L. Shi

TP63 Gene Mutations in Chinese P63 Syndrome Patients

W. Yin, X. Ye, L. Shi, 2010, Journal of dental research.

Novel mutation of SIK1 gene causing a mild form of pediatric epilepsy in a Chinese patient.

L. Shi, B. Zhu, Wenping Ma, 2022, Metabolic brain disease.

Novel mutation of SIK1 gene causing a mild form of pediatric epilepsy in a Chinese patient

L. Shi, B. Zhu, Tianjie Lv, 2021, Metabolic Brain Disease.

A novel locus for autosomal dominant hereditary gingival fibromatosis, GINGF3, maps to chromosome 2p22.3‐p23.3

L. Shi, Z. Bian, B. Peng, 2005, Clinical genetics.

Comprehensive population screening in the Ashkenazi Jewish population for recurrent disease‐causing variants

L. Edelmann, L. Shi, B. Webb, 2017, Clinical genetics.

Carrier screening of RTEL1 mutations in the Ashkenazi Jewish population

S. Savage, L. Edelmann, L. Shi, 2015, Clinical genetics.