Detalhe da pesquisa
1.
Changes of neurofilament light chain in patients with alcohol dependence following withdrawal and the genetic effect from ALDH2 Polymorphism.
Eur Arch Psychiatry Clin Neurosci
; 274(2): 423-432, 2024 Mar.
Artigo
em Inglês
| MEDLINE | ID: mdl-37314537
2.
Exploring concepts and trends in informal caregiver burden: systematic review using citation network and content analysis.
Aging Clin Exp Res
; 35(12): 2873-2885, 2023 Dec.
Artigo
em Inglês
| MEDLINE | ID: mdl-37907665
3.
Classifying Alzheimer's disease and normal subjects using machine learning techniques and genetic-environmental features.
J Formos Med Assoc
; 2023 Dec 02.
Artigo
em Inglês
| MEDLINE | ID: mdl-38044212
4.
Association of the D-amino acid oxidase gene with methadone dose in heroin dependent patients under methadone maintenance treatment.
J Hum Genet
; 67(5): 273-278, 2022 May.
Artigo
em Inglês
| MEDLINE | ID: mdl-34983973
5.
Increase in plasma CCL11 (Eotaxin-1) in patients with alcohol dependence and changes during detoxification.
Brain Behav Immun
; 99: 83-90, 2022 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-34571176
6.
Splice-Site Variants in the Gene Encoding GABA-A Receptor Delta Subunit Are Associated with Amphetamine Use in Patients under Methadone Maintenance Treatment.
Int J Mol Sci
; 24(1)2022 Dec 31.
Artigo
em Inglês
| MEDLINE | ID: mdl-36614162
7.
Multi-omics analysis identifies CpGs near G6PC2 mediating the effects of genetic variants on fasting glucose.
Diabetologia
; 64(7): 1613-1625, 2021 07.
Artigo
em Inglês
| MEDLINE | ID: mdl-33842983
8.
pWGBSSimla: a profile-based whole-genome bisulfite sequencing data simulator incorporating methylation QTLs, allele-specific methylations and differentially methylated regions.
Bioinformatics
; 36(3): 660-665, 2020 02 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-31397839
9.
Genetic polymorphisms in the opioid receptor delta 1 (OPRD1) gene are associated with methadone dose in methadone maintenance treatment for heroin dependence.
J Hum Genet
; 65(4): 381-386, 2020 Apr.
Artigo
em Inglês
| MEDLINE | ID: mdl-31907389
10.
Fine-mapping of lipid regions in global populations discovers ethnic-specific signals and refines previously identified lipid loci.
Hum Mol Genet
; 25(24): 5500-5512, 2016 12 15.
Artigo
em Inglês
| MEDLINE | ID: mdl-28426890
11.
GRK5 Is Associated with the Regulation of Methadone Dosage in Heroin Dependence.
Int J Neuropsychopharmacol
; 21(10): 910-917, 2018 10 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-30060048
12.
IGF1 Gene Is Associated With Triglyceride Levels In Subjects With Family History Of Hypertension From The SAPPHIRe And TWB Projects.
Int J Med Sci
; 15(10): 1035-1042, 2018.
Artigo
em Inglês
| MEDLINE | ID: mdl-30013445
13.
Genome-wide copy number variation analysis identified deletions in SFMBT1 associated with fasting plasma glucose in a Han Chinese population.
BMC Genomics
; 18(1): 591, 2017 08 08.
Artigo
em Inglês
| MEDLINE | ID: mdl-28789618
14.
SeqSIMLA2_exact: simulate multiple disease sites in large pedigrees with given disease status for diseases with low prevalence.
Bioinformatics
; 32(4): 557-62, 2016 Feb 15.
Artigo
em Inglês
| MEDLINE | ID: mdl-26515824
15.
An efficient gene-gene interaction test for genome-wide association studies in trio families.
Bioinformatics
; 32(12): 1848-55, 2016 06 15.
Artigo
em Inglês
| MEDLINE | ID: mdl-26873927
16.
FamPipe: An Automatic Analysis Pipeline for Analyzing Sequencing Data in Families for Disease Studies.
PLoS Comput Biol
; 12(6): e1004980, 2016 06.
Artigo
em Inglês
| MEDLINE | ID: mdl-27272119
17.
GCORE-sib: An efficient gene-gene interaction tool for genome-wide association studies based on discordant sib pairs.
BMC Bioinformatics
; 17(1): 273, 2016 Jul 08.
Artigo
em Inglês
| MEDLINE | ID: mdl-27391654
18.
SeqSIMLA2: simulating correlated quantitative traits accounting for shared environmental effects in user-specified pedigree structure.
Genet Epidemiol
; 39(1): 20-4, 2015 Jan.
Artigo
em Inglês
| MEDLINE | ID: mdl-25250827
19.
A multi-SNP association test for complex diseases incorporating an optimal P-value threshold algorithm in nuclear families.
BMC Genomics
; 16: 381, 2015 May 15.
Artigo
em Inglês
| MEDLINE | ID: mdl-25975968
20.
Evaluation of copy number variations reveals novel candidate genes in autism spectrum disorder-associated pathways.
Hum Mol Genet
; 21(15): 3513-23, 2012 Aug 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-22543975