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- Publisher Website: 10.1038/jhg.2012.11
- Scopus: eid_2-s2.0-84860300759
- PMID: 22301463
- WOS: WOS:000303416800005
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Article: SNP rs11190870 near LBX1 is associated with adolescent idiopathic scoliosis in southern Chinese
Title | SNP rs11190870 near LBX1 is associated with adolescent idiopathic scoliosis in southern Chinese | ||||||||||||
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Authors | |||||||||||||
Keywords | Adolescent idiopathic scoliosis Replication study rs11190870 Southern Chinese | ||||||||||||
Issue Date | 2012 | ||||||||||||
Publisher | Springer Japan. The Journal's web site is located at http://link.springer.de/link/service/journals/10038/index.htm | ||||||||||||
Citation | Journal Of Human Genetics, 2012, v. 57 n. 4, p. 244-246 How to Cite? | ||||||||||||
Abstract | A study was conducted to validate the most significant single nucleotide polymorphism (SNP) from a genome-wide association study of Japanese adolescent idiopathic scoliosis (AIS) patients in an independent southern Chinese population. In total, 300 AIS patients fulfilled the clinical criteria and 788 controls with MRI scans of the spine were included in the replication study. We employed case-control analysis to study the association of SNP rs11190870 near LBX1 (ladybird homeobox 1) with AIS in a southern Chinese population. The results suggest that SNP rs11190870 is significantly associated with AIS (P=9.1 × 10 -10; odds ratio1.85; 95% confidence interval=1.52-2.25). The results of this study confirm that SNP rs11190870 is associated with AIS. © 2012 The Japan Society of Human Genetics All rights reserved. | ||||||||||||
Persistent Identifier | http://hdl.handle.net/10722/147662 | ||||||||||||
ISSN | 2023 Impact Factor: 2.6 2023 SCImago Journal Rankings: 1.148 | ||||||||||||
ISI Accession Number ID |
Funding Information: This study was supported by grants from the Seed Funding Programme for Basic Research, the University of Hong Kong (HKU), the HKU Strategic Research Themes on Genomics and on Development & Reproduction, AOSPINE and the Tam Sai Kit Endowment Fund. We thank Josephine Lam for technical help. | ||||||||||||
References | |||||||||||||
Grants |
DC Field | Value | Language |
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dc.contributor.author | Fan, YH | en_HK |
dc.contributor.author | Song, YQ | en_HK |
dc.contributor.author | Chan, D | en_HK |
dc.contributor.author | Takahashi, Y | en_HK |
dc.contributor.author | Ikegawa, S | en_HK |
dc.contributor.author | Matsumoto, M | en_HK |
dc.contributor.author | Kou, I | en_HK |
dc.contributor.author | Cheah, KSE | en_HK |
dc.contributor.author | Sham, P | en_HK |
dc.contributor.author | Cheung, KMC | en_HK |
dc.contributor.author | Luk, KDK | en_HK |
dc.date.accessioned | 2012-05-29T06:05:20Z | - |
dc.date.available | 2012-05-29T06:05:20Z | - |
dc.date.issued | 2012 | en_HK |
dc.identifier.citation | Journal Of Human Genetics, 2012, v. 57 n. 4, p. 244-246 | en_HK |
dc.identifier.issn | 1434-5161 | en_HK |
dc.identifier.uri | http://hdl.handle.net/10722/147662 | - |
dc.description.abstract | A study was conducted to validate the most significant single nucleotide polymorphism (SNP) from a genome-wide association study of Japanese adolescent idiopathic scoliosis (AIS) patients in an independent southern Chinese population. In total, 300 AIS patients fulfilled the clinical criteria and 788 controls with MRI scans of the spine were included in the replication study. We employed case-control analysis to study the association of SNP rs11190870 near LBX1 (ladybird homeobox 1) with AIS in a southern Chinese population. The results suggest that SNP rs11190870 is significantly associated with AIS (P=9.1 × 10 -10; odds ratio1.85; 95% confidence interval=1.52-2.25). The results of this study confirm that SNP rs11190870 is associated with AIS. © 2012 The Japan Society of Human Genetics All rights reserved. | en_HK |
dc.language | eng | en_US |
dc.publisher | Springer Japan. The Journal's web site is located at http://link.springer.de/link/service/journals/10038/index.htm | en_HK |
dc.relation.ispartof | Journal of Human Genetics | en_HK |
dc.subject | Adolescent idiopathic scoliosis | en_HK |
dc.subject | Replication study | en_HK |
dc.subject | rs11190870 | en_HK |
dc.subject | Southern Chinese | en_HK |
dc.subject.mesh | Adolescent | en_HK |
dc.subject.mesh | Asian Continental Ancestry Group - genetics | en_HK |
dc.subject.mesh | Case-Control Studies | en_HK |
dc.subject.mesh | Child | en_HK |
dc.subject.mesh | Female | en_HK |
dc.subject.mesh | Gene Frequency | en_HK |
dc.subject.mesh | Genetic Predisposition to Disease | en_HK |
dc.subject.mesh | Genetics, Population | en_HK |
dc.subject.mesh | Genome-Wide Association Study | en_HK |
dc.subject.mesh | Homeodomain Proteins - genetics | en_HK |
dc.subject.mesh | Humans | en_HK |
dc.subject.mesh | Magnetic Resonance Imaging | en_HK |
dc.subject.mesh | Male | en_HK |
dc.subject.mesh | Odds Ratio | en_HK |
dc.subject.mesh | Polymorphism, Single Nucleotide | en_HK |
dc.subject.mesh | Scoliosis - genetics | en_HK |
dc.subject.mesh | Sex Factors | en_HK |
dc.subject.mesh | Transcription Factors - genetics | en_HK |
dc.subject.mesh | Young Adult | en_HK |
dc.title | SNP rs11190870 near LBX1 is associated with adolescent idiopathic scoliosis in southern Chinese | en_HK |
dc.type | Article | en_HK |
dc.identifier.email | Chan, D: chand@hku.hk | en_HK |
dc.identifier.email | Cheah, KSE: hrmbdkc@hku.hk | en_HK |
dc.identifier.email | Sham, P: pcsham@hku.hk | en_HK |
dc.identifier.email | Cheung, KMC: cheungmc@hku.hk | en_HK |
dc.identifier.email | Luk, KDK: hcm21000@hku.hk | en_HK |
dc.identifier.authority | Chan, D=rp00540 | en_HK |
dc.identifier.authority | Cheah, KSE=rp00342 | en_HK |
dc.identifier.authority | Sham, P=rp00459 | en_HK |
dc.identifier.authority | Cheung, KMC=rp00387 | en_HK |
dc.identifier.authority | Luk, KDK=rp00333 | en_HK |
dc.description.nature | link_to_subscribed_fulltext | en_US |
dc.identifier.doi | 10.1038/jhg.2012.11 | en_HK |
dc.identifier.pmid | 22301463 | - |
dc.identifier.scopus | eid_2-s2.0-84860300759 | en_HK |
dc.identifier.hkuros | 200628 | - |
dc.relation.references | http://www.scopus.com/mlt/select.url?eid=2-s2.0-84860300759&selection=ref&src=s&origin=recordpage | en_HK |
dc.identifier.volume | 57 | en_HK |
dc.identifier.issue | 4 | en_HK |
dc.identifier.spage | 244 | en_HK |
dc.identifier.epage | 246 | en_HK |
dc.identifier.isi | WOS:000303416800005 | - |
dc.publisher.place | Japan | en_HK |
dc.relation.project | Developmental genomics and skeletal research | - |
dc.identifier.scopusauthorid | Fan, YH=37461378000 | en_HK |
dc.identifier.scopusauthorid | Song, YQ=47761560700 | en_HK |
dc.identifier.scopusauthorid | Chan, D=7402216545 | en_HK |
dc.identifier.scopusauthorid | Takahashi, Y=37108651300 | en_HK |
dc.identifier.scopusauthorid | Ikegawa, S=7102780383 | en_HK |
dc.identifier.scopusauthorid | Matsumoto, M=35429991100 | en_HK |
dc.identifier.scopusauthorid | Kou, I=22985136000 | en_HK |
dc.identifier.scopusauthorid | Cheah, KSE=35387746200 | en_HK |
dc.identifier.scopusauthorid | Sham, P=34573429300 | en_HK |
dc.identifier.scopusauthorid | Cheung, KMC=7402406754 | en_HK |
dc.identifier.scopusauthorid | Luk, KDK=7201921573 | en_HK |
dc.identifier.issnl | 1434-5161 | - |