The genetics of handedness and dyslexia

The genetics of handedness and dyslexia

<p>The population level bias towards right-handedness in humans implies left-hemisphere dominance for fine motor control. Left-handedness and reduced cerebral asymmetry have been linked to neurodevelopmental disorders such as dyslexia. Understanding the biology of these traits at a genetic lev...

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Bibliografiske detaljer
Hovedforfatter:	Brandler, W
Andre forfattere:	Monaco, A
Format:	Thesis
Sprog:	English
Udgivet:	2014
Fag:	Genetics (life sciences) Behavioural Neuroscience Bioinformatics (life sciences) Neurogenetics Genetics (medical sciences)

Lignende værker

The chromosome 6p22 haplotype associated with dyslexia reduces the expression of KIAA0319, a novel gene involved in neuronal migration
af: Paracchini, S, et al.
Udgivet: (2006)

The genetic relationship between handedness and neurodevelopmental disorders
af: Brandler, W, et al.
Udgivet: (2014)

Molecular Genetics of Language Impairment
af: Nudel, R
Udgivet: (2015)

Investigating the roles of zinc finger homeobox 3 in circadian rhythms
af: Edwards, JK
Udgivet: (2013)

Genetic basis of neurocognitive decline and reduced white-matter integrity in normal human brain aging
af: Glahn, D, et al.
Udgivet: (2013)

Functional characterisation of synuclein-based novel genetic mouse models
af: Anwar, S
Udgivet: (2011)

Comparative neurotranscriptomics in mammals and birds
af: Belgard, TG
Udgivet: (2011)

Genetic architecture of declarative memory: implications for complex illnesses
af: Bearden, C, et al.
Udgivet: (2012)

The genetics of amyotrophic lateral sclerosis
af: Schymick, J
Udgivet: (2009)

Functional genomics analyses of neuropsychiatric and neurodevelopmental disorders
af: Steinberg, J
Udgivet: (2014)

Blood pressure and cerebral white matter share common genetic factors in Mexican Americans
af: Kochunov, P, et al.
Udgivet: (2011)

Transcriptional brain networks and their key regulators across the human lifespan
af: Wehrspaun, CC
Udgivet: (2014)

Intergenic long noncoding RNAs provide a novel layer of post-transcriptional regulation in development and disease
af: Tan, J
Udgivet: (2014)

Genes contributing to variation in fear-related behaviour
af: Krohn, J, et al.
Udgivet: (2013)

Identifying causative elements within structural variants associated with developmental disorders
af: Boulding, H
Udgivet: (2013)

P-selectin expression tracks cerebral atrophy in Mexican-Americans
af: Kochunov, P, et al.
Udgivet: (2012)

Social Isolation and Enrichment Induce Unique miRNA Signatures in the Prefrontal Cortex and Behavioral Changes in Mice
af: Natalia Popa, et al.
Udgivet: (2020-12-01)

Reduced white matter integrity in sibling pairs discordant for bipolar disorder
af: Sprooten, E, et al.
Udgivet: (2013)

On genetic variants underlying common disease
af: Hechter, E
Udgivet: (2011)

A method for the identification of biological pathways
af: Honti, F
Udgivet: (2014)

Protocadherin 11X/Y a human-speciﬁc gene pair: an immunohistochemical survey of fetal and adult brains
af: Priddle, T, et al.
Udgivet: (2013)

The estimation of recombination rates from population genetic data
af: Auton, A
Udgivet: (2007)

Reproducing speech intervals in the sub-hundred millisecond (ms) range with a translocation in 7q31
af: Garcia-Bellido, P
Udgivet: (2013)

Subplate populations in normal and pathological cortical development
af: Oeschger, F
Udgivet: (2011)

Characterisation of pitch: an early onset model of sensorineural deafness
af: Carrott, L
Udgivet: (2014)

Model systems for exploring new therapeutic interventions and disease mechanisms in spinal muscular atrophies (SMAs)
af: Sleigh, JN
Udgivet: (2012)

The effect of manipulating the expression of the NR2B subunit of the NMDA receptor on learning and memory
af: Hoon, A
Udgivet: (2011)

Identification of epigenetic regulators of RNA editing mechanisms
af: Buss, G
Udgivet: (2023)

Intersecting doublesex neurons underlying sexual behaviours in Drosophila melanogaster
af: Pavlou, H
Udgivet: (2014)

Neuroanatomical screening and analysis of transgenic and ENU induced mutagenised mice
af: Edwards, A
Udgivet: (2011)

Investigation of dyslexia and SLI risk variants in reading- and language-impaired subjects
af: Newbury, D, et al.
Udgivet: (2011)

Recurrent activating ACVR1 mutations in diffuse intrinsic pontine glioma
af: Taylor, K, et al.
Udgivet: (2014)

Murine Cep290 phenotypes are modified by genetic backgrounds and provide an impetus for investigating disease modifier alleles [version 1; referees: 2 approved]
af: Simon Ramsbottom, et al.
Udgivet: (2015-08-01)

Functional characterisation of a multiple sclerosis-associated genetic variant
af: Gregory, A
Udgivet: (2012)

Molecular mechanisms of recombination hotspots in humans
af: Noor, N
Udgivet: (2013)

Whole-genome analysis of the transcriptional network underlying male sexual behaviour in Drosophila melanogaster
af: Ashley, E, et al.
Udgivet: (2012)

An integrated genomic approach for the identification and analysis of single nucleotide polymorphisms that affect cancer in humans
af: Repapi, E
Udgivet: (2013)

Statistical challenges in the detection of mutation and variation using high throughput sequencing
af: Pfeifer, S
Udgivet: (2012)

Human population structure and demographic history using genetic markers
af: Wilson, J, et al.
Udgivet: (2002)

Functional genomics of severe sepsis and septic shock
af: Radhakrishnan, J
Udgivet: (2013)