Published in Genes Brain Behav on April 08, 2015
PLINK: a tool set for whole-genome association and population-based linkage analyses. Am J Hum Genet (2007) 209.92
METAL: fast and efficient meta-analysis of genomewide association scans. Bioinformatics (2010) 21.21
Genome-wide association scan of tag SNPs identifies a susceptibility locus for lung cancer at 15q25.1. Nat Genet (2008) 16.17
Biological insights from 108 schizophrenia-associated genetic loci. Nature (2014) 16.13
A simple correction for multiple testing for single-nucleotide polymorphisms in linkage disequilibrium with each other. Am J Hum Genet (2004) 14.76
Cholinergic nicotinic receptor genes implicated in a nicotine dependence association study targeting 348 candidate genes with 3713 SNPs. Hum Mol Genet (2006) 13.16
Meta-analysis and imputation refines the association of 15q25 with smoking quantity. Nat Genet (2010) 8.55
GWAF: an R package for genome-wide association analyses with family data. Bioinformatics (2009) 3.81
Multiple distinct risk loci for nicotine dependence identified by dense coverage of the complete family of nicotinic receptor subunit (CHRN) genes. Am J Med Genet B Neuropsychiatr Genet (2009) 2.86
Ethnic- and gender-specific association of the nicotinic acetylcholine receptor alpha4 subunit gene (CHRNA4) with nicotine dependence. Hum Mol Genet (2005) 2.80
Relations among speech, language, and reading disorders. Annu Rev Psychol (2009) 2.46
DCDC2 is associated with reading disability and modulates neuronal development in the brain. Proc Natl Acad Sci U S A (2005) 2.35
Genes and the parsing of cognitive processes. Trends Cogn Sci (2004) 1.97
Strong genetic evidence of DCDC2 as a susceptibility gene for dyslexia. Am J Hum Genet (2005) 1.94
Haplotype spanning TTC12 and ANKK1, flanked by the DRD2 and NCAM1 loci, is strongly associated to nicotine dependence in two distinct American populations. Hum Mol Genet (2006) 1.94
Strong evidence that KIAA0319 on chromosome 6p is a susceptibility gene for developmental dyslexia. Am J Hum Genet (2005) 1.93
Variant BDNF (Val66Met) impact on brain structure and function. Cogn Affect Behav Neurosci (2006) 1.85
Investigation of dyslexia and SLI risk variants in reading- and language-impaired subjects. Behav Genet (2010) 1.67
Significant association of BDNF haplotypes in European-American male smokers but not in European-American female or African-American smokers. Am J Med Genet B Neuropsychiatr Genet (2005) 1.55
Association of haplotypic variants in DRD2, ANKK1, TTC12 and NCAM1 to alcohol dependence in independent case control and family samples. Hum Mol Genet (2007) 1.55
Pleiotropic effects of a chromosome 3 locus on speech-sound disorder and reading. Am J Hum Genet (2004) 1.36
Multiple cholinergic nicotinic receptor genes affect nicotine dependence risk in African and European Americans. Genes Brain Behav (2010) 1.35
Evolution of heterogeneity (I2) estimates and their 95% confidence intervals in large meta-analyses. PLoS One (2012) 1.33
Genetic advances in the study of speech and language disorders. Neuron (2010) 1.33
Significant association of ANKK1 and detection of a functional polymorphism with nicotine dependence in an African-American sample. Neuropsychopharmacology (2008) 1.31
DCDC2, KIAA0319 and CMIP are associated with reading-related traits. Biol Psychiatry (2011) 1.29
Genetic variants of FOXP2 and KIAA0319/TTRAP/THEM2 locus are associated with altered brain activation in distinct language-related regions. J Neurosci (2012) 1.28
Genetically determined measures of striatal D2 signaling predict prefrontal activity during working memory performance. PLoS One (2010) 1.24
The genetic bases of speech sound disorders: evidence from spoken and written language. J Speech Lang Hear Res (2006) 1.22
Increased expression of the dyslexia candidate gene DCDC2 affects length and signaling of primary cilia in neurons. PLoS One (2011) 1.22
Linkage of speech sound disorder to reading disability loci. J Child Psychol Psychiatry (2005) 1.21
Resequencing of nicotinic acetylcholine receptor genes and association of common and rare variants with the Fagerström test for nicotine dependence. Neuropsychopharmacology (2010) 1.17
Exploring the transcriptome of ciliated cells using in silico dissection of human tissues. PLoS One (2012) 1.06
Risk gene variants for nicotine dependence in the CHRNA5-CHRNA3-CHRNB4 cluster are associated with cognitive performance. Am J Med Genet B Neuropsychiatr Genet (2010) 1.05
Association of specific haplotypes of neurotrophic tyrosine kinase receptor 2 gene (NTRK2) with vulnerability to nicotine dependence in African-Americans and European-Americans. Biol Psychiatry (2006) 1.05
A dyslexia-associated variant in DCDC2 changes gene expression. Behav Genet (2010) 1.04
Efficient association study design via power-optimized tag SNP selection. Ann Hum Genet (2008) 1.01
The CHRNA5-A3-B4 gene cluster in nicotine addiction. Mol Psychiatry (2011) 1.01
Single nucleotide polymorphisms in ANKK1 and the dopamine D2 receptor gene affect cognitive outcome shortly after traumatic brain injury: a replication and extension study. Brain Inj (2008) 1.01
Perception and awareness of phonemes in phonologically impaired children. Eur J Disord Commun (1992) 1.00
Investigation of the DCDC2 intron 2 deletion/compound short tandem repeat polymorphism in a large German dyslexia sample. Psychiatr Genet (2008) 1.00
A functional polymorphism in the succinate-semialdehyde dehydrogenase (aldehyde dehydrogenase 5 family, member A1) gene is associated with cognitive ability. Mol Psychiatry (2004) 0.99
Follow-up of children with early expressive phonology disorders. J Learn Disabil (2004) 0.98
Reduced visuospatial performance in children with the D2 dopamine receptor A1 allele. Behav Genet (1995) 0.98
The nuclear transcription factor PKNOX2 is a candidate gene for substance dependence in European-origin women. PLoS One (2011) 0.97
Alleles of a polymorphic ETV6 binding site in DCDC2 confer risk of reading and language impairment. Am J Hum Genet (2013) 0.94
BDNF up-regulates alpha7 nicotinic acetylcholine receptor levels on subpopulations of hippocampal interneurons. Mol Cell Neurosci (2006) 0.91
Genetic variant in KIAA0319, but not in DYX1C1, is associated with risk of dyslexia: an integrated meta-analysis. Am J Med Genet B Neuropsychiatr Genet (2012) 0.90
Mapping for dyslexia and related cognitive trait loci provides strong evidence for further risk genes on chromosome 6p21. Am J Med Genet B Neuropsychiatr Genet (2010) 0.90
Glutamate and choline levels predict individual differences in reading ability in emergent readers. J Neurosci (2014) 0.89
Brain-derived neurotrophic factor and trkB signaling in parasympathetic neurons: relevance to regulating alpha7-containing nicotinic receptors and synaptic function. J Neurosci (2004) 0.89
Genetic analysis of dyslexia candidate genes in the European cross-linguistic NeuroDys cohort. Eur J Hum Genet (2013) 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
Postsynaptic action of brain-derived neurotrophic factor attenuates alpha7 nicotinic acetylcholine receptor-mediated responses in hippocampal interneurons. J Neurosci (2008) 0.88
The dyslexia-associated gene DCDC2 is required for spike-timing precision in mouse neocortex. Biol Psychiatry (2013) 0.87
Association between polymorphisms of the dopamine receptor D2 and catechol-o-methyl transferase genes and cognitive function. Behav Genet (2010) 0.87
Literacy outcomes of children with early childhood speech sound disorders: impact of endophenotypes. J Speech Lang Hear Res (2011) 0.87
Characterization of the DYX2 locus on chromosome 6p22 with reading disability, language impairment, and IQ. Hum Genet (2014) 0.87
Variation in the nicotinic acetylcholine receptor gene cluster CHRNA5-CHRNA3-CHRNB4 and its interaction with recent tobacco use influence cognitive flexibility. Neuropsychopharmacology (2010) 0.87
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
Linguistic grammar learning and DRD2-TAQ-IA polymorphism. PLoS One (2013) 0.83
Effect of the TaqIA polymorphism on ethanol response in the brain. Psychiatry Res (2009) 0.82
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
Associations of prenatal nicotine exposure and the dopamine related genes ANKK1 and DRD2 to verbal language. PLoS One (2013) 0.81
Heritability estimation for speech-sound traits with developmental trajectories. Behav Genet (2010) 0.79
Association between AVPR1A, DRD2, and ASPM and endophenotypes of communication disorders. Psychiatr Genet (2014) 0.76
Methods for dietary fiber, neutral detergent fiber, and nonstarch polysaccharides in relation to animal nutrition. J Dairy Sci (1991) 30.74
TAN-1, the human homolog of the Drosophila notch gene, is broken by chromosomal translocations in T lymphoblastic neoplasms. Cell (1991) 10.06
Cloning and structural analysis of cDNAs for bcl-2 and a hybrid bcl-2/immunoglobulin transcript resulting from the t(14;18) translocation. Cell (1986) 7.34
Lipid bilayer thickness varies linearly with acyl chain length in fluid phosphatidylcholine vesicles. J Mol Biol (1983) 6.67
Quantitative trait locus for reading disability on chromosome 6. Science (1994) 6.07
Clinical Pharmacogenetics Implementation Consortium guidelines for thiopurine methyltransferase genotype and thiopurine dosing. Clin Pharmacol Ther (2011) 5.44
Chromosomal translocation t(1;19) results in synthesis of a homeobox fusion mRNA that codes for a potential chimeric transcription factor. Cell (1990) 4.60
Clinical Pharmacogenetics Implementation Consortium Guidelines for CYP2C9 and VKORC1 genotypes and warfarin dosing. Clin Pharmacol Ther (2011) 4.42
Diagnosis of chronic myeloid and acute lymphocytic leukemias by detection of leukemia-specific mRNA sequences amplified in vitro. Proc Natl Acad Sci U S A (1988) 4.40
Characterization of the cytoplasm of Escherichia coli K-12 as a function of external osmolarity. Implications for protein-DNA interactions in vivo. J Mol Biol (1991) 3.73
Monoclonal antibody and enzymatic profiles of human malignant T-lymphoid cells and derived cell lines. Cancer Res (1984) 3.67
Homozygous deletion of the alpha- and beta 1-interferon genes in human leukemia and derived cell lines. Proc Natl Acad Sci U S A (1988) 3.67
Clinical Pharmacogenetics Implementation Consortium guidelines for cytochrome P450-2C19 (CYP2C19) genotype and clopidogrel therapy. Clin Pharmacol Ther (2011) 3.53
Attenuation of isoproterenol-mediated vasodilatation in blacks. N Engl J Med (1995) 3.25
Identification of a gene, MLL, that spans the breakpoint in 11q23 translocations associated with human leukemias. Proc Natl Acad Sci U S A (1991) 3.25
Executive function deficits in high-functioning autistic individuals: relationship to theory of mind. J Child Psychol Psychiatry (1991) 3.18
Molecular basis of ethnic differences in drug disposition and response. Annu Rev Pharmacol Toxicol (2001) 2.86
lyl-1, a novel gene altered by chromosomal translocation in T cell leukemia, codes for a protein with a helix-loop-helix DNA binding motif. Cell (1989) 2.84
The effect of common polymorphisms of the beta2-adrenergic receptor on agonist-mediated vascular desensitization. N Engl J Med (2001) 2.74
Clinical Pharmacogenetics Implementation Consortium guidelines for CYP2C19 genotype and clopidogrel therapy: 2013 update. Clin Pharmacol Ther (2013) 2.73
Novel mutations in the connexin 26 gene (GJB2) that cause autosomal recessive (DFNB1) hearing loss. Am J Hum Genet (1998) 2.51
Origins of the osmoprotective properties of betaine and proline in Escherichia coli K-12. J Bacteriol (1992) 2.34
LAI inversion algorithm based on directional reflectance kernels. J Environ Manage (2006) 2.31
Quantitative-trait locus for specific language and reading deficits on chromosome 6p. Am J Hum Genet (1999) 2.26
Integration of genetic, clinical, and INR data to refine warfarin dosing. Clin Pharmacol Ther (2010) 2.21
Fusion of the leucine zipper gene HLF to the E2A gene in human acute B-lineage leukemia. Science (1992) 2.19
TUNEL-positive ganglion cells in human primary open-angle glaucoma. Arch Ophthalmol (1997) 2.11
Bacteriorhodopsin remains dispersed in fluid phospholipid bilayers over a wide range of bilayer thicknesses. J Mol Biol (1983) 2.07
Linkage of autosomal dominant hearing loss to the short arm of chromosome 1 in two families. N Engl J Med (1994) 2.03
Differential phosphorylation and localization of the transcription factor UBF in vivo in response to serum deprivation. In vitro dephosphorylation of UBF reduces its transactivation properties. J Biol Chem (1992) 2.02
The percentage of consonants correct (PCC) metric: extensions and reliability data. J Speech Lang Hear Res (1997) 2.01
Inhibition of P-glycoprotein-mediated drug transport: A unifying mechanism to explain the interaction between digoxin and quinidine [seecomments]. Circulation (1999) 2.01
Intact and impaired memory functions in autism. Child Dev (1996) 2.00
A reliable method for evaluating drug compliance in children with cancer. Cancer (1979) 2.00
Clinical pharmacogenetics implementation consortium guidelines for thiopurine methyltransferase genotype and thiopurine dosing: 2013 update. Clin Pharmacol Ther (2013) 1.99
Common region on chromosome 14 in T-cell leukemia and lymphoma. Science (1984) 1.98
A comparison of the neuropsychological profiles of the DSM-IV subtypes of ADHD. J Abnorm Child Psychol (2001) 1.97
Understanding of others' intentions in children with autism. J Autism Dev Disord (2001) 1.94
Specific reading disability: identification of an inherited form through linkage analysis. Science (1983) 1.94
Comorbidity of reading disability and attention-deficit/hyperactivity disorder: differences by gender and subtype. J Learn Disabil (2004) 1.92
Genetic influences on learning disabilities and speech and language disorders. Child Dev (1983) 1.90
A comparison of the cognitive deficits in reading disability and attention-deficit/hyperactivity disorder. J Abnorm Psychol (2001) 1.88
Fusion of an immunoglobulin variable gene and a T cell receptor constant gene in the chromosome 14 inversion associated with T cell tumors. Cell (1985) 1.87
Drug-induced haemolysis masquerading as blackwater fever. Cent Afr J Med (1987) 1.82
Analysis of the phosphorylation, DNA-binding and dimerization properties of the RNA polymerase I transcription factors UBF1 and UBF2. Nucleic Acids Res (1992) 1.69
Psychiatric comorbidity in children and adolescents with reading disability. J Child Psychol Psychiatry (2000) 1.66
Spelling errors and reading fluency in compensated adult dyslexics. Ann Dyslexia (1991) 1.66
Executive function and social communication deficits in young autistic children. J Child Psychol Psychiatry (1993) 1.60
Changing patterns of medication use in patients with rheumatoid arthritis in a Medicaid population. Rheumatology (Oxford) (2008) 1.59
Identification and functional characterization of a new CYP2C9 variant (CYP2C9*5) expressed among African Americans. Mol Pharmacol (2001) 1.59
Expression of a distinctive BCR-ABL oncogene in Ph1-positive acute lymphocytic leukemia (ALL). Science (1988) 1.59
Imitation and pantomime in high-functioning adolescents with autism spectrum disorders. Child Dev (1996) 1.58
A long-term dose-response study of mitomycin in glaucoma filtration surgery. Arch Ophthalmol (1997) 1.58
Phenotypic involvement in females with the FMR1 gene mutation. Am J Ment Retard (1998) 1.58
Asperger's syndrome: evidence of an empirical distinction from high-functioning autism. J Child Psychol Psychiatry (1991) 1.57
Heterogeneity of genomic fusion of BCR and ABL in Philadelphia chromosome-positive acute lymphoblastic leukemia. Proc Natl Acad Sci U S A (1988) 1.56
A chromosome 14 inversion in a T-cell lymphoma is caused by site-specific recombination between immunoglobulin and T-cell receptor loci. Nature (1986) 1.55
Ahmed glaucoma valve implant vs trabeculectomy in the surgical treatment of glaucoma: a randomized clinical trial. Am J Ophthalmol (2000) 1.54
Mutations in the KCNQ4 gene are responsible for autosomal dominant deafness in four DFNA2 families. Hum Mol Genet (1999) 1.54
Pair distribution functions of bacteriorhodopsin and rhodopsin in model bilayers. Biophys J (1983) 1.54
A randomized double-blind trial of oral L-arginine for treatment of interstitial cystitis. J Urol (1999) 1.53
NMR structural analysis of a membrane protein: bacteriorhodopsin peptide backbone orientation and motion. Biochemistry (1985) 1.53
Prospective results of a standardized algorithm based on hemodynamic status for managing pediatric solid organ injury. J Am Coll Surg (2001) 1.50
Atherosclerosis in rheumatoid arthritis and systemic lupus erythematosus. Clin Exp Rheumatol (2008) 1.46
Executive functions in young children with autism. Child Dev (1999) 1.45
Treatment of CNS relapse in children with acute lymphoblastic leukemia: A Pediatric Oncology Group study. J Clin Oncol (1993) 1.45
A new fused transcript in Philadelphia chromosome positive acute lymphocytic leukaemia. Nature (1987) 1.42
Human gamma-aminobutyric acid B receptor gene: complementary DNA cloning, expression, chromosomal location, and genomic organization. Biol Psychiatry (1998) 1.42
CYP3A activity in African American and European American men: population differences and functional effect of the CYP3A4*1B5'-promoter region polymorphism. Clin Pharmacol Ther (2000) 1.42
Novel cardiovascular risk prediction models in patients with systemic lupus erythematosus. Lupus (2011) 1.41
rUBF, an RNA polymerase I transcription factor from rats, produces DNase I footprints identical to those produced by xUBF, its homolog from frogs. Mol Cell Biol (1990) 1.41
The gene for enhancer binding proteins E12/E47 lies at the t(1;19) breakpoint in acute leukemias. Science (1989) 1.41
Educational program for physicians to reduce use of non-steroidal anti-inflammatory drugs among community-dwelling elderly persons: a randomized controlled trial. Med Care (2001) 1.41
The sodium-retaining effect of renal nerve activity in the cat: role of angiotensin formation. Clin Sci Mol Med (1976) 1.41
Bacterial infection induces nitric oxide synthase in human neutrophils. J Clin Invest (1997) 1.40
Obtaining an accepted Investigational New Drug application to operate an umbilical cord blood bank. Transfusion (1999) 1.39
Testicular temperatures measured by thermistor probe and contact thermography. Fertil Steril (1990) 1.39
Quantitative trait locus for reading disability: correction. Science (1995) 1.37
Twin study of the etiology of comorbidity between reading disability and attention-deficit/hyperactivity disorder. Am J Med Genet (2000) 1.36
Phonological processing skills and deficits in adult dyslexics. Child Dev (1990) 1.35
A common beta1-adrenergic receptor polymorphism (Arg389Gly) affects blood pressure response to beta-blockade. Clin Pharmacol Ther (2003) 1.34
Hypoxia limits differentiation and up-regulates expression and activity of prostaglandin H synthase 2 in cultured trophoblast from term human placenta. Am J Obstet Gynecol (1999) 1.33
Allelic, genotypic and phenotypic distributions of S-mephenytoin 4'-hydroxylase (CYP2C19) in healthy Caucasian populations of European descent throughout the world. Pharmacogenetics (1999) 1.33
ACR 20: clinical or statistical significance? Arthritis Rheum (1999) 1.32
Evidence for linkage and association with reading disability on 6p21.3-22. Am J Hum Genet (2002) 1.31
Haplotype analysis of hemochromatosis: evaluation of different linkage-disequilibrium approaches and evolution of disease chromosomes. Am J Hum Genet (1997) 1.31
Separation and characterization of the soluble and insoluble components of insoluble laminaran. Carbohydr Res (1974) 1.31
Word identification in reading and the promise of subsymbolic psycholinguistics. Psychol Rev (1990) 1.31
Neuropsychology of early-treated phenylketonuria: specific executive function deficits. Child Dev (1990) 1.31
Are there emotion perception deficits in young autistic children? J Child Psychol Psychiatry (1990) 1.29
Application of a new leaf area index algorithm to China's landmass using MODIS data for carbon cycle research. J Environ Manage (2006) 1.29
Arg389Gly beta 1-adrenoceptor polymorphism varies in frequency among different ethnic groups but does not alter response in vivo. Pharmacogenetics (2001) 1.28