Qi Yang

6PUBLICATIONS
7CO-AUTHORS
Gene mappingDevelopmental genetics (incl. sex determination)Epigenetics (incl. genome methylation and epigenomics)Nanomedicine
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Publications (6)

|Apr 09, 2026
Novel Compound Heterozygous Variants in the COG5 Gene Causing Fetal Hydrops and Skeletal Dysplasia.

Qi Yang, Wei He, Qiang Zhang

|Jan 14, 2026
Clinical and Genetic Analysis of SMARCC2-Related Diseases in Three Chinese Patients.

Shan Ou, Shujie Zhang, Qi Yang

|Nov 29, 2025
Novel Compound Heterozygous Variants in the TCTN2 Gene Causing Meckel-Gruber Syndrome 8 in a Non-Consanguineous Chinese Family.

Qi Yang, Wei He, Qiang Zhang

|Feb 20, 2025
Unmasking a Recessive Allele by a Rare Interstitial Deletion at 10q26.13q26.2: Prenatal Diagnosis of MMP21 -Related Disorder and Further Refine INSYN2A Involvement in the Postnatal Cognitive Phenotype.

Jiasun Su, Shujie Zhang, Wei Li

|Feb 26, 2024
Novel variants in TNRC6B cause global developmental delay with speech and behavioral abnormalities, short stature, low body weight, café-au-lait spots, and metabolic abnormality.

Qi Yang, Shan Ou, Xunzhao Zhou

|Jan 29, 2024
A genetic variant in the MAST1 gene is associated with mega-corpus-callosum syndrome with hypoplastic cerebellar vermis, in a fetus.

Sheng Yi, Xianglian Tang, Fei Chen

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Frequent Collaborators

4 joint publications

Sheng Yi

2 joint publications

Zailong Qin

2 joint publications

Qiang Zhang

2 joint publications

Qinle Zhang