A transcription map of the 6p22.3 reading disability locus identifying candidate genes

por Londin, Eric R, Meng, Haiying, Gruen, Jeffrey R
Publicado 2003

Sex‐specific associations between traumatic experiences and resting‐state functional connectivity in the Philadelphia Neurodevelopmental Cohort

por Wang, Shiying, Malins, Jeffrey G., Zhang, Heping, Gruen, Jeffrey R.
Publicado 2021

DCDC2 READ1 regulatory element: how temporal processing differences may shape language

por Tang, Kevin, DeMille, Mellissa M. C., Frijters, Jan C., Gruen, Jeffrey R.
Publicado 2020

Phonological Awareness Mediates the Relationship between DCDC2 and Reading Performance with the Influence of Home Environment

por Li, Miao, DeMille, Mellissa, Lovett, Maureen, Bosson-Heenan, Joan, Frijters, Jan, Gruen, Jeffrey
Publicado 2023

Functional impact of a single nucleotide polymorphism in the OPRD1 promoter region

por Zhang, Huiping, Gelernter, Joel, Gruen, Jeffrey R., Kranzler, Henry R., Herman, Aryeh I., Simen, Arthur A.
Publicado 2010

Molecular diagnostic testing for Klinefelter syndrome and other male sex chromosome aneuploidies

por Hager, Karl, Jennings, Kori, Hosono, Seiyu, Howell, Susan, Gruen, Jeffrey R, Tartaglia, Nicole R, Rinder, Henry M
Publicado 2012

Dyslexia associated gene KIAA0319 regulates cell cycle during human neuroepithelial cell development

por Paniagua, Steven, Cakir, Bilal, Hu, Yue, Kiral, Ferdi Ridvan, Tanaka, Yoshiaki, Xiang, Yangfei, Patterson, Benjamin, Gruen, Jeffrey R., Park, In-Hyun
Publicado 2022

Associations of Prenatal Nicotine Exposure and the Dopamine Related Genes ANKK1 and DRD2 to Verbal Language

por Eicher, John D., Powers, Natalie R., Cho, Kelly, Miller, Laura L., Mueller, Kathryn L., Ring, Susan M., Tomblin, J. Bruce, Gruen, Jeffrey R.
Publicado 2013

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

The Rosetta Phenotype Harmonization Method Facilitates Finding a Relationship Quantitative Trait Locus for a Complex Cognitive Trait

por Petrill, Stephen A., Klamer, Brett G., Buyske, Steven, Willcutt, Erik G., Gruen, Jeffrey R., Francis, David J., Flax, Judy F., Brzustowicz, Linda M., Bartlett, Christopher W.
Publicado 2023

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

A molecular-genetic and imaging-genetic approach to specific comprehension difficulties in children

por Li, Miao, Malins, Jeffrey G., DeMille, Mellissa M. C., Lovett, Maureen W., Truong, Dongnhu T., Epstein, Katherine, Lacadie, Cheryl, Mehta, Chintan, Bosson-Heenan, Joan, Gruen, Jeffrey R., Frijters, Jan C.
Publicado 2018

Worldwide distribution of the DCDC2 READ1 regulatory element and its relationship with phoneme variation across languages

por DeMille, Mellissa M. C., Tang, Kevin, Mehta, Chintan M., Geissler, Christopher, Malins, Jeffrey G., Powers, Natalie R., Bowen, Beatrice M., Adams, Andrew K., Truong, Dongnhu T., Frijters, Jan C., Gruen, Jeffrey R.
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

Family Income, Parental Education and Brain Structure in Children and Adolescents

por Noble, Kimberly G., Houston, Suzanne M., Brito, Natalie H., Bartsch, Hauke, Kan, Eric, Kuperman, Joshua M., Akshoomoff, Natacha, Amaral, David G., Bloss, Cinnamon S., Libiger, Ondrej, Schork, Nicholas J., Murray, Sarah S., Casey, B. J., Chang, Linda, Ernst, Thomas M., Frazier, Jean A., Gruen, Jeffrey R., Kennedy, David N., Zijl, Peter Van, Mostofsky, Stewart, Kaufmann, Walter E., Kenet, Tal, Dale, Anders M., Jernigan, Terry L., Sowell, Elizabeth R.
Publicado 2015

Dyslexia and language impairment associated genetic markers influence cortical thickness and white matter in typically developing children

por Eicher, John D., Montgomery, Angela M., Akshoomoff, Natacha, Amaral, David G., Bloss, Cinnamon S., Libiger, Ondrej, Schork, Nicholas J., Darst, Burcu F., Casey, B. J., Chang, Linda, Ernst, Thomas, Frazier, Jean, Kaufmann, Walter E., Keating, Brian, Kenet, Tal, Kennedy, David, Mostofsky, Stewart, Murray, Sarah S., Sowell, Elizabeth R., Bartsch, Hauke, Kuperman, Joshua M., Brown, Timothy T., Hagler, Donald J., Dale, Anders M., Jernigan, Terry L., Gruen, Jeffrey R.
Publicado 2015

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

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