Yuzhi Zuo

发表

Molecular therapeutic strategies for FGFR3 gene-related skeletal dysplasia

Zhihong Wu, G. Qiu, N. Wu, 2017, Journal of Molecular Medicine.

Development of a nomogram combining multiparametric magnetic resonance imaging and PSA‐related parameters to enhance the detection of clinically significant cancer across different region

Yi Zhou, Z. Ji, Han-Zhong Li, 2022, The Prostate.

Multifocal Paraganglioma and Pheochromocytoma Due to Truncated SDHD Mutation.

Zhihong Wu, Han-Zhong Li, Yuzhi Zuo, 2018, Urology.

Association between ADAMTS‐4 gene polymorphism and lumbar disc degeneration in Chinese Han population

Hong Zhao, Jun Chen, Guixing Qiu, 2016, Journal of orthopaedic research : official publication of the Orthopaedic Research Society.

Spinal and sacroiliac involvement in SAPHO syndrome: A single center study of a cohort of 354 patients.

Zhihong Wu, Wenrui Xu, Weihong Zhang, 2019, Seminars in arthritis and rheumatism.

Synovitis, acne, pustulosis, hyperostosis and osteitis syndrome: a single centre study of a cohort of 164 patients.

Chen Li, Zhihong Wu, Wenrui Xu, 2016, Rheumatology.

The genetic implication of scoliosis in osteogenesis imperfecta: a review.

Zhihong Wu, N. Wu, Yangzhong Zhou, 2017, Journal of spine surgery.

Phenotype expansion of variants affecting p38 MAPK signaling in hypospadias patients

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

Phenotypic heterogeneity of intellectual disability in patients with congenital insensitivity to pain with anhidrosis: A case report and literature review

Zhihong Wu, P. Giampietro, G. Qiu, 2018, The Journal of international medical research.

Multiple inferior vena cava aneurysms mimic a retroperitoneal tumor: a case report

Z. Ji, Yuzhi Zuo, Zhongming Huang, 2020, BMC Urology.

Recent Advances in Technique and Clinical Outcomes of Minimally Invasive Spine Surgery in Adult Scoliosis

Zhihong Wu, N. Wu, Sen Liu, 2017, Chinese medical journal.

Progress and perspective of TBX6 gene in congenital vertebral malformations

Zhihong Wu, P. Giampietro, G. Qiu, 2016, Oncotarget.

Genetic polymorphisms of GPR126 are functionally associated with PUMC classifications of adolescent idiopathic scoliosis in a Northern Han population

Zhihong Wu, G. Qiu, N. Wu, 2018, Journal of cellular and molecular medicine.

Identification of novel FBN1 variations implicated in congenital scoliosis

Zhihong Wu, Shuyang Zhang, G. Qiu, 2019, Journal of Human Genetics.

TBX6-associated congenital scoliosis (TACS) as a clinically distinguishable subtype of congenital scoliosis: further evidence supporting the compound inheritance and TBX6 gene dosage model

J. Lupski, Zhihong Wu, Yiping Shen, 2019, Genetics in Medicine.

The coexistence of copy number variations (CNVs) and single nucleotide polymorphisms (SNPs) at a locus can result in distorted calculations of the significance in associating SNPs to disease

J. Lupski, You-Qiang Song, Zhihong Wu, 2018, Human Genetics.

The genetic landscape and clinical implications of vertebral anomalies in VACTERL association

Zhihong Wu, P. Giampietro, G. Qiu, 2016, Journal of Medical Genetics.

TBX6-associated congenital scoliosis (TACS) as a clinically distinguishable subtype of congenital scoliosis: further evidence supporting the compound inheritance and TBX6 gene dosage model

J. Lupski, Zhihong Wu, Yiping Shen, 2019, Genetics in Medicine.

Efficacy of bisphosphonates in patients with synovitis, acne, pustulosis, hyperostosis, and osteitis syndrome: a prospective open study.

Zhihong Wu, Wenrui Xu, Weihong Zhang, 2019, Clinical and experimental rheumatology.

Three patterns of osteoarticular involvement in SAPHO syndrome: a cluster analysis based on whole body bone scintigraphy of 157 patients.

Weihong Zhang, N. Wu, Wen Zhang, 2019, Rheumatology.

Genetic and molecular mechanism for distinct clinical phenotypes conveyed by allelic truncating mutations implicated in FBN1

J. Lupski, Zhihong Wu, Shuyang Zhang, 2019, bioRxiv.

Expanding the mutation and phenotype spectrum of MYH3-associated skeletal disorders

J. Lupski, Zhihong Wu, A. Nordgren, 2022, NPJ genomic medicine.

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.

Whole-spine Computed Tomography Findings in SAPHO Syndrome

Wenrui Xu, Weihong Zhang, N. Wu, 2017, The Journal of Rheumatology.

Genetic Polymorphism of LBX1 Is Associated With Adolescent Idiopathic Scoliosis in Northern Chinese Han Population

Zhihong Wu, Hong Zhao, X. Weng, 2017, Spine.

Comparative analysis of serum proteome in congenital scoliosis patients with TBX6 haploinsufficiency – a first report pointing to lipid metabolism

Zhihong Wu, Jian Wang, Jianxiong Shen, 2017, Journal of cellular and molecular medicine.

The coexistence of copy number variations (CNVs) and single nucleotide polymorphisms (SNPs) at a locus can result in distorted calculations of the significance in associating SNPs to disease

J. Lupski, You-Qiang Song, Zhihong Wu, 2018, Human Genetics.

Hsa_circ_0085576 promotes clear cell renal cell carcinoma tumorigenesis and metastasis through the miR-498/YAP1 axis

Z. Ji, Yuzhi Zuo, Guanghua Liu, 2020, Aging.

Change in the cause of inpatient mortality after arthroplasty: a retrospective study

X. Weng, G. Qiu, Jin Lin, 2019, Journal of Orthopaedic Surgery and Research.

Comprehensive prediction of immune microenvironment and hot and cold tumor differentiation in cutaneous melanoma based on necroptosis-related lncRNA

Xing Guo, Yuzhi Zuo, Miao Zhang, 2023, Scientific reports.

Genetic polymorphisms of PAX1 are functionally associated with different PUMC types of adolescent idiopathic scoliosis in a northern Chinese Han population.

Zhihong Wu, Jianxiong Shen, G. Qiu, 2019, Gene.

Whole-Genome Methylation Analysis of Phenotype Discordant Monozygotic Twins Reveals Novel Epigenetic Perturbation Contributing to the Pathogenesis of Adolescent Idiopathic Scoliosis

Zhihong Wu, Jianxiong Shen, G. Qiu, 2019, Front. Bioeng. Biotechnol..