Yuan-Tsong Chen
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Taiwanese physician scientist
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Biology Philosophy
Yuan-Tsong Chen's Degrees
- Masters Medicine National Taiwan University
- PhD Biochemistry University of Texas Southwestern Medical Center
Why Is Yuan-Tsong Chen Influential?
(Suggest an Edit or Addition)According to Wikipedia, Yuan-Tsong Chen is a Taiwanese physician scientist, notable for his work on human genetic disorders. He is the director emeritus and distinguished research fellow of the Institute of Biomedical Sciences, Academia Sinica, Taiwan, and also tenured professor of pediatrics of Duke University Chen was a 2019 awardee of Taiwan's , as were Yuan-Pern Lee and Wei Fu-chan.
Yuan-Tsong Chen's Published Works
Number of citations in a given year to any of this author's works
Total number of citations to an author for the works they published in a given year. This highlights publication of the most important work(s) by the author
Published Works
- Medical genetics: A marker for Stevens–Johnson syndrome (2004) (1586)
- Genome-wide trans-ancestry meta-analysis provides insight into the genetic architecture of type 2 diabetes susceptibility (2014) (933)
- HLA-B*5801 allele as a genetic marker for severe cutaneous adverse reactions caused by allopurinol. (2005) (901)
- Granulysin is a key mediator for disseminated keratinocyte death in Stevens-Johnson syndrome and toxic epidermal necrolysis (2008) (656)
- Genetic susceptibility to carbamazepine-induced cutaneous adverse drug reactions (2006) (609)
- Meta-analysis of genome-wide association studies identifies eight new loci for type 2 diabetes in east Asians (2011) (581)
- Mapping Human Genetic Diversity in Asia (2009) (559)
- Meta-analysis of genome-wide association studies identifies common variants associated with blood pressure variation in east Asians (2011) (534)
- FASTSNP: an always up-to-date and extendable service for SNP function analysis and prioritization (2006) (533)
- Carbamazepine-induced toxic effects and HLA-B*1502 screening in Taiwan. (2011) (496)
- A novel functional VKORC1 promoter polymorphism is associated with inter-individual and inter-ethnic differences in warfarin sensitivity. (2005) (476)
- Genetic associations at 53 loci highlight cell types and biological pathways relevant for kidney function (2016) (388)
- Recombinant human acid α-glucosidase enzyme therapy for infantile glycogen storage disease type II: Results of a phase I/II clinical trial (2001) (372)
- PSORS2 is due to mutations in CARD14. (2012) (351)
- A Genome-Wide Association Study Identifies Susceptibility Variants for Type 2 Diabetes in Han Chinese (2010) (325)
- Trans-ancestry genome-wide association study identifies 12 genetic loci influencing blood pressure and implicates a role for DNA methylation (2015) (285)
- Meta-analysis identifies multiple loci associated with kidney function–related traits in east Asian populations (2012) (264)
- Type I glycogen storage diseases: disorders of the glucose-6-phosphatase complex. (2002) (263)
- Common risk allele in aromatic antiepileptic-drug induced Stevens-Johnson syndrome and toxic epidermal necrolysis in Han Chinese. (2010) (263)
- Direct interaction between HLA-B and carbamazepine activates T cells in patients with Stevens-Johnson syndrome. (2012) (252)
- Shared and restricted T-cell receptor use is crucial for carbamazepine-induced Stevens-Johnson syndrome. (2011) (232)
- Early Detection of Pompe Disease by Newborn Screening Is Feasible: Results From the Taiwan Screening Program (2008) (217)
- The impact of antibodies on clinical outcomes in diseases treated with therapeutic protein: Lessons learned from infantile Pompe disease (2011) (212)
- Population structure of Han Chinese in the modern Taiwanese population based on 10,000 participants in the Taiwan Biobank project. (2016) (192)
- Pompe Disease in Infants: Improving the Prognosis by Newborn Screening and Early Treatment (2009) (188)
- Identification of type 2 diabetes loci in 433,540 East Asian individuals (2019) (188)
- Clinical Pharmacogenetics Implementation Consortium Guideline for HLA Genotype and Use of Carbamazepine and Oxcarbazepine: 2017 Update (2018) (167)
- Type II collagen gene variants and inherited osteonecrosis of the femoral head. (2005) (163)
- Human leukocyte antigens and drug hypersensitivity (2007) (160)
- Two new susceptibility loci for Kawasaki disease identified through genome-wide association analysis (2012) (158)
- Use of HLA-B*58:01 genotyping to prevent allopurinol induced severe cutaneous adverse reactions in Taiwan: national prospective cohort study (2015) (143)
- Variant GADL1 and response to lithium therapy in bipolar I disorder. (2014) (139)
- Long contiguous stretches of homozygosity in the human genome (2006) (125)
- Mitochondrial GLUT10 facilitates dehydroascorbic acid import and protects cells against oxidative stress: mechanistic insight into arterial tortuosity syndrome. (2010) (125)
- Association analyses of East Asian individuals and trans‐ancestry analyses with European individuals reveal new loci associated with cholesterol and triglyceride levels (2017) (119)
- A Genome-Wide Association Study Reveals a Quantitative Trait Locus of Adiponectin on CDH13 That Predicts Cardiometabolic Outcomes (2011) (119)
- HLA-B*1502-bound peptides: implications for the pathogenesis of carbamazepine-induced Stevens-Johnson syndrome. (2007) (113)
- ENU mutagenesis identifies mice with mitochondrial branched-chain aminotransferase deficiency resembling human maple syrup urine disease. (2004) (103)
- Measurement of Pre-Existing IgG and IgM Antibodies against Polyethylene Glycol in Healthy Individuals. (2016) (102)
- Identification of Novel Susceptibility Loci for Kawasaki Disease in a Han Chinese Population by a Genome-Wide Association Study (2011) (97)
- Genome-wide expression profiles of subchondral bone in osteoarthritis (2013) (94)
- Han Chinese Cell and Genome Bank in Taiwan: Purpose, Design and Ethical Considerations (2006) (93)
- The putative glucose 6-phosphate translocase gene is mutated in essentially all cases of glycogen storage disease type I non-a (1999) (91)
- Multi-ancestry genetic study of type 2 diabetes highlights the power of diverse populations for discovery and translation (2020) (88)
- AAV vector-mediated reversal of hypoglycemia in canine and murine glycogen storage disease type Ia. (2008) (84)
- Genetic determinants of antithyroid drug-induced agranulocytosis by human leukocyte antigen genotyping and genome-wide association study (2015) (82)
- Dysregulation of C/EBPα by mutant Huntingtin causes the urea cycle deficiency in Huntington's disease (2007) (80)
- Pharmacogenomics of adverse drug reactions: implementing personalized medicine. (2012) (78)
- Comparison of maltose and acarbose as inhibitors of maltase-glucoamylase activity in assaying acid α-glucosidase activity in dried blood spots for the diagnosis of infantile Pompe disease (2006) (75)
- Genome-Wide Association Study of Young-Onset Hypertension in the Han Chinese Population of Taiwan (2009) (74)
- Molecular genetic basis and prevalence of glycogen storage disease type IIIA in the Faroe Islands (2001) (74)
- Genetic predisposition of life-threatening antiepileptic-induced skin reactions (2010) (74)
- Glucose tetrasaccharide as a biomarker for monitoring the therapeutic response to enzyme replacement therapy for Pompe disease. (2005) (72)
- Mice with Alopecia, Osteoporosis, and Systemic Amyloidosis Due to Mutation in Zdhhc13, a Gene Coding for Palmitoyl Acyltransferase (2010) (72)
- CXCL10/IP-10 is a biomarker and mediator for Kawasaki disease. (2015) (71)
- Type I glycogen storage disease: Kidney involvement, pathogenesis and its treatment (2004) (70)
- Nephrotic Syndrome Complicating α-Glucosidase Replacement Therapy for Pompe Disease (2004) (69)
- Outer Membrane Protein I of Pseudomonas aeruginosa Is a Target of Cationic Antimicrobial Peptide/Protein* (2010) (69)
- Efficacy of gene therapy for a prototypical lysosomal storage disease (GSD-II) is critically dependent on vector dose, transgene promoter, and the tissues targeted for vector transduction. (2002) (65)
- Tissue-specific inactivation of murine M6P/IGF2R. (2003) (65)
- Overlapping high‐resolution copy number alterations in cancer genomes identified putative cancer genes in hepatocellular carcinoma (2010) (64)
- Chromosomal and genetic alterations in human hepatocellular adenomas associated with type Ia glycogen storage disease. (2009) (64)
- Analysis of a glucose tetrasaccharide elevated in Pompe disease by stable isotope dilution-electrospray ionization tandem mass spectrometry. (2003) (61)
- Genome-Wide Association Study of Treatment Refractory Schizophrenia in Han Chinese (2012) (60)
- Interethnic analyses of blood pressure loci in populations of East Asian and European descent (2018) (59)
- Genome-wide analysis of copy number variations identifies PARK2 as a candidate gene for autism spectrum disorder (2016) (59)
- Over-expression of AURKA, SKA3 and DSN1 contributes to colorectal adenoma to carcinoma progression (2016) (59)
- Nephrotic syndrome complicating alpha-glucosidase replacement therapy for Pompe disease. (2004) (58)
- Mutations in the SLC2A10 gene cause arterial abnormalities in mice. (2008) (57)
- Genome-wide association studies in East Asians identify new loci for waist-hip ratio and waist circumference (2016) (56)
- Dysregulation of C/EBPalpha by mutant Huntingtin causes the urea cycle deficiency in Huntington's disease. (2007) (53)
- A comparison of major histocompatibility complex SNPs in Han Chinese residing in Taiwan and Caucasians. (2006) (53)
- Glycogen storage disease type I: diagnosis and phenotype/genotype correlation (2007) (52)
- PrimerZ: streamlined primer design for promoters, exons and human SNPs (2007) (51)
- Role of S-Palmitoylation by ZDHHC13 in Mitochondrial function and Metabolism in Liver (2017) (48)
- Neonatal hypotonia and cardiomyopathy secondary to type IV glycogenosis (1994) (48)
- HLA-B genotyping to detect carbamazepine-induced Stevens-Johnson syndrome: implications for personalizing medicine. (2005) (47)
- Genome-wide Trans-ethnic Meta-analysis Identifies Seven Genetic Loci Influencing Erythrocyte Traits and a Role for RBPMS in Erythropoiesis. (2017) (46)
- 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 (2006) (45)
- A new nucleic acid-based agent inhibits cytotoxic T lymphocyte-mediated immune disorders. (2013) (44)
- VarioWatch: providing large-scale and comprehensive annotations on human genomic variants in the next generation sequencing era (2012) (43)
- A genome-wide association study identifies a novel susceptibility locus for the immunogenicity of polyethylene glycol (2017) (43)
- Replication of genome‐wide association signals of type 2 diabetes in Han Chinese in a prospective cohort (2012) (42)
- A recent update of pharmacogenomics in drug-induced severe skin reactions. (2012) (42)
- A Single-Base Deletion in the 3′-Coding Region of Glycogen-Debranching Enzyme Is Prevalent in Glycogen Storage Disease Type IIIA in a Population of North African Jewish Patients (1997) (41)
- Glycogen-branching enzyme deficiency leads to abnormal cardiac development: novel insights into glycogen storage disease IV. (2011) (40)
- Genome-wide association study in NSAID-induced acute urticaria/angioedema in Spanish and Han Chinese populations. (2013) (39)
- Glycogen storage disease type IV: novel mutations and molecular characterization of a heterogeneous disorder (2010) (38)
- ENU mutagenesis identifies mice with cardiac fibrosis and hepatic steatosis caused by a mutation in the mitochondrial trifunctional protein beta-subunit. (2006) (38)
- Loss of GPNMB Causes Autosomal-Recessive Amyloidosis Cutis Dyschromica in Humans. (2018) (38)
- Immunologic basis for allopurinol-induced severe cutaneous adverse reactions: HLA-B*58:01-restricted activation of drug-specific T cells and molecular interaction. (2015) (38)
- Identification of differentially expressed microRNAs in human hepatocellular adenoma associated with type I glycogen storage disease: a potential utility as biomarkers (2014) (37)
- A promoter sequence variant of ZNF750 is linked with familial psoriasis. (2008) (35)
- Glycogen storage in multiple muscles of old GSD‐II mice can be rapidly cleared after a single intravenous injection with a modified adenoviral vector expressing hGAA (2005) (34)
- Glycogen storage disease type IIIa in curly-coated retrievers. (2007) (32)
- Identification of susceptibility gene associated with female primary Sjögren’s syndrome in Han Chinese by genome-wide association study (2016) (32)
- Association of circadian genes with diurnal blood pressure changes and non-dipper essential hypertension: a genetic association with young-onset hypertension (2014) (32)
- Knock-in human FGFR3 achondroplasia mutation as a mouse model for human skeletal dysplasia (2017) (31)
- A single-base deletion in the 3'-coding region of glycogen-debranching enzyme is prevalent in glycogen storage disease type IIIA in a population of North African Jewish patients (1997) (30)
- A nonsense mutation due to a single base insertion in the 3′‐coding region of glycogen debranching enzyme gene associated with a severe phenotype in a patient with glycogen storage disease type IIIa (1997) (30)
- Fractures in children with Pompe disease: a potentiallong-term complication (2007) (29)
- Erratum: HLA-B*5801 allele as a genetic marker for severe cutaneous adverse reactions caused by allopurinol (Proceedings of the National Academy of Sciences of the United States of America (March 15, 2005) 102, 11 (4134-4139)) (2005) (29)
- Mouse model of glycogen storage disease type III. (2014) (28)
- Pharmacogenomics for personalized pain medicine. (2016) (27)
- Non‐lethal congenital hypotonia due to glycogen storage disease type IV (2006) (27)
- Palmitoyl Acyltransferase, Zdhhc13, Facilitates Bone Mass Acquisition by Regulating Postnatal Epiphyseal Development and Endochondral Ossification: A Mouse Model (2014) (27)
- Molecular profile and copy number analysis of sporadic colorectal cancer in Taiwan (2011) (26)
- Genome-wide transcriptome analysis to further understand neutrophil activation and lncRNA transcript profiles in Kawasaki disease (2019) (25)
- Genome-wide association study identifies novel susceptibility loci for migraine in Han Chinese resided in Taiwan (2018) (25)
- A genome-wide survey of copy number variations in Han Chinese residing in Taiwan. (2009) (25)
- Intragenic microdeletion of RUNX2 is a novel mechanism for cleidocranial dysplasia (2008) (24)
- Antimicrobial Properties of an Immunomodulator - 15 kDa Human Granulysin (2016) (24)
- A large-scale survey of genetic copy number variations among Han Chinese residing in Taiwan (2008) (24)
- Glycogen storage disease type I: diagnosis and phenotype/genotype correlation (2002) (24)
- Functional analysis of novel SNPs and mutations in human and mouse genomes (2008) (23)
- Recombinant Human Acid α-Glucosidase Corrects Acidα-Glucosidase-Deficient Human Fibroblasts, Quail Fibroblasts, and Quail Myoblasts (1998) (23)
- SLC2A10 genetic polymorphism predicts development of peripheral arterial disease in patients with type 2 diabetes. SLC2A10 and PAD in type 2 diabetes (2010) (21)
- A Case of Congenital Glycogen Storage Disease Type IV With a Novel GBE1 Mutation (2008) (21)
- Loss of PTPRM Associates with the Pathogenic Development of Colorectal Adenoma-Carcinoma Sequence (2015) (20)
- Mutations in medium chain acyl-CoA dehydrogenase deficiency (1990) (18)
- Defects in Metabolism of Carbohydrates (2005) (18)
- Homozygosity Mapping and Whole-Genome Sequencing Links a Missense Mutation in POMGNT1 to Autosomal Recessive Retinitis Pigmentosa. (2016) (18)
- Sibling phenotype concordance in classical infantile Pompe disease (2007) (17)
- Both IgM and IgG Antibodies against Polyethylene Glycol Can Alter the Biological Activity of Methoxy Polyethylene Glycol-Epoetin Beta in Mice (2019) (17)
- Garlic Accelerates Red Blood Cell Turnover and Splenic Erythropoietic Gene Expression in Mice: Evidence for Erythropoietin-Independent Erythropoiesis (2010) (16)
- Determinants of the Over-Anticoagulation Response during Warfarin Initiation Therapy in Asian Patients Based on Population Pharmacokinetic-Pharmacodynamic Analyses (2014) (16)
- Association of an IGHV3-66 gene variant with Kawasaki disease (2020) (16)
- Alglucosidase alfa enzyme replacement therapy as a therapeutic approach for glycogen storage disease type III. (2013) (15)
- GenoWatch: a disease gene mining browser for association study (2008) (15)
- Novel susceptibility gene for nonfamilial hypokalemic periodic paralysis (2016) (15)
- Association of the Congenital Neuromuscular Form of Glycogen Storage Disease Type IV With a Large Deletion and Recurrent Frameshift Mutation (2012) (15)
- Cyclic Alopecia and Abnormal Epidermal Cornification in Zdhhc13-Deficient Mice Reveal the Importance of Palmitoylation in Hair and Skin Differentiation. (2015) (15)
- Pharmacogenetics of toxic epidermal necrolysis (2010) (14)
- Use of the Biopharmaceutics Drug Disposition Classification System (BDDCS) to Help Predict the Occurrence of Idiosyncratic Cutaneous Adverse Drug Reactions Associated with Antiepileptic Drug Usage (2016) (14)
- A genome-wide association study links small-vessel ischemic stroke to autophagy (2017) (14)
- Genetics of Severe Drug Hypersensitivity Reactions in Han Chinese (2007) (13)
- Prenatal diagnosis of Pompe's disease (type ii glycogenosis) in chorionic villus biopsy using maltose as a substrate (1992) (13)
- MPDA: Microarray pooled DNA analyzer (2008) (13)
- Prenatal diagnosis and carrier detection for glycogen storage disease type III using polymorphic DNA markers (1998) (13)
- Glycogen Storage Disease Type I (2016) (13)
- Longitudinal Evaluation of an N-Ethyl-N-Nitrosourea-Created Murine Model with Normal Pressure Hydrocephalus (2009) (12)
- Predicting HLA genotypes using unphased and flanking single-nucleotide polymorphisms in Han Chinese population (2014) (12)
- Prenatal diagnosis of glycogen storage disease type IV using PCR‐based DNA mutation analysis (1999) (12)
- T-cell receptor and carbamazepine-induced Stevens–Johnson syndrome and toxic epidermal necrolysis: understanding a hypersensitivity reaction (2012) (12)
- Identification of functional single nucleotide polymorphisms in the branchpoint site (2017) (12)
- Protein Palmitoylation by ZDHHC13 Protects Skin against Microbial-Driven Dermatitis. (2017) (11)
- Identification of a submicroscopic 3.2 Mb chromosomal 16q12.2‐13 deletion in a child with short stature, mild developmental delay, and craniofacial anomalies, by high‐density oligonucleotide array‐a recognizable syndrome (2010) (10)
- Expression of catalytically active human multifunctional glycogen‐debranching enzyme and lysosomal acid alpha‐glucosidase in insect cells (1996) (10)
- Genome‐wide copy number analysis using copy number inferring tool (CNIT) and DNA pooling (2008) (9)
- Alternative Splicing in Acad8 Resulting a Mitochondrial Defect and Progressive Hepatic Steatosis in Mice (2011) (9)
- Prenatal diagnosis in glycogen storage diseases (2002) (9)
- Filamin B Loss‐of‐Function Mutation in Dimerization Domain Causes Autosomal‐Recessive Spondylocarpotarsal Synostosis Syndrome with Rib Anomalies (2017) (9)
- Novel DNA sequence variations of cytochrome P450 genes in the Han Chinese population. (2009) (9)
- Immunoglobulin profiling identifies unique signatures in patients with Kawasaki disease during intravenous immunoglobulin treatment (2018) (8)
- Purification of recombinant human precursor acid α‐glucosidase (1997) (8)
- A Mutation in Cartilage Oligomeric Matrix Protein (COMP) Causes Early‐Onset Osteoarthritis in a Large Kindred Study (2011) (8)
- Palmitoyl acyltransferase activity of ZDHHC13 regulates skin barrier development partly by controlling PADi3 and TGM1 protein stability. (2020) (8)
- Genetic Polymorphisms of Metabolic Enzymes and the Pharmacokinetics of Indapamide in Taiwanese Subjects (2013) (8)
- A new analysis tool for individual-level allele frequency for genomic studies (2010) (7)
- SAQC: SNP Array Quality Control (2011) (6)
- Inter-Individual Differences in Baseline Coagulation Activities and Their Implications for International Normalized Ratio Control During Warfarin Initiation Therapy (2012) (6)
- De novo MECP2 duplication derived from paternal germ line result in dysmorphism and developmental delay. (2014) (6)
- Genetic epidemiological study doesn't support GLA IVS4+919G>A variant is a significant mutation in Fabry disease. (2017) (6)
- Brain Abscess in Glycogen Storage Disease Type Ib (1991) (5)
- A large kindred of early-onset osteoarthritis of the knee and hip: excluding the link to COL2A1 gene. (2009) (5)
- 7th Drug hypersensitivity meeting: part two (2016) (4)
- An integrated analysis tool for analyzing hybridization intensities and genotypes using new-generation population-optimized human arrays (2016) (3)
- Type III glycogen storage disease: An adult case with mild disease but complete absence of debrancher protein (1991) (3)
- Enrichment of Prevotella intermedia in human colorectal cancer and its additive effects with Fusobacterium nucleatum on the malignant transformation of colorectal adenomas (2022) (3)
- Identification of susceptibility gene associated with female primary Sjögren’s syndrome in Han Chinese by genome-wide association study (2016) (2)
- 339. Sustained, High-Level Expression of Human Acid Alpha-Glucosidase and Correction of Glycogen Storage Disease Type II (GSD II) with an Adeno-Associated Virus 8 (AAV2/8) Vector Containing a Liver-Specific Promoter (2004) (2)
- Erratum: Early, sustained efficacy of adeno-associated virus vector-mediated gene therapy in glycogen storage disease type Ia (Gene Therapy (2006) vol. 13 (1281-1289) 10.1038/sj.gt.3302774) (2006) (1)
- S.9. Genome-Wide Association Studies and the Selective T Cell Receptor (TCR) Usage of CD8+T Cells in Patients with Carbamazepine-Induced Stevens-Johnson Syndrome (2009) (1)
- . Genomic Medicine in Taiwan: Research and Developments (2012) (1)
- A prospective study of HLA*B-5801 genotyping in preventing allopurinol- induced severe cutaneous adverse reactions (2014) (1)
- CHRONIC RENAL DISEASE IN TYPE I GLYCCGEN STORAGE DISEASE (1987) (1)
- Risk assessment of adverse drug reactions (2004) (1)
- S30-7 PROSPECTIVE STUDY OF WARFARIN DOSAGE REQUIREMENTS BASED ON CYP2C9 AND VKORC1 GENOTYPES (2007) (1)
- Isolation and characterization of the mouse P1-450 chromosomal gene. (1982) (1)
- Identification of mutations in Type IV glycogen storage disease (1994) (1)
- ENU mutagenesis identifies mice with cardiac fibrosis and hepatic steatosis caused by a mutation in the mitochondrial trifunctional protein b -subunit (2006) (1)
- Genetic susceptibility and pharmacogenomics of severe cutaneous adverse drug reactions (2010) (1)
- Animal Model Tissue-Specific Inactivation of Murine M6P/IGF2R (2003) (0)
- Abstract 60: FcR + CD4 + T Cells as a Specific Subset of IL-17-producing Cells Controlled by BATF/IRF8: Novel Insights Into Etiology of Kawasaki Disease (2015) (0)
- Gluconeogenesis treatment of type II. (2001) (0)
- Genetic Polymorphisms of Metabolic Enzymes and the Pharmacokinetics of Indapamide in Taiwanese Subjects (2013) (0)
- Abstract TP134: Genome Wide Association Studies in Han Chinese Populations Identify Novel Susceptibility Loci for Specific Ischemic Stroke Subtypes (2016) (0)
- A Genome-Wide Association Study of Non-Steroidal Antiinflammatory Drugs (NSAIDs)-Induced Acute Urticaria in the Spanish Population (2013) (0)
- Predicting HLA genotypes using unphased and flanking single-nucleotide polymorphisms in Han Chinese population (2014) (0)
- 487. Liver-Targeted Gene Therapy in Glycogen Storage Disease Type Ia (GSD-Ia) Requires Widespread, Regulated Glucose-6-phosphatase (2006) (0)
- Abstract 518: Identification of differentially expressed microRNAs in human hepatocellular adenoma associated with type I glycogen storage disease: a potential utility as biomarkers (2014) (0)
- Corrigendum to "Efficacy of Helper-dependent Adenovirus Vector-mediated Gene Therapy in Murine Glycogen Storage Disease Type Ia". (2007) (0)
- 211. Development of Helper-Dependent Adenovirus (HDAd) Vectors for Gene Therapy in the Mouse Model for Glycogen Storage Disease Type Ia (GSD-Ia) (2006) (0)
- Risk assessment of negative drug reactions (2004) (0)
- Faculty Opinions recommendation of Stevens-Johnson syndrome/toxic epidermal necrolysis mouse model generated by using PBMCs and the skin of patients. (2013) (0)
- Concurrent direct human leukocyte antigen (HLA) genotyping and genome-wide association study (GWAS) reveal major genetic determinants of anti-thyroid drug-induced agranulocytosis. (2015) (0)
- Precision Medicine for Kawasaki Disease (2015) (0)
- No Deletion of CFHL1 and CFHL3 Genes in Age-Related Macular Degeneration (2007) (0)
- Baseline serum WFA+-M2BP level is a strong predictor of response to pegylated interferon-α in HBeAg-positive chronic hepatitis B patients (2017) (0)
- sugar/polyol transport facilitators Nomenclature of the GLUT/SLC2A family of (2011) (0)
- 159 COMPARISON OF GENE EXPRESSION PROFILES BETWEEN NORMAL AND SCLEROSIS REGIONS OF HUMAN OSTEOARTHRITIC SUBCHONDRAL BONE (2010) (0)
- Abstract O.30: Novel Biomarker for Early Diagnosis of Kawasaki Diseases (2015) (0)
- Role of S-Palmitoylation by ZDHHC13 in Mitochondrial function and Metabolism in Liver (2017) (0)
- Table 2. [G6PC Pathogenic Variants Discussed in This GeneReview]. (2016) (0)
- Identification of functional single nucleotide polymorphisms in the branchpoint site (2017) (0)
- A genome-wide association study identifies a novel susceptibility locus for the immunogenicity of polyethylene glycol (2017) (0)
- An integrated analysis tool for analyzing hybridization intensities and genotypes using new-generation population-optimized human arrays (2016) (0)
- Table 3. [SLC37A4 Pathogenic Variants Discussed in This GeneReview]. (2016) (0)
- Genetic Susceptibility to Severe Adverse Drug Reactions: Perspective for Future Medicine (2006) (0)
- Identi fi cation of PTCSC 3 as a Novel Locus for Large-Vessel Ischemic Stroke : A Genome-Wide Association Study (2016) (0)
- Table 1. [Molecular Genetic Testing Used in Glycogen Storage Disease Type I]. (2016) (0)
- List of Contributors (2021) (0)
- Treatment of Wilson’s disease (2017) (0)
- Important role of abnormal glycogen structure in the development of liver cirrhosis and progression to hepatocellular carcinoma in patients with glycogen storage disease type-III (2007) (0)
- Prenatal Diagnosis of Disorders of Carbohydrate Metabolism (2010) (0)
- Faculty Opinions recommendation of A randomized trial of icatibant in ACE-inhibitor-induced angioedema. (2016) (0)
- Glycogen storage disease III subtypes and muscle weakness during childhood (1999) (0)
- Associated With Cirrhosis and (1993) (0)
- Correlations between the enantio- and regio-selective metabolisms of warfarin. (2017) (0)
- 1054. Development of Adeno-Associated Virus (AAV) Vectors for Gene Therapy in the Mouse Model for Glycogen Storage Disease Type Ia (GSD-Ia) (2004) (0)
- Composition and method for modulating fibroblast growth factor receptor 3 activation (2018) (0)
- Faculty of 1000 evaluation for T-cells from HLA-B*57:01+ human subjects are activated with abacavir through two independent pathways and induce cell death by multiple mechanisms. (2013) (0)
- Use of the Biopharmaceutics Drug Disposition Classification System (BDDCS) to Help Predict the Occurrence of Idiosyncratic Cutaneous Adverse Drug Reactions Associated with Antiepileptic Drug Usage (2016) (0)
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Yuan-Tsong Chen is affiliated with the following schools:
