Published in Psychiatr Genet on October 01, 2014
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Further evidence of pleiotropy influencing speech and language: analysis of the DYX8 region. Hum Hered (2007) 0.93
Linking neurogenetics and individual differences in language learning: the dopamine hypothesis. Cortex (2012) 0.92
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The derived allele of ASPM is associated with lexical tone perception. PLoS One (2012) 0.89
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Phonological processing and reading in children with speech sound disorders. Am J Speech Lang Pathol (2007) 0.86
An assessment of transmission disequilibrium between quantitative measures of childhood problem behaviors and DRD2/Taql and DRD4/48bp-repeat polymorphisms. Behav Genet (2004) 0.84
Association between the A1 allele of the DRD2 gene and reduced verbal abilities in adolescence and early adulthood. J Neural Transm (Vienna) (2010) 0.83
Distinguishing groups of children with persistent speech disorder: findings from a prospective population study. Logoped Phoniatr Vocol (2011) 0.82
Speech-Sound Disorders and Attention-Deficit/Hyperactivity Disorder Symptoms. Top Lang Disord (2012) 0.81
Associations of prenatal nicotine exposure and the dopamine related genes ANKK1 and DRD2 to verbal language. PLoS One (2013) 0.81
No evidence for association and linkage disequilibrium between dyslexia and markers of four dopamine-related genes. Eur Child Adolesc Psychiatry (2003) 0.81
From dopaminergic genes to psychiatric disorders. Neurotox Res (2007) 0.80
Vasopressin modulates male squirrel monkeys' behavior during social separation. Eur J Pharmacol (1991) 0.76
MYH9 is associated with nondiabetic end-stage renal disease in African Americans. Nat Genet (2008) 9.50
A randomized trial of adenotonsillectomy for childhood sleep apnea. N Engl J Med (2013) 5.99
Poor predictive validity of the Bayley Scales of Infant Development for cognitive function of extremely low birth weight children at school age. Pediatrics (2005) 5.17
Genetic variants near TIMP3 and high-density lipoprotein-associated loci influence susceptibility to age-related macular degeneration. Proc Natl Acad Sci U S A (2010) 4.30
Chronic conditions, functional limitations, and special health care needs of school-aged children born with extremely low-birth-weight in the 1990s. JAMA (2005) 3.89
Seven new loci associated with age-related macular degeneration. Nat Genet (2013) 3.81
Apolipoprotein L1 gene variants associate with hypertension-attributed nephropathy and the rate of kidney function decline in African Americans. Kidney Int (2012) 3.46
Grades I-II intraventricular hemorrhage in extremely low birth weight infants: effects on neurodevelopment. J Pediatr (2006) 2.60
Genome-wide meta-analyses of multiancestry cohorts identify multiple new susceptibility loci for refractive error and myopia. Nat Genet (2013) 2.36
Meta-analysis of genome scans of age-related macular degeneration. Hum Mol Genet (2005) 2.34
Increased behavioral morbidity in school-aged children with sleep-disordered breathing. Pediatrics (2004) 2.26
Familial clustering of chronic kidney disease. Semin Dial (2007) 1.95
Short- and long-term social outcomes following pediatric traumatic brain injury. J Int Neuropsychol Soc (2004) 1.92
TbMP57 is a 3' terminal uridylyl transferase (TUTase) of the Trypanosoma brucei editosome. Mol Cell (2003) 1.88
The Family Investigation of Nephropathy and Diabetes (FIND): design and methods. J Diabetes Complications (2005) 1.87
Cognitive and academic consequences of bronchopulmonary dysplasia and very low birth weight: 8-year-old outcomes. Pediatrics (2003) 1.86
EPHA2 is associated with age-related cortical cataract in mice and humans. PLoS Genet (2009) 1.82
Genome-wide linkage study of retinal vessel diameters in the Beaver Dam Eye Study. Hypertension (2006) 1.80
Social outcomes in childhood brain disorder: a heuristic integration of social neuroscience and developmental psychology. Psychol Bull (2007) 1.79
Behavioral outcomes and evidence of psychopathology among very low birth weight infants at age 20 years. Pediatrics (2004) 1.73
Long-term behavior problems following pediatric traumatic brain injury: prevalence, predictors, and correlates. J Pediatr Psychol (2003) 1.71
Examining the relative influence of familial, genetic, and environmental covariate information in flexible risk models. Proc Natl Acad Sci U S A (2009) 1.68
Genome-wide scan for estimated glomerular filtration rate in multi-ethnic diabetic populations: the Family Investigation of Nephropathy and Diabetes (FIND). Diabetes (2007) 1.61
Four novel Loci (19q13, 6q24, 12q24, and 5q14) influence the microcirculation in vivo. PLoS Genet (2010) 1.57
Long-term attention problems in children with traumatic brain injury. J Am Acad Child Adolesc Psychiatry (2005) 1.56
Social problem-solving skills in children with traumatic brain injury: long-term outcomes and prediction of social competence. Child Neuropsychol (2002) 1.55
A prospective study of short- and long-term neuropsychological outcomes after traumatic brain injury in children. Neuropsychology (2002) 1.55
A whole-genome screen of a quantitative trait of age-related maculopathy in sibships from the Beaver Dam Eye Study. Am J Hum Genet (2003) 1.53
Mathematical assumptions versus biological reality: myths in affected sib pair linkage analysis. Am J Hum Genet (2004) 1.52
Assessing cognitive outcomes in a rural African population: development of a neuropsychological battery in Kilifi District, Kenya. J Int Neuropsychol Soc (2004) 1.52
The epidemiology of retinal reticular drusen. Am J Ophthalmol (2007) 1.50
A new method for grading the severity of keratoconus: the Keratoconus Severity Score (KSS). Cornea (2006) 1.49
Placental lesions as predictors of cerebral palsy and abnormal neurocognitive function at school age in extremely low birth weight infants (<1 kg). Pediatr Dev Pathol (2007) 1.49
Learning disabilities in children with very low birthweight: prevalence, neuropsychological correlates, and educational interventions. J Learn Disabil (2005) 1.46
Variation of cognition and achievement with sleep-disordered breathing in full-term and preterm children. Arch Pediatr Adolesc Med (2006) 1.46
Health-related quality of life of children and adolescents after traumatic brain injury. Pediatrics (2002) 1.44
Genome scan of M. tuberculosis infection and disease in Ugandans. PLoS One (2008) 1.41
Outcomes of late preterm birth: who is at risk and for what? Am J Obstet Gynecol (2012) 1.41
Neurobehavioural outcomes of mild head injury in children and adolescents. Pediatr Rehabil (2005) 1.40
Longitudinal trajectories of postconcussive symptoms in children with mild traumatic brain injuries and their relationship to acute clinical status. Pediatrics (2009) 1.37
Pleiotropic effects of a chromosome 3 locus on speech-sound disorder and reading. Am J Hum Genet (2004) 1.36
Association of polymorphisms in the hepatocyte growth factor gene promoter with keratoconus. Invest Ophthalmol Vis Sci (2011) 1.29
Heritability of the severity of diabetic retinopathy: the FIND-Eye study. Invest Ophthalmol Vis Sci (2008) 1.29
Long-term executive function deficits in children with traumatic brain injuries: assessment using the Behavior Rating Inventory of Executive Function (BRIEF). Child Neuropsychol (2002) 1.22
Variants in the Wilms' tumor gene are associated with focal segmental glomerulosclerosis in the African American population. Physiol Genomics (2005) 1.22
The genetic bases of speech sound disorders: evidence from spoken and written language. J Speech Lang Hear Res (2006) 1.22
Candidate gene association study for diabetic retinopathy in persons with type 2 diabetes: the Candidate gene Association Resource (CARe). Invest Ophthalmol Vis Sci (2011) 1.22
The family environment as a moderator of psychosocial outcomes following traumatic brain injury in young children. Neuropsychology (2010) 1.20
Mitochondrial DNA variants of respiratory complex I that uniquely characterize haplogroup T2 are associated with increased risk of age-related macular degeneration. PLoS One (2009) 1.19
Genetic association and gene-gene interaction analyses in African American dialysis patients with nondiabetic nephropathy. Am J Kidney Dis (2011) 1.19
Predicting longitudinal patterns of functional deficits in children with traumatic brain injury. Neuropsychology (2009) 1.19
A sarcoidosis genetic linkage consortium: the sarcoidosis genetic analysis (SAGA) study. Sarcoidosis Vasc Diffuse Lung Dis (2005) 1.18
Toll-like receptor polymorphisms and age-related macular degeneration. Invest Ophthalmol Vis Sci (2008) 1.18
Clinically significant behavior problems during the initial 18 months following early childhood traumatic brain injury. Rehabil Psychol (2010) 1.17
Dimensions of postconcussive symptoms in children with mild traumatic brain injuries. J Int Neuropsychol Soc (2009) 1.16
Management of pediatric mild traumatic brain injury: a neuropsychological review from injury through recovery. Clin Neuropsychol (2007) 1.15
Counselor-assisted problem solving (CAPS) improves behavioral outcomes in older adolescents with complicated mild to severe TBI. J Head Trauma Rehabil (2014) 1.14
Associations of executive function with sleepiness and sleep duration in adolescents. Pediatrics (2009) 1.14
Cognitive reserve as a moderator of postconcussive symptoms in children with complicated and uncomplicated mild traumatic brain injury. J Int Neuropsychol Soc (2009) 1.13
Linkage analyses of four regions previously implicated in dyslexia: confirmation of a locus on chromosome 15q. Am J Med Genet B Neuropsychiatr Genet (2004) 1.12
Toward diagnostic and phenotype markers for genetically transmitted speech delay. J Speech Lang Hear Res (2005) 1.12
Cognitive outcomes for extremely preterm/extremely low birth weight children in kindergarten. J Int Neuropsychol Soc (2011) 1.11
A genome-wide association study identifies a potential novel gene locus for keratoconus, one of the commonest causes for corneal transplantation in developed countries. Hum Mol Genet (2011) 1.11
A prospective study of long-term caregiver and family adaptation following brain injury in children. J Head Trauma Rehabil (2002) 1.10
Large scale international replication and meta-analysis study confirms association of the 15q14 locus with myopia. The CREAM consortium. Hum Genet (2012) 1.09
Variation in the lysyl oxidase (LOX) gene is associated with keratoconus in family-based and case-control studies. Invest Ophthalmol Vis Sci (2012) 1.09
Relationship of Fuchs endothelial corneal dystrophy severity to central corneal thickness. Arch Ophthalmol (2012) 1.08
Traumatic brain injuries in early childhood: initial impact on the family. J Dev Behav Pediatr (2008) 1.08
Family burden and parental distress following mild traumatic brain injury in children and its relationship to post-concussive symptoms. J Pediatr Psychol (2008) 1.07
Genomewide linkage scan for diabetic renal failure and albuminuria: the FIND study. Am J Nephrol (2011) 1.07
Nine loci for ocular axial length identified through genome-wide association studies, including shared loci with refractive error. Am J Hum Genet (2013) 1.06
Behavior disorders in extremely preterm/extremely low birth weight children in kindergarten. J Dev Behav Pediatr (2012) 1.06
The relationship of cataract and cataract extraction to age-related macular degeneration: the Beaver Dam Eye Study. Ophthalmology (2012) 1.06
Developmental sequelae in preterm infants having a diagnosis of bronchopulmonary dysplasia: analysis using a severity-based classification system. Arch Pediatr Adolesc Med (2007) 1.05
A 32 kb critical region excluding Y402H in CFH mediates risk for age-related macular degeneration. PLoS One (2011) 1.05
Evidence for a major gene influence on tumor necrosis factor-alpha expression in tuberculosis: path and segregation analysis. Hum Hered (2005) 1.05
Kinetoplastid RNA editing ligases: complex association, characterization, and substrate requirements. Mol Biochem Parasitol (2003) 1.05
Linkage and association analysis of candidate genes for TB and TNFalpha cytokine expression: evidence for association with IFNGR1, IL-10, and TNF receptor 1 genes. Hum Genet (2007) 1.04
The distribution of long range admixture linkage disequilibrium in an African-American population. Hum Hered (2002) 1.03
Complement factor H and hemicentin-1 in age-related macular degeneration and renal phenotypes. Hum Mol Genet (2007) 1.03
Race as a moderator of parent and family outcomes following pediatric traumatic brain injury. J Pediatr Psychol (2002) 1.02
Speech sound disorder influenced by a locus in 15q14 region. Behav Genet (2006) 1.02
Structural equation model-based genome scan for the metabolic syndrome. BMC Genet (2003) 1.02
Prediction of age-related macular degeneration in the general population: the Three Continent AMD Consortium. Ophthalmology (2013) 1.02
Risk alleles in CFH and ARMS2 and the long-term natural history of age-related macular degeneration: the Beaver Dam Eye Study. JAMA Ophthalmol (2013) 1.01
CKD increases the risk of age-related macular degeneration. J Am Soc Nephrol (2008) 1.01
Harmonizing the classification of age-related macular degeneration in the three-continent AMD consortium. Ophthalmic Epidemiol (2014) 1.01
Endoribonuclease activities of Trypanosoma brucei mitochondria. Mol Biochem Parasitol (2002) 1.00
A multicenter study to map genes for Fuchs endothelial corneal dystrophy: baseline characteristics and heritability. Cornea (2012) 1.00