Christopher Mathew

2023

Kaposi sarcoma-associated herpesvirus, HIV-1 and Kaposi sarcoma risk in black South Africans diagnosed with cancer during antiretroviral treatment rollout

Motlhale, M., Mathew, C., Lewis, C. & Sitas, F., 15 May 2023, In: International Journal of Cancer. 152, 10, p. 2081-2089 9 p.

Research output: Contribution to journal › Article › peer-review

Open Access

2022

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 journal › Review article › peer-review

Open Access

8 Citations (Scopus)

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 journal › Article › peer-review

Open Access

File

1 Citation (Scopus)

37 Downloads (Pure)

2020

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 journal › Article › peer-review

Open Access

File

12 Citations (Scopus)

239 Downloads (Pure)

2019

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 journal › Article › peer-review

Open Access

File

8 Citations (Scopus)

116 Downloads (Pure)

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 journal › Article › peer-review

Open Access

File

17 Citations (Scopus)

242 Downloads (Pure)

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., Sept 2019, In: Gut. 68, 9, p. 1537-1540

Research output: Contribution to journal › Letter › peer-review

Open Access

23 Citations (Scopus)

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 journal › Article › peer-review

Open Access

3 Citations (Scopus)

2018

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 journal › Article › peer-review

Open Access

File

1 Citation (Scopus)

212 Downloads (Pure)

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 journal › Article › peer-review

Open Access

File

12 Citations (Scopus)

168 Downloads (Pure)

2017

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 othersTremelling, 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 journal › Article › peer-review

Open Access

File

109 Citations (Scopus)

83 Downloads (Pure)

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 journal › Article › peer-review

Open Access

File

352 Citations (Scopus)

58 Downloads (Pure)

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 othersHart, 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 journal › Letter › peer-review

Open Access

File

665 Citations (Scopus)

92 Downloads (Pure)

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 othersMenya, 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 journal › Review article › peer-review

124 Citations (Scopus)

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 othersChallis, 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 journal › Article › peer-review

Open Access

70 Citations (Scopus)

2016

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 othersLek, 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 journal › Article › peer-review

Open Access

File

41 Citations (Scopus)

134 Downloads (Pure)

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 journal › Article › peer-review

Open Access

File

6 Citations (Scopus)

162 Downloads (Pure)

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 journal › Article › peer-review

Open Access

File

10 Citations (Scopus)

213 Downloads (Pure)

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 journal › Article › peer-review

Open Access

File

15 Citations (Scopus)

214 Downloads (Pure)

2015

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 journal › Article › peer-review

25 Citations (Scopus)

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 journal › Article › peer-review

13 Citations (Scopus)

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 othersMelén, 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 journal › Article › peer-review

Open Access

262 Citations (Scopus)

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 othersSatsangi, 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 journal › Article › peer-review

Open Access

47 Citations (Scopus)

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 othersSudlow, 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 journal › Article › peer-review

80 Citations (Scopus)

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 othersSawcer, 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 journal › Article › peer-review

30 Citations (Scopus)

2014

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 othersD'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 journal › Article › peer-review

Open Access

25 Citations (Scopus)

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 othersBakker, 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 journal › Article › peer-review

39 Citations (Scopus)

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 othersWood, 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 journal › Article › peer-review

16 Citations (Scopus)

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 othersDe 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 journal › Article › peer-review

Open Access

File

193 Citations (Scopus)

156 Downloads (Pure)

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 othersDronov, 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 journal › Article › peer-review

Open Access

71 Citations (Scopus)

2013

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 othersBoehm, 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 journal › Article › peer-review

122 Citations (Scopus)

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 othersPontes, 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 journal › Letter › peer-review

Open Access

File

83 Citations (Scopus)

150 Downloads (Pure)

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 othersBulik-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 journal › Article › peer-review

1171 Citations (Scopus)

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 othersRunz, 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., Sept 2013, In: Hepatology. 58, 3, p. 1074-1083 10 p., N/A.

Research output: Contribution to journal › Article › peer-review

132 Citations (Scopus)

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 othersMein, 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 journal › Letter › peer-review

158 Citations (Scopus)

2012

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 othersPembrey, 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 journal › Article › peer-review

327 Citations (Scopus)

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 othersTrembath, 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 journal › Article › peer-review

248 Citations (Scopus)

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 othersvan 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 journal › Article › peer-review

146 Citations (Scopus)

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 journal › Article › peer-review

39 Citations (Scopus)

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 journal › Article › peer-review

Open Access

26 Citations (Scopus)

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 othersMurphy, 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 journal › Article › peer-review

343 Citations (Scopus)

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 othersColeman, 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 journal › Article › peer-review

136 Citations (Scopus)

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 othersAchkar, 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 journal › Article › peer-review

3470 Citations (Scopus)

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 othersEstivill, 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 journal › Article › peer-review

748 Citations (Scopus)

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 othersGlass, 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 journal › Letter › peer-review

36 Citations (Scopus)

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 journal › Article › peer-review

126 Citations (Scopus)

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 journal › Article › peer-review

164 Citations (Scopus)

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 journal › Meeting abstract › peer-review

16 Citations (Scopus)

2011

Association of a deletion of GSTT2B with an altered risk of oesophageal squamous cell carcinoma in a South African population: a case-control study

Matejcic, M., Li, D., Prescott, N. J., Lewis, C. M., Mathew, C. G. & Parker, M. I., 2011, In: PLoS ONE. 6, 12, e29366.

Research output: Contribution to journal › Article › peer-review

28 Citations (Scopus)

AUTOPHAGY GENE POLYMORPHISMS INFLUENCE THE INTERACTION OF E COLI AND MACROPHAGES IN CROHN'S DISEASE

Elliott, T., Prescott, N., Hudspith, B., Rayment, N., Hermon-Taylor, J., Brostoff, J., Mathew, C. & Sanderson, J. D., 2011, In: Gut. 60, p. A61 - A61

Research output: Contribution to journal › Meeting abstract

32 Citations (Scopus)

Christopher Mathew

Research output

Search results