Bixia Zheng

13PUBLICATIONS
19CO-AUTHORS
Epigenetics (incl. genome methylation and epigenomics)Cancer geneticsGenomicsNeural engineeringCardiology (incl. cardiovascular diseases)
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Publications (13)

|Sep 20, 2026
Monoallelic SH2B1 Variants in Neurodevelopmental Disorders: Phenotypic Expansion and Functional Characterization of Rare Variants.

|Jul 28, 2026
Rare Biallelic CTU2 Variants in an Individual With CAKUT: Clinical Characterization and Minigene Splicing Analysis.

|Nov 27, 2025
Inactivating GNAS complex locus variants impair G protein-coupled receptor signaling and cause multiple suture craniosynostosis in humans and zebrafish.

Qing Yan, Wei Zhou, Han Li

|Oct 24, 2025
De novo missense variants in BAIAP2 are associated with developmental and epileptic encephalopathies.

Gang Zhang, Yaping Lu, Lingling Xie

|Oct 08, 2025
Age at disease onset and risk of chronic kidney disease in patients with heterozygous disease-causing variants in COL4A3 and COL4A4.

Ningning Hu, Lei Sun, Xuantong Dai

|May 12, 2025
Genetic Insights Into Craniosynostosis: Identification of Novel IL11RA Variants in Chinese Pediatric Patients.

Ziwei Liu, Ding Zhou, Chunli Wang

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Frequent Collaborators

3 joint publications

Wei Zhou

2 joint publications

Aihua Zhang

1 joint publications

Qian Shen

1 joint publications

Sophia Schneider