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Discovery of 42 genome-wide significant loci associated with dyslexia (vol 54, pg 1621, 2022) Doust, Catherine B.; Fontanillas, Pierre P.; Eising, Else F.; Gordon, Scott R.; Wang, Zhengjun K.; Alagoz, Goekberk G.; Molz, Barbara C.; St Pourcain, Beate D.; Francks, Clyde J.; Marioni, Riccardo E. G.; Zhao, Jinging; Paracchini, Silvia C.; Talcott, Joel B. E.; Monaco, Anthony P.; DeFries, John; Pennington, Bruce; Smith, Shelley; Wright, Margaret; Martin, Nicholas; Bates, Timothy; Fisher, Simon; Luciano, Michelle Share Save
Hypothesis-driven genome-wide association studies provide novel insights into genetics of reading disabilities Price, Kaitlyn M.; Wigg, Karen G.; Eising, Else; Feng, Yu; Blokland, Kirsten; Wilkinson, Margaret; Kerr, Elizabeth N.; Guger, Sharon L.; Abbondanza, Filippo; Allegrini, Andrea G.; Andlauer, Till F. M.; Bates, Timothy C.; Bernard, Manon; Bonte, Milene; Boomsma, Dorret I.; Bourgeron, Thomas; Brandeis, Daniel; Carreiras, Manuel; Ceroni, Fabiola; Csepe, Valeria; Dale, Philip S.; DeFries, John C.; de Jong, Peter F.; Demonet, Jean Francois; de Zeeuw, Eveline L.; Franken, Marie-Christine J.; Francks, Clyde; Gerritse, Margot; Gialluisi, Alessandro; Gordon, Scott D.; Gruen, Jeffrey R.; Hayiou-Thomas, Marianna E.; Hernandez-Cabrera, Juan; Hottenga, Jouke-Jan; Hulme, Charles; Jansen, Philip R.; Kere, Juha; Koomar, Tanner; Landerl, Karin; Leonard, Gabriel T.; Liao, Zhijie; Luciano, Michelle; Lyytinen, Heikki; Martin, Nicholas G.; Martinelli, Angela; Maurer, Urs; Michaelson, Jacob J.; Mirza-Schreiber, Nazanin; Moll, Kristina; Monaco, Anthony P.; Morgan, Angela T.; Mueller-Myhsok, Bertram; Newbury, Dianne F.; Noethen, Markus M.; Olson, Richard K.; Paracchini, Silvia; Paus, Tomas; Pausova, Zdenka; Pennell, Craig E.; Pennington, Bruce F.; Plomin, Robert J.; Ramus, Franck; Reilly, Sheena; Richer, Louis; Rimfeld, Kaili; Schulte-Korne, Gerd; Shapland, Chin Yang; Simpson, Nuala H.; Smith, Shelley D.; Snowling, Margaret J.; St Pourcain, Beate; Stein, John F.; Talcott, Joel B.; Tiemeier, Henning; Tomblin, J. Bruce; Truong, Dongnhu T.; van Bergen, Elsje; van der Schroeff, Marc P.; Van Donkelaar, Marjolein; Verhoef, Ellen; Wang, Carol A.; Watkins, Kate E.; Whitehouse, Andrew J. O.; Willcutt, Erik G.; Wright, Margaret J.; Zhu, Gu; Fisher, Simon E.; Lovett, Maureen W.; Strug, Lisa J.; Barr, Cathy L. Share Save
Discovery of 42 genome-wide significant loci associated with dyslexia Doust, Catherine; Fontanillas, Pierre; Eising, Else; Gordon, Scott D.; Wang, Zhengjun; Alagoz, Gokberk; Molz, Barbara; St Pourcain, Beate; Francks, Clyde; Marioni, Riccardo E.; Zhao, Jingjing; Paracchini, Silvia; Talcott, Joel B.; Monaco, Anthony P.; Stein, John F.; Gruen, Jeffrey R.; Olson, Richard K.; Willcutt, Erik G.; DeFries, John C.; Pennington, Bruce F.; Smith, Shelley D.; Wright, Margaret J.; Martin, Nicholas G.; Auton, Adam; Bates, Timothy C.; Fisher, Simon E.; Luciano, Michelle Share Save
Genome-wide analyses of individual differences in quantitatively assessed reading- and language-related skills in up to 34,000 people Eising, Else; Mirza-Schreiber, Nazanin; de Zeeuw, Eveline L.; Wang, Carol A.; Truong, Dongnhu T.; Allegrini, Andrea G.; Shapland, Chin Yang; Zhu, Gu; Wigg, Karen G.; Gerritse, Margot L.; Molz, Barbara; Alagoz, Gokberk; Gialluisi, Alessandro; Abbondanza, Filippo; Rimfeld, Kaili; van Donkelaar, Marjolein; Liao, Zhijie; Jansen, Philip R.; Andlauer, Till F. M.; Bates, Timothy C.; Bernard, Manon; Blokland, Kirsten; Bonte, Milene; Borglum, Anders D.; Bourgeron, Thomas; Brandeis, Daniel; Ceronihh, Fabiola; Csepe, Valeria; Dale, Philip S.; de Jong, Peter F.; DeFries, John C.; Demonet, Jean-Francois; Demontis, Ditte; Feng, Yu; Gordon, Scott D.; Guger, Sharon L.; Hayiou-Thomas, Marianna E.; Hernandez-Cabrera, Juan A.; Hottenga, Jouke-Jan; Hulme, Charles; Kere, Juha; Kerr, Elizabeth N.; Koomar, Tanner; Landerl, Karin; Leonard, Gabriel T.; Lovett, Maureen W.; Lyytinen, Heikki; Martin, Nicholas G.; Martinelli, Angela; Maurer, Urs; Michaelson, Jacob J.; Moll, Kristina; Monaco, Anthony P.; Morgan, Angela T.; Nothen, Markus M.; Pausova, Zdenka; Pennell, Craig E.; Pennington, Bruce F.; Price, Kaitlyn M.; Rajagopal, Veera M.; Ramus, Franck; Richer, Louis; Simpson, Nuala H.; Smith, Shelley D.; Snowling, Margaret J.; Stein, John; Struguuu, Lisa J.; Talcott, Joel B.; Tiemeier, Henning; van der Schroeff, Marc P.; Verhoef, Ellen; Watkins, Kate E.; Wilkinson, Margaret; Wright, Margaret J.; Barr, Cathy L.; Boomsma, Dorret, I; Carreiras, Manuel; Franken, Marie-Christine J.; Gruen, Jeffrey R.; Luciano, Michelle; Muller-Myhsok, Bertram; Newbury, Dianne F.; Olson, Richard K.; Paracchini, Silvia; Paus, Tomas; Plomin, Robert; Reilly, Sheena; Schulte-Korn, Gerd; Tomblin, J. Bruce; Bergen, Elsjevan; Whitehouse, Andrew J. O.; Willcutt, Erik G.; St Pourcain, Beate; Francks, Clyde; Fisher, Simon E. Share Save
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The Importance of Bringing Transplantation Tolerance to the Clinic Cosimi, A. Benedict; Ascher, Nancy L.; Emond, Jean C.; Kaufman, Dixon B.; Madsen, Joren C.; Miller, Joshua; Monaco, Anthony P.; Montgomery, Robert A.; Newell, Kenneth A.; Sanchez-Fueyo, Alberto; Sarwal, Minnie M.; Scandling, John D.; Strober, Samuel; Todo, Satoru; Weir, Matthew R.; Sachs, David H. Share Save
Genome-wide association study reveals new insights into the heritability and genetic correlates of developmental dyslexia Gialluisi, Alessandro; Andlauer, Till F. M.; Mirza-Schreiber, Nazanin; Moll, Kristina; Becker, Jessica; Hoffmann, Per; Ludwig, Kerstin U.; Czamara, Darina; St Pourcain, Beate; Honbolygo, Ferenc; Toth, Denes; Csepe, Valeria; Huguet, Guillaume; Chaix, Yves; Iannuzzi, Stephanie; Demonet, Jean-Francois; Morris, Andrew P.; Hulslander, Jacqueline; Willcutt, Erik G.; DeFries, John C.; Olson, Richard K.; Smith, Shelley D.; Pennington, Bruce F.; Vaessen, Anniek; Maurer, Urs; Lyytinen, Heikki; Peyrard-Janvid, Myriam; Leppanen, Paavo H. T.; Brandeis, Daniel; Bonte, Milene; Stein, John F.; Talcott, Joel B.; Fauchereau, Fabien; Wilcke, Arndt; Kirsten, Holger; Mueller, Bent; Francks, Clyde; Bourgeron, Thomas; Monaco, Anthony P.; Ramus, Franck; Landerl, Karin; Kere, Juha; Scerri, Thomas S.; Paracchini, Silvia; Fisher, Simon E.; Schumacher, Johannes; Noethen, Markus M.; Mueller-Myhsok, Bertram; Schulte-Koerne, Gerd Share Save
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Even late may still be brain, but be careful Fiori, P.; Corbo, A.; Corbo, G.; Iorillo, L.; Capaldo, G.; Botticella, F.; Dragonetti, C.; Morella, A.; Pellecchia, A.; Bellizzi, G.; Pelosi, C.; Savino, P.; Alberico, M.; Benigni, G.; De Caro, M.; Guerriero, B.; Pace, E.; Mazza, E.; Tammaro, C.; Giannetti, L. M.; Monaco, A. Share Save
Genome-wide association scan identifies new variants associated with a cognitive predictor of dyslexia Gialluisi, Alessandro; Andlauer, Till F. M.; Mirza-Schreiber, Nazanin; Moll, Kristina; Becker, Jessica; Hoffmann, Per; Ludwig, Kerstin U.; Czamara, Darina; St Pourcain, Beate; Brandler, William; Honbolygo, Ferenc; Toth, Denes; Csepe, Valeria; Huguet, Guillaume; Morris, Andrew P.; Hulslander, Jacqueline; Willcutt, Erik G.; DeFries, John C.; Olson, Richard K.; Smith, Shelley D.; Pennington, Bruce F.; Vaessen, Anniek; Maurer, Urs; Lyytinen, Heikki; Peyrard-Janvid, Myriam; Leppanen, Paavo H. T.; Brandeis, Daniel; Bonte, Milene; Stein, John F.; Talcott, Joel B.; Fauchereau, Fabien; Wilcke, Arndt; Francks, Clyde; Bourgeron, Thomas; Monaco, Anthony P.; Ramus, Franck; Landerl, Karin; Kere, Juha; Scerri, Thomas S.; Paracchini, Silvia; Fisher, Simon E.; Schumacher, Johannes; Noethen, Markus M.; Mueller-Myhsok, Bertram; Schulte-Koerne, Gerd Share Save
Human VPS13A is associated with multiple organelles and influences mitochondrial morphology and lipid droplet motility Yeshaw, Wondwossen M.; van der Zwaag, Marianne; Pinto, Francesco; Lahaye, Liza L.; Faber, Anita I. E.; Gomez-Sanchez, Ruben; Dolga, Amalia M.; Poland, Conor; Monaco, Anthony P.; van IJzendoorn, Sven C. D.; Grzeschik, Nicola A.; Velayos-Baeza, Antonio; Sibon, Ody C. M. Share Save
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The DCDC2 deletion is not a risk factor for dyslexia Scerri, T. S.; Macpherson, E.; Martinelli, A.; Wa, W. C.; Monaco, A. P.; Stein, J.; Zheng, M.; Ho, C. Suk-Han; McBride, C.; Snowling, M.; Hulme, C.; Hayiou-Thomas, M. E.; Waye, M. M. Y.; Talcott, J. B.; Paracchini, S. Share Save
Further evidence for a parent-of-origin effect at the NOP9 locus on language-related phenotypes Pettigrew, Kerry A.; Frinton, Emily; Nudel, Ron; Chan, May T. M.; Thompson, Paul; Hayiou-Thomas, Marianna E.; Talcott, Joel B.; Stein, John; Monaco, Anthony P.; Hulme, Charles; Snowling, Margaret J.; Newbury, Dianne F.; Paracchini, Silvia Share Save
The handedness-associated PCSK6 locus spans an intronic promoter regulating novel transcripts Shore, Robert; Covill, Laura; Pettigrew, Kerry A.; Brandler, William M.; Diaz, Rebeca; Xu, Yiwang; Tello, Javier A.; Talcott, Joel B.; Newbury, Dianne F.; Stein, John; Monaco, Anthony P.; Paracchini, Silvia Share Save
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