Yang Zeng

Chengdu, China

Last Updated: 09/26/2026

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Found 16 publications

Aztreonam-Avibactam Resistance Due to Synergistic Interplay of ampC-Related Mutations in Carbapenem-Resistant Enterobacter spp.

Aztreonam-Avibactam Resistance Due to Synergistic Interplay of ampC-Related Mutations in Carbapenem-Resistant Enterobacter spp.

Journal: The Journal of infectious diseases

Published: March 13, 2026

Enhanced invasiveness promotes the dominance of a widely-distributed carbapenem-resistant virulence-plasmid-carrying Klebsiella pneumoniae sublineage.

Enhanced invasiveness promotes the dominance of a widely-distributed carbapenem-resistant virulence-plasmid-carrying Klebsiella pneumoniae sublineage.

Journal: Nature communications

Published: June 30, 2025

A miniaturized liver function detection system with machine learning enhancing strategy.

A miniaturized liver function detection system with machine learning enhancing strategy.

Journal: Biosensors & bioelectronics

Published: February 15, 2025

A prenatal case misunderstood as specimen confusion: 46,XY/46,XY chimerism.

A prenatal case misunderstood as specimen confusion: 46,XY/46,XY chimerism.

Journal: BMC pregnancy and childbirth

Published: November 03, 2023

Defining the scope of extended NIPS in Western China: evidence from a large cohort of fetuses with normal ultrasound scans.

Defining the scope of extended NIPS in Western China: evidence from a large cohort of fetuses with normal ultrasound scans.

Journal: BMC pregnancy and childbirth

Published: March 10, 2023

NGS-based targeted sequencing identified six novel variants in patients with Duchenne/Becker muscular dystrophy from southwestern China.

NGS-based targeted sequencing identified six novel variants in patients with Duchenne/Becker muscular dystrophy from southwestern China.

Journal: BMC medical genomics

Published: February 15, 2023

Prenatal phenotype of Wolf-Hirschhorn syndrome: A case series and literature review.

Prenatal phenotype of Wolf-Hirschhorn syndrome: A case series and literature review.

Journal: Molecular genetics & genomic medicine

Published: December 20, 2022

Application of copy number variation squencing for prenatal diagnosis

Application of copy number variation squencing for prenatal diagnosis

Journal: Zhonghua yi xue yi chuan xue za zhi = Zhonghua yixue yichuanxue zazhi = Chinese journal of medical genetics

Published: September 09, 2022

Does isolated nuchal translucency from 2.5 to 2.9 mm increase the risk of fetal chromosome disease?

Does isolated nuchal translucency from 2.5 to 2.9 mm increase the risk of fetal chromosome disease?

Journal: Molecular genetics and genomics : MGG

Published: July 04, 2022

Analysis of autosomal dominant genes impacted by copy number loss in 24,844 fetuses without structural abnormalities.

Analysis of autosomal dominant genes impacted by copy number loss in 24,844 fetuses without structural abnormalities.

Journal: BMC genomics

Published: October 14, 2021

Copy number variation sequencing combined with quantitative fluorescence polymerase chain reaction in clinical application of pregnancy loss.

Copy number variation sequencing combined with quantitative fluorescence polymerase chain reaction in clinical application of pregnancy loss.

Journal: Journal of assisted reproduction and genetics

Published: December 20, 2020

Influence of the detection of parent-of-origin on the pregnancy outcomes of fetuses with copy number variation of unknown significance.

Influence of the detection of parent-of-origin on the pregnancy outcomes of fetuses with copy number variation of unknown significance.

Journal: Scientific reports

Published: February 17, 2020

Showing 1-12 of 16

Last Updated: 09/26/2026