臺灣學術機構典藏系統 (Taiwan Academic Institutional Repository, TAIR)

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Showing items 26-35 of 156 (16 Page(s) Totally)
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Institution	Date	Title	Author
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

Showing items 26-35 of 156 (16 Page(s) Totally)
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