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ABO genotyping with next-generation sequencing to resolve heterogeneity in donors with serology discrepancies.
Published in:
2018
By:
- Wu, Ping Chun;
- Lin, Yin‐Hung;
- Tsai, Lei Fang;
- Chen, Ming Hung;
- Chen, Pei‐Lung;
- Pai, Shun‐Chung;
- Lin, Yin-Hung;
- Chen, Pei-Lung;
- Pai, Shun-Chung
Publication type:
journal article
A clinical and genetic study of early-onset and familial parkinsonism in taiwan: An integrated approach combining gene dosage analysis and next-generation sequencing.
Published in:
2019
By:
- Lin, Chin‐Hsien;
- Chen, Pei‐Lung;
- Tai, Chun‐Hwei;
- Lin, Hang‐I;
- Chen, Chih‐Shan;
- Chen, Meng‐Ling;
- Wu, Ruey‐Meei;
- Lin, Chin-Hsien;
- Chen, Pei-Lung;
- Tai, Chun-Hwei;
- Lin, Hang-I;
- Chen, Chih-Shan;
- Chen, Meng-Ling;
- Wu, Ruey-Meei
Publication type:
journal article
The Clinical Contribution of Full-Field Electroretinography and 8-Year Experiences of Application in a Tertiary Medical Center.
Published in:
Journal of Personalized Medicine, 2021, v. 11, n. 10, p. 1022, doi. 10.3390/jpm11101022
By:
- Yang, Jung-Je;
- Huang, Chu-Hsuan;
- Yang, Chang-Hao;
- Yang, Chung-May;
- Lin, Chao-Wen;
- Ho, Tzyy-Chang;
- Lin, Chang-Ping;
- Hsieh, Yi-Ting;
- Yeh, Po-Ting;
- Lai, Tso-Ting;
- Chen, Pei-Lung;
- Chen, Ta-Ching
Publication type:
Article
Identification of nine novel variants across PAX3, SOX10, EDNRB, and MITF genes in Waardenburg syndrome with next‐generation sequencing.
Published in:
Molecular Genetics & Genomic Medicine, 2022, v. 10, n. 12, p. 1, doi. 10.1002/mgg3.2082
By:
- Lee, Chen‐Yu;
- Lo, Ming‐Yu;
- Chen, You‐Mei;
- Lin, Pei‐Hsuan;
- Hsu, Chuan‐Jen;
- Chen, Pei‐Lung;
- Wu, Chen‐Chi;
- Hsu, Jacob Shujui
Publication type:
Article
Genetic study of young‐onset dementia using targeted gene panel sequencing in Taiwan.
Published in:
American Journal of Medical Genetics. Part B: Neuropsychiatric Genetics, 2021, v. 186, n. 2, p. 67, doi. 10.1002/ajmg.b.32836
By:
- Hsu, Jung‐Lung;
- Lin, Chin‐Hsien;
- Chen, Pei‐Lung;
- Lin, Kun‐Ju;
- Chen, Ta‐Fu
Publication type:
Article
Risk factors related to age at diagnosis of pancreatic cancer: a retrospective cohort pilot study.
Published in:
2022
By:
- Lin, Ro-Ting;
- Chen, Pei-Lung;
- Yang, Chi-Ying;
- Yeh, Chun-Chieh;
- Lin, Chun-Che;
- Huang, Wen-Hsin;
- Chung, An-Ko;
- Lin, Jaw-Town
Publication type:
journal article
Long-Term Cochlear Implant Outcomes in Children with GJB2 and SLC26A4 Mutations.
Published in:
PLoS ONE, 2015, v. 10, n. 9, p. 1, doi. 10.1371/journal.pone.0138575
By:
- Wu, Che-Ming;
- Ko, Hui-Chen;
- Tsou, Yung-Ting;
- Lin, Yin-Hung;
- Lin, Ju-Li;
- Chen, Chin-Kuo;
- Chen, Pei-Lung;
- Wu, Chen-Chi
Publication type:
Article
Application of Massively Parallel Sequencing to Genetic Diagnosis in Multiplex Families with Idiopathic Sensorineural Hearing Impairment.
Published in:
PLoS ONE, 2013, v. 8, n. 2, p. 1, doi. 10.1371/journal.pone.0057369
By:
- Wu, Chen-Chi;
- Lin, Yin-Hung;
- Lu, Ying-Chang;
- Chen, Pei-Jer;
- Yang, Wei-Shiung;
- Hsu, Chuan-Jen;
- Chen, Pei-Lung
Publication type:
Article
Metabolic Syndromes as Important Comorbidities in Patients of Inherited Retinal Degenerations: Experiences from the Nationwide Health Database and a Large Hospital-Based Cohort.
Published in:
International Journal of Environmental Research & Public Health, 2021, v. 18, n. 4, p. 2065, doi. 10.3390/ijerph18042065
By:
- Chiou, Guann-Jye;
- Huang, Ding-Siang;
- Hu, Fung-Rong;
- Yang, Chung-May;
- Yang, Chang-Hao;
- Huang, Ching-Wen;
- Lin, Jou-Wei;
- Lin, Chao-Wen;
- Ho, Tzyy-Chang;
- Hsieh, Yi-Ting;
- Lai, Tso-Ting;
- Chen, Ho-Min;
- Chen, Pei-Lung;
- Hsiao, Chuhsing Kate;
- Chen, Ta-Ching;
- Cavallo, Pierpaolo
Publication type:
Article
Genetic characteristics and epidemiology of inherited retinal degeneration in Taiwan.
Published in:
NPJ Genomic Medicine, 2021, v. 6, n. 1, p. 1, doi. 10.1038/s41525-021-00180-1
By:
- Chen, Ta-Ching;
- Huang, Ding-Siang;
- Lin, Chao-Wen;
- Yang, Chang-Hao;
- Yang, Chung-May;
- Wang, Victoria Y.;
- Lin, Jou-Wei;
- Luo, Allen Chilun;
- Hu, Fung-Rong;
- Chen, Pei-Lung
Publication type:
Article
High prevalence of exon-13 variants in USH2A-related retinal dystrophies in Taiwanese population.
Published in:
Orphanet Journal of Rare Diseases, 2024, v. 19, n. 1, p. 1, doi. 10.1186/s13023-024-03238-2
By:
- Lin, Yu-Wei;
- Huang, Yu-Shu;
- Lin, Chien-Yu;
- Lin, Chao-Wen;
- Wu, Chen-Chi;
- Yang, Chang-Hao;
- Yang, Chung-May;
- Chen, Pei-Lung;
- Chen, Ta-Ching
Publication type:
Article
Concurrent exome-targeted next-generation sequencing and single nucleotide polymorphism array to identify the causative genetic aberrations of isolated Mayer-Rokitansky-Küster-Hauser syndrome.
Published in:
2015
By:
- Chen, Mei-Jou;
- Wei, Shin-Yi;
- Yang, Wei-Shiung;
- Wu, Tsai-Tzu;
- Li, Huei-Ying;
- Ho, Hong-Nerng;
- Yang, Yu-Shih;
- Chen, Pei-Lung
Publication type:
journal article
Identification 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 review.
Published in:
2017
By:
- Ying-Fa Chen;
- Yung-Yee Chang;
- Min-Yu Lan;
- Pei-Lung Chen;
- Chin-Hsien Lin;
- Chen, Ying-Fa;
- Chang, Yung-Yee;
- Lan, Min-Yu;
- Chen, Pei-Lung;
- Lin, Chin-Hsien
Publication type:
journal article
Intrafamilial phenotypic heterogeneity in a Taiwanese family with a MAPT p.R5H mutation: a case report and literature review.
Published in:
2017
By:
- Hui-Chi Lin;
- Chin-Hsien Lin;
- Pei-Lung Chen;
- Shih-Jung Cheng;
- Pei-Hao Chen;
- Lin, Hui-Chi;
- Lin, Chin-Hsien;
- Chen, Pei-Lung;
- Cheng, Shih-Jung;
- Chen, Pei-Hao
Publication type:
journal article
Genetic determinants of antithyroid drug-induced agranulocytosis by human leukocyte antigen genotyping and genome-wide association study.
Published in:
Nature Communications, 2015, v. 6, n. 7, p. 7633, doi. 10.1038/ncomms8633
By:
- Chen, Pei-Lung;
- Shih, Shyang-Rong;
- Wang, Pei-Wen;
- Lin, Ying-Chao;
- Chu, Chen-Chung;
- Lin, Jung-Hsin;
- Chen, Szu-Chi;
- Chang, Ching-Chung;
- Huang, Tien-Shang;
- Tsai, Keh Sung;
- Tseng, Fen-Yu;
- Wang, Chih-Yuan;
- Lu, Jin-Ying;
- Chiu, Wei-Yih;
- Chang, Chien-Ching;
- Chen, Yu-Hsuan;
- Chen, Yuan-Tsong;
- Fann, Cathy Shen-Jang;
- Yang, Wei-Shiung;
- Chang, Tien-Chun
Publication type:
Article
Genetics in neovascular age‐related macular degeneration susceptibility and treatment response to anti‐VEGF intravitreal injection: A case series study.
Published in:
Clinical & Experimental Ophthalmology, 2024, v. 52, n. 6, p. 655, doi. 10.1111/ceo.14388
By:
- Chang, Fang‐Yu;
- Huang, Chu‐Hsuan;
- Yang, Chang‐Hao;
- Chang, Jung‐Tzu;
- Yang, Chung‐May;
- Ho, Tzzy‐Chang;
- Hsieh, Yi‐Ting;
- Lai, Tso‐Ting;
- Lin, Chao‐Wen;
- Lin, Chang‐Pin;
- Chen, Yi‐Chieh;
- Lai, Ying‐Ju;
- Chen, Pei‐Lung;
- Hsu, Jacob Shujui;
- Chen, Ta‐Ching
Publication type:
Article
An integrative approach for pediatric auditory neuropathy spectrum disorders: revisiting etiologies and exploring the prognostic utility of auditory steady-state response.
Published in:
Scientific Reports, 2020, v. 10, n. 1, p. 1, doi. 10.1038/s41598-020-66877-y
By:
- Lin, Pei-Hsuan;
- Hsu, Chuan-Jen;
- Lin, Yin-Hung;
- Lin, Yi-Hsin;
- Yang, Shu-Yu;
- Yang, Ting-Hua;
- Chen, Pei-Lung;
- Wu, Chen-Chi;
- Liu, Tien-Chen
Publication type:
Article
Distinctive genetic variation of long‐segment Hirschsprung's disease in Taiwan.
Published in:
Neurogastroenterology & Motility, 2019, v. 31, n. 11, p. N.PAG, doi. 10.1111/nmo.13665
By:
- Yang, Wendy;
- Chen, Szu‐Chieh;
- Lai, Jin‐Yao;
- Ming, Yung‐Ching;
- Chen, Jeng‐Chang;
- Chen, Pei‐Lung
Publication type:
Article
Comparison of clinical and neuroimaging features between NOTCH3 mutations and nongenetic spontaneous intracerebral haemorrhage.
Published in:
European Journal of Neurology, 2022, v. 29, n. 11, p. 3243, doi. 10.1111/ene.15485
By:
- Chen, Chih‐Hao;
- Chu, Yung‐Tsai;
- Chen, Ya‐Fang;
- Ko, Tzu‐Yu;
- Cheng, Yu‐Wen;
- Lee, Ming‐Jen;
- Chen, Pei‐Lung;
- Tang, Sung‐Chun;
- Jeng, Jiann‐Shing
Publication type:
Article
Genetic Underpinnings and Audiological Characteristics in Children With Unilateral Sensorineural Hearing Loss.
Published in:
Otolaryngology-Head & Neck Surgery, 2023, v. 169, n. 5, p. 1299, doi. 10.1002/ohn.354
By:
- Lee, Chen‐Yu;
- Lin, Pei‐Hsuan;
- Chiang, Yu‐Ting;
- Tsai, Cheng‐Yu;
- Yang, Shu‐Yu;
- Chen, You‐Mei;
- Li, Chao‐Hsuan;
- Lu, Chun‐Yi;
- Liu, Tien‐Chen;
- Hsu, Chuan‐Jen;
- Chen, Pei‐Lung;
- Hsu, Jacob Shujui;
- Wu, Chen‐Chi
Publication type:
Article
Comprehensive Etiologic Analyses in Pediatric Cochlear Implantees and the Clinical Implications.
Published in:
Biomedicines, 2022, v. 10, n. 8, p. N.PAG, doi. 10.3390/biomedicines10081846
By:
- Lee, Chee-Yee;
- Lin, Pei-Hsuan;
- Tsai, Cheng-Yu;
- Chiang, Yu-Ting;
- Chiou, Hong-Ping;
- Chiang, Ko-Yin;
- Chen, Pei-Lung;
- Hsu, Jacob Shu-Jui;
- Liu, Tien-Chen;
- Wu, Hung-Pin;
- Wu, Chen-Chi;
- Hsu, Chuan-Jen
Publication type:
Article
Cochlear Implantation Outcomes in Patients with Auditory Neuropathy Spectrum Disorder of Genetic and Non-Genetic Etiologies: A Multicenter Study.
Published in:
Biomedicines, 2022, v. 10, n. 7, p. N.PAG, doi. 10.3390/biomedicines10071523
By:
- Lin, Pei-Hsuan;
- Wu, Hung-Pin;
- Wu, Che-Ming;
- Chiang, Yu-Ting;
- Hsu, Jacob Shujui;
- Tsai, Cheng-Yu;
- Wang, Han;
- Tseng, Li-Hui;
- Chen, Pey-Yu;
- Yang, Ting-Hua;
- Hsu, Chuan-Jen;
- Chen, Pei-Lung;
- Wu, Chen-Chi;
- Liu, Tien-Chen
Publication type:
Article
The 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 Mice.
Published in:
Arthritis & Rheumatology, 2018, v. 70, n. 11, p. 1866, doi. 10.1002/art.40555
By:
- Jhou, Jyun‐Pei;
- Yu, I‐Shing;
- Hwai, Haw;
- Chen, Chih‐Shan;
- Chen, Pei‐Lung;
- Tzeng, Shiang‐Jong
Publication type:
Article
Comprehensive human leukocyte antigen genotyping of patients with type 1 diabetes mellitus in Taiwan.
Published in:
Pediatric Diabetes, 2018, v. 19, n. 4, p. 699, doi. 10.1111/pedi.12645
By:
- Tung, Yi‐Ching;
- Fann, Cathy S‐J;
- Chang, Chien‐Ching;
- Chu, Chen‐Chung;
- Yang, Wei‐Shiung;
- Hwu, Wuh‐Liang;
- Chen, Pei‐Lung;
- Tsai, Wen‐Yu
Publication type:
Article
Metabolomics facilitates differential diagnosis in common inherited retinal degenerations by exploring their profiles of serum metabolites.
Published in:
Nature Communications, 2024, v. 15, n. 1, p. 1, doi. 10.1038/s41467-024-47911-3
By:
- Wang, Wei-Chieh;
- Huang, Chu-Hsuan;
- Chung, Hsin-Hsiang;
- Chen, Pei-Lung;
- Hu, Fung-Rong;
- Yang, Chang-Hao;
- Yang, Chung-May;
- Lin, Chao-Wen;
- Hsu, Cheng-Chih;
- Chen, Ta-Ching
Publication type:
Article
Revisiting Genetic Epidemiology with a Refined Targeted Gene Panel for Hereditary Hearing Impairment in the Taiwanese Population.
Published in:
Genes, 2023, v. 14, n. 4, p. 880, doi. 10.3390/genes14040880
By:
- Lee, Yen-Hui;
- Tsai, Cheng-Yu;
- Lu, Yue-Sheng;
- Lin, Pei-Hsuan;
- Chiang, Yu-Ting;
- Yang, Ting-Hua;
- Hsu, Jacob Shu-Jui;
- Hsu, Chuan-Jen;
- Chen, Pei-Lung;
- Liu, Tien-Chen;
- Wu, Chen-Chi
Publication type:
Article
Genetic Spectrum and Characteristics of Hereditary Optic Neuropathy in Taiwan.
Published in:
Genes, 2021, v. 12, n. 9, p. 1378, doi. 10.3390/genes12091378
By:
- Lin, Chao-Wen;
- Huang, Ching-Wen;
- Luo, Allen Chilun;
- Chou, Yuh-Tsyr;
- Huang, Yu-Shu;
- Chen, Pei-Lung;
- Chen, Ta-Ching
Publication type:
Article
Hereditary Hearing Impairment with Cutaneous Abnormalities.
Published in:
Genes, 2021, v. 12, n. 1, p. 43, doi. 10.3390/genes12010043
By:
- Lee, Tung-Lin;
- Lin, Pei-Hsuan;
- Chen, Pei-Lung;
- Hong, Jin-Bon;
- Wu, Chen-Chi
Publication type:
Article
Genotypes Predispose Phenotypes—Clinical Features and Genetic Spectrum of ABCA4 -Associated Retinal Dystrophies.
Published in:
Genes, 2020, v. 11, n. 12, p. 1421, doi. 10.3390/genes11121421
By:
- Sung, Yu-Chi;
- Yang, Chang-Hao;
- Yang, Chung-May;
- Lin, Chao-Wen;
- Huang, Ding-Siang;
- Huang, Yu-Shu;
- Hu, Fung-Rong;
- Chen, Pei-Lung;
- Chen, Ta-Ching
Publication type:
Article
Genetic Epidemiology and Clinical Features of Hereditary Hearing Impairment in the Taiwanese Population.
Published in:
Genes, 2019, v. 10, n. 10, p. 772, doi. 10.3390/genes10100772
By:
- Wu, Chen-Chi;
- Tsai, Cheng-Yu;
- Lin, Yi-Hsin;
- Chen, Pey-Yu;
- Lin, Pei-Hsuan;
- Cheng, Yen-Fu;
- Wu, Che-Ming;
- Lin, Yin-Hung;
- Lee, Chee-Yee;
- Erdenechuluun, Jargalkhuu;
- Liu, Tien-Chen;
- Chen, Pei-Lung;
- Hsu, Chuan-Jen
Publication type:
Article
Unique spectra of deafness-associated mutations in Mongolians provide insights into the genetic relationships among Eurasian populations.
Published in:
PLoS ONE, 2018, v. 13, n. 12, p. 1, doi. 10.1371/journal.pone.0209797
By:
- Erdenechuluun, Jargalkhuu;
- Lin, Yin-Hung;
- Ganbat, Khongorzul;
- Bataakhuu, Delgermaa;
- Makhbal, Zaya;
- Tsai, Cheng-Yu;
- Lin, Yi-Hsin;
- Chan, Yen-Hui;
- Hsu, Chuan-Jen;
- Hsu, Wei-Chung;
- Chen, Pei-Lung;
- Wu, Chen-Chi
Publication type:
Article
Transcriptome Analysis of Mesenchymal Progenitor Cells Revealed Molecular Insights into Metabolic Dysfunction and Inflammation in Polycystic Ovary Syndrome.
Published in:
International Journal of Molecular Sciences, 2024, v. 25, n. 14, p. 7948, doi. 10.3390/ijms25147948
By:
- Huang, Mei-Chi;
- Chen, Pei-Lung;
- Hsu, Chia-Lang
Publication type:
Article
Genotype-phenotype correlations of adult-onset PLA2G6-associated Neurodegeneration: case series and literature review.
Published in:
2020
By:
- Chu, Yung-Tsai;
- Lin, Han-Yi;
- Chen, Pei-Lung;
- Lin, Chin-Hsien
Publication type:
journal article
Phenome-wide analysis of Taiwan Biobank reveals novel glycemia-related loci and genetic risks for diabetes.
Published in:
Communications Biology, 2022, v. 5, n. 1, p. 1, doi. 10.1038/s42003-022-04168-0
By:
- Lee, Chia-Jung;
- Chen, Ting-Huei;
- Lim, Aylwin Ming Wee;
- Chang, Chien-Ching;
- Sie, Jia-Jyun;
- Chen, Pei-Lung;
- Chang, Su-Wei;
- Wu, Shang-Jung;
- Hsu, Chia-Lin;
- Hsieh, Ai-Ru;
- Yang, Wei-Shiung;
- Fann, Cathy S. J.
Publication type:
Article
Different clinical and genetic features of Alagille patients with progressive disease versus a jaundice‐free course.
Published in:
JGH Open, 2022, v. 6, n. 12, p. 839, doi. 10.1002/jgh3.12830
By:
- Chiang, Che‐Ming;
- Jeng, Yung‐Ming;
- Ho, Ming‐Chih;
- Lai, Ming‐Wei;
- Li, Huei‐Ying;
- Chen, Pei‐Lung;
- Lee, Ni‐Chung;
- Wu, Jia‐Feng;
- Chiu, Yu‐Chun;
- Liou, Bang‐Yu;
- Ni, Yen‐Hsuan;
- Hsu, Hong‐Yuan;
- Chang, Mei‐Hwei;
- Chen, Huey‐Ling
Publication type:
Article
Linkage of Graves’ disease to the human leucocyte antigen region in the Chinese-Han population in Taiwan.
Published in:
Clinical Endocrinology, 2007, v. 66, n. 5, p. 646, doi. 10.1111/j.1365-2265.2007.02787.x
By:
- Chen, Pei-Lung;
- Fann, Cathy Shen-Jang;
- Chang, Chien-Ching;
- Wu, I-Lin;
- Chiu, Wei-Yih;
- Lin, Chin-Yu;
- Yang, Wei-Shiung;
- Chang, Tien-Chun
Publication type:
Article
Cochlear implantation in LEOPARD syndrome: Our experience with three patients.
Published in:
Clinical Otolaryngology, 2022, v. 47, n. 2, p. 341, doi. 10.1111/coa.13895
By:
- Wu, Ping‐Che;
- Tsai, Cheng‐Yu;
- Lin, Pei‐Hsuan;
- Chou, Pao‐Hsuan;
- Huang, Fang‐Lih;
- Chen, Pei‐Lung;
- Shiao, Jiun‐Yih;
- Liu, Tien‐Chen;
- Hsu, Chuan‐Jen;
- Huang, Chang‐Wei;
- Wu, Chen‐Chi
Publication type:
Article

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