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Gene × Environment interactions in speech sound disorder predict language and preliteracy outcomes.
Published in:
Development & Psychopathology, 2007, v. 19, n. 4, p. 1047, doi. 10.1017/S0954579407000533
By:
- MCGRATH, LAUREN M.;
- PENNINGTON, BRUCE F.;
- WILLCUTT, ERIK G.;
- BOADA, RICHARD;
- SHRIBERG, LAWRENCE D.;
- SMITH, SHELLEY D.
Publication type:
Article
Measuring neurodevelopmental effects of polygenic risk for Alzheimer's disease via longitudinal study of brain and cognitive variables in periadolescent children: Genetics/genetic factors of Alzheimer's disease.
Published in:
Alzheimer's & Dementia: The Journal of the Alzheimer's Association, 2020, v. 16, n. 11, p. 1, doi. 10.1002/alz.044805
By:
- Warren, David E.;
- Phipps, Connor J.;
- Eckel, Medea;
- Rangel, Anthony;
- Heller, Abi M.;
- Maerlender, Arthur C.;
- Phatak, Vaishali S.;
- Cramer, Justin A.;
- Blair, James;
- Murman, Daniel L.;
- Smith, Shelley D.
Publication type:
Article
National Deaf Register as a Resource for Hereditary Deafness Research.
Published in:
Annals of the New York Academy of Sciences, 1991, v. 630, n. 1, p. 292, doi. 10.1111/j.1749-6632.1991.tb19609.x
By:
- ING, PAUL S.;
- WERNIMONT, BRENDA M.;
- SMITH, SHELLEY D.;
- KIMBERLING, WILLIAM J.
Publication type:
Article
Recurrence Risks.
Published in:
Annals of the New York Academy of Sciences, 1991, v. 630, n. 1, p. 203, doi. 10.1111/j.1749-6632.1991.tb19589.x
By:
- SMITH, SHELLEY D.
Publication type:
Article
Evidence for Major Gene Transmission of Developmental Dyslexia.
Published in:
JAMA: Journal of the American Medical Association, 1991, v. 266, n. 11, p. 1527, doi. 10.1001/jama.1991.03470110073036
By:
- Pennington, Bruce F.;
- Gilger, Jeffrey W.;
- Pauls, David;
- Smith, Sandra A.;
- Smith, Shelley D.;
- DeFries, John C.
Publication type:
Article
Independent genome-wide scans identify a chromosome 18 quantitative-trait locus influencing dyslexia.
Published in:
Nature Genetics, 2002, v. 30, n. 1, p. 86, doi. 10.1038/ng792
By:
- Fisher, Simon E.;
- Francks, Clyde;
- Marlow, Angela J.;
- MacPhie, I. Laurence;
- Newbury, Dianne F.;
- Cardon, Lon R.;
- Ishikawa-Brush, Yumiko;
- Richardson, Alex J.;
- Talcott, Joel B.;
- Gayán, Javier;
- Olson, Richard K.;
- Pennington, Bruce F.;
- Smith, Shelley D.;
- DeFries, John C.;
- Stein, John F.;
- Monaco, Anthony P.
Publication type:
Article
Identification of Candidate Genes for Dyslexia Susceptibility on Chromosome 18.
Published in:
PLoS ONE, 2010, v. 5, n. 10, p. 1, doi. 10.1371/journal.pone.0013712
By:
- 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.
Publication type:
Article
Refinement of the 6p21.3 quantitative trait locus influencing dyslexia: linkage and association analyses.
Published in:
Human Genetics, 2004, v. 115, n. 2, p. 128, doi. 10.1007/s00439-004-1126-6
By:
- Deffenbacher, Karen E.;
- Kenyon, Judith B.;
- Hoover, Denise M.;
- Olson, Richard K.;
- Pennington, Bruce F.;
- DeFries, John C.;
- Smith, Shelley D.
Publication type:
Article
Genome-wide association scan identifies new variants associated with a cognitive predictor of dyslexia.
Published in:
Translational Psychiatry, 2019, v. 9, n. 1, p. 1, doi. 10.1038/s41398-019-0402-0
By:
- 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.
Publication type:
Article
Is phonology bypassed in normal or dyslexic development?
Published in:
1987
By:
- Pennington, Bruce F.;
- Lefty, Dianne L.;
- van Orden, Guy C.;
- Bookman, Myra O.;
- Smith, Shelley D.;
- Pennington, B F;
- Lefly, D L;
- Van Orden, G C;
- Bookman, M O;
- Smith, S D
Publication type:
journal article
Reading Disability and Chromosome 6p21.3: Evaluation of MOG as a Candidate Gene.
Published in:
Journal of Learning Disabilities, 2001, v. 34, n. 6, p. 512, doi. 10.1177/002221940103400604
By:
- Smith, Shelley D.;
- Kelley, Philip M.;
- Askew, James W.;
- Hoover, Denise M.;
- Deffenbacher, Karen E.;
- Gayán, Javier;
- Brower, Amy M.;
- Olson, Richard K.
Publication type:
Article
Molecular approaches to the genetic analysis of specific reading disbility.
Published in:
Human Biology, 1998, v. 70, n. 2, p. 239
By:
- Smith, Shelley D.;
- Kelley, Philip M.;
- Brower, Amy M.
Publication type:
Article
Pedigree-Based Gene Mapping Supports Previous Loci and Reveals Novel Suggestive Loci in Specific Language Impairment.
Published in:
Journal of Speech, Language & Hearing Research, 2020, v. 63, n. 12, p. 4046, doi. 10.1044/2020_JSLHR-20-00102
By:
- Andres, Erin M.;
- Kelsey Earnest, Kathleen;
- Smith, Shelley D.;
- Rice, Mabel L.;
- Hashim Raza, Muhammad
Publication type:
Article
Collaborative analysis of DRD4 and DAT genotypes in population-defined ADHD subtypes.
Published in:
Journal of Child Psychology, 2005, v. 46, n. 10, p. 1067, doi. 10.1111/j.1469-7610.2005.01517.x
By:
- Todd, Richard D.;
- Huang, Hongyan;
- Smalley, Susan L.;
- Nelson, Stanley F.;
- Willcutt, Erik G.;
- Pennington, Bruce F.;
- Smith, Shelley D.;
- Faraone, Stephen V.;
- Neuman, Rosalind J.
Publication type:
Article
Linkage of speech sound disorder to reading disability loci.
Published in:
Journal of Child Psychology, 2005, v. 46, n. 10, p. 1057, doi. 10.1111/j.1469-7610.2005.01534.x
By:
- Smith, Shelley D.;
- Pennington, Bruce F.;
- Boada, Richard;
- Shriberg, Lawrence D.
Publication type:
Article
Spelling errors in adults with a form of familial dyslexia.
Published in:
1986
By:
- Pennington, Bruce F.;
- McCabe, Linda L.;
- Smith, Shelley D.;
- Lefly, Dianne L.;
- Bookman, Myra O.;
- Kimberling, William J.;
- Lubs, Herbert A.;
- Pennington, B F;
- McCabe, L L;
- Smith, S D;
- Lefly, D L;
- Bookman, M O;
- Kimberling, W J;
- Lubs, H A
Publication type:
journal article
Genetic Influences on Learning Disabilities and Speech and Language Disorders.
Published in:
Child Development, 1983, v. 54, n. 2, p. 369, doi. 10.2307/1129698
By:
- Pennington, Bruce F.;
- Smith, Shelley D.
Publication type:
Article
A Family Based Association Study of DRD4, DAT1, and 5HTT and Continuous Traits of Attention-Deficit Hyperactivity Disorder.
Published in:
Behavior Genetics, 2011, v. 41, n. 1, p. 165, doi. 10.1007/s10519-010-9437-y
By:
- Bidwell, L. Cinnamon;
- Willcutt, Erik G.;
- McQueen, Matthew B.;
- DeFries, John C.;
- Olson, Richard K.;
- Smith, Shelley D.;
- Pennington, Bruce F.
Publication type:
Article
Differential Genetic Etiology of Reading Component Processes as a Function of IQ.
Published in:
Behavior Genetics, 2002, v. 32, n. 3, p. 181, doi. 10.1023/A:1016069012111
By:
- Knopik, Valerie S.;
- Smith, Shelley D.;
- Cardon, Lon;
- Pennington, Bruce;
- Gayan, Javier;
- Olson, Richard K.;
- DeFries, John C.
Publication type:
Article
Etiology of Reading Difficulties and Rapid Naming: The Colorado Twin Study of Reading Disability.
Published in:
Behavior Genetics, 2001, v. 31, n. 6, p. 625, doi. 10.1023/A:1013305730430
By:
- Davis, Chayna J.;
- Gayán, Javier;
- Knopik, Valerie S.;
- Smith, Shelley D.;
- Cardon, Lon R.;
- Pennington, Bruce F.;
- Olson, Richard K.;
- DeFries, John C.
Publication type:
Article
Deafness linked to DFNA2: one locus but how many genes?
Published in:
Nature Genetics, 1999, v. 21, n. 3, p. 263, doi. 10.1038/6778
By:
- Hauwe, Peter Van;
- Coucke, Paul J.;
- Declau, Frank;
- Kunst, Henricus;
- Ensink, Robbert J.;
- Marres, Henri A.;
- Cremers, Cor W.R.J.;
- Djelantik, Bulantrisna;
- Smith, Shelley D.;
- Kelley, Phil;
- Heyning, Paul H. Van de;
- Camp, Guy Van
Publication type:
Article
Novel mutation in the KCNQ4 gene in a large kindred with dominant progressive hearing loss.
Published in:
Human Mutation, 1999, v. 14, n. 6, p. 493, doi. 10.1002/(SICI)1098-1004(199912)14:6<493::AID-HUMU8>3.0.CO;2-P
By:
- Talebizadeh, Zohreh;
- Kelley, Philip M.;
- Askew, James W.;
- Beisel, Kirk W.;
- Smith, Shelley D.
Publication type:
Article
Mutations in the KCNQ4 gene are responsible for autosomal dominant deafness in four DFNA2 families.
Published in:
Human Molecular Genetics, 1999, v. 8, n. 7, p. 1321, doi. 10.1093/hmg/8.7.1321
By:
- Coucke, Paul J.;
- Hauwe, Peter Van;
- Kelley, Philip M.;
- Kunst, Henricus;
- Schatteman, Isabelle;
- Van Velzen, Desiree;
- Meyers, Johan;
- Ensink, Robbert J.;
- Verstreken, Margriet;
- Declau, Frank;
- Marres, Henri;
- Kastury, Kumar;
- Bhasin, Shalender;
- McGuirt, Wyman T.;
- Smith, Richard J.H.;
- Cremers, Cor W.R.J.;
- Van de Heyning, Paul;
- Willems, Patrick J.;
- Smith, Shelley D.;
- Van Camp, Guy
Publication type:
Article
Localization of a gene for non-syndromic hearing loss (DFNA5) to chromosome 7p15.
Published in:
Human Molecular Genetics, 1995, v. 4, n. 11, p. 2159
By:
- Camp, Guy Van;
- Coucke, Paul;
- Balemans, Wendy;
- Van Velzen, Désirée;
- Van de Bilt, Caroline;
- Van Laer, Lut;
- Smith, Richard J.H.;
- Fukushima, Kunihiro;
- Padberg, George W.;
- Frants, Rune R.;
- Heyning, Paul Van de;
- Smith, Shelley D.;
- Huizing, Egbert H.;
- Willems, Patrick J.
Publication type:
Article
Phonological processing skills and deficits in adult dyslexics.
Published in:
Child Development, 1990, v. 61, n. 6, p. 1753, doi. 10.2307/1130836
By:
- Pennington, Bruce F.;
- Van Orden, Guy C.;
- Smith, Shelley D.;
- Green, Phyllis A.;
- Haith, Marshall M.
Publication type:
Article
Cytogentic studies of a patient with mosaicism of isochromosome 13q and a dicentric (Y; 13) translocation showing differential centromeric activity.
Published in:
Clinical Genetics, 1983, v. 24, n. 3, p. 194, doi. 10.1111/j.1399-0004.1983.tb02239.x
By:
- Ing, Paul S.;
- Smith, Shelley D.
Publication type:
Article

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