Sheng Yi

9PUBLICATIONS
10CO-AUTHORS
Developmental genetics (incl. sex determination)Epigenetics (incl. genome methylation and epigenomics)Gene expression (incl. microarray and other genome-wide approaches)NanomedicineNeurogenetics
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Publications (9)

|Jan 24, 2026
Clinical and Molecular Characterization of Five Additional Individuals With SATB2-Associated Syndrome in Guangxi.

Sheng Yi, Qinle Zhang, Fei Chen

|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 13, 2025
The Genetics of 241 Fetuses With Talipes Equinovarus: A 8-Year Monocentric Retrospective Study.

Pingshan Pan, Dongbing Huang, Jiangxuan Wei

|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

5 joint publications

Zailong Qin

4 joint publications

Qi Yang

2 joint publications

Jiasun Su

2 joint publications

Mengting Li