(Q36564234)

14 August 2017

Association of rs11190870 near LBX1 with adolescent idiopathic scoliosis susceptibility in a Han Chinese population (English)

1 reference

adolescent idiopathic scoliosis

14 August 2017

1 reference

1 reference

1 reference

5

Zezhang Zhu

1 reference

14 August 2017

7

Yong Qiu

1 reference

14 August 2017

2

Xusheng Qiu

1 reference

14 August 2017

6

Bangping Qian

1 reference

14 August 2017

Hua Jiang

1

1 reference

14 August 2017

Jin Dai

series ordinal

3

1 reference

14 August 2017

Huang Yan

series ordinal

4

1 reference

14 August 2017

21 October 2012

1 reference

14 August 2017

European Spine Journal

1 reference

14 August 2017

22

1 reference

14 August 2017

2

1 reference

14 August 2017

282-286

1 reference

Genome-wide association studies of adolescent idiopathic scoliosis suggest candidate susceptibility genes.

14 August 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3555620

Idiopathic scoliosis: cracking the genetic code and what does it mean?

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3555620

Top theories for the etiopathogenesis of adolescent idiopathic scoliosis.

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3555620

Genome-wide association studies: progress in identifying genetic biomarkers in common, complex diseases.

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3555620

Postural imbalance in non-treated adolescent idiopathic scoliosis at different periods of progression

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3555620

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

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3555620

Genome-wide association studies for complex traits: consensus, uncertainty and challenges

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3555620

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

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3555620

CHD7 gene polymorphisms are associated with susceptibility to idiopathic scoliosis.

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3555620

The search for idiopathic scoliosis genes

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3555620

Lbx1 and Tlx3 are opposing switches in determining GABAergic versus glutamatergic transmitter phenotypes

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3555620

Genome-wide association studies for common diseases and complex traits

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3555620

The Iliac apophysis; an invaluable sign in the management of scoliosis

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3555620

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

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3555620

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

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3555620

Etiology of idiopathic scoliosis: current trends in research

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3555620

The aetiology of idiopathic scoliosis: biomechanical and neuromuscular factors

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3555620

Genetic relationship of populations in China

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3555620

Mouse Lbx1 and human LBX1 define a novel mammalian homeobox gene family related to the Drosophila lady bird genes

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3555620

Idiopathic scoliosis and the central nervous system: a motor control problem. The Harrington lecture, 1983. Scoliosis Research Society.

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3555620

Replication of past candidate loci for common diseases and phenotypes in 100 genome-wide association studies

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3555620

Scoliosis: incidence and natural history. A prospective epidemiological study

28 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3555620

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

28 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3555620

Molecular characterization and expression patterns of Lbx1 in porcine skeletal muscle

21 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3555620

Balance control in adolescents with idiopathic scoliosis and disturbed somatosensory function

21 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3555620

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

21 September 2018

1 reference

Crossref

https://api.crossref.org/works/10.1007%2FS00586-012-2532-4

Impaired Dynamic Balance Control in Adolescents With Idiopathic Scoliosis and Abnormal Somatosensory Evoked Potentials

21 January 2018

1 reference

Crossref

https://api.crossref.org/works/10.1007%2FS00586-012-2532-4

Adolescent idiopathic scoliosis

21 January 2018

1 reference

12 December 2020

Is the central nervous system a causative factor in idiopathic scoliosis?

1 reference

12 December 2020

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

1 reference

12 December 2020

Scoliosis prevalence: a call for a statement of terms

1 reference

12 December 2020

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

1 reference

12 December 2020

Sensory deprivation and balance control in idiopathic scoliosis adolescent

1 reference

12 December 2020

Evolution and migration history of the Chinese population inferred from Chinese Y-chromosome evidence

1 reference

12 December 2020

10.1007/S00586-012-2532-4

Identifiers

DOI

1 reference

14 August 2017

1 reference

14 August 2017

PubMed publication ID

23096252

1 reference