Genome-wide association study identifies novel susceptible loci and highlights Wnt/beta-catenin pathway in the development of adolescent idiopathic scoliosis-Reference-Cited by-同舟云学术

Genome-wide association study identifies novel susceptible loci and highlights Wnt/beta-catenin pathway in the development of adolescent idiopathic scoliosis

Published:2017-02-28 Issue:8 Volume:26 Page:1577-1583
ISSN:0964-6906
Container-title:Human Molecular Genetics
language:en
Short-container-title:

Author:

Zhu Zezhang¹²,Xu Leilei¹²,Leung-Sang Tang Nelson²³⁴,Qin Xiaodong¹²,Feng Zhenhua¹²,Sun Weixiang¹²,Zhu Weiguo¹²,Shi Benlong¹,Liu Peng⁵,Mao Saihu¹²,Qiao Jun¹,Liu Zhen¹,Sun Xu¹,Li Fangcai⁶,Chun-Yiu Cheng Jack²⁷,Qiu Yong¹²

Affiliation:

1. Department of Spine Surgery, The Drum Tower Hospital of Nanjing University Medical School, Nanjing 210008, P.R. China

2. Joint Scoliosis Research Center of The Chinese University of Hong Kong and Nanjing University, Nanjing 210008 & Hong Kong 999077, P.R. China

3. Department of Chemical Pathology and School of Biomedical Sciences, Faculty of Medicine, The Chinese University of Hong Kong, Hong Kong 999077, P.R. China

4. Li Ka Shing Institute of Health Sciences, Faculty of Medicine, The Chinese University of Hong Kong, Hong Kong 999077, P.R. China

5. Department of Orthopaedics, China-Japan Union Hospital of Jilin University, Changchun 130116, P.R. China

6. Department of Orthopaedics, The Second Affiliated Hospital of Zhejiang University School of Medicine, Hangzhou 310002, P.R. China

7. Department of Orthopaedics and Traumatology, Faculty of Medicine, The Chinese University of Hong Kong, Hong Kong 999077, P.R. China

Funder

Science and Technology Project of Jiangsu Province’s Clinical Medicine

Jiangsu Province’s Key Medical Center

Natural Science Foundation of China

Natural Science Foundation of Jiangsu Province

Nanjing Medical Science and technology development Foundation

Publisher

Oxford University Press (OUP)

Subject

Genetics(clinical),Genetics,Molecular Biology,General Medicine

Link

http://academic.oup.com/hmg/article-pdf/26/8/1577/13629085/ddx045.pdf

Reference41 articles.

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2. Rare variants in FBN1 and FBN2 are associated with severe adolescent idiopathic scoliosis;Buchan;Hum. Mol. Genet,2014

3. CHD7 gene polymorphisms are associated with susceptibility to idiopathic scoliosis;Gao;Am. J. Hum. Genet,2007

4. Association between genetic determinants of peak height velocity during puberty and predisposition to adolescent idiopathic scoliosis;Mao;Spine (Phila Pa 1976),2013

5. Investigation of the 53 Markers in a DNA-Based Prognostic Test Revealing New Predisposition Genes for Adolescent Idiopathic Scoliosis;Xu;Spine (Phila Pa 1976,2015

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