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...

पूर्ण विवरण

ग्रंथसूची विवरण
मुख्य लेखक:	Brandler, W
अन्य लेखक:	Monaco, A
स्वरूप:	थीसिस
भाषा:	English
प्रकाशित:	2014
विषय:	Genetics (life sciences) Behavioural Neuroscience Bioinformatics (life sciences) Neurogenetics Genetics (medical sciences)

समान संसाधन

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The genetic relationship between handedness and neurodevelopmental disorders
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Genetic basis of neurocognitive decline and reduced white-matter integrity in normal human brain aging
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Functional characterisation of synuclein-based novel genetic mouse models
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Comparative neurotranscriptomics in mammals and birds
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Genetic architecture of declarative memory: implications for complex illnesses
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The genetics of amyotrophic lateral sclerosis
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Functional genomics analyses of neuropsychiatric and neurodevelopmental disorders
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प्रकाशित: (2014)

Blood pressure and cerebral white matter share common genetic factors in Mexican Americans
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Transcriptional brain networks and their key regulators across the human lifespan
द्वारा: Wehrspaun, CC
प्रकाशित: (2014)

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

Genes contributing to variation in fear-related behaviour
द्वारा: Krohn, J, और अन्य
प्रकाशित: (2013)

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

P-selectin expression tracks cerebral atrophy in Mexican-Americans
द्वारा: Kochunov, P, और अन्य
प्रकाशित: (2012)

Social Isolation and Enrichment Induce Unique miRNA Signatures in the Prefrontal Cortex and Behavioral Changes in Mice
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प्रकाशित: (2020-12-01)

Reduced white matter integrity in sibling pairs discordant for bipolar disorder
द्वारा: Sprooten, E, और अन्य
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On genetic variants underlying common disease
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प्रकाशित: (2011)

A method for the identification of biological pathways
द्वारा: Honti, F
प्रकाशित: (2014)

Protocadherin 11X/Y a human-speciﬁc gene pair: an immunohistochemical survey of fetal and adult brains
द्वारा: Priddle, T, और अन्य
प्रकाशित: (2013)

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

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

Subplate populations in normal and pathological cortical development
द्वारा: Oeschger, F
प्रकाशित: (2011)

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

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

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

Identification of epigenetic regulators of RNA editing mechanisms
द्वारा: Buss, G
प्रकाशित: (2023)

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

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

Investigation of dyslexia and SLI risk variants in reading- and language-impaired subjects
द्वारा: Newbury, D, और अन्य
प्रकाशित: (2011)

Recurrent activating ACVR1 mutations in diffuse intrinsic pontine glioma
द्वारा: Taylor, K, और अन्य
प्रकाशित: (2014)

Murine Cep290 phenotypes are modified by genetic backgrounds and provide an impetus for investigating disease modifier alleles [version 1; referees: 2 approved]
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Functional characterisation of a multiple sclerosis-associated genetic variant
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Molecular mechanisms of recombination hotspots in humans
द्वारा: Noor, N
प्रकाशित: (2013)

Whole-genome analysis of the transcriptional network underlying male sexual behaviour in Drosophila melanogaster
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प्रकाशित: (2012)

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

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

Human population structure and demographic history using genetic markers
द्वारा: Wilson, J, और अन्य
प्रकाशित: (2002)

Functional genomics of severe sepsis and septic shock
द्वारा: Radhakrishnan, J
प्रकाशित: (2013)