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Research Outputs

  1. 2017
  2. 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

  3. 2015
  4. Association between the COMT gene and neurological abnormalities and poorer executive function in psychosis

    Tosato, S., Ira, E., Russo, M., Iyegbe, C., Lasalvia, A., Di Forti, M., Morgan, K., Bonetto, C., Morgan, C., De Rossi, M., Nicolau, S., Chan, R. C. K., Reis Marques, T., Collier, D. A., Reichenberg, A., Murray, R. M., Tansella, M., Ruggeri, M. & Dazzan, P., 15 Dec 2015, In : Psychiatry Research. 230, 2, p. 742-743 2 p.

    Research output: Contribution to journalLetter

  5. 2013
  6. 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

  7. 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

  8. 2012
  9. Therapygenetics: the 5HTTLPR and response to psychological therapy

    Eley, T. C., Hudson, J. L., Creswell, C., Tropeano, M., Lester, K. J., Cooper, P., Farmer, A., Lewis, C. M., Lyneham, H. J., Rapee, R. M., Uher, R., Zavos, H. M. S. & Collier, D. A., Mar 2012, In : Molecular Psychiatry. 17, 3, p. 236 - 237 2 p.

    Research output: Contribution to journalLetter

  10. 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

  11. 2011
  12. The impact of the CACNA1C gene polymorphism on frontolimbic function in bipolar disorder

    Jogia, J., Ruberto, G., Lelli-Chiesa, G., Vassos, E., Maieru, M., Tatarelli, R., Girardi, P., Collier, D. & Frangou, S., Nov 2011, In : Molecular Psychiatry. 16, 11, p. 1070-1071 2 p.

    Research output: Contribution to journalLetter

  13. 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

  14. Gene-environment interaction in anorexia nervosa: relevance of non-shared environment and the serotonin transporter gene

    Karwautz, A. F. K., Wagner, G., Waldherr, K., Nader, I. W., Fernandez-Aranda, F., Estivill, X., Holliday, J., Collier, D. A. & Treasure, J. L., Jun 2011, In : Molecular Psychiatry. 16, 6, p. 590 - 592 3 p.

    Research output: Contribution to journalLetter

  15. Genome-Wide Association Study of Hoarding Traits

    Perroud, N., Guipponi, M., Pertusa, A., Fullana, M. A., Iervolino, A. C., Cherkas, L., Spector, T., Collier, D. & Mataix-Cols, D., Mar 2011, In : American Journal of Medical Genetics. Part B: Neuropsychiatric Genetics. 156B, 2, p. 240 - 242 3 p.

    Research output: Contribution to journalLetter

  16. Replication of association of 3p21.1 with susceptibility to bipolar disorder but not major depression

    Breen, G., Lewis, C. M., Vassos, E., Pergadia, M. L., Blackwood, D. H. R., Boomsma, D. I., Penninx, B., Sullivan, P. F., Pedroso, I., Collier, D. & McGuffin, P., Jan 2011, In : Nature Genetics. 43, 1, p. 3 - 5 3 p.

    Research output: Contribution to journalLetter

  17. 2010
  18. 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

  19. 2009
  20. Effects of the CACNA1C risk allele for bipolar disorder on cerebral gray matter volume in healthy individuals

    Kempton, M. J., Ruberto, G., Vassos, E., Tatarelli, R., Girardi, P., Collier, D. & Frangou, S., 1 Dec 2009, In : The American Journal of Psychiatry. 166, 12, p. 1413-1414 2 p., N/A.

    Research output: Contribution to journalLetter

  21. 2008
  22. The functional MMP-9 microsatellite marker is not associated with episodic memory in humans

    Vassos, E., Ma, X., Fiotti, N., Wang, D., Sham, P. C., Liu, X., Wang, Y., Yan, C., Meng, H., Deng, W., Collier, D. A. & Li, T., Oct 2008, In : Psychiatric Genetics. 18, 5, p. 252 - 252 1 p., N/A.

    Research output: Contribution to journalLetter

  23. 2007
  24. 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

  25. No association between a promoter polymorphism in the noradrenaline transporter gene and anorexia nervosa

    Hu, X., Karwautz, A., Wagner, G., Holliday, J., Li, T., Treasure, J. & Collier, D. A., Aug 2007, In : Psychiatric Genetics. 17, 4, p. 247 - 248 2 p.

    Research output: Contribution to journalLetter

  26. 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

  27. 2005
  28. 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

  29. 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

  30. 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

  31. 2004
  32. No association between polymorphisms of methylenetetrahydrofolate reductase gene and schizophrenia in both Chinese and Scottish populations

    Yu, L., Li, T., Robertson, Z., Dean, J., Gu, N. F., Feng, G. Y., Yates, P., Sinclair, M., Crombie, C., Collier, D. A., Walker, N., He, L. & St Clair, D., Dec 2004, In : Molecular Psychiatry. 9, 12, p. 1063 - 1065 3 p.

    Research output: Contribution to journalLetter

  33. 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

  34. 2003
  35. 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

  36. 2000
  37. 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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