Evidence for linkage and association with reading disability on 6p21.3-22. - Wikidata - wikimedia - TriplyDB

Evidence for linkage and association with reading disability on 6p21.3-22.

Evidence for linkage and association with reading disability on 6p21.3-22.

http://www.wikidata.org/entity/Q35764638

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A transcription map of the 6p22.3 reading disability locus identifying candidate genes Genetics of dyslexia: the evolving landscape DCDC2 is associated with reading disability and modulates neuronal development in the brain.Strong evidence that KIAA0319 on chromosome 6p is a susceptibility gene for developmental dyslexia.A 77-kilobase region of chromosome 6p22.2 is associated with dyslexia in families from the United Kingdom and from the United States.Strong genetic evidence of DCDC2 as a susceptibility gene for dyslexia.Dyslexia and DCDC2: normal variation in reading and spelling is associated with DCDC2 polymorphisms in an Australian population sample DCDC2, KIAA0319 and CMIP are associated with reading-related traits DCDC2 genetic variants and susceptibility to developmental dyslexia Opposite Associations between Individual KIAA0319 Polymorphisms and Developmental Dyslexia Risk across Populations: A Stratified Meta-Analysis by the Study Population.Dyslexia and language impairment associated genetic markers influence cortical thickness and white matter in typically developing children Association of short-term memory with a variant within DYX1C1 in developmental dyslexia Imaging-genetics in dyslexia: connecting risk genetic variants to brain neuroimaging and ultimately to reading impairments.The genetics of reading disabilities: from phenotypes to candidate genes Progress towards a cellular neurobiology of reading disability.Characterization of the DYX2 locus on chromosome 6p22 with reading disability, language impairment, and IQ Genetic variation in the KIAA0319 5' region as a possible contributor to dyslexia Reading and language disorders: the importance of both quantity and quality.Pleiotropic effects of a chromosome 3 locus on speech-sound disorder and reading.Highly significant linkage to the SLI1 locus in an expanded sample of individuals affected by specific language impairment.A genomewide scan for intelligence identifies quantitative trait loci on 2q and 6p.A theoretical molecular network for dyslexia: integrating available genetic findings.Dyslexia: nature and nurture.Attentional gating in primary visual cortex: a physiological basis for dyslexia.The genetics of developmental dyslexia.Replication of reported linkages for dyslexia and spelling and suggestive evidence for novel regions on chromosomes 4 and 17.In search of the perfect phenotype: an analysis of linkage and association studies of reading and reading-related processes.Analysis of dyslexia candidate genes in the Raine cohort representing the general Australian population.Developmental dyslexia: genetic dissection of a complex cognitive trait.Pleiotropic functions of EAPII/TTRAP/TDP2: cancer development, chemoresistance and beyond Motor sequencing deficit as an endophenotype of speech sound disorder: a genome-wide linkage analysis in a multigenerational family.Mutation in CEP63 co-segregating with developmental dyslexia in a Swedish family Genomewide scan for real-word reading subphenotypes of dyslexia: novel chromosome 13 locus and genetic complexity.A whole-genome scan and fine-mapping linkage study of auditory-visual synesthesia reveals evidence of linkage to chromosomes 2q24, 5q33, 6p12, and 12p12 KIAA0319 gene polymorphisms are associated with developmental dyslexia in Chinese Uyghur children.DCDC2 gene polymorphisms are associated with developmental dyslexia in Chinese Uyghur children.Molecular genetics of dyslexia: an overview.An examination of candidate gene SNPs for dyslexia in an Indian sample.Approach to epigenetic analysis in language disorders CTNND2-a candidate gene for reading problems and mild intellectual disability.

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P2860

Evidence for linkage and association with reading disability on 6p21.3-22.

http://www.wikidata.org/entity/Q35764638

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Evidence for linkage and association with reading disability on 6p21.3-22.

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Evidence for linkage and association with reading disability on 6p21.3-22.

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Evidence for linkage and association with reading disability on 6p21.3-22.

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Evidence for linkage and association with reading disability on 6p21.3-22.

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Evidence for linkage and association with reading disability on 6p21.3-22.

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American Journal of Human Genetics

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Evidence for linkage and association with reading disability on 6p21.3-22.

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D E Kaplan

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F Wood

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P2860

A frameshift mutation in NOD2 associated with susceptibility to Crohn's disease

Chromosome 6p influences on different dyslexia-related cognitive processes: further confirmation

Quantitative-trait locus for specific language and reading deficits on chromosome 6p

Transmission test for linkage disequilibrium: the insulin gene region and insulin-dependent diabetes mellitus (IDDM)

Susceptibility loci for distinct components of developmental dyslexia on chromosomes 6 and 15

Functional disruption in the organization of the brain for reading in dyslexia

A new gene (DYX3) for dyslexia is located on chromosome 2

Association of NOD2 leucine-rich repeat variants with susceptibility to Crohn's disease

Merlin--rapid analysis of dense genetic maps using sparse gene flow trees

Quantitative trait locus for reading disability on chromosome 6

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