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Research Outputs

  1. 2017
  2. Acne and Telomere Length: A New Spectrum between Senescence and Apoptosis Pathways

    Ribero, S., Sanna, M., Visconti, A., Navarini, A., Aviv, A., Glass, D., Spector, T. D., Smith, C., Simpson, M., Barker, J., Mangino, M., Falchi, M. & Bataille, V., Feb 2017, In : Journal of Investigative Dermatology. 137, 2, p. 513-515

    Research output: Contribution to journalLetter

  3. Genome-wide association study implicates immune activation of multiple integrin genes in inflammatory bowel disease

    de Lange, K. M., Moutsianas, L., Lee, J. C., Lamb, C. A., Luo, Y., Kennedy, N. A., Jostins, L., Rice, D. L., Gutierrez-Achury, J., Ji, S-G., Heap, G., Nimmo, E. R., Edwards, C., Henderson, P., Mowat, C., Sanderson, J., Satsangi, J., Simmons, A., Wilson, D. C., Tremelling, M. & 12 others, Hart, A., Mathew, C. G., Newman, W. G., Parkes, M., Lees, C. W., Uhlig, H., Hawkey, C., Prescott, N. J., Ahmad, T., Mansfield, J. C., Anderson, C. A. & Barrett, J. C., 2017, In : Nature Genetics. 49, 2, p. 256-261

    Research output: Contribution to journalLetter

  4. 2016
  5. Hidradenitis suppurativa: Haploinsufficiency of gamma-secretase components does not affect gamma-secretase enzyme activity in vitro

    Pink, A. E., Dafou, D., Desai, N., Holmes, O., Hobbs, C., Smith, C. H., Mortimer, P., Simpson, M. A., Trembath, R. C. & Barker, J. N., 28 Jul 2016, In : British Journal of Dermatology.

    Research output: Contribution to journalLetter

  6. 2014
  7. Psoriatic arthritis screening tools: study design and methodologic challenges - reply from authors

    Coates, L. C., Aslam, T., Al Balushi, F., Burden, A. D., Burden-Teh, E., Caperon, A. R., Cerio, R., Chattopadhyay, C., Chinoy, H., Goodfield, M. J. D., Kay, L., Kelly, S., Kirkham, B., Lovell, C. R., Marzo-Ortega, H., McHugh, N., Murphy, R., Reynolds, N. J., Smith, C. H., Stewart, E. J. C. & 4 others, Warren, R. B., Waxman, R., Wilson, H. E. & Helliwell, P. S., Apr 2014, In : British Journal of Dermatology. 170, 4, p. 995-996 2 p.

    Research output: Contribution to journalLetter

  8. Generalized Pustular Eruptions: Time to Adapt the Disease Taxonomy to the Genetic Architecture?

    Navarini, A. A., Valeyrie-Allanore, L., Setta-Kaffetzi, N., Barker, J. N., Capon, F., Creamer, D., Roujeau, J-C., Sekula, P., Simpson, M. A., Trembath, R. C., Mockenhaupt, M. & Smith, C. H., Feb 2014, In : Journal of Investigative Dermatology. 134, 2, p. 580-581 2 p.

    Research output: Contribution to journalLetter

  9. Loss of IL36RN Function Does Not Confer Susceptibility to Psoriasis Vulgaris

    Berki, D. M., Mahil, S. K., David Burden, A., Trembath, R. C., Smith, C. H., Capon, F. & Barker, J. N., Jan 2014, In : Journal of Investigative Dermatology. 134, 1, p. 271-273 3 p.

    Research output: Contribution to journalLetter

  10. 2013
  11. Rare Variations in IL36RN in Severe Adverse Drug Reactions Manifesting as Acute Generalized Exanthematous Pustulosis

    Navarini, A. A., Valeyrie-Allanore, L., Setta-Kaffetzi, N., Barker, J. N., Capon, F., Creamer, D., Roujeau, J-C., Sekula, P., Simpson, M. A., Trembath, R. C., Mockenhaupt, M. & Smith, C. H., Jul 2013, In : Journal of Investigative Dermatology. 133, 7, p. 1904-1907 4 p.

    Research output: Contribution to journalLetter

  12. Negligible impact of rare autoimmune-locus coding-region variants on missing heritability

    Hunt, K. A., Mistry, V., Bockett, N. A., Ahmad, T., Ban, M., Barker, J. N., Barrett, J. C., Blackburn, H., Brand, O., Burren, O., Capon, F., Compston, A., Gough, S. C. L., Jostins, L., Kong, Y., Lee, J. C., Lek, M., MacArthur, D. G., Mansfield, J. C., Mathew, C. G. & 17 others, Mein, C. A., Mirza, M., Nutland, S., Onengut-Gumuscu, S., Papouli, E., Parkes, M., Rich, S. S., Sawcer, S., Satsangi, J., Simmonds, M. J., Trembath, R. C., Walker, N. M., Wozniak, E., Todd, J. A., Simpson, M. A., Plagnol, V. & van Heel, D. A., 13 Jun 2013, In : NATURE. 498, 7453, p. 232-235 4 p.

    Research output: Contribution to journalLetter

  13. Common variants in the HLA-DRB1-HLA-DQA1 HLA class II region are associated with susceptibility to visceral leishmaniasis

    Fakiola, M., Strange, A., Cordell, H. J., Miller, E. N., Pirinen, M., Su, Z., Mishra, A., Mehrotra, S., Monteiro, G. R., Band, G., Bellenguez, C., Dronov, S., Edkins, S., Freeman, C., Giannoulatou, E., Gray, E., Hunt, S. E., Lacerda, H. G., Langford, C., Pearson, R. & 31 others, Pontes, N. N., Rai, M., Singh, S. P., Smith, L., Sousa, O., Vukcevic, D., Bramon-Bosch, E., Brown, M. A., Casas, J. P., Corvin, A., Duncanson, A., Jankowski, J., Markus, H. S., Mathew, C., Palmer, C. N. A., Plomin, R., Rautanen, A., Sawcer, S. J., Trembath, R. C., Viswanathan, A. C., Wood, N. W., Wilson, M. E., Deloukas, P., Peltonen, L., Christiansen, F., Witt, C., Jeronimo, S. M. B., Sundar, S., Spencer, C. C. A., Blackwell, J. M. & LeishGEN Consortium, 1 Feb 2013, In : Nature Genetics. 45, 2, p. 208-213 6 p.

    Research output: Contribution to journalLetter

  14. Rare Pathogenic Variants in IL36RN Underlie a Spectrum of Psoriasis-Associated Pustular Phenotypes

    Setta-Kaffetzi, N., Navarini, A. A., Patel, V. M., Pullabhatla, V., Pink, A., Choon, S-E., Allen, M. A., Burden, A. D., Griffiths, C. E. M., Seyger, M. M. B., Kirby, B., Trembath, R. C., Simpson, M. A., Smith, C. H., Capon, F. & Barker, J. N., 10 Jan 2013, In : Journal of Investigative Dermatology. 133, 5, p. 1366-1369 4 p.

    Research output: Contribution to journalLetter

  15. 2012
  16. Rare and functional SIAE variants are not associated with autoimmune disease risk in up to 66,924 individuals of European ancestry

    Hunt, K. A., Smyth, D. J., Balschun, T., Ban, M., Mistry, V., Ahmad, T., Anand, V., Barrett, J. C., Bhaw-Rosun, L., Bockett, N. A., Brand, O. J., Brouwer, E., Concannon, P., Cooper, J. D., Dias, K-R. M., van Diemen, C. C., Dubois, P. C., Edkins, S., Foelster-Holst, R., Fransen, K. & 45 others, Glass, D. N., Heap, G. A. R., Hofmann, S., Huizinga, T. W. J., Hunt, S., Langford, C., Lee, J., Mansfield, J., Marrosu, M. G., Mathew, C. G., Mein, C. A., Mueller-Quernheim, J., Nutland, S., Onengut-Gumuscu, S., Ouwehand, W., Pearce, K., Prescott, N. J., Posthumus, M. D., Potter, S., Rosati, G., Sambrook, J., Satsangi, J., Schreiber, S., Shtir, C., Simmonds, M. J., Sudman, M., Thompson, S. D., Toes, R., Trynka, G., Vyse, T. J., Walker, N. M., Weidinger, S., Zhernakova, A., Zoledziewska, M., Weersma, R. K., Gough, S. C. L., Sawcer, S., Wijmenga, C., Parkes, M., Cucca, F., Franke, A., Deloukas, P., Rich, S. S., Todd, J. A. & van Heel, D. A., Jan 2012, In : Nature Genetics. 44, 1, p. 3 - 5 3 p.

    Research output: Contribution to journalLetter

  17. 2011
  18. Genetic risk and a primary role for cell-mediated immune mechanisms in multiple sclerosis

    Sawcer, S., Hellenthal, G., Pirinen, M., Spencer, C. C. A., Patsopoulos, N. A., Moutsianas, L., Dilthey, A., Su, Z., Freeman, C., Hunt, S. E., Edkins, S., Gray, E., Booth, D. R., Potter, S. C., Goris, A., Band, G., Oturai, A. B., Strange, A., Saarela, J., Bellenguez, C. & 222 others, Fontaine, B., Gillman, M., Hemmer, B., Gwilliam, R., Zipp, F., Jayakumar, A., Martin, R., Leslie, S., Hawkins, S., Giannoulatou, E., D'alfonso, S., Blackburn, H., Boneschi, F. M., Liddle, J., Harbo, H. F., Perez, M. L., Spurkland, A., Waller, M. J., Mycko, M. P., Ricketts, M., Comabella, M., Hammond, N., Kockum, I., McCann, O. T., Ban, M., Whittaker, P., Kemppinen, A., Weston, P., Hawkins, C., Widaa, S., Zajicek, J., Dronov, S., Robertson, N., Bumpstead, S. J., Barcellos, L. F., Ravindrarajah, R., Abraham, R., Alfredsson, L., Ardlie, K., Aubin, C., Baker, A., Baker, K., Baranzini, S. E., Bergamaschi, L., Bergamaschi, R., Bernstein, A., Berthele, A., Boggild, M., Bradfield, J. P., Brassat, D., Broadley, S. A., Buck, D., Butzkueven, H., Capra, R., Carroll, W. M., Cavalla, P., Celius, E. G., Cepok, S., Chiavacci, R., Clerget-Darpoux, F., Clysters, K., Comi, G., Cossburn, M., Cournu-Rebeix, I., Cox, M. B., Cozen, W., Cree, B. A. C., Cross, A. H., Cusi, D., Daly, M. J., Davis, E., de Bakker, P. I. W., Debouverie, M., D'hooghe, M. B., Dixon, K., Dobosi, R., Dubois, B., Ellinghaus, D., Elovaara, I., Esposito, F., Fontenille, C., Foote, S., Franke, A., Galimberti, D., Ghezzi, A., Glessner, J., Gomez, R., Gout, O., Graham, C., Grant, S. F. A., Guerini, F. R., Hakonarson, H., Hall, P., Hamsten, A., Hartung, H-P., Heard, R. N., Heath, S., Hobart, J., Hoshi, M., Infante-Duarte, C., Ingram, G., Ingram, W., Islam, T., Jagodic, M., Kabesch, M., Kermode, A. G., Kilpatrick, T. J., Kim, C., Klopp, N., Koivisto, K., Larsson, M., Lathrop, M., Lechner-Scott, J. S., Leone, M. A., Leppa, V., Liljedahl, U., Bomfim, I. L., Lincoln, R. R., Link, J., Liu, J., Lorentzen, A. R., Lupoli, S., Macciardi, F., Mack, T., Marriott, M., Martinelli, V., Mason, D., McCauley, J. L., Mentch, F., Mero, I-L., Mihalova, T., Montalban, X., Mottershead, J., Myhr, K-M., Naldi, P., Ollier, W., Page, A., Palotie, A., Pelletier, J., Piccio, L., Pickersgill, T., Piehl, F., Pobywajlo, S., Quach, H. L., Ramsay, P. P., Reunanen, M., Reynolds, R., Rioux, J., Rodegher, M., Roesner, S., Rubio, J. P., Rueckert, I-M., Salvetti, M., Salvi, E., Santaniello, A., Schaefer, C. A., Schreiber, S., Schulze, C., Scott, R. J., Sellebjerg, F., Selmaj, K. W., Sexton, D., Shen, L., Simms-Acuna, B., Skidmore, S., Sleiman, P. M. A., Smestad, C., Sorensen, P. S., Sondergaard, H. B., Stankovich, J., Strange, R. C., Sulonen, A-M., Sundqvist, E., Syvaenen, A-C., Taddeo, F., Taylor, B., Blackwell, J. M., Tienari, P., Bramon, E., Tourbah, A., Brown, M. A., Tronczynska, E., Casas, J. P., Tubridy, N., Corvin, A., Vickery, J., Jankowski, J., Villoslada, P., Markus, H. S., Wang, K., Mathew, C. G., Wason, J., Palmer, C. N. A., Wichmann, H-E., Plomin, R., Willoughby, E., Rautanen, A., Winkelmann, J., Wittig, M., Trembath, R. C., Yaouanq, J., Viswanathan, A. C., Zhang, H., Wood, N. W., Zuvich, R., Deloukas, P., Langford, C., Duncanson, A., Oksenberg, J. R., Pericak-Vance, M. A., Haines, J. L., Olsson, T., Hillert, J., Ivinson, A. J., De Jager, P. L., Peltonen, L., Stewart, G. J., Hafler, D. A., Hauser, S. L., McVean, G., Donnelly, P. & Compston, A., 11 Aug 2011, In : NATURE. 476, 7359, p. 214 - 219 6 p.

    Research output: Contribution to journalLetter

  19. 2010
  20. Genome-wide meta-analysis increases to 71 the number of confirmed Crohn's disease susceptibility loci

    Franke, A., McGovern, D. P. B., Barrett, J. C., Wang, K., Radford-Smith, G. L., Ahmad, T., Lees, C. W., Balschun, T., Lee, J., Roberts, R., Anderson, C. A., Bis, J. C., Bumpstead, S., Ellinghaus, D., Festen, E. M., Georges, M., Green, T., Haritunians, T., Jostins, L., Latiano, A. & 76 others, Mathew, C. G., Montgomery, G. W., Prescott, N. J., Raychaudhuri, S., Rotter, J. I., Schumm, P., Sharma, Y., Simms, L. A., Taylor, K. D., Whiteman, D., Wijmenga, C., Baldassano, R. N., Barclay, M., Bayless, T. M., Brand, S., Buening, C., Cohen, A., Colombel, J-F., Cottone, M., Stronati, L., Denson, T., De Vos, M., D'Inca, R., Dubinsky, M., Edwards, C., Florin, T., Franchimont, D., Gearry, R., Glas, J., Van Gossum, A., Guthery, S. L., Halfvarson, J., Verspaget, H. W., Hugot, J-P., Karban, A., Laukens, D., Lawrance, I., Lemann, M., Levine, A., Libioulle, C., Louis, E., Mowat, C., Newman, W., Panes, J., Phillips, A., Proctor, D. D., Regueiro, M., Russell, R., Rutgeerts, P., Sanderson, J., Sans, M., Seibold, F., Steinhart, A. H., Stokkers, P. C. F., Torkvist, L., Kullak-Ublick, G., Wilson, D., Walters, T., Targan, S. R., Brant, S. R., Rioux, J. D., D'Amato, M., Weersma, R. K., Kugathasan, S., Griffiths, A. M., Mansfield, J. C., Vermeire, S., Duerr, R. H., Silverberg, M. S., Satsangi, J., Schreiber, S., Cho, J. H., Annese, V., Hakonarson, H., Daly, M. J. & Parkes, M., Dec 2010, In : Nature Genetics. 42, 12, p. 1118 - U121 9 p.

    Research output: Contribution to journalLetter

  21. The development of sarcoidosis on antitumour necrosis factor therapy: a paradox

    Pink, A. E., Fonia, A., Smith, C. H. & Barker, J. N. W. N., Sep 2010, In : British Journal of Dermatology. 163, 3, p. 648 - 649 2 p.

    Research output: Contribution to journalLetter

  22. 2007
  23. Interleukin-23R arg381 gln is associated with susceptibility to Crohn's disease but not with phenotype in an Italian population - Reply

    Tremelling, M., Lees, C., Mansfiel, J., Mathew, C., Jewell, D., Satsangi, J. & Parkes, M., Sep 2007, In : Gastroenterology. 133, 3, p. 1051 - 1052 2 p.

    Research output: Contribution to journalLetter

  24. Combined evidence from three large British association studies rejects TUCAN/CARD8 as an IBD susceptibility gene

    Fisher, S. A., Mirza, M. M., Onnie, C. M., Soars, D., Lewis, C. M., Prescott, N. J., Mathew, C. G., Sanderson, J., Forbes, A., Todhunter, C., Donaldson, P. & Mansfield, J., May 2007, In : Gastroenterology. 132, 5, p. 2078 - 2080 3 p.

    Research output: Contribution to journalLetter

  25. 2005
  26. A human ortholog of archaeal DNA repair protein Hef is defective in Fanconi anemia complementation group M.

    Meetei, A. R., Medhurst, A., Ling, C., Xue, Y., Singh, T. R., Bier, P., Steltenpool, J., Stone, S., Dokal, I., Mathew, C. G., Hoatlin, M., Joenje, H., de Winter, J. P. & Wang, W., Sep 2005, In : Nature Genetics. 37, 9, p. 958 - 963 6 p.

    Research output: Contribution to journalLetter

  27. No association of the NFKB1 promoter polymorphism with ulcerative colitis in a British case control cohort.

    Mirza, M. M., Fisher, S. A., Onnie, C., Sanderson, J., Forbes, A., Lewis, C. M. & Mathew, C. G., Aug 2005, In : Gut. 54, 8, p. 1205 - 1206 2 p.

    Research output: Contribution to journalLetter

  28. Muramyl dipeptide and toll-like receptor sensitivity in NOD2-associated Crohn's disease.

    van Heel, D. A., Ghosh, S., Butler, M., Lundberg, A. M. C., Ahmad, T., McGovern, D. P. B., Onnie, C., Negoro, K., Goldthorpe, S., Foxwell, B. M. J., Mathew, C. G., Forbes, A., Jewell, D. P. & Playford, R. J., 2005, In : The Lancet. 365, 9473, p. 1794 - 1796 3 p.

    Research output: Contribution to journalLetter

  29. 2004
  30. Genetic association between EPHX1 and Crohn's disease: population stratification, genotyping error, or random chance?

    Cuthbert, A. P., Fisher, S. A., Lewis, C. M., Mathew, C. G., Sanderson, J. & Forbes, A., 2004, In : Gut. 53, 9, p. 1386 - 1386 1 p.

    Research output: Contribution to journalLetter

  31. 2003
  32. Lack of association between the C3435T MDR1 gene polymorphism and inflammatory bowel disease in two independent northern European populations

    Croucher, P. J. P., Mascheretti, S., Foelsch, U. R., Hampe, J., Schreiber, S. & Mathew, C. G., Dec 2003, In : Gastroenterology. 125, 6, p. 1919 - 1920 2 p.

    Research output: Contribution to journalLetter

  33. 2000
  34. Low prevalence of germline BRCA1 mutations in early onset breast cancer without a family history

    Ellis, D., Greenman, J., Hodgson, S., McCall, S., Lalloo, F., Cameron, J., Izatt, L., Scott, G., Jacobs, C., Watts, S., Chorley, W., Perrett, C., Macdermot, K., Mohammed, S., Evans, G. & Mathew, C. G., 2000, In : Journal of Medical Genetics. 37, 10, p. 792 - 794 3 p.

    Research output: Contribution to journalLetter

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