公開日期 | 標題 | 作者 | 來源出版物 | scopus | WOS | 全文 |
2020 | Prediction Model for Audiological Outcomes in Patients With GJB2 Mutations | Chen P.-Y.; Lin Y.-H.; TIEN-CHEN LIU ; Lin Y.-H.; LI-HUI TSENG ; TING-HUA YANG ; PEI-LUNG CHEN ; Chen-Chi Wu ; Hsu C.-J. | Ear and hearing | 15 | 16 | |
2022 | Profiling genes encoding the adaptive immune receptor repertoire with gAIRR Suite | Lin, Mao-Jan; Lin, Yu-Chun; Chen, Nae-Chyun; Luo, Allen Chilun; Lai, Sheng-Kai; Hsu, Chia-Lang; Jacob Shujui Hsu ; Chen, Chien-Yu; WEI-SHIUNG YANG ; PEI-LUNG CHEN | Frontiers in Immunology | 1 | 1 | |
2001 | Progress in genetic study on graves' disease | PEI-LUNG CHEN ; TIEN-CHUN CHANG | Journal of Internal Medicine of Taiwan | | | |
2021 | Rare manifestations and malignancies in tuberous sclerosis complex: findings from the TuberOus SClerosis registry to increAse disease awareness (TOSCA) | Sauter M.; Belousova E.; Benedik M.P.; Carter T.; Cottin V.; Curatolo P.; Dahlin M.; D’Amato L.; d’Aug?res G.B.; de Vries P.J.; Ferreira J.C.; Feucht M.; Fladrowski C.; Hertzberg C.; Jozwiak S.; Lawson J.A.; Macaya A.; Marques R.; Nabbout R.; O’Callaghan F.; Qin J.; Sander V.; Shah S.; Takahashi Y.; Touraine R.; Youroukos S.; Zonnenberg B.; Jansen A.; Kingswood J.C.; Shinohara N.; Horie S.; Kubota M.; Tohyama J.; Imai K.; Kaneda M.; Kaneko H.; Uchida Y.; Kirino T.; Endo S.; Inoue Y.; Uruno K.; Serdaroglu A.; Yapici Z.; Anlar B.; Altunbasak S.; Lvova O.; Belyaev O.V.; Agranovich O.; Levitina E.V.; Maksimova Y.V.; Karas A.; Jiang Y.; Zou L.; Xu K.; Zhang Y.; Luan G.; Zhang Y.; Wang Y.; Jin M.; Ye D.; Liao W.; Zhou L.; Liu J.; Liao J.; Yan B.; Deng Y.; Jiang L.; Liu Z.; Huang S.; Li H.; Kim K.; PEI-LUNG CHEN ; Lee H.-F.; Tsai J.-D.; Chi C.-S.; Huang C.-C.; Riney K.; Yates D.; Kwan P.; Likasitwattanakul S.; Nabangchang C.; Chomtho L.T.K.; Katanyuwong K.; Sriudomkajorn S.; Wilmshurst J.; Segel R.; Gilboa T.; Tzadok M.; Valevski A.F.; Papathanasopoulos P.; Papavasiliou A.S.; Giannakodimos S.; Gatzonis S.; Pavlou E.; Tzoufi M.; Vergeer A.M.H.; Dhooghe M.; Verhelst H.; Roelens F.; Nassogne M.C.; Defresne P.; De Waele L.; Leroy P.; Demonceau N.; Legros B.; Van Bogaert P.; Ceulemans B.; Dom L.; Castelnau P.; De Saint Martin A.; Riquet A.; Milh M.; Cances C.; Pedespan J.-M.; Ville D.; Roubertie A.; Auvin S.; Berquin P.; Richelme C.; Allaire C.; Gueden S.; Tich S.N.T.; Godet B.; Rojas M.L.R.F.; Planas J.C.; Bermejo A.M.; Dura P.S.; Aparicio S.R.; Gonzalez M.J.M.; Pison J.L.; Barca M.O.B.; Laso E.L.; Luengo O.A.; Rodriguez F.J.A.; Dieguez I.M.; Salas A.C.; Carrera I.M.; Salcedo E.M.; Petri M.E.Y.; Candela R.C.; da Conceicao Carrilho I.; Vieira J.P.; da Silva Oliveira Monteiro J.P.; de Oliveira Ferreira Leao M.J.S.; Luis C.S.M.R.; Mendonca C.P.; Endziniene M.; Strautmanis J.; Talvik I.; Canevini M.P.; Gambardella A.; Pruna D.; Buono S.; Fontana E.; Bernardina B.D.; Burloiu C.; Cosma I.S.B.; Vintan M.A.; Popescu L.; Zitterbart K.; Payerova J.; Bratsky L.; Zilinska Z.; Gruber-Sedlmayr U.; Baumann M.; Haberlandt E.; Rostasy K.; Pataraia E.; Elmslie F.; Johnston C.A.; Crawford P.; Uldall P.; Uvebrant P.; Rask O.; Bjoernvold M.; Brodtkorb E.; Sloerdahl A.; Solhoff R.; Jaatun M.S.G.; Mandera M.; Radzikowska E.J.; Wysocki M.; Fischereder M.; Kurlemann G.; Wilken B.; Wiemer-Kruel A.; Budde K.; Marquard K.; Knuf M.; Hahn A.; Hartmann H.; Merkenschlager A.; Trollmann R.; the TOSCA investigators | Orphanet Journal of Rare Diseases | 12 | 10 | |
2010 | Replication of an association of a common variant in the Reelin gene (RELN) with schizophrenia in Ashkenazi Jewish women | Liu Y.; PEI-LUNG CHEN ; McGrath J.; Wolyniec P.; Fallin D.; Nestadt G.; Liang K.-Y.; Pulver A.; Valle D.; Avramopoulos D. | Psychiatric Genetics | 39 | 34 | |
2023 | Reply | TA-CHING CHEN ; PEI-LUNG CHEN ; Chen, Yi Chieh; CHANG-HAO YANG ; CHUNG-MAY YANG | Retina | 0 | 0 | |
2023 | Revisiting Genetic Epidemiology with a Refined Targeted Gene Panel for Hereditary Hearing Impairment in the Taiwanese Population | Lee, Yen-Hui; Tsai, Cheng-Yu; Lu, Yue-Sheng; PEI-HSUAN LIN ; Chiang Yu-ting; TING-HUA YANG ; Jacob Shujui Hsu ; Hsu, Chuan-Jen; PEI-LUNG CHEN ; TIEN-CHEN LIU ; CHEN-CHI WU | Genes | 0 | 0 | |
2022 | Risk factors related to age at diagnosis of pancreatic cancer: a retrospective cohort pilot study | Lin, Ro-Ting; PEI-LUNG CHEN ; Yang, Chi-Ying; Yeh, Chun-Chieh; Lin, Chun-Che; Huang, Wen-Hsin; Chung, An-Ko; JAW-TOWN LIN | BMC Gastroenterology | 2 | 2 | |
2018 | Serum 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 Taiwan | FEN-YU TSENG ; Chen Y.-T.; Chi Y.-C.; PEI-LUNG CHEN ; WEI-SHIUNG YANG | Medicine (United States) | 4 | 3 | |
2016 | Serum levels of follistatin are positively associated with serum-free thyroxine levels in patients with hyperthyroidism or euthyroidism | FEN-YU TSENG ; Chen Y.-T.; Chi Y.-C.; PEI-LUNG CHEN ; WEI-SHIUNG YANG | Medicine (United States) | 5 | 4 | |
2019 | Serum 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 study | FEN-YU TSENG ; Chen Y.-T.; Chi Y.-C.; PEI-LUNG CHEN ; WEI-SHIUNG YANG | Medicine | 5 | 5 | |
2016 | Serum Spot 14 concentration is negatively associated with thyroid-stimulating hormone level | Chen Y.-T.; FEN-YU TSENG ; PEI-LUNG CHEN ; Chi Y.-C.; DER-SHENG HAN ; WEI-SHIUNG YANG | Medicine (United States) | 3 | 3 | |
2023 | SLCO1B1 and SLCO1B3 genetic mutations in Taiwanese patients with Rotor syndrome | Cheng, Ya-Yuan; KAI-CHI CHANG ; PEI-LUNG CHEN ; Yeung, Chun-Yan; Liou, Bang-Yu; HUEY-LING CHEN | Journal of the Formosan Medical Association | 0 | 0 | |
2014 | STAT3 mediates regorafenib-induced apoptosis in hepatocellular carcinoma | Tai 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 | 79 | 72 | |
2019 | Targeted Next-Generation Sequencing Facilitates Genetic Diagnosis and Provides Novel Pathogenetic Insights into Deafness with Enlarged Vestibular Aqueduct | Lin Y.-H.; Chen-Chi Wu ; Lin Y.-H.; Lu Y.-C.; Chen C.-S.; TIEN-CHEN LIU ; PEI-LUNG CHEN ; Hsu C.-J. | Journal of Molecular Diagnostics | 10 | 7 | |
2018 | Thyrotropin receptor antibodies and a genetic hint in antithyroid drug-induced adverse drug reactions | LIN-CHAU CHANG ; Chang C.-C.; PEI-LUNG CHEN ; Wang S.-H.; Chen Y.-H.; Tsai Y.-H.; SHYANG-RONG SHIH ; WEI-YIH CHIU ; Fann C.S.-J.; WEI-SHIUNG YANG ; TIEN-CHUN CHANG | Expert Opinion on Drug Safety | 5 | 5 | |
2023 | Traits of Patients With Pituitary Tumors in Multiple Endocrine Neoplasia Type 1 and Comparing Different Mutation Status | Lin, Kuan-Yu; YU-TING KUO ; MEI-FANG CHENG ; PEI-LUNG CHEN ; HSIU-PO WANG ; TSU-YAO CHENG ; CHIA-HSUIN CHANG ; HSIANG-FONG KAO ; SHIH-HUNG YANG ; HUNG-YUAN LI ; CHIA-HUNG LIN ; Chou, Yuh-Tsyr; Chung, An-Ko; WAN-CHEN WU ; JIN-YING LU ; CHIH-YUAN WANG ; Hsih, Wen-Hui; Wen, Chen-Yu; WEI-SHIUNG YANG ; SHYANG-RONG SHIH | The Journal of clinical endocrinology and metabolism | 0 | 0 | |
2006 | Translational repression restricts expression of the C. elegans Nanos homolog NOS-2 to the embryonic germline | D'Agostino I.; Merritt C.; PEI-LUNG CHEN ; Seydoux G.; Subramaniam K. | Developmental Biology | 62 | 63 | |
2013 | Tuberous sclerosis complex diagnostic criteria update: Recommendations of the 2012 international tuberous sclerosis complex consensus conference | PEI-LUNG CHEN | Pediatric Neurology | 1127 | 949 | |
2013 | Tuberous sclerosis complex surveillance and management: recommendations of the 2012 International Tuberous Sclerosis Complex Consensus Conference | PEI-LUNG CHEN ; Northrup, Hope | Pediatric neurology | 663 | 545 | |