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Research at St Andrews

Silvia Paracchini

Person

  1. 2019
  2. Published

    A novel mutation in SPART gene causes a severe neurodevelopmental delay due to mitochondrial dysfunction with Complex I impairments and altered pyruvate metabolism

    Diquigiovanni, C., Bergamini, C., Diaz, R., Liparulo, I., Bianco, F., Masin, L., Baldassarro, V. A., Rizzardi, N., Tranchina, A., Bruscherini, F., Wischmeijer, A., Pippucci, T., Scarano, E., Cordelli, D. M., Fato, R., Seri, M., Paracchini, S. & Bonora, E., 1 Oct 2019, In : FASEB Journal. 33, 10, p. 11284-11302 19 p.

    Research output: Contribution to journalArticle

  3. Published
  4. Published

    Functional characterization of ATP2C2, a risk factor for language disorders

    Martinelli, A., Diaz, R., Feliciotti, I., Pitt, S. & Paracchini, S., 2019, In : European Neuropsychopharmacology. 29, p. 1194-1195 2 p.

    Research output: Contribution to journalAbstract

  5. E-pub ahead of print

    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., 11 Feb 2019, In : Translational Psychiatry. 9, 15 p., 77.

    Research output: Contribution to journalArticle

  6. Published

    Genomic imprinting as a window into human language evolution

    Hitchcock, T., Paracchini, S. & Gardner, A., Jun 2019, In : BioEssays. 41, 6, 11 p., 1800212.

    Research output: Contribution to journalArticle

  7. Published
  8. Published

    Prevalence and heritability of handedness in a Chinese twin and singleton sample

    Zheng, M., McBride, C., Ho, C. S-H., Chan, J. K-C., Choy, K. W. & Paracchini, S., 22 Oct 2019, In : PsyArXiv. 31 p.

    Research output: Contribution to journalArticle

  9. Published
  10. Published
  11. Published
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