| Issue Date | Title | Author(s) | Source | scopus | WOS | Fulltext/Archive link |
|---|---|---|---|---|---|---|
| 2018 | A 1204-single nucleotide polymorphism and insertion–deletion polymorphism panel for massively parallel sequencing analysis of DNA mixtures | Hwa 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 | 17 | ||
| 2018 | ABO genotyping with next-generation sequencing to resolve heterogeneity in donors with serology discrepancies | Wu P.C.; Lin Y.-H.; Tsai L.F.; Chen M.H.; PEI-LUNG CHEN ; Pai S.-C. | Transfusion | 21 | ||
| 2013 | Application of Massively Parallel Sequencing to Genetic Diagnosis in Multiplex Families with Idiopathic Sensorineural Hearing Impairment | Wu C.-C.; Lin Y.-H.; Lu Y.-C.; Chen P.-J.; Yang W.-S.; Hsu C.-J.; PEI-LUNG CHEN | PLoS ONE | 41 | ||
| 2015 | Association between serum levels of adipocyte fatty acid-binding protein and free thyroxine | Tseng 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) | 6 | ||
| 2020 | Burden of Illness and Quality of Life in Tuberous Sclerosis Complex: Findings From the TOSCA Study | PEI-LUNG CHEN | Frontiers in Neurology | 7 | ||
| 2020 | Cerebral microbleeds in autosomal dominant polycystic kidney disease | Tsai 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 | 2 | ||
| 2019 | A clinical and genetic study of early-onset and familial parkinsonism in taiwan: An integrated approach combining gene dosage analysis and next-generation sequencing | Lin C.-H.; PEI-LUNG CHEN ; Tai C.-H.; Lin H.-I.; Chen C.-S.; Chen M.-L.; Wu R.-M. | Movement Disorders | 36 | ||
| 2022 | A Clinical and Integrated Genetic Study of Isolated and Combined Dystonia in Taiwan | Wu M.-C.; Chang Y.-Y.; Lan M.-Y.; Chen Y.-F.; Tai C.-H.; Lin Y.-F.; Tsai S.-F.; PEI-LUNG CHEN ; Lin C.-H. | Journal of Molecular Diagnostics | 0 | 0 | |
| 2019 | Clinical characteristics of subependymal giant cell astrocytoma in tuberous sclerosis complex | PEI-LUNG CHEN | Frontiers in Neurology | 8 | ||
| 2021 | The clinical contribution of full-field electroretinography and 8-year experiences of application in a tertiary medical center | Yang J.-J.; Huang C.-H.; Yang C.-H.; Yang C.-M.; Lin C.-W.; Ho T.-C.; Lin C.-P.; Hsieh Y.-T.; Yeh P.-T.; Lai T.-T.; PEI-LUNG CHEN ; Chen T.-C. | Journal of Personalized Medicine | 0 | ||
| 2016 | Clinical heterogeneity of LRRK2 p.I2012T mutation | Fan 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 | 11 | ||
| 2011 | Clinical implication of the C allele of the ITPKC gene SNP rs28493229 in kawasaki disease: Association with disease susceptibility and BCG scar reactivation | Lin 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 | 47 | ||
| 2021 | Clinical manifestations and genetic characteristics in the Taiwan thoracic aortic aneurysm and dissection cohort - a prospective cohort study | Duan D.-M.; Chiu H.-H.; PEI-LUNG CHEN ; Yeh P.-T.; Yu C.-W.; Yang K.-C.; Yu C.-C. | Journal of the Formosan Medical Association | 0 | ||
| 2022 | Cochlear implantation in LEOPARD syndrome: Our experience with three patients | Wu P.-C.; Tsai C.-Y.; Lin P.-H.; Chou P.-H.; Huang F.-L.; PEI-LUNG CHEN ; Shiao J.-Y.; Liu T.-C.; Hsu C.-J.; Huang C.-W.; Wu C.-C. | Clinical Otolaryngology | 0 | 0 | |
| 2012 | Common genetic mutations in the start codon of the SDH subunit D gene among Chinese families with familial head and neck paragangliomas | Wang 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 | 9 | ||
| 2011 | Comprehensive genotyping in two homogeneous Graves' disease samples reveals major and novel HLA association alleles | PEI-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 | 45 | ||
| 2018 | Comprehensive human leukocyte antigen genotyping of patients with type 1 diabetes mellitus in Taiwan | Tung 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 | 2 | ||
| 2015 | Concurrent exome-targeted next-generation sequencing and single nucleotide polymorphism array to identify the causative genetic aberrations of isolated Mayer-Rokitansky-K?ster-Hauser syndrome | Chen 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 | 12 | ||
| 2019 | Distinctive genetic variation of long-segment Hirschsprung's disease in Taiwan | Yang W.; Chen S.-C.; Lai J.-Y.; Ming Y.-C.; Chen J.-C.; PEI-LUNG CHEN | Neurogastroenterology and Motility | 1 | ||
| 2017 | Early 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 article | Liu 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 | 12 |
