISMS.
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- Alzheimer's & Dementia: The Journal of the Alzheimer's Association, 2017, v. 13, p. P589, doi. 10.1016/j.jalz.2017.07.220
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- Publication type:
- Article
Molecular genetics of early-onset Alzheimer's disease revisited.
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- Alzheimer's & Dementia: The Journal of the Alzheimer's Association, 2016, v. 12, n. 6, p. 733, doi. 10.1016/j.jalz.2016.01.012
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- Article
C-terminal neurogranin is increased in cerebrospinal fluid but unchanged in plasma in Alzheimer's disease.
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- Alzheimer's & Dementia: The Journal of the Alzheimer's Association, 2015, v. 11, n. 12, p. 1461, doi. 10.1016/j.jalz.2015.05.012
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- Publication type:
- Article
A 22-single nucleotide polymorphism Alzheimer's disease risk score correlates with family history, onset age, and cerebrospinal fluid Aβ42.
- Published in:
- Alzheimer's & Dementia: The Journal of the Alzheimer's Association, 2015, v. 11, n. 12, p. 1452, doi. 10.1016/j.jalz.2015.02.013
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- Publication type:
- Article
The identification of high-penetrant loss-of-function mutations in abca7 in Alzheimer’s disease.
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- Alzheimer's & Dementia: The Journal of the Alzheimer's Association, 2015, v. 11, n. 7, p. P854, doi. 10.1016/j.jalz.2015.08.022
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- Publication type:
- Article
Targeted re-sequencing of sorl1 in early-onset Alzheimer’s dementia: The european early onset dementia consortium.
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- Alzheimer's & Dementia: The Journal of the Alzheimer's Association, 2015, v. 11, n. 7, p. P253, doi. 10.1016/j.jalz.2015.07.484
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- Publication type:
- Article
Development of novel elisas for the quantification of both pan-ApoE and ApoE4 proteins in CSF and blood, and ApoE ε4 phenotyping.
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- Alzheimer's & Dementia: The Journal of the Alzheimer's Association, 2015, v. 11, n. 7, p. P510, doi. 10.1016/j.jalz.2015.06.609
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- Publication type:
- Article
Rare variants in PLD3 do not increase risk in a belgian cohort of early-onset Alzheimer dementia patients.
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- Alzheimer's & Dementia: The Journal of the Alzheimer's Association, 2015, v. 11, n. 7, p. P626, doi. 10.1016/j.jalz.2015.06.883
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- Publication type:
- Article
Massive parallel gene panel sequencing in a belgian ftld cohort of causal genes associated with diverse neurodegenerative brain diseases.
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- Alzheimer's & Dementia: The Journal of the Alzheimer's Association, 2015, v. 11, n. 7, p. P251, doi. 10.1016/j.jalz.2015.07.311
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- Publication type:
- Article
Analysis of sqstm1 in patients with early-onset alzheimer's disease.
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- Alzheimer's & Dementia: The Journal of the Alzheimer's Association, 2014, v. 10, p. P135, doi. 10.1016/j.jalz.2014.04.077
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- Article
Genetic association and interaction of Alzheimer's risk genes CLU, CR1, BIN1, PICALM and MS4A in a Flanders-Belgian cohort
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- 2012
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- Abstract