Neurobiology and neurogenetics of dyslexia (Q58227231)

https://api.crossref.org/works/10.1016%2FS2173-5808%2820%2970105-7

7 January 2021

Dyslexia (specific reading disability).

1 reference

https://api.crossref.org/works/10.1016%2FS2173-5808%2820%2970105-7

7 January 2021

The education of dyslexic children from childhood to young adulthood

1 reference

https://api.crossref.org/works/10.1016%2FS2173-5808%2820%2970105-7

7 January 2021

Reading disabilities: the case of Chinese, Japanese, and English

1 reference

https://api.crossref.org/works/10.1016%2FS2173-5808%2820%2970105-7

7 January 2021

Evidence That Dyslexia May Represent the Lower Tail of a Normal Distribution of Reading Ability

1 reference

https://api.crossref.org/works/10.1016%2FS2173-5808%2820%2970105-7

7 January 2021

Genes, brain, and cognition: a roadmap for the cognitive scientist

1 reference

https://api.crossref.org/works/10.1016%2FS2173-5808%2820%2970105-7

7 January 2021

The genetic lexicon of dyslexia

1 reference

https://api.crossref.org/works/10.1016%2FS2173-5808%2820%2970105-7

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS2173-5808%2820%2970105-7

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS2173-5808%2820%2970105-7

7 January 2021

Disruption of the neural response to rapid acoustic stimuli in dyslexia: evidence from functional MRI

1 reference

https://api.crossref.org/works/10.1016%2FS2173-5808%2820%2970105-7

7 January 2021

Specific reading disability: differences in contrast sensitivity as a function of spatial frequency.

1 reference

https://api.crossref.org/works/10.1016%2FS2173-5808%2820%2970105-7

7 January 2021

https://api.crossref.org/works/10.1016%2FS2173-5808%2820%2970105-7

1 reference

7 January 2021

Lobular Patterns of Cerebellar Activation in Verbal Working-Memory and Finger-Tapping Tasks as Revealed by Functional MRI

1 reference

https://api.crossref.org/works/10.1016%2FS2173-5808%2820%2970105-7

7 January 2021

Physiological and anatomical evidence for a magnocellular defect in developmental dyslexia

1 reference

https://api.crossref.org/works/10.1016%2FS2173-5808%2820%2970105-7

7 January 2021

To see but not to read; the magnocellular theory of dyslexia

1 reference

https://api.crossref.org/works/10.1016%2FS2173-5808%2820%2970105-7

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS2173-5808%2820%2970105-7

7 January 2021

Functional connectivity of the angular gyrus in normal reading and dyslexia

1 reference

https://api.crossref.org/works/10.1016%2FS2173-5808%2820%2970105-7

7 January 2021

Disruption of posterior brain systems for reading in children with developmental dyslexia

1 reference

https://api.crossref.org/works/10.1016%2FS2173-5808%2820%2970105-7

7 January 2021

Language-specific tuning of visual cortex? Functional properties of the Visual Word Form Area

1 reference

https://api.crossref.org/works/10.1016%2FS2173-5808%2820%2970105-7

7 January 2021

The visual word form area: expertise for reading in the fusiform gyrus

1 reference

https://api.crossref.org/works/10.1016%2FS2173-5808%2820%2970105-7

7 January 2021

Development of neural systems for reading

1 reference

https://api.crossref.org/works/10.1016%2FS2173-5808%2820%2970105-7

7 January 2021

Neurobiological studies of reading and reading disability

1 reference

https://api.crossref.org/works/10.1016%2FS2173-5808%2820%2970105-7

7 January 2021

The relation of phoneme discrimination, lexical access, and short-term memory: A case study and interactive activation account

1 reference

https://api.crossref.org/works/10.1016%2FS2173-5808%2820%2970105-7

7 January 2021

Neuroimaging studies of the cerebellum: language, learning and memory

1 reference

https://api.crossref.org/works/10.1016%2FS2173-5808%2820%2970105-7

7 January 2021

Developmental dyslexia: four consecutive patients with cortical anomalies

1 reference

https://api.crossref.org/works/10.1016%2FS2173-5808%2820%2970105-7

7 January 2021

Developmental dyslexia in women: neuropathological findings in three patients

1 reference

https://api.crossref.org/works/10.1016%2FS2173-5808%2820%2970105-7

7 January 2021

Cytoarchitectonic abnormalities in developmental dyslexia: A case study

1 reference

https://api.crossref.org/works/10.1016%2FS2173-5808%2820%2970105-7

7 January 2021

Reading impairment in the neuronal migration disorder of periventricular nodular heterotopia

1 reference

https://api.crossref.org/works/10.1016%2FS2173-5808%2820%2970105-7

7 January 2021

Microstructure of temporo-parietal white matter as a basis for reading ability: evidence from diffusion tensor magnetic resonance imaging

1 reference

https://api.crossref.org/works/10.1016%2FS2173-5808%2820%2970105-7

7 January 2021

Children's reading performance is correlated with white matter structure measured by diffusion tensor imaging

1 reference

https://api.crossref.org/works/10.1016%2FS2173-5808%2820%2970105-7

7 January 2021

When all hypotheses are right: a multifocal account of dyslexia.

1 reference

https://api.crossref.org/works/10.1016%2FS2173-5808%2820%2970105-7

7 January 2021

Developmental dyslexia

1 reference

https://api.crossref.org/works/10.1016%2FS2173-5808%2820%2970105-7

7 January 2021

Neuroanatomical markers for dyslexia: a review of dyslexia structural imaging studies

1 reference

https://api.crossref.org/works/10.1016%2FS2173-5808%2820%2970105-7

7 January 2021

Dyslexia: cultural diversity and biological unity

1 reference

https://api.crossref.org/works/10.1016%2FS2173-5808%2820%2970105-7

7 January 2021

A meta-analysis of functional neuroimaging studies of dyslexia.

1 reference

https://api.crossref.org/works/10.1016%2FS2173-5808%2820%2970105-7

7 January 2021

Effective brain connectivity in children with reading difficulties during phonological processing

1 reference

https://api.crossref.org/works/10.1016%2FS2173-5808%2820%2970105-7

7 January 2021

Neural systems for compensation and persistence: young adult outcome of childhood reading disability

1 reference

https://api.crossref.org/works/10.1016%2FS2173-5808%2820%2970105-7

7 January 2021

Subliminal convergence of Kanji and Kana words: further evidence for functional parcellation of the posterior temporal cortex in visual word perception

1 reference

https://api.crossref.org/works/10.1016%2FS2173-5808%2820%2970105-7

7 January 2021

A structural-functional basis for dyslexia in the cortex of Chinese readers

1 reference

https://api.crossref.org/works/10.1016%2FS2173-5808%2820%2970105-7

7 January 2021

The genetic basis of dyslexia

1 reference

https://api.crossref.org/works/10.1016%2FS2173-5808%2820%2970105-7

7 January 2021

Neural deficits in children with dyslexia ameliorated by behavioral remediation: evidence from functional MRI.

1 reference

https://api.crossref.org/works/10.1016%2FS2173-5808%2820%2970105-7

7 January 2021

Temporal processing deficits of language-learning impaired children ameliorated by training

1 reference

https://api.crossref.org/works/10.1016%2FS2173-5808%2820%2970105-7

7 January 2021

Language comprehension in language-learning impaired children improved with acoustically modified speech

1 reference

https://api.crossref.org/works/10.1016%2FS2173-5808%2820%2970105-7

7 January 2021

Psychiatric endophenotypes and the development of valid animal models.

1 reference

https://api.crossref.org/works/10.1016%2FS2173-5808%2820%2970105-7

7 January 2021

Evidence for a genetic aetiology in reading disability of twins

1 reference

https://api.crossref.org/works/10.1016%2FS2173-5808%2820%2970105-7

7 January 2021

A twin study of genetic influences on reading and spelling ability and disability

1 reference

https://api.crossref.org/works/10.1016%2FS2173-5808%2820%2970105-7

7 January 2021

Phonological and orthographic components of word recognition. A PET-rCBF study

1 reference

https://api.crossref.org/works/10.1016%2FS2173-5808%2820%2970105-7

7 January 2021

Causal models of reading disability: a twin study

1 reference

https://api.crossref.org/works/10.1016%2FS2173-5808%2820%2970105-7

7 January 2021

Association of the KIAA0319 dyslexia susceptibility gene with reading skills in the general population.

1 reference

https://api.crossref.org/works/10.1016%2FS2173-5808%2820%2970105-7

7 January 2021

Evidence for major gene transmission of developmental dyslexia

1 reference

https://api.crossref.org/works/10.1016%2FS2173-5808%2820%2970105-7

7 January 2021

Segregation analysis of phenotypic components of learning disabilities. II. Phonological decoding

1 reference

https://api.crossref.org/works/10.1016%2FS2173-5808%2820%2970105-7

7 January 2021

Association study designs for complex diseases

1 reference

https://api.crossref.org/works/10.1016%2FS2173-5808%2820%2970105-7

7 January 2021

The human lexinome: genes of language and reading

1 reference

https://api.crossref.org/works/10.1016%2FS2173-5808%2820%2970105-7

7 January 2021

The genetic basis of complex human behaviors

1 reference

https://api.crossref.org/works/10.1016%2FS2173-5808%2820%2970105-7

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS2173-5808%2820%2970105-7

7 January 2021

Functional genomics of neural and behavioral plasticity

1 reference

https://api.crossref.org/works/10.1016%2FS2173-5808%2820%2970105-7

7 January 2021

Tangled webs: tracing the connections between genes and cognition

1 reference

https://api.crossref.org/works/10.1016%2FS2173-5808%2820%2970105-7

7 January 2021

The genetics of developmental dyslexia

1 reference

https://api.crossref.org/works/10.1016%2FS2173-5808%2820%2970105-7

7 January 2021

Evidence for linkage of spelling disability to chromosome 15

1 reference

https://api.crossref.org/works/10.1016%2FS2173-5808%2820%2970105-7

7 January 2021

Family-based association mapping provides evidence for a gene for reading disability on chromosome 15q

1 reference

https://api.crossref.org/works/10.1016%2FS2173-5808%2820%2970105-7

7 January 2021

A candidate gene for developmental dyslexia encodes a nuclear tetratricopeptide repeat domain protein dynamically regulated in brain

1 reference

https://api.crossref.org/works/10.1016%2FS2173-5808%2820%2970105-7

7 January 2021

The tetratricopeptide repeat: a structural motif mediating protein-protein interactions

1 reference

https://api.crossref.org/works/10.1016%2FS2173-5808%2820%2970105-7

7 January 2021

The complex of TFII-I, PARP1, and SFPQ proteins regulates the DYX1C1 gene implicated in neuronal migration and dyslexia

1 reference

https://api.crossref.org/works/10.1016%2FS2173-5808%2820%2970105-7

7 January 2021

Disruption of neuronal migration by RNAi of Dyx1c1 results in neocortical and hippocampal malformations

1 reference

https://api.crossref.org/works/10.1016%2FS2173-5808%2820%2970105-7

7 January 2021

DYX1C1 functions in neuronal migration in developing neocortex

1 reference

https://api.crossref.org/works/10.1016%2FS2173-5808%2820%2970105-7

7 January 2021

Developmental disruptions and behavioral impairments in rats following in utero RNAi of Dyx1c1.

1 reference

https://api.crossref.org/works/10.1016%2FS2173-5808%2820%2970105-7

7 January 2021

Learning-associated activation of nuclear MAPK, CREB and Elk-1, along with Fos production, in the rat hippocampus after a one-trial avoidance learning: abolition by NMDA receptor blockade

1 reference

https://api.crossref.org/works/10.1016%2FS2173-5808%2820%2970105-7

7 January 2021

Modulation of taste-induced Elk-1 activation by identified neurotransmitter systems in the insular cortex of the behaving rat.

1 reference

https://api.crossref.org/works/10.1016%2FS2173-5808%2820%2970105-7

7 January 2021

Association of short-term memory with a variant within DYX1C1 in developmental dyslexia

1 reference

https://api.crossref.org/works/10.1016%2FS2173-5808%2820%2970105-7

7 January 2021

Further evidence for DYX1C1 as a susceptibility factor for dyslexia

1 reference

https://api.crossref.org/works/10.1016%2FS2173-5808%2820%2970105-7

7 January 2021

The first candidate gene for dyslexia: Turning the page of a new chapter of research

1 reference

https://api.crossref.org/works/10.1016%2FS2173-5808%2820%2970105-7

7 January 2021

A quantitative-trait locus on chromosome 6p influences different aspects of developmental dyslexia

1 reference

https://api.crossref.org/works/10.1016%2FS2173-5808%2820%2970105-7

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS2173-5808%2820%2970105-7

7 January 2021

Use of multivariate linkage analysis for dissection of a complex cognitive trait

1 reference

https://api.crossref.org/works/10.1016%2FS2173-5808%2820%2970105-7

7 January 2021

Refinement of the 6p21.3 quantitative trait locus influencing dyslexia: linkage and association analyses

1 reference

https://api.crossref.org/works/10.1016%2FS2173-5808%2820%2970105-7

7 January 2021

DCDC2 is associated with reading disability and modulates neuronal development in the brain

1 reference

https://api.crossref.org/works/10.1016%2FS2173-5808%2820%2970105-7

7 January 2021

Male sexual dysfunction in mice bearing targeted mutant alleles of the PEA3 ets gene

1 reference

https://api.crossref.org/works/10.1016%2FS2173-5808%2820%2970105-7

7 January 2021

Neurotrophins and netrins require calcineurin/NFAT signaling to stimulate outgrowth of embryonic axons

1 reference

https://api.crossref.org/works/10.1016%2FS2173-5808%2820%2970105-7

7 January 2021

Doublecortin is a developmentally regulated, microtubule-associated protein expressed in migrating and differentiating neurons

1 reference

https://api.crossref.org/works/10.1016%2FS2173-5808%2820%2970105-7

7 January 2021

A novel CNS gene required for neuronal migration and involved in X-linked subcortical laminar heterotopia and lissencephaly syndrome

1 reference

https://api.crossref.org/works/10.1016%2FS2173-5808%2820%2970105-7

7 January 2021

Postnatal analysis of the effect of embryonic knockdown and overexpression of candidate dyslexia susceptibility gene homolog Dcdc2 in the rat

1 reference

https://api.crossref.org/works/10.1016%2FS2173-5808%2820%2970105-7

7 January 2021

Strong genetic evidence of DCDC2 as a susceptibility gene for dyslexia

1 reference

https://api.crossref.org/works/10.1016%2FS2173-5808%2820%2970105-7

7 January 2021

The role of gene DCDC2 in German dyslexics.

1 reference

https://api.crossref.org/works/10.1016%2FS2173-5808%2820%2970105-7

7 January 2021

A 77-kilobase region of chromosome 6p22.2 is associated with dyslexia in families from the United Kingdom and from the United States

1 reference

https://api.crossref.org/works/10.1016%2FS2173-5808%2820%2970105-7

7 January 2021

Strong evidence that KIAA0319 on chromosome 6p is a susceptibility gene for developmental dyslexia

1 reference

https://api.crossref.org/works/10.1016%2FS2173-5808%2820%2970105-7

7 January 2021

A transcription map of the 6p22.3 reading disability locus identifying candidate genes

1 reference

https://api.crossref.org/works/10.1016%2FS2173-5808%2820%2970105-7

7 January 2021

The chromosome 6p22 haplotype associated with dyslexia reduces the expression of KIAA0319, a novel gene involved in neuronal migration

1 reference

https://api.crossref.org/works/10.1016%2FS2173-5808%2820%2970105-7

7 January 2021

The dyslexia-associated gene KIAA0319 encodes highly N- and O-glycosylated plasma membrane and secreted isoforms

1 reference

https://api.crossref.org/works/10.1016%2FS2173-5808%2820%2970105-7

7 January 2021

Alternative splicing in the dyslexia-associated gene KIAA0319

1 reference

https://api.crossref.org/works/10.1016%2FS2173-5808%2820%2970105-7

7 January 2021

Further evidence that the KIAA0319 gene confers susceptibility to developmental dyslexia

1 reference

https://api.crossref.org/works/10.1016%2FS2173-5808%2820%2970105-7

7 January 2021

A haplotype spanning KIAA0319 and TTRAP is associated with normal variation in reading and spelling ability

1 reference

https://api.crossref.org/works/10.1016%2FS2173-5808%2820%2970105-7

7 January 2021

Investigation of interaction between DCDC2 and KIAA0319 in a large German dyslexia sample

1 reference

https://api.crossref.org/works/10.1016%2FS2173-5808%2820%2970105-7

7 January 2021

Genes, cognition and dyslexia: learning to read the genome

1 reference

https://api.crossref.org/works/10.1016%2FS2173-5808%2820%2970105-7

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS2173-5808%2820%2970105-7

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS2173-5808%2820%2970105-7

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS2173-5808%2820%2970105-7

7 January 2021

A locus on 2p12 containing the co-regulated MRPL19 and C2ORF3 genes is associated to dyslexia

1 reference

https://api.crossref.org/works/10.1016%2FS2173-5808%2820%2970105-7

7 January 2021

The human mitochondrial ribosomal protein genes: mapping of 54 genes to the chromosomes and implications for human disorders

1 reference

https://api.crossref.org/works/10.1016%2FS2173-5808%2820%2970105-7

7 January 2021

Molecular analysis of the GCF gene identifies revisions to the cDNA and amino acid sequences(1)

1 reference

https://api.crossref.org/works/10.1016%2FS2173-5808%2820%2970105-7

7 January 2021

Evidence for a susceptibility locus on chromosome 6q influencing phonological coding dyslexia

1 reference

https://api.crossref.org/works/10.1016%2FS2173-5808%2820%2970105-7

7 January 2021

The axon guidance receptor gene ROBO1 is a candidate gene for developmental dyslexia

1 reference

https://api.crossref.org/works/10.1016%2FS2173-5808%2820%2970105-7

7 January 2021

Breakthroughs in the search for dyslexia candidate genes

1 reference

https://api.crossref.org/works/10.1016%2FS2173-5808%2820%2970105-7

7 January 2021

Roundabout controls axon crossing of the CNS midline and defines a novel subfamily of evolutionarily conserved guidance receptors

1 reference

https://api.crossref.org/works/10.1016%2FS2173-5808%2820%2970105-7

7 January 2021

Slit proteins prevent midline crossing and determine the dorsoventral position of major axonal pathways in the mammalian forebrain

1 reference

https://api.crossref.org/works/10.1016%2FS2173-5808%2820%2970105-7

7 January 2021

Hierarchical organization of guidance receptors: silencing of netrin attraction by slit through a Robo/DCC receptor complex

1 reference

https://api.crossref.org/works/10.1016%2FS2173-5808%2820%2970105-7

7 January 2021

A dominant gene for developmental dyslexia on chromosome 3

1 reference

https://api.crossref.org/works/10.1016%2FS2173-5808%2820%2970105-7

7 January 2021

Prevalence of speech delay in 6-year-old children and comorbidity with language impairment

1 reference

https://api.crossref.org/works/10.1016%2FS2173-5808%2820%2970105-7

7 January 2021

Pleiotropic effects of a chromosome 3 locus on speech-sound disorder and reading

1 reference

https://api.crossref.org/works/10.1016%2FS2173-5808%2820%2970105-7

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS2173-5808%2820%2970105-7

7 January 2021

Developmental dyslexia: genetic dissection of a complex cognitive trait

1 reference

https://api.crossref.org/works/10.1016%2FS2173-5808%2820%2970105-7

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS2173-5808%2820%2970105-7

7 January 2021

Secretin, glucagon, gastric inhibitory polypeptide, parathyroid hormone, and related peptides in the regulation of the hypothalamus- pituitary-adrenal axis.

1 reference

https://api.crossref.org/works/10.1016%2FS2173-5808%2820%2970105-7

7 January 2021

Secretin facilitates GABA transmission in the cerebellum.

1 reference

https://api.crossref.org/works/10.1016%2FS2173-5808%2820%2970105-7

7 January 2021

Molecular cloning of a novel human gene (D11S4896E) at chromosomal region 11p15.5

1 reference

https://api.crossref.org/works/10.1016%2FS2173-5808%2820%2970105-7

7 January 2021

Identification and characterization of MTR1, a novel gene with homology to melastatin (MLSN1) and the trp gene family located in the BWS-WT2 critical region on chromosome 11p15.5 and showing allele-specific expression

1 reference

https://api.crossref.org/works/10.1016%2FS2173-5808%2820%2970105-7

7 January 2021

Ras and Rap control AMPA receptor trafficking during synaptic plasticity

1 reference

https://api.crossref.org/works/10.1016%2FS2173-5808%2820%2970105-7

7 January 2021

Studies of the c-Harvey-Ras gene in psychiatric disorders

1 reference

https://api.crossref.org/works/10.1016%2FS2173-5808%2820%2970105-7

7 January 2021

A haplotype relative risk study of the dopamine D4 receptor (DRD4) exon III repeat polymorphism and attention deficit hyperactivity disorder (ADHD).

1 reference

https://api.crossref.org/works/10.1016%2FS2173-5808%2820%2970105-7

7 January 2021

Evidence for linkage of a tandem duplication polymorphism upstream of the dopamine D4 receptor gene (DRD4) with attention deficit hyperactivity disorder (ADHD).

1 reference

https://api.crossref.org/works/10.1016%2FS2173-5808%2820%2970105-7

7 January 2021

Attention-deficit hyperactivity disorder: a study of association with both the dopamine transporter gene and the dopamine D4 receptor gene

1 reference

https://api.crossref.org/works/10.1016%2FS2173-5808%2820%2970105-7

7 January 2021

Association of DRD4 with attention problems in normal childhood development

1 reference

https://api.crossref.org/works/10.1016%2FS2173-5808%2820%2970105-7

7 January 2021

Language abilities in children with attention deficit hyperactivity disorder, reading disabilities, and normal controls

1 reference

https://api.crossref.org/works/10.1016%2FS2173-5808%2820%2970105-7

7 January 2021

https://api.crossref.org/works/10.1016%2FS2173-5808%2820%2970105-7

1 reference

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS2173-5808%2820%2970105-7

7 January 2021

Distribution of D4 dopamine receptor in rat brain with sequence-specific antibodies

1 reference

https://api.crossref.org/works/10.1016%2FS2173-5808%2820%2970105-7

7 January 2021

Cosegregation of balanced translocation (1;2) with retarded speech development and dyslexia

1 reference

https://api.crossref.org/works/10.1016%2FS2173-5808%2820%2970105-7

7 January 2021

Suggestive linkage of developmental dyslexia to chromosome 1p34-p36.

1 reference

https://api.crossref.org/works/10.1016%2FS2173-5808%2820%2970105-7

7 January 2021

The KIAA0319-like (KIAA0319L) gene on chromosome 1p34 as a candidate for reading disabilities

1 reference

https://api.crossref.org/works/10.1016%2FS2173-5808%2820%2970105-7

7 January 2021

Linkage to chromosome 1p36 for attention-deficit/hyperactivity disorder traits in school and home settings

1 reference

https://api.crossref.org/works/10.1016%2FS2173-5808%2820%2970105-7

7 January 2021

Genomewide scan identifies susceptibility locus for dyslexia on Xq27 in an extended Dutch family

1 reference

https://api.crossref.org/works/10.1016%2FS2173-5808%2820%2970105-7

7 January 2021

Common and specific gender influences on individual differences in reading performance: a twin study

1 reference

https://api.crossref.org/works/10.1016%2FS2173-5808%2820%2970105-7

7 January 2021

Sex differences in developmental reading disability: new findings from 4 epidemiological studies

1 reference

https://api.crossref.org/works/10.1016%2FS2173-5808%2820%2970105-7

7 January 2021

Intragenic loss of function mutations demonstrate the primary role of FMR1 in fragile X syndrome

1 reference

https://api.crossref.org/works/10.1016%2FS2173-5808%2820%2970105-7

7 January 2021

Molecular-clinical correlations in males with an expanded FMR1 mutation

1 reference

https://api.crossref.org/works/10.1016%2FS2173-5808%2820%2970105-7

7 January 2021

Prader-Willi-like phenotype in fragile X syndrome

1 reference

https://api.crossref.org/works/10.1016%2FS2173-5808%2820%2970105-7

7 January 2021

Understanding the molecular basis of fragile X syndrome

1 reference

https://api.crossref.org/works/10.1016%2FS2173-5808%2820%2970105-7

7 January 2021

Experience-dependent plasticity of dendritic spines in the developing rat barrel cortex in vivo

1 reference

https://api.crossref.org/works/10.1016%2FS2173-5808%2820%2970105-7

7 January 2021

A decade of molecular studies of fragile X syndrome

1 reference

https://api.crossref.org/works/10.1016%2FS2173-5808%2820%2970105-7

7 January 2021

Synaptic regulation of protein synthesis and the fragile X protein

1 reference

https://api.crossref.org/works/10.1016%2FS2173-5808%2820%2970105-7

7 January 2021

Genomewide scan for real-word reading subphenotypes of dyslexia: novel chromosome 13 locus and genetic complexity

1 reference

https://api.crossref.org/works/10.1016%2FS2173-5808%2820%2970105-7

7 January 2021

A major susceptibility locus for specific language impairment is located on 13q21.

1 reference

https://api.crossref.org/works/10.1016%2FS2173-5808%2820%2970105-7

7 January 2021

Speech and language impairment and oromotor dyspraxia due to deletion of 7q31 that involves FOXP2.

1 reference

https://api.crossref.org/works/10.1016%2FS2173-5808%2820%2970105-7

7 January 2021

Deciphering the genetic basis of speech and language disorders

1 reference

https://api.crossref.org/works/10.1016%2FS2173-5808%2820%2970105-7

7 January 2021

Genetic influences on language impairment and phonological short-term memory.

1 reference

https://api.crossref.org/works/10.1016%2FS2173-5808%2820%2970105-7

7 January 2021

Apparently balanced t(1;7)(q21.3;q34) in an infant with Coffin-Siris syndrome

1 reference

https://api.crossref.org/works/10.1016%2FS2173-5808%2820%2970105-7

7 January 2021

Candidate region for Coffin-Siris syndrome at 7q32-->34.

1 reference

https://api.crossref.org/works/10.1016%2FS2173-5808%2820%2970105-7

7 January 2021

The Coffin-Siris syndrome: data on mental development, language, behavior and social skills in 12 children.

1 reference

https://api.crossref.org/works/10.1016%2FS2173-5808%2820%2970105-7

7 January 2021

Incorporating language phenotypes strengthens evidence of linkage to autism

1 reference

https://api.crossref.org/works/10.1016%2FS2173-5808%2820%2970105-7

7 January 2021

Molecular genetic delineation of a deletion of chromosome 13q12-->q13 in a patient with autism and auditory processing deficits

1 reference

https://api.crossref.org/works/10.1016%2FS2173-5808%2820%2970105-7

7 January 2021

A centrosomal mechanism involving CDK5RAP2 and CENPJ controls brain size

1 reference

https://api.crossref.org/works/10.1016%2FS2173-5808%2820%2970105-7

7 January 2021

Protein 4.1 R-135 interacts with a novel centrosomal protein (CPAP) which is associated with the gamma-tubulin complex

1 reference

https://api.crossref.org/works/10.1016%2FS2173-5808%2820%2970105-7

7 January 2021

Identification of a novel microtubule-destabilizing motif in CPAP that binds to tubulin heterodimers and inhibits microtubule assembly

1 reference

https://api.crossref.org/works/10.1016%2FS2173-5808%2820%2970105-7

7 January 2021

Primary microcephaly: new approaches for an old disorder

1 reference

https://api.crossref.org/works/10.1016%2FS2173-5808%2820%2970105-7

7 January 2021

https://api.crossref.org/works/10.1016%2FS2173-5808%2820%2970105-7

1 reference

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS2173-5808%2820%2970105-7

7 January 2021

Identification of novel dyslexia candidate genes through the analysis of a chromosomal deletion

1 reference

https://api.crossref.org/works/10.1016%2FS2173-5808%2820%2970105-7

7 January 2021

Evidence that GRIP, a PDZ-domain protein which is expressed in the embryonic forebrain, co-activates transcription with DLX homeodomain proteins

1 reference

https://api.crossref.org/works/10.1016%2FS2173-5808%2820%2970105-7

7 January 2021

Functional roles of protein interactions with AMPA and kainate receptors

1 reference

https://api.crossref.org/works/10.1016%2FS2173-5808%2820%2970105-7

7 January 2021

Do different components of working memory underlie different subgroups of reading disabilities?

1 reference

https://api.crossref.org/works/10.1016%2FS2173-5808%2820%2970105-7

7 January 2021

Cloning, genomic organization and expression pattern of a novel Drosophila gene, the disco-interacting protein 2 (dip2), and its murine homolog

1 reference

https://api.crossref.org/works/10.1016%2FS2173-5808%2820%2970105-7

7 January 2021

Identification of a human centrosomal calmodulin-binding protein that shares homology with pericentrin

1 reference

https://api.crossref.org/works/10.1016%2FS2173-5808%2820%2970105-7

7 January 2021

Dyslexia--a molecular disorder of neuronal migration: the 2004 Norman Geschwind Memorial Lecture

1 reference

https://api.crossref.org/works/10.1016%2FS2173-5808%2820%2970105-7

7 January 2021

From genes to behavior in developmental dyslexia

1 reference

https://api.crossref.org/works/10.1016%2FS2173-5808%2820%2970105-7

7 January 2021

Mutations in filamin 1 prevent migration of cerebral cortical neurons in human periventricular heterotopia.

1 reference

https://api.crossref.org/works/10.1016%2FS2173-5808%2820%2970105-7

7 January 2021

Reading impairment in the neuronal migration disorder of periventricular nodular heterotopia

1 reference

https://api.crossref.org/works/10.1016%2FS2173-5808%2820%2970105-7

7 January 2021

Bridging cognition, the brain and molecular genetics: evidence from Williams syndrome

1 reference

https://api.crossref.org/works/10.1016%2FS2173-5808%2820%2970105-7

7 January 2021

The structure of genetic influences on general cognitive, language, phonological, and reading abilities

1 reference

https://api.crossref.org/works/10.1016%2FS2173-5808%2820%2970105-7

7 January 2021