Huakang Du

发表

A Recurrent Rare SOX9 Variant (M469V) is Associated with Congenital Vertebral Malformations.

Zhihong Wu, G. Qiu, N. Wu, 2019, Current gene therapy.

Phenotype expansion of variants affecting p38 MAPK signaling in hypospadias patients

Zhihong Wu, G. Qiu, Hengqiang Zhao, 2022, Orphanet Journal of Rare Diseases.

Global competence of medical students: An assessment scale and preliminary investigation in China

Yihan Cao, Huakang Du, Yunying Feng, 2019, PloS one.

Dissection of mendelian predisposition and complex genetic architecture of craniovertebral junction malformation

Zhihong Wu, Hengqiang Zhao, N. Wu, 2022, Human Genetics.

Delineation of dual molecular diagnosis in patients with skeletal deformity

Zhihong Wu, G. Qiu, N. Wu, 2022, Orphanet Journal of Rare Diseases.

Aberrant interaction between mutated ADAMTSL2 and LTBP4 is associated with adolescent idiopathic scoliosis.

G. Qiu, Hengqiang Zhao, Yuchen Niu, 2021, Gene.

Epidemiology and Phenotypic Characteristics of Dual Molecular Diagnosis Cases in Skeletal Abnormality

Zhihong Wu, G. Qiu, N. Wu, 2021 .

Cost-effectiveness analysis of using the TBX6-associated congenital scoliosis risk score (TACScore) in genetic diagnosis of congenital scoliosis

Zhihong Wu, G. Qiu, Hengqiang Zhao, 2020, Orphanet Journal of Rare Diseases.

Factors and predictive model associated with perioperative complications after long fusion in the treatment of adult non-degenerative scoliosis

Hong Zhao, Jianxiong Shen, G. Qiu, 2020, BMC Musculoskeletal Disorders.

The Progress of CRISPR/Cas9-Mediated Gene Editing in Generating Mouse/Zebrafish Models of Human Skeletal Diseases

Zhihong Wu, G. Qiu, N. Wu, 2019, Computational and structural biotechnology journal.

Rare variant association analyses reveal the significant contribution of carbohydrate metabolic disturbance in severe adolescent idiopathic scoliosis

Zhifa Zheng, Xi Cheng, Huakang Du, 2024, Journal of Medical Genetics.