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List of works by Zhengfeng Xu

A De Novo heterozygous frameshift mutation identified in BCL11B causes neurodevelopmental disorder by whole exome sequencing

scientific article published on 25 July 2019

A novel splice site mutation in the UBE2A gene leads to aberrant mRNA splicing in a Chinese patient with X-linked intellectual disability type Nascimento

scientific article published on 30 September 2019

An enrichment method to increase cell-free fetal DNA fraction and significantly reduce false negatives and test failures for non-invasive prenatal screening: a feasibility study

scientific article published on 11 April 2019

Analysis of microbial differences in amniotic fluid between advanced and normal age pregnant women

publication published on 27 July 2021

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

scientific article published on 18 February 2020

Clinical application of targeted next-generation sequencing in fetuses with congenital heart defect

scientific article published on 25 June 2018

Comprehensive evaluation of genetic variants in fetuses with congenital heart defect using chromosomal microarray analysis and exome sequencing

scientific article published on 03 November 2020

Diagnosis of Shashi-Pena Syndrome Caused by Chromosomal Rearrangement Using Nanopore Sequencing

scientific article published on 23 November 2021

Genetic analysis of 62 Chinese families with Duchenne muscular dystrophy and strategies of prenatal diagnosis in a single center

scientific article published on 14 November 2019

Identification and characterization of a novel 43-bp deletion mutation of the ATP7B gene in a Chinese patient with Wilson's disease: a case report.

scientific article published on 12 April 2018

Molecular diagnostic in fetuses with isolated congenital anomalies of the kidney and urinary tract by whole-exome sequencing

scientific article published on 11 August 2020

Perinatal outcomes following cell-free DNA screening in >32 000 women: Clinical follow-up data from a single tertiary center

scientific article published on 27 July 2018

Pregnancy outcomes of rare autosomal trisomies results in non‐invasive prenatal screening: clinical follow‐up data from a single tertiary centre

scientific article published in 2022

Systematic analysis of copy-number variations associated with early pregnancy loss

scientific article published on 01 January 2020

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