<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Ludwig KU</submitter><funding>Medical Research Council</funding><pagination>e229</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC3591001</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>3</volume><pubmed_abstract>The ability to perform mathematical tasks is required in everyday life. Although heritability estimates suggest a genetic contribution, no previous study has conclusively identified a genetic risk variant for mathematical performance. Research has shown that the prevalence of mathematical disabilities is increased in children with dyslexia. We therefore correlated genome-wide data of 200 German children with spelling disability, with available quantitative data on mathematic ability. Replication of the top findings in additional dyslexia samples revealed that rs133885 was a genome-wide significant marker for mathematical abilities (P(comb) = 7.71 × 10(-10), n = 699), with an effect size of 4.87%. This association was also found in a sample from the general population (P = 0.048, n = 1080),</pubmed_abstract><journal>Translational psychiatry</journal><pubmed_title>A common variant in myosin-18B contributes to mathematical abilities in children with dyslexia and intraparietal sulcus variability in adults.</pubmed_title><pmcid>PMC3591001</pmcid><funding_grant_id>G0500079(73692)</funding_grant_id><funding_grant_id>G500079</funding_grant_id><funding_grant_id>G9817803B</funding_grant_id><funding_grant_id>G0500079</funding_grant_id><pubmed_authors>Ludwig KU</pubmed_authors><pubmed_authors>Becker J</pubmed_authors><pubmed_authors>Czisch M</pubmed_authors><pubmed_authors>Davis OS</pubmed_authors><pubmed_authors>Landerl K</pubmed_authors><pubmed_authors>Warnke A</pubmed_authors><pubmed_authors>Nothen MM</pubmed_authors><pubmed_authors>Plomin R</pubmed_authors><pubmed_authors>Alexander M</pubmed_authors><pubmed_authors>Czamara D</pubmed_authors><pubmed_authors>Docherty SJ</pubmed_authors><pubmed_authors>Muller-Myhsok B</pubmed_authors><pubmed_authors>Schumacher J</pubmed_authors><pubmed_authors>Spieler D</pubmed_authors><pubmed_authors>Moll K</pubmed_authors><pubmed_authors>Hoffmann P</pubmed_authors><pubmed_authors>Samann P</pubmed_authors><pubmed_authors>Bruder J</pubmed_authors><pubmed_authors>Schulte-Korne G</pubmed_authors></additional><is_claimable>false</is_claimable><name>A common variant in myosin-18B contributes to mathematical abilities in children with dyslexia and intraparietal sulcus variability in adults.</name><description>The ability to perform mathematical tasks is required in everyday life. Although heritability estimates suggest a genetic contribution, no previous study has conclusively identified a genetic risk variant for mathematical performance. Research has shown that the prevalence of mathematical disabilities is increased in children with dyslexia. We therefore correlated genome-wide data of 200 German children with spelling disability, with available quantitative data on mathematic ability. Replication of the top findings in additional dyslexia samples revealed that rs133885 was a genome-wide significant marker for mathematical abilities (P(comb) = 7.71 × 10(-10), n = 699), with an effect size of 4.87%. This association was also found in a sample from the general population (P = 0.048, n = 1080),</description><dates><release>2013-01-01T00:00:00Z</release><publication>2013 Feb</publication><modification>2026-05-05T10:44:26.695Z</modification><creation>2026-04-07T21:37:44.917Z</creation></dates><accession>S-EPMC3591001</accession><cross_references><pubmed>23423138</pubmed><doi>10.1038/tp.2012.148</doi></cross_references></HashMap>