Xia Zhu

Yangtze River Fisheries Research Institute
Wuhan, 430223, China

Last Updated: 09/26/2026

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Found 8 publications

Cloning and functional characterization of Pcficolin1 and Pcficolin2 in red swamp crayfish (Procambarus clarkii).

Cloning and functional characterization of Pcficolin1 and Pcficolin2 in red swamp crayfish (Procambarus clarkii).

Journal: Fish & shellfish immunology
Published: December 12, 2025

Incidence, distribution, disease spectrum, and genetic deficits of congenital heart defects in China: implementation of prenatal ultrasound screening identified 18,171 affected fetuses from 2,452,249 pregnancies.

Incidence, distribution, disease spectrum, and genetic deficits of congenital heart defects in China: implementation of prenatal ultrasound screening identified 18,171 affected fetuses from 2,452,249 pregnancies.

Journal: Cell & bioscience
Published: June 06, 2023

The impacts of economy policy uncertainty on peer effects of firms R&D investment: Based on LDA machine learning and regression statistical modeling approach.

The impacts of economy policy uncertainty on peer effects of firms R&D investment: Based on LDA machine learning and regression statistical modeling approach.

Journal: PloS one
Published: May 11, 2023

The VANGL1 P384R variant cause both neural tube defect and Klippel-Feil syndrome.

The VANGL1 P384R variant cause both neural tube defect and Klippel-Feil syndrome.

Journal: Molecular genetics & genomic medicine
Published: March 10, 2021

Genomic architecture of fetal central nervous system anomalies using whole-genome sequencing.

Genomic architecture of fetal central nervous system anomalies using whole-genome sequencing.

Journal: NPJ genomic medicine
Published: October 26, 2020

Identification of a novel de novo mutation of ENG gene in a fetus with pulmonary arteriovenous malformation.

Identification of a novel de novo mutation of ENG gene in a fetus with pulmonary arteriovenous malformation.

Journal: Clinical genetics
Published: July 14, 2020

Novel compound heterozygous variants in the STIL gene identified in a Chinese family with presentation of foetal microcephaly.

Novel compound heterozygous variants in the STIL gene identified in a Chinese family with presentation of foetal microcephaly.

Journal: European journal of medical genetics
Published: April 23, 2020

First-Trimester Cranial Ultrasound Markers of Open Spina Bifida.

First-Trimester Cranial Ultrasound Markers of Open Spina Bifida.

Journal: Journal of ultrasound in medicine : official journal of the American Institute of Ultrasound in Medicine
Published: March 02, 2020
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Last Updated: 09/26/2026