出版者更正:儿童多动症症状和诊断的全基因组关联荟萃分析确定了新的基因座和潜在的效应基因。

IF 29 1区 生物学 Q1 GENETICS & HEREDITY
Camiel M van der Laan, Hill F Ip, Marijn Schipper, Jouke-Jan Hottenga, Beate St Pourcain, Tetyana Zayats, René Pool, Eva M L Krapohl, Isabell Brikell, María Soler Artigas, Judit Cabana-Domínguez, Natalia Llonga, Ilja M Nolte, Koen Bolhuis, Teemu Palviainen, Hadi Zafarmand, Scott Gordon, Fazil Aliev, S Alexandra Burt, Carol A Wang, Gretchen Saunders, Ville Karhunen, Daniel E Adkins, Richard Border, Roseann E Peterson, Joseph A Prinz, Elisabeth Thiering, Natàlia Vilor-Tejedor, Tarunveer S Ahluwalia, Andrea Allegrini, Kaili Rimfeld, Qi Chen, Yi Lu, Joanna Martin, Rosa Bosch, Josep Antoni Ramos-Quiroga, Alexander Neumann, Judith Ensink, Katrina L Grasby, José J Morosoli, Xiaoran Tong, Shelby Marrington, James G Scott, Andrey A Shabalin, Robin Corley, Luke M Evans, Karen Sugden, Silvia Alemany, Lærke Sass, Rebecca Vinding, Erik A Ehli, Fiona A Hagenbeek, Eske M Derks, Henrik Larsson, Harold Snieder, Charlotte Cecil, Alyce M Whipp, Tellervo Korhonen, Eero Vuoksimaa, Richard J Rose, André G Uitterlinden, Jan Haavik, Jennifer R Harris, Øyvind Helgeland, Stefan Johansson, Gun Peggy S Knudsen, Pal Rasmus Njolstad, Qing Lu, Alina Rodriguez, Anjali K Henders, Abdullah Mamun, Jackob M Najman, Sandy Brown, Christian Hopfer, Kenneth Krauter, Chandra A Reynolds, Andrew Smolen, Michael Stallings, Sally Wadsworth, Tamara L Wall, Lindon Eaves, Judy L Silberg, Allison Miller, Alexandra Havdahl, Sabrina Llop, Maria-Jose Lopez-Espinosa, Klaus Bønnelykke, Jordi Sunyer, Louise Arseneault, Marie Standl, Joachim Heinrich, Joseph Boden, John Pearson, John Horwood, Martin Kennedy, Richie Poulton, Hermine H Maes, John Hewitt, William E Copeland, Christel M Middeldorp, Gail M Williams, Naomi Wray, Marjo-Riitta Järvelin, Matt McGue, William Iacono, Avshalom Caspi, Terrie E Moffitt, Andrew J O Whitehouse, Craig E Pennell, Kelly L Klump, Chang Jiang, Danielle M Dick, Ted Reichborn-Kjennerud, Nicholas G Martin, Sarah E Medland, Tanja Vrijkotte, Jaakko Kaprio, Henning Tiemeier, George Davey Smith, Catharina A Hartman, Albertine J Oldehinkel, Miquel Casas, Marta Ribasés, Paul Lichtenstein, Sebastian Lundström, Robert Plomin, Meike Bartels, Michel G Nivard, Dorret I Boomsma
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Whipp, Tellervo Korhonen, Eero Vuoksimaa, Richard J Rose, André G Uitterlinden, Jan Haavik, Jennifer R Harris, Øyvind Helgeland, Stefan Johansson, Gun Peggy S Knudsen, Pal Rasmus Njolstad, Qing Lu, Alina Rodriguez, Anjali K Henders, Abdullah Mamun, Jackob M Najman, Sandy Brown, Christian Hopfer, Kenneth Krauter, Chandra A Reynolds, Andrew Smolen, Michael Stallings, Sally Wadsworth, Tamara L Wall, Lindon Eaves, Judy L Silberg, Allison Miller, Alexandra Havdahl, Sabrina Llop, Maria-Jose Lopez-Espinosa, Klaus Bønnelykke, Jordi Sunyer, Louise Arseneault, Marie Standl, Joachim Heinrich, Joseph Boden, John Pearson, John Horwood, Martin Kennedy, Richie Poulton, Hermine H Maes, John Hewitt, William E Copeland, Christel M Middeldorp, Gail M Williams, Naomi Wray, Marjo-Riitta Järvelin, Matt McGue, William Iacono, Avshalom Caspi, Terrie E Moffitt, Andrew J O Whitehouse, Craig E Pennell, Kelly L Klump, Chang Jiang, Danielle M Dick, Ted Reichborn-Kjennerud, Nicholas G Martin, Sarah E Medland, Tanja Vrijkotte, Jaakko Kaprio, Henning Tiemeier, George Davey Smith, Catharina A Hartman, Albertine J Oldehinkel, Miquel Casas, Marta Ribasés, Paul Lichtenstein, Sebastian Lundström, Robert Plomin, Meike Bartels, Michel G Nivard, Dorret I Boomsma","doi":"10.1038/s41588-025-02383-z","DOIUrl":null,"url":null,"abstract":"","PeriodicalId":18985,"journal":{"name":"Nature genetics","volume":" ","pages":""},"PeriodicalIF":29.0000,"publicationDate":"2025-09-29","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Publisher Correction: Genome-wide association meta-analysis of childhood ADHD symptoms and diagnosis identifies new loci and potential effector genes.\",\"authors\":\"Camiel M van der Laan, Hill F Ip, Marijn Schipper, Jouke-Jan Hottenga, Beate St Pourcain, Tetyana Zayats, René Pool, Eva M L Krapohl, Isabell Brikell, María Soler Artigas, Judit Cabana-Domínguez, Natalia Llonga, Ilja M Nolte, Koen 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Publisher Correction: Genome-wide association meta-analysis of childhood ADHD symptoms and diagnosis identifies new loci and potential effector genes.
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来源期刊
Nature genetics
Nature genetics 生物-遗传学
CiteScore
43.00
自引率
2.60%
发文量
241
审稿时长
3 months
期刊介绍: Nature Genetics publishes the very highest quality research in genetics. It encompasses genetic and functional genomic studies on human and plant traits and on other model organisms. Current emphasis is on the genetic basis for common and complex diseases and on the functional mechanism, architecture and evolution of gene networks, studied by experimental perturbation. Integrative genetic topics comprise, but are not limited to: -Genes in the pathology of human disease -Molecular analysis of simple and complex genetic traits -Cancer genetics -Agricultural genomics -Developmental genetics -Regulatory variation in gene expression -Strategies and technologies for extracting function from genomic data -Pharmacological genomics -Genome evolution
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