Wenyan Huang

10PUBLICATIONS
13CO-AUTHORS
Infant and child healthMolecular targetsImmunogenetics (incl. genetic immunology)AutoimmunityNeurogenetics
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Publications (10)

|Oct 29, 2026
Early clinical manifestations and long-term renal outcomes by genotype in children with X-linked Alport syndrome.

|Sep 15, 2026
Tubule-Specific RGC-32 Knockout Exhibits Direct and Progressive Aggravating Activity Against Renal Function in an Ischemia-Reperfusion Mouse Model.

|Sep 13, 2026
From Undifferentiated Connective Tissue Disease to Common Variable Immunodeficiency: A Novel NFKB1 Mutation in a Pediatric Case.

|Aug 04, 2026
Remission of Nephrotic Proteinuria after Liver Transplantation in a Case of Abernethy Malformation Type Ib and Membranoproliferative Glomerulonephritis.

|Jul 15, 2026
A Novel FN1 Nucleotide Variant c.3051G>C (p.Trp1017Cys) in a Pediatric Patient with Fibronectin Glomerulopathy: Case Report and Literature Review.

|May 04, 2026
A Novel Col4a5-G814fs Knock-In Mouse Model Reveals Phenotypic Heterogeneity Among Truncating COL4A5 Mutations in X-Linked Alport Syndrome.

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Frequent Collaborators

2 joint publications

Yingqi Lin

2 joint publications

Lei Sun

1 joint publications

Yu-Jie Hu

1 joint publications

Bing-Xue Huang