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...

Descrizione completa

Dettagli Bibliografici
Autore principale:	Brandler, W
Altri autori:	Monaco, A
Natura:	Tesi
Lingua:	English
Pubblicazione:	2014
Soggetti:	Genetics (life sciences) Behavioural Neuroscience Bioinformatics (life sciences) Neurogenetics Genetics (medical sciences)

Documenti analoghi

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

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

Molecular Genetics of Language Impairment
di: Nudel, R
Pubblicazione: (2015)

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

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

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

Comparative neurotranscriptomics in mammals and birds
di: Belgard, TG
Pubblicazione: (2011)

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

The genetics of amyotrophic lateral sclerosis
di: Schymick, J
Pubblicazione: (2009)

Functional genomics analyses of neuropsychiatric and neurodevelopmental disorders
di: Steinberg, J
Pubblicazione: (2014)

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

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

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

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

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

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

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

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

On genetic variants underlying common disease
di: Hechter, E
Pubblicazione: (2011)

A method for the identification of biological pathways
di: Honti, F
Pubblicazione: (2014)

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

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

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

Subplate populations in normal and pathological cortical development
di: Oeschger, F
Pubblicazione: (2011)

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

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

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

Identification of epigenetic regulators of RNA editing mechanisms
di: Buss, G
Pubblicazione: (2023)

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

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

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

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

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

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

Molecular mechanisms of recombination hotspots in humans
di: Noor, N
Pubblicazione: (2013)

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

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

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

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

Functional genomics of severe sepsis and septic shock
di: Radhakrishnan, J
Pubblicazione: (2013)