Polygenic threshold model with sex dimorphism in adolescent idiopathic scoliosis: the Carter effect.

Rare variants in FBN1 and FBN2 are associated with severe adolescent idiopathic scoliosis. Hum Mol Genet (2014) 1.02

Are copy number variants associated with adolescent idiopathic scoliosis? Clin Orthop Relat Res (2014) 0.97

A PAX1 enhancer locus is associated with susceptibility to idiopathic scoliosis in females. Nat Commun (2015) 0.88

A polygenic burden of rare variants across extracellular matrix genes among individuals with adolescent idiopathic scoliosis. Hum Mol Genet (2015) 0.84

Participation of sex hormones in multifactorial pathogenesis of adolescent idiopathic scoliosis. Int Orthop (2015) 0.81

Higher genetic threshold for progressive adolescent idiopathic scoliosis in male individuals: commentary on an article by Lisa M. Kruse, MD, et al.: "Polygenic threshold model with sex dimorphism in adolescent idiopathic scoliosis: the Carter effect". J Bone Joint Surg Am (2012) 0.75

Effects of bracing in adolescents with idiopathic scoliosis. N Engl J Med (2013) 6.02

DICER1 mutations in familial pleuropulmonary blastoma. Science (2009) 3.82

Genome-wide copy number variation in epilepsy: novel susceptibility loci in idiopathic generalized and focal epilepsies. PLoS Genet (2010) 3.39

Fairness to all: gender and sex in scientific reporting. Clin Orthop Relat Res (2013) 2.98

Factors predictive of outcome after use of the Ponseti method for the treatment of idiopathic clubfeet. J Bone Joint Surg Am (2004) 2.87

Mutations in the gene PRRT2 cause paroxysmal kinesigenic dyskinesia with infantile convulsions. Cell Rep (2011) 2.17

Genome-wide association studies of adolescent idiopathic scoliosis suggest candidate susceptibility genes. Hum Mol Genet (2011) 1.83

Treatment of the complex idiopathic clubfoot. Clin Orthop Relat Res (2006) 1.75

A new dynamic foot abduction orthosis for clubfoot treatment. J Pediatr Orthop (2007) 1.66

Update on clubfoot: etiology and treatment. Clin Orthop Relat Res (2009) 1.49

Two novel point mutations in the long-range SHH enhancer in three families with triphalangeal thumb and preaxial polydactyly. Am J Med Genet A (2007) 1.41

Early results of the Ponseti method for the treatment of clubfoot in distal arthrogryposis. J Bone Joint Surg Am (2008) 1.40

Complications of titanium elastic nails for pediatric femoral shaft fractures. J Pediatr Orthop (2003) 1.38

Design of the Bracing in Adolescent Idiopathic Scoliosis Trial (BrAIST). Spine (Phila Pa 1976) (2013) 1.34

A new approach to the treatment of congenital vertical talus. J Child Orthop (2007) 1.31

Impact of congenital talipes equinovarus etiology on treatment outcomes. Dev Med Child Neurol (2008) 1.25

Asymmetric lower-limb malformations in individuals with homeobox PITX1 gene mutation. Am J Hum Genet (2008) 1.21

Incomplete penetrance and phenotypic variability characterize Gdf6-attributable oculo-skeletal phenotypes. Hum Mol Genet (2009) 1.14

Complications after titanium elastic nailing of pediatric tibial fractures. J Pediatr Orthop (2007) 1.12

Polygenic threshold model with sex dimorphism in clubfoot inheritance: the Carter effect. J Bone Joint Surg Am (2008) 1.11

Complications after pinning of supracondylar distal humerus fractures. J Pediatr Orthop (2010) 1.10

Validity and reliability of intraoperative monitoring in pediatric spinal deformity surgery: a 23-year experience of 3436 surgical cases. Spine (Phila Pa 1976) (2010) 1.09

Copy number variants and infantile spasms: evidence for abnormalities in ventral forebrain development and pathways of synaptic function. Eur J Hum Genet (2011) 1.08

BRAF(V600E) mutation is a negative prognosticator in pediatric ganglioglioma. Acta Neuropathol (2013) 1.08

Familial isolated clubfoot is associated with recurrent chromosome 17q23.1q23.2 microduplications containing TBX4. Am J Hum Genet (2010) 1.05

Exome sequencing identifies an MYH3 mutation in a family with distal arthrogryposis type 1. J Bone Joint Surg Am (2011) 1.03

Early reduction, arthrotomy, and cannulated screw fixation in unstable slipped capital femoral epiphysis treatment. J Pediatr Orthop (2002) 1.02

Use of the Ponseti method for recurrent clubfoot following posteromedial release. Indian J Orthop (2008) 1.02

Voltage-gated potassium channel KCNV2 (Kv8.2) contributes to epilepsy susceptibility. Proc Natl Acad Sci U S A (2011) 1.02

Results of the Ponseti method in patients with clubfoot associated with arthrogryposis. Iowa Orthop J (2008) 1.01

Genetic linkage localizes an adolescent idiopathic scoliosis and pectus excavatum gene to chromosome 18 q. Spine (Phila Pa 1976) (2009) 1.01

Are copy number variants associated with adolescent idiopathic scoliosis? Clin Orthop Relat Res (2014) 0.97

Mutations in the GABRA1 and EFHC1 genes are rare in familial juvenile myoclonic epilepsy. Epilepsy Res (2006) 0.96

Diaphyseal derotational osteotomy with intramedullary fixation for correction of excessive femoral anteversion in children. J Pediatr Orthop (2005) 0.96

HOXD10 M319K mutation in a family with isolated congenital vertical talus. J Orthop Res (2006) 0.96

Editorial: Estimating survivorship in the face of competing risks. Clin Orthop Relat Res (2015) 0.96

Pitx1 haploinsufficiency causes clubfoot in humans and a clubfoot-like phenotype in mice. Hum Mol Genet (2011) 0.95

Pilocytic astrocytoma in a child with Noonan syndrome. Pediatr Blood Cancer (2009) 0.95

Early results of the Ponseti method for the treatment of clubfoot associated with myelomeningocele. J Bone Joint Surg Am (2009) 0.94

Antegrade intramedullary nailing of pediatric femoral fractures using an interlocking pediatric femoral nail and a lateral trochanteric entry point. J Pediatr Orthop (2009) 0.94

A minimally invasive treatment protocol for the congenital dislocation of the knee. J Pediatr Orthop (2010) 0.93

Skeletal muscle contractile gene (TNNT3, MYH3, TPM2) mutations not found in vertical talus or clubfoot. Clin Orthop Relat Res (2009) 0.93

Intramedullary nailing of femoral fractures in children through the lateral aspect of the greater trochanter using a modified rigid humeral intramedullary nail: preliminary results of a new technique in 15 children. J Orthop Trauma (2004) 0.93

Urgent reduction, fixation, and arthrotomy for unstable slipped capital femoral epiphysis. J Pediatr Orthop (2010) 0.91

Altered transmission of HOX and apoptotic SNPs identify a potential common pathway for clubfoot. Am J Med Genet A (2009) 0.91

Active management of financial conflicts of interest on the Editorial Board of CORR. Clin Orthop Relat Res (2013) 0.91

Magnetic resonance angiography in clubfoot and vertical talus: a feasibility study. Clin Orthop Relat Res (2009) 0.91

Vascular abnormalities correlate with decreased soft tissue volumes in idiopathic clubfoot. Clin Orthop Relat Res (2010) 0.91

Complications and outcomes of open pediatric forearm fractures. J Pediatr Orthop (2003) 0.90

Combined midfoot osteotomy for severe forefoot adductus. J Pediatr Orthop (2002) 0.89

Absence of HOXD10 mutations in idiopathic clubfoot and sporadic vertical talus. Clin Orthop Relat Res (2007) 0.89

Management of juvenile idiopathic scoliosis. J Bone Joint Surg Am (2007) 0.89

MYBPC1 mutations impair skeletal muscle function in zebrafish models of arthrogryposis. Hum Mol Genet (2013) 0.88

Genetics of clubfoot. J Pediatr Orthop B (2012) 0.87

Evaluation of CAND2 and WNT7a as candidate genes for congenital idiopathic clubfoot. Clin Orthop Relat Res (2009) 0.87

Skeletal muscle abnormalities and genetic factors related to vertical talus. Clin Orthop Relat Res (2010) 0.86

Case report: Congenital knee dislocation in a patient with larsen syndrome and a novel filamin B mutation. Clin Orthop Relat Res (2008) 0.86

Minimally invasive approach for the treatment of non-isolated congenital vertical talus. J Bone Joint Surg Am (2012) 0.86

Variants in genes that encode muscle contractile proteins influence risk for isolated clubfoot. Am J Med Genet A (2011) 0.85

Evaluation of GPR50, hMel-1B, and ROR-alpha melatonin-related receptors and the etiology of adolescent idiopathic scoliosis. J Pediatr Orthop (2010) 0.85

Axial distribution of myosin binding protein-C is unaffected by mutations in human cardiac and skeletal muscle. J Muscle Res Cell Motil (2012) 0.85

Smoking and socio-economic status in the etiology and severity of Legg-Calvé-Perthes' disease. J Pediatr Orthop B (2004) 0.84

Copy number analysis of 413 isolated talipes equinovarus patients suggests role for transcriptional regulators of early limb development. Eur J Hum Genet (2012) 0.84

Femoral deformity in tibia vara. J Bone Joint Surg Am (2006) 0.84

Kinesin family member 6 (kif6) is necessary for spine development in zebrafish. Dev Dyn (2014) 0.84

A comparison of monolateral and circular external fixation of unstable diaphyseal tibial fractures in children. J Pediatr Orthop B (2003) 0.83

Variable hand and foot abnormalities in family with congenital vertical talus and CDMP-1 gene mutation. J Orthop Res (2005) 0.83

Evidence for an additional locus for split hand/foot malformation in chromosome region 8q21.11-q22.3. Am J Med Genet A (2006) 0.83

Outcome of hemiepiphyseal stapling for late-onset tibia vara. J Bone Joint Surg Am (2005) 0.83

Arthroscopic findings at the time of patellar realignment surgery in adolescents. J Pediatr Orthop (2007) 0.83

Interobserver and intraobserver reliability in the evaluation of mechanical axis deviation. J Pediatr Orthop (2009) 0.82

Adolescent patellofemoral pain: implicating the medial patellofemoral ligament as the main pain generator. J Child Orthop (2008) 0.81

Clubfoot: etiology and treatment: editorial comment. Clin Orthop Relat Res (2009) 0.80

Duplication within the SEPT9 gene associated with a founder effect in North American families with hereditary neuralgic amyotrophy. Hum Mol Genet (2009) 0.80

Serial casting for neuromuscular flatfoot and vertical talus in an adolescent with hereditary spastic paraplegia. Pediatr Phys Ther (2014) 0.79

Rigid pediatric pes planovalgus: conservative and surgical treatment options. Clin Podiatr Med Surg (2010) 0.79

Design and descriptive data of the randomized Clubfoot Foot Abduction Brace Length of Treatment Study (FAB24). J Pediatr Orthop B (2017) 0.79

Surgical treatment of traumatic pediatric humeral diaphyseal fractures with titanium elastic nails. J Child Orthop (2009) 0.78

Common polymorphisms in human lysyl oxidase genes are not associated with the adolescent idiopathic scoliosis phenotype. BMC Med Genet (2011) 0.78

Flexor digitorum accessorius longus muscle is associated with familial idiopathic clubfoot. J Pediatr Orthop (2005) 0.78

Defining the phenotype to discover the genotype. Neurology (2006) 0.78