Wanyu Fu

14PUBLICATIONS
2CO-AUTHORS
NeonatologyNeurology and neuromuscular diseasesGene expression (incl. microarray and other genome-wide approaches)Developmental genetics (incl. sex determination)Gene mapping
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Publications (14)

|Jul 23, 2026
Prenatal Etiology Diagnosis of Rare Compound Heterozygous PROC Gene Variants in a Fetus With Ocular Ultrasonic Anomaly Using Whole Exome Sequencing.

|Jul 10, 2026
Prenatal Diagnosis and Functional Analysis of Two Compound Heterozygous Variants in the KLHL40 Gene Causing Nemaline Myopathy 8.

|May 11, 2026
Identification of Two Novel Variants in CRYGD and OCRL Genes in the Chinese Population With Hereditary Congenital Cataracts Using Whole Exome Sequencing.

|Apr 14, 2025
Long-Read Sequencing Identified a Large Novel δ/β-Globin Gene Deletion in a Chinese Family.

Jianlong Zhuang, Yu Zheng, Yuying Jiang

|Aug 27, 2024
Whole Exome Sequencing Revealing a Novel PBX1 Gene Variant in a Chinese Family Causing Recurrent Neonatal Death.

Nan Huang, Hegan Zhang, Zhengping Huang

|May 20, 2024
Prenatal diagnosis of fetuses with absent/hypoplastic nasal bone in second-trimester using chromosomal microarray analysis.

Xinying Chen, Yuying Jiang, Shuhong Zeng

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Frequent Collaborators

2 joint publications

Wanyu Fu

1 joint publications

Chunnuan Chen