Published in Am J Hum Genet on January 20, 2004
The axon guidance receptor gene ROBO1 is a candidate gene for developmental dyslexia. PLoS Genet (2005) 2.02
EPHA2 is associated with age-related cortical cataract in mice and humans. PLoS Genet (2009) 1.82
Highly significant linkage to the SLI1 locus in an expanded sample of individuals affected by specific language impairment. Am J Hum Genet (2004) 1.63
Convergent genetic linkage and associations to language, speech and reading measures in families of probands with Specific Language Impairment. J Neurodev Disord (2009) 1.57
Genetics of developmental dyslexia. Eur Child Adolesc Psychiatry (2009) 1.38
Gene X environment interactions in reading disability and attention-deficit/hyperactivity disorder. Dev Psychol (2009) 1.36
High risk of reading disability and speech sound disorder in rolandic epilepsy families: case-control study. Epilepsia (2007) 1.35
Genetic advances in the study of speech and language disorders. Neuron (2010) 1.33
Inter-relationships among behavioral markers, genes, brain and treatment in dyslexia and dysgraphia. Future Neurol (2010) 1.26
Heritability of specific language impairment depends on diagnostic criteria. Genes Brain Behav (2007) 1.22
A nonword repetition task for speakers with misarticulations: the Syllable Repetition Task (SRT). J Speech Lang Hear Res (2009) 1.17
The genetics of reading disabilities: from phenotypes to candidate genes. Front Psychol (2013) 1.12
Association of reading disabilities with regions marked by acetylated H3 histones in KIAA0319. Am J Med Genet B Neuropsychiatr Genet (2010) 1.05
Genetics of dyslexia: the evolving landscape. J Med Genet (2007) 0.99
Globularity and language-readiness: generating new predictions by expanding the set of genes of interest. Front Psychol (2014) 0.94
Common variation near ROBO2 is associated with expressive vocabulary in infancy. Nat Commun (2014) 0.94
Pleiotropic effects of DCDC2 and DYX1C1 genes on language and mathematics traits in nuclear families of developmental dyslexia. Behav Genet (2010) 0.93
Motor sequencing deficit as an endophenotype of speech sound disorder: a genome-wide linkage analysis in a multigenerational family. Psychiatr Genet (2012) 0.88
Speaking genes or genes for speaking? Deciphering the genetics of speech and language. J Child Psychol Psychiatry (2009) 0.88
Children with comorbid speech sound disorder and specific language impairment are at increased risk for attention-deficit/hyperactivity disorder. J Abnorm Child Psychol (2007) 0.87
Literacy outcomes of children with early childhood speech sound disorders: impact of endophenotypes. J Speech Lang Hear Res (2011) 0.87
A multigenerational family study of oral and hand motor sequencing ability provides evidence for a familial speech sound disorder subtype. Top Lang Disord (2011) 0.85
Reading skills of students with speech sound disorders at three stages of literacy development. Lang Speech Hear Serv Sch (2013) 0.81
KIAA0319 and ROBO1: evidence on association with reading and pleiotropic effects on language and mathematics abilities in developmental dyslexia. J Hum Genet (2014) 0.81
Etiologies and molecular mechanisms of communication disorders. J Dev Behav Pediatr (2010) 0.81
Language Impairments in ASD Resulting from a Failed Domestication of the Human Brain. Front Neurosci (2016) 0.80
Subtyping Children With Speech Sound Disorders by Endophenotypes. Top Lang Disord (2011) 0.79
Heritability estimation for speech-sound traits with developmental trajectories. Behav Genet (2010) 0.79
The genetics of reading disability in an often excluded sample: novel loci suggested for reading disability in Rolandic epilepsy. PLoS One (2012) 0.79
Approach to epigenetic analysis in language disorders. J Neurodev Disord (2011) 0.78
Oral and hand movement speeds are associated with expressive language ability in children with speech sound disorder. J Psycholinguist Res (2012) 0.78
A common haplotype of KIAA0319 contributes to the phonological awareness skill in Chinese children. Behav Brain Funct (2014) 0.78
At the height of fashion: what genetics can teach us about neurodevelopmental disabilities. Curr Opin Neurol (2009) 0.77
Association between AVPR1A, DRD2, and ASPM and endophenotypes of communication disorders. Psychiatr Genet (2014) 0.76
Characterization of a complex chromosomal rearrangement using chromosome, FISH, and microarray assays in a girl with multiple congenital abnormalities and developmental delay. Mol Cytogenet (2014) 0.75
The DYX2 locus and neurochemical signaling genes contribute to speech sound disorder and related neurocognitive domains. Genes Brain Behav (2015) 0.75
Genome-Wide Studies of Specific Language Impairment. Curr Behav Neurosci Rep (2014) 0.75
Genomic sequencing of a dyslexia susceptibility haplotype encompassing ROBO1. J Neurodev Disord (2016) 0.75
When does speech sound disorder matter for literacy? The role of disordered speech errors, co-occurring language impairment and family risk of dyslexia. J Child Psychol Psychiatry (2016) 0.75
Merlin--rapid analysis of dense genetic maps using sparse gene flow trees. Nat Genet (2001) 53.16
Genetic dissection of complex traits: guidelines for interpreting and reporting linkage results. Nat Genet (1995) 49.77
The investigation of linkage between a quantitative trait and a marker locus. Behav Genet (1972) 24.92
Searching for genetic determinants in the new millennium. Nature (2000) 17.50
Haseman and Elston revisited. Genet Epidemiol (2000) 7.23
Quantitative trait locus for reading disability on chromosome 6. Science (1994) 6.07
A variance component approach to dichotomous trait linkage analysis using a threshold model. Genet Epidemiol (1997) 3.33
Adding further power to the Haseman and Elston method for detecting linkage in larger sibships: weighting sums and differences. Hum Hered (2003) 3.33
Rapid "automatized" naming (R.A.N): dyslexia differentiated from other learning disabilities. Neuropsychologia (1976) 3.00
A new gene (DYX3) for dyslexia is located on chromosome 2. J Med Genet (1999) 2.72
A prospective study of the relationship between specific language impairment, phonological disorders and reading retardation. J Child Psychol Psychiatry (1990) 2.67
Susceptibility loci for distinct components of developmental dyslexia on chromosomes 6 and 15. Am J Hum Genet (1997) 2.65
Nonword repetition as a behavioural marker for inherited language impairment: evidence from a twin study. J Child Psychol Psychiatry (1996) 2.54
Independent genome-wide scans identify a chromosome 18 quantitative-trait locus influencing dyslexia. Nat Genet (2001) 2.48
A quantitative-trait locus on chromosome 6p influences different aspects of developmental dyslexia. Am J Hum Genet (1999) 2.38
Localisation of a gene implicated in a severe speech and language disorder. Nat Genet (1998) 2.33
Prevalence of speech delay in 6-year-old children and comorbidity with language impairment. J Speech Lang Hear Res (1999) 2.31
Quantitative-trait locus for specific language and reading deficits on chromosome 6p. Am J Hum Genet (1999) 2.26
The percentage of consonants correct (PCC) metric: extensions and reliability data. J Speech Lang Hear Res (1997) 2.01
Developmental dyslexia: genetic dissection of a complex cognitive trait. Nat Rev Neurosci (2002) 1.97
A genomewide scan identifies two novel loci involved in specific language impairment. Am J Hum Genet (2002) 1.96
Four new speech and prosody-voice measures for genetics research and other studies in developmental phonological disorders. J Speech Hear Res (1993) 1.80
Neural basis of an inherited speech and language disorder. Proc Natl Acad Sci U S A (1998) 1.76
Early reading development in children at family risk for dyslexia. Child Dev (2001) 1.70
Definition of the phenotype. Adv Genet (2001) 1.68
Evidence for linkage of spelling disability to chromosome 15. Am J Hum Genet (1998) 1.65
A genomewide scan for loci involved in attention-deficit/hyperactivity disorder. Am J Hum Genet (2002) 1.63
Use of multivariate linkage analysis for dissection of a complex cognitive trait. Am J Hum Genet (2003) 1.62
Clinical assessment of oropharyngeal motor development in young children. J Speech Hear Disord (1987) 1.52
Suggestive linkage of developmental dyslexia to chromosome 1p34-p36. Lancet (1993) 1.51
Major locus analysis for quantitative traits. Am J Hum Genet (1979) 1.48
An examination of word frequency and neighborhood density in the development of spoken-word recognition. Mem Cognit (1997) 1.44
Pre-literacy skills of subgroups of children with speech sound disorders. J Child Psychol Psychiatry (2004) 1.39
Heritability of poor language achievement among twins. J Speech Lang Hear Res (1998) 1.39
Quantitative trait locus for reading disability: correction. Science (1995) 1.37
A genome scan for developmental dyslexia confirms linkage to chromosome 2p11 and suggests a new locus on 7q32. J Med Genet (2003) 1.35
A dominant gene for developmental dyslexia on chromosome 3. J Med Genet (2001) 1.33
Evidence for linkage and association with reading disability on 6p21.3-22. Am J Hum Genet (2002) 1.31
Sample size requirements to control for stochastic variation in magnitude and location of allele-sharing linkage statistics in affected sibling pairs. Ann Hum Genet (2001) 1.29
Word-frequency and phonological-neighborhood effects on verbal short-term memory. J Exp Psychol Learn Mem Cogn (2002) 1.28
A study of developmental speech and language disorders in twins. J Speech Hear Res (1992) 1.19
Toward an understanding of developmental language and reading disorders. J Speech Hear Disord (1986) 1.17
Speech production/phonological deficits in reading-disordered children. J Learn Disabil (1986) 1.15
Structural equation model-based genome scan for the metabolic syndrome. BMC Genet (2003) 1.02
Pedigree analysis of children with phonology disorders. J Learn Disabil (1992) 1.00
Linkage studies suggest a possible locus for developmental dyslexia on chromosome 1p. Am J Med Genet (2001) 0.99
Follow-up of children with early expressive phonology disorders. J Learn Disabil (2004) 0.98
Continuing the search for dyslexia genes on 6p. Am J Med Genet B Neuropsychiatr Genet (2003) 0.97
Supportive evidence for the DYX3 dyslexia susceptibility gene in Canadian families. J Med Genet (2002) 0.93
Speech production skills of nuclear family members of children with phonology disorders. Lang Speech (1998) 0.90
The growth of lexical constraints on spoken word recognition. Percept Psychophys (1990) 0.89
Segregation analysis of speech and language disorders. Behav Genet (1993) 0.89
Familial dyslexia: neurocognitive and genetic correlation in a large Finnish family. Dev Med Child Neurol (2002) 0.88
Predicting reading problems in at-risk children. J Speech Hear Res (1991) 0.87
Genetic linkage analysis with dyslexia: evidence for linkage of spelling disability to chromosome 15. Eur Child Adolesc Psychiatry (1999) 0.85
A follow-up study of children with phonologic disorders of unknown origin. J Speech Hear Disord (1988) 0.85
Evidence for a susceptibility locus on chromosome 6q influencing phonological coding dyslexia. Am J Med Genet (2001) 0.84
Fine mapping of the chromosome 2p12-16 dyslexia susceptibility locus: quantitative association analysis and positional candidate genes SEMA4F and OTX1. Psychiatr Genet (2002) 0.84
A familial study of severe phonological disorders. J Speech Hear Res (1989) 0.83
Familial aggregation of phonological disorders: results from a 28-year follow-up. J Speech Hear Res (1995) 0.83
MYH9 is associated with nondiabetic end-stage renal disease in African Americans. Nat Genet (2008) 9.50
Optimal two-stage genotyping in population-based association studies. Genet Epidemiol (2003) 6.01
A generalized combinatorial approach for detecting gene-by-gene and gene-by-environment interactions with application to nicotine dependence. Am J Hum Genet (2007) 4.46
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
Seven new loci associated with age-related macular degeneration. Nat Genet (2013) 3.81
Natural selection on EPAS1 (HIF2alpha) associated with low hemoglobin concentration in Tibetan highlanders. Proc Natl Acad Sci U S A (2010) 3.78
Apolipoprotein L1 gene variants associate with hypertension-attributed nephropathy and the rate of kidney function decline in African Americans. Kidney Int (2012) 3.46
Improved power by use of a weighted score test for linkage disequilibrium mapping. Am J Hum Genet (2006) 3.36
Adding further power to the Haseman and Elston method for detecting linkage in larger sibships: weighting sums and differences. Hum Hered (2003) 3.33
Choosing an optimal method to combine P-values. Stat Med (2009) 3.15
Improved survival rates with increased neurodevelopmental disability for extremely low birth weight infants in the 1990s. Pediatrics (2005) 3.06
The genetic basis of complex traits: rare variants or "common gene, common disease"? Methods Mol Biol (2007) 3.01
A unified association analysis approach for family and unrelated samples correcting for stratification. Am J Hum Genet (2008) 3.00
Dissection of genomewide-scan data in extended families reveals a major locus and oligogenic susceptibility for age-related macular degeneration. Am J Hum Genet (2003) 2.92
Detecting rare variants for complex traits using family and unrelated data. Genet Epidemiol (2010) 2.80
Ethnic- and gender-specific association of the nicotinic acetylcholine receptor alpha4 subunit gene (CHRNA4) with nicotine dependence. Hum Mol Genet (2005) 2.80
Improved neurodevelopmental outcomes for extremely low birth weight infants in 2000-2002. Pediatrics (2007) 2.45
Premature myocardial infarction novel susceptibility locus on chromosome 1P34-36 identified by genomewide linkage analysis. Am J Hum Genet (2004) 2.36
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
A prospective study of short- and long-term outcomes after traumatic brain injury in children: behavior and achievement. Neuropsychology (2002) 2.34
Linkage analysis of a complex disease through use of admixed populations. Am J Hum Genet (2004) 2.21
Using the optimal receiver operating characteristic curve to design a predictive genetic test, exemplified with type 2 diabetes. Am J Hum Genet (2008) 2.20
Single- and multilocus allelic variants within the GABA(B) receptor subunit 2 (GABAB2) gene are significantly associated with nicotine dependence. Am J Hum Genet (2005) 2.18
A powerful method of combining measures of association and Hardy-Weinberg disequilibrium for fine-mapping in case-control studies. Stat Med (2006) 2.18
Odds ratio based multifactor-dimensionality reduction method for detecting gene-gene interactions. Bioinformatics (2006) 2.08
Whole genome scan for obstructive sleep apnea and obesity in African-American families. Am J Respir Crit Care Med (2004) 2.03
Reduced ventricular shunt rate in very preterm infants with severe intraventricular hemorrhage: an institutional experience. J Neurosurg Pediatr (2012) 1.98
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
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
Self-reported race and genetic admixture. N Engl J Med (2006) 1.85
A subset of familial colorectal neoplasia kindreds linked to chromosome 9q22.2-31.2. Proc Natl Acad Sci U S A (2003) 1.84
The meaning of interaction. Hum Hered (2010) 1.83
EPHA2 is associated with age-related cortical cataract in mice and humans. PLoS Genet (2009) 1.82
A whole-genome scan for obstructive sleep apnea and obesity. Am J Hum Genet (2002) 1.81
Genome-wide linkage study of retinal vessel diameters in the Beaver Dam Eye Study. Hypertension (2006) 1.80
Genome-wide scans for diabetic nephropathy and albuminuria in multiethnic populations: the family investigation of nephropathy and diabetes (FIND). Diabetes (2007) 1.79
Academic achievement of adolescents born with extremely low birth weight. Acta Paediatr (2012) 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
A combinatorial approach to detecting gene-gene and gene-environment interactions in family studies. Am J Hum Genet (2008) 1.57
A prospective study of short- and long-term neuropsychological outcomes after traumatic brain injury in children. Neuropsychology (2002) 1.55
Improving power in contrasting linkage-disequilibrium patterns between cases and controls. Am J Hum Genet (2007) 1.55
The effect of maternal milk on neonatal morbidity of very low-birth-weight infants. Arch Pediatr Adolesc Med (2003) 1.54
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
A genome-wide scan to identify loci for smoking rate in the Framingham Heart Study population. BMC Genet (2003) 1.50
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
Log-linear model-based multifactor dimensionality reduction method to detect gene gene interactions. Bioinformatics (2007) 1.44
Genetics of the apnea hypopnea index in Caucasians and African Americans: I. Segregation analysis. Genet Epidemiol (2002) 1.44
Detecting rare and common variants for complex traits: sibpair and odds ratio weighted sum statistics (SPWSS, ORWSS). Genet Epidemiol (2011) 1.43
Sampling correction in linkage analysis. Genet Epidemiol (2004) 1.43
Genome scan of M. tuberculosis infection and disease in Ugandans. PLoS One (2008) 1.41
Plasma aldosterone is independently associated with the metabolic syndrome. Hypertension (2006) 1.40
Are linkage analysis and the collection of family data dead? Prospects for family studies in the age of genome-wide association. Hum Hered (2007) 1.39
Pre-literacy skills of subgroups of children with speech sound disorders. J Child Psychol Psychiatry (2004) 1.39
Infrequent detection of germline allele-specific expression of TGFBR1 in lymphoblasts and tissues of colon cancer patients. Cancer Res (2009) 1.38
What influences literacy outcome in children with speech sound disorder? J Speech Lang Hear Res (2009) 1.37
Haplotype analysis indicates an association between the DOPA decarboxylase (DDC) gene and nicotine dependence. Hum Mol Genet (2005) 1.36
Post-concussive symptoms in children with mild traumatic brain injury. Neuropsychology (2010) 1.32
A genomewide search finds major susceptibility loci for nicotine dependence on chromosome 10 in African Americans. Am J Hum Genet (2006) 1.31
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
Statistical interaction in human genetics: how should we model it if we are looking for biological interaction? Nat Rev Genet (2010) 1.28
Two-level Haseman-Elston regression for general pedigree data analysis. Genet Epidemiol (2005) 1.28
Identification of a major locus for age-related cortical cataract on chromosome 6p12-q12 in the Beaver Dam Eye Study. Proc Natl Acad Sci U S A (2004) 1.27
Hip fracture incidence in nursing home residents and community-dwelling older people, Washington State, 1993-1995. J Am Geriatr Soc (2002) 1.25
The power of independent types of genetic information to detect association in a case-control study design. Genet Epidemiol (2008) 1.24
Outcomes of extremely low birth weight (<1 kg) and extremely low gestational age (<28 weeks) infants with bronchopulmonary dysplasia: effects of practice changes in 2000 to 2003. Pediatrics (2008) 1.24
Risk factors for speech delay of unknown origin in 3-year-old children. Child Dev (2003) 1.24
Adaptive two-stage analysis of genetic association in case-control designs. Hum Hered (2007) 1.23
CYP3A5 and ABCB1 genes influence blood pressure and response to treatment, and their effect is modified by salt. Hypertension (2007) 1.23
The genetic bases of speech sound disorders: evidence from spoken and written language. J Speech Lang Hear Res (2006) 1.22
Variants in the Wilms' tumor gene are associated with focal segmental glomerulosclerosis in the African American population. Physiol Genomics (2005) 1.22
Correlates of lactation in mothers of very low birth weight infants. Pediatrics (2002) 1.22
Single-marker and two-marker association tests for unphased case-control genotype data, with a power comparison. Genet Epidemiol (2010) 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
Linkage of speech sound disorder to reading disability loci. J Child Psychol Psychiatry (2005) 1.21
Long-term neuropsychological outcomes of very low birth weight: associations with early risks for periventricular brain insults. J Int Neuropsychol Soc (2004) 1.21