TY - JOUR
AU - Cuellar-Partida, Gabriel
AU - Tung, Joyce Y
AU - Eriksson, Nicholas
AU - Albrecht, Eva
AU - Aliev, Fazil
AU - Andreassen, Ole A
AU - Barroso, Inês
AU - Beckmann, Jacques S
AU - Boks, Marco P
AU - Boomsma, Dorret I
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AU - Breteler, Monique
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AU - Chasman, Daniel I
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AU - Davies, Gail
AU - de Geus, Eco J C
AU - Deary, Ian J
AU - Deloukas, Panos
AU - Dick, Danielle M
AU - Duffy, David L
AU - Eriksson, Johan G
AU - Esko, Tõnu
AU - Feenstra, Bjarke
AU - Geller, Frank
AU - Gieger, Christian
AU - Giegling, Ina
AU - Gordon, Scott D
AU - Han, Jiali
AU - Hansen, Thomas F
AU - Hartmann, Annette M
AU - Hayward, Caroline
AU - Heikkilä, Kauko
AU - Hicks, Andrew A
AU - Hirschhorn, Joel N
AU - Hottenga, Jouke-Jan
AU - Huffman, Jennifer E
AU - Hwang, Liang-Dar
AU - Ikram, M Arfan
AU - Kaprio, Jaakko
AU - Kemp, John P
AU - Khaw, Kay-Tee
AU - Klopp, Norman
AU - Konte, Bettina
AU - Kutalik, Zoltan
AU - Lahti, Jari
AU - Li, Xin
AU - Loos, Ruth J F
AU - Luciano, Michelle
AU - Magnusson, Sigurdur H
AU - Mangino, Massimo
AU - Marques-Vidal, Pedro
AU - Martin, Nicholas G
AU - McArdle, Wendy L
AU - McCarthy, Mark I
AU - Medina-Gomez, Carolina
AU - Melbye, Mads
AU - Melville, Scott A
AU - Metspalu, Andres
AU - Milani, Lili
AU - Mooser, Vincent
AU - Nelis, Mari
AU - Nyholt, Dale R
AU - O'Connell, Kevin S
AU - Ophoff, Roel A
AU - Palmer, Cameron
AU - Palotie, Aarno
AU - Palviainen, Teemu
AU - Pare, Guillaume
AU - Paternoster, Lavinia
AU - Peltonen, Leena
AU - Penninx, Brenda W J H
AU - Polasek, Ozren
AU - Pramstaller, Peter P
AU - Prokopenko, Inga
AU - Raikkonen, Katri
AU - Ripatti, Samuli
AU - Rivadeneira, Fernando
AU - Rudan, Igor
AU - Rujescu, Dan
AU - Smit, Johannes H
AU - Smith, George Davey
AU - Smoller, Jordan W
AU - Soranzo, Nicole
AU - Spector, Tim D
AU - Pourcain, Beate St
AU - Starr, John M
AU - Stefánsson, Hreinn
AU - Steinberg, Stacy
AU - Teder-Laving, Maris
AU - Thorleifsson, Gudmar
AU - Stefánsson, Kári
AU - Timpson, Nicholas J
AU - Uitterlinden, André G
AU - van Duijn, Cornelia M
AU - van Rooij, Frank J A
AU - Vink, Jaqueline M
AU - Vollenweider, Peter
AU - Vuoksimaa, Eero
AU - Waeber, Gérard
AU - Wareham, Nicholas J
AU - Warrington, Nicole
AU - Waterworth, Dawn
AU - Werge, Thomas
AU - Wichmann, H-Erich
AU - Widen, Elisabeth
AU - Willemsen, Gonneke
AU - Wright, Alan F
AU - Wright, Margaret J
AU - Xu, Mousheng
AU - Zhao, Jing Hua
AU - Kraft, Peter
AU - Hinds, David A
AU - Lindgren, Cecilia M
AU - Mägi, Reedik
AU - Neale, Benjamin M
AU - Evans, David M
AU - Medland, Sarah E
TI - Genome-wide association study identifies 48 common genetic variants associated with handedness.
JO - Nature human behaviour
VL - 5
IS - 1
SN - 2397-3374
CY - London
PB - Nature Research
M1 - DZNE-2021-00872
SP - 59 - 70
PY - 2021
AB - 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.
KW - Adult
KW - Aged
KW - Female
KW - Functional Laterality: genetics
KW - Gene Frequency: genetics
KW - Genetic Loci: genetics
KW - Genetic Variation: genetics
KW - Genome-Wide Association Study
KW - Humans
KW - Linkage Disequilibrium
KW - Male
KW - Middle Aged
KW - Polymorphism, Single Nucleotide: genetics
KW - Quantitative Trait, Heritable
KW - Sex Factors
LB - PUB:(DE-HGF)16
C6 - pmid:32989287
C2 - pmc:PMC7116623
DO - DOI:10.1038/s41562-020-00956-y
UR - https://pub.dzne.de/record/155704
ER -