Splice-altering variant in COL11A1 as a cause of nonsyndromic hearing loss DFNA37
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
Published in Genetics in medicine (01.04.2019)
Published in Genetics in medicine (01.04.2019)
Get full text
Journal Article
Understanding the complex etiologies of developmental disorders: behavioral and molecular genetic approaches
Willcutt, Erik G, Pennington, Bruce F, Duncan, Laramie, Smith, Shelley D, Keenan, Janice M, Wadsworth, Sally, Defries, John C, Olson, Richard K
Published in Journal of developmental and behavioral pediatrics (01.09.2010)
Published in Journal of developmental and behavioral pediatrics (01.09.2010)
Get more information
Journal Article
DCDC2 Is Associated with Reading Disability and Modulates Neuronal Development in the Brain
Haiying Meng, Smith, Shelley D., Karl Hager, Held, Matthew, Jonathan Liu, Olson, Richard K., Pennington, Bruce F., DeFries, John C., Gelernter, Joel, Thomas O'Reilly-Pol, Somlo, Stefan, Skudlarski, Pawel, Shaywitz, Sally E., Shaywitz, Bennett A., Karen Marchione, Wang, Yu, Murugan Paramasivam, LoTurco, Joseph J., Page, Grier P., Jeffrey R. Gruen
Published in Proceedings of the National Academy of Sciences - PNAS (22.11.2005)
Published in Proceedings of the National Academy of Sciences - PNAS (22.11.2005)
Get full text
Journal Article
Breakthroughs in the search for dyslexia candidate genes
McGrath, Lauren M., Smith, Shelley D., Pennington, Bruce F.
Published in Trends in molecular medicine (01.07.2006)
Published in Trends in molecular medicine (01.07.2006)
Get full text
Journal Article
A Family Based Association Study of DRD4, DAT1, and 5HTT and Continuous Traits of Attention-Deficit Hyperactivity Disorder
Bidwell, L. Cinnamon, Willcutt, Erik G., McQueen, Matthew B., DeFries, John C., Olson, Richard K., Smith, Shelley D., Pennington, Bruce F.
Published in Behavior genetics (2011)
Published in Behavior genetics (2011)
Get full text
Journal Article
Identification of candidate genes for dyslexia susceptibility on chromosome 18
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
Published in PloS one (28.10.2010)
Published in PloS one (28.10.2010)
Get full text
Journal Article
Quantitative trait locus for reading disability on chromosome 6p is pleiotropic for attention-deficit/hyperactivity disorder
Willcutt, Erik G, Pennington, Bruce F, Smith, Shelley D, Cardon, Lon R, Gayán, Javier, Knopik, Valerie S, Olson, Richard K, DeFries, John C
Published in American journal of medical genetics (08.04.2002)
Published in American journal of medical genetics (08.04.2002)
Get more information
Journal Article
Pedigree-Based Gene Mapping Supports Previous Loci and Reveals Novel Suggestive Loci in Specific Language Impairment
Andres, Erin M, Earnest, Kathleen Kelsey, Smith, Shelley D, Rice, Mabel L, Raza, Muhammad Hashim
Published in Journal of speech, language, and hearing research (01.12.2020)
Published in Journal of speech, language, and hearing research (01.12.2020)
Get full text
Journal Article
Neuropsychology and genetics of speech, language, and literacy disorders
Peterson, Robin L, McGrath, Lauren M, Smith, Shelley D, Pennington, Bruce F
Published in The Pediatric clinics of North America (01.06.2007)
Published in The Pediatric clinics of North America (01.06.2007)
Get more information
Journal Article
Multivariate genome-wide association study of rapid automatised naming and rapid alternating stimulus in Hispanic American and African–American youth
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
Published in Journal of medical genetics (01.08.2019)
Published in Journal of medical genetics (01.08.2019)
Get full text
Journal Article
The regulatory element READ1 epistatically influences reading and language, with both deleterious and protective alleles
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
Published in Journal of medical genetics (01.03.2016)
Published in Journal of medical genetics (01.03.2016)
Get full text
Journal Article
Enrichment of putatively damaging rare variants in the DYX2 locus and the reading-related genes CCDC136 and FLNC
Adams, Andrew K., Smith, Shelley D., Truong, Dongnhu T., Willcutt, Erik G., Olson, Richard K., DeFries, John C., Pennington, Bruce F., Gruen, Jeffrey R.
Published in Human genetics (01.11.2017)
Published in Human genetics (01.11.2017)
Get full text
Journal Article
Gene x Environment Interactions in Reading Disability and Attention-Deficit/Hyperactivity Disorder
Pennington, Bruce F, McGrath, Lauren M, Rosenberg, Jenni, Barnard, Holly, Smith, Shelley D, Willcutt, Erik G, Friend, Angela, DeFries, John C, Olson, Richard K
Published in Developmental psychology (01.01.2009)
Published in Developmental psychology (01.01.2009)
Get more information
Journal Article
Characterization of the DYX2 locus on chromosome 6p22 with reading disability, language impairment, and IQ
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.
Published in Human genetics (01.07.2014)
Published in Human genetics (01.07.2014)
Get full text
Journal Article
A 77-Kilobase Region of Chromosome 6p22.2 Is Associated with Dyslexia in Families From the United Kingdom and From the United States
Francks, Clyde, Paracchini, Silvia, Smith, Shelley D., Richardson, Alex J., Scerri, Tom S., Cardon, Lon R., Marlow, Angela J., MacPhie, I. Laurence, Walter, Janet, Pennington, Bruce F., Fisher, Simon E., Olson, Richard K., DeFries, John C., Stein, John F., Monaco, Anthony P.
Published in American journal of human genetics (01.12.2004)
Published in American journal of human genetics (01.12.2004)
Get full text
Journal Article
Detecting incipient inner-ear damage from impulse noise with otoacoustic emissions
Marshall, Lynne, Lapsley Miller, Judi A, Heller, Laurie M, Wolgemuth, Keith S, Hughes, Linda M, Smith, Shelley D, Kopke, Richard D
Published in The Journal of the Acoustical Society of America (01.02.2009)
Published in The Journal of the Acoustical Society of America (01.02.2009)
Get more information
Journal Article
Investigating the effects of copy number variants on reading and language performance
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
Published in Journal of neurodevelopmental disorders (15.05.2016)
Published in Journal of neurodevelopmental disorders (15.05.2016)
Get full text
Journal Article
Linkage of speech sound disorder to reading disability loci
Smith, Shelley D., Pennington, Bruce F., Boada, Richard, Shriberg, Lawrence D.
Published in Journal of child psychology and psychiatry (01.10.2005)
Published in Journal of child psychology and psychiatry (01.10.2005)
Get full text
Journal Article