Rare variant of HSPG2 is not involved in the development of adolescent idiopathic scoliosis: evidence from a large-scale replication study-Reference-Cited by-同舟云学术

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Rare variant of HSPG2 is not involved in the development of adolescent idiopathic scoliosis: evidence from a large-scale replication study

Published:2019-01-15 Issue:1 Volume:20 Page:
ISSN:1471-2474
Container-title:BMC Musculoskeletal Disorders
language:en
Short-container-title:BMC Musculoskelet Disord

Author:

Xia Chao,Xu Leilei,Xue Bingchuan,Sheng Fei,Qiu Yong,Zhu Zezhang

Funder

National Natural Science Foundation of China

Natural Science Foundation of Jiangsu Province

Nanjing Medical Science and technology development Foundation

Publisher

Springer Science and Business Media LLC

Subject

Orthopedics and Sports Medicine,Rheumatology

Link

http://link.springer.com/content/pdf/10.1186/s12891-019-2402-x.pdf

Reference39 articles.

1. Murray DW, Bulstrode CJ. The development of adolescent idiopathic scoliosis. Eur Spine J. 1996;5(4):251–7.

2. Kouwenhoven JW, Castelein RM. The pathogenesis of adolescent idiopathic scoliosis: review of the literature. Spine. 2008;33(26):2898–908.

3. Xu L, Qiu X, Sun X, Mao S, Liu Z, Qiao J, Qiu Y. Potential genetic markers predicting the outcome of brace treatment in patients with adolescent idiopathic scoliosis. Eur Spine J. 2011;20(10):1757–64.

4. Wei-Jun W, Xu S, Zhi-Wei W, Xu-Sheng Q, Zhen L, Yong Q. Abnormal anthropometric measurements and growth pattern in male adolescent idiopathic scoliosis. Eur Spine J. 2012;21(1):77–83.

5. Wang S, Qiu Y, Ma Z, Xia C, Zhu F, Zhu Z. Expression of Runx2 and type X collagen in vertebral growth plate of patients with adolescent idiopathic scoliosis. Connect Tissue Res. 2010;51(3):188–96.

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1. Knowledge mapping of idiopathic scoliosis genes and research hotspots (2002–2022): a bibliometric analysis;Frontiers in Pediatrics;2023-12-04

2. The Whole-Exome Sequencing of a Cohort of 19 Families with Adolescent Idiopathic Scoliosis (AIS): Candidate Pathways;Genes;2023-11-17

3. Understanding Musculoskeletal Disorders Through Next-Generation Sequencing;JBJS Reviews;2022-04

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