Common variants in left/right asymmetry genes and pathways are associated with relative hand skillA predominantly neolithic origin for Y-chromosomal DNA variation in North Africa.A 77-kilobase region of chromosome 6p22.2 is associated with dyslexia in families from the United Kingdom and from the United States.PCSK6 is associated with handedness in individuals with dyslexiaDCDC2, KIAA0319 and CMIP are associated with reading-related traitsY-chromosomal insights into the genetic impact of the caste system in IndiaPutative functional alleles of DYX1C1 are not associated with dyslexia susceptibility in a large sample of sibling pairs from the UKA Y chromosomal influence on prostate cancer risk: the multi-ethnic cohort studyAlternative splicing in the dyslexia-associated gene KIAA0319The chromosome 6p22 haplotype associated with dyslexia reduces the expression of KIAA0319, a novel gene involved in neuronal migrationInvestigation of dyslexia and SLI risk variants in reading- and language-impaired subjects.Hierarchical high-throughput SNP genotyping of the human Y chromosome using MALDI-TOF mass spectrometry.Haplotype-specific expression of exon 10 at the human MAPT locus.A common variant associated with dyslexia reduces expression of the KIAA0319 geneIdentification of candidate genes for dyslexia susceptibility on chromosome 18.An allele-specific gene expression assay to test the functional basis of genetic associations.Reading and language disorders: the importance of both quantity and quality.A large AZFc deletion removes DAZ3/DAZ4 and nearby genes from men in Y haplogroup NGenome-wide association analyses of child genotype effects and parent-of-origin effects in specific language impairment.Characterization of a family with rare deletions in CNTNAP5 and DOCK4 suggests novel risk loci for autism and dyslexia.Genome-wide screening for DNA variants associated with reading and language traitsThe genetic relationship between handedness and neurodevelopmental disorders.The dyslexia candidate locus on 2p12 is associated with general cognitive ability and white matter structure.The handedness-associated PCSK6 locus spans an intronic promoter regulating novel transcripts.The genetic lexicon of dyslexia.Association of the KIAA0319 dyslexia susceptibility gene with reading skills in the general population.Analysis of dyslexia candidate genes in the Raine cohort representing the general Australian population.Increased prevalence of sex chromosome aneuploidies in specific language impairment and dyslexiaDissection of genetic associations with language-related traits in population-based cohorts.Copy Number Variation Screen Identifies a Rare De Novo Deletion at Chromosome 15q13.1-13.3 in a Child with Language ImpairmentLack of replication for the myosin-18B association with mathematical ability in independent cohorts.CMIP and ATP2C2 modulate phonological short-term memory in language impairment.A new model organism for studying the catabolism of pyrimidines and purines.The DCDC2 deletion is not a risk factor for dyslexiaGenetic analysis of dyslexia candidate genes in the European cross-linguistic NeuroDys cohort.Advances in Dyslexia Genetics-New Insights Into the Role of Brain Asymmetries.The dyslexia-associated gene KIAA0319 encodes highly N- and O-glycosylated plasma membrane and secreted isoforms.Further evidence for a parent-of-origin effect at the NOP9 locus on language-related phenotypes.Reply to Repping et al.Further evidence that the KIAA0319 gene confers susceptibility to developmental dyslexia.
P50
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Silvia Paracchini
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2000-01-01T00:00:00Z
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