Published in Am J Med Genet B Neuropsychiatr Genet on August 15, 2003
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
Inter-relationships among behavioral markers, genes, brain and treatment in dyslexia and dysgraphia. Future Neurol (2010) 1.26
The genetics of reading disabilities: from phenotypes to candidate genes. Front Psychol (2013) 1.12
Linkage analyses of chromosomal region 18p11-q12 in dyslexia. J Neural Transm (Vienna) (2005) 0.89
Genome scan for spelling deficits: effects of verbal IQ on models of transmission and trait gene localization. Behav Genet (2010) 0.88
In search of the perfect phenotype: an analysis of linkage and association studies of reading and reading-related processes. Behav Genet (2011) 0.87
Genome scan for cognitive trait loci of dyslexia: Rapid naming and rapid switching of letters, numbers, and colors. Am J Med Genet B Neuropsychiatr Genet (2014) 0.83
Global processing speed in children with low reading ability and in children and adults with typical reading ability: exploratory factor analytic models. J Speech Lang Hear Res (2010) 0.82
Etiologies and molecular mechanisms of communication disorders. J Dev Behav Pediatr (2010) 0.81
Replicating genotype-phenotype associations. Nature (2007) 16.11
Functional impact of global rare copy number variation in autism spectrum disorders. Nature (2010) 14.66
Mapping autism risk loci using genetic linkage and chromosomal rearrangements. Nat Genet (2007) 14.05
Genetic relationship between five psychiatric disorders estimated from genome-wide SNPs. Nat Genet (2013) 8.02
Actionable, pathogenic incidental findings in 1,000 participants' exomes. Am J Hum Genet (2013) 4.06
A putative RUNX1 binding site variant between SLC9A3R1 and NAT9 is associated with susceptibility to psoriasis. Nat Genet (2003) 3.52
A genome-wide scan for common alleles affecting risk for autism. Hum Mol Genet (2010) 3.42
Case-control association testing in the presence of unknown relationships. Genet Epidemiol (2009) 2.63
Individual common variants exert weak effects on the risk for autism spectrum disorderspi. Hum Mol Genet (2012) 2.46
Relative burden of large CNVs on a range of neurodevelopmental phenotypes. PLoS Genet (2011) 2.46
Relationship inference from trios of individuals, in the presence of typing error. Am J Hum Genet (2001) 2.32
Identification of a novel gene on chromosome 7q11.2 interrupted by a translocation breakpoint in a pair of autistic twins. Genomics (2002) 2.16
Integrative analysis of RUNX1 downstream pathways and target genes. BMC Genomics (2008) 2.14
Genetic variation at the 22q11 PRODH2/DGCR6 locus presents an unusual pattern and increases susceptibility to schizophrenia. Proc Natl Acad Sci U S A (2002) 1.92
Comparison of multipoint linkage analyses for quantitative traits in the CEPH data: parametric LOD scores, variance components LOD scores, and Bayes factors. BMC Proc (2007) 1.84
Presence of alanine-to-valine substitutions in myofibrillogenesis regulator 1 in paroxysmal nonkinesigenic dyskinesia: confirmation in 2 kindreds. Arch Neurol (2005) 1.78
Comprehensive analysis of APOE and selected proximate markers for late-onset Alzheimer's disease: patterns of linkage disequilibrium and disease/marker association. Genomics (2007) 1.78
Anatomical correlates of dyslexia: frontal and cerebellar findings. Brain (2003) 1.64
Converging evidence for triple word form theory in children with dyslexia. Dev Neuropsychol (2006) 1.57
Genetic investigation of quantitative traits related to autism: use of multivariate polygenic models with ascertainment adjustment. Am J Hum Genet (2004) 1.51
Presence of large deletions in kindreds with autism. Am J Hum Genet (2002) 1.47
Gain-of-function ADCY5 mutations in familial dyskinesia with facial myokymia. Ann Neurol (2014) 1.47
Autosomal dominant familial dyskinesia and facial myokymia: single exome sequencing identifies a mutation in adenylyl cyclase 5. Arch Neurol (2012) 1.46
The N141I mutation in PSEN2: implications for the quintessential case of Alzheimer disease. Arch Neurol (2010) 1.46
Characteristics of genetic markers and maps for cost-effective genome screens using diallelic markers. Genet Epidemiol (2002) 1.44
A novel approach of homozygous haplotype sharing identifies candidate genes in autism spectrum disorder. Hum Genet (2011) 1.43
X-linked thrombocytopenia with thalassemia from a mutation in the amino finger of GATA-1 affecting DNA binding rather than FOG-1 interaction. Blood (2002) 1.41
Missense mutations in the regulatory domain of PKC gamma: a new mechanism for dominant nonepisodic cerebellar ataxia. Am J Hum Genet (2003) 1.36
Predicting response to early reading intervention from verbal IQ, reading-related language abilities, attention ratings, and verbal IQ-word reading discrepancy: failure to validate discrepancy method. J Learn Disabil (2004) 1.33
A score for Bayesian genome screening. Genet Epidemiol (2003) 1.33
Human phenotypes associated with GATA-1 mutations. Gene (2008) 1.24
The effect of algorithms on copy number variant detection. PLoS One (2010) 1.23
Executive functions in becoming writing readers and reading writers: note taking and report writing in third and fifth graders. Dev Neuropsychol (2006) 1.22
Evaluation of candidate genes for DYX1 and DYX2 in families with dyslexia. Am J Med Genet B Neuropsychiatr Genet (2007) 1.21
IFRD1 is a candidate gene for SMNA on chromosome 7q22-q23. Am J Hum Genet (2009) 1.21
GIGI: an approach to effective imputation of dense genotypes on large pedigrees. Am J Hum Genet (2013) 1.15
Executive functions for reading and writing in typical literacy development and dyslexia. J Clin Exp Neuropsychol (2008) 1.15
Replication of CNTNAP2 association with nonword repetition and support for FOXP2 association with timed reading and motor activities in a dyslexia family sample. J Neurodev Disord (2010) 1.13
Two sites in the MAPT region confer genetic risk for Guam ALS/PDC and dementia. Hum Mol Genet (2006) 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
The genetics of reading disabilities: from phenotypes to candidate genes. Front Psychol (2013) 1.12
Spinocerebellar ataxia type 14 caused by a mutation in protein kinase C gamma. Arch Neurol (2003) 1.08
Comparison of single-nucleotide polymorphisms and microsatellite markers for linkage analysis in the COGA and simulated data sets for Genetic Analysis Workshop 14: Presentation Groups 1, 2, and 3. Genet Epidemiol (2005) 1.07
Low-frequency signal changes reflect differences in functional connectivity between good readers and dyslexics during continuous phoneme mapping. Magn Reson Imaging (2006) 1.02
Abnormal fMRI Connectivity in Children with Dyslexia During a Phoneme Task: Before But Not After Treatment . J Neurolinguistics (2008) 1.01
Comparison of marker types and map assumptions using Markov chain Monte Carlo-based linkage analysis of COGA data. BMC Genet (2005) 1.01
A common VLDLR polymorphism interacts with APOE genotype in the prediction of carotid artery disease risk. J Lipid Res (2007) 0.99
Empirical significance values for linkage analysis: trait simulation using posterior model distributions from MCMC oligogenic segregation analysis. Genet Epidemiol (2008) 0.99
Identifying and predicting classes of response to explicit phonological spelling instruction during independent composing. J Learn Disabil (2008) 0.99
Reproducibility of proton MR spectroscopic imaging (PEPSI): comparison of dyslexic and normal-reading children and effects of treatment on brain lactate levels during language tasks. AJNR Am J Neuroradiol (2002) 0.99
Power of family-based association designs to detect rare variants in large pedigrees using imputed genotypes. Genet Epidemiol (2013) 0.98
MCMC-based linkage analysis for complex traits on general pedigrees: multipoint analysis with a two-locus model and a polygenic component. Genet Epidemiol (2007) 0.97
Genomewide scan for real-word reading subphenotypes of dyslexia: novel chromosome 13 locus and genetic complexity. Am J Med Genet B Neuropsychiatr Genet (2006) 0.96
Low-density lipoprotein particle size loci in familial combined hyperlipidemia: evidence for multiple loci from a genome scan. Arterioscler Thromb Vasc Biol (2004) 0.96
Genome-scan for IQ discrepancy in autism: evidence for loci on chromosomes 10 and 16. Hum Genet (2010) 0.96
Low clusterin levels in high-density lipoprotein associate with insulin resistance, obesity, and dyslipoproteinemia. Arterioscler Thromb Vasc Biol (2010) 0.96
Altered splicing of ATP6AP2 causes X-linked parkinsonism with spasticity (XPDS). Hum Mol Genet (2013) 0.95
Evidence of linkage of HDL level variation to APOC3 in two samples with different ascertainment. Hum Genet (2003) 0.95
A novel mutation in FHL1 in a family with X-linked scapuloperoneal myopathy: phenotypic spectrum and structural study of FHL1 mutations. J Neurol Sci (2010) 0.94
Combining family- and population-based imputation data for association analysis of rare and common variants in large pedigrees. Genet Epidemiol (2014) 0.93
Sensorineural deafness, distinctive facial features, and abnormal cranial bones: a new variant of Waardenburg syndrome? Am J Med Genet A (2008) 0.93
Identification of genetic loci underlying the phenotypic constructs of autism spectrum disorders. J Am Acad Child Adolesc Psychiatry (2011) 0.92
Genome scan for quantitative trait loci influencing HDL levels: evidence for multilocus inheritance in familial combined hyperlipidemia. Hum Genet (2005) 0.92
Effects of prior attention training on child dyslexics' response to composition instruction. Dev Neuropsychol (2006) 0.92
Estimation and visualization of identity-by-descent within pedigrees simplifies interpretation of complex trait analysis. Hum Hered (2011) 0.92
Identification of novel susceptibility loci for Guam neurodegenerative disease: challenges of genome scans in genetic isolates. Hum Mol Genet (2009) 0.91
Linkage and association of phospholipid transfer protein activity to LASS4. J Lipid Res (2011) 0.91
Extended intermarker linkage disequilibrium in the Afrikaners. Genome Res (2002) 0.91
Genome scan of a nonword repetition phenotype in families with dyslexia: evidence for multiple loci. Behav Genet (2008) 0.90
Evidence for three loci modifying age-at-onset of Alzheimer's disease in early-onset PSEN2 families. Am J Med Genet B Neuropsychiatr Genet (2010) 0.90
Functional magnetic resonance imaging sequential-finger movement activation differentiating good and poor writers. J Clin Exp Neuropsychol (2009) 0.89
MCMC multilocus lod scores: application of a new approach. Hum Hered (2005) 0.89
Genetic Analysis Workshop 15: gene expression analysis and approaches to detecting multiple functional loci. BMC Proc (2007) 0.89
Linguistic pattern analysis of misspellings of typically developing writers in grades 1-9. J Speech Lang Hear Res (2012) 0.89
Motor sequencing deficit as an endophenotype of speech sound disorder: a genome-wide linkage analysis in a multigenerational family. Psychiatr Genet (2012) 0.88
Deficits in sequential processing manifest in motor and linguistic tasks in a multigenerational family with childhood apraxia of speech. Clin Linguist Phon (2013) 0.88
Genome scan for spelling deficits: effects of verbal IQ on models of transmission and trait gene localization. Behav Genet (2010) 0.88
Oligogenic segregation analysis of hereditary prostate cancer pedigrees: evidence for multiple loci affecting age at onset. Int J Cancer (2003) 0.87
Joint linkage and association analysis with exome sequence data implicates SLC25A40 in hypertriglyceridemia. Am J Hum Genet (2013) 0.87
Contrasting identity-by-descent estimators, association studies, and linkage analyses using the Framingham Heart Study data. BMC Proc (2009) 0.87
Genetic and nongenetic sources of variation in phospholipid transfer protein activity. J Lipid Res (2009) 0.87
Two novel mutations in ABHD12: expansion of the mutation spectrum in PHARC and assessment of their functional effects. Hum Mutat (2013) 0.86
Dimensions of good and poor handwriting legibility in first and second graders: motor programs, visual-spatial arrangement, and letter formation parameter setting. Dev Neuropsychol (2006) 0.86
Familial aggregation of dyslexia phenotypes. II: paired correlated measures. Am J Med Genet (2002) 0.85