Yi-Yung Chen

发表

Chromosome 22q11.2 deletion syndrome: prenatal diagnosis, array comparative genomic hybridization characterization using uncultured amniocytes and literature review.

Chih-ping Chen, Jian-Pei Huang, S. Chern, 2013, Gene.

3q26.31-q29 duplication and 9q34.3 microdeletion associated with omphalocele, ventricular septal defect, abnormal first-trimester maternal serum screening and increased nuchal translucency: prenatal diagnosis and aCGH characterization.

Chih-ping Chen, S. Chern, Peih-Shan Wu, 2013, Gene.

Prenatal diagnosis and molecular cytogenetic characterization of mosaicism for a small supernumerary marker chromosome derived from chromosome 22 associated with cat eye syndrome.

Chih-ping Chen, T. Ko, Wayseen Wang, 2013, Gene.

Prenatal diagnosis of de novo interstitial deletions involving 5q23.1-q23.3 and 18q12.1-q12.3 by array CGH using uncultured amniocytes in a pregnancy with fetal interrupted aortic arch and atrial septal defect.

Chih-ping Chen, Ming-Chao Huang, S. Chern, 2013, Gene.

Prenatal diagnosis of a 15q11.2-q14 deletion of paternal origin associated with increased nuchal translucency, mosaicism for de novo multiple unbalanced translocations involving 15q11-q14, 5qter, 15qter, 17pter and 3qter and Prader-Willi syndrome.

Chih-ping Chen, S. Chern, Peih-Shan Wu, 2021, Taiwanese journal of obstetrics & gynecology.

Increased ubiquitination and reduced plasma membrane trafficking of placental amino acid transporter SNAT-2 in human IUGR

Madhulika B. Gupta, F. Rosario, T. Powell, 2015, Clinical science.

Angiogenesis in Differentiated Placental Multipotent Mesenchymal Stromal Cells Is Dependent on Integrin α5β1

Jian-Pei Huang, Chie-Pein Chen, Yi-Hsin Wu, 2009, PloS one.

Characteristics of early-onset neonatal sepsis caused by Escherichia coli.

Chie-Pein Chen, Yi-Yung Chen, Chen-Yu Chen, 2012, Taiwanese journal of obstetrics & gynecology.

Cri-du-chat (5p-) syndrome presenting with cerebellar hypoplasia and hypospadias: prenatal diagnosis and aCGH characterization using uncultured amniocytes.

Chih-ping Chen, Ming-Chao Huang, S. Chern, 2013, Gene.

1,25-Dihydroxy vitamin D3 stimulates system A amino acid transport in primary human trophoblast cells

T. Powell, T. Jansson, Yi-Yung Chen, 2017, Molecular and Cellular Endocrinology.

Prenatal diagnosis and molecular cytogenetic characterization of de novo partial trisomy 12q (12q24.21→qter) and partial monosomy 6q (6q27→qter) associated with coarctation of the aorta, ventriculomegaly and thickened nuchal fold.

Chih-ping Chen, S. Chern, Peih-Shan Wu, 2013, Gene.

Perinatal outcome of recurrent pre‐eclampsia versus pre‐eclampsia in nulliparas

Chie-Pein Chen, Yi-Yung Chen, T. Su, 2009, The journal of obstetrics and gynaecology research.

The reliability of transabdominal cervical length measurement in a low-risk obstetric population: Comparison with transvaginal measurement.

Chie-Pein Chen, Yi-Yung Chen, Liang-Kai Wang, 2015, Taiwanese journal of obstetrics & gynecology.

Prenatal diagnosis and molecular cytogenetic characterization of a small marker chromosome derived from Y chromosome.

Chih-ping Chen, Wayseen Wang, Yi-Yung Chen, 2011, Taiwanese journal of obstetrics & gynecology.

Prenatal diagnosis of low-level mosaicism for trisomy 21 by amniocentesis in a pregnancy associated with maternal uniparental disomy of chromosome 21 in the fetus and a favorable outcome.

Chih-ping Chen, T. Ko, S. Chern, 2020, Taiwanese journal of obstetrics & gynecology.

Down-regulation of placental folate transporters in intrauterine growth restriction.

Madhulika B. Gupta, T. Powell, T. Jansson, 2018, The Journal of nutritional biochemistry.

Chromosome 18p deletion syndrome presenting holoprosencephaly and premaxillary agenesis: prenatal diagnosis and aCGH characterization using uncultured amniocytes.

Chih-ping Chen, Jian-Pei Huang, S. Chern, 2013, Gene.

Chromosome 1p32-p31 deletion syndrome: prenatal diagnosis by array comparative genomic hybridization using uncultured amniocytes and association with NFIA haploinsufficiency, ventriculomegaly, corpus callosum hypogenesis, abnormal external genitalia, and intrauterine growth restriction.

Chih-ping Chen, S. Chern, Wayseen Wang, 2011, Taiwanese journal of obstetrics & gynecology.

The effect of conditioned medium derived from human placental multipotent mesenchymal stromal cells on neutrophils: possible implications for placental infection.

Jian-Pei Huang, Chie-Pein Chen, Yi-Hsin Wu, 2014, Molecular human reproduction.

Wolf-Hirschhorn (4p-) syndrome: prenatal diagnosis, molecular cytogenetic characterization and association with a 1.2-Mb microduplication at 8p22-p21.3 and a 1.1-Mb microduplication at 10p15.3 in a fetus with an apparently pure 4p deletion.

Chih-ping Chen, S. Chern, Wayseen Wang, 2011, Taiwanese journal of obstetrics & gynecology.

Acute fatty liver of pregnancy in a Taiwanese tertiary care center: a retrospective review.

Jian-Pei Huang, Chie-Pein Chen, Yi-Yung Chen, 2010, Taiwanese journal of obstetrics & gynecology.

First-trimester two-dimensional and three-dimensional ultrasound demonstration of craniofacial defects, abdominal wall defects and upper limb deficiency associated with limb-body wall complex.

Chih-ping Chen, Wayseen Wang, Yi-Yung Chen, 2011, Taiwanese journal of obstetrics & gynecology.

Prenatal Diagnosis of LimbeBody Wall Complex With Craniofacial Defects

Chih-ping Chen, Wayseen Wang, Yi-Yung Chen, 2022 .

17 – Placental Function in Intrauterine Growth Restriction

T. Jansson, Yi-Yung Chen, 2017 .

Prenatal diagnosis of mosaic trisomy 2 associated with abnormal maternal serum screening, oligohydramnios, intrauterine growth restriction, ventricular septal defect, preaxial polydactyly, and facial dysmorphism.

Chih-ping Chen, S. Chern, Peih-Shan Wu, 2013, Taiwanese journal of obstetrics & gynecology.

VACTERL association with hydrocephalus in a fetus conceived by in vitro fertilization and embryo transfer.

Chih-ping Chen, S. Chern, Wayseen Wang, 2013, Taiwanese journal of obstetrics & gynecology.

First-trimester sonographic demonstration of digynic triploidy.

Chih-ping Chen, S. Chern, Wayseen Wang, 2013, Taiwanese journal of obstetrics & gynecology.

Usefulness of interphase FISH on uncultured amniocytes for rapid confirmation of low-level trisomy 7 mosaicism in a pregnancy with fetal intrauterine growth restriction and microcephaly.

Chih-ping Chen, S. Chern, Wayseen Wang, 2012, Taiwanese journal of obstetrics & gynecology.

The effects of absent or reversed end-diastolic umbilical artery Doppler flow velocity.

Yi-Yung Chen, Chen-Yu Chen, Kuo‐Gon Wang, 2009, Taiwanese journal of obstetrics & gynecology.

Detection of a familial 1q21.1 microdeletion and concomitant CHD1L mutation in a fetus with oligohydramnios and bilateral renal dysplasia on prenatal ultrasound.

Chih-ping Chen, Jian-Pei Huang, S. Chern, 2019, Taiwanese journal of obstetrics & gynecology.

Detection of maternal transmission of a splicing mutation in the TSC2 gene following prenatal diagnosis of fetal cardiac rhabdomyomas mimicking congenital cystic adenomatoid malformation of the lung and cerebral tubers and awareness of a family history of maternal epilepsy.

Wan-Yuo Guo, Chih-ping Chen, S. Chern, 2013, Taiwanese journal of obstetrics & gynecology.

Prenatal diagnosis and molecular cytogenetic characterization of low-level mosaicism for tetrasomy 18p at amniocentesis in a pregnancy with a favorable outcome.

Chih-ping Chen, T. Ko, S. Chern, 2017, Taiwanese journal of obstetrics & gynecology.

Prenatal diagnosis and antenatal history of total anomalous pulmonary venous return.

Yi-Yung Chen, Chin-Yuan Hsu, 2006, Taiwanese journal of obstetrics & gynecology.

Prenatal diagnosis and array comparative genomic hybridization characterization of interstitial deletions of 8q23.3-q24.11 and 8q24.13 associated with Langer-Giedion syndrome, Cornelia de Lange syndrome and haploinsufficiency of TRPS1, RAD21 and EXT1.

Chih-ping Chen, S. Chern, Peih-Shan Wu, 2015, Taiwanese journal of obstetrics & gynecology.

Prenatal diagnosis of a distal 3p deletion associated with fetoplacental chromosomal discrepancy and confined placental mosaicism detected by array comparative genomic hybridization.

Chih-ping Chen, S. Chern, Peih-Shan Wu, 2013, Taiwanese journal of obstetrics & gynecology.

Rapid aneuploidy diagnosis by multiplex ligation-dependent probe amplification using uncultured amniocytes in pregnancy with major fetal structural abnormalities.

Chih-Long Chang, Chih-ping Chen, S. Chern, 2012, Taiwanese journal of obstetrics & gynecology.

Spontaneous rupture and massive hemoperitoneum from uterine leiomyomas and adenomyosis in a nongravid and unscarred uterus.

Chie-Pein Chen, Yi-Yung Chen, Liang-Kai Wang, 2015, Taiwanese journal of obstetrics & gynecology.

Monozygotic twins with trisomy 18 of paternal origin: prenatal diagnosis and molecular cytogenetic characterization in a pregnancy with one structurally abnormal living fetus and one intrauterine fetal demise.

Chih-ping Chen, S. Chern, Wayseen Wang, 2012, Taiwanese journal of obstetrics & gynecology.

Decreased placental folate transporter expression and activity in first and second trimester in obese mothers.

F. Rosario, T. Powell, T. Jansson, 2019, The Journal of nutritional biochemistry.

Unexplained shortening of the long bones in the third trimester as the only prenatal feature in a male fetus with 45,X/46,X,r(Y) mosaicism.

Chih-ping Chen, F. Tsai, Wayseen Wang, 2012, Taiwanese journal of obstetrics & gynecology.

Rapid aneuploidy diagnosis by multiplex ligation-dependent probe amplification and array comparative genomic hybridization in pregnancy with major congenital malformations.

Chih-Long Chang, Chih-ping Chen, Yeou-Lih Wang, 2011, Taiwanese journal of obstetrics & gynecology.

Rapid Diagnosis of Trisomy 18 Using Uncultured Amniocytes in Late Second Trimester in a Pregnancy with Fetal Congenital Heart Defects, Arthrogryposis, Omphalocele, and Mega Cisterna Magna

Chih-ping Chen, S. Chern, Peih-Shan Wu, 2012 .

Association between maternal benzodiazepine or Z-hypnotic use in early pregnancy and the risk of stillbirth, preterm birth, and small for gestational age: a nationwide, population-based cohort study in Taiwan.

F. Hsiao, Liang‐Kung Chen, K. Chan, 2023, The lancet. Psychiatry.

Effects of prenatal subjective well-being on birth outcomes and child development: A longitudinal study

Jian-Pei Huang, H. Au, Yi-Yung Chen, 2022, European Psychiatry.

Prenatal diagnosis and molecular genetic analysis of short rib-polydactyly syndrome type III (Verma-Naumoff) in a second-trimester fetus with a homozygous splice site mutation in intron 4 in the NEK1 gene.

Chih-ping Chen, S. Chern, Wayseen Wang, 2012, Taiwanese journal of obstetrics & gynecology.

Molecular cytogenetic characterization of del(X)(p22.33)mat and de novo dup(4)(q34.3q35.2) in a male fetus with multiple anomalies of facial dysmorphism, ventriculomegaly, congenital heart defects, short long bones and clinodactyly.

Chih-ping Chen, Jian-Pei Huang, S. Chern, 2023, Taiwanese journal of obstetrics & gynecology.

Chih-ping Chen, S. Chern, Wayseen Wang, 2011, Taiwanese journal of obstetrics & gynecology.