Detalhe da pesquisa
1.
An association test of the spatial distribution of rare missense variants within protein structures identifies Alzheimer's disease-related patterns.
Genome Res
; 32(4): 778-790, 2022 04.
Artigo
em Inglês
| MEDLINE | ID: mdl-35210353
2.
Sex-specific genetic architecture of late-life memory performance.
Alzheimers Dement
; 20(2): 1250-1267, 2024 Feb.
Artigo
em Inglês
| MEDLINE | ID: mdl-37984853
3.
Longitudinal change in memory performance as a strong endophenotype for Alzheimer's disease.
Alzheimers Dement
; 20(2): 1268-1283, 2024 Feb.
Artigo
em Inglês
| MEDLINE | ID: mdl-37985223
4.
Genetic heterogeneity: Challenges, impacts, and methods through an associative lens.
Genet Epidemiol
; 46(8): 555-571, 2022 12.
Artigo
em Inglês
| MEDLINE | ID: mdl-35924480
5.
Identification of novel genes for age-at-onset of Alzheimer's disease by combining quantitative and survival trait analyses.
Alzheimers Dement
; 19(7): 3148-3157, 2023 07.
Artigo
em Inglês
| MEDLINE | ID: mdl-36738287
6.
A haptoglobin (HP) structural variant alters the effect of APOE alleles on Alzheimer's disease.
Alzheimers Dement
; 19(11): 4886-4895, 2023 11.
Artigo
em Inglês
| MEDLINE | ID: mdl-37051669
7.
Admixture mapping identifies novel Alzheimer's disease risk regions in African Americans.
Alzheimers Dement
; 19(6): 2538-2548, 2023 06.
Artigo
em Inglês
| MEDLINE | ID: mdl-36539198
8.
One for all and all for One: Improving replication of genetic studies through network diffusion.
PLoS Genet
; 14(4): e1007306, 2018 04.
Artigo
em Inglês
| MEDLINE | ID: mdl-29684019
9.
Identification of seven novel loci associated with amino acid levels using single-variant and gene-based tests in 8545 Finnish men from the METSIM study.
Hum Mol Genet
; 27(9): 1664-1674, 2018 05 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-29481666
10.
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.
Artigo
em Inglês
| MEDLINE | ID: mdl-29857119
11.
Rare Functional Variant in TM2D3 is Associated with Late-Onset Alzheimer's Disease.
PLoS Genet
; 12(10): e1006327, 2016 Oct.
Artigo
em Inglês
| MEDLINE | ID: mdl-27764101
12.
Genetic Variation in Genes Underlying Diverse Dementias May Explain a Small Proportion of Cases in the Alzheimer's Disease Sequencing Project.
Dement Geriatr Cogn Disord
; 45(1-2): 1-17, 2018.
Artigo
em Inglês
| MEDLINE | ID: mdl-29486463
13.
Genome-wide association meta-analysis of neuropathologic features of Alzheimer's disease and related dementias.
PLoS Genet
; 10(9): e1004606, 2014 Sep.
Artigo
em Inglês
| MEDLINE | ID: mdl-25188341
14.
Systems biology approach to late-onset Alzheimer's disease genome-wide association study identifies novel candidate genes validated using brain expression data and Caenorhabditis elegans experiments.
Alzheimers Dement
; 13(10): 1133-1142, 2017 Oct.
Artigo
em Inglês
| MEDLINE | ID: mdl-28242297
15.
Transethnic genome-wide scan identifies novel Alzheimer's disease loci.
Alzheimers Dement
; 13(7): 727-738, 2017 Jul.
Artigo
em Inglês
| MEDLINE | ID: mdl-28183528
16.
Genomic variants, genes, and pathways of Alzheimer's disease: An overview.
Am J Med Genet B Neuropsychiatr Genet
; 174(1): 5-26, 2017 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-27943641
17.
SUCLG2 identified as both a determinator of CSF Aß1-42 levels and an attenuator of cognitive decline in Alzheimer's disease.
Hum Mol Genet
; 23(24): 6644-58, 2014 Dec 15.
Artigo
em Inglês
| MEDLINE | ID: mdl-25027320
18.
Global and local ancestry in African-Americans: Implications for Alzheimer's disease risk.
Alzheimers Dement
; 12(3): 233-43, 2016 Mar.
Artigo
em Inglês
| MEDLINE | ID: mdl-26092349
19.
Whole-exome sequencing links a variant in DHDDS to retinitis pigmentosa.
Am J Hum Genet
; 88(2): 201-6, 2011 Feb 11.
Artigo
em Inglês
| MEDLINE | ID: mdl-21295283
20.
Parkinsonism and distinct dementia patterns in a family with the MAPT R406W mutation.
Alzheimers Dement
; 10(3): 360-5, 2014 May.
Artigo
em Inglês
| MEDLINE | ID: mdl-23727082