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Shin-Wen Chen Selected Research

Pregnancy-Associated Plasma Protein-A (PAPP-A)

1/2023Molecular cytogenetic characterization of de novo concomitant distal 8p deletion of 8p23.3p23.1 and Xp and Xq deletion of Xp22.13q28 due to an unbalanced X;8 translocation detected by amniocentesis.
11/2022Prenatal diagnosis and molecular cytogenetic characterization of a de novo deletion of 4q34.1→qter associated with low PAPP-A and low PlGF in the first-trimester maternal serum screening, congenital heart defect on fetal ultrasound and a false negative non-invasive prenatal testing (NIPT) result.
3/2022Prenatal diagnosis and molecular cytogenetic characterization of mosaic ring chromosome 21 associated with low PAPP-A and low PlGF in the first-trimester maternal serum screening.
3/2022Detection of paternal origin of fetal de novo rea(21q;21q) down syndrome in a pregnancy of a young woman associated with an abnormal first-trimester maternal serum screening result.
1/2022Detection of maternal uniparental disomy 9 in association with low-level mosaic trisomy 9 at amniocentesis in a pregnancy associated with intrauterine growth restriction, abnormal first-trimester screening result (low PAPP-A and low PlGF), maternal preeclampsia and a favorable outcome.
11/2021Prenatal diagnosis of mosaic trisomy 16 by amniocentesis in a pregnancy associated with abnormal first-trimester screening result (low PAPP-A and low PlGF), intrauterine growth restriction and a favorable outcome.
9/2020Prenatal diagnosis of partial monosomy 2q (2q37.3→qter) and partial trisomy 10q (10q24.31→qter) of paternal origin associated with increased nuchal translucency and abnormal maternal serum screening results.

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Shin-Wen Chen Research Topics

Disease

30Uniparental Disomy
05/2023 - 04/2017
15Down Syndrome (Down's Syndrome)
01/2023 - 02/2017
6Trisomy (Trisomies)
05/2023 - 09/2020
5Fetal Growth Retardation (Intrauterine Growth Retardation)
05/2023 - 10/2017
5Trisomy 13 Syndrome
11/2022 - 12/2017
4Trisomy 18 Syndrome
05/2023 - 07/2020
2Aneuploidy (Aneuploid)
11/2022 - 07/2021
2Ring Chromosomes (Ring Chromosome)
03/2022 - 08/2017
2Pre-Eclampsia (Preeclampsia)
03/2022 - 01/2022
2Chromosome Aberrations (Chromosome Abnormalities)
05/2021 - 01/2020
2Spontaneous Abortion (Miscarriage)
09/2020 - 06/2017
2Oligohydramnios
09/2020 - 11/2019
2Ventricular Heart Septal Defects (Ventricular Septal Defect)
09/2019 - 06/2016
1Cystic Lymphangioma (Hygroma)
05/2023
1Turner Syndrome (Turner's Syndrome)
03/2023
1tetrasomy 9p Chromosome 9
01/2023
1Congenital Heart Defects (Congenital Heart Defect)
11/2022
1Male Infertility (Male Sterility)
09/2022
1Fetal Distress
03/2021
1Persistent Left Superior Vena Cava
03/2021
1Esophageal Atresia
03/2021
1Polyhydramnios
03/2021
115q24 Microdeletion
05/2020
1Pericardial Effusion
09/2019
1Cardiomegaly (Heart Hypertrophy)
09/2019
1Triploidy
12/2018
1Duplication 15q11-q13 Syndrome
10/2018
1Spinocerebellar Ataxias (Spinocerebellar Ataxia)
02/2018
1Isochromosomes
12/2017
1Attention Deficit Disorder with Hyperactivity (Attention Deficit Hyperactivity Disorder)
12/2016
1Intellectual Disability (Idiocy)
12/2016
1Obesity
12/2016
1Language Development Disorders (Semantic-Pragmatic Disorder)
06/2016

Drug/Important Bio-Agent (IBA)

40Genetic Markers (Genetic Marker)IBA
05/2023 - 06/2016
18DNA (Deoxyribonucleic Acid)IBA
05/2023 - 10/2018
12dimemorfan (AT 17)IBA
03/2023 - 02/2017
10dichlorobis(azomycin)platinum IIIBA
05/2023 - 10/2017
7Pregnancy-Associated Plasma Protein-A (PAPP-A)IBA
01/2023 - 09/2020
4Intercellular Signaling Peptides and Proteins (Growth Factors)IBA
01/2023 - 11/2021
1Cytochrome P-450 CYP1A2 (CYP1A2)IBA
05/2020
1Cholesterol Side-Chain Cleavage Enzyme (CYP11A1)IBA
05/2020
1Cytochrome P-450 CYP1A1 (CYP1A1)IBA
05/2020
1OligonucleotidesIBA
12/2017

Therapy/Procedure

3Ligation
03/2023 - 07/2022
2Cesarean Section (Caesarean Section)
03/2021 - 09/2020
1Treatment Delay
09/2022
1Gastric Balloon
03/2021