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Open AccessJournal ArticleDOI

Genome-wide association study identifies 48 common genetic variants associated with handedness

Gabriel Cuellar-Partida, +145 more
- 01 Jan 2021 - 
- Vol. 5, Iss: 1, pp 59-70
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TLDR
It is suggested that handedness is highly polygenic and that the genetic variants that predispose to left-handedness may underlie part of the association with some psychiatric disorders.
Abstract
Handedness has been extensively studied because of its relationship with language and the over-representation of left-handers in some neurodevelopmental disorders. Using data from the UK Biobank, 23andMe and the International Handedness Consortium, we conducted a genome-wide association meta-analysis of handedness (N = 1,766,671). We found 41 loci associated (P < 5 × 10−8) with left-handedness and 7 associated with ambidexterity. Tissue-enrichment analysis implicated the CNS in the aetiology of handedness. Pathways including regulation of microtubules and brain morphology were also highlighted. We found suggestive positive genetic correlations between left-handedness and neuropsychiatric traits, including schizophrenia and bipolar disorder. Furthermore, the genetic correlation between left-handedness and ambidexterity is low (rG = 0.26), which implies that these traits are largely influenced by different genetic mechanisms. Our findings suggest that handedness is highly polygenic and that the genetic variants that predispose to left-handedness may underlie part of the association with some psychiatric disorders. A genome-wide association study of 1.7 million individuals identified 41 genetic variants associated with left-handedness and 7 associated with ambidexterity. The genetic correlation between the traits was low, thereby implying different aetiologies.

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The universal protein resource (UniProt)

陈奕欣
TL;DR: The core activities include manual curation of protein sequences assisted by computational analysis, sequence archiving, development of a user-friendly UniProt website, and the provision of additional value-added information through cross-references to other databases.
Journal ArticleDOI

The genetic architecture of structural left-right asymmetry of the human brain

TL;DR: In this article, the authors performed multivariate genome-wide association scanning of cortical regional surface area and thickness asymmetries, and subcortical volume asymmetry, using data from 32,256 participants from the UK Biobank.
Journal ArticleDOI

Four meta-analyses across 164 studies on atypical footedness prevalence and its relation to handedness.

TL;DR: It was showed that the prevalence of atypical footedness ranges between 12.10% using the most conservative criterion of left-footedness to 23.7% including all left- and mixed-footers as a single non-right category, and that footing is a valuable phenotype for the study of lateral motor biases, its underlying genetics and neurodevelopment.
Posted ContentDOI

The genetic architecture of structural left-right asymmetry of the human brain

TL;DR: Genetic variants affecting brain asymmetry overlapped with those influencing autism, educational attainment and schizophrenia, consistent with a known role of the cytoskeleton in left-right axis determination in other organs of invertebrates and frogs.
References
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Journal ArticleDOI

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Adam Auton, +517 more
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TL;DR: The 1000 Genomes Project set out to provide a comprehensive description of common human genetic variation by applying whole-genome sequencing to a diverse set of individuals from multiple populations, and has reconstructed the genomes of 2,504 individuals from 26 populations using a combination of low-coverage whole-generation sequencing, deep exome sequencing, and dense microarray genotyping.
Journal ArticleDOI

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John T. Lonsdale, +129 more
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Journal ArticleDOI

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Journal ArticleDOI

The Universal Protein Resource (UniProt)

TL;DR: During 2004, tens of thousands of Knowledgebase records got manually annotated or updated; the UniProt keyword list got augmented by additional keywords; the documentation of the keywords and are continuously overhauling and standardizing the annotation of post-translational modifications.
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