Results 1-79 of 79 (Search time: 0.015 seconds).

Issue DateTitleAuthor(s)SourcescopusWOSFulltext/Archive link
12021Genetic characteristics and epidemiology of inherited retinal degeneration in TaiwanChen T.-C.; Huang D.-S.; Lin C.-W.; Yang C.-H.; Yang C.-M.; Wang V.Y.; Lin J.-W.; Luo A.C.; Hu F.-R.; PEI-LUNG CHEN npj Genomic Medicine
22021Genetic study of young-onset dementia using targeted gene panel sequencing in TaiwanHsu J.-L.; Lin C.-H.; PEI-LUNG CHEN ; Lin K.-J.; Chen T.-F.American Journal of Medical Genetics, Part B: Neuropsychiatric Genetics
32021Metabolic syndromes as important comorbidities in patients of inherited retinal degenerations: Experiences from the nationwide health database and a large hospital-based cohortChiou G.-J.; Huang D.-S.; Hu F.-R.; Yang C.-M.; Yang C.-H.; Huang C.-W.; Lin J.-W.; Lin C.-W.; Ho T.-C.; Hsieh Y.-T.; Lai T.-T.; Chen H.-M.; PEI-LUNG CHEN ; Hsiao C.K.; Chen T.-C.International Journal of Environmental Research and Public Health
42021Next-generation sequencing and bioinformatics to identify genetic causes of malignant hyperthermiaYeh H.-M.; Liao M.-H.; Chu C.-L.; Lin Y.-H.; Sun W.-Z.; Lai L.-P.; PEI-LUNG CHEN Journal of the Formosan Medical Association
52021Investigating DYT1 in a Taiwanese dystonia cohortWu M.-C.; Chang Y.-Y.; Chen Y.-F.; Lan M.-Y.; PEI-LUNG CHEN ; Tai C.-H.; Lin C.-H.Journal of the Formosan Medical Association
62021Hereditary hearing impairment with cutaneous abnormalitiesLee T.-L.; Lin P.-H.; PEI-LUNG CHEN ; Hong J.-B.; Wu C.-C.Genes
72020An integrative approach for pediatric auditory neuropathy spectrum disorders: revisiting etiologies and exploring the prognostic utility of auditory steady-state responseLin P.-H.; Hsu C.-J.; Lin Y.-H.; Lin Y.-H.; Yang S.-Y.; Yang T.-H.; PEI-LUNG CHEN ; Wu C.-C.; Liu T.-C.Scientific Reports
82020The efficacy and safety of topical rapamycin–calcitriol for facial angiofibromas in patients with tuberous sclerosis complex: a prospective, double-blind, randomized clinical trialPEI-LUNG CHEN ; Hong J.B.; Shen L.J.; Chen Y.T.; Wang S.J.; Liao Y.H.British Journal of Dermatology
92020Genotypes predispose phenotypes—clinical features and genetic spectrum of abca4-associated retinal dystrophiesSung Y.-C.; Yang C.-H.; Yang C.-M.; Lin C.-W.; Huang D.-S.; Huang Y.-S.; Hu F.-R.; PEI-LUNG CHEN ; Chen T.-C.Genes
102020Cerebral microbleeds in autosomal dominant polycystic kidney diseaseTsai L.-K.; PEI-LUNG CHEN ; Tsai H.-H.; Chen Y.-F.; Wu P.-C.; Jeng J.-S.; Huang J.-W.; Chu T.-S.; Kao J.T.-W.Journal of Stroke
112020Genotype-phenotype correlations of adult-onset PLA2G6-associated Neurodegeneration: Case series and literature reviewChu Y.-T.; Lin H.-Y.; PEI-LUNG CHEN ; Lin C.-H.BMC Neurology
122020Burden of Illness and Quality of Life in Tuberous Sclerosis Complex: Findings From the TOSCA StudyPEI-LUNG CHEN Frontiers in Neurology
132020Natural clusters of tuberous sclerosis complex (TSC)-associated neuropsychiatric disorders (TAND): New findings from the TOSCA TAND research projectPEI-LUNG CHEN Journal of Neurodevelopmental Disorders
142019Newly diagnosed and growing subependymal giant cell astrocytoma in adults with tuberous sclerosis complex: Results from the International TOSCA StudyPEI-LUNG CHEN Frontiers in Neurology
152019Clinical characteristics of subependymal giant cell astrocytoma in tuberous sclerosis complexPEI-LUNG CHEN Frontiers in Neurology
162019Epilepsy in tuberous sclerosis complex: Findings from the TOSCA StudyPEI-LUNG CHEN Epilepsia Open
172019Plectin Mutations in Progressive Familial Intrahepatic CholestasisWu S.-H.; Hsu J.S.; Chen H.-L.; Chien M.-M.; Wu J.-F.; Ni Y.-H.; Liou B.-Y.; Ho M.-C.; Jeng Y.-M.; Chang M.-H.; PEI-LUNG CHEN ; Chen H.-L.Hepatology
182019Distinctive genetic variation of long-segment Hirschsprung's disease in TaiwanYang W.; Chen S.-C.; Lai J.-Y.; Ming Y.-C.; Chen J.-C.; PEI-LUNG CHEN Neurogastroenterology and Motility
192019P53 ICE CRIM mouse: A tool to generate mutant allelic series in somatic cells and germ lines for cancer studiesFan H.-H.; Shing Yu I.; Lin Y.-H.; Wang S.-Y.; Liaw Y.-H.; PEI-LUNG CHEN ; Yang T.-L.; Lin S.-W.; Chen Y.-T.FASEB Journal
202019Genetic epidemiology and clinical features of hereditary hearing impairment in the Taiwanese populationWu C.-C.; Tsai C.-Y.; Lin Y.-H.; Chen P.-Y.; Lin P.-H.; Cheng Y.-F.; Wu C.-M.; Lin Y.-H.; Lee C.-Y.; Erdenechuluun J.; Liu T.-C.; PEI-LUNG CHEN ; Hsu C.-J.Genes
212019A clinical and genetic study of early-onset and familial parkinsonism in taiwan: An integrated approach combining gene dosage analysis and next-generation sequencingLin C.-H.; PEI-LUNG CHEN ; Tai C.-H.; Lin H.-I.; Chen C.-S.; Chen M.-L.; Wu R.-M.Movement Disorders
222019Targeted Next-Generation Sequencing Facilitates Genetic Diagnosis and Provides Novel Pathogenetic Insights into Deafness with Enlarged Vestibular AqueductLin Y.-H.; Wu C.-C.; Lin Y.-H.; Lu Y.-C.; Chen C.-S.; Liu T.-C.; PEI-LUNG CHEN ; Hsu C.-J.Journal of Molecular Diagnostics
232019HSD3B1 gene polymorphism and female pattern hair loss in women with polycystic ovary syndromeTu Y.-A.; Lin S.-J.; PEI-LUNG CHEN ; Chou C.-H.; Huang C.-C.; Ho H.-N.; Chen M.-J.Journal of the Formosan Medical Association
242019Serum levels of insulin-like growth factor 1 are negatively associated with log transformation of thyroid-stimulating hormone in Graves' disease patients with hyperthyroidism or subjects with euthyroidism: A prospective observational studyTseng F.-Y.; Chen Y.-T.; Chi Y.-C.; PEI-LUNG CHEN ; Yang W.-S.Medicine
252018Overview of the current status of familial hypercholesterolaemia care in over 60 countries - The EAS Familial Hypercholesterolaemia Studies Collaboration (FHSC)PEI-LUNG CHEN Atherosclerosis
262018Serum levels of fetuin-A are negatively associated with log transformation levels of thyroid-stimulating hormone in patients with hyperthyroidism or euthyroidism: An observational study at a medical center in TaiwanTseng F.-Y.; Chen Y.-T.; Chi Y.-C.; PEI-LUNG CHEN ; Yang W.-S.Medicine (United States)
272018Unique spectra of deafness-associated mutations in Mongolians provide insights into the genetic relationships among Eurasian populationsErdenechuluun J.; Lin Y.-H.; Ganbat K.; Bataakhuu D.; Makhbal Z.; Tsai C.-Y.; Lin Y.-H.; Chan Y.-H.; Hsu C.-J.; Hsu W.-C.; PEI-LUNG CHEN ; Wu C.-C.PLoS ONE
282018The Lupus-Associated Fcγ Receptor IIb–I232T Polymorphism Results in Impairment in the Negative Selection of Low-Affinity Germinal Center B Cells Via c-Abl in MiceJhou J.-P.; Yu I.-S.; Hwai H.; Chen C.-S.; PEI-LUNG CHEN ; Tzeng S.-J.Arthritis and Rheumatology
292018Identification of a novel LDLR disease-causing variant using capture-based next-generation sequencing screening of familial hypercholesterolemia patients in TaiwanHsiung Y.-C.; Lin P.-C.; Chen C.-S.; Tung Y.-C.; Yang W.-S.; PEI-LUNG CHEN ; Su T.-C.Atherosclerosis
302018Thyrotropin receptor antibodies and a genetic hint in antithyroid drug-induced adverse drug reactionsChang L.-C.; Chang C.-C.; PEI-LUNG CHEN ; Wang S.-H.; Chen Y.-H.; Tsai Y.-H.; Shih S.-R.; Chiu W.-Y.; Fann C.S.-J.; Yang W.-S.; Chang T.-C.Expert Opinion on Drug Safety
312018A 1204-single nucleotide polymorphism and insertion–deletion polymorphism panel for massively parallel sequencing analysis of DNA mixturesHwa H.-L.; Chung W.-C.; PEI-LUNG CHEN ; Lin C.-P.; Li H.-Y.; Yin H.-I.; Lee J.C.-I.Forensic Science International: Genetics
322018Oncogenic Function of a KIF5B-MET Fusion Variant in Non-Small Cell Lung CancerGow C.-H.; Liu Y.-N.; Li H.-Y.; Hsieh M.-S.; Chang S.-H.; Luo S.-C.; Tsai T.-H.; PEI-LUNG CHEN ; Tsai M.-F.; Shih J.-Y.Neoplasia (United States)
332018Comprehensive human leukocyte antigen genotyping of patients with type 1 diabetes mellitus in TaiwanTung Y.-C.; Fann C.S.-J.; Chang C.-C.; Chu C.-C.; Yang W.-S.; Hwu W.-L.; PEI-LUNG CHEN ; Tsai W.-Y.Pediatric Diabetes
342018Using Ion Torrent sequencing to study genetic mutation profiles of fatal thyroid cancersLu J.-Y.; Cheng W.-C.; Chen K.-Y.; Lin C.-C.; Chang C.-C.; Kuo K.-T.; PEI-LUNG CHEN Journal of the Formosan Medical Association
352018Prediction Model for Audiological Outcomes in Patients with GJB2 MutationsChen P.-Y.; Lin Y.-H.; Liu T.-C.; Lin Y.-H.; Tseng L.-H.; Yang T.-H.; PEI-LUNG CHEN ; Wu C.-C.; Hsu C.-J.Ear and Hearing
362018ABO genotyping with next-generation sequencing to resolve heterogeneity in donors with serology discrepanciesWu P.C.; Lin Y.-H.; Tsai L.F.; Chen M.H.; PEI-LUNG CHEN ; Pai S.-C.Transfusion
372017Early measurement of IL-10 predicts the outcomes of patients with acute respiratory distress syndrome receiving extracorporeal membrane oxygenation /631/250/127 /692/53/2422 /13 /13/21 /13/31 /45/23 articleLiu C.-H.; Kuo S.-W.; Ko W.-J.; Tsai P.-R.; Wu S.-W.; Lai C.-H.; Wang C.-H.; Chen Y.-S.; PEI-LUNG CHEN ; Liu T.-T.; Huang S.-C.; Jou T.-S.Scientific Reports
382017A novel missense variant in the nuclear localization signal of POU4F3 causes autosomal dominant non-syndromic hearing lossLin Y.-H.; Lin Y.-H.; Lu Y.-C.; Liu T.-C.; Chen C.-Y.; Hsu C.-J.; PEI-LUNG CHEN ; Wu C.-C.Scientific Reports
392017Identification of VPS35 p.D620N mutation-related Parkinson's disease in a Taiwanese family with successful bilateral subthalamic nucleus deep brain stimulation: A case report and literature reviewChen Y.-F.; Chang Y.-Y.; Lan M.-Y.; PEI-LUNG CHEN ; Lin C.-H.BMC Neurology
402017Intrafamilial phenotypic heterogeneity in a Taiwanese family with a MAPT p.R5H mutation: A case report and literature reviewLin H.-C.; Lin C.-H.; PEI-LUNG CHEN ; Cheng S.-J.; Chen P.-H.BMC Neurology
412017Identification of a novel HLA-B allele, HLA-B*40:238, in a Taiwanese individualLee H.-L.; Lai S.-K.; PEI-LUNG CHEN ; Chu C.-C.HLA
422016Serum Spot 14 concentration is negatively associated with thyroid-stimulating hormone levelChen Y.-T.; Tseng F.-Y.; PEI-LUNG CHEN ; Chi Y.-C.; Han D.-S.; Yang W.-S.Medicine (United States)
432016Clinical heterogeneity of LRRK2 p.I2012T mutationFan T.-S.; Wu R.-M.; PEI-LUNG CHEN ; Chen T.-F.; Li H.-Y.; Lin Y.-H.; Chen C.-Y.; Chen M.-L.; Tai C.-H.; Lin H.-I.; Lin C.-H.Parkinsonism and Related Disorders
442016Next generation sequencing yields the complete mitochondrial genome of the flathead mullet, Mugil cephalus cryptic species NWP2 (Teleostei: Mugilidae)Shen K.-N.; Yen T.-C.; Chen C.-H.; Li H.-Y.; PEI-LUNG CHEN ; Hsiao C.-D.Mitochondrial DNA. Part A, DNA mapping, sequencing, and analysis
452016Multiple gene sequencing for risk assessment in patients with early-onset or familial breast cancerLin P.-H.; Kuo W.-H.; Huang A.-C.; Lu Y.-S.; Lin C.-H.; Kuo S.-H.; Wang M.-Y.; Liu C.-Y.; Cheng F.T.-F.; Yeh M.-H.; Li H.-Y.; Yang Y.-H.; Hsu Y.-H.; Fan S.-C.; Li L.-Y.; Yu S.-L.; Chang K.-J.; PEI-LUNG CHEN ; Ni Y.-H.; Huang C.-S.Oncotarget
462016Follicular thyroid carcinoma with NRAS Q61K and GNAS R201H mutations that had a good 131I treatment responseLu J.-Y.; Hung P.-J.; PEI-LUNG CHEN ; Yen R.-F.; Kuo K.-T.; Yang T.-L.; Wang C.-Y.; Chang T.-C.; Huang T.-S.; Chang C.-C.Endocrinology, Diabetes and Metabolism Case Reports
472016KCNN2 polymorphisms and cardiac tachyarrhythmiasYu C.-C.; Chia-Ti T.; PEI-LUNG CHEN ; Wu C.-K.; Chiu F.-C.; Chiang F.-T.; Chen P.-S.; Chen C.-L.; Lin L.-Y.; Juang J.-M.; Ho L.-T.; La L.-P.; Yang W.-S.; Lin J.-L.Medicine (United States)
482016First step towards precision medicine for antithyroid drug-induced agranulocytosisPEI-LUNG CHEN ; Fann C.S.-J.; Shih S.-R.; Yang W.-S.; Chang T.-C.The Lancet Diabetes and Endocrinology
492016Serum levels of follistatin are positively associated with serum-free thyroxine levels in patients with hyperthyroidism or euthyroidismTseng F.-Y.; Chen Y.-T.; Chi Y.-C.; PEI-LUNG CHEN ; Yang W.-S.Medicine (United States)
502015Genetic determinants of antithyroid drug-induced agranulocytosis by human leukocyte antigen genotyping and genome-wide association studyPEI-LUNG CHEN ; Shih S.-R.; Wang P.-W.; Lin Y.-C.; Chu C.-C.; Lin J.-H.; Chen S.-C.; Chang C.-C.; Huang T.-S.; Tsai K.S.; Tseng F.-Y.; Wang C.-Y.; Lu J.-Y.; Chiu W.-Y.; Chang C.-C.; Chen Y.-H.; Chen Y.-T.; Fann C.S.-J.; Yang W.-S.; Chang T.-C.Nature Communications
512015Functional variants in DPYSL2 sequence increase risk of schizophrenia and suggest a link to mTOR signalingLiu Y.; Pham X.; Zhang L.; PEI-LUNG CHEN ; Burzynski G.; McGaughey D.M.; He S.; McGrath J.A.; Wolyniec P.; Fallin M.D.; Pierce M.S.; McCallion A.S.; Pulver A.E.; Avramopoulos D.; Valle D.G3: Genes, Genomes, Genetics
522015Concurrent exome-targeted next-generation sequencing and single nucleotide polymorphism array to identify the causative genetic aberrations of isolated Mayer-Rokitansky-K?ster-Hauser syndromeChen M.-J.; Wei S.-Y.; Yang W.-S.; Wu T.-T.; Li H.-Y.; Ho H.-N.; Yang Y.-S.; PEI-LUNG CHEN Human Reproduction
532015Association between serum levels of adipocyte fatty acid-binding protein and free thyroxineTseng F.-Y.; PEI-LUNG CHEN ; Chen Y.-T.; Chi Y.-C.; Shih S.-R.; Wang C.-Y.; Chen C.-L.; Yang W.-S.Medicine (United States)
542015Identifying children with poor cochlear implantation outcomes using massively parallel sequencingWu C.-C.; Lin Y.-H.; Liu T.-C.; Lin K.-N.; Yang W.-S.; Hsu C.-J.; PEI-LUNG CHEN ; Wu C.-M.Medicine (United States)
552015An isodicentric X chromosome with gonadal dysgenesis in a lady without prominent somatic features of Turner's syndrome. A case reportYu T.-Y.; Lin H.-S.; PEI-LUNG CHEN ; Huang T.-S.Journal of the Formosan Medical Association
562015Long-term cochlear implant outcomes in children with GJB2 and SLC26A4 mutationsWu C.-M.; Ko H.-C.; Tsou Y.-T.; Lin Y.-H.; Lin J.-L.; Chen C.-K.; PEI-LUNG CHEN ; Wu C.-C.PLoS ONE
572015Identification of a novel GATA3 mutation in a deaf Taiwanese family by massively parallel sequencingLin Y.-H.; Wu C.-C.; Hsu T.-Y.; Chiu W.-Y.; Hsu C.-J.; PEI-LUNG CHEN Mutation Research - Fundamental and Molecular Mechanisms of Mutagenesis
582014Predicting HLA genotypes using unphased and flanking single-nucleotide polymorphisms in Han Chinese populationHsieh A.-R.; Chang S.-W.; PEI-LUNG CHEN ; Chu C.-C.; Hsiao C.-L.; Yang W.-S.; Chang C.-C.; Wu J.-Y.; Chen Y.-T.; Chang T.-C.; Fann C.S.J.BMC Genomics
592014STAT3 mediates regorafenib-induced apoptosis in hepatocellular carcinomaTai W.-T.; Chu P.-Y.; Shiau C.-W.; Chen Y.-L.; Li Y.-S.; Hung M.-H.; Chen L.-J.; PEI-LUNG CHEN ; Su J.-C.; Lin P.-Y.; Yu H.-C.; Chen K.-F.Clinical Cancer Research
602014Genetic analysis of CARD14 in non-familial pityriasis rubra pilaris: A case seriesHong J.-B.; PEI-LUNG CHEN ; Chen Y.-T.; Tsai T.-F.Acta Dermato-Venereologica
612014A fault-tolerant method for HLA typing with PacBio dataChang C.-J.; PEI-LUNG CHEN ; Yang W.-S.; Chao K.-M.BMC Bioinformatics
622013Tuberous sclerosis complex surveillance and management: Recommendations of the 2012 international tuberous sclerosis complex consensus conferencePEI-LUNG CHEN Pediatric Neurology
632013Gene-wide tagging study of the effects of common genetic polymorphisms in the α subunits of the GABAA receptor on epilepsy treatment responseHung C.-C.; PEI-LUNG CHEN ; Huang W.-M.; Tai J.J.; Hsieh T.-J.; Ding S.-T.; Hsieh Y.-W.; Liou H.-H.Pharmacogenomics
642013Identification of a novel HLA-B allele, B*07:162, in a Taiwanese individualPEI-LUNG CHEN ; Lai S.-K.; Yang W.-S.; Chang T.-C.; Chu C.-C.Tissue Antigens
652013A genome-wide association analysis identifies novel susceptibility loci for coronary arterial lesions in patients with Kawasaki diseaseLin M.-T.; Hsu C.-L.; PEI-LUNG CHEN ; Yang W.-S.; Wang J.-K.; Fann C.S.J.; Wu M.-H.Translational Research
662013Application of Massively Parallel Sequencing to Genetic Diagnosis in Multiplex Families with Idiopathic Sensorineural Hearing ImpairmentWu C.-C.; Lin Y.-H.; Lu Y.-C.; Chen P.-J.; Yang W.-S.; Hsu C.-J.; PEI-LUNG CHEN PLoS ONE
672013Tuberous sclerosis complex diagnostic criteria update: Recommendations of the 2012 international tuberous sclerosis complex consensus conferencePEI-LUNG CHEN Pediatric Neurology
682012Common genetic mutations in the start codon of the SDH subunit D gene among Chinese families with familial head and neck paragangliomasWang C.-P.; Chen T.-C.; Chang Y.-L.; Ko J.-Y.; Yang T.-L.; Lo F.-Y.; Hu Y.-L.; PEI-LUNG CHEN ; Wu C.-C.; Lou P.-J.Oral Oncology
692011Clinical implication of the C allele of the ITPKC gene SNP rs28493229 in kawasaki disease: Association with disease susceptibility and BCG scar reactivationLin M.-T.; Wang J.-K.; Yeh J.-I.; Sun L.-C.; PEI-LUNG CHEN ; Wu J.-F.; Chang C.-C.; Lee W.-L.; Shen C.-T.; Wang N.-K.; Wu C.-S.; Yeh S.-Z.; Chen C.-A.; Chiu S.-N.; Wu M.-H.Pediatric Infectious Disease Journal
702011Comprehensive genotyping in two homogeneous Graves' disease samples reveals major and novel HLA association allelesPEI-LUNG CHEN ; Fann C.-S.-J.; Chu C.-C.; Chang C.-C.; Chang S.-W.; Hsieh H.-Y.; Lin M.; Yang W.-S.; Chang T.-C.PLoS ONE
712011Linkage and association on 8p21.2-p21.1 in schizophreniaFallin M.D.; Lasseter V.K.; Liu Y.; Avramopoulos D.; McGrath J.; Wolyniec P.S.; Nestadt G.; Liang K.-Y.; PEI-LUNG CHEN ; Valle D.; Pulver A.E.American Journal of Medical Genetics, Part B: Neuropsychiatric Genetics
722010Replication of an association of a common variant in the Reelin gene (RELN) with schizophrenia in Ashkenazi Jewish womenLiu Y.; PEI-LUNG CHEN ; McGrath J.; Wolyniec P.; Fallin D.; Nestadt G.; Liang K.-Y.; Pulver A.; Valle D.; Avramopoulos D.Psychiatric Genetics
732009Fine Mapping on Chromosome 10q22-q23 Implicates Neuregulin 3 in SchizophreniaPEI-LUNG CHEN ; Avramopoulos D.; Lasseter V.K.; McGrath J.A.; Fallin M.D.; Liang K.-Y.; Nestadt G.; Feng N.; Steel G.; Cutting A.S.; Wolyniec P.; Pulver A.E.; Valle D.American Journal of Human Genetics
742009Familiality of novel factorial dimensions of schizophreniaMcGrath J.A.; Avramopoulos D.; Lasseter V.K.; Wolyniec P.S.; Fallin M.D.; Liang K.-Y.; Nestadt G.; Thornquist M.H.; Luke J.R.; PEI-LUNG CHEN ; Valle D.; Pulver A.E.Archives of General Psychiatry
752009Human genetics of diabetes mellitus in TaiwanPEI-LUNG CHEN ; Yang W.-S.Frontiers in Bioscience
762008Family-based association study of cytotoxic T-lymphocyte antigen-4 with susceptibility to Graves' disease in Han population of TaiwanPEI-LUNG CHEN ; Fann C.S.-J.; Chang C.-C.; Wu I.-L.; Chiu W.-Y.; Lin C.-Y.; Yang W.-S.; Chang T.-C.Genes and Immunity
772007Linkage of Graves' disease to the human leucocyte antigen region in the Chinese-Han population in TaiwanPEI-LUNG CHEN ; Fann C.S.-J.; Chang C.-C.; Wu I.-L.; Chiu W.-Y.; Lin C.-Y.; Yang W.-S.; Chang T.-C.Clinical Endocrinology
782006Translational repression restricts expression of the C. elegans Nanos homolog NOS-2 to the embryonic germlineD'Agostino I.; Merritt C.; PEI-LUNG CHEN ; Seydoux G.; Subramaniam K.Developmental Biology
792001Progress in genetic study on graves' diseasePEI-LUNG CHEN ; Chang T.-C.Journal of Internal Medicine of Taiwan