Sheng Yi

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

|Aug 30, 2026
Clinical and genetic profiles of postnatal patients with skeletal dysplasia in Guangxi during 8 years: a single-center experience.

|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

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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