Genome-wide association study reveals new insights into the heritability and genetic correlates of developmental dyslexia Article Swipe

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Alessandro Gialluisi , Till F. M. Andlauer , Nazanin Mirza‐Schreiber , Kristina Moll , Jessica Becker , Per Hoffmann , Kerstin U. Ludwig , Darina Czamara , Beaté St Pourcain , Ferenc Honbolygó , Dénes Tóth , Valéria Csépe , Guillaume Huguet , Yves Chaix , Stéphanie Iannuzzi , Jean‐François Démonet , Andrew P. Morris , Jacqueline Hulslander , Erik G. Willcutt , John C. DeFries , Richard K. Olson , Shelley D. Smith , Bruce F. Pennington , Anniek Vaessen , Urs Maurer , Heikki Lyytinen , Myriam Peyrard‐Janvid , Paavo H. T. Leppänen , Daniel Brandeis , Milene Bonte , John Stein , Joel B. Talcott , Fabien Fauchereau , Arndt Wilcke , Holger Kirsten , Bent Müller , Clyde Francks , Thomas Bourgeron , Anthony P. Monaco , Franck Ramus , Karin Landerl , Juha Kere , Thomas Scerri , Silvia Paracchini , Simon E. Fisher , Johannes Schumacher , Markus M. Nöthen , Bertram Müller‐Myhsok , Gerd Schulte‐Körne ·

YOU? · · 2020 · Open Access · · DOI: https://doi.org/10.1038/s41380-020-00898-x

Related Topics

Heritability

Genome-Wide Association Study

Concepts

Heritability Genome-wide association study Dyslexia Single-nucleotide polymorphism Genetic association Missing heritability problem SNP Genetics Psychology Attention deficit hyperactivity disorder Bipolar disorder Biology Clinical psychology Gene Psychiatry Genotype Cognition Political science Law Reading (process)

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Type: article
Language: en
Landing Page: https://doi.org/10.1038/s41380-020-00898-x
PDF: https://www.nature.com/articles/s41380-020-00898-x.pdf
OA Status: hybrid
Cited By: 123
References: 105
Related Works: 10
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DOI: https://doi.org/10.1038/s41380-020-00898-x

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Title: Genome-wide association study reveals new insights into the heritability and genetic correlates of developmental dyslexia

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Language: en

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Publication year: 2020

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Publication date: 2020-10-14

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Authors: Alessandro Gialluisi, Till F. M. Andlauer, Nazanin Mirza‐Schreiber, Kristina Moll, Jessica Becker, Per Hoffmann, Kerstin U. Ludwig, Darina Czamara, Beaté St Pourcain, Ferenc Honbolygó, Dénes Tóth, Valéria Csépe, Guillaume Huguet, Yves Chaix, Stéphanie Iannuzzi, Jean‐François Démonet, Andrew P. Morris, Jacqueline Hulslander, Erik G. Willcutt, John C. DeFries, Richard K. Olson, Shelley D. Smith, Bruce F. Pennington, Anniek Vaessen, Urs Maurer, Heikki Lyytinen, Myriam Peyrard‐Janvid, Paavo H. T. Leppänen, Daniel Brandeis, Milene Bonte, John Stein, Joel B. Talcott, Fabien Fauchereau, Arndt Wilcke, Holger Kirsten, Bent Müller, Clyde Francks, Thomas Bourgeron, Anthony P. Monaco, Franck Ramus, Karin Landerl, Juha Kere, Thomas Scerri, Silvia Paracchini, Simon E. Fisher, Johannes Schumacher, Markus M. Nöthen, Bertram Müller‐Myhsok, Gerd Schulte‐Körne

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Landing page: https://doi.org/10.1038/s41380-020-00898-x

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Concepts: Heritability, Genome-wide association study, Dyslexia, Single-nucleotide polymorphism, Genetic association, Missing heritability problem, SNP, Genetics, Psychology, Attention deficit hyperactivity disorder, Bipolar disorder, Biology, Clinical psychology, Gene, Psychiatry, Genotype, Cognition, Political science, Law, Reading (process)

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Cited by: 123

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Citations by year (recent): 2025: 20, 2024: 27, 2023: 27, 2022: 23, 2021: 22

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References (count): 105

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