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    • Chih‐ping Chen
    • Chih‐Ping Chen

      Chih‐Ping Chen

      Department of Obstetrics and Gynecology, National Yang-Ming, University School of Medicine, Taipei, Taiwan; Institute of Clinical and Community Health Nursing, National Yang ...

       

       

      KOL Resume for Chih‐Ping Chen

      Year
      2021

      Department of Obstetrics and Gynecology, National Yang-Ming, University School of Medicine, Taipei, Taiwan; Institute of Clinical and Community Health Nursing, National Yang Ming Chiao Tung University, Taipei, Taiwan; Department of Obstetrics and Gynecology, Mackay Memorial, Hospital, Taipei, Taiwan; Department of Medical Research, Mackay Memorial Hospital, Taipei, Taiwan; Department of Biotechnology, Asia University, Taichung, Taiwan; School of Chinese Medicine, College of Chinese Medicine, China; Medical University, Taichung, Taiwan.

      2020

      Department of Medical Research, MacKay Memorial Hospital, Taipei, Taiwan

      School of Chinese Medicine, College of Chinese Medicine, China

      2018

      Department of Obstetrics and Gynecology, Mackay Memorial Hospital, Taipei, Taiwan

      2017

      Department of Medical Research, Mackay Memorial Hospital, Taipei, Taiwan, ROC

      2016

      Department of Biotechnology, Medical University, Taichung, Taiwan

      School of Chinese Medicine, College of Chinese Medicine, Taichung, China

      2015

      Department of Obstetrics and Gynecology, National Yang-Ming, University School of Medicine, Taipei, Taiwan

      2014

      Department of Medicine, Mackay Medical College, New Taipei City, Taiwan

      2013

      Department of Obstetrics and Gynecology, Mackay Memorial Hospital, Taipei City, Taiwan

      2012

      Department of Medical Research, Mackay Memorial Hospital, Taipei, Taiwan, Republic of China, .

      School of Chinese Medicine, College of Chinese Medicine, China Medical University, Taichung, Taipei, Taiwan

      2011

      Department of Obstetrics and Gynecology, Mackay Memorial Hospital, Taipei, Taiwan.

       

       

      Chih‐Ping Chen: Influence Statistics

      Sample of concepts for which Chih‐Ping Chen is among the top experts in the world.
      Concept World rank
      acgh analysis #1
      umbilical humans #1
      8q233q2411 #1
      hydronephrosis fetus #1
      gestation raa #1
      anomalies mds #1
      mosaic level #1
      bws pregnancy #1
      fetus oligohydramnios #1
      bilateral ventriculomegaly #1
      d9s1780 #1
      acgh analysis result #1
      17p133 deletion #1
      distal 11q deletion #1
      fluorescence infant human #1
      multiple adult anus #1
      21q112q211 #1
      polydactyly #1
      distal 12p #1
      uncultured #1
      induced adult diagnosis #1
      perinatal imaging findings #1
      15 amniocentesis #1
      prenatal diagnosis tof #1
      ssmc amniocentesis #1
      amniocentesis objective #1
      partial monosomy 9p #1
      8 amniocentesis #1
      mos 46xx #1
      prenatal ultrasound prognosis #1
      prenatal findings diagnosis #1
      thymic hypoplasia aplasia #1
      pair ventricular hernia #1
      raa prenatal diagnosis #1
      2 comparative #1
      adult chromosomes #1
      chorionic villi arr #1
      fluorescence infant birth #1
      prenatal adult chromosomes #1
      gestation microcephaly #1
      cord blood mlpa #1
      nek1 gene #1
      fetal ultrasound findings #1
      female holoprosencephaly humans #1
      meis2 haploinsufficiency tetralogy #1
      trisomy single colony #1
      2 amniocentesis #1
      cephalothoracopagus janiceps #1
      pair female hernia #1

       

      Prominent publications by Chih‐Ping Chen

      KOL-Index: 15367

      OBJECTIVE: This study aims at presenting prenatal diagnosis of mosaic trisomy 2 and reviewing the literature.

      MATERIALS, METHODS, AND RESULTS: A 32-year-old woman underwent amniocentesis at 21 weeks of gestation because of abnormal maternal serum biochemistry. Amniocentesis revealed a karyotype of 47,XY,+2[1]/46,XY[21] in in situ cultures. The single colony with trisomy 2 had two metaphase cells, and both had the karyotype of 47,XY,+2. Repeated amniocentesis was performed at 23 weeks of ...

      Known for Prenatal Diagnosis | Trisomy 2 | Uncultured Amniocytes | Single Colony | Fish Analysis
      KOL-Index: 14951

      OBJECTIVE: To present the prenatal diagnosis and molecular cytogenetic characterization of de novo partial trisomy 7p (7p15.3→pter) and partial monosomy 13q (13q33.3→qter) associated with Dandy-Walker malformation (DWM), abnormal skull development, microcephaly and multiple congenital anomalies.

      MATERIALS, METHODS AND RESULTS: A 42-year-old woman, gravida 6, para 1, was referred for amniocentesis at 18 weeks of gestation because of her advanced maternal age. Amniocentesis revealed an ...

      Known for Partial Monosomy | Prenatal Diagnosis | Abnormal Skull Development | Trisomy 7p | Situ Hybridization
      KOL-Index: 14107

      OBJECTIVE: To present prenatal diagnosis of true trisomy 7 mosaicism.

      MATERIALS, METHODS AND RESULTS: A 36-year-old woman underwent amniocentesis at 18 weeks of gestation. Amniocentesis revealed a karyotype of 47,XY,+7[20]/46,XY[9]. The parental karyotypes were normal. Repeated amniocentesis was performed at 20 weeks of gestation. Array comparative genomic hybridization (aCGH) analysis on uncultured amniocytes manifested a genomic gain in chromosome 7. Quantitative fluorescent polymerase ...

      Known for Uncultured Amniocytes | Trisomy 7 | Interphase Fish | Situ Hybridization | True Mosaicism
      KOL-Index: 14012

      OBJECTIVE: This study is aimed at prenatal diagnosis of mosaic trisomy 12 and reviewing the literature.

      MATERIALS AND METHODS: A 34-year-old woman underwent amniocentesis at 17 weeks of gestation because of advanced maternal age. Cytogenetic analysis of cultured amniocytes revealed a karyotype of 47,XX,+12[9]/46,XX[14]. She was referred to the hospital for genetic counseling. Repeated amniocentesis was performed at 22 weeks of gestation. Array comparative genomic hybridization (aCGH), ...

      Known for Mosaic Trisomy | Prenatal Diagnosis | Uncultured Amniocytes | Situ Hybridization | Cytogenetic Analysis
      KOL-Index: 13354

      OBJECTIVE: To present the prenatal magnetic resonance imaging (MRI) and ultrasound findings of Miller-Dieker lissencephaly syndrome (MDLS) associated with chromosome 17p13.3 deletion in a fetus.

      CASE REPORT: A 30-year-old, primigravid woman was referred to the hospital at 31 weeks' gestation because of intrauterine growth restriction (IUGR) and polyhydramnios detected by ultrasound. The pregnancy was uneventful until 31 weeks of gestation when IUGR and polyhydramnios were first noted. ...

      Known for Prenatal Diagnosis | Intrauterine Growth Restriction | Monosomy 17p | Ventriculomegaly Polyhydramnios | Human Pair
      KOL-Index: 12952

      OBJECTIVE: This study aimed at presenting prenatal diagnosis and molecular cytogenetic characterization of a small supernumerary marker chromosome (sSMC) derived from chromosome 8 by fluorescence in situ hybridization (FISH), quantitative fluorescent polymerase chain reaction (QF-PCR), and array comparative genomic hybridization (aCGH) on uncultured amniocytes.

      MATERIALS, METHODS, AND RESULTS: A 32-year-old woman underwent amniocentesis at 19 weeks of gestation because of fetal ...

      Known for Uncultured Amniocytes | Situ Hybridization | Interphase Fluorescence | Prenatal Diagnosis | Polymerase Chain
      KOL-Index: 12548

      OBJECTIVE: To present prenatal diagnosis of mosaic trisomy 8 and to review the literature.

      MATERIALS, METHODS, AND RESULTS: A 34-year-old woman underwent amniocentesis at 16 weeks of gestation because of advanced maternal age. Amniocentesis revealed a karyotype of 47,XY,+8[6]/46,XY[31]. Repeated amniocentesis at 21 weeks of gestation revealed a karyotype of 47,XY,+8[4]/46,XY[77]. Interphase fluorescence in situ hybridization analysis of uncultured amniocytes showed 25% (5/20) mosaicism ...

      Known for Mosaic Trisomy | Prenatal Diagnosis | Uncultured Amniocytes | Amniocentesis Karyotype | Interphase Fluorescence
      KOL-Index: 12324

      OBJECTIVE: To present molecular cytogenetic characterization of prenatally detected inverted duplication and deletion of 9p, or inv dup del(9p).

      MATERIALS, METHODS, AND RESULTS: A 35-year-old primigravid woman underwent amniocentesis at 16 weeks of gestation because of advanced maternal age. Amniocentesis revealed a derivative chromosome 9, or der(9) with additional material at the end of the short arm of one chromosome 9. Parental karyotypes were normal. Level II ultrasound showed ...

      Known for Situ Hybridization | Inv Dup | Prenatal Diagnosis | Comparative Genomic | Human Pair
      KOL-Index: 12317

      OBJECTIVE: To present prenatal diagnosis and molecular genetic analyses of mosaic trisomy 9.

      MATERIALS, METHODS AND RESULTS: A 35-year-old woman, gravida 3, para 1, underwent amniocentesis at 17 weeks of gestation because of her advanced maternal age. Amniocentesis revealed a karyotype of 47,XX,+9[3]/46,XX[6]. Repeat amniocentesis at 19 weeks of gestation revealed a karyotype of 47,XX,+9[6]/46,XX[19]. At 22 weeks of gestation, she was referred to a tertiary medical center for genetic ...

      Known for Mosaic Trisomy | Prenatal Diagnosis | Uncultured Amniocytes | Molecular Genetic | Amniocentesis Karyotype
      KOL-Index: 12215

      OBJECTIVE: To present prenatal diagnosis of mosaic trisomy 15 at amniocentesis.

      MATERIALS AND METHODS: A 37-year-old woman underwent amniocentesis at 17 weeks of gestation because of advanced maternal age. Cytogenetic analysis of cultured amniocytes revealed a karyotype of 47,XY,+15[2]/46,XY[17]. She was referred for repeated amniocentesis at 19 weeks of gestation. Array comparative genomic hybridization (aCGH), interphase fluorescence in situ hybridization (FISH) and quantitative ...

      Known for Mosaic Trisomy | Prenatal Diagnosis | Uncultured Amniocytes | Literature Review | Situ Hybridization
      KOL-Index: 11392

      OBJECTIVE: To report five cases of major congenital malformations associated with common aneuploidies detected by rapid aneuploidy diagnosis.

      CASE REPORTS: The fetus in the first case presented cebocephaly, semilobar holoprosencephaly, and tetralogy of Fallot on ultrasound at 25 gestational weeks. Cordocentesis using multiplex ligation-dependent probe amplification to detect aneuploidies of chromosomes X, Y, 13, 18, and 21 in uncultured cord blood revealed three copies of all targets on ...

      Known for Rapid Aneuploidy Diagnosis | Uncultured Amniocytes | Genomic Hybridization | Array Comparative | Multiplex Ligation
      KOL-Index: 11101

      OBJECTIVE: To present the perinatal findings and molecular cytogenetic analysis of a rare chromosomal abnormality involving structural and numerical abnormalities of chromosome 18.

      MATERIALS, METHODS AND RESULTS: A 36-year-old woman, gravida 5, para 3, underwent amniocentesis because of her advanced maternal age. Amniocentesis revealed a karyotype of 46,XY,r(18) [27]/45,XY,-18[5]/46,XY[5]. The parents decided to continue the pregnancy. Level II ultrasound revealed ventriculomegaly. At 38 ...

      Known for Ring Chromosome | Situ Hybridization | Comparative Genomic | Perinatal Findings | Human Pair
      KOL-Index: 10910

      OBJECTIVE: To present prenatal diagnosis and molecular cytogenetic characterization of a small supernumerary marker chromosome (sSMC) derived from chromosome 8 by multiplex ligation-dependent probe amplification (MLPA), fluorescence in situ hybridization (FISH), spectral karyotyping (SKY) and array comparative genomic hybridization (aCGH).

      CASE REPORT: A 42-year-old woman, gravida 6, para 3, underwent amniocentesis at 19 gestational weeks because of advanced maternal age. Amniocentesis ...

      Known for Prenatal Diagnosis | Chromosome 8 | Situ Hybridization | Molecular Cytogenetic | Supernumerary Marker
      KOL-Index: 10678

      OBJECTIVE: To investigate unbalanced and balanced acrocentric rearrangements involving chromosomes other than chromosome 21 at amniocentesis.

      MATERIALS AND METHODS: From January 1987 to September 2009, 31,194 amniocenteses were performed at Mackay Memorial Hospital, Taipei, Taiwan. Two cases with unbalanced acrocentric rearrangements involving chromosomes other than chromosome 21 from two families, and 24 cases with balanced acrocentric rearrangements involving chromosomes other than ...

      Known for Acrocentric Rearrangements | Chromosome 21 | Parental Carrier Status | Prenatal Diagnosis | Human Pair
      KOL-Index: 10627

      We report the prenatal diagnosis of partial trisomy 3p(3p23-->pter) and monosomy 7q(7q36-->qter) in a fetus with microcephaly, alobar holoprosencephaly and cyclopia. A 26-year-old primigravida woman was referred for genetic counselling at 23 gestational weeks due to sonographic findings of intra-uterine growth retardation and cranio-facial abnormalities. Level II ultrasonograms further demonstrated alobar holoprosencephaly, a proboscis above the eye and a single median orbit consistent ...

      Known for Prenatal Diagnosis | Alobar Holoprosencephaly | Partial Trisomy | Situ Hybridization | Human Pair

      Key People For Prenatal Diagnosis

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      #2
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      Chih‐Ping Chen:Expert Impact

      Concepts for whichChih‐Ping Chenhas direct influence:Prenatal diagnosis,  Human pair,  Situ hybridization,  Uncultured amniocytes,  Mosaic trisomy,  Partial monosomy,  Cultured amniocytes,  Prenatal ultrasound.

      Chih‐Ping Chen:KOL impact

      Concepts related to the work of other authors for whichfor which Chih‐Ping Chen has influence:Prenatal diagnosis,  Situ hybridization,  Human pair,  Uncultured amniocytes,  Ring chromosome,  Kawasaki disease,  Intellectual disability.


       

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      Department of Obstetrics and Gynecology, National Yang-Ming, University School of Medicine, Taipei, Taiwan; Institute of Clinical and Community Health Nursing, National Yang Ming Chiao Tung University, Taipei, Taiwan; Department of Obstetrics and Gyn

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