Detalles de la búsqueda
1.
Connecting dementia risk loci to the CSF proteome identifies pathophysiological leads for dementia.
Brain
; 2024 Mar 25.
Artículo
en Inglés
| MEDLINE | ID: mdl-38527854
2.
Genome-wide meta-analysis for Alzheimer's disease cerebrospinal fluid biomarkers.
Acta Neuropathol
; 144(5): 821-842, 2022 11.
Artículo
en Inglés
| MEDLINE | ID: mdl-36066633
3.
Amyloid-ß and APOE genotype predict memory decline in cognitively unimpaired older individuals independently of Alzheimer's disease polygenic risk score.
BMC Neurol
; 22(1): 484, 2022 Dec 15.
Artículo
en Inglés
| MEDLINE | ID: mdl-36522743
4.
Genome-wide association study identifies 74 loci associated with educational attainment.
Nature
; 533(7604): 539-42, 2016 05 26.
Artículo
en Inglés
| MEDLINE | ID: mdl-27225129
5.
Plasma amyloid ß levels are driven by genetic variants near APOE, BACE1, APP, PSEN2: A genome-wide association study in over 12,000 non-demented participants.
Alzheimers Dement
; 17(10): 1663-1674, 2021 10.
Artículo
en Inglés
| MEDLINE | ID: mdl-34002480
6.
The coarse-grained plaque: a divergent Aß plaque-type in early-onset Alzheimer's disease.
Acta Neuropathol
; 140(6): 811-830, 2020 12.
Artículo
en Inglés
| MEDLINE | ID: mdl-32926214
7.
PLCG2 protective variant p.P522R modulates tau pathology and disease progression in patients with mild cognitive impairment.
Acta Neuropathol
; 139(6): 1025-1044, 2020 06.
Artículo
en Inglés
| MEDLINE | ID: mdl-32166339
8.
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 Neuropathol
; 139(5): 959-962, 2020 05.
Artículo
en Inglés
| MEDLINE | ID: mdl-31955222
9.
Quality control and integration of genotypes from two calling pipelines for whole genome sequence data in the Alzheimer's disease sequencing project.
Genomics
; 111(4): 808-818, 2019 07.
Artículo
en Inglés
| MEDLINE | ID: mdl-29857119
10.
New insights into the genetics of primary open-angle glaucoma based on meta-analyses of intraocular pressure and optic disc characteristics.
Hum Mol Genet
; 26(2): 438-453, 2017 01 15.
Artículo
en Inglés
| MEDLINE | ID: mdl-28073927
11.
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 Neuropathol
; 138(2): 237-250, 2019 08.
Artículo
en Inglés
| MEDLINE | ID: mdl-31131421
12.
Rare Functional Variant in TM2D3 is Associated with Late-Onset Alzheimer's Disease.
PLoS Genet
; 12(10): e1006327, 2016 Oct.
Artículo
en Inglés
| MEDLINE | ID: mdl-27764101
13.
Association of MGMT and BIN1 genes with Alzheimer's disease risk across sex and APOE ε4 status.
Alzheimers Dement
; 20(3): 2282-2284, 2024 Mar.
Artículo
en Inglés
| MEDLINE | ID: mdl-38041824
14.
The Role of Age-Related Clonal Hematopoiesis in Genetic Sequencing Studies.
Am J Hum Genet
; 107(3): 575-576, 2020 09 03.
Artículo
en Inglés
| MEDLINE | ID: mdl-32888507
15.
Disentangling the biological pathways involved in early features of Alzheimer's disease in the Rotterdam Study.
Alzheimers Dement
; 14(7): 848-857, 2018 07.
Artículo
en Inglés
| MEDLINE | ID: mdl-29494809
16.
Association of branched-chain amino acids and other circulating metabolites with risk of incident dementia and Alzheimer's disease: A prospective study in eight cohorts.
Alzheimers Dement
; 14(6): 723-733, 2018 06.
Artículo
en Inglés
| MEDLINE | ID: mdl-29519576
17.
Circulating metabolites and general cognitive ability and dementia: Evidence from 11 cohort studies.
Alzheimers Dement
; 14(6): 707-722, 2018 06.
Artículo
en Inglés
| MEDLINE | ID: mdl-29316447
18.
Haplotype reference consortium panel: Practical implications of imputations with large reference panels.
Hum Mutat
; 38(8): 1025-1032, 2017 08.
Artículo
en Inglés
| MEDLINE | ID: mdl-28493391
19.
ARHGEF12 influences the risk of glaucoma by increasing intraocular pressure.
Hum Mol Genet
; 24(9): 2689-99, 2015 May 01.
Artículo
en Inglés
| MEDLINE | ID: mdl-25637523
20.
Gray matter heritability in family-based and population-based studies using voxel-based morphometry.
Hum Brain Mapp
; 38(5): 2408-2423, 2017 05.
Artículo
en Inglés
| MEDLINE | ID: mdl-28145022