The DOI matches its Crossref record; 30 of the 30 references it cites were found in a registry or an index.
Host–microbe interactions have shaped the genetic architecture of inflammatory bowel disease
Open accessAbstract
Crohn's disease and ulcerative colitis, the two common forms of inflammatory bowel disease (IBD), affect over 2.5 million people of European ancestry, with rising prevalence in other populations. Genome-wide association studies and subsequent meta-analyses of these two diseases as separate phenotypes have implicated previously unsuspected mechanisms, such as autophagy, in their pathogenesis and showed that some IBD loci are shared with other inflammatory diseases. Here we expand on the knowledge of relevant pathways by undertaking a meta-analysis of Crohn's disease and ulcerative colitis genome-wide association scans, followed by extensive validation of significant findings, with a combined total of more than 75,000 cases and controls. We identify 71 new associations, for a total of 163 IBD loci, that meet genome-wide significance thresholds. Most loci contribute to both phenotypes, and both directional (consistently favouring one allele over the course of human history) and balancing (favouring the retention of both alleles within populations) selection effects are evident. Many IBD loci are also implicated in other immune-mediated disorders, most notably with ankylosing spondylitis and psoriasis. We also observe considerable overlap between susceptibility loci for IBD and mycobacterial infection. Gene co-expression network analysis emphasizes this relationship, with pathways shared between host responses to mycobacteria and those predisposing to IBD.
Overview
The claims and statistics of this paper haven’t been checked yet.
Run the check — free, no account needed. It reads the open-access text and checks the sources it cites.
Integrity signals
Registry
Cites
Statistics
Verification
Claims the paper makes
The claims and statistics of this paper haven’t been checked yet.
Run the check — free, no account needed. It reads the open-access text and checks the sources it cites.
Claims other papers make about this one
Each is checked against this paper’s own text: does it say what the citing paper says it does?
The cited source says what the claim attributes to it.
In the citing paper
“Population-based, genome-wide–association studies followed by subsequent meta-analysis of population-based, genome-wide–association studies and immunochip data have identified more than 160 loci linked to IBD susceptibility (Jostins et al., 2012).”
From Targeting Janus Kinases and Signal Transducer and Activator of Transcription 3 To Treat Inflammation, Fibrosis, and Cancer: Rationale, Progress, and Caution (2020) · cites this paper as Jostins et al., 2012
In the citing paper
“Examples include the role of complement in the pathogenesis of acute macular degeneration38, synaptic pruning in schizophrenia64 and autophagy in inflammatory bowel disease65.”
From A brief history of human disease genetics (2020) · cites this paper as [65]
In the citing paper
“The 71 regulators significantly overlap with genes genetically associated with inflammatory bowel disease44 (11 of 71, p<10-9).”
From Dynamic regulatory network controlling TH17 cell differentiation (2013) · cites this paper as [44]
Self-check
Percentages, sums and reported differences re-computed from the paper’s own numbers.
The self-check needs the paper’s full text.
Citations
Cites
A General Framework for Weighted Gene Co-Expression Network Analysis
Zhang, B., & Horvath, S. (2005) · Statistical Applications in Genetics and Molecular Biology · doi:10.2202/1544-6115.1128 · Cited by 5,684
Self-citationMolodecky, N. A., Soon, I. S., Rabi, D. M., Ghali, W. A., Ferris, M., Chernoff, G., Benchimol, E. I., Panaccione, R., Ghosh, S., Barkema, H. W., et al. (2012) · Gastroenterology · doi:10.1053/j.gastro.2011.10.001 · Cited by 4,833
Hindorff, L. A., Sethupathy, P., Junkins, H. A., Ramos, E. M., Mehta, J. P., Collins, F. S., & Manolio, T. A. (2009) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0903103106 · Cited by 4,013
Genetics and pathogenesis of inflammatory bowel disease
Khor, B., Gardet, A., & Xavier, R. J. (2011) · Nature · doi:10.1038/nature10209 · Cited by 2,725
Self-citationFranke, 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., et al. (2010) · Nature Genetics · doi:10.1038/ng.717 · Cited by 2,520
Self-citationThe mystery of missing heritability: Genetic interactions create phantom heritability
Zuk, O., Hechter, E., Sunyaev, S. R., & Lander, E. S. (2012) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1119675109 · Cited by 1,542
Anderson, C., Boucher, G., Lees, C., Franke, A., D'Amato, M., Taylor, K., Lee, J., Goyette, P., Imieliński, M., Latiano, A., et al. (2011) · Nature Genetics · doi:10.1038/ng.764 · Cited by 1,361
Self-citationGenetics of gene expression and its effect on disease
Emilsson, V., Thorleifsson, G., Zhang, B., Leonardson, A. S., Zink, F., Zhu, J., Carlson, S., Helgason, A., Walters, G. B., Gunnarsdottir, S., et al. (2008) · Nature · doi:10.1038/nature06758 · Cited by 1,296
Self-citationSTAT3 Mutations in the Hyper-IgE Syndrome
Holland, S. M., DeLeo, F. R., Elloumi, H. Z., Hsu, A. P., Uzel, G., Brodsky, N. N., Freeman, A. F., Demidowich, A. P., Davis, J., Turner, M. L. C., et al. (2007) · New England Journal of Medicine · doi:10.1056/nejmoa073687 · Cited by 1,233
Dominant-negative mutations in the DNA-binding domain of STAT3 cause hyper-IgE syndrome
Minegishi, Y., Saitō, M., Tsuchiya, S., Tsuge, I., Takada, H., Hara, T., Kawamura, N., Ariga, T., Pašić, S., Stojković, O., et al. (2007) · Nature · doi:10.1038/nature06096 · Cited by 1,075
Cited by
Sorted by citations
Items 501–600 of 1,032
Functional Impacts of the Intestinal Microbiome in the Pathogenesis of Inflammatory Bowel Disease
Li, J. S. Y., Butcher, J., Mack, D. R., & Stintzi, A. (2014) · Inflammatory Bowel Diseases · doi:10.1097/mib.0000000000000215 · Cited by 152
Schwerd, T., Pandey, S., Yang, H., Bagola, K., Jameson, E., Jung, J., Lachmann, R., Shah, N., Patel, S. Y., Booth, C., et al. (2016) · Gut · doi:10.1136/gutjnl-2015-310382 · Cited by 156
Self-citationPutignani, L., CHIERICO, F. D., Vernocchi, P., Cicala, M., Cucchiara, S., & Dallapiccola, B. (2015) · Inflammatory Bowel Diseases · doi:10.1097/mib.0000000000000602 · Cited by 153
IL-10 in Humans: Lessons from the Gut, IL-10/IL-10 Receptor Deficiencies, and IL-10 Polymorphisms
Engelhardt, K. R., & Grimbacher, B. (2014) · Current topics in microbiology and immunology · doi:10.1007/978-3-662-43492-5_1 · Cited by 156
RIP1 inhibition blocks inflammatory diseases but not tumor growth or metastases
Patel, S. D., Webster, J. D., Varfolomeev, E. E., Kwon, Y. C., Cheng, J. H., Zhang, J., Dugger, D. L., Wickliffe, K. E., Maltzman, A., Sujatha-Bhaskar, S., et al. (2019) · Cell Death and Differentiation · doi:10.1038/s41418-019-0347-0 · Cited by 152
Mycobacterium paratuberculosis as a cause of Crohn’s disease
McNees, A. L., Markesich, D. C., Zayyani, N. R., & Graham, D. Y. (2015) · Expert Review of Gastroenterology & Hepatology · doi:10.1586/17474124.2015.1093931 · Cited by 149
Intestinal epithelial cell metabolism at the interface of microbial dysbiosis and tissue injury
Rath, E., & Haller, D. (2022) · Mucosal Immunology · doi:10.1038/s41385-022-00514-x · Cited by 159
Robinson, P. C., Claushuis, T. A. M., Cortés, A., Martin, T. M., Evans, D. M., Leo, P., Mukhopadhyay, P., Bradbury, L. A., Cremin, K., Harris, J., et al. (2014) · Arthritis & Rheumatology · doi:10.1002/art.38873 · Cited by 148
A RIPK2 inhibitor delays NOD signalling events yet prevents inflammatory cytokine production
Nachbur, U., Stafford, C. A., Bankovacki, A., Zhan, Y., Lindqvist, L., Fiil, B. K., Khakham, Y., Ko, H., Sandow, J. J., Falk, H., et al. (2015) · Nature Communications · doi:10.1038/ncomms7442 · Cited by 148
Why interleukin-10 supplementation does not work in Crohn’s disease patients
Marlow, G. (2013) · World Journal of Gastroenterology · doi:10.3748/wjg.v19.i25.3931 · Cited by 148
Gut mucosal DAMPs in IBD: from mechanisms to therapeutic implications
Boyapati, R. K., Rossi, A. G., Satsangi, J., & Ho, G. (2016) · Mucosal Immunology · doi:10.1038/mi.2016.14 · Cited by 150
Self-citationEnvironmental Enteric Dysfunction in Children
Syed, S., Ali, A., & Duggan, C. (2016) · Journal of Pediatric Gastroenterology and Nutrition · doi:10.1097/mpg.0000000000001147 · Cited by 148
Clinical Genomics for the Diagnosis of Monogenic Forms of Inflammatory Bowel Disease
Uhlig, H. H., Charbit‐Henrion, F., Kotlarz, D., Shouval, D. S., Schwerd, T., Strisciuglio, C., de Ridder, L., Limbergen, J. V., Macchi, M., Snapper, S. B., et al. (2020) · Journal of Pediatric Gastroenterology and Nutrition · doi:10.1097/mpg.0000000000003017 · Cited by 152
Self-citationLocation is important: differentiation between ileal and colonic Crohn’s disease
Atreya, R. N., & Siegmund, B. (2021) · Nature Reviews Gastroenterology & Hepatology · doi:10.1038/s41575-021-00424-6 · Cited by 150
Progress and promise in understanding the genetic basis of common diseases
Price, A. L., Spencer, C. C. A., & Donnelly, P. (2015) · Proceedings of the Royal Society B: Biological Sciences · doi:10.1098/rspb.2015.1684 · Cited by 147
Systems biology of asthma and allergic diseases: A multiscale approach
Bunyavanich, S., & Schadt, E. E. (2014) · Journal of Allergy and Clinical Immunology · doi:10.1016/j.jaci.2014.10.015 · Cited by 149
Self-citationHelicobacter species are potent drivers of colonic T cell responses in homeostasis and inflammation
Chai, J. N., Peng, Y., Rengarajan, S., Solomon, B. D., Ai, T. L., Shen, Z., Perry, J. S. A., Knoop, K. A., Tanoue, T., Narushima, S., et al. (2017) · Science Immunology · doi:10.1126/sciimmunol.aal5068 · Cited by 152
The emerging role of lncRNAs in inflammatory bowel disease
Yarani, R., Mirza, A. H., Kaur, S., & Pociot, F. (2018) · Experimental & Molecular Medicine · doi:10.1038/s12276-018-0188-9 · Cited by 147
Zinc: An underappreciated modulatory factor of brain function
Marger, L., Schubert, C. R., & Bertrand, D. (2014) · Biochemical Pharmacology · doi:10.1016/j.bcp.2014.08.002 · Cited by 150
Immunologic manifestations of autophagy
Deretic, V. P., Kimura, T., Timmins, G. S., Moseley, P. L., Chauhan, S., & Mandell, M. A. (2015) · Journal of Clinical Investigation · doi:10.1172/jci73945 · Cited by 150
Clinical Genomics in Inflammatory Bowel Disease
Uhlig, H. H., & Muise, A. M. (2017) · Trends in Genetics · doi:10.1016/j.tig.2017.06.008 · Cited by 152
Early cellular mechanisms of type I interferon-driven susceptibility to tuberculosis
Kotov, D. I., Lee, O. V., Fattinger, S. A., Langner, C. A., Guillen, J. V., Peters, J. M., Moon, A., Burd, E. M., Witt, K. C., Stetson, D. B., et al. (2023) · Cell · doi:10.1016/j.cell.2023.11.002 · Cited by 146
ATG16L1: A multifunctional susceptibility factor in Crohn disease
Salem, M. A., Ammitzboell, M., Nys, K., Seidelin, J. B., & Nielsen, O. H. (2015) · Autophagy · doi:10.1080/15548627.2015.1017187 · Cited by 166
XIAP deficiency syndrome in humans
Latour, S., & Aguilar, C. (2015) · Seminars in Cell and Developmental Biology · doi:10.1016/j.semcdb.2015.01.015 · Cited by 148
Hedin, C. R. H., McCarthy, N. E., Louis, P., Farquharson, F. M., McCartney, S. A., Taylor, K. M., Prescott, N. J., Murrells, T., Stagg, A. J., Whelan, K., et al. (2014) · Gut · doi:10.1136/gutjnl-2013-306226 · Cited by 147
Self-citationHuman Gut Microbiota: Toward an Ecology of Disease
Selber‐Hnatiw, S., Rukundo, B., Ahmadi, M., Akoubi, H., Al-Bizri, H., Aliu, A. F., Ambeaghen, T. U., Avetisyan, L., Bahar, I., Baird, A., et al. (2017) · Frontiers in Microbiology · doi:10.3389/fmicb.2017.01265 · Cited by 151
Role of autophagy in the pathogenesis of inflammatory bowel disease
Iida, T., Onodera, K., & Nakase, H. (2017) · World Journal of Gastroenterology · doi:10.3748/wjg.v23.i11.1944 · Cited by 151
Ma, W.-T., Chang, C. C.-C., Gershwin, M. E., & Lian, Z. (2017) · Journal of Autoimmunity · doi:10.1016/j.jaut.2017.07.003 · Cited by 146
Takagawa, T., Kitani, A., Fuss, I., Levine, B., Brant, S. R., Peter, I., Tajima, M., Nakamura, S., & Strober, W. (2018) · Science Translational Medicine · doi:10.1126/scitranslmed.aan8162 · Cited by 145
Self-citationGenomic modulators of gene expression in human neutrophils
Naranbhai, V., Fairfax, B. P., Makino, S., Humburg, P., Wong, D., Ng, E., Hill, A. V. S., & Knight, J. C. (2015) · Nature Communications · doi:10.1038/ncomms8545 · Cited by 147
Dheer, R., Santaolalla, R., Davies, J. M., Lang, J. K., Phillips, M. C., Pastorini, C., Vazquez-Pertejo, M. T., & Abreu, M. T. (2016) · Infection and Immunity · doi:10.1128/iai.01374-15 · Cited by 144
Rapid and Efficient Generation of Regulatory T Cells to Commensal Antigens in the Periphery
Nutsch, K., Chai, J. N., Ai, T. L., Russler-Germain, E. V., Feehley, T., Nagler‐Anderson, C., & Hsieh, C. (2016) · Cell Reports · doi:10.1016/j.celrep.2016.08.092 · Cited by 151
ER Stress and the UPR in Shaping Intestinal Tissue Homeostasis and Immunity
Coleman, O. I., & Haller, D. (2019) · Frontiers in Immunology · doi:10.3389/fimmu.2019.02825 · Cited by 147
Integrated microbiota and metabolite profiles link Crohn’s disease to sulfur metabolism
Metwaly, A., Dunkel, A., Waldschmitt, N., Raj, A. C. D., Lagkouvardos, I., Corraliza, A. M., Mayorgas, A., Martínez-Medina, M., Reiter, S., Schloter, M., et al. (2020) · Nature Communications · doi:10.1038/s41467-020-17956-1 · Cited by 146
The Genetics of Complex Cholestatic Disorders
Hirschfield, G. M., Chapman, R. W., Karlsen, T. H., Lammert, F., Lazaridis, K. N., & Mason, A. L. (2013) · Gastroenterology · doi:10.1053/j.gastro.2013.03.053 · Cited by 145
Self-citationUnifying immunology with informatics and multiscale biology
Kidd, B. A., Peters, L. A., Schadt, E. E., & Dudley, J. T. (2014) · Nature Immunology · doi:10.1038/ni.2787 · Cited by 145
Self-citationCells of the innate and adaptive immunity and their interactions in inflammatory bowel disease
Kmieć, Z., Cyman, M., & Ślebioda, T. J. (2017) · Advances in Medical Sciences · doi:10.1016/j.advms.2016.09.001 · Cited by 151
Westra, H.-J., Martínez‐Bonet, M., Önengüt-Gümüşcü, S., Lee, A., Luo, Y., Teslovich, N. C., Worthington, J., Martin, J. J., Huizinga, T. W. J., Klareskog, L., et al. (2018) · Nature Genetics · doi:10.1038/s41588-018-0216-7 · Cited by 147
Self-citationThe roles of SOCS 3 and STAT 3 in bacterial infection and inflammatory diseases
Gao, Y., Zhao, H., Wang, P., Wang, J., & Zou, L. (2018) · Scandinavian Journal of Immunology · doi:10.1111/sji.12727 · Cited by 143
Self-citationPopulation genetic tools for dissecting innate immunity in humans
Quintana‐Murci, L., & Clark, A. G. (2013) · Nature reviews. Immunology · doi:10.1038/nri3421 · Cited by 160
Vanhove, W., Peeters, P. M., Staelens, D., Schraenen, A., der Goten, J. V., Cleynen, I., Schepper, S. D., Lommel, L. V., Reynaert, N. L., Schuit, F. C., et al. (2015) · Inflammatory Bowel Diseases · doi:10.1097/mib.0000000000000535 · Cited by 144
Self-citationThe gut microbiota and inflammatory bowel diseases
Miyoshi, J., & Chang, E. B. (2016) · Translational research · doi:10.1016/j.trsl.2016.06.002 · Cited by 151
Lessons Learned From Trials Targeting Cytokine Pathways in Patients With Inflammatory Bowel Diseases
Abraham, C., Dulai, P. S., Vermeire, S., & Sandborn, W. J. (2016) · Gastroenterology · doi:10.1053/j.gastro.2016.10.018 · Cited by 142
Self-citationGenetics and epigenetics of IBD
Annese, V. (2020) · Pharmacological Research · doi:10.1016/j.phrs.2020.104892 · Cited by 149
Self-citationCholesteryl ester transfer protein (CETP) as a drug target for cardiovascular disease
Schmidt, A. F., Hunt, N. B., Gordillo‐Marañón, M., Charoen, P., Drenos, F., Casas, J. P., Mika Kivimaki, B., Lawlor, D. A., Giambartolomei, C., Papacosta, O., et al. (2021) · Nature Communications · doi:10.1038/s41467-021-25703-3 · Cited by 142
History of Inflammatory Bowel Diseases
Actis, G. C., Pellicano, R., Fagoonee, S., & Ribaldone, D. G. (2019) · Journal of Clinical Medicine · doi:10.3390/jcm8111970 · Cited by 140
The Cambridge Handbook of Personality Psychology
(2020) · Cambridge University Press eBooks · doi:10.1017/9781108264822 · Cited by 148
Mechanisms of Pediatric Inflammatory Bowel Disease
Peloquin, J. M., Goel, G., Villablanca, E. J., & Xavier, R. J. (2016) · Annual Review of Immunology · doi:10.1146/annurev-immunol-032414-112151 · Cited by 141
Self-citationGenetic Epidemiology of Psoriasis
Gupta, R., Debbaneh, M. G., & Liao, W. J. (2014) · Current Dermatology Reports · doi:10.1007/s13671-013-0066-6 · Cited by 141
Guo, H., Fortune, M. D., Burren, O. S., Schofield, E. C., Todd, J. A., & Wallace, C. (2015) · Human Molecular Genetics · doi:10.1093/hmg/ddv077 · Cited by 139
Fibrosis in Ulcerative Colitis
Gordon, I. O., Agrawal, N., Goldblum, J. R., Fiocchi, C., & Rieder, F. (2014) · Inflammatory Bowel Diseases · doi:10.1097/mib.0000000000000080 · Cited by 139
Lassen, K. G., McKenzie, C. I., Mari, M. C., Murano, T., Begun, J., Baxt, L. A., Goel, G., Villablanca, E. J., Kuo, S.-Y., Huang, H., et al. (2016) · Immunity · doi:10.1016/j.immuni.2016.05.007 · Cited by 142
Self-citationIntegrative functional genomics identifies regulatory mechanisms at coronary artery disease loci
Miller, C. L., Pjanic, M., Wang, T., Nguyen, T., Cohain, A. T., Lee, J. D., Matic, L. P., Hedin, U., Kundu, R. K., Majmudar, D., et al. (2016) · Nature Communications · doi:10.1038/ncomms12092 · Cited by 141
Self-citationCirculating and Fecal microRNAs as Biomarkers for Inflammatory Bowel Diseases
Schönauen, K., Le, N. N. H., von Arnim, U., Schulz, C., Malfertheiner, P., & Link, A. (2018) · Inflammatory Bowel Diseases · doi:10.1093/ibd/izy046 · Cited by 139
Salt-Inducible Kinases: Physiology, Regulation by cAMP, and Therapeutic Potential
Wein, M. N., Foretz, M., Fisher, D. E., Xavier, R. J., & Kronenberg, H. M. (2018) · Trends in Endocrinology and Metabolism · doi:10.1016/j.tem.2018.08.004 · Cited by 138
Self-citationA20 at the Crossroads of Cell Death, Inflammation, and AutoimmunityPreprint
Martens, A., & Loo, G. (2019) · Cold Spring Harbor Perspectives in Biology · doi:10.1101/cshperspect.a036418 · Cited by 142
Auer, P. L., Teumer, A., Schick, U. M., O'Shaughnessy, A., Lo, K. S., Chami, N., Carlson, C., de Denus, S., Dubé, M., Haessler, J., et al. (2014) · Nature Genetics · doi:10.1038/ng.2962 · Cited by 141
Self-citationIL-17+ CD8+ T cells: Differentiation, phenotype and role in inflammatory disease
Srenathan, U., Steel, K. J. A., & Taams, L. S. (2016) · Immunology Letters · doi:10.1016/j.imlet.2016.05.001 · Cited by 143
Genetic basis of myasthenia gravis – A comprehensive review
Avidan, N., Panse, R. L., Berrih‐Aknin, S., & Miller, A. (2013) · Journal of Autoimmunity · doi:10.1016/j.jaut.2013.12.001 · Cited by 148
Salzer, E., Kansu, A., Sic, H., Májek, P., İkincioğulları, A., Doğu, F., Serwas, N. K., Santos-Valente, E., Pickl, W. F., Bilić, I., et al. (2014) · Journal of Allergy and Clinical Immunology · doi:10.1016/j.jaci.2014.02.034 · Cited by 138
A20 controls intestinal homeostasis through cell-specific activities
Vereecke, L., Vieira‐Silva, S., Billiet, T., van Es, J. H., Guire, C. M., Slowicka, K., Sze, M., van den Born, M., Hertogh, G. D., Clevers, H. C., et al. (2014) · Nature Communications · doi:10.1038/ncomms6103 · Cited by 142
Self-citationMucosal Interactions between Genetics, Diet, and Microbiome in Inflammatory Bowel Disease
Basson, A. R., Trotter, A., Rodriguez‐Palacios, A., & Cominelli, F. (2016) · Frontiers in Immunology · doi:10.3389/fimmu.2016.00290 · Cited by 140
Roy, U., Gálvez, E. J. C., Iljazović, A., Lesker, T. R., Błażejewski, A. J., Pils, M. C., Heise, U., Huber, S., Flavell, R. A., & Strowig, T. (2017) · Cell Reports · doi:10.1016/j.celrep.2017.09.097 · Cited by 140
Pediatric Inflammatory Bowel Disease
Bouhuys, M., Lexmond, W. S., & van Rheenen, P. F. (2022) · PEDIATRICS · doi:10.1542/peds.2022-058037 · Cited by 136
Impact of probiotic supplements on microbiome diversity following antibiotic treatment of mice
Grazul, H., Kanda, L. L., & Gondek, D. (2016) · Gut Microbes · doi:10.1080/19490976.2016.1138197 · Cited by 135
Terao, C., Matsumura, T., Yoshifuji, H., Kirino, Y., Maejima, Y., Nakaoka, Y., Takahashi, M., Amiya, E., Tamura, N., Nakajima, T., et al. (2015) · Arthritis & Rheumatology · doi:10.1002/art.39157 · Cited by 135
Genome-wide Association Studies: Findings at the Major Histocompatibility Complex Locus in Psychosis
Corvin, A. P., & Morris, D. W. (2013) · Biological Psychiatry · doi:10.1016/j.biopsych.2013.09.018 · Cited by 136
Yamazaki, K., Umeno, J., Takahashi, A., Hirano, A., Johnson, T. A., Kumasaka, N., Morizono, T., Hosono, N., Kawaguchi, T., Takazoe, M., et al. (2012) · Gastroenterology · doi:10.1053/j.gastro.2012.12.021 · Cited by 136
Cleynen, I., Moerkercke, W. V., Billiet, T., Vandecandelaere, P., Casteele, N. V., Breynaert, C. M., Ballet, V., Ferrante, M., Noman, M., Assche, G. V., et al. (2015) · Annals of Internal Medicine · doi:10.7326/m15-0729 · Cited by 135
Self-citationLimbergen, J. V., Radford‐Smith, G. L., & Satsangi, J. J. (2014) · Nature Reviews Gastroenterology & Hepatology · doi:10.1038/nrgastro.2014.27 · Cited by 139
Self-citationLi, X., Zhang, Z., Li, L., Gong, W., Lazenby, A. J., Swanson, B. J., Herring, L. E., Asara, J. M., Singer, J. D., & Wen, H. (2017) · The Journal of Experimental Medicine · doi:10.1084/jem.20161105 · Cited by 138
Hancock, D. B., Guo, Y., Reginsson, G. W., Gaddis, N., Lutz, S. M., Sherva, R., Loukola, A., Minică, C. C., Markunas, C. A., Han, Y., et al. (2017) · Molecular Psychiatry · doi:10.1038/mp.2017.193 · Cited by 139
Blood-Derived DNA Methylation Signatures of Crohn's Disease and Severity of Intestinal Inflammation
Somineni, R. P., Venkateswaran, S., Kilaru, V., Marigorta, U. M., Mo, A., Okou, D. T., Kellermayer, R., Mondal, K., Cobb, D. O., Walters, T. D., et al. (2019) · Gastroenterology · doi:10.1053/j.gastro.2019.01.270 · Cited by 138
Self-citationShang, L., Liu, H., Yu, H., Chen, M., Yang, T., Zeng, X., & Qiao, S. (2021) · Antibiotics · doi:10.3390/antibiotics10060643 · Cited by 134
The spatial transcriptomic landscape of the healing mouse intestine following damage
Parigi, S. M., Larsson, L., Das, S., Flores, R. O. R., Frede, A., Tripathi, K. P., Diaz, O. E., Selin, K., Morales, R. A., Luo, X., et al. (2022) · Nature Communications · doi:10.1038/s41467-022-28497-0 · Cited by 139
Hypoxia and Mucosal Inflammation
Colgan, S. P., Campbell, E. L., & Kominsky, D. J. (2016) · Annual Review of Pathology Mechanisms of Disease · doi:10.1146/annurev-pathol-012615-044231 · Cited by 137
Fusobacterium nucleatum, inflammation, and immunity: the fire within human gut
Bashir, A., Miskeen, A. Y., Hazari, Y., Asrafuzzaman, S., & Fazili, K. M. (2015) · Tumor Biology · doi:10.1007/s13277-015-4724-0 · Cited by 139
The complex relationships between microglia, alpha-synuclein, and LRRK2 in Parkinson's disease
Schapansky, J., Nardozzi, J. D., & LaVoie, M. J. (2015) · Neuroscience · doi:10.1016/j.neuroscience.2014.09.049 · Cited by 132
Reduced sodium/proton exchanger NHE3 activity causes congenital sodium diarrhea
Janecke, A., Heinz‐Erian, P., Yin, J., Petersen, B., Franke, A., Lechner, S., Fuchs, I., Melançon, S. B., Uhlig, H. H., Travis, S. P. L., et al. (2015) · Human Molecular Genetics · doi:10.1093/hmg/ddv367 · Cited by 132
Self-citationEarly-onset Crohn’s disease and autoimmunity associated with a variant in CTLA-4
Zeißig, S., Petersen, B., Tomczak, M. F., Melum, E., Huc‐Claustre, E., Dougan, S. K., Laerdahl, J. K., Stade, B., Förster, M., Schreiber, S., et al. (2014) · Gut · doi:10.1136/gutjnl-2014-308541 · Cited by 139
Self-citationGenomic ATG16L1 risk allele-restricted Paneth cell ER stress in quiescent Crohn's disease
Deuring, J. J., Fuhler, G. M., Konstantinov, S. R., Peppelenbosch, M. P., Kuipers, E. J., de Haar, C. G., & van der Woude, C. J. (2013) · Gut · doi:10.1136/gutjnl-2012-303527 · Cited by 148
Mechanisms That Mediate the Development of Fibrosis in Patients With Crohnʼs Disease
Li, C., & Kuemmerle, J. F. (2014) · Inflammatory Bowel Diseases · doi:10.1097/mib.0000000000000043 · Cited by 136
Urine metabolome profiling of immune-mediated inflammatory diseases
Alonso, A., Julià, A., Vinaixa, M., Domènech, E., Fernández‐Nebro, A., Cañete, J. D. D., Ferrándiz, C., Tornero, J., Gisbert, J. P., Nos, P., et al. (2016) · BMC Medicine · doi:10.1186/s12916-016-0681-8 · Cited by 132
The autoimmunity–oral microbiome connection
Nikitakis, N. G., Papaioannou, W., Sakkas, L. I., & Kousvelari, E. E. (2016) · Oral Diseases · doi:10.1111/odi.12589 · Cited by 134
Shi, H. Y., Levy, A. N., Trivedi, H. D., Chan, F. K. L., Ng, S. C., & Ananthakrishnan, A. N. (2017) · Clinical Gastroenterology and Hepatology · doi:10.1016/j.cgh.2017.05.047 · Cited by 132
Self-citationD’Souza, W. N., Douangpanya, J., Mu, S., Jaeckel, P., Zhang, M., Maxwell, J. R., Rottman, J. B., Labitzke, K., Willee, A., Beckmann, H., et al. (2017) · PLoS ONE · doi:10.1371/journal.pone.0180190 · Cited by 136
Curcumin and Inflammatory Bowel Disease: Potential and Limits of Innovative Treatments
Brumatti, L. V., Marcuzzi, A., Tricarico, P. M., Zanin, V., Girardelli, M., & Bianco, A. M. (2014) · Molecules · doi:10.3390/molecules191221127 · Cited by 134
Ubiquitin Ligase TRIM62 Regulates CARD9-Mediated Anti-fungal Immunity and Intestinal Inflammation
Cao, Z., Conway, K. L., Heath, R. J. W., Rush, J. S., Leshchiner, E. S., Ramirez‐Ortiz, Z. G., Nedelsky, N. B., Huang, H., Ng, A., Gardet, A., et al. (2015) · Immunity · doi:10.1016/j.immuni.2015.10.005 · Cited by 137
Self-citationStallhofer, J., Friedrich, M., Konrad-Zerna, A., Wetzke, M., Lohse, P., Glas, J., Tillack‐Schreiber, C., Schnitzler, F., Beigel, F., & Brand, S. (2015) · Inflammatory Bowel Diseases · doi:10.1097/mib.0000000000000515 · Cited by 134
Self-citationPolygenic burdens on cell-specific pathways underlie the risk of rheumatoid arthritis
Ishigaki, K., Kochi, Y., Suzuki, A., Tsuchida, Y., Tsuchiya, H., Sumitomo, S., Yamaguchi, K., Nagafuchi, Y., Nakachi, S., Kato, R., et al. (2017) · Nature Genetics · doi:10.1038/ng.3885 · Cited by 133
Schäffler, H., Herlemann, D. P. R., Klinitzke, P., Berlin, P., Kreikemeyer, B., Jaster, R., & Lamprecht, G. (2018) · Journal of Digestive Diseases · doi:10.1111/1751-2980.12591 · Cited by 134
Regulatory T Cells and Immune Tolerance in the IntestinePreprint
Harrison, O. B., & Powrie, F. M. (2013) · Cold Spring Harbor Perspectives in Biology · doi:10.1101/cshperspect.a018341 · Cited by 137
Fortune, M. D., Guo, H., Burren, O. S., Schofield, E. C., Walker, N. M., Ban, M., Sawcer, S. J., Bowes, J., Worthington, J., Barton, A. C., et al. (2015) · Nature Genetics · doi:10.1038/ng.3330 · Cited by 130
Paneth cell defects in Crohn’s disease patients promote dysbiosis
Liu, T., Gurram, B., Baldridge, M. T., Head, R. D., Lam, V., Luo, C., Cao, Y., Simpson, P. M., Hayward, M., Holtz, M. L., et al. (2016) · JCI Insight · doi:10.1172/jci.insight.86907 · Cited by 134
Self-citationSelective autophagy of the adaptor TRIF regulates innate inflammatory signaling
Samie, M., Lim, J., Verschueren, E., Baughman, J. M., Peng, I., Wong, A., Kwon, Y. C., Şenbabaoğlu, Y., Hackney, J. A., Keir, M. E., et al. (2018) · Nature Immunology · doi:10.1038/s41590-017-0042-6 · Cited by 133
Kerner, G., Ramirez‐Alejo, N., Seeleuthner, Y., Yang, R., Ogishi, M., Cobat, A., Patin, É., Quintana‐Murci, L., Boisson‐Dupuis, S., Casanova, J., et al. (2019) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1903561116 · Cited by 130
Pharmacological activities and mechanisms of action of Pogostemon cablin Benth: a review
Junren, C., Xiaofang, X., Li, M.-T., Qiuyun, X., Li, G., Huiqiong, Z., Guanru, C., Xu, X., Yanpeng, Y., Peng, F., et al. (2021) · Chinese Medicine · doi:10.1186/s13020-020-00413-y · Cited by 134
Bank, S., Andersen, P. S., Burisch, J. M., Pedersen, N. K., Roug, S., Galsgaard, J., Turino, S. Y., Brodersen, J. B., Rashid, S., Rasmussen, B. K., et al. (2014) · PLoS ONE · doi:10.1371/journal.pone.0098815 · Cited by 129
Self-citationDiet, gut microbes, and the pathogenesis of inflammatory bowel diseases
Dolan, K. T., & Chang, E. B. (2016) · Molecular Nutrition & Food Research · doi:10.1002/mnfr.201600129 · Cited by 136
Nod2: A Critical Regulator of Ileal Microbiota and Crohn’s Disease
Sidiq, T., Yoshihama, S., Downs, I., & Kobayashi, K. S. (2016) · Frontiers in Immunology · doi:10.3389/fimmu.2016.00367 · Cited by 140
Metadata
- Authors
- The International IBD Genetics Consortium (IIBDGC), Jostins, L., Ripke, S., Weersma, R. K., Duerr, R. H., McGovern, D. P., Hui, K. Y., Lee, J. C., Philip Schumm, L., 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., 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., Glas, J., Haritunians, T., Hart, A., Hawkey, C., Hedl, M., Hu, X., Karlsen, T. H., Kupcinskas, L., Kugathasan, S., Latiano, A., Laukens, D., Lawrance, I. C., Lees, C. W., Louis, E., Mahy, G., Mansfield, J., Morgan, A. R., Mowat, C., Newman, W., Palmieri, O., Ponsioen, C. Y., Potocnik, U., Prescott, N. J., Regueiro, M., Rotter, J. I., Russell, R. K., Sanderson, J. D., Sans, M., Satsangi, J., Schreiber, S., Simms, L. A., Sventoraityte, J., Targan, S. R., Taylor, K. D., Tremelling, M., Verspaget, H. W., De Vos, M., Wijmenga, C., Wilson, D. C., Winkelmann, J., Xavier, R. J., Zeissig, S., Zhang, B., Zhang, C. K., Zhao, H., Silverberg, M. S., Annese, V., Hakonarson, H., Brant, S. R., Radford-Smith, G., Mathew, C. G., Rioux, J. D., Schadt, E. E., Daly, M. J., Franke, A., Parkes, M., Vermeire, S., Barrett, J. C., & Cho, J. H.
- Affiliations
- Wellcome Sanger Institute (GB)
- Broad Institute (US)
- University Medical Center Groningen (NL)
- University of Pittsburgh (US)
- Cedars-Sinai Medical Center (US)
- Yale University (US)
- University of Cambridge (GB)
- Harvard University (US)
- KU Leuven (BE)
- Guy's Hospital (GB)
- Montreal Heart Institute (CA)
- New Jersey Institute of Technology (US)
- Cleveland Clinic (US)
- Peninsula College of Medicine and Dentistry (GB)
- Université Libre de Bruxelles (BE)
- Regionshospitalet Viborg (DK)
- Royal Adelaide Hospital (AU)
- Christian-Albrechts-Universität zu Kiel (DE)
- Flinders University (AU)
- McGill University Health Centre (CA)
- Ludwig-Maximilians-Universität München (DE)
- Charité – Universitätsmedizin Berlin (DE)
- Icahn School of Medicine at Mount Sinai (US)
- University Hospital Bonn (DE)
- Karolinska Institutet (SE)
- Torbay Hospital (GB)
- University of Auckland (NZ)
- Christchurch Hospital (NZ)
- University of Liège (BE)
- Helmholtz Munich (DE)
- St Mark's Hospital (GB)
- Queen's Medical Centre (GB)
- Brigham and Women's Hospital (US)
- Oslo University Hospital (NO)
- Emory University (US)
- Casa Sollievo della Sofferenza (IT)
- Ghent University Hospital (BE)
- The University of Western Australia (AU)
- Western General Hospital (GB)
- Townsville Hospital (AU)
- Newcastle University (GB)
- Ninewells Hospital (GB)
- Manchester Academic Health Science Centre (GB)
- Amsterdam UMC Location University of Amsterdam (NL)
- Royal Hospital for Children (GB)
- St Thomas' Hospital (GB)
- Hospital Clínic de Barcelona (ES)
- QIMR Berghofer Medical Research Institute (AU)
- F. Widjaja Inflammatory Bowel Disease Institute (US)
- Norfolk and Norwich University Hospital (GB)
- Leiden University Medical Center (NL)
- Institut für Humangenetik (DE)
- Mount Sinai Hospital (CA)
- Children's Hospital of Philadelphia (US)
- Johns Hopkins University (US)
- Corresponding author
- Cho, Judy H
- ORCID
- Ripke, Stephan
- Weersma, Rinse K.
- Duerr, Richard H.
- McGovern, Dermot P.
- Hui, Ken Y.
- Lee, James C.
- Sharma, Yashoda
- Anderson, Carl A.
- Ning, Kaida
- Cleynen, Isabelle
- Spain, Sarah L.
- Raychaudhuri, Soumya
- Wei, Zhi
- Abraham, Clara
- Achkar, Jean-Paul
- Ahmad, Tariq
- Amininejad, Leila
- Ananthakrishnan, Ashwin N.
- Andersen, Vibeke
- Andrews, Jane M.
- Baidoo, Leonard
- Bampton, Peter A.
- Bitton, Alain
- Boucher, Gabrielle
- Brand, Stephan
- Cohain, Ariella
- Cichon, Sven
- D’Amato, Mauro
- Dubinsky, Marla
- Edwards, Cathryn
- Ellinghaus, David
- Ferguson, Lynnette R.
- Franchimont, Denis
- Gearry, Richard
- Georges, Michel
- Gieger, Christian
- Haritunians, Talin
- Hart, Ailsa
- Hu, Xinli
- Karlsen, Tom H.
- Kugathasan, Subra
- Latiano, Anna
- Laukens, Debby
- Lees, Charlie W.
- Louis, Edouard
- Mansfield, John
- Mowat, Craig
- Newman, William
- Palmieri, Orazio
- Ponsioen, Cyriel Y.
- Prescott, Natalie J.
- Regueiro, Miguel
- Rotter, Jerome I.
- Russell, Richard K.
- Sanderson, Jeremy D.
- Sans, Miquel
- Schreiber, Stefan
- Simms, Lisa A.
- Targan, Stephan R.
- Taylor, Kent D.
- Verspaget, Hein W.
- Wijmenga, Cisca
- Winkelmann, Juliane
- Xavier, Ramnik J.
- Zeissig, Sebastian
- Zhang, Bin
- Zhao, Hongyu
- Silverberg, Mark S.
- Annese, Vito
- Hakonarson, Hakon
- Brant, Steven R.
- Mathew, Christopher G.
- Rioux, John D.
- Schadt, Eric E.
- Daly, Mark J.
- Parkes, Miles
- Barrett, Jeffrey C.
- Cho, Judy H
- Venue
- Nature
- Published
- 2012-10-31
- Volume
- 491
- Issue
- 7422
- Pages
- 119-124
- ISSN
- 0028-0836 (ISSN-L)
- 1476-4687
- PMC
- PMC3491803
- OpenAlex
- W2143625465
- Cited by
- 4,722
- References
- 30
- Citations by year
- 2026: 169 · 2025: 221 · 2024: 303 · 2023: 296 · 2022: 314 · 2021: 345 · 2020: 360 · 2019: 384 · 2018: 374 · 2017: 404 · 2016: 444 · 2015: 422 · 2014: 424 · 2013: 247 · 2012: 13
- FWCI
- 43.39
- Type
- journal article
- Language
- en
- Open access
- bronze
- doi.org
- Licence
- www.springer.com/tdm (tdm)
- Locations
- Nature (publishedVersion)
- PubMed (publishedVersion)
- Pure Amsterdam UMC (publishedVersion)
- University of Groningen research database (University of Groningen / Centre for Information Technology) (publishedVersion)
- University of Southern Denmark Research Portal (University of Southern Denmark) (publishedVersion)
- Europe PMC (PubMed Central) (acceptedVersion)
- PubMed Central (acceptedVersion)
- ResearchOnline at James Cook University (James Cook University) (submittedVersion)
- UWA Profiles and Research Repository (UWA) (submittedVersion)
- Edinburgh Research Explorer (University of Edinburgh) (submittedVersion, other-oa)
- Lithuanian University of Health Sciences (submittedVersion)
- Rutgers University Community Repository (Rutgers University) (submittedVersion)
- Digital Access to Scholarship at Harvard (DASH) (Harvard University) (submittedVersion, cc-by)
- Data Archiving and Networked Services (DANS) (submittedVersion)
- Leiden Repository (Leiden University) (submittedVersion)
- Ghent University Academic Bibliography (Ghent University) (submittedVersion)
- BORIS (University Library Bern) (submittedVersion)
- CLOK (University of Central Lancashire) (submittedVersion)
- Digital Access to Libraries (Université catholique de Louvain (UCL), l'Université de Namur (UNamur) and the Université Saint-Louis (USL-B)) (submittedVersion)
- Adelaide Research & Scholarship (AR&S) (University of Adelaide) (submittedVersion)
- Dépôt institutionnel de l'Université libre de Bruxelles (Université Libre de Bruxelles) (submittedVersion)
- Discovery Research Portal (University of Dundee) (submittedVersion)
- Document Server@UHasselt (UHasselt) (submittedVersion)
- UCL Discovery (University College London) (submittedVersion)
- eScholarship (California Digital Library) (submittedVersion)
- Figshare (submittedVersion)
- ORCA Online Research @Cardiff (Cardiff University) (submittedVersion)
- IRIS Research product catalog (Sapienza University of Rome) (submittedVersion)
- Archivio Istituzionale della Ricerca - Università Vita-Salute San Raffaele (submittedVersion)
- Research Portal (King's College London) (submittedVersion)
- mediaTUM – the media and publications repository of the Technical University Munich (Technical University Munich) (submittedVersion)
- Open Repository and Bibliography (University of Liège) (submittedVersion)
- Research Explorer (The University of Manchester) (submittedVersion)
- Radboud Repository (Radboud University) (submittedVersion)
- UEA Digital Repository (University of East Anglia) (submittedVersion)
- University of Groningen research database (University of Groningen / Centre for Information Technology) (submittedVersion)
- Newcastle University ePrints (Newcastle Univesity)
- Funders
- Crohn's and Colitis Foundation of America (DK062422)
- Leona M. and Harry B. Helmsley Charitable Trust
- Wellcome Trust (085475/Z/08/Z, 068545/Z/02), 085475, G0000934, 083948/Z/07/Z, 068545, 089120, 090532, 085475/B/08/Z, 098051)
- Crohn's and Colitis Foundation
- Cedars-Sinai Medical Center
- National Institute for Health and Care Research (NF-SI-0508-10299, NF-SI-0611-10219)
- British Heart Foundation (G0000934)
- Diabetes UK
- King's College London
- Deutsche Forschungsgemeinschaft
- Bundesministerium für Bildung und Forschung
- Fonds De La Recherche Scientifique - FNRS
- Fonds Wetenschappelijk Onderzoek
- Ministero della Salute
- Örebro Universitet
- Crohn's and Colitis UK (M11-1)
- Karolinska Institutet
- Universitetssjukhuset Örebro
- Svenska Läkaresällskapet
- Exzellenzclusters Entzündungsforschung
- Versus Arthritis (18475)
- National Institutes of Health (G0000934, UL1TR000124, UL1TR000005, 068545/Z/02, M01-RR00425, DK062429, TR000124, RR00425, DK-063491, DK 043351, PO1DK046763)
- U.S. Public Health Service (UL1 TR000124, DK062413, PO1DK046763)
- Inflammatory Bowel and Immunobiology Research Institute
- Medical Research Council (098051, 068545/Z/02, G0000934)
- National Health and Medical Research Council (G0000934)
- Helmholtz Zentrum München
- Münchner Zentrum für Gesundheitswissenschaften
- National Human Genome Research Institute (DK062429, DK062422)
- National Cancer Institute (CA141743, R01CA141743)
- National Institute of General Medical Sciences (T32-GM07205, T32GM007205)
- National Institute of Allergy and Infectious Diseases (AI 062773, R01AI062773)
- National Institute of Diabetes and Digestive and Kidney Diseases (DK076984, DK063491, DK-06-2423, (DK043351, R01DK083756, P01DK046763, DK062429, DK062413, DK062420, R01DK055731, R21DK084554, R03DK076984, DK062429-S1, DK062418, DK 83756, DK062431, DK062422, K23DK097142, DK062432, U01DK062418, DK084554, U01DK062420, M01-RR00425, U01DK062429, U24DK062429, U01DK062413, U01DK062422, P30DK063491, U01DK062432, P30DK043351, U01DK062431, U01DK062423)
- National Institute of Child Health and Human Development
- National Center for Research Resources (M01RR000425, M01-RR00425)
- National Center for Advancing Translational Sciences
- Topics
- Health Sciences › Medicine › Gastroenterology › Inflammatory Bowel Disease
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Genetics › Genetic Associations and Epidemiology
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Gut microbiota and health
- Keywords
- inflammatory bowel disease, Crohn's disease, ulcerative colitis, host-microbe interactions, mycobacterial infection, immune-mediated diseases, ankylosing spondylitis, psoriasis, genetic susceptibility loci, balancing selection, directional selection, gene co-expression network
- MeSH terms
- Colitis, Ulcerative, Crohn Disease, Haplotypes, Humans, Mycobacterium, Mycobacterium Infections, Mycobacterium tuberculosis, Phenotype, Reproducibility of Results, Inflammatory Bowel Diseases, Genome, Human, Genetic Predisposition to Disease, Polymorphism, Single Nucleotide, Host-Pathogen Interactions, Genome-Wide Association Study
About these checks
Registry, retraction, Cites and statistics results are computed, not judged, with one exception: a printed reference that no index lists is read once by a model before it counts as a citation error. Claims are extracted by a model and kept only when their quote appears verbatim in the text; each cited source is then checked, with a model’s help, for whether it says what the claim relies on. Those verdicts can be wrong — read the claim’s quote and the cited source before relying on one.
Statistics and arithmetic are recomputed, not judged.
Confidence bands are shown only for fields calibrated on our annotated test set. None is calibrated yet, so no band is shown.
What counts as a claim ›How we measure confidence ›How we check this ›
Are you an author, or do you see a problem with this page? Request a review