about
Association between polymorphisms in the coagulation factor VII gene and coronary heart disease risk in different ethnicities: a meta-analysisAssociation between polymorphisms in the adiponectin gene and cardiovascular disease: a meta-analysis.Associations of epithelial sodium channel genes with blood pressure: the GenSalt studyGene-based association analysis identified novel genes associated with bone mineral density.Integrated Analyses of Gene Expression Profiles Digs out Common Markers for Rheumatic Diseases.Novel Genes Affecting Blood Pressure Detected Via Gene-Based Association Analysis.Identification and evaluation of lncRNA and mRNA integrative modules in human peripheral blood mononuclear cells.Integrative multi-omics analysis revealed SNP-lncRNA-mRNA (SLM) networks in human peripheral blood mononuclear cells.Correlation analyses revealed global microRNA-mRNA expression associations in human peripheral blood mononuclear cells.Identification of important genes associated with total cholesterol using bioinformatics analysis.Adiponectin levels and risk of coronary heart disease: a meta-analysis of prospective studies.Relative abundance of mature myostatin rather than total myostatin is negatively associated with bone mineral density in Chinese.Association of Plasma Irisin with Bone Mineral Density in a Large Chinese Population Using an Extreme Sampling Design.Functional analysis of single-nucleotide polymorphisms in the regulation of coactivator-associated arginine methyltransferase 1 expression and plasma homocysteine levels.Plasma gelsolin is associated with hip BMD in Chinese postmenopausal women.Detection of lncRNA-mRNA interaction modules by integrating eQTL with weighted gene co-expression network analysisRheumatoid arthritis-associated DNA methylation sites in peripheral blood mononuclear cellsGenome-Wide Identification of N-Methyladenosine (mA) SNPs Associated With Rheumatoid ArthritisSNPs rs10224002 in PRKAG2 may disturb gene expression and consequently affect hypertensionDetection of Putative Functional Single Nucleotide Polymorphisms in Blood Pressure Loci and Validation of Association Between Single Nucleotide Polymorphism in WBP1L and Hypertension in the Chinese Han Population[Genotype imputation: principle, methods and application in studies on genetic epidemiology]Detecting novel genes for low-density lipoprotein cholesterol in European population using bioinformatics analysisPutative functional SNPs in SLC22A3 and H3F3B might influence the development of CAD by regulating the lipid levelsGenome-wide identification of m6A-associated SNPs as potential functional variants for bone mineral densityIdentification of PBMC-expressed miRNAs for rheumatoid arthritisPhosphorylation-related SNPs influence lipid levels and rheumatoid arthritis risk by altering gene expression and plasma protein levelsMendelian randomization analysis revealed potential causal factors for systemic lupus erythematosusEpigenetically regulated co-expression network of genes significant for rheumatoid arthritisDetection of m6A-associated SNPs as potential functional variants for coronary artery diseaseIntegrative analysis identified mediation effects of lncRNAs on the correlations between methylation and mRNASmoking modifies the effect of two independent SNPs rs5063 and rs198358 of NPPA on central obesity in the Chinese Han populationGenome-wide enrichment of m6A-associated single-nucleotide polymorphisms in the lipid lociIntegrative analysis revealed potential causal genetic and epigenetic factors for multiple sclerosisMulti-omics integrative analysis identified SNP-methylation-mRNA: Interaction in peripheral blood mononuclear cellsAssociations among NPPA gene polymorphisms, serum ANP levels, and hypertension in the Chinese Han populationIntegrative Analysis Identified IRF6 and NDST1 as Potential Causal Genes for Ischemic StrokeExamination of the associations between m6A-associated single-nucleotide polymorphisms and blood pressureIdentification of Phosphorylation Associated SNPs for Blood Pressure, Coronary Artery Disease and Stroke from Genome-wide Association Studies
P50
Q33992017-F9981FE9-4992-492E-B463-820FD42D27D9Q34284227-59289C5B-0094-45BD-9DB9-F91B6C20AAD6Q35171131-F2E5FC8B-866B-4C3F-B407-F733DA9A3B81Q35219519-A1ED7359-E749-48AB-B0A5-6D8D360F7AE6Q35767935-96DD620D-2F5B-49BB-B556-F3942D4C58BBQ35773947-BC5E2D4B-C47E-4E82-8EC3-9A0CA6DE95FCQ38432407-CE4981D5-8D9E-4591-8A3B-8D3713328D57Q38752480-5F065F77-3604-43C2-AB7A-96BFCB78F85DQ40054338-DB87C147-1677-4698-93BD-E96DC051CA40Q40953425-662CE55F-B518-4921-B461-C440C98822D7Q44906832-0A9A337C-FCFB-4650-931B-2DDEE5D0E861Q47298043-9BF9CA2C-06C0-4C5B-A34C-5C48DA2817F5Q52628956-51988A34-7DF7-4581-B58D-A01640E34DADQ52652385-ACB2602C-0647-4EAF-B9EA-FE237477B505Q55229761-57B26734-7A87-4D23-B096-4D7128E9E516Q57046161-A39C80CA-8A19-4471-90A4-0FE49D9591CDQ57293175-A40C1F4F-B024-4DF1-B124-6AEC6063D175Q58801649-CD539053-27BC-4011-9514-217295EBEDFCQ64131451-161BAAF0-4FFA-46A7-B53B-BF0C068601BFQ64136007-5D5F84A1-0C34-4F7F-85DC-13E8457D0F30Q82915353-BA10B3FB-FEAB-4026-9509-9961935A3E64Q88691708-F3CE1BCF-CB95-4963-9501-74E5356C7505Q89078639-9AC2272E-888E-4795-BFBC-3E02B63ADEA8Q89450369-1EC83CB4-131C-440A-A649-6ACB0D692152Q90547455-EC8883C8-A717-449A-8109-F28EAD649D12Q90785129-185AAA7A-5EED-4399-962E-1A6F1ACD31F1Q91031325-77A47E97-0967-45A9-BF91-35070AB0566FQ91143670-9EB62B46-26FE-4BBA-9AEE-CAED850EA215Q91476774-92F30D99-46C7-4009-A898-B95647FD89B6Q91509639-D6ADB4AE-93A7-4852-8A87-393A019B9036Q91825386-BB53424B-F44D-431A-B907-A61E414C9A10Q91826392-A9634639-EA08-4F27-8333-359F9D86C357Q92009716-DF92CDF4-6E60-4FAC-A3CE-03B99929CBBAQ92151866-0B5847F5-1FCE-4E85-B13A-85766AE5C3CBQ92153970-8E3B524D-AD4D-4AC5-95A3-0F6448BE5123Q92478828-552A59F8-2E0D-4CAE-8464-D5D306BBE0F8Q92596509-FBF22254-F94E-4B63-9294-109CC9B57C2CQ92919672-C4BD115F-C292-4EFA-BA17-3883B8DE17AD
P50
description
investigador
@es
researcher
@en
wetenschapper
@nl
name
Xing-bo Mo
@en
Xing-bo Mo
@nl
type
label
Xing-bo Mo
@en
Xing-bo Mo
@nl
prefLabel
Xing-bo Mo
@en
Xing-bo Mo
@nl
P31
P496
0000-0001-8956-4918