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Selective feticide in dichorionic diamniotic (DCDA) twins complicated with previable premature rupture of membrane before 24 weeks may be a safe therapeutic alternative to ongoing pregnancy

BMC pregnancy and childbirth, 2024-02, Vol.24 (1), p.166-166, Article 166

2024

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Pregnancies complicated with functioning adrenal adenomas causing severe obstetric outcomes: a 20-year experience at a tertiary center

BMC endocrine disorders, 2024-07, Vol.24 (1), p.122-8, Article 122

2024

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Intertwin nuchal translucency difference predicts the chance of co-twin death after fetal reduction in dichorionic triplet pregnancies: a retrospective analysis study

BMC pregnancy and childbirth, 2023-10, Vol.23 (1), p.1-747, Article 747

2023

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The use of high-resolution SNP arrays to detect congenital cardiac defects

The journal of maternal-fetal & neonatal medicine, 2024-12, Vol.37 (1), p.2301831-2301831

2024

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Contribution of genetic variants to congenital heart defects in both singleton and twin fetuses: a Chinese cohort study

Molecular cytogenetics, 2024-01, Vol.17 (1), p.2-2, Article 2

2024

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The Role of MALAT1 in Regulating the Proangiogenic Functions, Invasion, and Migration of Trophoblasts in Selective Fetal Growth Restriction

Biomolecules (Basel, Switzerland), 2024-08, Vol.14 (8), p.988

2024

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Integrative profiling of extrachromosomal circular DNA in placenta and maternal plasma provides insights into the biology of fetal growth restriction and reveals potential biomarkers

Frontiers in genetics, 2023-07, Vol.14, p.1128082-1128082

2023

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Prenatal diagnosis of dent disease type I with a nonsense pathogenic variant in CLCN5: a case study

BMC medical genomics, 2024-01, Vol.17 (1), p.34-34, Article 34

2024

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Evaluation of a Microhaplotype-Based Noninvasive Prenatal Test in Twin Gestations: Determination of Paternity, Zygosity, and Fetal Fraction

Genes, 2020-12, Vol.12 (1), p.26

2020

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Increased expression and altered methylation of HERVWE1 in the human placentas of smaller fetuses from monozygotic, dichorionic, discordant twins

PloS one, 2012-03, Vol.7 (3), p.e33503-e33503

2012

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Case Report: Low-Level Maternal Mosaicism of a Novel CREBBP Variant Causes Recurrent Rubinstein-Taybi Syndrome in Two Siblings of a Chinese Family

Frontiers in genetics, 2021-03, Vol.12, p.640992

2021

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Chromosomal Uniparental Disomy 16 and Fetal Intrauterine Growth Restriction

European journal of obstetrics & gynecology and reproductive biology, 2017-04, Vol.211, p.1-7

2017

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Prenatal treatment of severe fetal hemolytic disease due to anti-M alloimmunization by serial intrauterine transfusions

Taiwanese journal of obstetrics & gynecology, 2017-06, Vol.56 (3), p.379-381

2017

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Clinical value of genetic analysis in prenatal diagnosis of short femur

Molecular genetics & genomic medicine, 2019-11, Vol.7 (11), p.e978-n/a

2019

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Is an analysis of copy number variants necessary for various types of kidney ultrasound anomalies in fetuses?

Molecular cytogenetics, 2019-07, Vol.12 (Suppl 1), p.31-31, Article 31

2019

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Sub-kHz-Linewidth Wavelength-Tunable Single-Frequency Ring-Cavity Fiber Laser for C- and L-Band Operation

Journal of lightwave technology, 2021-07, Vol.39 (14), p.4794-4799

2021

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Effect of MSX1 on the cellular function of cardiomyocytes

Gene, 2024-07, Vol.916, p.148419-148419, Article 148419

2024

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An Incidental Detection of a Rare UPD in SNP-Array Based PGT-SR: A Case Report

Reproductive sciences (Thousand Oaks, Calif.), 2024-09, Vol.31 (9), p.2893-2899

2024

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Estrogen-related receptor γ regulates expression of 17β-hydroxysteroid dehydrogenase type 1 in fetal growth restriction

Placenta (Eastbourne), 2018-07, Vol.67, p.38-44

2018

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Hemolytic disease of the fetus and newborn due to alloanti‐M: three Chinese case reports and a review of the literature

Transfusion (Philadelphia, Pa.), 2019-01, Vol.59 (1), p.385-395

2019

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Potential role of microRNA-424 in regulating ERRγ to suppress trophoblast proliferation and invasion in fetal growth restriction

Placenta (Eastbourne), 2019-08, Vol.83, p.57-62

2019

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Unusual twinning: Additional findings during prenatal diagnosis of twin zygosity by single nucleotide polymorphism (SNP) array

Prenatal diagnosis, 2018-05, Vol.38 (6), p.428-434

2018

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CXCR2 is decreased in preeclamptic placentas and promotes human trophoblast invasion through the Akt signaling pathway

Placenta (Eastbourne), 2016-07, Vol.43, p.17-25

2016

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High-Precision Tunable Single-Frequency Fiber Laser at 1.5 μm Based on Self-Injection Locking

IEEE photonics technology letters, 2022-06, Vol.34 (12), p.633-636

2022

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Discordant phenotypes in monozygotic twins with 16p11.2 microdeletions including the SH2B1 gene

American journal of medical genetics. Part A, 2017-08, Vol.173 (8), p.2284-2288

2017

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Selective feticide in dichorionic diamniotic (DCDA) twins complicated with previable premature rupture of membrane before 24 weeks may be a safe therapeutic alternative to ongoing pregnancy

Pregnancies complicated with functioning adrenal adenomas causing severe obstetric outcomes: a 20-year experience at a tertiary center

Intertwin nuchal translucency difference predicts the chance of co-twin death after fetal reduction in dichorionic triplet pregnancies: a retrospective analysis study

The use of high-resolution SNP arrays to detect congenital cardiac defects

Contribution of genetic variants to congenital heart defects in both singleton and twin fetuses: a Chinese cohort study

The Role of MALAT1 in Regulating the Proangiogenic Functions, Invasion, and Migration of Trophoblasts in Selective Fetal Growth Restriction

Integrative profiling of extrachromosomal circular DNA in placenta and maternal plasma provides insights into the biology of fetal growth restriction and reveals potential biomarkers

Prenatal diagnosis of dent disease type I with a nonsense pathogenic variant in CLCN5: a case study

Evaluation of a Microhaplotype-Based Noninvasive Prenatal Test in Twin Gestations: Determination of Paternity, Zygosity, and Fetal Fraction

Increased expression and altered methylation of HERVWE1 in the human placentas of smaller fetuses from monozygotic, dichorionic, discordant twins

Case Report: Low-Level Maternal Mosaicism of a Novel CREBBP Variant Causes Recurrent Rubinstein-Taybi Syndrome in Two Siblings of a Chinese Family

Chromosomal Uniparental Disomy 16 and Fetal Intrauterine Growth Restriction

Prenatal treatment of severe fetal hemolytic disease due to anti-M alloimmunization by serial intrauterine transfusions

Clinical value of genetic analysis in prenatal diagnosis of short femur

Is an analysis of copy number variants necessary for various types of kidney ultrasound anomalies in fetuses?

Sub-kHz-Linewidth Wavelength-Tunable Single-Frequency Ring-Cavity Fiber Laser for C- and L-Band Operation

Effect of MSX1 on the cellular function of cardiomyocytes

An Incidental Detection of a Rare UPD in SNP-Array Based PGT-SR: A Case Report

Estrogen-related receptor γ regulates expression of 17β-hydroxysteroid dehydrogenase type 1 in fetal growth restriction

Hemolytic disease of the fetus and newborn due to alloanti‐M: three Chinese case reports and a review of the literature

Potential role of microRNA-424 in regulating ERRγ to suppress trophoblast proliferation and invasion in fetal growth restriction

Unusual twinning: Additional findings during prenatal diagnosis of twin zygosity by single nucleotide polymorphism (SNP) array

CXCR2 is decreased in preeclamptic placentas and promotes human trophoblast invasion through the Akt signaling pathway

High-Precision Tunable Single-Frequency Fiber Laser at 1.5 μm Based on Self-Injection Locking

Discordant phenotypes in monozygotic twins with 16p11.2 microdeletions including the SH2B1 gene

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