P3373
Genome-wide association study of young-onset hypertension in the Han Chinese population of TaiwanMice with alopecia, osteoporosis, and systemic amyloidosis due to mutation in Zdhhc13, a gene coding for palmitoyl acyltransferaseHLA-B*5801 allele as a genetic marker for severe cutaneous adverse reactions caused by allopurinolPharmacogenomics for personalized pain medicineHomozygosity Mapping and Whole-Genome Sequencing Links a Missense Mutation in POMGNT1 to Autosomal Recessive Retinitis PigmentosaHuman leukocyte antigens and drug hypersensitivityMedical genetics: a marker for Stevens-Johnson syndromeMapping human genetic diversity in AsiaGarlic accelerates red blood cell turnover and splenic erythropoietic gene expression in mice: evidence for erythropoietin-independent erythropoiesisAntimicrobial Properties of an Immunomodulator - 15 kDa Human GranulysinENU mutagenesis identifies mice with cardiac fibrosis and hepatic steatosis caused by a mutation in the mitochondrial trifunctional protein beta-subunitENU mutagenesis identifies mice with mitochondrial branched-chain aminotransferase deficiency resembling human maple syrup urine diseaseGenome-wide association study of treatment refractory schizophrenia in Han ChineseIdentification of novel susceptibility Loci for kawasaki disease in a Han chinese population by a genome-wide association studyA genome-wide association study identifies susceptibility variants for type 2 diabetes in Han ChineseGenome-wide trans-ancestry meta-analysis provides insight into the genetic architecture of type 2 diabetes susceptibilityTwo new susceptibility loci for Kawasaki disease identified through genome-wide association analysis.Meta-analysis of genome-wide association studies identifies eight new loci for type 2 diabetes in east Asians.Association analyses of East Asian individuals and trans-ancestry analyses with European individuals reveal new loci associated with cholesterol and triglyceride levels.MPDA: microarray pooled DNA analyzer.Functional analysis of novel SNPs and mutations in human and mouse genomes.A large-scale survey of genetic copy number variations among Han Chinese residing in TaiwanVKORC1 haplotypes in five East-Asian populations and Indians.A new analysis tool for individual-level allele frequency for genomic studies.SLC2A10 genetic polymorphism predicts development of peripheral arterial disease in patients with type 2 diabetes. SLC2A10 and PAD in type 2 diabetes.Outer membrane protein I of Pseudomonas aeruginosa is a target of cationic antimicrobial peptide/protein.SAQC: SNP array quality control.HLA-B*1502-bound peptides: implications for the pathogenesis of carbamazepine-induced Stevens-Johnson syndrome.Determinants of the over-anticoagulation response during warfarin initiation therapy in Asian patients based on population pharmacokinetic-pharmacodynamic analysesMitochondrial GLUT10 facilitates dehydroascorbic acid import and protects cells against oxidative stress: mechanistic insight into arterial tortuosity syndrome.A novel functional VKORC1 promoter polymorphism is associated with inter-individual and inter-ethnic differences in warfarin sensitivity.Trans-ancestry genome-wide association study identifies 12 genetic loci influencing blood pressure and implicates a role for DNA methylation.Genetic susceptibility to carbamazepine-induced cutaneous adverse drug reactions.FASTSNP: an always up-to-date and extendable service for SNP function analysis and prioritization.Common risk allele in aromatic antiepileptic-drug induced Stevens-Johnson syndrome and toxic epidermal necrolysis in Han Chinese.Novel DNA sequence variations of cytochrome P450 genes in the Han Chinese population.Replication and meta-analysis of GWAS identified susceptibility loci in Kawasaki disease confirm the importance of B lymphoid tyrosine kinase (BLK) in disease susceptibility.Molecular profile and copy number analysis of sporadic colorectal cancer in Taiwan.Palmitoyl acyltransferase, Zdhhc13, facilitates bone mass acquisition by regulating postnatal epiphyseal development and endochondral ossification: a mouse model.Meta-analysis of genome-wide association studies identifies common variants associated with blood pressure variation in east Asians.
P50
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P50
description
Taiwanese physician scientist
@en
geneticus
@nl
name
Yuan-Tsong Chen
@ast
Yuan-Tsong Chen
@en
Yuan-Tsong Chen
@es
陳垣崇
@zh
type
label
Yuan-Tsong Chen
@ast
Yuan-Tsong Chen
@en
Yuan-Tsong Chen
@es
陳垣崇
@zh
altLabel
YT Chen
@en
prefLabel
Yuan-Tsong Chen
@ast
Yuan-Tsong Chen
@en
Yuan-Tsong Chen
@es
陳垣崇
@zh
P1048
P108
P21
P214
29146573954238102551
P2456
P31
P3373
P3874
yuan-tsong-chen
P569
1948-09-24T00:00:00Z
P6023
2071118476_Yuan-Tsong_Chen
P734
P7859
viaf-29146573954238102551