• 6144 Citations
  • 42 h-Index
1975 …2019

Research output per year

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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.

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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


Project: Research project


    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


    Project: Research project


    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


    Project: Research project

  • Research Output

    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
  • 8 Scopus citations

    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
  • 3 Scopus citations

    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., 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

  • 10 Scopus citations

    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

  • 16 Scopus citations

    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

  • 1 Scopus citations