Zhengye Zhao - Publications

Erratum to "Deep insights and clinical benefits from the comprehensive cohort of fetal skeletal dysplasia in China"[Journal of Genetics and Genomics 52 (2025) 1524-1536].

Journal: Journal of genetics and genomics = Yi chuan xue bao

Published: February 16, 2026

The Smallest Worthwhile Effect as a Promising Alternative to the MCID in Estimating PROMs for Adult Idiopathic Scoliosis.

Journal: The Journal of bone and joint surgery. American volume

Published: August 05, 2025

Deep insights and clinical benefits from the comprehensive cohort of fetal skeletal dysplasia in China.

Journal: Journal of genetics and genomics = Yi chuan xue bao

Published: May 21, 2025

The association between scoliosis research society-22r and cosmetic parameters in female patients with adolescent idiopathic scoliosis.

Journal: European spine journal : official publication of the European Spine Society, the European Spinal Deformity Society, and the European Section of the Cervical Spine Research Society

Published: April 28, 2025

Factors influencing the quality of life following posterior approach surgical treatment in adolescents with idiopathic scoliosis: A 2-year follow-up study.

Journal: Journal of orthopaedic surgery and research

Published: April 03, 2025

Core planar cell polarity genes VANGL1 and VANGL2 in predisposition to congenital vertebral malformations.

Journal: Proceedings of the National Academy of Sciences of the United States of America

Published: April 26, 2024

Integrating deep phenotyping with genetic analysis: a comprehensive workflow for diagnosis and management of rare bone diseases.

Journal: Orphanet journal of rare diseases

Published: April 02, 2024

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

Journal: Journal of medical genetics

Published: October 02, 2023

Unraveling the genetic architecture of congenital vertebral malformation with reference to the developing spine.

Journal: Nature communications

Published: September 02, 2023

SIGMA leverages protein structural information to predict the pathogenicity of missense variants.

Journal: Cell reports methods

Published: March 16, 2023

Disruptive NADSYN1 Variants Implicated in Congenital Vertebral Malformations.

Journal: Genes

Published: August 24, 2021

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

Journal: American journal of human genetics

Published: May 21, 2021