Edinburgh Research Explorer

Prof Tim Aitman

Chair of Molecular Pathology and Genetics

  1. 2020
  2. Impulsivity is a heritable trait in rodents and associated with a novel quantitative trait locus on chromosome 1

    Jupp, B., Pitzoi, S., Petretto, E., Mar, A. C., Oliver, Y. P., Jordan, E. R., Taylor, S., Atanur, S., Srivastava, P. K., Saar, K., Hübner, N., Sommer, W., Staehlin, O., Spanagel, R., Robinson, E. S., Schumann, G., Moreno, M., Everitt, B. J., Robbins, T. W., Aitman, T. J. & 1 others, Dalley, J. W., 21 Apr 2020, In : Scientific Reports.

    Research output: Contribution to journalArticle

  3. Spatial transcriptomics identifies spatially dysregulated expression of GRM3 and USP47 in amyotrophic lateral sclerosis

    Gregory, J. M., McDade, K., Livesey, M. R., Croy, I., Marion de Proce, S., Aitman, T., Chandran, S. & Smith, C., 10 Jan 2020, In : Neuropathology and Applied Neurobiology.

    Research output: Contribution to journalArticle

  4. 2019
  5. An actionable KCNH2 Long QT Syndrome variant detected by sequence and haplotype analysis in a population research cohort

    Kerr, S., Klaric, L., Halachev, M., Hayward, C., Boutin, T., Meynert, A. M., Semple, C. A., Tuiskula, A. M., Swan, H., Santoyo-Lopez, J., Vitart, V., Haley, C., Dean, J., Miedzybrodzka, Z., Aitman, T. J. & Wilson, J. F., 29 Jul 2019, In : Scientific Reports. 9, 10964.

    Research output: Contribution to journalArticle

  6. Camk2n1 is a negative regulator of blood pressure, left ventricular mass, insulin sensitivity and promotes adiposity

    Alfazema, N., Barrier, M., Marion de Proce, S., Menzies, R., Nicholas Carter, R., Diaz, A. G., Moyon, B., Webster, Z., Bellamy, C. O. C., Arends, M. J., Stimson, R. H., Morton, N. M., Aitman, T. J. & Coan, P., 22 Jul 2019, In : Hypertension.

    Research output: Contribution to journalArticle

  7. Germline selection shapes human mitochondrial DNA diversity

    NIHR BioResource-Rare Dis, 100000 Genomes Project-Rare Dis & Tomlinson, I., 24 May 2019, In : Science. 364, 6442, p. 749-+ 59 p.

    Research output: Contribution to journalArticle

  8. Whole genome sequencing reveals that genetic conditions are frequent in intensively ill children

    NIHR BioResource-Rare Dis & Next Generation Children Project, May 2019, In : Intensive Care Medicine. 45, 5, p. 627-636 10 p.

    Research output: Contribution to journalArticle

  9. Bi-allelic Loss-of-Function CACNA1B Mutations in Progressive Epilepsy-Dyskinesia

    Deciphering Developmental Disorders Study, UK10K Consortium & NIHR BioResource, 11 Apr 2019, In : American Journal of Human Genetics. 104, 5, p. 948-956 9 p.

    Research output: Contribution to journalArticle

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