Handedness and its genetic influences are associated with structural asymmetries of the cerebral cortex in 31,864 individuals.
Zhiqiang Sha,Antonietta Pepe,Antonietta Pepe,Antonietta Pepe,Dick Schijven,Amaia Carrion-Castillo,James M Roe,René Westerhausen,Marc Joliot,Marc Joliot,Marc Joliot,Simon E. Fisher,Simon E. Fisher,Fabrice Crivello,Fabrice Crivello,Fabrice Crivello,Clyde Francks,Clyde Francks +17 more
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In this paper, structural brain image data from 28,802 right handers and 3,062 left handers were resampled to a symmetrical surface template, and mapped asymmetries for each of 8,681 vertices across the cerebral cortex in each individual.Abstract:
Roughly 10% of the human population is left-handed, and this rate is increased in some brain-related disorders. The neuroanatomical correlates of hand preference have remained equivocal. We resampled structural brain image data from 28,802 right-handers and 3,062 left-handers (UK Biobank population dataset) to a symmetrical surface template, and mapped asymmetries for each of 8,681 vertices across the cerebral cortex in each individual. Left-handers compared to right-handers showed average differences of surface area asymmetry within the fusiform cortex, the anterior insula, the anterior middle cingulate cortex, and the precentral cortex. Meta-analyzed functional imaging data implicated these regions in executive functions and language. Polygenic disposition to left-handedness was associated with two of these regional asymmetries, and 18 loci previously linked with left-handedness by genome-wide screening showed associations with one or more of these asymmetries. Implicated genes included six encoding microtubule-related proteins: TUBB, TUBA1B, TUBB3, TUBB4A, MAP2, and NME7-mutations in the latter can cause left to right reversal of the visceral organs. There were also two cortical regions where average thickness asymmetry was altered in left-handedness: on the postcentral gyrus and the inferior occipital cortex, functionally annotated with hand sensorimotor and visual roles. These cortical thickness asymmetries were not heritable. Heritable surface area asymmetries of language-related regions may link the etiologies of hand preference and language, whereas nonheritable asymmetries of sensorimotor cortex may manifest as consequences of hand preference.read more
Citations
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Subtly altered topological asymmetry of brain structural covariance networks in autism spectrum disorder across 43 datasets from the ENIGMA consortium
Zhiqiang Sha,Omar Ismail +1 more
TL;DR: In this paper , the authors used cortical thickness data from 1455 individuals with ASD and 1560 controls, across 43 independent datasets of the ENIGMA consortium's ASD Working Group, to assess hemispheric asymmetries of intra-individual structural covariance networks, using graph theory-based topological metrics.
Journal ArticleDOI
Limb Preference in Animals: New Insights into the Evolution of Manual Laterality in Hominids
TL;DR: A recent review as discussed by the authors highlights the contribution of comparative research to the understanding of human handedness' evolutionary and developmental pathways, by distinguishing animal forelimb asymmetries for functionally different actions, potentially depending on different hemispheric specializations.
Journal ArticleDOI
Large-scale differences in functional organization of left- and right-handed individuals using whole-brain, data-driven analysis of connectivity
TL;DR: In this article , the authors compared functional connectomes of left and right-handed individuals at the whole brain level and found that the functional connectivity of left- and righthanded individuals are not specific to networks of interest, but extend across every region of the brain.
Journal ArticleDOI
The evolution and biological correlates of hand preferences in anthropoid primates
TL;DR: For example, the authors found that human right-handedness represents an unparalleled extreme among anthropoids and found taxa displaying population-level handedness to be rare, while human lateralization patterns do not align with trends found among other anthropoids, suggesting that unique selective pressures gave rise to the unusual hand preferences of our species.
Posted ContentDOI
Large-scale analysis of structural brain asymmetries in schizophrenia via the ENIGMA consortium
Dick Schijven,Merel Postema,Masaki Fukunaga,Junya Matsumoto,Kenichiro Miura,Sonja M C de Zwarte,Neeltje E.M. van Haren,Wiepke Cahn,Hilleke E. Hulshoff Pol,René S. Kahn,Rosa Ayesa-Arriola,Victor Ortiz-García de la Foz,Diana Tordesillas-Gutiérrez,Javier Vázquez-Bourgon,Benedicto Crespo-Facorro,Dag Alnæs,A Dahl,Lars T. Westlye,Ingrid Agartz,Ole A. Andreassen,Erik G. Jönsson,Peter Kochunov,Jason M. Bruggemann,Stanley V. Catts,Patricia T. Michie,Bryan J. Mowry,Yann Quidé,Paul E. Rasser,Ulrich Schall,Rodney J. Scott,Vaughan J. Carr,Melissa J. Green,Frans Henskens,Carmel M. Loughland,Christos Pantelis,Cynthia Shannon Weickert,Thomas W. Weickert,Lieuwe de Haan,Katharina Brosch,Juliane Pfarr,Kai Ringwald,Frederike Stein,Andreas Jansen,Tilo Kircher,Igor Nenadic,Bernd Krämer,Oliver Gruber,Theodore D. Satterthwaite,Juan R. Bustillo,Daniel H. Mathalon,Adrian Preda,Vince D. Calhoun,Judith M. Ford,Steven G. Potkin,Jingxu Chen,Yunlong Tan,Zhen Wang,H. Xiang,Fengmei Fan,Fabio Bernardoni,Stefan Ehrlich,Paola Fuentes-Claramonte,Maria Angeles Garcia-Leon,Amalia Guerrero-Pedraza,Raymond Salvador,Salvador Sarró,Edith Pomarol-Clotet,Valentina Ciullo,Fabrizio Piras,Daniel James Vecchio,Nerisa Banaj,Gianfranco Spalletta,Stijn Michielse,Therese van Amelsvoort,Erin W. Dickie,Aristotle N. Voineskos,Kang Sim,Simone Ciufolini,Paola Dazzan,Robin M. Murray,Woo-Sung Kim,Y. Chung,Christina Andreou,André Schmidt,Stefan Borgwardt,Andrew M. McIntosh,Heather C. Whalley,Stephen M. Lawrie,S.S. Du Plessis,Hilmar K. Luckhoff,Freda Scheffler,Robin Emsley,Dominik Grotegerd,Rebekka Lencer,Udo Dannlowski,Jesse T. Edmond,Kelly Rootes-Murdy,Julia M. Stephen,Andrew R. Mayer,Linda A. Antonucci,Leonardo Fazio,Giulio Pergola,Alessandro Bertolini,Covadonga M. Díaz-Caneja,Joost Janssen,Noemi Lois,Celso Arango,Alexander Tomyshev,Irina V. Lebedeva,Simon Cervenka,Carl M. Sellgren,Foivos Georgiadis,Matthias Kirschner,Stefan Kaiser,Tomas Hajek,Antonin Skoch,Filip Spaniel,Minah Kim,Yoo Bin Kwak,Sanghoon Oh,Jun Soo Kwon,Anthony A. James,Geor Bakker,Christian Knöchel,Michael Stäblein,Viola Oertel,Anne Uhlmann,Fleur M. Howells,Dan J. Stein,Henk Temmingh,Ana M. Díaz-Zuluaga,Julian A Pineda-Zapata,Carlos López-Jaramillo,Stephanie Homan,Ellen Ji,Werner Surbeck,Philipp Homan,Simon E. Fisher,Barbara Franke,David C. Glahn,Ruben C. Gur,Ryota Hashimoto,Neda Jahanshad,Eileen Luders,Sarah E. Medland,Paul M. Thompson,Jessica A. Turner,Theo G.M. van Erp,Clyde Francks +148 more
TL;DR: Small case-control differences of brain macro-structural asymmetry may manifest due to more substantial differences at the molecular, cytoarchitectonic or circuit levels, with functional relevance for lateralized cognitive processes in schizophrenia.
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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
UK biobank: an open access resource for identifying the causes of a wide range of complex diseases of middle and old age
Cathie Sudlow,John Gallacher,Naomi E. Allen,Valerie Beral,Paul Burton,John Danesh,Paul Downey,Paul Elliott,Jane Green,Martin J Landray,Bette Liu,Paul M. Matthews,Giok Ong,Jill P. Pell,Alan J. Silman,Alan Young,Tim Sprosen,Tim Peakman,Rory Collins +18 more
TL;DR: The UK Biobank is described, a large population-based prospective study, established to allow investigation of the genetic and non-genetic determinants of the diseases of middle and old age.
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GCTA: a tool for genome-wide complex trait analysis.
TL;DR: The GCTA software is a versatile tool to estimate and partition complex trait variation with large GWAS data sets and focuses on the function of estimating the variance explained by all the SNPs on the X chromosome and testing the hypotheses of dosage compensation.
Journal ArticleDOI
The UK Biobank resource with deep phenotyping and genomic data
Clare Bycroft,Colin Freeman,Desislava Petkova,Desislava Petkova,Gavin Band,Lloyd T. Elliott,Kevin Sharp,Allan Motyer,Damjan Vukcevic,Olivier Delaneau,Olivier Delaneau,Jared O'Connell,Adrian Cortes,Adrian Cortes,Samantha Welsh,Alan Young,Mark Effingham,Gil McVean,Stephen Leslie,Naomi E. Allen,Peter Donnelly,Jonathan Marchini +21 more
TL;DR: Deep phenotype and genome-wide genetic data from 500,000 individuals from the UK Biobank is described, describing population structure and relatedness in the cohort, and imputation to increase the number of testable variants to 96 million.
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Common SNPs explain a large proportion of the heritability for human height
Jian Yang,Beben Benyamin,Brian P. McEvoy,Scott D. Gordon,Anjali K. Henders,Dale R. Nyholt,Pamela A. F. Madden,Andrew C. Heath,Nicholas G. Martin,Grant W. Montgomery,Michael E. Goddard,Peter M. Visscher +11 more
TL;DR: Evidence is provided that the remaining heritability is due to incomplete linkage disequilibrium between causal variants and genotyped SNPs, exacerbated by causal variants having lower minor allele frequency than the SNPs explored to date.
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