About: Yuan-Tsong Chen

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Taiwanese physician scientist

Attributes	Values
rdf:type	Item
description	geneticus (nl) Taiwanese physician scientist (en) 台灣醫學科學家 (zh)
rdfs:label	Yuan-Tsong Chen (en) Yuan-Tsong Chen (es) Yuan-Tsong Chen (sq) Yuan-Tsong Chen (ast) 陳垣崇 (ja) 陳垣崇 (zh)
skos:prefLabel	Yuan-Tsong Chen (en) Yuan-Tsong Chen (es) Yuan-Tsong Chen (sq) Yuan-Tsong Chen (ast) 陳垣崇 (ja) 陳垣崇 (zh)
name	Yuan-Tsong Chen (en) Yuan-Tsong Chen (es) Yuan-Tsong Chen (sq) Yuan-Tsong Chen (ast) 陳垣崇 (ja) 陳垣崇 (zh)
ResearchGate contributions ID	wds:Q8933624-a25c9c56-41ee-28b9-4268-8b8af3401725
ResearchGate contributions ID	2071118476_Yuan-Tsong_Chen
instance of	wds:Q8933624-AC0A4FF0-3F49-4F20-9753-FD9121A6CDD9
instance of	Homo sapiens
NCL ID	wds:Q8933624-3858efd1-418f-7db1-88dd-8bf92e8a1101
Google Knowledge Graph ID	wds:Q8933624-9818B037-F7A3-428C-8255-B60EB7E2C560
Google Knowledge Graph ID	http://g.co/kg/g/155qfrff
NCL ID	000003227
Google Knowledge Graph ID	/g/155qfrff
Justia Patents inventor ID	wds:Q8933624-d55dc25a-4483-c6b6-a946-5d22f21131fa
Justia Patents inventor ID	yuan-tsong-chen
skos:altLabel	YT Chen (en)
occupation	wds:Q8933624-CFB86B63-6B1D-4966-B842-9B61D9BEC8BF wds:Q8933624-c556fef7-48f3-a670-675d-07eed4df252d
employer	wds:Q8933624-AEED4E9C-D8E2-4E3A-95F6-49C3A14DDBA5
sex or gender	wds:Q8933624-37DBE3C2-B794-4B8C-93B5-0B1E62604E32
VIAF ID	wds:Q8933624-c921c643-46c3-33ab-295c-ff59f63aa3aa
DBLP author ID	wds:Q8933624-426a04f5-491f-569d-9168-4a9099271cad
country of citizenship	wds:Q8933624-355497C6-FC1A-414B-A4FC-6F610E78C18C
sibling	wds:Q8933624-b3ab48ed-4a59-7229-fb8d-541aa2ffdb03
date of birth	wds:Q8933624-ABA9B1E3-488E-4105-8D62-51BBC7D32093
educated at	wds:Q8933624-1467F8B7-9799-4F8B-9A0F-B27B3F0A0AB8 wds:Q8933624-14A4D768-7C43-437C-B20F-DB24DBDFA74A
family name	wds:Q8933624-9C08040A-9A62-4A3F-ADE9-E8D3D7BB22BC
WorldCat Identities ID (superseded)	wds:Q8933624-2F564684-1910-4AC8-9B09-252BA07569F2
VIAF ID	http://viaf.org/viaf/29146573954238102551
DBLP author ID	https://dblp.org/pid/77/3430.rdf
occupation	geneticist medical researcher
employer	Duke University
sex or gender	male
VIAF ID	29146573954238102551
DBLP author ID	77/3430
country of citizenship	Republic of China
sibling	Alice Lin-Tsing Yu
date of birth	1948-09-24 00:00:00Z (xsd:dateTime)
educated at	National Taiwan University Columbia University
family name	Chen
WorldCat Identities ID (superseded)	viaf-29146573954238102551
is about of	https://www.wikidata.org/wiki/Special:EntityData/Q8933624 Yuan-Tsong Chen https://zh.wikipedia.org/wiki/%E9%99%B3%E5%9E%A3%E5%B4%87
is author of	Genome-wide trans-ancestry meta-analysis provides insight into the genetic architecture of type 2 diabetes susceptibility Genetic susceptibility to carbamazepine-induced cutaneous adverse drug reactions. Association analyses of East Asian individuals and trans-ancestry analyses with European individuals reveal new loci associated with cholesterol and triglyceride levels Genome-wide analysis of copy number variations identifies PARK2 as a candidate gene for autism spectrum disorder Genetic predisposition of life-threatening antiepileptic-induced skin reactions. Meta-analysis identifies multiple loci associated with kidney function-related traits in east Asian populations Direct interaction between HLA-B and carbamazepine activates T cells in patients with Stevens-Johnson syndrome. Replication of genome-wide association signals of type 2 diabetes in Han Chinese in a prospective cohort. Long contiguous stretches of homozygosity in the human genome A common SCN5A polymorphism attenuates a severe cardiac phenotype caused by a nonsense SCN5A mutation in a Chinese family with an inherited cardiac conduction defect A novel functional VKORC1 promoter polymorphism is associated with inter-individual and inter-ethnic differences in warfarin sensitivity. Mapping human genetic diversity in Asia Identification of novel susceptibility Loci for kawasaki disease in a Han chinese population by a genome-wide association study Two new susceptibility loci for Kawasaki disease identified through genome-wide association analysis Use of HLA-B58:01 genotyping to prevent allopurinol induced severe cutaneous adverse reactions in Taiwan: national prospective cohort study Trans-ancestry genome-wide association study identifies 12 genetic loci influencing blood pressure and implicates a role for DNA methylation HLA-B5801 allele as a genetic marker for severe cutaneous adverse reactions caused by allopurinol Medical genetics: a marker for Stevens-Johnson syndrome HLA-B*1502-bound peptides: implications for the pathogenesis of carbamazepine-induced Stevens-Johnson syndrome. Genome-wide association study of young-onset hypertension in the Han Chinese population of Taiwan Glycogen-branching enzyme deficiency leads to abnormal cardiac development: novel insights into glycogen storage disease IV. Pharmacogenomics of adverse drug reactions: implementing personalized medicine ENU mutagenesis identifies mice with mitochondrial branched-chain aminotransferase deficiency resembling human maple syrup urine disease FASTSNP: an always up-to-date and extendable service for SNP function analysis and prioritization. A large-scale survey of genetic copy number variations among Han Chinese residing in Taiwan Shared and restricted T-cell receptor use is crucial for carbamazepine-induced Stevens-Johnson syndrome AAV vector-mediated reversal of hypoglycemia in canine and murine glycogen storage disease type Ia. Mitochondrial GLUT10 facilitates dehydroascorbic acid import and protects cells against oxidative stress: mechanistic insight into arterial tortuosity syndrome Outer membrane protein I of Pseudomonas aeruginosa is a target of cationic antimicrobial peptide/protein A genome-wide association study identifies susceptibility variants for type 2 diabetes in Han Chinese Han Chinese cell and genome bank in Taiwan: purpose, design and ethical considerations A genome-wide association study reveals a quantitative trait locus of adiponectin on CDH13 that predicts cardiometabolic outcomes Meta-analysis of genome-wide association studies identifies eight new loci for type 2 diabetes in east Asians Meta-analysis of genome-wide association studies identifies common variants associated with blood pressure variation in east Asians Identification of differentially expressed microRNAs in human hepatocellular adenoma associated with type I glycogen storage disease: a potential utility as biomarkers

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