• 5978 Citations
  • 42 h-Index
1975 …2019
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Fingerprint Dive into the research topics where Shelley D Smith is active. These topic labels come from the works of this person. Together they form a unique fingerprint.

  • 3 Similar Profiles
Reading Medicine & Life Sciences
Dyslexia Medicine & Life Sciences
Genes Medicine & Life Sciences
Hearing Loss Medicine & Life Sciences
Language Medicine & Life Sciences
Chromosomes Medicine & Life Sciences
Quantitative Trait Loci Medicine & Life Sciences
Deafness Medicine & Life Sciences

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Projects 1984 2019

The Molecular Biology of Neurosensory Systems

Walsh, E. J., Gurumurthy, C., Eudy, J. D., Smith, S. D., Wert, D. & Gurumurthy, C. B.

National Institutes of Health

9/5/148/31/19

Project: Research project

Genes
biology
mentoring
Molecular biology
DNA
Dyslexia
Reading
Genes
Phenotype
Nuclear Family
Deafness
Hearing Loss
Genes
Organism Cloning
Dominant Genes

DIFFERENTIAL DIAGNOSIS IN LEARNING DISABILITIES

Smith, S. D., Keenan, J., Wadsworth, S., Wilcutt, E., Wise, B., Defries, J., Pennington, B., Pennington, B., De Fries, J. & Olson, R.

National Institutes of Health

9/30/9011/30/16

Project: Research project

Genetic Linkage
Reading
Learning Disorders
Genes
Mathematics

CENTER FOR HEARING LOSS IN CHILDREN

Stelmachowicz, P. G., Brookhouser, P. E., Neely, S. T., Walsh, E. J., Moeller, M. P., Smith, S. D., Higgins, M., Nittrouer, S. & Warr, W.

National Institutes of Health

9/30/908/31/01

Project: Research project

Hearing Loss
Hearing aids
Audition
Cochlea
Continuing Education

Research Output 1975 2019

1 Citation (Scopus)

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

Gialluisi, A., Andlauer, T. F. M., Mirza-Schreiber, N., Moll, K., Becker, J., Hoffmann, P., Ludwig, K. U., Czamara, D., St Pourcain, B., Brandler, W., Honbolygó, F., Tóth, D., Csépe, V., Huguet, G., Morris, A. P., Hulslander, J., Willcutt, E. G., DeFries, J. C., Olson, R. K., Smith, S. D. & 25 others, Pennington, B. F., Vaessen, A., Maurer, U., Lyytinen, H., Peyrard-Janvid, M., Leppänen, P. H. T., Brandeis, D., Bonte, M., Stein, J. F., Talcott, J. B., Fauchereau, F., Wilcke, A., Francks, C., Bourgeron, T., Monaco, A. P., Ramus, F., Landerl, K., Kere, J., Scerri, T. S., Paracchini, S., Fisher, S. E., Schumacher, J., Nöthen, M. M., Müller-Myhsok, B. & Schulte-Körne, G., Dec 1 2019, In : Translational Psychiatry. 9, 1, 77.

Research output: Contribution to journalArticle

Open Access
Dyslexia
Genome-Wide Association Study
Attention Deficit Disorder with Hyperactivity
Reading
Genome
1 Citation (Scopus)

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

Pediatric, Imaging, Neurocognition, and Genetics Consortium, Aug 1 2019, In : Journal of medical genetics. 56, 8, p. 557-566 10 p.

Research output: Contribution to journalArticle

Open Access
Genome-Wide Association Study
Hispanic Americans
African Americans
Reading
Epigenomics
1 Citation (Scopus)

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

Booth, K. T., Askew, J. W., Talebizadeh, Z., Huygen, P. L. M., Eudy, J. D., Kenyon, J., Hoover, D., Hildebrand, M. S., Smith, K. R., Bahlo, M., Kimberling, W. J., Smith, R. J. H., Azaiez, H. & Smith, S. D., Apr 1 2019, In : Genetics in Medicine. 21, 4, p. 948-954 7 p.

Research output: Contribution to journalArticle

Exome
Deafness
RNA Splicing
RNA Splice Sites
Hearing Loss
9 Citations (Scopus)

Next-gen sequencing identifies non-coding variation disrupting miRNA-binding sites in neurological disorders

Devanna, P., Chen, X. S., Ho, J., Gajewski, D., Smith, S. D., Gialluisi, A., Francks, C., Fisher, S. E., Newbury, D. F. & Vernes, S. C., May 1 2018, In : Molecular Psychiatry. 23, 5, p. 1375-1384 10 p.

Research output: Contribution to journalArticle

Nervous System Diseases
MicroRNAs
Binding Sites
Language
Inborn Genetic Diseases
1 Citation (Scopus)

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

Adams, A. K., Smith, S. D., Truong, D. T., Willcutt, E. G., Olson, R. K., DeFries, J. C., Pennington, B. F. & Gruen, J. R., Nov 1 2017, In : Human genetics. 136, 11-12, p. 1395-1405 11 p.

Research output: Contribution to journalArticle

Reading
Genes
Alleles
Chromosomes, Human, Pair 7
Learning Disorders