| scholarly article | Q13442814 |
| P356 | DOI | 10.1002/JOR.22090 |
| P698 | PubMed publication ID | 22362628 |
| P50 | author | Nelson Leung-Sang Tang | Q37839560 |
| Jack Chun-Yiu Cheng | Q57693740 | ||
| P2093 | author name string | Vivian W Y Hung | |
| Hiu-Yan Yeung | |||
| Kwong-Man Lee | |||
| Tsz-Ping Lam | |||
| Chen Di Liao | |||
| Bobby Kin-Wah Ng | |||
| Hau-Man Yeung | |||
| P2860 | cites work | Heritability in the genomics era — concepts and misconceptions | Q22122010 |
| The genetics of autistic disorders and its clinical relevance: a review of the literature | Q22250987 | ||
| Role of Genes and Environments for Explaining Alzheimer Disease | Q22253029 | ||
| Schizophrenia as a complex trait: evidence from a meta-analysis of twin studies | Q28190066 | ||
| Assignment of a locus for autosomal dominant idiopathic scoliosis (IS) to human chromosome 17p11 | Q28208125 | ||
| Eye Color Changes Past Early Childhood | Q29541140 | ||
| New disease gene location and high genetic heterogeneity in idiopathic scoliosis. | Q34170982 | ||
| Genetic liability of type 1 diabetes and the onset age among 22,650 young Finnish twin pairs: a nationwide follow-up study | Q34186708 | ||
| The search for idiopathic scoliosis genes | Q34502567 | ||
| Genome-wide association studies of adolescent idiopathic scoliosis suggest candidate susceptibility genes. | Q34627021 | ||
| Melatonin receptor 1B (MTNR1B) gene polymorphism is associated with the occurrence of adolescent idiopathic scoliosis. | Q34651172 | ||
| Aetiology of idiopathic scoliosis: current concepts | Q35624652 | ||
| CHD7 gene polymorphisms are associated with susceptibility to idiopathic scoliosis. | Q35752651 | ||
| Genetic association of complex traits: using idiopathic scoliosis as an example | Q36833934 | ||
| A genetic locus for adolescent idiopathic scoliosis linked to chromosome 19p13.3. | Q37218363 | ||
| Clinical effectiveness of school screening for adolescent idiopathic scoliosis: a large population-based retrospective cohort study | Q43830610 | ||
| Genetic heritability of a shallow anterior chamber in Chinese families with primary angle closure glaucoma | Q46133032 | ||
| Costs of school scoliosis screening: a large, population-based study. | Q46870543 | ||
| Heritability of body size and muscle strength in young adulthood: a study of one million Swedish men. | Q47247194 | ||
| Genetic and environmental factors in epilepsy: a population-based study of 11900 Danish twin pairs. | Q50568648 | ||
| Psoriasis in Norwegian twins: contribution of genetic and environmental effects. | Q51902378 | ||
| Association study of BMP4, IL6, Leptin, MMP3, and MTNR1B gene promoter polymorphisms and adolescent idiopathic scoliosis. | Q54392918 | ||
| Familial Resemblance and Heritability | Q57315997 | ||
| Fine mapping of the MHC Class III region demonstrates association of AIF1 and rheumatoid arthritis | Q57667629 | ||
| A Relook Into the Association of the Estrogen Receptor α Gene (PvuII, XbaI) and Adolescent Idiopathic Scoliosis | Q57955061 | ||
| RUS skeletal maturity of children in Beijing | Q58298280 | ||
| P433 | issue | 9 | |
| P921 | main subject | heritability | Q1503548 |
| P304 | page(s) | 1464-1469 | |
| P577 | publication date | 2012-02-23 | |
| P1433 | published in | Journal of Orthopaedic Research | Q6295700 |
| P1476 | title | Genetic epidemiology and heritability of AIS: A study of 415 Chinese female patients. | |
| P478 | volume | 30 |
| Q36068737 | A Functional SNP in BNC2 Is Associated with Adolescent Idiopathic Scoliosis |
| Q35193960 | A PAX1 enhancer locus is associated with susceptibility to idiopathic scoliosis in females |
| Q51095091 | A meta-analysis identifies adolescent idiopathic scoliosis association with LBX1 locus in multiple ethnic groups. |
| Q57399091 | A multi-ethnic meta-analysis confirms the association of rs6570507 with adolescent idiopathic scoliosis |
| Q89216494 | Adolescent idiopathic scoliosis |
| Q91655679 | Association between ladybird homeobox 1 gene polymorphisms and adolescent idiopathic scoliosis: A MOOSE-compliant meta-analysis |
| Q64074361 | Association of Circulating YKL-40 Levels and CHI3L1 Variants with the Risk of Spinal Deformity Progression in Adolescent Idiopathic Scoliosis |
| Q49334724 | Etiological Theories of Adolescent Idiopathic Scoliosis: Past and Present |
| Q35061914 | Exome sequencing identifies a rare HSPG2 variant associated with familial idiopathic scoliosis |
| Q37456533 | Family history and its association to curve size and treatment in 1,463 patients with idiopathic scoliosis |
| Q28072651 | Genetics and pathogenesis of idiopathic scoliosis |
| Q58553609 | Genome-wide meta-analysis and replication studies in multiple ethnicities identify novel adolescent idiopathic scoliosis susceptibility loci |
| Q35078933 | Haplotypes at LBX1 have distinct inheritance patterns with opposite effects in adolescent idiopathic scoliosis |
| Q57173968 | Idiopathic Scoliosis Families Highlight Actin-Based and Microtubule-Based Cellular Projections and Extracellular Matrix in Disease Etiology |
| Q35053538 | Mechanism of right thoracic adolescent idiopathic scoliosis at risk for progression; a unifying pathway of development by normal growth and imbalance |
| Q57455770 | The Role of Vitamin D in the Pathogenesis of Adolescent Idiopathic Scoliosis |
| Q90482836 | The cartilage matrisome in adolescent idiopathic scoliosis |
| Q36718750 | Whither the etiopathogenesis (and scoliogeny) of adolescent idiopathic scoliosis? Incorporating presentations on scoliogeny at the 2012 IRSSD and SRS meetings |
Search more.