Dense-map genome scan for dyslexia supports loci at 4q13, 16p12, 17q22; suggests novel locus at 7q36. (Q48276055)

10 February 2018

title

Dense-map genome scan for dyslexia supports loci at 4q13, 16p12, 17q22; suggests novel locus at 7q36. (English)

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10 February 2018

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L L Field

1

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10 February 2018

K Shumansky

2

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J Ryan

3

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D Truong

4

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E Swiergala

5

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B J Kaplan

6

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language of work or name

English

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publication date

7 December 2012

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10 February 2018

Genes, Brain and Behavior

published in

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10 February 2018

volume

12

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issue

1

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10 February 2018

page(s)

56-69

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10 February 2018

Handling marker-marker linkage disequilibrium: pedigree analysis with clustered markers

cites work

1 reference

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

21 January 2018

1 reference

Attention-deficit/hyperactivity disorder in a population isolate: linkage to loci at 4q13.2, 5q33.3, 11q22, and 17p11.

21 January 2018

1 reference

A common variant of the latrophilin 3 gene, LPHN3, confers susceptibility to ADHD and predicts effectiveness of stimulant medication

21 January 2018

1 reference

A genomewide screen for autism-spectrum disorders: evidence for a major susceptibility locus on chromosome 3q25-27

21 January 2018

1 reference

Lmo4 and Clim1 progressively delineate cortical projection neuron subtypes during development

21 January 2018

1 reference

A whole-genome scan in 164 Dutch sib pairs with attention-deficit/hyperactivity disorder: suggestive evidence for linkage on chromosomes 7p and 15q.

21 January 2018

1 reference

Replication of reported linkages for dyslexia and spelling and suggestive evidence for novel regions on chromosomes 4 and 17.

21 January 2018

1 reference

Discrimination of speech sounds by children with dyslexia: comparisons with chronological age and reading level controls.

21 January 2018

1 reference

Incorporating language phenotypes strengthens evidence of linkage to autism.

21 January 2018

1 reference

Genome scan of a nonword repetition phenotype in families with dyslexia: evidence for multiple loci

21 January 2018

1 reference

Genome-wide analyses of exonic copy number variants in a family-based study point to novel autism susceptibility genes

21 January 2018

1 reference

A role for PKC in mediating stress-induced prefrontal cortical structural plasticity and cognitive function.

21 January 2018

1 reference

The Engrailed homeobox genes determine the different foliation patterns in the vermis and hemispheres of the mammalian cerebellum

21 January 2018

1 reference

Protein kinase A-dependent phosphorylation of B/K protein

21 January 2018

1 reference

Gender ratios in children with reading disability and their affected relatives: a commentary

21 January 2018

1 reference

Evidence for a genetic aetiology in reading disability of twins.

21 January 2018

1 reference

Screening of human LPHN3 for variants with a potential impact on ADHD susceptibility

21 January 2018

1 reference

Absence of linkage of phonological coding dyslexia to chromosome 6p23-p21.3 in a large family data set.

21 January 2018

1 reference

Independent genome-wide scans identify a chromosome 18 quantitative-trait locus influencing dyslexia.

21 January 2018

1 reference

Deletion of Atoh1 disrupts Sonic Hedgehog signaling in the developing cerebellum and prevents medulloblastoma

21 January 2018

1 reference

Fine mapping of the chromosome 2p12-16 dyslexia susceptibility locus: quantitative association analysis and positional candidate genes SEMA4F and OTX1.

21 January 2018

1 reference

Crossinhibitory activities of Ngn1 and Math1 allow specification of distinct dorsal interneurons

21 January 2018

1 reference

The neurological basis of developmental dyslexia: an overview and working hypothesis

21 January 2018

1 reference

Wide phenotypic variability in families with holoprosencephaly and a sonic hedgehog mutation

21 January 2018

1 reference

A dyslexia susceptibility locus (DYX7) linked to dopamine D4 receptor (DRD4) region on chromosome 11p15.5.

21 January 2018

1 reference

Ignoring linkage disequilibrium among tightly linked markers induces false-positive evidence of linkage for affected sib pair analysis

21 January 2018

1 reference

Mammalian Brain Morphogenesis and Midline Axon Guidance Require Heparan Sulfate

21 January 2018

1 reference

A genomewide screen for autism: strong evidence for linkage to chromosomes 2q, 7q, and 16p.

21 January 2018

1 reference

Attention-Deficit/Hyperactivity Disorder and Comorbid Disruptive Behavior Disorders: Evidence of Pleiotropy and New Susceptibility Loci

21 January 2018

1 reference

ARP3beta, the gene encoding a new human actin-related protein, is alternatively spliced and predominantly expressed in brain neuronal cells.

21 January 2018

1 reference

Regulation of a remote Shh forebrain enhancer by the Six3 homeoprotein

21 January 2018

1 reference

A genome scan for developmental dyslexia confirms linkage to chromosome 2p11 and suggests a new locus on 7q32

21 January 2018

1 reference

Identification of a novel intronic enhancer responsible for the transcriptional regulation of musashi1 in neural stem/progenitor cells.

21 January 2018

1 reference

In vivo Atoh1 targetome reveals how a proneural transcription factor regulates cerebellar development

21 January 2018

1 reference

Allele-sharing models: LOD scores and accurate linkage tests

21 January 2018

1 reference

Genetic dissection of complex traits: guidelines for interpreting and reporting linkage results

21 January 2018

1 reference

A genome-wide search for alleles and haplotypes associated with autism and related pervasive developmental disorders on the Faroe Islands

21 January 2018

1 reference

Effects of stratification in the analysis of affected-sib-pair data: benefits and costs

21 January 2018

1 reference

Potential target genes of EMX2 include Odz/Ten-M and other gene families with implications for cortical patterning

21 January 2018

1 reference

Rare copy number variation discovery and cross-disorder comparisons identify risk genes for ADHD.

21 January 2018

1 reference

A genomewide screen for autism susceptibility loci

21 January 2018

1 reference

Genome-wide scan of reading ability in affected sibling pairs with attention-deficit/hyperactivity disorder: unique and shared genetic effects

21 January 2018

1 reference

SNP sets and reading ability: testing confirmation of a 10-SNP set in a population sample.

21 January 2018

1 reference

Lhx2 selector activity specifies cortical identity and suppresses hippocampal organizer fate.

21 January 2018

1 reference

Structural variation of chromosomes in autism spectrum disorder

21 January 2018

1 reference

Quantitative trait locus association scan of early reading disability and ability using pooled DNA and 100K SNP microarrays in a sample of 5760 children

21 January 2018

1 reference

Disturbances in the secretion of neurotransmitters in IA-2/IA-2beta null mice: changes in behavior, learning and lifespan

21 January 2018

1 reference

Attention deficit hyperactivity disorder: fine mapping supports linkage to 5p13, 6q12, 16p13, and 17p11.

21 January 2018

1 reference

Involvement of fibroblast growth factor (FGF)18-FGF8 signaling in specification of left-right asymmetry and brain and limb development of the chick embryo.

21 January 2018

1 reference

Specific deficits in component reading and language skills: genetic and environmental influences.

21 January 2018

1 reference

Supportive evidence for the DYX3 dyslexia susceptibility gene in Canadian families

21 January 2018

1 reference

Haplotypes in the gene encoding protein kinase c-beta (PRKCB1) on chromosome 16 are associated with autism

21 January 2018

1 reference

PLINK: a tool set for whole-genome association and population-based linkage analyses

21 January 2018

1 reference

Theories of developmental dyslexia: insights from a multiple case study of dyslexic adults

21 January 2018

1 reference

A genome scan in multigenerational families with dyslexia: Identification of a novel locus on chromosome 2q that contributes to phonological decoding efficiency.

21 January 2018

1 reference

Contribution of LPHN3 to the genetic susceptibility to ADHD in adulthood: a replication study.

21 January 2018

1 reference

RNA-binding protein Musashi family: roles for CNS stem cells and a subpopulation of ependymal cells revealed by targeted disruption and antisense ablation

21 January 2018

1 reference

Impairments in phonological processing and nonverbal intellectual function in parents of children with autism.

21 January 2018

1 reference

Family-based studies indicate association of Engrailed 2 gene with autism in an Indian population.

21 January 2018

1 reference

Dyslexia (specific reading disability).

21 January 2018

1 reference

Differential genetic etiology of reading difficulties as a function of IQ: an update

21 January 2018

1 reference

Understanding comorbidity: a twin study of reading disability and attention-deficit/hyperactivity disorder

21 January 2018

1 reference

Developmental and regional expression of heparan sulfate sulfotransferase genes in the mouse brain.

21 January 2018

1 reference

Bivariate linkage scan for reading disability and attention-deficit/hyperactivity disorder localizes pleiotropic loci

21 January 2018

1 reference

Confirmation of a dyslexia susceptibility locus on chromosome 1p34-p36 in a set of 100 Canadian families

21 January 2018

1 reference

21 January 2018

Identifiers

DOI

10.1111/GBB.12003

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10 February 2018

PubMed ID

23190410

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10 February 2018