Hao Wei

发表

De Novo SMARCC2 Variant in a Chinese Woman with Coffin-Siris Syndrome 8: a Case Report with Mild Intellectual Disability and Endocrinopathy

Junjie Chen, Z. Qin, Qinle Zhang, 2022, Journal of Molecular Neuroscience.

Clinical application of whole-exome sequencing: A retrospective, single-center study

Z. Qin, Jiasun Su, Qiang Zhang, 2021, Experimental and therapeutic medicine.

Two novel compound heterozygous variants of LTBP4 in a Chinese infant with cutis laxa type IC and a review of the related literature

Z. Qin, Jiasun Su, Qiang Zhang, 2020, BMC Medical Genomics.

Novel Synonymous and Frameshift Variants in the TRIP12 Gene Identified in 2 Chinese Patients With Intellectual Disability

Z. Qin, Qinle Zhang, Fei Chen, 2022, Neurology: Genetics.

Screening of Graves' disease susceptibility genes by whole exome sequencing in a three-generation family

Miaosheng Li, Wangen Li, Hao Wei, 2020, BMC medical genomics.

Case Report: Variations in the ALPL Gene in Chinese Patients With Hypophosphatasia

Z. Qin, Qiang Zhang, Shang Yi, 2021, Frontiers in Genetics.

Two novel compound heterozygous variants of LTBP4 in a Chinese infant with cutis laxa type IC and a review of the related literature

Z. Qin, Qiang Zhang, Shang Yi, 2020, BMC medical genomics.

Single-cell RNA sequencing of neural stem cells derived from human trisomic iPSCs reveals the abnormalities during neural differentiation of Down syndrome

F. Zeng, Jiajun Qiu, Yanna Liu, 2023, Frontiers in Molecular Neuroscience.