Published in Am J Hum Genet on July 09, 2010
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A systematic review of association studies of common variants associated with idiopathic congenital talipes equinovarus (ICTEV) in humans in the past 30 years. Springerplus (2016) 0.76
The 2017 ABJS Nicolas Andry Award: Advancing Personalized Medicine for Clubfoot Through Translational Research. Clin Orthop Relat Res (2017) 0.75
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Factors predictive of outcome after use of the Ponseti method for the treatment of idiopathic clubfeet. J Bone Joint Surg Am (2004) 2.87
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Tbx4 and tbx5 acting in connective tissue are required for limb muscle and tendon patterning. Dev Cell (2010) 1.22
Asymmetric lower-limb malformations in individuals with homeobox PITX1 gene mutation. Am J Hum Genet (2008) 1.21
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Dual hindlimb control elements in the Tbx4 gene and region-specific control of bone size in vertebrate limbs. Development (2008) 1.19
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Identification of a recurrent microdeletion at 17q23.1q23.2 flanked by segmental duplications associated with heart defects and limb abnormalities. Am J Hum Genet (2010) 0.95
Clubfoot and developmental dysplasia of the hip: value of screening hip radiographs in children with clubfoot. J Pediatr Orthop (2003) 0.95
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Factors predictive of outcome after use of the Ponseti method for the treatment of idiopathic clubfeet. J Bone Joint Surg Am (2004) 2.87
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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
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Expression of novel Alzheimer's disease risk genes in control and Alzheimer's disease brains. PLoS One (2012) 1.48
Polygenic threshold model with sex dimorphism in adolescent idiopathic scoliosis: the Carter effect. J Bone Joint Surg Am (2012) 1.46
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
Myosin binding protein C1: a novel gene for autosomal dominant distal arthrogryposis type 1. Hum Mol Genet (2010) 1.32
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
Lack of C9ORF72 coding mutations supports a gain of function for repeat expansions in amyotrophic lateral sclerosis. Neurobiol Aging (2013) 1.08
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
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
Mutations in the GABRA1 and EFHC1 genes are rare in familial juvenile myoclonic epilepsy. Epilepsy Res (2006) 0.96
Candidate genes for alcohol preference identified by expression profiling in alcohol-preferring and -nonpreferring reciprocal congenic rats. Genome Biol (2010) 0.96
Editorial: Estimating survivorship in the face of competing risks. Clin Orthop Relat Res (2015) 0.96
Identification of candidate genes for alcohol preference by expression profiling of congenic rat strains. Alcohol Clin Exp Res (2007) 0.95
Pilocytic astrocytoma in a child with Noonan syndrome. Pediatr Blood Cancer (2009) 0.95
Pitx1 haploinsufficiency causes clubfoot in humans and a clubfoot-like phenotype in mice. Hum Mol Genet (2011) 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
Vascular abnormalities correlate with decreased soft tissue volumes in idiopathic clubfoot. Clin Orthop Relat Res (2010) 0.91
Magnetic resonance angiography in clubfoot and vertical talus: a feasibility study. Clin Orthop Relat Res (2009) 0.91
Complications and outcomes of open pediatric forearm fractures. J Pediatr Orthop (2003) 0.90
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
Combined midfoot osteotomy for severe forefoot adductus. J Pediatr Orthop (2002) 0.89
MYBPC1 mutations impair skeletal muscle function in zebrafish models of arthrogryposis. Hum Mol Genet (2013) 0.88
Evaluation of a commercially available focused aCGH platform for the detection of constitutional chromosome anomalies. Am J Med Genet A (2007) 0.87
Evaluation of CAND2 and WNT7a as candidate genes for congenital idiopathic clubfoot. Clin Orthop Relat Res (2009) 0.87
Genetics of clubfoot. J Pediatr Orthop B (2012) 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
Femoral deformity in tibia vara. J Bone Joint Surg Am (2006) 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
Kinesin family member 6 (kif6) is necessary for spine development in zebrafish. Dev Dyn (2014) 0.84
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
A comparison of monolateral and circular external fixation of unstable diaphyseal tibial fractures in children. J Pediatr Orthop B (2003) 0.83
Arthroscopic findings at the time of patellar realignment surgery in adolescents. J Pediatr Orthop (2007) 0.83
Variable hand and foot abnormalities in family with congenital vertical talus and CDMP-1 gene mutation. J Orthop Res (2005) 0.83
A multiplex assay for the detection and mapping of complex glycerol kinase deficiency. Clin Chem (2006) 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