LRRTM1 on chromosome 2p12 is a maternally suppressed gene that is associated paternally with handedness and schizophrenia
about
Web-based, participant-driven studies yield novel genetic associations for common traitsCommon variants in left/right asymmetry genes and pathways are associated with relative hand skillPolymorphisms in leucine-rich repeat genes are associated with autism spectrum disorder susceptibility in populations of European ancestryAdvances in autism genetics: on the threshold of a new neurobiologyTruncating mutations in NRXN2 and NRXN1 in autism spectrum disorders and schizophreniaDecreased prevalence of left-handedness among females with male co-twins: evidence suggesting prenatal testosterone transfer in humans?Disease-associated epigenetic changes in monozygotic twins discordant for schizophrenia and bipolar disorderPCSK6 is associated with handedness in individuals with dyslexiaMeta-analysis of genome-wide association studies identifies common variants in CTNNA2 associated with excitement-seeking.LRRTMs and neuroligins bind neurexins with a differential code to cooperate in glutamate synapse developmentGenetic influences on handedness: data from 25,732 Australian and Dutch twin familiesLeucine-rich repeat transmembrane proteins are essential for maintenance of long-term potentiationNeuroligins/LRRTMs prevent activity- and Ca2+/calmodulin-dependent synapse elimination in cultured neuronsLRRTM2 functions as a neurexin ligand in promoting excitatory synapse formationComplex tasks force hand laterality and technological behaviour in naturalistically housed chimpanzees: inferences in hominin evolutionForelimb preferences in human beings and other species: multiple models for testing hypotheses on lateralizationOrigin and loss of nested LRRTM/α-catenin genes during vertebrate evolutionGenetic Consideration of Schizotypal Traits: A ReviewPsychosis and autism as diametrical disorders of the social brainLRRTM1-deficient mice show a rare phenotype of avoiding small enclosures--a tentative mouse model for claustrophobia-like behaviour.An unbiased expression screen for synaptogenic proteins identifies the LRRTM protein family as synaptic organizersImpaired cognitive function and altered hippocampal synapse morphology in mice lacking Lrrtm1, a gene associated with schizophreniaIt's All in the Family: Brain Asymmetry and Syntactic Processing of Word ClassLeft brain, right brain: facts and fantasiesHuman brain evolution: harnessing the genomics (r)evolution to link genes, cognition, and behaviorThe evolution and genetics of cerebral asymmetryGenome-wide association and meta-analysis of bipolar disorder in individuals of European ancestryA Comparative Study Of Nerve Conduction Velocity Between Left And Right Handed SubjectsThe relation between lateralisation, early start of training, and amount of practice in musicians: a contribution to the problem of handedness classification.Atypically rightward cerebral asymmetry in male adults with autism stratifies individuals with and without language delay.The impact of gene expression regulation on evolution of extracellular signaling pathways.Left-handedness and language lateralization in children.Hemispheric asymmetries: the comparative view.A linear structural equation model for covert verb generation based on independent component analysis of FMRI data from children and adolescents.A cell surface interaction network of neural leucine-rich repeat receptors.Neurodevelopmental effects of chronic exposure to elevated levels of pro-inflammatory cytokines in a developing visual system.Language laterality in autism spectrum disorder and typical controls: a functional, volumetric, and diffusion tensor MRI study.Multilocus genetic models of handedness closely resemble single-locus models in explaining family data and are compatible with genome-wide association studies.Cognitive Control Processes and Functional Cerebral Asymmetries: Association with Variation in the Handedness-Associated Gene LRRTM1.Cerebral asymmetries: complementary and independent processes.
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P2860
LRRTM1 on chromosome 2p12 is a maternally suppressed gene that is associated paternally with handedness and schizophrenia
description
2007 nî lūn-bûn
@nan
2007 թուականի Դեկտեմբերին հրատարակուած գիտական յօդուած
@hyw
2007 թվականի դեկտեմբերին հրատարակված գիտական հոդված
@hy
2007年の論文
@ja
2007年論文
@yue
2007年論文
@zh-hant
2007年論文
@zh-hk
2007年論文
@zh-mo
2007年論文
@zh-tw
2007年论文
@wuu
name
LRRTM1 on chromosome 2p12 is a ...... h handedness and schizophrenia
@ast
LRRTM1 on chromosome 2p12 is a ...... h handedness and schizophrenia
@en
LRRTM1 on chromosome 2p12 is a ...... h handedness and schizophrenia
@en-gb
LRRTM1 on chromosome 2p12 is a ...... h handedness and schizophrenia
@nl
type
label
LRRTM1 on chromosome 2p12 is a ...... h handedness and schizophrenia
@ast
LRRTM1 on chromosome 2p12 is a ...... h handedness and schizophrenia
@en
LRRTM1 on chromosome 2p12 is a ...... h handedness and schizophrenia
@en-gb
LRRTM1 on chromosome 2p12 is a ...... h handedness and schizophrenia
@nl
prefLabel
LRRTM1 on chromosome 2p12 is a ...... h handedness and schizophrenia
@ast
LRRTM1 on chromosome 2p12 is a ...... h handedness and schizophrenia
@en
LRRTM1 on chromosome 2p12 is a ...... h handedness and schizophrenia
@en-gb
LRRTM1 on chromosome 2p12 is a ...... h handedness and schizophrenia
@nl
P2093
P2860
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LRRTM1 on chromosome 2p12 is a ...... h handedness and schizophrenia
@en
P2093
A J Richardson
A P Monaco
B S Abrahams
D H Geschwind
D St Clair
E Z McAuley
P2860
P2888
P304
1129-39, 1057
P3181
P356
10.1038/SJ.MP.4002053
P407
P577
2007-12-01T00:00:00Z
P5875
P6179
1034646284