King's College London

Research portal

Professor Christopher Mathew

  1. Lifestyle factors associated with sex differences in Kaposi sarcoma incidence among adult black South Africans: A case-control study

    Motlhale, M., Sitas, F., Bradshaw, D., Chen, W. C., Singini, M. G., de Villiers, C. B., Lewis, C. M., Muchengeti, M., Waterboer, T., Mathew, C. G., Newton, R. & Singh, E., 30 Jun 2022, In: Cancer Epidemiology. 78, 102158.

    Research output: Contribution to journalArticlepeer-review

  2. Epidemiology of Kaposi's sarcoma in sub-Saharan Africa

    Motlhale, M., Sitas, F., Bradshaw, D., Chen, W. C., Singini, M. G., de Villiers, C. B., Lewis, C. M., Muchengeti, M., Waterboer, T., Mathew, C. G., Newton, R. & Singh, E., Jun 2022, In: Cancer Epidemiology. 78, 102167.

    Research output: Contribution to journalReview articlepeer-review

  3. Johannesburg Cancer Study (JCS): contribution to knowledge and opportunities arising from 20 years of data collection in an African setting

    Chen, W. C., Singh, E., Muchengeti, M., Bradshaw, D., Mathew, C. G., Babb de Villiers, C., Lewis, C. M., Waterboer, T., Newton, R. & Sitas, F., Apr 2020, In: Cancer Epidemiology. 65, 101701.

    Research output: Contribution to journalArticlepeer-review

  4. IBD BioResource: An Open-Access Platform of 25 000 Patients to Accelerate Research in Crohn's and Colitis

    Parkes, M., Prescott, N., Mathew, C., Sanderson, J. & Irving, P., Sep 2019, In: Gut. 68, 9, p. 1537-1540

    Research output: Contribution to journalLetterpeer-review

  5. Genetic and Inflammatory Biomarkers Classify Small Intestine Inflammation in Asymptomatic First-degree Relatives of Patients With Crohn's Disease

    Taylor, K. M., Hanscombe, K. B., Prescott, N. J., Iniesta, R., Traylor, M., Taylor, N. S., Fong, S., Powell, N., Irving, P. M., Anderson, S. H., Mathew, C. G., Lewis, C. M. & Sanderson, J. D., 14 Jun 2019, (E-pub ahead of print) In: Clinical Gastroenterology and Hepatology : the official clinical practice journal of the American Gastroenterological Association.

    Research output: Contribution to journalArticlepeer-review

  6. Association of genetic variants in CHEK2 with oesophageal squamous cell carcinoma in the South African Black population

    Chen, W. C., Bye, H., Matejcic, M., Amar, A., Govender, D., Khew, Y. W., Beynon, V., Kerr, R., Singh, E., Prescott, N. J., Lewis, C. M., Babb de Villiers, C., Parker, M. I. & Mathew, C. G., Apr 2019, In: Carcinogenesis. 40, 4, p. 513-520 8 p., bgz026.

    Research output: Contribution to journalArticlepeer-review

  7. The relationship between environmental exposure and genetic architecture of the 2q33 locus with esophageal cancer in South Africa

    Matejcic, M., Mathew, C. G. & Iqbal Parker, M., 1 Jan 2019, In: Frontiers in Genetics. 10, MAY, 406.

    Research output: Contribution to journalArticlepeer-review

  8. Exome array analysis of adverse reactions to fluoropyrimidine-based therapy for gastrointestinal cancer

    Traylor, M., Walker, J. L., Corrigan, A. A., Hernandez, M. A., Newhouse, S. J., Folarin, A. A., Patel, H., Ross, P. J., Sanderson, J. D., Spicer, J., Prescott, N. J., Mathew, C. G., Marinaki, A. M. & Lewis, C. M., 1 May 2018, In: PLoS ONE. 13, 5, 11 p., e0188911.

    Research output: Contribution to journalArticlepeer-review

  9. Exome Sequencing and Genotyping Identify a Rare Variant in NLRP7 Gene Associated With Ulcerative Colitis

    Onoufriadis, A., Stone, K., Katsiamides, A., Amar, A., Omar, Y., de Lange, K. M., Taylor, K., Barrett, J. C., Pollok, R., Hayee, BH., Mansfield, J. C., Sanderson, J. D., Simpson, M. A., Mathew, C. G. & Prescott, N. J., Mar 2018, In: Journal of Crohn's & colitis. 12, 3, p. 321–326

    Research output: Contribution to journalArticlepeer-review

  10. Fine-mapping inflammatory bowel disease loci to single-variant resolution

    International Inflammatory Bowel Disease Genetics Consortium, 13 Jul 2017, In: NATURE. 547, 7662, p. 173-178 6 p.

    Research output: Contribution to journalArticlepeer-review

  11. Mutations in DONSON disrupt replication fork stability and cause microcephalic dwarfism

    Reynolds, J. J., Bicknell, L. S., Carroll, P., Higgs, M. R., Shaheen, R., Murray, J. E., Papadopoulos, D. K., Leitch, A., Murina, O., Tarnauskaitė, Ž., Wessel, S. R., Zlatanou, A., Vernet, A., von Kriegsheim, A., Mottram, R. M. A., Logan, C. V., Bye, H., Li, Y., Brean, A., Maddirevula, S. & 42 others, Challis, R. C., Skouloudaki, K., Almoisheer, A., Alsaif, H. S., Amar, A., Prescott, N. J., Bober, M. B., Duker, A., Faqeih, E., Seidahmed, M. Z., Al Tala, S., Alswaid, A., Ahmed, S., Al-Aama, J. Y., Altmüller, J., Al Balwi, M., Brady, A. F., Chessa, L., Cox, H., Fischetto, R., Heller, R., Henderson, B. D., Hobson, E., Nürnberg, P., Percin, E. F., Peron, A., Spaccini, L., Quigley, A. J., Thakur, S., Wise, C. A., Yoon, G., Alnemer, M., Tomancak, P., Yigit, G., Taylor, A. M. R., Reijns, M. A. M., Simpson, M. A., Cortez, D., Alkuraya, F. S., Mathew, C. G., Jackson, A. P. & Stewart, G. S., 1 Apr 2017, In: Nature Genetics. 49, 4, p. 537-549

    Research output: Contribution to journalArticlepeer-review

  12. Exploring the genetic architecture of inflammatory bowel disease by whole-genome sequencing identifies association at ADCY7

    Luo, Y., de Lange, K. M., Jostins, L., Moutsianas, L., Randall, J., Kennedy, N. A., Lamb, C. A., McCarthy, S., Ahmad, T., Edwards, C., Serra, E. G., Hart, A., Hawkey, C., Mansfield, J. C., Mowat, C., Newman, W. G., Nichols, S., Pollard, M., Satsangi, J., Simmons, A. & 10 others, Tremelling, M., Uhlig, H., Wilson, D. C., Lee, J. C., Prescott, N. J., Lees, C. W., Mathew, C. G., Parkes, M., Barrett, J. C. & Anderson, C. A., 1 Feb 2017, In: Nature Genetics. 49, 2, p. 186-192

    Research output: Contribution to journalArticlepeer-review

  13. 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., 1 Feb 2017, In: Nature Genetics. 49, 2, p. 256-261

    Research output: Contribution to journalLetterpeer-review

  14. International cancer seminars: A focus on esophageal squamous cell carcinoma

    Murphy, G., McCormack, V., Abedi-Ardekani, B., Arnold, M., Camargo, M. C., Dar, N. A., Dawsey, S. M., Etemadi, A., Fitzgerald, R. C., Fleischer, D. E., Freedman, N. D., Goldstein, A. M., Gopa, S., Hashemian, M., Hu, N., Hyland, P. L., Kaimila, B., Kamangar, F., Malekzadeh, R., Mathew, C. G. & 19 others, Menya, D., Mulima, G., M. Mwachiro, M., Mwasamwaja, A., Pritchett, N., Qiao, Y. L., Ribeiro-Pinto, L. F., Ricciardone, M., Schüz, J., Sitas, F., Taylor, P. R., Van Loon, K., Wang, S. M., Wei, W. Q., Wild, C. P., Wu, C., Abnet, C. C., Chanock, S. J. & Brennan, P., 2017, In: Annals of oncology : official journal of the European Society for Medical Oncology / ESMO. 28, 9, p. 2086-2093 8 p.

    Research output: Contribution to journalReview articlepeer-review

  15. A protein-truncating R179X variant in RNF186 confers protection against ulcerative colitis

    Rivas, M. A., Graham, D., Sulem, P., Stevens, C., Desch, A. N., Goyette, P., Gudbjartsson, D., Jonsdottir, I., Thorsteinsdottir, U., Degenhardt, F., Mucha, S., Kurki, M. I., Li, D., D'Amato, M., Annese, V., Vermeire, S., Weersma, R. K., Halfvarson, J., Paavola-Sakki, P., Lappalainen, M. & 31 others, Lek, M., Cummings, B., Tukiainen, T., Haritunians, T., Halme, L., Koskinen, L. L. E., Ananthakrishnan, A. N., Luo, Y., Heap, G. A., Visschedijk, M. C., MacArthur, D. G., Ahmad, T., Anderson, C. A., Brant, S. R., Duerr, R. H., Silverberg, M. S., Cho, J. H., Palotie, A., Saavalainen, P., Kontula, K., Färkkilä, M., McGovern, D. P. B., Franke, A., Stefansson, K., Rioux, J. D., Xavier, R. J., Daly, M. J., Hawkey, C., Mathew, C., Prescott, N. & UK IBD Genetics Consortium, 9 Aug 2016, In: Nature Communications. 7, 12342.

    Research output: Contribution to journalArticlepeer-review

  16. Genetic Association Analysis Reveals Differences in the Contribution of NOD2 Variants to the Clinical Phenotypes of Orofacial Granulomatosis

    Mentzer, A., Nayee, S., Omar, Y., Hullah, E., Taylor, K., Goel, R., Bye, H., Shembesh, T., Elliott, T. R., Campbell, H., Patel, P., Nolan, A., Mansfield, J., Challacombe, S., Escudier, M., Mathew, C. G., Sanderson, J. D. & Prescott, N. J., Jul 2016, In: Inflammatory Bowel Diseases. 22, 7, p. 1552-1558 7 p.

    Research output: Contribution to journalArticlepeer-review

  17. Genome-wide rare copy number variation screening in ulcerative colitis identifies potential susceptibility loci

    Saadati, H. R., Wittig, M., Helbig, I., Häsler, R., Anderson, C. A., Mathew, C. G., Kupcinskas, L., Parkes, M., Karlsen, T. H., Rosenstiel, P., Schreiber, S. & Franke, A., 1 Apr 2016, In: BMC Medical Genetics. 17, 1, 26.

    Research output: Contribution to journalArticlepeer-review

  18. Copy number variation of scavenger-receptor cysteine-rich domains within DMBT1 and Crohn's disease

    Polley, S., Prescott, N., Nimmo, E., Veal, C., Vind, I., Munkholm, P., Fode, P., Mansfield, J., Skyt Andersen, P., Satsangi, J., G Mathew, C. & Hollox, E. J., 27 Jan 2016, (E-pub ahead of print) In: European journal of human genetics : EJHG.

    Research output: Contribution to journalArticlepeer-review

  19. The genetic associations of acute anterior uveitis and their overlap with the genetics of ankylosing spondylitis

    Robinson, P. C., Leo, P. J., Pointon, J. J., Cremin, K., Bradbury, L. A., Donnelly (chair), P., Barroso (deputy Chair), I., M Blackwell, J., Bramon, E., Brown, M. A., Casas, J. P., Corvin, A., Deloukas, P., Duncanson, A., Jankowski, J., Markus, H. S., Mathew, C. G., Palmer, C. N., Plomin, R., Rautanen, A. & 59 others, Sawcer, S. J., Trembath, R. C., Viswanathan, A. C., Wood, N. W., Spencer, C. C., Band, G., Bellenguez, C., Freeman, C., Hellenthal, G., Giannoulatou, E., Pirinen, M., Pearson, R., Strange, A., Su, Z., Vukcevic, D., Donnelly, P., Langford, C., Hunt, S. E., Edkins, S., Gwilliam, R., Blackburn, H., Bumpstead, S. J., Dronov, S., Gillman, M., Gray, E., Hammond, N., Jayakumar, A., Mccann, O. T., Liddle, J., Potter, S. C., Ravindrarajah, R., Ricketts, M., Waller, M., Weston, P., Widaa, S., Whittaker, P., Barroso, I., Deloukas, P., Mathew (chair), C. G., Blackwell, J. M., Brown, M. A., Corvin, A., Spencer, C. C. A., Mccloskey, E., Eisman, J., Jones, G., Nicholson, G., Eastell, R., Sambrook, P., Prince, R., Dennison, E., Reid, I., Wark, J., Stebbings, S., Harrison, A. A., Evans, D. M., Duncan, E. L., Wordsworth, B. P. & Brown, M. A., 26 Nov 2015, (E-pub ahead of print) In: GENES AND IMMUNITY. 17, 1, p. 46-51

    Research output: Contribution to journalArticlepeer-review

  20. Novel insights into the genetics of smoking behaviour, lung function, and chronic obstructive pulmonary disease (UK BiLEVE): A genetic association study in UK Biobank

    Wain, L. V., Shrine, N., Miller, S., Jackson, V. E., Ntalla, I., Artigas, M. S., Billington, C. K., Kheirallah, A. K., Allen, R., Cook, J. P., Probert, K., Obeidat, M., Bossé, Y., Hao, K., Postma, D. S., Paré, P. D., Ramasamy, A., Mägi, R., Mihailov, E., Reinmaa, E. & 138 others, Melén, E., O'Connell, J., Frangou, E., Delaneau, O., Freeman, C., Petkova, D., McCarthy, M., Sayers, I., Deloukas, P., Hubbard, R., Pavord, I., Hansell, A. L., Thomson, N. C., Zeggini, E., Morris, A. P., Marchini, J., Strachan, D. P., Tobin, M. D., Hall, I. P., Farrall, M., Barroso, I., Anderson, C. A., Botía, J., Vandrocova, J., Guelfi, S., D'Sa, K., Ryten, M., Trabzuni, D., Matarin, M., Hardy, J. A., Weale, M. E., Varghese, V., Forabosco, P., Farmer, A., McGuffin, P., Zgaga, L., Wilson, J. F., Wild, S. H., Campbell, H., Rudan, I., Smith, C., Walker, R., Liu, J. Z., Tozzi, F., Muglia, P., Waterworth, D. M., Pillai, S. G., Yuan, X., Mooser, V., Middleton, L., Kooner, J., Chambers, J. C., Berrettini, W., Knouff, C. W., Waeber, G., Vollenweider, P., Preisig, M., Wareham, N. J., Zhao, J. H., Loos, R. J. F., Khaw, K. T., Grundy, S., Barter, P., Mahley, R., Kesaniemi, A., McPherson, R., Vincent, J. B., Strauss, J., Kennedy, J. L., Day, R., Matthews, K., Bakke, P., Gulsvik, A., Lucae, S., Ising, M., Brueckl, T., Horstmann, S., Wichmann, H. E., Rawal, R., Wichmann, H. E., Lamina, C., Dahmen, N., Polasek, O., Kolcic, I., Huffman, J., Campbell, S., Vitart, V., Hayward, C., Wright, A. F., Burnett, M. S., Devaney, J. M., Pichard, A. D., Kent, K. M., Satler, L., Lindsay, J. M., Waksman, R., Epstein, S., Reilly, M. P., Li, M., Qu, L., Wilensky, R., Matthai, W., Hakonarson, H. H., Rader, D. J., Ellinghaus, D., Lieb, W., Franke, A., Uda, M., Busonero, F., Terracciano, A., Schlessinger, D., Xiao, X., Scheet, P., St Clair, D., Rujescu, D., Abecasis, G. R., Grabe, H. J., Teumer, A., Völzke, H., Petersmann, A., John, U., Wright, B. J., Thompson, J. R., Balmforth, A. J., Hall, A. S., Samani, N. J., Ahmad, T., Mathew, C. G., Parkes, M., Satsangi, J., Caulfield, M., Munroe, P. B., Dominiczak, A., Worthington, J., Thomson, W., Eyre, S., Barton, A. & Francks, C., Oct 2015, In: The Lancet Respiratory Medicine. 3, 10, p. 769-781 13 p.

    Research output: Contribution to journalArticlepeer-review

  21. Lamina propria macrophage phenotypes in relation to Escherichia coli in Crohn's disease

    Elliott, T. R., Rayment, N. B., Hudspith, B., Hands, R. E., Taylor, K., Parkes, G. C., Prescott, N. J., Petrovska, L., Hermon-Taylor, J., Brostoff, J., Boussioutas, A., Mathew, C. G., Bustin, S. A. & Sanderson, J. D., 3 Jul 2015, In: BMC GASTROENTEROLOGY. 15, 75.

    Research output: Contribution to journalArticlepeer-review

  22. Shared genetic basis for migraine and ischemic stroke: A genome-wide analysis of common variants

    Malik, R., Freilinger, T., Winsvold, B. S., Anttila, V., Vander Heiden, J., Traylor, M., De Vries, B., Holliday, E. G., Terwindt, G. M., Sturm, J., Bis, J. C., Hopewell, J. C., Ferrari, M. D., Rannikmae, K., Wessman, M., Kallela, M., Kubisch, C., Fornage, M., Meschia, J. F., Lehtimaki, T. & 105 others, Sudlow, C., Clarke, R., Chasman, D. I., Mitchell, B. D., Maguire, J., Kaprio, J., Farrall, M., Raitakari, O. T., Kurth, T., Ikram, M. A., Reiner, A. P., Longstreth, W. T., Rothwell, P. M., Strachan, D. P., Sharma, P., Seshadri, S., Quaye, L., Cherkas, L., Schurks, M., Rosand, J., Ligthart, L., Boncoraglio, G. B., Davey Smith, G., Van Duijn, C. M., Stefansson, K., Worrall, B. B., Nyholt, D. R., Markus, H. S., Van Den Maagdenberg, A. M. J. M., Cotsapas, C., Zwart, J. A., Palotie, A., Dichgans, M., Thorsteinsdottir, U., Destefano, A. L., Levi, C., Gretarsdottir, S., Donnelly, P., Barroso, I., Blackwell, J. M., Bramon, E., Brown, M. A., Casas, J. P., Corvin, A., Deloukas, P., Duncanson, A., Jankowski, J., Markus, H. S., Mathew, C. G., Palmer, C. NA., Plomin, R., Rautanen, A., Sawcer, S. J., Trembath F, R. C., Viswanathan, A. C., Wood, N. W., Spencer, C. CA., Band, G., Bellengues, C., Freeman, C., Hellenthal, G., Giannoulatou, E., Pirinen, M., Pearson, R., Strange, A., Su, Z., Vukcevic, D., Langford, C., Hunt, S. E., Edkind, S., Gwilliam, R., Blackburn, H., Bumpstead, S. J., Dronv, S., Gillman, M., Gray, E., Hammond, N., Jayakumar, A., Mccann, O. T., Liddle, J., Potter, S. C., Ravindrarajah, R., Rickette, M., Waller, M., Weston, P., Widaa, S., Whittaker, P., Gormley, P., Bettella, F., Mcmahon, G., Todt, U., Palta, P., Hamalainen, E., Steinberg, S., Stefansson, H., Farkkila, M., Artto, V., Kaunisto, M. A., Schoenen, J., Frants, R. R., Borck, G., Gobel, H., Heinze, A., Heinze-kuhn, K. & Muller-myhsok, B., 26 May 2015, In: Neurology. 84, 21, p. 2132-2145 14 p., 21 .

    Research output: Contribution to journalArticlepeer-review

  23. Pooled Sequencing of 531 Genes in Inflammatory Bowel Disease Identifies an Associated Rare Variant in BTNL2 and Implicates Other Immune Related Genes

    Prescott, N. J., Lehne, B., Stone, K., Lee, J. C., Taylor, K., Knight, J., Papouli, E., Mirza, M. M., Simpson, M. A., Spain, S. L., Lu, G., Fraternali, F., Bumpstead, S. J., Gray, E., Amar, A., Bye, H., Green, P., Chung-Faye, G., Hayee, BH., Pollok, R. & 10 others, Satsangi, J., Parkes, M., Barrett, J. C., Mansfield, J. C., Sanderson, J., Lewis, C. M., Weale, M. E., Schlitt, T., Mathew, C. G. & UK IBD Genetics Consortium, 11 Feb 2015, In: PL o S Genetics. 11, 2, 19 p., e1004955.

    Research output: Contribution to journalArticlepeer-review

  24. Defective macrophage handling of Escherichia coli in Crohn's disease

    Elliott, T. R., Hudspith, B. N., Rayment, N. B., Prescott, N. J., Petrovska, L., Hermon-Taylor, J., Brostoff, J., Boussioutas, A., Mathew, C. G. & Sanderson, J. D., 2015, In: Journal of Gastroenterology and Hepatology.

    Research output: Contribution to journalArticlepeer-review

  25. Pharmacogenetic meta-analysis of genome-wide association studies of LDL cholesterol response to statins

    Postmus, I., Trompet, S., Deshmukh, H. A., Barnes, M. R., Li, X., Warren, H. R., Chasman, D. I., Zhou, K., Arsenault, B. J., Donnelly, L. A., Wiggins, K. L., Avery, C. L., Griffin, P., Feng, Q., Taylor, K. D., Li, G., Evans, D. S., Smith, A. V., De Keyser, C. E., Johnson, A. D. & 142 others, De Craen, A. J. M., Stott, D. J., Buckley, B. M., Ford, I., Westendorp, R. G. J., Eline Slagboom, P., Sattar, N., Munroe, P. B., Sever, P., Poulter, N., Stanton, A., Shields, D. C., O???brien, E., Shaw-hawkins, S., Ida Chen, Y., Nickerson, D. A., Smith, J. D., Pierre Dub??, M., Matthijs Boekholdt, S., Kees Hovingh, G., Kastelein, J. J. P., Mckeigue, P. M., Betteridge, J., Neil, A., Durrington, P. N., Doney, A., Carr, F., Morris, A., Mccarthy, M. I., Groop, L., Ahlqvist, E., Bis, J. C., Rice, K., Smith, N. L., Lumley, T., Whitsel, E. A., St??rmer, T., Boerwinkle, E., Ngwa, J. S., O???donnell, C. J., Vasan, R. S., Wei, W., Wilke, R. A., Liu, C., Sun, F., Guo, X., Heckbert, S. R., Post, W., Sotoodehnia, N., Arnold, A. M., Stafford, J. M., Ding, J., Herrington, D. M., Kritchevsky, S. B., Eiriksdottir, G., Launer, L. J., Harris, T. B., Chu, A. Y., Giulianini, F., Macfadyen, J. G., Barratt, B. J., Nyberg, F., Stricker, B. H., Uitterlinden, A. G., Hofman, A., Rivadeneira, F., Emilsson, V., Franco, O. H., Ridker, P. M., Gudnason, V., Liu, Y., Denny, J. C., Ballantyne, C. M., Rotter, J. I., Adrienne Cupples, L., Psaty, B. M., Palmer, C. N. A., Tardif, J., Colhoun, H. M., Hitman, G., Krauss, R. M., Wouter Jukema, J., Caulfield, M. J., Donnelly, P., Barroso, I., Blackwell, J. M., Bramon, E., Brown, M. A., Casas, J. P., Corvin, A., Deloukas, P., Duncanson, A., Jankowski, J., Markus, H. S., Mathew, C. G., Palmer, C. N. A., Plomin, R., Rautanen, A., Sawcer, S. J., Trembath, R., Viswanathan, A. C., Wood, N. W., Spencer, C. C. A., Band, G., Bellenguez, C., Freeman, C., Hellenthal, G., Giannoulatou, E., Pirinen, M., Pearson, R., Strange, A., Su, Z., Vukcevic, D., Donnelly, P., Langford, C., Hunt, S. E., Edkins, S., Gwilliam, R., Blackburn, H., Bumpstead, S. J., Dronov, S., Gillman, M., Gray, E., Hammond, N., Jayakumar, A., Mccann, O. T., Liddle, J., Potter, S. C., Ravindrarajah, R., Ricketts, M., Waller, M., Weston, P., Widaa, S., Whittaker, P., Barroso, I., Deloukas, P., Mathew, C. G., Blackwell, J. M., Brown, M. A., Corvin, A., Mccarthy, M. I. & Spencer, C. C. A., 28 Oct 2014, In: Nature Communications. 5, 5068.

    Research output: Contribution to journalArticlepeer-review

  26. The correlation between reading and mathematics ability at age twelve has a substantial genetic component

    Davis, O. S. P., Band, G., Pirinen, M., Haworth, C. M. A., Meaburn, E. L., Kovas, Y., Harlaar, N., Docherty, S. J., Hanscombe, K. B., Trzaskowski, M., Curtis, C. J. C., Strange, A., Freeman, C., Bellenguez, C., Su, Z., Vukcevic, D., Langford, C., Deloukas, P., Hunt, S., Gray, E. & 30 others, Dronov, S., Potter, S. C., Tashakkori-Ghanbaria, A., Edkins, S., Bumpstead, S. J., Blackwell, J. M., Bramon, E., Brown, M. A., Casas, J. P., Corvin, A., Duncanson, A., Jankowski, J. A. Z., Markus, H. S., Mathew, C. G., Palmer, C. N. A., Rautanen, A., Sawcer, S. J., Trembath, R. C., Viswanathan, A. C., Wood, N. W., Barroso, I., Peltonen, L., Dale, P. S., Petrill, S. A., Schalkwyk, L. S., Craig, I. W., Lewis, C. M., Price, T. S., Plomin, R. & Wellcome Trust Case Control Consortium, 8 Jul 2014, In: Nature Communications. 5, 6 p., 4204.

    Research output: Contribution to journalArticlepeer-review

  27. A genome-wide association analysis of a broad psychosis phenotype identifies three loci for further investigation

    Bramon, E., Pirinen, M., Strange, A., Lin, K., Freeman, C., Bellenguez, C., Su, Z., Band, G., Pearson, R., Vukcevic, D., Langford, C., Deloukas, P., Hunt, S., Gray, E., Dronov, S., Potter, S. C., Tashakkori-Ghanbaria, A., Edkins, S., Bumpstead, S. J., Arranz, M. J. & 31 others, Bakker, S., Bender, S., Bruggeman, R., Cahn, W., Chandler, D., Collier, D. A., Crespo-Facorro, B., Dazzan, P., de Haan, L., Di Forti, M., Dragović, M., Giegling, I., Hall, J., Iyegbe, C., Jablensky, A., Kravariti, E., Mata, I., McDonald, C., Pariante, C. M., Picchioni, M., Shaikh, M., Toulopoulou, T., Van Os, J., Walshe, M., Mathew, C. G., Plomin, R., Trembath, R. C., Lewis, C. M., Murray, R. M., Powell, J. & Psychosis Endophenotypes International Consortium, 1 Mar 2014, In: Biological psychiatry. 75, 5, p. 386-397 12 p.

    Research output: Contribution to journalArticlepeer-review

  28. A gene pathway analysis highlights the role of cellular adhesion molecules in multiple sclerosis susceptibility

    Damotte, V., Guillot-noel, L., Patsopoulos, N. A., Madireddy, L., El Behi, M., Ban, M., Baranzini, S., Barcellos, L., Beecham, G., Beecham, A., Bernardinelli, L., Booth, D., Bos, S., Buck, D., Bush, W., Comabella, M., Compston, A., Cotsapas, C., Cournu-rebeix, I., Cree, B. & 118 others, D'alfonso, S., Daly, M., Damotte, V., Davis, M., De Bakker, P., De Jager, P. L., Dubois, B., Esposito, F., Fontaine, B., Goris, A., Gourraud, P., Green, T., Gulowsen Celius, E., Hadjixenofontos, A., Hafler, D., Haines, J., Flinstad, H. F., Hauser, S., Hawkins, C., Hemmer, B., Hillert, J., Hintzen, R., Horáková, D., Ivinson, A. J., Kemppinen, A., Kira, J., Kockum, I., Lincoln, R., Martin, R., Martinelli Boneschi, F., Mccauley, J. L., Mero, I., Oksenberg, J., Olsson, T., Oturai, A., Palotie, A., Patsopoulos, N., Pericak-vance, M., Rioux, J., Saarela, J., Sawcer, S., Schnetz-boutaud, N., Sellebjerg, F., Soendergaard, H., Soelberg Sorensen, P., Spurkland, A., Stankovich, J., Stewart, G., Taylor, B., Ticca, A., West, S., Zipp, F., Donnelly, P., Barroso, I., Blackwell, J. M., Bramon, E., Brown, M. A., Casas, J. P., Corvin, A., Jankowski, J., Markus, H. S., Mathew, C. G., Palmer, C. N. A., Plomin, R., Rautanen, A., Sawcer, S., Trembath, R. C., Viswanathan, A. C., Wood, N. W., Spencer, C. C. A., Band, G., Bellenguez, C., Freeman, C., Hellenthal, G., Giannoulatou, E., Pirinen, M., Pearson, R., Strange, A., Su, Z., Vukcevic, D., Donnelly, P., Langford, C., Hunt, S. E., Edkins, S., Gwilliam, R., Blackburn, H., Bumpstead, S. J., Dronov, S., Gillman, M., Gray, E., Hammond, N., Jayakumar, A., Mccann, O. T., Liddle, J., Potter, S. C., Ravindrarajah, R., Ricketts, M., Waller, M. J., Weston, P., Widaa, S., Whittaker, P., Barroso, I., Deloukas, P., Dilthey, A., Leslie, S., Moutsianas, L., Perez, M. L., Mcvean, G., Mathew, C. G., Blackwell, J. M., Brown, M. A., Corvin, A., Mccarthy, M. I., Spencer, C. C. A., De Jager, P. L., Baranzini, S. E., Cournu-rebeix, I. & Fontaine, B., Mar 2014, In: GENES AND IMMUNITY. 15, 2, p. 126-132 7 p., N/A.

    Research output: Contribution to journalArticlepeer-review

  29. Genome-wide estimates of inbreeding in unrelated individuals and their association with cognitive ability

    Power, R., Nagoshi, C., Defries, J. C., Donnelly, P., Barroso, I., Blackwell, J. M., Bramon, E., Brown, M. A., Casas, J. P., Corvin, A., Deloukas, P., Duncanson, A., Jankowski, J., Markus, H. S., Mathew, C. G., Palmer, C. N., Rautanen, A., Sawcer, S. J., Trembath, R. C., Viswanathan, A. C. & 41 others, Wood, N. W., Spencer, C. C. A., Band, G., Bellenguez, C., Freeman, C., Hellenthal, G., Giannoulatou, E., Pirinen, M., Pearson, R., Strange, A., Su, Z., Vukcevic, D., Donnelly, P., Langford, C., Hunt, S. E., Edkins, S., Gwilliam, R., Blackburn, H., Bumpstead, S. J., Dronov, S., Gillman, M., Gray, E., Hammond, N., Jayakumar, A., Mccann, O. T., Liddle, J., Potter, S. C., Ravindrarajah, R., Ricketts, M., Waller, M., Weston, P., Widaa, S., Whittaker, P., Barroso, I., Deloukas, P., Mathew, C. G., Blackwell, J. M., Brown, M. A., Corvin, A., Spencer, C. C. A. & Plomin, R., Mar 2014, In: European Journal of Human Genetics. 22, 3, p. 386-390 5 p.

    Research output: Contribution to journalArticlepeer-review

  30. Genome-wide association analysis identifies 13 new risk loci for schizophrenia

    Ripke, S., O'dushlaine, C., Chambert, K., Moran, J. L., K??hler, A. K., Akterin, S., Bergen, S. E., Collins, A. L., Crowley, J. J., Fromer, M., Kim, Y., Lee, S. H., Magnusson, P. K. E., Sanchez, N., Stahl, E. A., Williams, S., Wray, N. R., Xia, K., Bettella, F., Borglum, A. D. & 15 others, Bulik-sullivan, B. K., Cormican, P., Craddock, N., De Leeuw, C., Durmishi, N., Gill, M., Lin, K., Neale, B. M., Powell, J., Riley, B. P., Walters, J. T., Multicenter Genetic Studies of Schizophrenia Consortium, Psychosis Endophenotypes International Consortium, Wellcome Trust Case Consortium 2 & Purcell, S., Oct 2013, In: Nature Genetics. 45, 10, p. 1150-1159 10 p.

    Research output: Contribution to journalArticlepeer-review

  31. Genome-wide association analysis in primary sclerosing cholangitis and ulcerative colitis identifies risk loci at GPR35 and TCF4

    Ellinghaus, D., Folseraas, T., Holm, K., Ellinghaus, E., Melum, E., Balschun, T., Laerdahl, J. K., Shiryaev, A., Gotthardt, D. N., Weismüller, T. J., Schramm, C., Wittig, M., Bergquist, A., Björnsson, E., Marschall, H-U., Vatn, M., Teufel, A., Rust, C., Gieger, C., Wichmann, H-E. & 17 others, Runz, H., Sterneck, M., Rupp, C., Braun, F., Weersma, R. K., Wijmenga, C., Ponsioen, C. Y., Mathew, C. G., Rutgeerts, P., Vermeire, S., Schrumpf, E., Hov, J. R., Manns, M. P., Boberg, K. M., Schreiber, S., Franke, A. & Karlsen, T. H., Sep 2013, In: Hepatology. 58, 3, p. 1074-1083 10 p., N/A.

    Research output: Contribution to journalArticlepeer-review

  32. Association Between Variants of PRDM1 and NDP52 and Crohn's Disease, Based on Exome Sequencing and Functional Studies

    Ellinghaus, D., Zhang, H., Zeissig, S., Lipinski, S., Till, A., Jiang, T., Stade, B., Bromberg, Y., Ellinghaus, E., Keller, A., Rivas, M. A., Skieceviciene, J., Doncheva, N. T., Liu, X., Liu, Q., Jiang, F., Forster, M., Mayr, G., Albrecht, M., Haesler, R. & 41 others, Boehm, B. O., Goodall, J., Berzuini, C. R., Lee, J., Andersen, V., Vogel, U., Kupcinskas, L., Kayser, M., Krawczak, M., Nikolaus, S., Weersma, R. K., Ponsioen, C. Y., Sans, M., Wijmenga, C., Strachan, D. P., McAardle, W. L., Vermeire, S., Rutgeerts, P., Sanderson, J., Mathew, C. G., Vatn, M. H., Wang, J., Noethen, M. M., Duerr, R. H., Buening, C., Brand, S., Glas, J., Winkelmann, J., Illig, T., Latiano, A., Annese, V., Halfvarson, J., D'Amato, M., Daly, M. J., Nothnagel, M., Karlsen, T. H., Subramani, S., Rosenstiel, P., Schreiber, S., Parkes, M. & Franke, A., Aug 2013, In: Gastroenterology. 145, 2, p. 339-347 9 p.

    Research output: Contribution to journalArticlepeer-review

  33. 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 journalLetterpeer-review

  34. 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 journalLetterpeer-review

  35. Seven newly identified loci for autoimmune thyroid disease

    Wellcome Trust Case Control Consortium, 1 Dec 2012, In: Human Molecular Genetics. 21, 23, p. 5202-5208 7 p.

    Research output: Contribution to journalArticlepeer-review

  36. Bayesian refinement of association signals for 14 loci in 3 common diseases

    Maller, J. B., McVean, G., Byrnes, J., Vukcevic, D., Palin, K., Su, Z., Howson, J. M. M., Auton, A., Myers, S., Morris, A., Pirinen, M., Brown, M. A., Burton, P. R., Caulfield, M. J., Compston, A., Farrall, M., Hall, A. S., Hattersley, A. T., Hill, A. V. S., Mathew, C. G. & 18 others, Pembrey, M., Satsangi, J., Stratton, M. R., Worthington, J., Craddock, N., Hurles, M., Ouwehand, W., Parkes, M., Rahman, N., Duncanson, A., Todd, J. A., Kwiatkowski, D. P., Samani, N. J., Gough, S. C. L., McCarthy, M. I., Deloukas, P., Donnelly, P. & Wellcome Trust Case Control Consortium, Dec 2012, In: Nature Genetics. 44, 12, p. 1294-1301 8 p.

    Research output: Contribution to journalArticlepeer-review

  37. Identification of 15 new psoriasis susceptibility loci highlights the role of innate immunity

    Tsoi, L. C., Spain, S. L., Knight, J., Ellinghaus, E., Stuart, P. E., Capon, F., Ding, J., Li, Y., Tejasvi, T., Gudjonsson, J. E., Kang, H. M., Allen, M. H., McManus, R., Novelli, G., Samuelsson, L., Schalkwijk, J., Ståhle, M., Burden, A. D., Smith, C. H., Cork, M. J. & 31 others, Estivill, X., Bowcock, A. M., Krueger, G. G., Weger, W., Worthington, J., Tazi-Ahnini, R., Nestle, F. O., Hayday, A., Hoffmann, P., Winkelmann, J., Wijmenga, C., Langford, C., Edkins, S., Andrews, R., Blackburn, H., Strange, A., Band, G., Pearson, R. D., Vukcevic, D., Spencer, C. C. A., Onoufriadis, A., Weale, M. E., Campbell, L. E., Mathew, C. G., Plomin, R., Viswanathan, A. C., Gray, E., Weston, P., Barker, J. N. W. N., Trembath, R. C. & Collaborative Association Study of Psoriasis (CASP), Dec 2012, In: Nature Genetics. 44, 12, p. 1341-1348 8 p.

    Research output: Contribution to journalArticlepeer-review

  38. Host-microbe interactions have shaped the genetic architecture of inflammatory bowel disease

    Jostins, L., Ripke, S., Weersma, R. K., Duerr, R. H., McGovern, D. P., Hui, K. Y., Lee, J. C., Schumm, L. P., Sharma, Y., Anderson, C. A., Essers, J., Mitrovic, M., Ning, K., Cleynen, I., Theatre, E., Spain, S. L., Raychaudhuri, S., Goyette, P., Wei, Z., Abraham, C. & 31 others, Achkar, J-P., Ahmad, T., Amininejad, L., Ananthakrishnan, A. N., Andersen, V., Andrews, J. M., Baidoo, L., Balschun, T., Bampton, P. A., Bitton, A., Boucher, G., Brand, S., Büning, C., Cohain, A., Cichon, S., D'Amato, M., De Jong, D., Devaney, K. L., Dubinsky, M., Edwards, C., Ellinghaus, D., Ferguson, L. R., Franchimont, D., Fransen, K., Gearry, R., Georges, M., Gieger, C., Prescott, N. J., Sanderson, J., Mathew, C. G. & International IBD Genetics Consortium (IIBDGC), 1 Nov 2012, In: NATURE. 491, 7422, p. 119-124 6 p.

    Research output: Contribution to journalArticlepeer-review

  39. Distinct genetic association at the PLCE1 locus with oesophageal squamous cell carcinoma in the South African population

    Bye, H., Prescott, N. J., Lewis, C. M., Matejcic, M., Moodley, L., Robertson, B., van Rensburg, C., Parker, M. I. & Mathew, C. G., Nov 2012, In: Carcinogenesis. 33, 11, p. 2155-2161 7 p.

    Research output: Contribution to journalArticlepeer-review

  40. Genome-Wide Association Study Implicates HLA-C*01:02 as a Risk Factor at the Major Histocompatibility Complex Locus in Schizophrenia

    Strange, A., Riley, B. P., Spencer, C. C. A., Morris, D. W., Pirinen, M., O'Dushlaine, C. T., Su, Z., Maher, B. S., Freeman, C., Cormican, P., Bellenguez, C., Kenny, E. M., Band, G., Wormley, B., Donohoe, G., Dilthey, A., Moutsianas, L., Quinn, E., Edkins, S., Judge, R. & 31 others, Coleman, K., Hunt, S., Tropea, D., Roche, S., Cummings, L., Kelleher, E., McKeon, P., Dinan, T., McDonald, C., Murphy, K. C., O'Callaghan, E., O'Neill, F. A., Waddington, J. L., Walsh, D., Giannoulatou, E., Langford, C., Deloukas, P., Gray, E., Dronov, S., Potter, S., Pearson, R., Vukcevic, D., Tashakkori-Ghanbaria, A., Blackwell, J. M., Bramon, E., Brown, M. A., Casas, J. P., Mathew, C. G., Plomin, R., Trembath, R. C. & Wellcome Trust Case Control Consor, SGENE Consortium, Schizophrenia Working Grp Psychiat, Irish Schizophrenia Genomics Conso, 15 Oct 2012, In: Biological psychiatry. 72, 8, p. 620-628 9 p.

    Research output: Contribution to journalArticlepeer-review

  41. Common variants at the MHC locus and at chromosome 16q24.1 predispose to Barrett's esophagus

    Su, Z., Gay, L. J., Strange, A., Palles, C., Band, G., Whiteman, D. C., Lescai, F., Langford, C., Nanji, M., Edkins, S., van der Winkel, A., Levine, D., Sasieni, P., Bellenguez, C., Howarth, K., Freeman, C., Trudgill, N., Tucker, A. T., Pirinen, M., Peppelenbosch, M. P. & 32 others, van der Laan, L. J. W., Kuipers, E. J., Drenth, J. P. H., Peters, W. H., Reynolds, J. V., Kelleher, D. P., McManus, R., Grabsch, H., Prenen, H., Bisschops, R., Krishnadath, K., Siersema, P. D., van Baal, J. W. P. M., Middleton, M., Petty, R., Gillies, R., Burch, N., Bhandari, P., Paterson, S., Edwards, C., Penman, I., Vaidya, K., Ang, Y., Murray, I., Patel, P., Ye, W., Mullins, P., Mathew, C. G., Plomin, R., Trembath, R. C., Esophageal Adenocarcinoma Genetics & Wellcome Trust Case Control Consor, Oct 2012, In: Nature Genetics. 44, 10, p. 1131-1136 8 p., N/A.

    Research output: Contribution to journalArticlepeer-review

  42. Effect of communicating DNA based risk assessments for Crohn's disease on smoking cessation: randomised controlled trial

    Hollands, G. J., Whitwell, S. C. L., Parker, R. A., Prescott, N. J., Forbes, A., Sanderson, J., Mathew, C. G., Lewis, C. M., Watts, S., Sutton, S., Armstrong, D., Kinmonth, A. L., Prevost, A. T. & Marteau, T. M., 20 Jul 2012, In: British Medical Journal. 345, 7870, 12 p., e4708.

    Research output: Contribution to journalArticlepeer-review

  43. TOWARDS INDIVIDUALISED RISK PREDICTION FOR CROHN'S DISEASE

    Taylor, K. M., Prescott, N. J., Anderson, S. H., Irving, P. M., West, S. L., Crouch, D. J. M., Mathew, C. G., Sanderson, J. D. & Lewis, C. M., Jul 2012, In: Gut. 61, p. A72-A72 1 p.

    Research output: Contribution to journalMeeting abstractpeer-review

  44. Smokers with active Crohn's disease have a clinically relevant dysbiosis of the gastrointestinal microbiota

    Benjamin, J. L., Hedin, C. R. H., Koutsoumpas, A., Ng, S. C., McCarthy, N. E., Prescott, N. J., Pessoa-Lopes, P., Mathew, C. G., Sanderson, J., Hart, A. L., Kamm, M. A., Knight, S. C., Forbes, A., Stagg, A. J., Lindsay, J. O. & Whelan, K., Jun 2012, In: Inflammatory Bowel Diseases. 18, 6, p. 1092-1100 9 p.

    Research output: Contribution to journalArticlepeer-review

  45. Combined Analysis of Genome-wide Association Studies for Crohn Disease and Psoriasis Identifies Seven Shared Susceptibility Loci

    Ellinghaus, D., Ellinghaus, E., Nair, R. P., Stuart, P. E., Esko, T., Metspalu, A., Debrus, S., Raelson, J. V., Tejasvi, T., Belouchi, M., West, S. L., Barker, J. N., Koks, S., Kingo, K., Balschun, T., Palmieri, O., Annese, V., Gieger, C., Wichmann, H. E., Kabesch, M. & 10 others, Trembath, R. C., Mathew, C. G., Abecasis, G. R., Weidinger, S., Nikolaus, S., Schreiber, S., Elder, J. T., Weichenthal, M., Nothnagel, M. & Franke, A., 6 Apr 2012, In: American Journal of Human Genetics. 90, 4, p. 636-647 12 p.

    Research output: Contribution to journalArticlepeer-review

  46. Genome-wide association study identifies a variant in HDAC9 associated with large vessel ischemic stroke

    Bellenguez, C., Bevan, S., Gschwendtner, A., Spencer, C. C. A., Burgess, A. I., Pirinen, M., Jackson, C. A., Traylor, M., Strange, A., Su, Z., Band, G., Syme, P. D., Malik, R., Pera, J., Norrving, B., Lemmens, R., Freeman, C., Schanz, R., James, T., Poole, D. & 68 others, Murphy, L., Segal, H., Cortellini, L., Cheng, Y-C., Woo, D., Nalls, M. A., Mueller-Myhsok, B., Meisinger, C., Seedorf, U., Ross-Adams, H., Boonen, S., Wloch-Kopec, D., Valant, V., Slark, J., Furie, K., Delavaran, H., Langford, C., Deloukas, P., Edkins, S., Hunt, S., Gray, E., Dronov, S., Peltonen, L., Gretarsdottir, S., Thorleifsson, G., Thorsteinsdottir, U., Stefansson, K., Boncoraglio, G. B., Parati, E. A., Attia, J., Holliday, E., Levi, C., Franzosi, M-G., Goel, A., Helgadottir, A., Blackwell, J. M., Bramon, E., Brown, M. A., Casas, J. P., Corvin, A., Duncanson, A., Jankowski, J., Mathew, C. G., Palmer, C. N. A., Plomin, R., Rautanen, A., Sawcer, S. J., Trembath, R. C., Viswanathan, A. C., Wood, N. W., Worrall, B. B., Kittner, S. J., Mitchell, B. D., Kissela, B., Meschia, J. F., Thijs, V., Lindgren, A., Macleod, M. J., Slowik, A., Walters, M., Rosand, J., Sharma, P., Farrall, M., Sudlow, C. L. M., Rothwell, P. M., Dichgans, M., Donnelly, P. & Markus, H. S., Mar 2012, In: Nature Genetics. 44, 3, p. 328 - U141 6 p.

    Research output: Contribution to journalArticlepeer-review

  47. 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 journalLetterpeer-review

  48. Population-specific genetic associations with oesophageal squamous cell carcinoma in South Africa

    Bye, H., Prescott, N. J., Matejcic, M., Rose, E., Lewis, C. M., Parker, M. I. & Mathew, C. G., 16 Sep 2011, In: Carcinogenesis. 32, 12, p. 1855-1861 7 p.

    Research output: Contribution to journalArticlepeer-review

  49. 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 journalLetterpeer-review

  50. Interaction between ERAP1 and HLA-B27 in ankylosing spondylitis implicates peptide handling in the mechanism for HLA-B27 in disease susceptibility

    Evans, D. M., Spencer, C. C. A., Pointon, J. J., Su, Z., Harvey, D., Kochan, G., Opperman, U., Dilthey, A., Pirinen, M., Stone, M. A., Appleton, L., Moutsianis, L., Leslie, S., Wordsworth, T., Kenna, T. J., Karaderi, T., Thomas, G. P., Ward, M. M., Weisman, M. H., Farrar, C. & 73 others, Bradbury, L. A., Danoy, P., Inman, R. D., Maksymowych, W., Gladman, D., Rahman, P., Morgan, A., Marzo-Ortega, H., Bowness, P., Gaffney, K., Gaston, J. S. H., Smith, M., Bruges-Armas, J., Couto, A-R., Sorrentino, R., Paladini, F., Ferreira, M. A., Xu, H., Liu, Y., Jiang, L., Lopez-Larrea, C., Diaz-Pena, R., Lopez-Vazquez, A., Zayats, T., Band, G., Bellenguez, C., Blackburn, H., Blackwell, J. M., Bramon, E., Bumpstead, S. J., Casas, J. P., Corvin, A., Craddock, N., Deloukas, P., Dronov, S., Duncanson, A., Edkins, S., Freeman, C., Gillman, M., Gray, E., Gwilliam, R., Hammond, N., Hunt, S. E., Jankowski, J., Jayakumar, A., Langford, C., Liddle, J., Markus, H. S., Mathew, C. G., McCann, O. T., McCarthy, M. I., Palmer, C. N. A., Peltonen, L., Plomin, R., Potter, S. C., Rautanen, A., Ravindrarajah, R., Ricketts, M., Samani, N., Sawcer, S. J., Strange, A., Trembath, R. C., Viswanathan, A. C., Waller, M., Weston, P., Whittaker, P., Widaa, S., Wood, N. W., McVean, G., Reveille, J. D., Wordsworth, B. P., Brown, M. A. & Donnelly, P., Aug 2011, In: Nature Genetics. 43, 8, p. 761 - 767 7 p.

    Research output: Contribution to journalArticlepeer-review

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