Jin Han

发表

Chromosome microarray analysis in the investigation of children with congenital heart disease

C. Liao, F. Fu, Ru Li, 2017, BMC Pediatrics.

The Genetic and Clinical Outcomes in Fetuses With Isolated Fetal Growth Restriction: A Chinese Single-Center Retrospective Study

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

Prenatal exome sequencing in fetuses with congenital heart defects

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

Prenatal diagnosis of thalassemia in twin pregnancies in mainland China

Dongzhi Li, Xin Yang, L. Zhen, 2016, Journal of obstetrics and gynaecology : the journal of the Institute of Obstetrics and Gynaecology.

Rapid prenatal diagnosis of skeletal dysplasia using medical trio exome sequencing: Benefit for prenatal counseling and pregnancy management

Wenjie Liu, C. Liao, Dongzhi Li, 2020, Prenatal diagnosis.

Prenatal diagnosis of foetuses with congenital abnormalities and duplication of the MECP2 region.

G. Xie, C. Liao, Dongzhi Li, 2014, Gene.

Outcome of isolated enlarged cisterna magna identified in utero: experience at a single medical center in mainland China

C. Liao, Dongzhi Li, F. Fu, 2017, Prenatal diagnosis.

NDUFA4 enhances neuron growth by triggering growth factors and inhibiting neuron apoptosis through Bcl-2 and cytochrome C mediated signaling pathway.

C. Liao, Dongzhi Li, T. Lei, 2018, American journal of translational research.

Early prenatal detection of triploidy: a 9-year experience in mainland China

Dongzhi Li, L. Zhen, M. Pan, 2019, 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.

Maternal serum PlGF (placental growth factor) in Chinese women in the first trimester undergoing screening for Down syndrome.

H. Cuckle, D. Sahota, C. Liao, 2016, European journal of obstetrics, gynecology, and reproductive biology.

Compound heterozygous mutation of the ASXL3 gene causes autosomal recessive congenital heart disease

C. Liao, Dongzhi Li, T. Lei, 2020, Human 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.

Exome sequencing improves genetic diagnosis of fetal increased nuchal translucency

Dongzhi Li, Xin Yang, L. Zhen, 2020, Prenatal diagnosis.

Identification of differential microRNAs and messenger RNAs resulting from ASXL transcriptional regulator 3 knockdown during during heart development

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

Fetal akinesia: The application of clinical exome sequencing in cases with decreased fetal movement.

Dongzhi Li, Xin Yang, Yu Yang, 2021, European journal of obstetrics, gynecology, and reproductive biology.

Novel FREM1 mutations are associated with severe hydrocephalus and shortened limbs in a prenatal case.

Dongzhi Li, Lv-Yin Huang, Jin Han, 2017, European Journal of Obstetrics, Gynecology, and Reproductive Biology.

Compound heterozygous mutation of the ASXL3 gene causes autosomal recessive congenital heart disease

C. Liao, Dongzhi Li, T. Lei, 2020, Human Genetics.

Prenatal diagnosis of Miller-Dieker syndrome/PAFAH1B1-related lissencephaly: Ultrasonography and genetically investigative results.

Dongzhi Li, L. Zhen, X. Jing, 2022, European journal of obstetrics, gynecology, and reproductive biology.

Prenatal diagnosis of 17q12 deletion syndrome: a retrospective case series

Dongzhi Li, L. Zhen, X. Jing, 2019, Journal of obstetrics and gynaecology : the journal of the Institute of Obstetrics and Gynaecology.

Prenatal Diagnosis of PPP2R1A-Related Neurodevelopmental Disorders Using Whole Exome Sequencing: Clinical Report and Review of Literature

C. Liao, T. Lei, F. Fu, 2023, Genes.

Prenatal diagnosis of fetuses with increased nuchal translucency using an approach based on quantitative fluorescent polymerase chain reaction and genomic microarray.

C. Liao, Dongzhi Li, Ru Li, 2016, European journal of obstetrics, gynecology, and reproductive biology.

Impact of cell-free fetal DNA on early invasive prenatal diagnosis at a Chinese reference maternal medicine center

Dongzhi Li, Xin Yang, L. Zhen, 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.

Case Report: Early diagnosis of lethal multiple pterygium syndrome with micrognathia: Two novel mutations in the CHRND gene

Ru Li, Xin Yang, Jin Han, 2023, Frontiers in Genetics.

Genetic Analysis and Sonography Characteristics in Fetus with SHOX Haploinsufficiency

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

Further genetic testing in prenatal cases of nonimmune hydrops fetalis with a normal array: a targeted panel or exome?

Dongzhi Li, Jin Han, 2021, American journal of obstetrics and gynecology.

The Trend in Timing of Prenatal Diagnosis for Thalassemia at a Chinese Tertiary Obstetric Center

Dongzhi Li, L. Zhen, Yu Yang, 2020, Hemoglobin.

Risk factors associated with fetal pleural effusion in prenatal diagnosis: a retrospective study in a single institute in Southern China

C. Liao, Dongzhi Li, Q. Deng, 2019, Journal of obstetrics and gynaecology : the journal of the Institute of Obstetrics and Gynaecology.

The indications for early prenatal diagnosis of trisomy 18: a 7-year experience at mainland China

Dongzhi Li, Xin Yang, L. Zhen, 2018, 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.

Prenatal diagnosis of Wolf-Hirschhorn syndrome: Ultrasonography and molecular karyotyping results.

Dongzhi Li, Xin Yang, L. Zhen, 2018, European journal of obstetrics, gynecology, and reproductive biology.

Prenatal diagnosis of ultrasound soft markers in a single medical center of mainland China

Ru Li, Xin Yang, L. Zhen, 2023, Molecular Cytogenetics.

How to make an accurate diagnosis of fetal pyriform sinus fistula in utero: experience at a single medical center in mainland China.

C. Liao, Dongzhi Li, F. Fu, 2018, European journal of obstetrics, gynecology, and reproductive biology.

The Two-Stage Ensemble Learning Model Based on Aggregated Facial Features in Screening for Fetal Genetic Diseases

Jin Han, Fanfan Zhu, Hang Zhou, 2023, International journal of environmental research and public health.

What can be inferred if the fetal increased nuchal translucency thickness changes?

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

Prenatal detection of 1p36 deletion syndrome: ultrasound findings and microarray testing results

C. Liao, Dongzhi Li, Xin Yang, 2019, 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.

Prenatal persistent left superior vena cava in low population: Not a benign vascular anomaly.

Dongzhi Li, Xin Yang, L. Zhen, 2022, Taiwanese journal of obstetrics & gynecology.

Application of noninvasive prenatal testing in pregnancies with fetal double bubble sign: Is it feasible?

Dongzhi Li, Xin Yang, L. Zhen, 2018, Prenatal diagnosis.

Prenatal Diagnosis and Prognosis of Fetal Hyperechogenic Kidney: A Study of 80 Cases

C. Liao, Ru Li, L. Zhen, 2021 .

Non-invasive prenatal testing: impact on invasive prenatal diagnosis at a mainland Chinese tertiary medical center

Dongzhi Li, Xin Yang, L. Zhen, 2016, 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.

First-trimester combined screening for trisomy 21 in women at risk for α-thalassemia

C. Liao, Dongzhi Li, Xin Yang, 2015, 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.

Use of noninvasive prenatal screening with cell-free DNA in late pregnancy with sonographic soft markers.

Dongzhi Li, Xin Yang, L. Zhen, 2020, European journal of obstetrics, gynecology, and reproductive biology.

Fetal Pyruvate Kinase Deficiency Identified Incidentally in a Chinese Family at Risk for α-Thalassemia

Dongzhi Li, Jian Li, Jin Han, 2021, Indian Journal of Hematology and Blood Transfusion.

Prenatal Diagnosis of Talipes Equinovarus by Ultrasound and Chromosomal Microarray Analysis: A Chinese Single-Center Retrospective Study

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

[Value of chromosomal microarray analysis for fetuses with duodenal obstruction].

C. Liao, F. Fu, Ru Li, 2021, Zhonghua yi xue yi chuan xue za zhi = Zhonghua yixue yichuanxue zazhi = Chinese journal of medical genetics.

What would be missed in the first trimester if nuchal translucency measurement is replaced by cell free DNA foetal aneuploidy screening?

Dongzhi Li, Xin Yang, L. Zhen, 2018, Journal of obstetrics and gynaecology : the journal of the Institute of Obstetrics and Gynaecology.

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

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

PT/NBL ratio assessment at mid-trimester in prenatal screening for Down syndrome in a Chinese population

C. Liao, Dongzhi Li, Xin Yang, 2014, 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.

Maternal serum ADAM12 in Chinese women undergoing screening for aneuploidy in the first trimester

D. Sahota, C. Liao, Dongzhi Li, 2010, 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.

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.

A Deep-Learning-Based Method Can Detect Both Common and Rare Genetic Disorders in Fetal Ultrasound

C. Liao, Ru Li, Xin Yang, 2023, Biomedicines.

Combining deep learning and intelligent biometry to extract ultrasound standard planes and assess early gestational weeks.

Huiying Liang, Longjiang E, Yuanyuan Pei, 2023, European Radiology.

Whole exome sequencing as a diagnostic adjunct to clinical testing in fetuses with structural abnormalities

C. Liao, Dongzhi Li, T. Lei, 2017, Ultrasound in obstetrics & gynecology : the official journal of the International Society of Ultrasound in Obstetrics and Gynecology.

ASXL3 gene mutations inhibit cell proliferation and promote cell apoptosis in mouse cardiomyocytes by upregulating lncRNA NONMMUT063967.2

C. Liao, Dongzhi Li, T. Lei, 2023, Biochemistry and biophysics reports.

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

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

Prenatal control of Hb Bart’s hydrops fetalis: a two-year experience at a mainland Chinese hospital

C. Liao, Dongzhi Li, Ru Li, 2015, 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.

Tumor markers in cord blood: A predictor of fetal malignant neoplasm?

Dongzhi Li, L. Zhen, M. Pan, 2021, European journal of obstetrics, gynecology, and reproductive biology.

Non-invasive prenatal detection of haemoglobin Bart's disease by cardiothoracic ratio during the first trimester.

C. Liao, Dongzhi Li, Xin Yang, 2015, European Journal of Obstetrics, Gynecology, and Reproductive Biology.

Exome sequencing improves genetic diagnosis of congenital orofacial clefts

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

Case report: A novel mosaic nonsense mutation of PCDH19 in a Chinese male with febrile epilepsy

Yan Lu, Jin Han, Ruibin Huang, 2022, Frontiers in Neurology.

An Innovative Three-Stage Model for Prenatal Genetic Disorder Detection Based on Region-of-Interest in Fetal Ultrasound

Jin Han, Long Lu, Hang Zhou, 2023, Bioengineering.

A 1st-trimester combined screening test in pregnant women of advanced maternal age in a Chinese population

C. Liao, Dongzhi Li, Xin Yang, 2015, Journal of obstetrics and gynaecology : the journal of the Institute of Obstetrics and Gynaecology.

Prenatal Diagnosis of Fetus With Transaldolase Deficiency Identifies Compound Heterozygous Variants: A Case Report

L. Zhen, S. Mei, Jin Han, 2022, Frontiers in Genetics.

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

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

Prenatal diagnosis and outcomes in fetuses with duplex kidney

F. Fu, Ru Li, Lushan Li, 2024, International journal of gynaecology and obstetrics: the official organ of the International Federation of Gynaecology and Obstetrics.

First trimester findings of decidual polyp: Caution to avoid polypectomy.

Dongzhi Li, Xin Yang, L. Zhen, 2020, European journal of obstetrics, gynecology, and reproductive biology.

Congenital extrahepatic portosystemic shunt: An unusual feature in cardio-facio-cutaneous syndrome.

Dongzhi Li, L. Zhen, Jin Han, 2022, European journal of obstetrics, gynecology, and reproductive biology.