Edinburgh Research Explorer

Centre for Genomic and Experimental Medicine

Organisational unit: Research Centre

  1. Understanding the evolving phenotype of vascular complications in telomere biology disorders

    Clinical Care Consortium for Telomere-associated Ailments (CCCTAA), 25 Aug 2018, In : Angiogenesis.

    Research output: Contribution to journalArticle

  2. Unordered arrangement of chromosomes in the nuclei of chicken spermatozoa

    Solovei, I., Joffe, B., Hori, T., Thomson, P., Mizuno, S. & MacGregor, H., 1 Jun 1998, In : Chromosoma. 107, 3, p. 184 188 p.

    Research output: Contribution to journalArticle

  3. Unravelling the GSK3β-related genotypic interaction network influencing hippocampal volume in recurrent major depressive disorder

    Inkster, B., Simmons, A., Cole, J. H., Schoof, E., Linding, R., Nichols, T., Muglia, P., Holsboer, F., Sämann, P. G., McGuffin, P., Fu, C. H. Y., Miskowiak, K., Matthews, P. M., Zai, G. & Nicodemus, K., Oct 2018, In : Psychiatric Genetics. 28, 5, p. 77-84 8 p.

    Research output: Contribution to journalArticle

  4. Unravelling the complex genetics of inflammatory bowel disease

    Russell, R. K., Wilson, D. C. & Satsangi, J., Jul 2004, In : Archives of Disease in Childhood Fetal and Neonatal Edition. 89, 7, p. 598-603 6 p.

    Research output: Contribution to journalArticle

  5. Unusual cutaneous features associated with a heterozygous gain-of-function mutation in IFIH1: overlap between Aicardi-Goutières and Singleton-Merten syndromes

    Bursztejn, A-C., Briggs, T. A., del Toro Duany, Y., Anderson, B. H., O'Sullivan, J., Williams, S. G., Bodemer, C., Fraitag, S., Gebhard, F., Leheup, B., Lemelle, I., Oojageer, A., Raffo, E., Schmitt, E., Rice, G. I., Hur, S. & Crow, Y. J., Dec 2015, In : British journal of dermatology. 173, 6, p. 1505-13 9 p.

    Research output: Contribution to journalArticle

  6. Unveiling the mysteries of the genetics of osteoporosis

    Alonso, N. & Ralston, S. H., Oct 2014, In : Journal of Endocrinological Investigation . 37, 10, p. 925-934 10 p.

    Research output: Contribution to journalLiterature review

  7. Update on the UK CF Gene Therapy Consortium Multidoes, non-viral, gene therapy trial

    Alton, E. W., Boyd, C., Cheng, S. H., Cunningham, S., Davies, J. C., Gill, D. R., Griesenbach, U., Higgins, T. E., Hyde, S. C., Innes, J. A., Murray, G. D. & Porteous, D., Oct 2012, In : Human Gene Therapy. 23, 10, p. A30-A30 1 p.

    Research output: Contribution to journalMeeting abstract

  8. Upper Gastrointestinal Involvement in Pediatric Crohn's Disease Reply

    Van Limbergen, J., Wilson, D. C., Russell, R. K., Drummond, H. E. & Satsangi, J., Jun 2009, In : Gastroenterology. 136, 7, p. 2409-2410 2 p.

    Research output: Contribution to journalLetter

  9. Use of Ruxolitinib in COPA syndrome manifesting as life-threatening alveolar hemorrhage

    Frémond, M-L., Legendre, M., Fayon, M., Clement, A., Filhol-Blin, E., Richard, N., Berdah, L., Roullaud, S., Rice, G. I., Bondet, V., Duffy, D., Sileo, C., Ducou le Pointe, H., Begueret, H., Coulomb l'Hermine, A., Neven, B., Amselem, S., Crow, Y. & Nathan, N., 30 Oct 2019, In : Thorax.

    Research output: Contribution to journalArticle