Shelley D Smith, PhD

Professor

  • 5909 Citations
  • 42 h-Index
1975 …2019
If you made any changes in Pure, your changes will be visible here soon.

Fingerprint Fingerprint is based on mining the text of the experts' scientific documents to create an index of weighted terms, which defines the key subjects of each individual researcher.

  • 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

Network Recent external collaboration on country level. Dive into details by clicking on the dots.

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

  • 5909 Citations
  • 42 h-Index
  • 97 Article
  • 2 Chapter

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

Truong, D. T., Adams, A. K., Paniagua, S., Frijters, J. C., Boada, R., Hill, D. E., Lovett, M. W., Mahone, E. M., Willcutt, E. G., Wolf, M., Defries, J. C., Gialluisi, A., Francks, C., Fisher, S. E., Olson, R. K., Pennington, B. F., Smith, S. D., Bosson-Heenan, J. & Gruen, J. R., Jan 1 2019, In : Journal of Medical Genetics.

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., Jan 1 2018, (Accepted/In press) In : Genetics in Medicine.

Research output: Contribution to journalArticle

Exome
Deafness
RNA Splicing
RNA Splice Sites
Hearing Loss
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., Sep 2 2017, (Accepted/In press) In : Human Genetics. p. 1-11 11 p.

Research output: Contribution to journalArticle

Reading
Genes
Alleles
Chromosomes, Human, Pair 7
Learning Disorders
7 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., Mar 14 2017, (Accepted/In press) In : Molecular Psychiatry.

Research output: Contribution to journalArticle

Nervous System Diseases
MicroRNAs
Binding Sites
Language
Inborn Genetic Diseases
7 Citations (Scopus)

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

Gialluisi, A., Visconti, A., Willcutt, E. G., Smith, S. D., Pennington, B. F., Falchi, M., DeFries, J. C., Olson, R. K., Francks, C. & Fisher, S. E., 2016, In : Journal of Neurodevelopmental Disorders. 8, 1, 17.

Research output: Contribution to journalArticle

Reading
Language
Contactins
alpha Catenin
Genome