Correction: Identification of Candidate Genes for Dyslexia Susceptibility on Chromosome 18.

Autor: Thomas S. Scerri, Silvia Paracchini, Andrew Morris, I. Laurence MacPhie, Joel Talcott, John Stein, Shelley D. Smith, Bruce F. Pennington, Richard K. Olson, John C. DeFries, Anthony P. Monaco, Alex J. Richardson

Publikováno v: PLoS ONE, Vol 5, Iss 12 (2010)

Externí odkaz: https://doaj.org/article/56870a7de1124cf78a766b8829820f65

Rapid auditory processing and medial geniculate nucleus anomalies in Kiaa0319 knockout mice

Autor: Peter A. Perrino, Renee Y. Chasse, Anthony P. Monaco, Zoltán Molnár, Antonio Velayos‐Baeza, R. Holly Fitch

Publikováno v: Genes, Brain and Behavior. 21

Developmental dyslexia is a common neurodevelopmental disorder characterized by difficulties in reading and writing. Although underlying biological and genetic mechanisms remain unclear, anomalies in phonological processing and auditory processing ha

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::65460adcafef1dc2a48dc56bbf2e7fc2
https://doi.org/10.1111/gbb.12808

Genome-wide association analyses of individual differences in quantitatively assessed reading- and language-related skills in up to 34,000 people

Autor: Kristina Moll, Liao Z, Feng Y, Price Km, Gruen, Scott D. Gordon, Else Eising, Bruce F. Pennington, Daniel Brandeis, Veera M. Rajagopal, Franken Mj, Bertram Müller-Myhsok, Tomblin Jb, Nazanin Mirza-Schreiber, Henning Tiemeier, Molz B, Silvia Paracchini, Wigg Kg, Beate St Pourcain, Guger Sl, van de Schroeff Mm, Alessandro Gialluisi, Simon E. Fisher, Carol A. Wang, Andrea G. Allegrini, Angela T Morgan, Cathy L. Barr, Erik G. Willcutt, Tanner Koomar, Jacob J. Michaelson, Truong Dt, Filippo Abbondanza, Hernández-Cabrera Ja, Reilly S, Timothy C. Bates, Markus M. Nöthen, Chin Yang Shapland, Gerritse M, Charles Hulme, Marianna E. Hayiou-Thomas, Blokland K, Lisa J. Strug, Robert Plomin, John F. Stein, Kerr En, D.I. Boomsma, Nicholas G. Martin, Dianne F. Newbury, Richard K. Olson, Clyde Francks, van Donkelaar M, J-J Hottenga, Michelle Luciano, Gökberk Alagöz, de Zeeuw El, Thomas Bourgeron, Craig E. Pennell, Margaret J. Wright, Anders D. Børglum, Kate E. Watkins, Andlauer Tfm, Fabiola Ceroni, Manon Bernard, Ditte Demontis, Kaili Rimfeld, Wilkinson M, Margaret J. Snowling, Andrew J. O. Whitehouse, John C. DeFries, Richer L, T. Paus, Maureen W. Lovett, Angela Martinelli, Joel B. Talcott, Gerd Schulte-Körne, Nuala H. Simpson, Zdenka Pausova, Manuel Carreiras, Anthony P. Monaco, Philip S. Dale, Gu Zhu, Ellen Verhoef, Philip R. Jansen, Karin Landerl, Shelley D. Smith, Franck Ramus, van Bergen E, Urs Maurer, Heikki Lyytinen, de Jong Pf

The use of spoken and written language is a capacity that is unique to humans. Individual differences in reading- and language-related skills are influenced by genetic variation, with twin-based heritability estimates of 30-80%, depending on the trai

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::d8719ed9c469bb55bb59c834789f72a9
https://doi.org/10.1101/2021.11.04.466897

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

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

Publikováno v: Mol. Psychiatry 26, 3004–3017 (2021)
Molecular Psychiatry
Molecular Psychiatry, 26, pp. 3004-3017
Molecular Psychiatry, 26(7), 3004-3017. Nature Publishing Group
Molecular Psychiatry, Nature Publishing Group, 2020, ⟨10.1038/s41380-020-00898-x⟩
Molecular Psychiatry, 2020, ⟨10.1038/s41380-020-00898-x⟩
Molecular psychiatry, vol. 26, no. 7, pp. 3004-3017
Molecular Psychiatry, 26, 3004-3017

Funding: AG and TFMA were supported by the Munich Cluster for Systems Neurology (SyNergy). AG 535 was supported by Fondazione Umberto Veronesi. SP is a Royal Society University Research fellow. BMM, CF, BSP and SEF are supported by the Max Planck Soc

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::15bf0ba70912f8d3d7892d2d155e9037
https://push-zb.helmholtz-muenchen.de/frontdoor.php?source_opus=60321

Infection and Malignancy Outweigh Cardiovascular Mortality in Kidney Transplant Recipients: Post Hoc Analysis of the FAVORIT Trial

Autor: Jiankang Liu, John A. D'Elia, Brian Claggett, Suphamai Bunnapradist, Peter V. Finn, Anthony P. Monaco, Larry A. Weinrauch, Matthew R. Weir

Publikováno v: The American Journal of Medicine. 131:165-172

Objective Now that long-term survival after successful renal transplantation is no longer limited by excessive cardiovascular risk, the primary care physician should consider that infection and malignancy are leading noncardiovascular causes of death

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2fb16ad3177ddf7e2c7b252570ce7bcf
https://doi.org/10.1016/j.amjmed.2017.08.038