T. Zhang

发表

Tobacco exposure primes the secretion of CCL21 positively associated with tertiary lymphoid structure and response to immunotherapy

Lin Xu, Gaochao Dong, W. Xia, 2023, Journal for ImmunoTherapy of Cancer.

A genotype-first analysis in a cohort of Mullerian anomaly

Zhihong Wu, G. Qiu, Hengqiang Zhao, 2022, Journal of Human Genetics.

Exome-wide Analysis of De Novo and Rare Genetic Variants in Patients With Brain Arteriovenous Malformation

Zhihong Wu, Kun Wang, Hengqiang Zhao, 2022, Neurology.

Heterozygous Recurrent Mutations Inducing Dysfunction of ROR2 Gene in Patients With Short Stature

Zhihong Wu, Hengqiang Zhao, N. Wu, 2021, Frontiers in Cell and Developmental Biology.

Identification of Novel FBN2 Variants in a Cohort of Congenital Contractural Arachnodactyly

Zhihong Wu, G. Qiu, N. Wu, 2022, Frontiers in Genetics.

Whole-genome methylation analysis reveals novel epigenetic perturbations of congenital scoliosis

Zhihong Wu, Hengqiang Zhao, N. Wu, 2021, Molecular therapy. Nucleic acids.

Retrospective Analysis of Associated Anomalies in 636 Patients with Operatively Treated Congenital Scoliosis

Jianxiong Shen, G. Qiu, N. Wu, 2023, The Journal of bone and joint surgery. American volume.

PhenoApt leverages clinical expertise to prioritize candidate genes via machine learning.

Y. Ming, G. Qiu, Hengqiang Zhao, 2022, American journal of human genetics.

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

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

TBX6 as a cause of a combined skeletal‐kidney dysplasia syndrome

H. Hakonarson, P. Giampietro, Erum A. Hartung, 2022, American journal of medical genetics. Part A.

Functional characteristics of a broad spectrum of TBX6 variants in Mayer-Rokitansky-Küster-Hauser syndrome.

J. Lupski, R. Gibbs, S. Jhangiani, 2022, Genetics in medicine : official journal of the American College of Medical Genetics.

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

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

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.

Genetics of the Growing Spine

K. Cheung, Nan Wu, Sen Zhao, 2022, The Growing Spine.

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.

De novo variants in H3-3A and H3-3B are associated with neurodevelopmental delay, dysmorphic features, and structural brain abnormalities

J. Rosenfeld, J. Lupski, Zhihong Wu, 2021, NPJ genomic medicine.

De novo variants in H3-3A and H3-3B are associated with neurodevelopmental delay, dysmorphic features, and structural brain abnormalities

J. Rosenfeld, J. Lupski, Zhihong Wu, 2021, npj Genomic Medicine.

Deciphering the mutational signature of congenital limb malformations

Zhihong Wu, G. Qiu, N. Wu, 2021, Molecular therapy. Nucleic acids.

Phenotype expansion of variants affecting p38 MAPK signaling in hypospadias patients

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

Delineation of dual molecular diagnosis in patients with skeletal deformity

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

The utility of hierarchical genetic testing in paediatric liver disease

Zhihong Wu, Xianghui Qi, N. Wu, 2022, Liver international : official journal of the International Association for the Study of the Liver.

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

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

Variants Affecting the C-Terminal of CSF1R Cause Congenital Vertebral Malformation Through a Gain-of-Function Mechanism

Zhihong Wu, G. Qiu, N. Wu, 2021, Frontiers in Cell and Developmental Biology.

The Mutational Landscape of PTK7 in Congenital Scoliosis and Adolescent Idiopathic Scoliosis

Zhihong Wu, G. Qiu, Hengqiang Zhao, 2021, Genes.

Recent advances in clinical genetics and genomics

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

Novel FGFR1 Variants Are Associated with Congenital Scoliosis

Zhihong Wu, N. Wu, Yang Yang, 2021, Genes.

Molecular Diagnostic Yield of Exome Sequencing and Chromosomal Microarray in Short Stature: A Systematic Review and Meta-Analysis.

Zefu Chen, Z. Wu, T. Zhang, 2023, JAMA pediatrics.

Exploring the association between congenital vertebral malformations and neural tube defects

Z. Wu, Nan Wu, Yongyu Ye, 2023, Journal of medical genetics.

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.

Does the presence of programmable implanted devices in patients with early onset scoliosis alter typical operative and postoperative practices? A survey of spine surgeons

Sara J. Morgan, Brian A. Kelly, Todd F. Ritzman, 2022, Spine Deformity.