SNP rs11190870 near LBX1 is associated with adolescent idiopathic scoliosis in southern Chinese (Q83388357)

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22 January 2020

title

SNP rs11190870 near LBX1 is associated with adolescent idiopathic scoliosis in southern Chinese (English)

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adolescent idiopathic scoliosis

22 January 2020

main subject

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1

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22 January 2020

Kenneth M Cheung

10

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22 January 2020

author name string

You-Qiang Song

2

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22 January 2020

Danny Chan

3

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22 January 2020

Yohei Takahashi

4

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22 January 2020

Shiro Ikegawa

5

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22 January 2020

Morio Matsumoto

6

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22 January 2020

Ikuyo Kou

7

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22 January 2020

Kathryn S E Cheah

8

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22 January 2020

Pak Sham

9

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22 January 2020

Keith D K Luk

11

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22 January 2020

publication date

2 February 2012

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Journal of Human Genetics

22 January 2020

published in

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volume

57

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issue

4

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page(s)

244-246

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Adolescent idiopathic scoliosis

22 January 2020

cites work

1 reference

https://api.crossref.org/works/10.1038%2FJHG.2012.11

7 January 2021

Adolescent idiopathic scoliosis

1 reference

https://api.crossref.org/works/10.1038%2FJHG.2012.11

7 January 2021

Sexual dimorphism in adolescent idiopathic scoliosis

1 reference

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7 January 2021

Recent advances in the aetiology of adolescent idiopathic scoliosis

1 reference

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7 January 2021

Etiology of idiopathic scoliosis: current trends in research

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7 January 2021

Genetic Association Study of Growth Hormone Receptor and Idiopathic Scoliosis

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https://api.crossref.org/works/10.1038%2FJHG.2012.11

7 January 2021

Understanding genetic factors in idiopathic scoliosis, a complex disease of childhood

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https://api.crossref.org/works/10.1038%2FJHG.2012.11

7 January 2021

Localization of susceptibility to familial idiopathic scoliosis

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https://api.crossref.org/works/10.1038%2FJHG.2012.11

7 January 2021

CHD7 gene polymorphisms are associated with susceptibility to idiopathic scoliosis.

1 reference

https://api.crossref.org/works/10.1038%2FJHG.2012.11

7 January 2021

A genetic locus for adolescent idiopathic scoliosis linked to chromosome 19p13.3.

1 reference

https://api.crossref.org/works/10.1038%2FJHG.2012.11

7 January 2021

Idiopathic scoliosis: identification of candidate regions on chromosome 19p13

1 reference

https://api.crossref.org/works/10.1038%2FJHG.2012.11

7 January 2021

Assignment of two loci for autosomal dominant adolescent idiopathic scoliosis to chromosomes 9q31.2-q34.2 and 17q25.3-qtel

1 reference

https://api.crossref.org/works/10.1038%2FJHG.2012.11

7 January 2021

Assignment of a locus for autosomal dominant idiopathic scoliosis (IS) to human chromosome 17p11

1 reference

https://api.crossref.org/works/10.1038%2FJHG.2012.11

7 January 2021

A novel locus for adolescent idiopathic scoliosis on chromosome 12p

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https://api.crossref.org/works/10.1038%2FJHG.2012.11

7 January 2021

Genetic analysis of structural elastic fiber and collagen genes in familial adolescent idiopathic scoliosis

1 reference

https://api.crossref.org/works/10.1038%2FJHG.2012.11

7 January 2021

Evidence of a linkage between matrilin-1 gene (MATN1) and idiopathic scoliosis

1 reference

https://api.crossref.org/works/10.1038%2FJHG.2012.11

7 January 2021

Association of estrogen receptor gene polymorphisms with susceptibility to adolescent idiopathic scoliosis.

1 reference

https://api.crossref.org/works/10.1038%2FJHG.2012.11

7 January 2021

Melatonin receptor 1B (MTNR1B) gene polymorphism is associated with the occurrence of adolescent idiopathic scoliosis.

1 reference

https://api.crossref.org/works/10.1038%2FJHG.2012.11

7 January 2021

Polymorphism in vitamin D receptor is associated with bone mineral density in patients with adolescent idiopathic scoliosis

1 reference

https://api.crossref.org/works/10.1038%2FJHG.2012.11

7 January 2021

Genomic polymorphisms of G-protein estrogen receptor 1 are associated with severity of adolescent idiopathic scoliosis

1 reference

https://api.crossref.org/works/10.1038%2FJHG.2012.11

7 January 2021

Promoter polymorphism of matrilin-1 gene predisposes to adolescent idiopathic scoliosis in a Chinese population

1 reference

https://api.crossref.org/works/10.1038%2FJHG.2012.11

7 January 2021

A genome-wide association study identifies common variants near LBX1 associated with adolescent idiopathic scoliosis.

1 reference

https://api.crossref.org/works/10.1038%2FJHG.2012.11

7 January 2021

A high-throughput SNP typing system for genome-wide association studies

1 reference

https://api.crossref.org/works/10.1038%2FJHG.2012.11

7 January 2021

METAL: fast and efficient meta-analysis of genomewide association scans

1 reference

https://api.crossref.org/works/10.1038%2FJHG.2012.11

7 January 2021

A Relook Into the Association of the Estrogen Receptor α Gene (PvuII, XbaI) and Adolescent Idiopathic Scoliosis

1 reference

https://api.crossref.org/works/10.1038%2FJHG.2012.11

7 January 2021

Replication study of the association between adolescent idiopathic scoliosis and two estrogen receptor genes

1 reference

https://api.crossref.org/works/10.1038%2FJHG.2012.11

7 January 2021

Lack of association between adolescent idiopathic scoliosis and previously reported single nucleotide polymorphisms in MATN1, MTNR1B, TPH1, and IGF1 in a Japanese population

1 reference

https://api.crossref.org/works/10.1038%2FJHG.2012.11

7 January 2021

Identifiers

DOI

10.1038/JHG.2012.11

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:22301463%20AND%20SRC:MED&resulttype=core&format=json

22 January 2020

1 reference