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  • 禾馨團隊 論文列表
    1. Raised maternal serum placenta growth factor concentration during the second trimester is associated with Down syndrome. Su YN, Hsu JJ, Lee CN, Cheng WF, Kung CC, Hsieh FJ. Prenat Diagn. 2002 Jan;22(1):8-12.
    2. Decreased maternal serum placenta growth factor in early second trimester and preeclampsia. Su YN, Lee CN, Cheng WF, Shau WY, Chow SN, Hsieh FJ. Obstet Gynecol. 2001 Jun;97(6):898-904.
    3. Resolution of high uterine artery pulsatility index and notching following sildenafil citrate treatment in a growth-restricted pregnancy. Lin TH, Su YN, Shih JC, Hsu HC, Lee CN. Ultrasound Obstet Gynecol. 2012 Feb 20.
    4. Carrier screening for spinal muscular atrophy (SMA) in 107,611 pregnant women during the period 2005-2009: a prospective population-based cohort study. Su YN, Hung CC, Lin SY, Chen FY, Chern JP, Tsai C, Chang TS, Yang CC, Li H, Ho HN, Lee CN. PLoS One. 2011 Feb 25;6(2):e17067.
    5. Rapid prenatal diagnosis of spinal muscular atrophy by denaturing high-performance liquid chromatography system. Shaw SW, Cheng PJ, Chang SD, Lin YT, Hung CC, Chen CP, Su YN. Acta Obstet Gynecol Scand. 2008;87(9):960-8.
    6. Quantification of relative gene dosage by single-base extension and high-performance liquid chromatography: application to the SMN1/SMN2 gene. Hung CC, Lee CN, Chen CP, Jong YJ, Chen CA, Cheng WF, Lin WL, Su YN. Anal Chem. 2005 Nov 1;77(21):6960-8.
    7. Quantitative analysis of SMN1 and SMN2 genes based on DHPLC: a highly efficient and reliable carrier-screening test. Su YN, Hung CC, Li H, Lee CN, Cheng WF, Tsao PN, Chang MC, Yu CL, Hsieh WS, Lin WL, Hsu SM. Hum Mutat. 2005 May;25(5):460-7.
    8. Clinical utility of array comparative genomic hybridisation for prenatal diagnosis: a cohort study of 3171 pregnancies. Lee CN, Lin SY, Lin CH, Shih JC, Lin TH, Su YN. BJOG. 2012 Feb 7.
    9. Re: Microarray application in prenatal diagnosis: a position statement from the cytogenetics working group of the Italian Society of Human Genetics (SIGU), November 2011. Lee CN, Lin SY, Lin CH, Shih JC, Lin TH, Su YN. Ultrasound Obstet Gynecol. 2012 May;39(5):603-4.
    10. Should array CGH be applied to all routine prenatal care?, Lin TH, Lin SY, Lee CN, Shih JC, Su YN, Prenat Diagn. 2012 (accepted)
    11. Prenatal diagnosis of a fetus with a de novo trisomy 12p by array-comparative genomic hybridization (array-CGH). Hung CC, Lin CH, Lin SY, Shin JC, Lee CN, Su YN. Gene. 2012 Mar 10;495(2):178-82.
    12. Second-trimester maternal serum quadruple test for Down syndrome screening: a Taiwanese population-based study. Shaw SW, Lin SY, Lin CH, Su YN, Cheng PJ, Lee CN, Chen CP. Taiwan J Obstet Gynecol. 2010 Mar;49(1):30-4.
    13. An update of preimplantation genetic diagnosis in gene diseases, chromosomal translocation, and aneuploidy screening. Chang LJ, Chen SU, Tsai YY, Hung CC, Fang MY, Su YN, Yang YS. Clin Exp Reprod Med. 2011 Sep;38(3):126-34.
    14. Successful application of the strategy of blastocyst biopsy, vitrification, whole genome amplification, and thawed embryo transfer for preimplantation genetic diagnosis of neurofibromatosis type 1. Chen YL, Hung CC, Lin SY, Fang MY, Tsai YY, Chang LJ, Lee CN, Su YN, Chen SU, Yang YS. Taiwan J Obstet Gynecol. 2011 Mar;50(1):74-8.
    15. Preimplantation genetic diagnosis (embryo screening) for enlarged vestibular aqueduct due to SLC26A4 mutation. Wu CC, Lin SY, Su YN, Fang MY, Chen SU, Hsu CJ. Audiol Neurootol. 2010;15(5):311-7.
    16. Preimplantation genetic diagnosis of beta-thalassemia using real-time polymerase chain reaction with fluorescence resonance energy transfer hybridization probes. Hung CC, Chen SU, Lin SY, Fang MY, Chang LJ, Tsai YY, Lin LT, Yang YS, Lee CN, Su YN. Anal Biochem. 2010 May 1;400(1):69-77.
    17. PGD of beta-thalassaemia and HLA haplotypes using OmniPlex whole genome amplification. Chen SU, Su YN, Fang MY, Chang LJ, Tsai YY, Lin LT, Lee CN, Yang YS. Reprod Biomed Online. 2008 Nov;17(5):699-705.
    18. Newborn genetic screening for hearing impairment: a preliminary study at a tertiary center. Wu CC, Hung CC, Lin SY, Hsieh WS, Tsao PN, Lee CN, Su YN, Hsu CJ. PLoS One. 2011;6(7):e22314.
    19. Quantitative and qualitative analyses of the SNRPN gene using real-time PCR with melting curve analysis. Hung CC, Lin SY, Lin SP, Chen CP, Chen LY, Lee CN, Su YN. J Mol Diagn. 2011 Nov;13(6):609-13.
    20. Low penetrance of retinoblastoma for p.V654L mutation of the RB1 gene. Hung CC, Lin SY, Lee CN, Chen CP, Lin SP, Chao MC, Chiou SS, Su YN. BMC Med Genet. 2011 May 26;12:76.
    21. Mutation spectrum of the fibrillin-1 (FBN1) gene in Taiwanese patients with Marfan syndrome. Hung CC, Lin SY, Lee CN, Cheng HY, Lin SP, Chen MR, Chen CP, Chang CH, Lin CY, Yu CC, Chiu HH, Cheng WF, Ho HN, Niu DM, Su YN. Ann Hum Genet. 2009 Nov;73(Pt 6):559-67.
    22. Identification of fibrillin-1 gene mutations in Marfan syndrome by high-resolution melting analysis. Hung CC, Lin SY, Lee CN, Cheng HY, Lin CY, Chang CH, Chiu HH, Yu CC, Lin SP, Cheng WF, Ho HN, Niu DM, Su YN. Anal Biochem. 2009 Jun 15;389(2):102-6. Epub 2009 Mar 27.
    23. Identification of CpG methylation of the SNRPN gene by methylation-specific multiplex PCR. Hung CC, Lin SY, Lin SP, Niu DM, Lee NC, Cheng WF, Chen CP, Lin WL, Lee CN, Su YN. Electrophoresis. 2009 Jan;30(2):410-6.
    24. Comparison of the mismatch-specific endonuclease method and denaturing high-performance liquid chromatography for the identification of HBB gene mutations. Hung CC, Su YN, Lin CY, Chang YF, Chang CH, Cheng WF, Chen CA, Lee CN, Lin WL. BMC Biotechnol. 2008 Aug 12;8:62.
    25. Mutation spectrum of 122 hemophilia A families from Taiwanese population by LD-PCR, DHPLC, multiplex PCR and evaluating the clinical application of HRM. Lin SY, Su YN, Hung CC, Tsay W, Chiou SS, Chang CT, Ho HN, Lee CN. BMC Med Genet. 2008 Jun 20;9:53.
    26. Identification of deletion and duplication genotypes of the PMP22 gene using PCR-RFLP, competitive multiplex PCR, and multiplex ligation-dependent probe amplification: a comparison. Hung CC, Lee CN, Lin CY, Cheng WF, Chen CA, Hsieh ST, Yang CC, Jong YJ, Su YN, Lin WL. Electrophoresis. 2008 Feb;29(3):618-25.
    27. Genotyping of the G1138A mutation of the FGFR3 gene in patients with achondroplasia using high-resolution melting analysis. Hung CC, Lee CN, Chang CH, Jong YJ, Chen CP, Hsieh WS, Su YN, Lin WL. Clin Biochem. 2008 Feb;41(3):162-6. Epub 2007 Sep 6.
    28. Use of multiplex PCR and CE for gene dosage quantification and its biomedical applications for SMN, PMP22, and alpha-globin genes. Hung CC, Chien SC, Lin CY, Chang CH, Chang YF, Jong YJ, Hsieh ST, Hsieh WS, Liu MS, Lin WL, Lee CN, Su YN. Electrophoresis. 2007 Aug;28(16):2826-34.
    29. Molecular assay of -alpha(3.7) and -alpha(4.2) deletions causing alpha-thalassemia by denaturing high-performance liquid chromatography. Hung CC, Lee CN, Chen CP, Jong YJ, Hsieh WS, Lin WL, Su YN, Hsu SM. Clin Biochem. 2007 Jul;40(11):817-21. Epub 2007 Apr 6.
    30. Rapid prenatal diagnosis of Duchenne muscular dystrophy with gene duplications by ion-pair reversed-phase high-performance liquid chromatography coupled with competitive multiplex polymerase chain reaction strategy. Huang WY, Hung CC, Lee CN, Su YN, Chen CP. Prenat Diagn. 2007 Jul;27(7):653-6.
    31. Unequal crossover recombination - population screening for PHOX2B gene polyalanine polymorphism using CE. Hung CC, Su YN, Tsao PN, Chen PC, Lin SJ, Lin CH, Mu SC, Liu CA, Chang YC, Lin WL, Hsieh WS, Hsu SM. Electrophoresis. 2007 Mar;28(6):894-9.
    32. Quantitative assay of deletion or duplication genotype by capillary electrophoresis system: Application in Prader-Willi syndrome and Duchenne muscular dystrophy. Hung CC, Chen CP, Lin SP, Chien SC, Lee CN, Cheng WF, Hsieh WS, Liu MS, Su YN, Lin WL. Clin Chem. 2006 Dec;52(12):2203-10. Epub 2006 Oct 13.
    33. Molecular and clinical analyses of 84 patients with tuberous sclerosis complex. Hung CC, Su YN, Chien SC, Liou HH, Chen CC, Chen PC, Hsieh CJ, Chen CP, Lee WT, Lin WL, Lee CN. BMC Med Genet. 2006 Sep 18;7:72.
    34. A rapid and reliable detection system for the analysis of PMP22 gene dosage by MP/DHPLC assay. Lin CY, Su YN, Lee CN, Hung CC, Cheng WF, Lin WL, Chen CA, Hsieh ST. J Hum Genet. 2006;51(3):227-35. Epub 2006 Feb 4.
    35. Denaturing HPLC coupled with multiplex PCR for rapid detection of large deletions in Duchenne muscular dystrophy carriers. Hung CC, Su YN, Lin CY, Yang CC, Lee WT, Chien SC, Lin WL, Lee CN. Clin Chem. 2005 Jul;51(7):1252-6.
    36. Rapid detection of FGFR3 gene mutation in achondroplasia by DHPLC system-coupling heteroduplex and fluorescence-enhanced primer-extension analysis. Su YN, Lee CN, Chien SC, Hung CC, Chien YH, Chen CA. J Hum Genet. 2004;49(8):399-403. Epub 2004 Jun 18.
    37. Rapid detection of beta-globin gene (HBB) mutations coupling heteroduplex and primer-extension analysis by DHPLC. Su YN, Lee CN, Hung CC, Chen CA, Cheng WF, Tsao PN, Yu CL, Hsieh FJ. Hum Mutat. 2003 Oct;22(4):326-36.
    38. AdimFlu-S(®) influenza A (H1N1) vaccine during pregnancy: the Taiwanese Pharmacovigilance Survey. Lin TH, Lin SY, Lin CH, Lin RI, Lin HC, Chiu TH, Cheng PJ, Lee CN. Vaccine. 2012 Mar 30;30(16):2671-5.
  • 國際論文-胎兒心臟外露異位與3D高清晰度(HD)渲染圖像(上)
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