Qiuxia Yu

发表

Whole‐exome sequencing in the evaluation of fetal congenital anomalies of the kidney and urinary tract detected by ultrasonography

C. Liao, Dongzhi Li, T. Lei, 2020, Prenatal diagnosis.

Prenatal exome sequencing in fetuses with congenital heart defects

C. Liao, Dongzhi Li, F. Fu, 2020, Clinical genetics.

Application of exome sequencing for prenatal diagnosis of fetal structural anomalies: clinical experience and lessons learned from a cohort of 1618 fetuses

C. Liao, P. Fang, Dongzhi Li, 2022, Genome Medicine.

Prenatal Diagnosis and Outcomes in Fetuses with Hemivertebra

C. Liao, Dongzhi Li, T. Lei, 2022, Genes.

Prenatal exome sequencing in fetuses with callosal anomalies

C. Liao, Dongzhi Li, T. Lei, 2022, Prenatal diagnosis.

Prenatal diagnosis of Coffin‐Siris syndrome: What are the fetal features?

Dongzhi Li, Qiuxia Yu, L. Zhen, 2022, Prenatal diagnosis.

Prenatal isolated clubfoot increases the risk for clinically significant exome sequencing results

Dongzhi Li, Qiuxia Yu, L. Zhen, 2022, Prenatal diagnosis.

The Value of a Comprehensive Genomic Evaluation in Prenatal Diagnosis of Genetic Diseases: A Retrospective Study

C. Liao, Dongzhi Li, F. Fu, 2022, Genes.

Contribution of maternal mosaicism to false-positive chromosome X loss associated with noninvasive prenatal testing

C. Liao, Dongzhi Li, F. Fu, 2022, The journal of maternal-fetal & neonatal medicine : the official journal of the European Association of Perinatal Medicine, the Federation of Asia and Oceania Perinatal Societies, the International Society of Perinatal Obstetricians.

Genetic Analysis and Sonography Characteristics in Fetus with SHOX Haploinsufficiency

C. Liao, F. Fu, Ru Li, 2023, Genes.

Prenatal diagnosis of 21 fetuses with balanced chromosomal abnormalities (BCAs) using whole-genome sequencing

C. Liao, Dongzhi Li, Weiyue Gu, 2022, Frontiers in Genetics.

Pregnancy outcome of autosomal aneuploidies other than common trisomies detected by noninvasive prenatal testing in routine clinical practice

C. Liao, Dongzhi Li, Ru Li, 2018, Prenatal diagnosis.

Prenatal Diagnosis of Chromosome 16p11.2 Microdeletion

C. Liao, Dongzhi Li, T. Lei, 2022, Genes.

Genetic tests aid in counseling of fetuses with cerebellar vermis defects

C. Liao, Ru Li, Qiuxia Yu, 2020, Prenatal diagnosis.

First trimester megacystis caused by a homozygous variant in MYL9.

Dongzhi Li, Qiuxia Yu, L. Zhen, 2022, European journal of obstetrics, gynecology, and reproductive biology.

Nonimmune hydrops fetalis: Genetic analysis and clinical outcome

C. Liao, T. Lei, F. Fu, 2020, Prenatal diagnosis.

A novel splicing mutation of ARHGAP29 is associated with nonsyndromic cleft lip with or without cleft palate

Shaoqing Wu, C. Liao, Dongzhi Li, 2020, The journal of maternal-fetal & neonatal medicine : the official journal of the European Association of Perinatal Medicine, the Federation of Asia and Oceania Perinatal Societies, the International Society of Perinatal Obstetricians.

Whole exome sequencing improves genetic diagnosis of fetal clubfoot

C. Liao, T. Lei, F. Fu, 2022, Human Genetics.

Fetal phenotype of Cornelia de Lange syndrome with a molecular confirmation.

Qiuxia Yu, L. Zhen, X. Jing, 2023, European journal of obstetrics, gynecology, and reproductive biology.

Aicardi-Goutières syndrome: The need for clinical vigilance in fetuses with sonographic features of congenital infection.

Dongzhi Li, Qiuxia Yu, Gui-lan Chen, 2023, European journal of obstetrics, gynecology, and reproductive biology.

Genetic diagnosis of fetal microcephaly at a single tertiary center in China

C. Liao, T. Lei, F. Fu, 2023, Frontiers in Genetics.

Identification of a Novel Mutation in the 3′ Untranslated Region of the β-Globin Gene (HBB:c.*132C>G) in a Chinese Family

Dongzhi Li, Qiuxia Yu, F. Jiang, 2022, Hemoglobin.

All‐trans‐retinoid acid induces the differentiation of P19 cells into neurons involved in the PI3K/Akt/GSK3β signaling pathway

C. Liao, Dongzhi Li, T. Lei, 2020, Journal of cellular biochemistry.

Genetic causes of isolated and severe fetal growth restriction in normal chromosomal microarray analysis

C. Liao, T. Lei, F. Fu, 2022, International journal of gynaecology and obstetrics: the official organ of the International Federation of Gynaecology and Obstetrics.

Case Report: Two Novel L1CAM Mutations in Two Unrelated Chinese Families With X-Linked Hydrocephalus

C. Liao, Dongzhi Li, F. Fu, 2022, Frontiers in Genetics.

Prenatal Diagnosis of Intragenic HNF1B Variant-Associated Renal Disease by Exome Sequencing

Dongzhi Li, Qiuxia Yu, X. Jing, 2022, Molecular Syndromology.

Ndufa4 Regulates the Proliferation and Apoptosis of Neurons via miR-145a-5p/Homer1/Ccnd2

C. Liao, Dongzhi Li, T. Lei, 2023, Molecular Neurobiology.

Exome sequencing improves genetic diagnosis of congenital orofacial clefts

C. Liao, T. Lei, F. Fu, 2023, Frontiers in genetics.

Fetal macrocephaly in late pregnancy: don't forget overgrowth syndromes

Qiuxia Yu, L. Zhen, D. Li, 2023, Ultrasound in obstetrics & gynecology : the official journal of the International Society of Ultrasound in Obstetrics and Gynecology.

Prenatal diagnosis in the fetal hyperechogenic kidneys: assessment using chromosomal microarray analysis and exome sequencing

C. Liao, T. Lei, F. Fu, 2023, Human Genetics.

Phenotypic and genotypic analysis of 11 fetal cases with Bardet-Biedl syndrome.

Qiuxia Yu, L. Zhen, Yun-Jing Wen, 2024, Prenatal diagnosis.