A multi-ethnic meta-analysis confirms the association of rs6570507 with adolescent idiopathic scoliosis

References

Page 1

	Year	Citations
Second-generation PLINK: rising to the challenge of larger and richer datasets Christopher Chang, Carson C. Chow, Laurent CAM Tellier, GigaScience	2015	13.1K
The Genotype-Tissue Expression (GTEx) pilot analysis: Multitissue gene regulation in humans Kristin G. Ardlie, David S. DeLuca, Ayellet V. Segrè, Science	2015	5.5K
Rare-Variant Association Testing for Sequencing Data with the Sequence Kernel Association Test Michael C. Wu, Seunggeun Lee, Tianxi Cai, The American Journal of Human Genetics BioinformaticsGenome-wide Association StudyMedicineGeneticsRare-variant Association Testing	2011	2.5K
Chromatin architecture reorganization during stem cell differentiation Jesse R. Dixon, Inkyung Jung, Siddarth Selvaraj, Nature	2015	1.7K
Data quality control in genetic case-control association studies Carl A. Anderson, Fredrik Pettersson, Geraldine M Clarke, Nature Protocols Genome-wide Association StudyData Quality ControlEngineeringGenotype-phenotype AssociationGenetics	2010	1.4K
Deep resequencing of GWAS loci identifies independent rare variants associated with inflammatory bowel disease Manuel A. Rivas, Mélissa Beaudoin, Agnès Gardet, Nature Genetics Genome-wide Association StudyMedicineGeneticsImmunologyGenetic Epidemiology	2011	776
A strategy to discover genes that carry multi-allelic or mono-allelic risk for common diseases: A cohort allelic sums test (CAST) Stephan Morgenthaler, William G. Thilly Mutation research. Fundamental and molecular mechanisms of mutagenesis Genome-wide Association StudyDisease SusceptibilityAllelic VariantMedicineGenetics	2006	520
Rare MTNR1B variants impairing melatonin receptor 1B function contribute to type 2 diabetes Amélie Bonnefond, Nathalie Clément, Katherine A. Fawcett, Nature Genetics Metabolic SyndromeSleepRare Mtnr1b VariantsMedicineDiabetes	2012	361
A rare penetrant mutation in CFH confers high risk of age-related macular degeneration Soumya Raychaudhuri, Oleg Iartchouk, Kimberly Chin, Nature Genetics Ocular DiseaseMendelian DisorderOphthalmologyGenetic DisorderGenetics	2011	324
A genome-wide association study identifies common variants near LBX1 associated with adolescent idiopathic scoliosis Yohei Takahashi, Ikuyo Kou, Atsushi Takahashi, Nature Genetics Genetic DisorderMedicineGeneticsGenetic EpidemiologyPathology	2011	266

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