| 臺大學術典藏 |
2022-09-21T23:33:13Z |
Cochlear Implantation Outcomes in Patients with Auditory Neuropathy Spectrum Disorder of Genetic and Non-Genetic Etiologies: A Multicenter Study
|
PEI-HSUAN LIN; Wu, Hung Pin; Wu, Che Ming; Chiang, Yu Ting; Jacob Shujui Hsu; Tsai, Cheng Yu; Wang, Han; LI-HUI TSENG; Chen, Pey Yu; TING-HUA YANG; Hsu, Chuan Jen; PEI-LUNG CHEN; CHEN-CHI WU; TIEN-CHEN LIU |
| 臺大學術典藏 |
2022-09-21T23:33:13Z |
Comprehensive Etiologic Analyses in Pediatric Cochlear Implantees and the Clinical Implications
|
Lee, Chee Yee; PEI-HSUAN LIN; Tsai, Cheng Yu; Chiang, Yu Ting; Chiou, Hong Ping; Chiang, Ko Yin; PEI-LUNG CHEN; Hsu, Jacob Shu Jui; TIEN-CHEN LIU; Wu, Hung Pin; CHEN-CHI WU; Hsu, Chuan Jen |
| 臺大學術典藏 |
2022-09-21T23:32:48Z |
Genotypes Influence Clinical Progression in EYS-Associated Retinitis Pigmentosa
|
Lo, Jui En; Cheng, Chia Yi; CHANG-HAO YANG; CHUNG-MAY YANG; YI-CHIEH CHEN; Huang, Yu Shu; PEI-LUNG CHEN; TA-CHING CHEN |
| 臺大學術典藏 |
2022-04-21T23:17:57Z |
PREDICTED PROTEIN STRUCTURE VARIATIONS INDICATE THE CLINICAL PRESENTATION OF CYP4V2 -RELATED BIETTI CRYSTALLINE DYSTROPHY
|
Chan, Li Wei; Sung, Yu Chi; Wu, Dung Chi; CHIEN-YU CHEN; CHANG-HAO YANG; CHUNG-MAY YANG; PEI-LUNG CHEN; TA-CHING CHEN |
| 臺大學術典藏 |
2022-04-14T23:27:41Z |
Genetic analysis of a family presenting with coexisting cerebral cavernous malformations and polycystic kidney disease
|
Hsieh, Pei Feng; SHIH-YAO LIU; CHIH-HAO CHEN; PEI-LUNG CHEN; SUNG-CHUN TANG; JIANN-SHING JENG |
| 臺大學術典藏 |
2022-03-14T23:45:55Z |
Evaluation of using WGS/WES to characterize ACMG actionable genes in genetic testing reports
|
Yang, Wen Tse; Wu, Dong Chi; Liu, Jen Feng; JIN-BON HONG; Wu, June Tai; PEI-LUNG CHEN; CHIEN-YU CHEN |
| 臺大學術典藏 |
2022-03-14T23:45:35Z |
A Clinical and Integrated Genetic Study of Isolated and Combined Dystonia in Taiwan
|
Wu, Meng Chen; Chang, Yung Yee; Lan, Min Yu; Chen, Ying Fa; CHUN-HWEI TAI; Lin, Yung Feng; Tsai, Shih Feng; PEI-LUNG CHEN; CHIN-HSIEN LIN |
| 臺大學術典藏 |
2022-03-09T08:01:39Z |
Evaluation of using WGS/WES to characterize ACMG actionable genes in genetic testing reports
|
Yang W.-T.; Wu D.-C.; Liu J.-F.; Hong J.-B.; Wu J.-T.; PEI-LUNG CHEN; Chen C.-Y. |
| 臺大學術典藏 |
2022-03-09T08:01:39Z |
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. |
| 臺大學術典藏 |
2022-03-09T08:01:38Z |
Genetic spectrum and characteristics of hereditary optic neuropathy in Taiwan
|
Lin C.-W.; Huang C.-W.; Luo A.C.; Chou Y.-T.; Huang Y.-S.; PEI-LUNG CHEN; Chen T.-C. |
| 臺大學術典藏 |
2022-03-09T08:01:38Z |
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. |
| 臺大學術典藏 |
2022-03-09T08:01:38Z |
Hearing Impairment with Monoallelic GJB2 Variants: A GJB2 Cause or Non-GJB2 Cause?
|
Lin Y.-H.; Wu P.-C.; Tsai C.-Y.; Lin Y.-H.; Lo M.-Y.; Hsu S.-J.; Lin P.-H.; Erdenechuluun J.; Wu H.-P.; Hsu C.-J.; Wu C.-C.; PEI-LUNG CHEN |
| 臺大學術典藏 |
2022-03-09T08:01:37Z |
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. |
| 臺大學術典藏 |
2022-03-09T08:01:37Z |
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 |
| 臺大學術典藏 |
2022-03-09T08:01:36Z |
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. |
| 臺大學術典藏 |
2021-12-21T23:17:41Z |
Cochlear implantation in LEOPARD syndrome: Our experience with three patients
|
Wu, Ping Che; Tsai, Cheng Yu; PEI-HSUAN LIN; Chou, Pao Hsuan; Huang, Fang Lih; PEI-LUNG CHEN; Shiao, Jiun Yih; TIEN-CHEN LIU; Hsu, Chuan Jen; Huang, Chang Wei; CHEN-CHI WU |
| 臺大學術典藏 |
2021-11-21T23:19:43Z |
The clinical contribution of full-field electroretinography and 8-year experiences of application in a tertiary medical center
|
Yang, Jung Je; Huang, Chu Hsuan; CHANG-HAO YANG; CHUNG-MAY YANG; Lin, Chao Wen; TZYY-CHANG HO; CHANG-PING LIN; Hsieh, Yi Ting; PO-TING YEH; TSO-TING LAI; PEI-LUNG CHEN; TA-CHING CHEN |
| 臺大學術典藏 |
2021-10-21T23:28:17Z |
Hearing Impairment with Monoallelic GJB2 Variants: A GJB2 Cause or Non-GJB2 Cause?
|
Lin, Yi Hsin; Wu, Ping Che; Tsai, Cheng Yu; Lin, Yin Hung; Lo, Ming Yu; Hsu, Shu Jui; PEI-HSUAN LIN; Erdenechuluun, Jargalkhuu; Wu, Hung Pin; Hsu, Chuan Jen; CHEN-CHI WU; PEI-LUNG CHEN |
| 臺大學術典藏 |
2021-09-21T23:20:14Z |
Genetic spectrum and characteristics of hereditary optic neuropathy in Taiwan
|
Lin, Chao Wen; Huang, Ching Wen; Luo, Allen Chilun; Chou, Yuh Tsyr; Huang, Yu Shu; PEI-LUNG CHEN; TA-CHING CHEN |
| 臺大學術典藏 |
2021-07-15T05:32:21Z |
Investigating DYT1 in a Taiwanese dystonia cohort
|
Wu, Meng Chen; Chang, Yung Yee; Chen, Ying Fa; Lan, Min Yu; PEI-LUNG CHEN; CHUN-HWEI TAI; CHIN-HSIEN LIN |
| 臺大學術典藏 |
2021-07-06T02:04:19Z |
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. |
| 臺大學術典藏 |
2021-07-06T02:04:19Z |
Progress in genetic study on graves' disease
|
PEI-LUNG CHEN; Chang T.-C. |
| 臺大學術典藏 |
2021-07-06T02:04:18Z |
Linkage of Graves' disease to the human leucocyte antigen region in the Chinese-Han population in Taiwan
|
PEI-LUNG CHEN; Fann C.S.-J.; Chang C.-C.; Wu I.-L.; Chiu W.-Y.; Lin C.-Y.; Yang W.-S.; Chang T.-C. |
| 臺大學術典藏 |
2021-07-06T02:04:18Z |
Human genetics of diabetes mellitus in Taiwan
|
PEI-LUNG CHEN; Yang W.-S. |
| 臺大學術典藏 |
2021-07-06T02:04:18Z |
Family-based association study of cytotoxic T-lymphocyte antigen-4 with susceptibility to Graves' disease in Han population of Taiwan
|
PEI-LUNG CHEN; Fann C.S.-J.; Chang C.-C.; Wu I.-L.; Chiu W.-Y.; Lin C.-Y.; Yang W.-S.; Chang T.-C. |
| 臺大學術典藏 |
2021-07-06T02:04:17Z |
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. |
| 臺大學術典藏 |
2021-07-06T02:04:17Z |
Fine Mapping on Chromosome 10q22-q23 Implicates Neuregulin 3 in Schizophrenia
|
PEI-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. |
| 臺大學術典藏 |
2021-07-06T02:04:17Z |
Familiality of novel factorial dimensions of schizophrenia
|
McGrath 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. |
| 臺大學術典藏 |
2021-07-06T02:04:16Z |
Linkage and association on 8p21.2-p21.1 in schizophrenia
|
Fallin 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. |
| 臺大學術典藏 |
2021-07-06T02:04:16Z |
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. |
| 臺大學術典藏 |
2021-07-06T02:04:16Z |
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. |
| 臺大學術典藏 |
2021-07-06T02:04:15Z |
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 |
| 臺大學術典藏 |
2021-07-06T02:04:15Z |
A genome-wide association analysis identifies novel susceptibility loci for coronary arterial lesions in patients with Kawasaki disease
|
Lin M.-T.; Hsu C.-L.; PEI-LUNG CHEN; Yang W.-S.; Wang J.-K.; Fann C.S.J.; Wu M.-H. |
| 臺大學術典藏 |
2021-07-06T02:04:15Z |
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. |
| 臺大學術典藏 |
2021-07-06T02:04:14Z |
Tuberous sclerosis complex surveillance and management: Recommendations of the 2012 international tuberous sclerosis complex consensus conference
|
Krueger D.A.; Northrup H.; Krueger D.A.; Roberds S.; Smith K.; Sampson J.; Korf B.; Kwiatkowski D.J.; Mowat D.; Nellist M.; Povey S.; de Vries P.; Byars A.; Dunn D.; Ess K.; Hook D.; Jansen A.; King B.; Sahin M.; Whittemore V.; Thiele E.; Bebin E.M.; Chugani H.T.; Crino P.; Curatolo P.; Holmes G.; Nabbout R.; O'Callaghan F.; Wheless J.; Wu J.; Darling T.N.; Cowen E.W.; Gosnell E.; Hebert A.; Mlynarczyk G.; Soltani K.; Teng J.; Wataya-Kaneda M.; Witman P.M.; Kingswood C.; Bissler J.; Budde K.; Hulbert J.; Guay-Woodford L.; Sauter M.; Zonneberg B.; J??wiak S.; Bartels U.; Berhouma M.; Franz D.N.; Koenig M.K.; Roach E.S.; Roth J.; Wang H.; Weiner H.; McCormack F.X.; Almoosa K.; Brody A.; Burger C.; Cottin V.; Finlay G.; Glass J.; Henske E.P.; Johnson S.; Kotloff R.; Lynch D.; Moss J.; Rhu J.; Da Silva A.T.; Young L.R.; Knilans T.; Hinton R.; Prakash A.; Romp R.; Singh A.D.; Debroy A.; PEI-LUNG CHEN; Sparagana S.; Frost M.D.; International Tuberous Sclerosis Complex Consensus Group; PEI-LUNG CHEN |
| 臺大學術典藏 |
2021-07-06T02:04:14Z |
Identification of a novel HLA-B allele, B*07:162, in a Taiwanese individual
|
PEI-LUNG CHEN; Lai S.-K.; Yang W.-S.; Chang T.-C.; Chu C.-C. |
| 臺大學術典藏 |
2021-07-06T02:04:13Z |
Genetic analysis of CARD14 in non-familial pityriasis rubra pilaris: A case series
|
Hong J.-B.; PEI-LUNG CHEN; Chen Y.-T.; Tsai T.-F. |
| 臺大學術典藏 |
2021-07-06T02:04:13Z |
Gene-wide tagging study of the effects of common genetic polymorphisms in the α subunits of the GABAA receptor on epilepsy treatment response
|
Hung C.-C.; PEI-LUNG CHEN; Huang W.-M.; Tai J.J.; Hsieh T.-J.; Ding S.-T.; Hsieh Y.-W.; Liou H.-H. |
| 臺大學術典藏 |
2021-07-06T02:04:13Z |
Tuberous sclerosis complex diagnostic criteria update: Recommendations of the 2012 international tuberous sclerosis complex consensus conference
|
Northrup H.; Krueger D.A.; Roberds S.; Smith K.; Sampson J.; Korf B.; Kwiatkowski D.J.; Mowat D.; Nellist M.; Povey S.; de Vries P.; Byars A.; Dunn D.; Ess K.; Hook D.; Jansen A.; King B.; Sahin M.; Whittemore V.; Thiele E.; Bebin E.M.; Chugani H.T.; Crino P.; Curatolo P.; Holmes G.; Nabbout R.; O'Callaghan F.; Wheless J.; Wu J.; Darling T.N.; Cowen E.W.; Gosnell E.; Hebert A.; Mlynarczyk G.; Soltani K.; Teng J.; Wataya-Kaneda M.; Witman P.M.; Kingswood C.; Bissler J.; Budde K.; Hulbert J.; Guay-Woodford L.; Sauter M.; Zonneberg B.; J??wiak S.; Bartels U.; Berhouma M.; Franz D.N.; Koenig M.K.; Roach E.S.; Roth J.; Wang H.; Weiner H.; McCormack F.X.; Almoosa K.; Brody A.; Burger C.; Cottin V.; Finlay G.; Glass J.; Henske E.P.; Johnson S.; Kotloff R.; Lynch D.; Moss J.; Rhu J.; Da Silva A.T.; Young L.R.; Knilans T.; Hinton R.; Prakash A.; Romp R.; Singh A.D.; Debroy A.; PEI-LUNG CHEN; Sparagana S.; Frost M.D.; International Tuberous Sclerosis Complex Consensus Group; PEI-LUNG CHEN |
| 臺大學術典藏 |
2021-07-06T02:04:12Z |
Predicting HLA genotypes using unphased and flanking single-nucleotide polymorphisms in Han Chinese population
|
Hsieh 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. |
| 臺大學術典藏 |
2021-07-06T02:04:12Z |
A fault-tolerant method for HLA typing with PacBio data
|
Chang C.-J.; PEI-LUNG CHEN; Yang W.-S.; Chao K.-M. |
| 臺大學術典藏 |
2021-07-06T02:04:11Z |
An isodicentric X chromosome with gonadal dysgenesis in a lady without prominent somatic features of Turner's syndrome. A case report
|
Yu T.-Y.; Lin H.-S.; PEI-LUNG CHEN; Huang T.-S. |
| 臺大學術典藏 |
2021-07-06T02:04:11Z |
Identification of a novel GATA3 mutation in a deaf Taiwanese family by massively parallel sequencing
|
Lin Y.-H.; Wu C.-C.; Hsu T.-Y.; Chiu W.-Y.; Hsu C.-J.; PEI-LUNG CHEN |
| 臺大學術典藏 |
2021-07-06T02:04:11Z |
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. |
| 臺大學術典藏 |
2021-07-06T02:04:10Z |
Functional variants in DPYSL2 sequence increase risk of schizophrenia and suggest a link to mTOR signaling
|
Liu 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. |
| 臺大學術典藏 |
2021-07-06T02:04:09Z |
Identifying children with poor cochlear implantation outcomes using massively parallel sequencing
|
Wu C.-C.; Lin Y.-H.; Liu T.-C.; Lin K.-N.; Yang W.-S.; Hsu C.-J.; PEI-LUNG CHEN; Wu C.-M. |
| 臺大學術典藏 |
2021-07-06T02:04:09Z |
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. |
| 臺大學術典藏 |
2021-07-06T02:04:08Z |
Genetic determinants of antithyroid drug-induced agranulocytosis by human leukocyte antigen genotyping and genome-wide association study
|
PEI-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. |
| 臺大學術典藏 |
2021-07-06T02:04:08Z |
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 |
| 臺大學術典藏 |
2021-07-06T02:04:07Z |
Multiple gene sequencing for risk assessment in patients with early-onset or familial breast cancer
|
Lin 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.; Lin 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. |
