Approach to epigenetic analysis in language disorders

por Smith, Shelley D.
Publicado 2011

Convergent genetic linkage and associations to language, speech and reading measures in families of probands with Specific Language Impairment

por Rice, Mabel L., Smith, Shelley D., Gayán, Javier
Publicado 2009

Pedigree-Based Gene Mapping Supports Previous Loci and Reveals Novel Suggestive Loci in Specific Language Impairment

por Andres, Erin M., Earnest, Kathleen Kelsey, Smith, Shelley D., Rice, Mabel L., Raza, Muhammad Hashim
Publicado 2020

Enrichment of putatively damaging rare variants in the DYX2 locus and the reading-related genes CCDC136 and FLNC

por Adams, Andrew K., Smith, Shelley D., Truong, Dongnhu T., Willcutt, Erik G., Olson, Richard K., DeFries, John C., Pennington, Bruce F., Gruen, Jeffrey R.
Publicado 2017

Investigating the effects of copy number variants on reading and language performance

por Gialluisi, Alessandro, Visconti, Alessia, Willcutt, Erik G., Smith, Shelley D., Pennington, Bruce F., Falchi, Mario, DeFries, John C., Olson, Richard K., Francks, Clyde, Fisher, Simon E.
Publicado 2016

The regulatory element READ1 epistatically influences reading and language, with both deleterious and protective alleles

por Powers, Natalie R, Eicher, John D, Miller, Laura L, Kong, Yong, Smith, Shelley D, Pennington, Bruce F, Willcutt, Erik G, Olson, Richard K, Ring, Susan M, Gruen, Jeffrey R
Publicado 2016

Identification of Candidate Genes for Dyslexia Susceptibility on Chromosome 18

por Scerri, Thomas S., Paracchini, Silvia, Morris, Andrew, MacPhie, I. Laurence, Talcott, Joel, Stein, John, Smith, Shelley D., Pennington, Bruce F., Olson, Richard K., DeFries, John C., Monaco, Anthony P.
Publicado 2010

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

por Scerri, Thomas S., Paracchini, Silvia, Morris, Andrew, MacPhie, I. Laurence, Talcott, Joel, Stein, John, Smith, Shelley D., Pennington, Bruce F., Olson, Richard K., DeFries, John C., Monaco, Anthony P., Richardson, Alex J.
Publicado 2010

Splice-altering variant in COL11A1 as a cause of nonsyndromic hearing loss DFNA37

por Booth, Kevin T., Askew, James W., Talebizadeh, Zohreh, Huygen, Patrick L. M., Eudy, James, Kenyon, Judith, Hoover, Denise, Hildebrand, Michael S., Smith, Katherine R., Bahlo, Melanie, Kimberling, William J., Smith, Richard J. H., Azaiez, Hela, Smith, Shelley D.
Publicado 2018

Characterization of the DYX2 locus on chromosome 6p22 with reading disability, language impairment, and IQ

por Eicher, John D., Powers, Natalie R., Miller, Laura L., Mueller, Kathryn L., Mascheretti, Sara, Marino, Cecilia, Willcutt, Erik G., DeFries, John C., Olson, Richard K., Smith, Shelley D., Pennington, Bruce F., Tomblin, J. Bruce, Ring, Susan M., Gruen, Jeffrey R.
Publicado 2014

Multivariate genome-wide association study of rapid automatised naming and rapid alternating stimulus in Hispanic American and African–American youth

por Truong, Dongnhu Thuy, Adams, Andrew Kenneth, Paniagua, Steven, Frijters, Jan C, Boada, Richard, Hill, Dina E, Lovett, Maureen W, Mahone, E Mark, Willcutt, Erik G, Wolf, Maryanne, Defries, John C, Gialluisi, Alessandro, Francks, Clyde, Fisher, Simon E, Olson, Richard K, Pennington, Bruce F, Smith, Shelley D, Bosson-Heenan, Joan, Gruen, Jeffrey R
Publicado 2019

Author Correction: Discovery of 42 genome-wide significant loci associated with dyslexia

por Doust, Catherine, Fontanillas, Pierre, Eising, Else, Gordon, Scott D., Wang, Zhengjun, Alagöz, Gökberk, Molz, Barbara, Pourcain, Beate St, 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
Publicado 2023

Discovery of 42 genome-wide significant loci associated with dyslexia

por Doust, Catherine, Fontanillas, Pierre, Eising, Else, Gordon, Scott D., Wang, Zhengjun, Alagöz, Gökberk, Molz, Barbara, Pourcain, Beate St, 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
Publicado 2022

The Aromatase Gene CYP19A1: Several Genetic and Functional Lines of Evidence Supporting a Role in Reading, Speech and Language

por Anthoni, Heidi, Sucheston, Lara E., Lewis, Barbara A., Tapia-Páez, Isabel, Fan, Xiaotang, Zucchelli, Marco, Taipale, Mikko, Stein, Catherine M., Hokkanen, Marie-Estelle, Castrén, Eero, Pennington, Bruce F., Smith, Shelley D., Olson, Richard K., Tomblin, J. Bruce, Schulte-Körne, Gerd, Nöthen, Markus, Schumacher, Johannes, Müller-Myhsok, Bertram, Hoffmann, Per, Gilger, Jeffrey W., Hynd, George W., Nopola-Hemmi, Jaana, Leppanen, Paavo H. T., Lyytinen, Heikki, Schoumans, Jacqueline, Nordenskjöld, Magnus, Spencer, Jason, Stanic, Davor, Boon, Wah Chin, Simpson, Evan, Mäkelä, Sari, Gustafsson, Jan-Åke, Peyrard-Janvid, Myriam, Iyengar, Sudha, Kere, Juha
Publicado 2012

Genome-wide association scan identifies new variants associated with a cognitive predictor of dyslexia

por 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, Honbolygó, Ferenc, Tóth, Dénes, Csépe, Valéria, 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, Leppänen, 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, Nöthen, Markus M., Müller-Myhsok, Bertram, Schulte-Körne, Gerd
Publicado 2019

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

por Gialluisi, Alessandro, Andlauer, Till F. M., Mirza-Schreiber, Nazanin, Moll, Kristina, Becker, Jessica, Hoffmann, Per, Ludwig, Kerstin U., Czamara, Darina, Pourcain, Beate St, Honbolygó, Ferenc, Tóth, Dénes, Csépe, Valéria, 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, Leppänen, Paavo H. T., Brandeis, Daniel, Bonte, Milene, Stein, John F., Talcott, Joel B., Fauchereau, Fabien, Wilcke, Arndt, Kirsten, Holger, Müller, Bent, Francks, Clyde, Bourgeron, Thomas, Monaco, Anthony P., Ramus, Franck, Landerl, Karin, Kere, Juha, Scerri, Thomas S., Paracchini, Silvia, Fisher, Simon E., Schumacher, Johannes, Nöthen, Markus M., Müller-Myhsok, Bertram, Schulte-Körne, Gerd
Publicado 2020

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

por 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, Alagöz, Gökberk, 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, Børglum, Anders D., Bourgeron, Thomas, Brandeis, Daniel, Ceroni, Fabiola, Csépe, Valéria, Dale, Philip S., de Jong, Peter F., DeFries, John C., Démonet, Jean-François, Demontis, Ditte, Feng, Yu, Gordon, Scott D., Guger, Sharon L., Hayiou-Thomas, Marianna E., Hernández-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., Nöthen, 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, Strug, 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, Müller-Myhsok, Bertram, Newbury, Dianne F., Olson, Richard K., Paracchini, Silvia, Paus, Tomáš, Plomin, Robert, Reilly, Sheena, Schulte-Körne, Gerd, Tomblin, J. Bruce, van Bergen, Elsje, Whitehouse, Andrew J. O., Willcutt, Erik G., St Pourcain, Beate, Francks, Clyde, Fisher, Simon E.
Publicado 2022