Detalhe da pesquisa
1.
Exploring the genetic diversity of the Japanese population: Insights from a large-scale whole genome sequencing analysis.
PLoS Genet
; 19(12): e1010625, 2023 Dec.
Artigo
em Inglês
| MEDLINE | ID: mdl-38060463
2.
Natural Selection Signatures in the Hondo and Ryukyu Japanese Subpopulations.
Mol Biol Evol
; 40(10)2023 Oct 04.
Artigo
em Inglês
| MEDLINE | ID: mdl-37903429
3.
Molecular subtypes of lung adenocarcinoma present distinct immune tumor microenvironments.
Cancer Sci
; 2024 Mar 25.
Artigo
em Inglês
| MEDLINE | ID: mdl-38527308
4.
Identification of potential blood-based biomarkers for frailty by using an integrative approach.
Gerontology
; 2024 Mar 14.
Artigo
em Inglês
| MEDLINE | ID: mdl-38484720
5.
Whole-genome sequencing reveals novel ethnicity-specific rare variants associated with Alzheimer's disease.
Mol Psychiatry
; 27(5): 2554-2562, 2022 05.
Artigo
em Inglês
| MEDLINE | ID: mdl-35264725
6.
Early-onset Alzheimer Disease Associated With Neuromyelitis Optica Spectrum Disorder.
Alzheimer Dis Assoc Disord
; 37(1): 85-87, 2023.
Artigo
em Inglês
| MEDLINE | ID: mdl-35838179
7.
Trans-ethnic genomic informed risk assessment for Alzheimer's disease: An International Hundred K+ Cohorts Consortium study.
Alzheimers Dement
; 19(12): 5765-5772, 2023 Dec.
Artigo
em Inglês
| MEDLINE | ID: mdl-37450379
8.
A functional variant of SHARPIN confers increased risk of late-onset Alzheimer's disease.
J Hum Genet
; 67(4): 203-208, 2022 Apr.
Artigo
em Inglês
| MEDLINE | ID: mdl-34737388
9.
Network-based meta-analysis and the candidate gene association studies reveal novel ethnicity-specific variants in MFSD3 and MRPL43 associated with dementia with Lewy bodies.
Am J Med Genet B Neuropsychiatr Genet
; 189(5): 139-150, 2022 07.
Artigo
em Inglês
| MEDLINE | ID: mdl-35765761
10.
Structural and numerical Y chromosomal variations in elderly men identified through multiplex ligation-dependent probe amplification.
J Hum Genet
; 66(12): 1181-1184, 2021 Dec.
Artigo
em Inglês
| MEDLINE | ID: mdl-34108640
11.
Association of an IGHV3-66 gene variant with Kawasaki disease.
J Hum Genet
; 66(5): 475-489, 2021 May.
Artigo
em Inglês
| MEDLINE | ID: mdl-33106546
12.
A rare functional variant of SHARPIN attenuates the inflammatory response and associates with increased risk of late-onset Alzheimer's disease.
Mol Med
; 25(1): 20, 2019 06 20.
Artigo
em Inglês
| MEDLINE | ID: mdl-31216982
13.
CRISPR/Cas9-mediated knock-in cells of the late-onset Alzheimer's disease-risk variant, SHARPIN G186R, reveal reduced NF-κB pathway and accelerated Aß secretion.
J Hum Genet
; 69(5): 171-176, 2024 May.
Artigo
em Inglês
| MEDLINE | ID: mdl-38351238
14.
Molecular genetics of coronary artery disease.
J Hum Genet
; 61(1): 71-7, 2016 Jan.
Artigo
em Inglês
| MEDLINE | ID: mdl-26134515
15.
A functional SNP in FLT1 increases risk of coronary artery disease in a Japanese population.
J Hum Genet
; 61(5): 435-41, 2016 May.
Artigo
em Inglês
| MEDLINE | ID: mdl-26791355
16.
Integrating genetic, transcriptional, and functional analyses to identify 5 novel genes for atrial fibrillation.
Circulation
; 130(15): 1225-35, 2014 Oct 07.
Artigo
em Inglês
| MEDLINE | ID: mdl-25124494
17.
A functional SNP in PSMA6 confers risk of myocardial infarction in the Japanese population.
Nat Genet
; 38(8): 921-5, 2006 Aug.
Artigo
em Inglês
| MEDLINE | ID: mdl-16845397
18.
Renin-angiotensin-aldosterone system polymorphisms and 5-year mortality in survivors of acute myocardial infarction: a report from the Osaka Acute Coronary Insufficiency Study.
Int Heart J
; 55(3): 190-6, 2014.
Artigo
em Inglês
| MEDLINE | ID: mdl-24806378
19.
The HLA-DRB1*09:01-DQB1*03:03 haplotype is associated with the risk for late-onset Alzheimer's disease in APOE [Formula: see text]4-negative Japanese adults.
NPJ Aging
; 10(1): 3, 2024 Jan 02.
Artigo
em Inglês
| MEDLINE | ID: mdl-38167405
20.
Polygenic effects on the risk of Alzheimer's disease in the Japanese population.
Alzheimers Res Ther
; 16(1): 45, 2024 Feb 27.
Artigo
em Inglês
| MEDLINE | ID: mdl-38414085