Detalhe da pesquisa
1.
Family history aggregation unit-based tests to detect rare genetic variant associations with application to the Framingham Heart Study.
Am J Hum Genet
; 109(4): 738-749, 2022 04 07.
Artigo
em Inglês
| MEDLINE | ID: mdl-35316615
2.
Key variants via the Alzheimer's Disease Sequencing Project whole genome sequence data.
Alzheimers Dement
; 20(5): 3290-3304, 2024 May.
Artigo
em Inglês
| MEDLINE | ID: mdl-38511601
3.
Evaluation of population stratification adjustment using genome-wide or exonic variants.
Genet Epidemiol
; 44(7): 702-716, 2020 10.
Artigo
em Inglês
| MEDLINE | ID: mdl-32608112
4.
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.
Artigo
em Inglês
| MEDLINE | ID: mdl-34002480
5.
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
6.
Six Novel Loci Associated with Circulating VEGF Levels Identified by a Meta-analysis of Genome-Wide Association Studies.
PLoS Genet
; 12(2): e1005874, 2016 Feb.
Artigo
em Inglês
| MEDLINE | ID: mdl-26910538
7.
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
8.
Exome Chip Analysis Identifies Low-Frequency and Rare Variants in MRPL38 for White Matter Hyperintensities on Brain Magnetic Resonance Imaging.
Stroke
; 49(8): 1812-1819, 2018 08.
Artigo
em Inglês
| MEDLINE | ID: mdl-30002152
9.
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
10.
Evaluation of logistic regression models and effect of covariates for case-control study in RNA-Seq analysis.
BMC Bioinformatics
; 18(1): 91, 2017 Feb 06.
Artigo
em Inglês
| MEDLINE | ID: mdl-28166718
11.
Polygenic Overlap Between C-Reactive Protein, Plasma Lipids, and Alzheimer Disease.
Circulation
; 131(23): 2061-2069, 2015 Jun 09.
Artigo
em Inglês
| MEDLINE | ID: mdl-25862742
12.
Novel microRNA discovery using small RNA sequencing in post-mortem human brain.
BMC Genomics
; 17(1): 776, 2016 10 04.
Artigo
em Inglês
| MEDLINE | ID: mdl-27716130
13.
PLD3 variants in population studies.
Nature
; 520(7545): E2-3, 2015 Apr 02.
Artigo
em Inglês
| MEDLINE | ID: mdl-25832410
14.
Genome-wide linkage analyses of non-Hispanic white families identify novel loci for familial late-onset Alzheimer's disease.
Alzheimers Dement
; 12(1): 2-10, 2016 Jan.
Artigo
em Inglês
| MEDLINE | ID: mdl-26365416
15.
Genome-wide association study for circulating tissue plasminogen activator levels and functional follow-up implicates endothelial STXBP5 and STX2.
Arterioscler Thromb Vasc Biol
; 34(5): 1093-101, 2014 May.
Artigo
em Inglês
| MEDLINE | ID: mdl-24578379
16.
Comprehensive research synopsis and systematic meta-analyses in Parkinson's disease genetics: The PDGene database.
PLoS Genet
; 8(3): e1002548, 2012.
Artigo
em Inglês
| MEDLINE | ID: mdl-22438815
17.
Predicting stroke through genetic risk functions: the CHARGE Risk Score Project.
Stroke
; 45(2): 403-12, 2014 Feb.
Artigo
em Inglês
| MEDLINE | ID: mdl-24436238
18.
Ischemic stroke is associated with the ABO locus: the EuroCLOT study.
Ann Neurol
; 73(1): 16-31, 2013 Jan.
Artigo
em Inglês
| MEDLINE | ID: mdl-23381943
19.
Bone mineral density and the risk of incident dementia: A meta-analysis.
J Am Geriatr Soc
; 72(1): 194-200, 2024 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-37933827
20.
Frequency of Variants in Mendelian Alzheimer's Disease Genes within the Alzheimer's Disease Sequencing Project (ADSP).
medRxiv
; 2024 Mar 29.
Artigo
em Inglês
| MEDLINE | ID: mdl-37961373