Yan Wang

Zhengfeng Xu, P. Hu, Yan Wang, 2020, Ultrasound in obstetrics & gynecology : the official journal of the International Society of Ultrasound in Obstetrics and Gynecology.

Identification of chromosomal abnormalities in early pregnancy loss using a high-throughput ligation-dependent probe amplification-based assay.

Zhengfeng Xu, P. Hu, Zhengwen Jiang, 2020, The Journal of molecular diagnostics : JMD.

Current attitudes and preconceptions towards expanded carrier screening in the Eastern Chinese reproductive-aged population

Zhengfeng Xu, P. Hu, Yan Wang, 2021, Journal of Assisted Reproduction and Genetics.

A De Novo Mutation in DYRK1A Causes Syndromic Intellectual Disability: A Chinese Case Report

Gang Liu, Zhengfeng Xu, P. Hu, 2019, Front. Genet..

Analyzing false‐negative results detected in low‐risk non‐invasive prenatal screening cases

Zhengfeng Xu, P. Hu, D. Liang, 2020, Molecular genetics & genomic medicine.

1q25.2-q31.3 Deletion in a female with mental retardation, clinodactyly, minor facial anomalies but no growth retardation

Zhengfeng Xu, P. Hu, L. Yi, 2013, Molecular Cytogenetics.

Molecular characterization of ring chromosome 18 by low-coverage next generation sequencing

R. Sun, Zhengfeng Xu, P. Hu, 2015, BMC Medical Genetics.

Analysis of chromosome 22q11 copy number variations by multiplex ligation-dependent probe amplification for prenatal diagnosis of congenital heart defect

Gang Liu, Zhengfeng Xu, P. Hu, 2015, Molecular Cytogenetics.

Analysis of Biomarkers for Congenital Heart Disease Based on Maternal Amniotic Fluid Metabolomics

Tao Jiang, Zhengfeng Xu, Yun Sun, 2021, Frontiers in Cardiovascular Medicine.

Reproductive outcomes in couples with sporadic miscarriage after embryonic chromosomal microarray analysis

Yiming Li, Zhengfeng Xu, Yan Wang, 2023, Annals of medicine.

A novel 11p13 microdeletion encompassing PAX6 in a Chinese Han family with aniridia, ptosis and mental retardation

Zhengfeng Xu, P. Hu, L. Yi, 2015, Molecular Cytogenetics.

Optical genome mapping for detection of chromosomal aberrations in prenatal diagnosis

Zhengfeng Xu, Qinxin Zhang, Yan Wang, 2023, Acta obstetricia et gynecologica Scandinavica.

Young LINE-1 transposon 5′ UTRs marked by elongation factor ELL3 function as enhancers to regulate naïve pluripotency in embryonic stem cells

Chengqi Lin, Zhuojuan Luo, Shiqi Zhu, 2023, Nature Cell Biology.

Clinical application of whole‐genome low‐coverage next‐generation sequencing to detect and characterize balanced chromosomal translocations

Asan, Y. Wang, Y. Lin, 2017, Clinical genetics.

Prenatal Diagnosis of Recurrent Distal 1q21.1 Duplication in Three Fetuses With Ultrasound Anomalies

Zhengfeng Xu, P. Hu, D. Ma, 2018, Front. Genet..

11q13.3q13.4 deletion plus 9q21.13q21.33 duplication in an affected girl arising from a familial four-way balanced chromosomal translocation.

Zhengfeng Xu, Qinxin Zhang, Yan Wang, 2023, Molecular Genetics & Genomic Medicine.

Peptidomic Analysis of Fetal Heart Tissue for Identification of Endogenous Peptides Involved in Tetralogy of Fallot.

Zhengfeng Xu, D. Ma, D. Liang, 2017, DNA and cell biology.

A capillary electrophoresis-based variant hotspot genotyping method for rapid and reliable analysis of the phenylalanine hydroxylase gene in the Chinese Han population.

Zhengfeng Xu, Zhengwen Jiang, Yan Wang, 2021, Clinica chimica acta; international journal of clinical chemistry.

Creatine Kinase-MM/Proto-oncogene Tyrosine-Protein Kinase Receptor as a Sensitive Indicator for Duchenne Muscular Dystrophy Carriers.

Zhengfeng Xu, D. Hong, D. Ma, 2024, Molecular Neurobiology.

Systematic analysis of copy number variants of uncertain significance partially overlapping with the haploinsufficient or triplosensitive genes in clinical testing

Zhengfeng Xu, Yan Wang, Ping Hu, 2023, Annals of medicine.