Search results

• 2008

  Additional filaggrin polymorphisms in early-onset and persistent atopic eczema

  Brown, SJ., Sandilands, A., Zhao, Y., Liao, H., Relton, CL., Meggitt, SJ., Reynolds, NJ., Barker, JN., Trembath, RC., Cordell, HJ. & McLean, WH., 2008, In: British Journal of Dermatology. 159, p. 1241 - 1242 2 p.

  Research output: Contribution to journal › Poster abstract

• Genetic and functional evidence for a role of the interleukin 23 pathway in the pathogenesis of psoriasis

  di Meglio, P., Tonel, G., Capon, F., Conrad, C., Oldham, E., Kastelein, R., Lanchbury, J., Barker, J., Trembath, R. & Nestle, F., 2008, In: British Journal of Dermatology. 158, 4, p. 890 - 890 1 p.

  Research output: Contribution to journal › Poster abstract
• 2006

  A genome-wide scan and HCRTR2 candidate gene analysis in a European cluster headache cohort.

  Baumber, L., Sjostrand, C., Leone, M., Harty, H., Bussone, G., Hillert, J., Trembath, RC. & Russell, MB., Jun 2006, In: Cephalalgia. 26, 11, p. 1363 - 1364 2 p.

  Research output: Contribution to journal › Poster abstract

  68 Citations (Scopus)

• Functional characterisation of genome sequence variation.

  Nasim, T., Gouri, AG., Patel, B. & Trembath, RC., 2006, In: Journal of Medical Genetics. 43, p. S87 - S87

  Research output: Contribution to journal › Poster abstract

• Further refinement of the SPG11 critical interval in a consanguineous family with autosomal recessive hereditary spastic paraplegia and thin corpus callosum.

  Baumber, L. & Trembath, RC., 2006, In: Journal of Medical Genetics. 43, p. S82 - S82

  Research output: Contribution to journal › Poster abstract
• 2003

  Functional interaction between BMPR2 and Tctex-1, a light chain of Dynein, is isoform-specific and disrupted by mutations underlying primary pulmonary hypertension.

  Machado, R. D., Rudarakanchana, N., Morrell, N. & Trembath, R., 2003, In: American Journal of Human Genetics. 73, 5, p. 543 1 p., 2193.

  Research output: Contribution to journal › Poster abstract
• 2002

  A Crohn's syndrome-associated insertion polymorphism (3020incC) in the NOD2 gene is not associated with psoriasis vulgaris, palmo-plantar pustulosis (PPP) or guttate psoriasis.

  Young, C., Allen, M. H., Cuthbert, A., Ameen, M., Veal, C., Leman, J., Burden, A. D., Kirby, B., Griffiths, C. E. M., Mathew, C. G., Trembath, R. C. & Barker, J. N. W., 2002, In: British Journal of Dermatology. 146, 4, p. 733 1 p., P2.

  Research output: Contribution to journal › Poster abstract

• Analysis of a dense SNP based map in a psoriatic cohort defines genetic variation at PSORS1, the major psoriasis susceptibility locus.

  Veal, C. D., Capon, F., Allen, M. H., Heath, E. K., Evans, J., Jones, A., Patel, S., Burden, D., Tillman, D., Barker, J. N. W. N. & Trembath, R. C., 2002, In: American Journal of Human Genetics. 71, 4, p. 447 1 p., 1622.

  Research output: Contribution to journal › Poster abstract

• Linkage of psoriasis to the MHC and evidence for additional loci in a large cohort (International Psoriasis Genetics Consortium).

  Elder, JT., Barker, JN., Burden, D., Chia, N., Christophers, E., Daly, M., Helms, C., Henseler, T., Jenisch, S., Menter, A., Mistry, R., Nair, RP., Stuart, PE., Tillman, D., Veal, C., Voorhees, JJ., Trembath, R. & Bowcock, AM., 2002, In: Journal of Investigative Dermatology. 119, 1, p. 266 1 p., 353.

  Research output: Contribution to journal › Poster abstract

• Mutation screening of SLC26A4 by DHPLC.

  Prasad, S. D., Kolln, K. A., Cucci, R. A., Van Hauwe, P., Coucke, P., Trembath, R., Van Camp, G. & Smith, R. J. H., 2002, In: American Journal of Human Genetics. 71, 4, p. 375 1 p.

  Research output: Contribution to journal › Poster abstract