Human genetic variation and the gut microbiome in disease
Abstract
Taxonomic and functional changes to the composition of the gut microbiome have been implicated in multiple human diseases. Recent microbiome genome-wide association studies reveal that variants in many human genes involved in immunity and gut architecture are associated with an altered composition of the gut microbiome. Although many factors can affect the microbial organisms residing in the gut, a number of recent findings support the hypothesis that certain host genetic variants predispose an individual towards microbiome dysbiosis. This condition, in which the normal microbiome population structure is disturbed, is a key feature in disorders of metabolism and immunity.
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Differences in microbiome diversity are partially attributed to genotype and sex.
“Differences in microbiome diversity have been shown to be partially attributed by genotype and sex [79–83].”
From Gut microbiota changes in children with autism spectrum disorder: a systematic review (2020) · cites this paper as [83]
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1 retracted
Million, M., Angelakis, E., Maraninchi, M., Henry, M., Giorgi, R., Valero, R., Vialettes, B., & Raoult, D. (2013) · International Journal of Obesity · doi:10.1038/ijo.2013.20 · Cited by 362 · see citing works
RetractedStructure, function and diversity of the healthy human microbiome
The Human Microbiome Project Consortium (2012) · Nature · doi:10.1038/nature11234 · Cited by 11,726 · see citing works
Diet rapidly and reproducibly alters the human gut microbiome
David, L. A., Maurice, C. F., Carmody, R. N., Gootenberg, D. B., Button, J. E., Wolfe, B. E., Ling, A. V., Devlin, A. S., Varma, Y., Fischbach, M. A., et al. (2014) · Nature · doi:10.1038/nature12820 · Cited by 10,100 · see citing works
A core gut microbiome in obese and lean twins
Turnbaugh, P. J., Hamady, M., Yatsunenko, T., Cantarel, B. L., Duncan, A., Ley, R. E., Sogin, M. L., Jones, W. J., Roe, B. A., Affourtit, J. P., et al. (2009) · Nature · doi:10.1038/nature07540 · Cited by 7,823 · see citing works
Changes of Intestinal Functions in Liver Cirrhosis
Fukui, H., & Wiest, R. (2016) · Inflammatory Intestinal Diseases · doi:10.1159/000444436 · Cited by 6,820 · see citing works
Association of NOD2 leucine-rich repeat variants with susceptibility to Crohn's disease
Hugot, J.-P., Chamaillard, M., Zouali, H., Lesage, S., Cézard, J.-P., Belaiche, J., Almer, S., Tysk, C., O'Morain, C. A., Gassull, M., et al. (2001) · Nature · doi:10.1038/35079107 · Cited by 5,591 · see citing works
Revised Estimates for the Number of Human and Bacteria Cells in the Body
Sender, R., Fuchs, S., & Milo, R. (2016) · PLOS Biology · doi:10.1371/journal.pbio.1002533 · Cited by 5,425 · see citing works
A frameshift mutation in NOD2 associated with susceptibility to Crohn's disease
Ogura, Y., Bonen, D. K., Inohara, N., Nicolae, D. L., Chen, F. F., Ramos, R., Britton, H., Moran, T., Karaliuskas, R., Duerr, R. H., et al. (2001) · Nature · doi:10.1038/35079114 · Cited by 5,030 · see citing works
Frank, D. N., St. Amand, A. L., Feldman, R. A., Boedeker, E. C., Harpaz, N., & Pace, N. R. (2007) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0706625104 · Cited by 4,611 · see citing works
Everard, A., Belzer, C., Geurts, L., Ouwerkerk, J. P., Druart, C., Bindels, L. B., Guiot, Y., Derrien, M., Muccioli, G. G., Delzenne, N. M., et al. (2013) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1219451110 · Cited by 4,511 · see citing works
Unravelling the pathogenesis of inflammatory bowel disease
Xavier, R. J., & Podolsky, D. K. (2007) · Nature · doi:10.1038/nature06005 · Cited by 4,364 · see citing works
Self-citationGut Microbiota from Twins Discordant for Obesity Modulate Metabolism in Mice
Ridaura, V. K., Faith, J. J., Rey, F. E., Cheng, J., Duncan, A. E., Kau, A. L., Griffin, N. W., Lombard, V., Henrissat, B., Bain, J. R., et al. (2013) · Science · doi:10.1126/science.1241214 · Cited by 3,788 · see citing works
Evolution of mammals and their gut microbes
Ley, R. E., Hamady, M., Lozupone, C., Turnbaugh, P. J., Ramey, R. R., Bircher, J. S., Schlegel, M. L., Tucker, T. A., Schrenzel, M. D., Knight, R., et al. (2008) · Science · doi:10.1126/science.1155725 · Cited by 3,747 · see citing works
The Treatment-Naive Microbiome in New-Onset Crohn’s Disease
Gevers, D., Kugathasan, S., Denson, L. A., Vázquez-Baeza, Y., Van Treuren, W., Ren, B., Schwager, E., Knights, D., Song, S. J., Yassour, M., et al. (2014) · Cell Host & Microbe · doi:10.1016/j.chom.2014.02.005 · Cited by 3,220 · see citing works
Self-citationHuman Genetics Shape the Gut Microbiome
Goodrich, J. K., Waters, J. L., Poole, A. C., Sutter, J. L., Koren, O., Blekhman, R., Beaumont, M., Van Treuren, W., Knight, R., Bell, J. T., et al. (2014) · Cell · doi:10.1016/j.cell.2014.09.053 · Cited by 3,164 · see citing works
Genetics and pathogenesis of inflammatory bowel disease
Khor, B., Gardet, A., & Xavier, R. J. (2011) · Nature · doi:10.1038/nature10209 · Cited by 2,629 · see citing works
Self-citationGut biogeography of the bacterial microbiota
Donaldson, G. P., Lee, S. M., & Mazmanian, S. K. (2016) · Nature Reviews Microbiology · doi:10.1038/nrmicro3552 · Cited by 2,535 · see citing works
Nod2 Is a General Sensor of Peptidoglycan through Muramyl Dipeptide (MDP) Detection
Girardin, S. E., Boneca, I. G., Viala, J., Chamaillard, M., Labigne-Roussel, A., Thomas, G. D., Philpott, D. J., & Sansonetti, P. J. (2003) · Journal of Biological Chemistry · doi:10.1074/jbc.c200651200 · Cited by 2,397 · see citing works
Sayin, S. I., Wahlström, A., Felin, J., Jäntti, S., Marschall, H.-U., Bamberg, K., Angelin, B., Hyötyläinen, T., Orešič, M., & Bäckhed, F. (2013) · Cell Metabolism · doi:10.1016/j.cmet.2013.01.003 · Cited by 2,331 · see citing works
The inner of the two Muc2 mucin-dependent mucus layers in colon is devoid of bacteria
Johansson, M. E. V., Phillipson, M., Petersson, J., Velcich, A., Holm, L., & Hansson, G. C. (2008) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0803124105 · Cited by 2,200 · see citing works
Akkermansia muciniphila gen. nov., sp. nov., a human intestinal mucin-degrading bacterium
Derrien, M., Vaughan, E. E., Plugge, C. M., & de Vos, W. M. (2004) · International Journal of Systematic and Evolutionary Microbiology · doi:10.1099/ijs.0.02873-0 · Cited by 2,094 · see citing works
The Long-Term Stability of the Human Gut Microbiota
Faith, J. J., Guruge, J. L., Charbonneau, M., Subramanian, S., Seedorf, H., Goodman, A. L., Clemente, J. C., Knight, R., Heath, A. C., Leibel, R. L., et al. (2013) · Science · doi:10.1126/science.1237439 · Cited by 2,058 · see citing works
Nod2-Dependent Regulation of Innate and Adaptive Immunity in the Intestinal Tract
Kobayashi, K. S., Chamaillard, M., Ogura, Y., Henegariu, O., Inohara, N., Núñez, G., & Flavell, R. A. (2005) · Science · doi:10.1126/science.1104911 · Cited by 1,776 · see citing works
Metagenomic microbial community profiling using unique clade-specific marker genes
Segata, N., Waldron, L., Ballarini, A., Narasimhan, V., Jousson, O., & Huttenhower, C. (2012) · Nature Methods · doi:10.1038/nmeth.2066 · Cited by 1,776 · see citing works
Host Recognition of Bacterial Muramyl Dipeptide Mediated through NOD2
Inohara, N., Ogura, Y., Fontalba, A., Gutierrez, O., Pons, F., Crespo, J., Fukase, K., Inamura, S., Kusumoto, S., Hashimoto, M., et al. (2003) · Journal of Biological Chemistry · doi:10.1074/jbc.c200673200 · Cited by 1,694 · see citing works
The Framingham Heart Study and the epidemiology of cardiovascular disease: a historical perspective
Mahmood, S. S., Levy, D., Vasan, R. S., & Wang, T. J. (2014) · The Lancet · doi:10.1016/s0140-6736(13)61752-3 · Cited by 1,622 · see citing works
Convergent adaptation of human lactase persistence in Africa and Europe
Tishkoff, S. A., Reed, F. A., Ranciaro, A., Voight, B. F., Babbitt, C. C., Silverman, J. S., Powell, K., Mortensen, H. M., Hirbo, J. B., Osman, M., et al. (2007) · Nature Genetics · doi:10.1038/ng1946 · Cited by 1,615 · see citing works
New genetic loci link adipose and insulin biology to body fat distribution
The ADIPOGen Consortium, Shungin, D., The CARDIOGRAMplusC4D Consortium, The CKDGen Consortium, The GEFOS Consortium, The GENIE Consortium, The, G. L. G. C., The, I. C. B. P., The International Endogene Consortium, Study, T. L. C., et al. (2015) · Nature · doi:10.1038/nature14132 · Cited by 1,580 · see citing works
Unravelling the effects of the environment and host genotype on the gut microbiome
Spor, A., Koren, O., & Ley, R. (2011) · Nature Reviews Microbiology · doi:10.1038/nrmicro2540 · Cited by 1,509 · see citing works
Lamas, B., Richard, M. L., Leducq, V., Pham, H.-P., Michel, M.-L., Da Costa, G., Bridonneau, C., Jegou, S., Hoffmann, T. W., Natividad, J. M., et al. (2016) · Nature Medicine · doi:10.1038/nm.4102 · Cited by 1,482 · see citing works
Self-citationTranskingdom Control of Microbiota Diurnal Oscillations Promotes Metabolic Homeostasis
Thaiss, C. A., Zeevi, D., Levy, M., Zilberman-Schapira, G., Suez, J., Tengeler, A. C., Abramson, L., Katz, M. N., Korem, T., Zmora, N., et al. (2014) · Cell · doi:10.1016/j.cell.2014.09.048 · Cited by 1,449 · see citing works
Png, C. W., Lindén, S. K., Gilshenan, K. S., Zoetendal, E. G., McSweeney, C. S., Sly, L. I., McGuckin, M. A., & Florin, T. H. J. (2010) · American Journal of Gastroenterology · doi:10.1038/ajg.2010.281 · Cited by 1,364 · see citing works
The composition of the gut microbiota throughout life, with an emphasis on early life
Rodríguez, J. M., Murphy, K., Stanton, C., Ross, R. P., Kober, O. I., Juge, N., Avershina, E., Rudi, K., Narbad, A., Jenmalm, M. C., et al. (2015) · Microbial Ecology in Health and Disease · doi:10.3402/mehd.v26.26050 · Cited by 1,320 · see citing works
Human susceptibility and resistance to Norwalk virus infection
Lindesmith, L. C., Moe, C. L., Marionneau‐Lambot, S., Ruvoën‐Clouet, N., Jiang, X., Lindblad, L., Stewart, P. W., Pendu, J. L., & Baric, R. S. (2003) · Nature Medicine · doi:10.1038/nm860 · Cited by 1,119 · see citing works
Diet dominates host genotype in shaping the murine gut microbiota
Carmody, R. N., Gerber, G. K., Luevano, J. M., Gatti, D. M., Somes, L., Svenson, K. L., & Turnbaugh, P. J. (2015) · Cell Host & Microbe · doi:10.1016/j.chom.2014.11.010 · Cited by 1,103 · see citing works
Hampe, J., Cuthbert, A. P., Croucher, P. J. P., Mirza, M. M., Mascheretti, S., Fisher, S. A., Frenzel, H., King, K., Hasselmeyer, A., Macpherson, A. J., et al. (2001) · The Lancet · doi:10.1016/s0140-6736(00)05063-7 · Cited by 1,090 · see citing works
Interactions between commensal fungi and the C-type lectin receptor Dectin-1 influence colitis
Iliev, I. D., Funari, V. A., Taylor, K. D., Nguyen, Q., Reyes, C. N., Strom, S. P., Brown, J., Becker, C. A., Fleshner, P. R., Dubinsky, M., et al. (2012) · Science · doi:10.1126/science.1221789 · Cited by 1,073 · see citing works
Metabolic Reconstruction for Metagenomic Data and Its Application to the Human Microbiome
Abubucker, S., Segata, N., Goll, J. B., Schubert, A. M., Izard, J., Cantarel, B. L., Rodriguez-Mueller, B., Zucker, J., Thiagarajan, M., Henrissat, B., et al. (2012) · PLoS Computational Biology · doi:10.1371/journal.pcbi.1002358 · Cited by 1,050 · see citing works
Genetic determinants of the gut microbiome in UK twins
Goodrich, J. K., Davenport, E. R., Beaumont, M., Jackson, M. A., Knight, R., Ober, C., Spector, T. D., Bell, J. T., Clark, A. G., & Ley, R. E. (2016) · Cell Host & Microbe · doi:10.1016/j.chom.2016.04.017 · Cited by 1,048 · see citing works
Yassour, M., Vatanen, T., Siljander, H., Hämäläinen, A.-M., Härkönen, T., Ryhänen, S. J., Franzosa, E. A., Vlamakis, H., Huttenhower, C., Gevers, D., et al. (2016) · Science Translational Medicine · doi:10.1126/scitranslmed.aad0917 · Cited by 1,043 · see citing works
Self-citationEcology drives a global network of gene exchange connecting the human microbiome
Smillie, C. S., Smith, M. B., Friedman, J., Cordero, O. X., David, L. A., & Alm, E. J. (2011) · Nature · doi:10.1038/nature10571 · Cited by 953 · see citing works
Mapping of a susceptibility locus for Crohn's disease on chromosome 16
Hugot, J., Laurent‐Puig, P., Gower‐Rousseau, C., Olson, J. M., Lee, J. C., Beaugerie, L., Naom, I., Dupas, J., Gossum, A. V., Af, G. D. T. D., et al. (1996) · Nature · doi:10.1038/379821a0 · Cited by 950 · see citing works
Mucin glycan foraging in the human gut microbiome
Tailford, L. E., Crost, E. H., Kavanaugh, D. W., & Juge, N. (2015) · Frontiers in Genetics · doi:10.3389/fgene.2015.00081 · Cited by 851 · see citing works
Wehkamp, J., Harder, J., Weichenthal, M., Schwab, M. G., Schäffeler, E., Schlee, M., Herrlinger, K. R., Stallmach, A., Noack, F., Fritz, P., et al. (2004) · Gut · doi:10.1136/gut.2003.032805 · Cited by 823 · see citing works
Lewis, J. D., Chen, E. Z., Baldassano, R. N., Otley, A. R., Griffiths, A. M., Lee, D., Bittinger, K., Bailey, A., Friedman, E. S., Hoffmann, C., et al. (2015) · Cell Host & Microbe · doi:10.1016/j.chom.2015.09.008 · Cited by 823 · see citing works
The effect of host genetics on the gut microbiome
Bonder, M. J., Kurilshikov, A., Tigchelaar, E. F., Mujagic, Z., Imhann, F., Vila, A. V., Deelen, P., Vatanen, T., Schirmer, M., Smeekens, S. P., et al. (2016) · Nature Genetics · doi:10.1038/ng.3663 · Cited by 819 · see citing works
Self-citationThe host shapes the gut microbiota via fecal microRNA
Liu, S., da Cunha, A. P., Rezende, R. M., Cialic, R., Wei, Z., Bry, L., Comstock, L. E., Gandhi, R., & Weiner, H. L. (2016) · Cell Host & Microbe · doi:10.1016/j.chom.2015.12.005 · Cited by 808 · see citing works
Host genetic variation impacts microbiome composition across human body sites
Blekhman, R., Goodrich, J. K., Huang, K., Sun, Q., Bukowski, R., Bell, J. T., Spector, T. D., Keinan, A., Ley, R. E., Gevers, D., et al. (2015) · Genome Biology · doi:10.1186/s13059-015-0759-1 · Cited by 745 · see citing works
Aberrant expansion of segmented filamentous bacteria in IgA-deficient gut
Suzuki, K., Meek, B., Doi, Y., Muramatsu, M., Chiba, T., Honjo, T., & Fagarasan, S. (2004) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0307317101 · Cited by 721 · see citing works
Collado, M. C., Derrien, M., Isolauri, E., de Vos, W. M., & Salminen, S. (2007) · Applied and Environmental Microbiology · doi:10.1128/aem.01477-07 · Cited by 706 · see citing works
Comparison of fermentation reactions in different regions of the human colon
Macfarlane, G. T., Gibson, G. R., & Cummings, J. H. (1992) · Journal of Applied Bacteriology · doi:10.1111/j.1365-2672.1992.tb04882.x · Cited by 676 · see citing works
NOD proteins: regulators of inflammation in health and disease
Philpott, D. J., Sorbara, M. T., Robertson, S. J., Croitoru, K., & Girardin, S. E. (2014) · Nature Reviews Immunology · doi:10.1038/nri3565 · Cited by 668 · see citing works
The Mucin Degrader Akkermansia muciniphila Is an Abundant Resident of the Human Intestinal Tract
Derrien, M., Collado, M. C., Amor, K. B., Salminen, S., & de Vos, W. M. (2007) · Applied and Environmental Microbiology · doi:10.1128/aem.01226-07 · Cited by 659 · see citing works
Wang, J., Thingholm, L. B., Skiecevičienė, J., Rausch, P., Kummen, M., Hov, J. R., Degenhardt, F., Heinsen, F.-A., Rühlemann, M. C., Szymczak, S., et al. (2016) · Nature Genetics · doi:10.1038/ng.3695 · Cited by 625 · see citing works
Ruiz-Palacios, G. M., Cervantes-Villar, L. E., Ramos, P., Chávez‐Munguía, B., & Newburg, D. S. (2003) · Journal of Biological Chemistry · doi:10.1074/jbc.m207744200 · Cited by 608 · see citing works
NOD2-mediated dysbiosis predisposes mice to transmissible colitis and colorectal cancer
Couturier-Maillard, A., Sécher, T., Rehman, A., Normand, S., Arcangelis, A. D., Häsler, R., Huot, L., Grandjean, T., Bressenot, A., Delanoye, A., et al. (2013) · Journal of Clinical Investigation · doi:10.1172/jci62236 · Cited by 571 · see citing works
Kelly, R. J., Rouquier, S., Giorgi, D., Lennon, G. G., & Lowe, J. B. (1995) · Journal of Biological Chemistry · doi:10.1074/jbc.270.9.4640 · Cited by 570 · see citing works
Cospeciation of gut microbiota with hominids
Moeller, A. H., Caro‐Quintero, A., Mjungu, D. C., Georgiev, A. V., Lonsdorf, E. V., Muller, M. N., Pusey, A. E., Peeters, M., Hahn, B. H., & Ochman, H. (2016) · Science · doi:10.1126/science.aaf3951 · Cited by 570 · see citing works
Nod2 is required for the regulation of commensal microbiota in the intestine
Petnicki-Ocwieja, T., Hrncir, T., Liu, Y.-J., Biswas, A., Hudcovic, T., Tlaskalova-Hogenova, H., & Kobayashi, K. S. (2009) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0907722106 · Cited by 564 · see citing works
The outer mucus layer hosts a distinct intestinal microbial niche
Li, H., Limenitakis, J. P., Fuhrer, T., Geuking, M. B., Lawson, M. A., Wyss, M., Brugiroux, S., Keller, I., Macpherson, J. A., Rupp, S., et al. (2015) · Nature Communications · doi:10.1038/ncomms9292 · Cited by 511 · see citing works
Fucose sensing regulates bacterial intestinal colonization
Pacheco, A. R., Curtis, M. M., Ritchie, J. M., Munera, D., Waldor, M. K., Moreira, C. G., & Sperandio, V. (2012) · Nature · doi:10.1038/nature11623 · Cited by 499 · see citing works
Evolutionary Relationships of Wild Hominids Recapitulated by Gut Microbial Communities
Ochman, H., Worobey, M., Kuo, C., Ndjango, J.-B. N., Peeters, M., Hahn, B. H., & Hugenholtz, P. (2010) · PLoS Biology · doi:10.1371/journal.pbio.1000546 · Cited by 498 · see citing works
Advances in inflammatory bowel disease pathogenesis: linking host genetics and the microbiome
Knights, D., Lassen, K. G., & Xavier, R. J. (2013) · Gut · doi:10.1136/gutjnl-2012-303954 · Cited by 468 · see citing works
Self-citationAssociation of host genome with intestinal microbial composition in a large healthy cohort
GEM Project Research Consortium, Turpin, W., Espin-Garcia, O., Xu, W., Silverberg, M. S., Kevans, D., Smith, M. I., Guttman, D. S., Griffiths, A., Panaccione, R., et al. (2016) · Nature Genetics · doi:10.1038/ng.3693 · Cited by 460 · see citing works
α‐Defensins in human innate immunity
Lehrer, R. I., & Lu, W. (2011) · Immunological Reviews · doi:10.1111/j.1600-065x.2011.01082.x · Cited by 426 · see citing works
van Passel, M. W. J., Kant, R., Zoetendal, E. G., Plugge, C. M., Derrien, M., Malfatti, S., Chain, P., Woyke, T., Palva, A., de Vos, W. M., et al. (2011) · PLoS ONE · doi:10.1371/journal.pone.0016876 · Cited by 425 · see citing works
Complex host genetics influence the microbiome in inflammatory bowel disease
Knights, D., Silverberg, M. S., Weersma, R. K., Gevers, D., Dijkstra, G., Huang, H., Tyler, A. D., van Sommeren, S., Imhann, F., Stempak, J. M., et al. (2014) · Genome Medicine · doi:10.1186/s13073-014-0107-1 · Cited by 418 · see citing works
Self-citationAntimicrobial peptide resistance mediates resilience of prominent gut commensals during inflammation
Cullen, T. W., Schofield, W. B., Barry, N. A., Putnam, E. E., Rundell, E. A., Trent, M. S., Degnan, P. H., Booth, C. J., Yu, H., & Goodman, A. L. (2015) · Science · doi:10.1126/science.1260580 · Cited by 395 · see citing works
Genetic and environmental control of host-gut microbiota interactions
Org, E., Parks, B. W., Joo, J. W. J., Emert, B., Schwartzman, W., Kang, E. Y., Mehrabian, M., Pan, C., Knight, R., Gunsalus, R., et al. (2015) · Genome Research · doi:10.1101/gr.194118.115 · Cited by 381 · see citing works
The Environmental Determinants of Diabetes in the Young (TEDDY) study: study design
The TEDDY Study Group (2007) · Pediatric Diabetes · doi:10.1111/j.1399-5448.2007.00269.x · Cited by 363 · see citing works
Bacteria from Diverse Habitats Colonize and Compete in the Mouse Gut
Seedorf, H., Griffin, N. W., Ridaura, V. K., Reyes, A., Cheng, J., Rey, F. E., Smith, M. I., Simon, G. M., Scheffrahn, R. H., Woebken, D., et al. (2014) · Cell · doi:10.1016/j.cell.2014.09.008 · Cited by 361 · see citing works
Fritz, J. H., Girardin, S. E., Fitting, C., Werts, C., Mengin‐Lecreulx, D., Caroff, M., Cavaillon, J., Philpott, D. J., & Adib‐Conquy, M. (2005) · European Journal of Immunology · doi:10.1002/eji.200526286 · Cited by 355 · see citing works
Xie, H., Guo, R., Zhong, H., Feng, Q., Lan, Z., Qin, B., Ward, K. J., Jackson, M. A., Xia, Y., Chen, X., et al. (2016) · Cell Systems · doi:10.1016/j.cels.2016.10.004 · Cited by 341 · see citing works
Human Symbionts Use a Host-Like Pathway for Surface Fucosylation
Coyne, M. J., Reinap, B., Lee, M. M., & Comstock, L. E. (2005) · Science · doi:10.1126/science.1106469 · Cited by 304 · see citing works
Adherent-invasive Escherichia coli in inflammatory bowel disease
Rolhion, N., & Darfeuille–Michaud, A. (2007) · Inflammatory Bowel Diseases · doi:10.1002/ibd.20176 · Cited by 299 · see citing works
An integrative view of microbiome-host interactions in inflammatory bowel diseases
Wlodarska, M., Kostic, A. D., & Xavier, R. J. (2015) · Cell Host & Microbe · doi:10.1016/j.chom.2015.04.008 · Cited by 287 · see citing works
Self-citationKashyap, P. C., Marcobal, A., Ursell, L. K., Smits, S. A., Sonnenburg, E. D., Costello, E. K., Higginbottom, S. K., Domino, S. E., Holmes, S. P., Relman, D. A., et al. (2013) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1306070110 · Cited by 285 · see citing works
Akkermansia muciniphila mediates negative effects of IFNγ on glucose metabolism
Greer, R. L., Dong, X., de Moraes, A. C. F., Zielke, R. A., Fernandes, G. D. R., Peremyslova, E., Vasquez‐Perez, S., Schoenborn, A. A., Gomes, E. P., Pereira, A. C., et al. (2016) · Nature Communications · doi:10.1038/ncomms13329 · Cited by 277 · see citing works
Chassaing, B., Rolhion, N., de Vallée, A., Salim, S. Y., Prorok-Hamon, M., Neut, C., Campbell, B. J., Söderholm, J. D., Hugot, J., Colombel, J., et al. (2011) · Journal of Clinical Investigation · doi:10.1172/jci44632 · Cited by 267 · see citing works
Genome-Wide Association Studies of the Human Gut Microbiota
Davenport, E., Cusanovich, D. A., Michelini, K., Barreiro, L. B., Ober, C., & Gilad, Y. (2015) · PLoS ONE · doi:10.1371/journal.pone.0140301 · Cited by 253 · see citing works
Azcárate-Peril, M. A., Ritter, A. J., Savaiano, D. A., Monteagudo-Mera, A., Anderson, C., Magness, S. T., & Klaenhammer, T. R. (2017) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1606722113 · Cited by 246 · see citing works
Heritable components of the human fecal microbiome are associated with visceral fat
Beaumont, M., Goodrich, J. K., Jackson, M. A., Yet, İ., Davenport, E., Vieira‐Silva, S., Debelius, J. W., Pallister, T., Mangino, M., Raes, J., et al. (2016) · Genome biology · doi:10.1186/s13059-016-1052-7 · Cited by 239 · see citing works
Macfarlane, S., Woodmansey, E. J., & Macfarlane, G. T. (2005) · Applied and Environmental Microbiology · doi:10.1128/aem.71.11.7483-7492.2005 · Cited by 235 · see citing works
Folseraas, T., Melum, E., Rausch, P., Juran, B. D., Ellinghaus, E., Shiryaev, A., Laerdahl, J. K., Ellinghaus, D., Schramm, C., Weismüller, T. J., et al. (2012) · Journal of Hepatology · doi:10.1016/j.jhep.2012.03.031 · Cited by 232 · see citing works
Reprograming of gut microbiome energy metabolism by the FUT2 Crohn’s disease risk polymorphism
Tong, M., McHardy, I. H., Ruegger, P. M., Goudarzi, M., Kashyap, P., Haritunians, T., Li, X., Graeber, T. G., Schwager, E., Huttenhower, C., et al. (2014) · The ISME Journal · doi:10.1038/ismej.2014.64 · Cited by 209 · see citing works
Cavanaugh, J. A. (2001) · The American Journal of Human Genetics · doi:10.1086/320119 · Cited by 199 · see citing works
Lahti, L., Salonen, A., Kekkonen, R. A., Salojärvi, J., Jalanka, J., Palva, A., Orešič, M., & de Vos, W. M. (2013) · PeerJ · doi:10.7717/peerj.32 · Cited by 196 · see citing works
Lapaquette, P., Bringer, M.-A., & Darfeuille–Michaud, A. (2012) · Cellular Microbiology · doi:10.1111/j.1462-5822.2012.01768.x · Cited by 194 · see citing works
NOD2 and Crohn’s Disease: Loss or Gain of Function?
Eckmann, L., & Karin, M. (2005) · Immunity · doi:10.1016/j.immuni.2005.06.004 · Cited by 185 · see citing works
Seaweeds for umami flavour in the New Nordic Cuisine
Mouritsen, O. G., Williams, L., Bjerregaard, R., & Duelund, L. (2012) · Flavour · doi:10.1186/2044-7248-1-4 · Cited by 177 · see citing works
Sokol, H., Conway, K. L., Zhang, M., Choi, M., Morin, B., Cao, Z., Villablanca, E. J., Li, C., Wijmenga, C., Yun, S. H., et al. (2013) · Gastroenterology · doi:10.1053/j.gastro.2013.05.047 · Cited by 161 · see citing works
Self-citationAging and the human gut microbiota—from correlation to causality
Saraswati, S., & Sitaraman, R. (2015) · Frontiers in Microbiology · doi:10.3389/fmicb.2014.00764 · Cited by 153 · see citing works
Li, D., Achkar, J., Haritunians, T., Jacobs, J. P., Hui, K. Y., D’Amato, M., Brand, S., Radford‐Smith, G. L., Halfvarson, J., Niess, J. H., et al. (2016) · Gastroenterology · doi:10.1053/j.gastro.2016.06.051 · Cited by 152 · see citing works
Self-citationMucin Function in Inflammatory Bowel Disease
Boltin, D., Perets, T. T., Vilkin, A., & Niv, Y. (2012) · Journal of Clinical Gastroenterology · doi:10.1097/mcg.0b013e3182688e73 · Cited by 151 · see citing works
A prominent glycyl radical enzyme in human gut microbiomes metabolizes trans -4-hydroxy- l -proline
Levin, B. J., Huang, Y. Y., Peck, S. C., Wei, Y., Campo, A. M.-D., Marks, J. A., Franzosa, E. A., Huttenhower, C., & Balskus, E. P. (2017) · Science · doi:10.1126/science.aai8386 · Cited by 142 · see citing works
FUT2 Nonsecretor Status Links Type 1 Diabetes Susceptibility and Resistance to Infection
Smyth, D. J., Cooper, J. D., Howson, J. M. M., Pamela, C., Downes, K., Mistry, T., Stevens, H. E., Walker, N. M., & Todd, J. A. (2011) · Diabetes · doi:10.2337/db11-0638 · Cited by 133 · see citing works
A genetic variant near olfactory receptor genes influences cilantro preference
Eriksson, N., Wu, S., Do, C. B., Kiefer, A. K., Tung, J. Y., Mountain, J. L., Hinds, D. A., & Francke, U. (2012) · Flavour · doi:10.1186/2044-7248-1-22 · Cited by 128 · see citing works
Molecular classification of Crohn's disease reveals two clinically relevant subtypes
Weiser, M., Simon, J. M., Kochar, B. D., Tovar, A., Israel, J. W., Robinson, A., Gipson, G. R., Schaner, M. S., Herfarth, H. H., Sartor, R. B., et al. (2016) · Gut · doi:10.1136/gutjnl-2016-312518 · Cited by 127 · see citing works
Advantages and limitations of genomics in prokaryotic taxonomy
Sentausa, E., & Fournier, P. (2013) · Clinical Microbiology and Infection · doi:10.1111/1469-0691.12181 · Cited by 121 · see citing works
Coyne, M. J., Chatzidaki‐Livanis, M., Paoletti, L. C., & Comstock, L. E. (2008) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0804220105 · Cited by 112 · see citing works
Ikehara, Y., Nishihara, S., Yasutomi, H., Kitamura, T., Matsuo, K., Shimizu, N., Inada, K., Kodera, Y., Yamamura, Y., Narimatsu, H., et al. (2001) · PubMed · Cited by 108 · see citing works
Inflammatory Bowel Disease Genetics: Nod2
Cho, J. H., & Abraham, C. (2006) · Annual Review of Medicine · doi:10.1146/annurev.med.58.061705.145024 · Cited by 105 · see citing works
Parmar, A., Alakulppi, N. S., Paavola–Sakki, P., Kurppa, K., Halme, L., Färkkilä, M. A., Turunen, U., Lappalainen, M., KONTULA, K. K., Kaukinen, K., et al. (2012) · Tissue Antigens · doi:10.1111/tan.12016 · Cited by 98 · see citing works
Neuron-enriched RNA-binding Proteins Regulate Pancreatic Beta Cell Function and Survival
Juan‐Mateu, J., Rech, T. H., Villate, O., Lizárraga-Mollinedo, E., Wendt, A., Turatsinze, J., Brondani, L. D. A., Nardelli, T. R., Nogueira, T. C., Esguerra, J. L. S., et al. (2017) · Journal of Biological Chemistry · doi:10.1074/jbc.m116.748335 · Cited by 70 · see citing works
Genome‐Wide Association of BMI in African Americans
Ng, M. C. Y., Hester, J. M., Wing, M. R., Li, J., Xu, J., Hicks, P. J., Roh, B. H., Lu, L., Divers, J., Langefeld, C. D., et al. (2011) · Obesity · doi:10.1038/oby.2011.154 · Cited by 63 · see citing works
Speakman, J. R. (2013) · Human Heredity · doi:10.1159/000353585 · Cited by 61 · see citing works
Analysis of a Capsular Polysaccharide Biosynthesis Locus ofBacteroides fragilis
Comstock, L. E., Coyne, M. J., Tzianabos, A. O., Pantosti, A., Onderdonk, A. B., & Kasper, D. L. (1999) · Infection and Immunity · doi:10.1128/iai.67.7.3525-3532.1999 · Cited by 55 · see citing works
Colonic mucin glycoproteins in health and disease.
Smith, A. C., & Podolsky, D. K. (1986) · PubMed · Cited by 54 · see citing works
Possible role of blood-group secretory substances in the aetiology of cholera
Chaudhuri, A., & Cr, D. (1978) · Transactions of the Royal Society of Tropical Medicine and Hygiene · doi:10.1016/0035-9203(78)90031-7 · Cited by 53 · see citing works
Walley, A. J., Jacobson, P., Falchi, M., Bottolo, L., Andersson‐Assarsson, J. C., Petretto, E. G., Bonnefond, A., Vaillant, E., Lecœur, C., Vatin, V., et al. (2011) · International Journal of Obesity · doi:10.1038/ijo.2011.22 · Cited by 51 · see citing works
Cassese, A., Raciti, G. A., Fiory, F., Nigro, C., Ulianich, L., Castanò, I., D’Esposito, V., Terracciano, D., Pastore, L., Formisano, P., et al. (2013) · PLoS ONE · doi:10.1371/journal.pone.0060555 · Cited by 12 · see citing works
Chen, J., Chen, L., Sanséau, P., Freudenberg, J., & Rajpal, D. K. (2016) · Physiological Reports · doi:10.14814/phy2.12793 · Cited by 12 · see citing works
Inflammatory Bowel Disease Genetics
Cotterill, L. (2011) · Research Explorer (The University of Manchester) · Cited by 11 · see citing works
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MAFLD: a consensus-driven proposed nomenclature for metabolic associated fatty liver disease
Eslam, M., Sanyal, A. J., George, J., Sanyal, A., Neuschwander-Tetri, B., Tiribelli, C., Kleiner, D. E., Brunt, E., Bugianesi, E., Yki-Järvinen, H., et al. (2020) · Gastroenterology · doi:10.1053/j.gastro.2019.11.312 · Cited by 3,286 · see citing works
Multi-omics of the gut microbial ecosystem in inflammatory bowel diseases
Lloyd-Price, J., Arze, C., Ananthakrishnan, A. N., Schirmer, M., Avila-Pacheco, J., Poon, T. W., Andrews, E., Ajami, N. J., Bonham, K. S., Brislawn, C. J., et al. (2019) · Nature · doi:10.1038/s41586-019-1237-9 · Cited by 3,143 · see citing works
Self-citationIntegrative omics for health and disease
Karczewski, K. J., & Snyder, M. P. (2018) · Nature Reviews Genetics · doi:10.1038/nrg.2018.4 · Cited by 1,158 · see citing works
Turecki, G., Brent, D. A., Gunnell, D., O’Connor, R. C., Oquendo, M. A., Pirkis, J., & Stanley, B. H. (2019) · Nature Reviews Disease Primers · doi:10.1038/s41572-019-0121-0 · Cited by 1,074 · see citing works
The Human Gut Microbiome: From Association to Modulation
Schmidt, T. S. B., Raes, J., & Bork, P. (2018) · Cell · doi:10.1016/j.cell.2018.02.044 · Cited by 845 · see citing works
Dietary metabolism, the gut microbiome, and heart failure
Tang, W. H. W., Li, D. Y., & Hazen, S. L. (2019) · Nature Reviews Cardiology · doi:10.1038/s41569-018-0108-7 · Cited by 789 · see citing works
MahmoudianDehkordi, S., Arnold, M., Nho, K., Ahmad, S., Jia, W., Xie, G., Louie, G., Kueider‐Paisley, A., Moseley, M. A., Thompson, J. W., et al. (2019) · Alzheimer's & Dementia · doi:10.1016/j.jalz.2018.07.217 · Cited by 706 · see citing works
Gut microbiota utilize immunoglobulin A for mucosal colonization
Donaldson, G. P., Ladinsky, M. S., Yu, K. B., Sanders, J. G., Yoo, B. B., Chou, W., Conner, M. E., Earl, A. M., Knight, R. D., Björkman, P. J., et al. (2018) · Science · doi:10.1126/science.aaq0926 · Cited by 633 · see citing works
Gut microbiota and Covid-19- possible link and implications
Dhar, D., & Mohanty, A. (2020) · Virus Research · doi:10.1016/j.virusres.2020.198018 · Cited by 608 · see citing works
Effect of host genetics on the gut microbiome in 7,738 participants of the Dutch Microbiome Project
Lopera-Maya, E. A., Kurilshikov, A., van der Graaf, A., Hu, S., Andreu-Sánchez, S., Chen, L., Vila, A. V., Gacesa, R., Sinha, T., Collij, V., et al. (2022) · Nature Genetics · doi:10.1038/s41588-021-00992-y · Cited by 553 · see citing works
A plant genetic network for preventing dysbiosis in the phyllosphere
Chen, T., Nomura, K., Wang, X., Sohrabi, R., Xu, J. H., Yao, L., Paasch, B. C., Ma, L. M., Kremer, J. M., Cheng, Y., et al. (2020) · Nature · doi:10.1038/s41586-020-2185-0 · Cited by 560 · see citing works
The Super-Donor Phenomenon in Fecal Microbiota Transplantation
Wilson, B. C., Vatanen, T., Cutfield, W. S., & O'Sullivan, J. M. (2019) · Frontiers in Cellular and Infection Microbiology · doi:10.3389/fcimb.2019.00002 · Cited by 420 · see citing works
Synthetic microbiota reveal priority effects and keystone strains in the Arabidopsis phyllosphere
Carlström, C. I., Field, C. M., Bortfeld‐Miller, M., Müller, B., Sunagawa, S., & Vorholt, J. A. (2019) · Nature Ecology & Evolution · doi:10.1038/s41559-019-0994-z · Cited by 406 · see citing works
The Ruminococci: key symbionts of the gut ecosystem
Reau, A. J. L., & Suen, G. (2018) · The Journal of Microbiology · doi:10.1007/s12275-018-8024-4 · Cited by 394 · see citing works
A predictive index for health status using species-level gut microbiome profiling
Gupta, V. K., Kim, M., Bakshi, U., Cunningham, K. Y., Davis, J. M., Lazaridis, K. N., Nelson, H., Chia, N., & Sung, J. (2020) · Nature Communications · doi:10.1038/s41467-020-18476-8 · Cited by 338 · see citing works
Microbiome and colorectal cancer: Roles in carcinogenesis and clinical potential
Saus, E., Iraola‐Guzmán, S., Willis, J. R., Brunet‐Vega, A., & Gabaldón, T. (2019) · Molecular Aspects of Medicine · doi:10.1016/j.mam.2019.05.001 · Cited by 348 · see citing works
Human microbiome: an academic update on human body site specific surveillance and its possible role
Dekaboruah, E., Suryavanshi, M. V., Chettri, D., & Verma, A. K. (2020) · Archives of Microbiology · doi:10.1007/s00203-020-01931-x · Cited by 345 · see citing works
Genetic contributions to NAFLD: leveraging shared genetics to uncover systems biology
Eslam, M., & George, J. (2019) · Nature Reviews Gastroenterology & Hepatology · doi:10.1038/s41575-019-0212-0 · Cited by 310 · see citing works
Gut Microbiota Dysbiosis: Pathogenesis, Diseases, Prevention, and Therapy
Shen, Y., Fan, N., Ma, S., Cheng, X., Yang, X., & Wang, G. (2025) · MedComm · doi:10.1002/mco2.70168 · Cited by 364 · see citing works
Mucosal fungi promote gut barrier function and social behavior via Type 17 immunity
Leonardi, I., Gao, I. H., Lin, W.-Y., Allen, M., Li, X. V., Fiers, W. D., De Celie, M. B., Putzel, G. G., Yantiss, R. K., Johncilla, M., et al. (2022) · Cell · doi:10.1016/j.cell.2022.01.017 · Cited by 307 · see citing works
TMAO: how gut microbiota contributes to heart failure
Zhang, Y., Wang, Y., Ke, B., & Du, J. (2020) · Translational research · doi:10.1016/j.trsl.2020.08.007 · Cited by 306 · see citing works
The gut microbiome and hypertension
O’Donnell, J. A., Zheng, T., Méric, G., & Marques, F. Z. (2023) · Nature Reviews Nephrology · doi:10.1038/s41581-022-00654-0 · Cited by 294 · see citing works
Bacteroides utilization for dietary polysaccharides and their beneficial effects on gut health
Cheng, J., Hu, J., Geng, F., & Nie, S. (2022) · Food Science and Human Wellness · doi:10.1016/j.fshw.2022.04.002 · Cited by 281 · see citing works
Pinpointing secondary metabolites that shape the composition and function of the plant microbiome
Jacoby, R. P., Kopřivová, A., & Kopřiva, S. (2020) · Journal of Experimental Botany · doi:10.1093/jxb/eraa424 · Cited by 265 · see citing works
Wu, J., Li, Q., & Fu, X. (2019) · Translational Oncology · doi:10.1016/j.tranon.2019.03.003 · Cited by 254 · see citing works
H3Africa: current perspectives
Mulder, N., Abimiku, A., Adebamowo, S. N., de Vries, J., Matimba, A., Olowoyo, P., Ramsay, M., Skelton, M., & Stein, D. J. (2018) · Pharmacogenomics and Personalized Medicine · doi:10.2147/pgpm.s141546 · Cited by 244 · see citing works
Maternal vertical transmission affecting early-life microbiota development
Wang, S., Ryan, C. A., Boyaval, P., Dempsey, E. M., Ross, R. P., & Stanton, C. (2020) · Trends in Microbiology · doi:10.1016/j.tim.2019.07.010 · Cited by 243 · see citing works
Healthy Human Gastrointestinal Microbiome: Composition and Function After a Decade of Exploration
Ruan, W. H., Engevik, M. A., Spinler, J. K., & Versalovic, J. A. (2020) · Digestive Diseases and Sciences · doi:10.1007/s10620-020-06118-4 · Cited by 240 · see citing works
Analysis of 1135 gut metagenomes identifies sex-specific resistome profiles
Sinha, T., Vich Vila, A., Garmaeva, S., Jankipersadsing, S. A., Imhann, F., Collij, V., Bonder, M. J., Jiang, X., Gurry, T., Alm, E. J., et al. (2019) · Gut Microbes · doi:10.1080/19490976.2018.1528822 · Cited by 208 · see citing works
Chen, L., Reeve, J., Zhang, L., Huang, S., Wang, X., & Chen, J. (2018) · PeerJ · doi:10.7717/peerj.4600 · Cited by 225 · see citing works
Thapa, S., Mishra, J., Arora, N. K., Mishra, P., Li, H., O’Hair, J., Bhatti, S., & Zhou, S. (2020) · Reviews in Environmental Science and Bio/Technology · doi:10.1007/s11157-020-09536-y · Cited by 223 · see citing works
One Health Relationships Between Human, Animal, and Environmental Microbiomes: A Mini-Review
Trinh, P., Zaneveld, J., Safranek, S. M., & Rabinowitz, P. M. (2018) · Frontiers in Public Health · doi:10.3389/fpubh.2018.00235 · Cited by 215 · see citing works
Cohen, L. J., Cho, J. H., Gevers, D., & Chu, H. (2019) · Gastroenterology · doi:10.1053/j.gastro.2019.03.017 · Cited by 201 · see citing works
Martínez, I., Maldonado-Gomez, M. X., Gomes-Neto, J. C., Kittana, H., Ding, H., Schmaltz, R., Joglekar, P., Cardona, R. J., Marsteller, N. L., Kembel, S. W., et al. (2018) · eLife · doi:10.7554/elife.36521 · Cited by 199 · see citing works
Gut epithelial TSC1/mTOR controls RIPK3-dependent necroptosis in intestinal inflammation and cancer
Xie, Y., Zhao, Y., Shi, L., Li, W., Chen, K., Li, M., Chen, X., Zhang, H., Li, T., Matsuzawa, Y., et al. (2020) · Journal of Clinical Investigation · doi:10.1172/jci133264 · Cited by 198 · see citing works
Probiotics: Versatile Bioactive Components in Promoting Human Health
Sharifi‐Rad, J., Rodrigues, C. F., Stojanović-Radić, Z. Z., Dimitrijević, M., Aleksić, A., Neffe‐Skocińska, K., Zielińska, D., Kołożyn‐Krajewska, D., Salehi, B., Prabu, S. M., et al. (2020) · Medicina · doi:10.3390/medicina56090433 · Cited by 195 · see citing works
Inflammatory Bowel Disease: A Review of Pre-Clinical Murine Models of Human Disease
Katsandegwaza, B., Horsnell, W. G. C., & Smith, K. A. (2022) · International Journal of Molecular Sciences · doi:10.3390/ijms23169344 · Cited by 191 · see citing works
B Vitamins and Their Roles in Gut Health
Hossain, K. S., Amarasena, S., & Mayengbam, S. (2022) · Microorganisms · doi:10.3390/microorganisms10061168 · Cited by 188 · see citing works
Delgado, B., Bach, À., Guasch, I., González, C., Elcoso, G., Pryce, J. E., & González-Recio, Ó. (2019) · Scientific Reports · doi:10.1038/s41598-018-36673-w · Cited by 186 · see citing works
The Th17/Treg Cell Balance: A Gut Microbiota-Modulated Story
Cheng, H., Guan, X., Chen, D., & Ma, W. (2019) · Microorganisms · doi:10.3390/microorganisms7120583 · Cited by 181 · see citing works
Microbial transmission, colonisation and succession: from pregnancy to infancy
Xiao, L., & Zhao, F. (2023) · Gut · doi:10.1136/gutjnl-2022-328970 · Cited by 183 · see citing works
Alonso, R., Pisa, D., Fernández-Fernández, A. M., & Carrasco, L. (2018) · Frontiers in Aging Neuroscience · doi:10.3389/fnagi.2018.00159 · Cited by 165 · see citing works
Role of gut microbiota in intestinal wound healing and barrier function
Alam, A., & Neish, A. (2018) · Tissue Barriers · doi:10.1080/21688370.2018.1539595 · Cited by 166 · see citing works
Potential Use of Marine Seaweeds as Prebiotics: A Review
López-Santamarina, A., Miranda, J. M., Mondragón, A. D. C., Lamas, A., Cardelle‐Cobas, A., Franco, C. M., & Cepeda, A. (2020) · Molecules · doi:10.3390/molecules25041004 · Cited by 162 · see citing works
Lavoie, S., Conway, K. L., Lassen, K. G., Jijon, H. B., Pan, H., Chun, E., Michaud, M., Lang, J. K., Gallini, C. A., Dreyfuss, J. M., et al. (2019) · eLife · doi:10.7554/elife.39982 · Cited by 153 · see citing works
Self-citationMicrobiome therapeutics: exploring the present scenario and challenges
Yadav, M., & Chauhan, N. S. (2021) · Gastroenterology report · doi:10.1093/gastro/goab046 · Cited by 157 · see citing works
Exploring rhizo-microbiome transplants as a tool for protective plant-microbiome manipulation
Jiang, G., Zhang, Y., Gan, G., Li, W., Wan, W., Jiang, Y., Yang, T., Zhang, Y., Xu, Y., Wang, Y., et al. (2022) · ISME Communications · doi:10.1038/s43705-022-00094-8 · Cited by 152 · see citing works
Gut microbiota changes in children with autism spectrum disorder: a systematic review
Ho, L. K. H., Tong, V. J. W., Syn, N., Nagarajan, N., Tham, E. H., Tay, S. K., Shorey, S., Tambyah, P. A., & Law, E. C. N. (2020) · Gut Pathogens · doi:10.1186/s13099-020-0346-1 · Cited by 149 · see citing works
Stinson, L. F., Payne, M. S., & Keelan, J. A. (2018) · Frontiers in Medicine · doi:10.3389/fmed.2018.00135 · Cited by 147 · see citing works
Chen, Z., Han, S., Zhou, D., Zhou, S., & Jia, G. (2019) · Nanoscale · doi:10.1039/c9nr07580a · Cited by 137 · see citing works
Genetic determinants of gut microbiota composition and bile acid profiles in mice
Kemis, J. H., Linke, V., Barrett, K. L., Boehm, F. J., Traeger, L. L., Keller, M. P., Rabaglia, M. E., Schueler, K. L., Stapleton, D. S., Gatti, D. M., et al. (2019) · PLOS Genetics · doi:10.1371/journal.pgen.1008073 · Cited by 136 · see citing works
The Human Microbiota and Asthma
Heul, A. V., Planer, J. D., & Kau, A. L. (2018) · Clinical Reviews in Allergy & Immunology · doi:10.1007/s12016-018-8719-7 · Cited by 127 · see citing works
Chen, Z., Zhou, D., Han, S., Zhou, S., & Jia, G. (2019) · Particle and Fibre Toxicology · doi:10.1186/s12989-019-0332-2 · Cited by 126 · see citing works
Role of the Intestinal Epithelium and Its Interaction With the Microbiota in Food Allergy
Ali, A. S., HuiYing, T., & Kaiko, G. E. (2020) · Frontiers in Immunology · doi:10.3389/fimmu.2020.604054 · Cited by 124 · see citing works
Host and microbiome multi-omics integration: applications and methodologies
Wang, Q., Wang, K., Wu, W., Giannoulatou, E., Ho, J. W. K., & Li, L. (2019) · Biophysical Reviews · doi:10.1007/s12551-018-0491-7 · Cited by 122 · see citing works
Nanotechnology for Targeted Detection and Removal of Bacteria: Opportunities and Challenges
Hajipour, M. J., Saei, A. A., Walker, E. D., Conley, B., Omidi, Y., Lee, K., & Mahmoudi, M. (2021) · Advanced Science · doi:10.1002/advs.202100556 · Cited by 121 · see citing works
Novel mechanisms and clinical trial endpoints in intestinal fibrosis*
Wang, J., Lin, S., Brown, J. M., Wagoner, D. R. V., Fiocchi, C., & Rieder, F. (2021) · Immunological Reviews · doi:10.1111/imr.12974 · Cited by 119 · see citing works
Impact of the gut microbiota on the m6A epitranscriptome of mouse cecum and liver
Jabs, S., Biton, A., Bécavin, C., Nahori, M., Ghozlane, A., Pagliuso, A., Spanò, G., Guérineau, V., Touboul, D., Gianetto, Q. G., et al. (2020) · Nature Communications · doi:10.1038/s41467-020-15126-x · Cited by 120 · see citing works
Host and Microbiome Genome-Wide Association Studies: Current State and Challenges
Awany, D., Allali, I., Dalvie, S., Hemmings, S. M. J., Mwaikono, K. S., Thomford, N. E., Gomez, A. M., Mulder, N., & Chimusa, E. R. (2019) · Frontiers in Genetics · doi:10.3389/fgene.2018.00637 · Cited by 108 · see citing works
Host genetic determinants of the gut microbiota of wild mice
Suzuki, T. A., Phifer‐Rixey, M., Mack, K. L., Sheehan, M. J., Lin, D., Bi, K., & Nachman, M. W. (2019) · Molecular Ecology · doi:10.1111/mec.15139 · Cited by 108 · see citing works
Anticancer drug discovery from Chinese medicinal herbs
Huang, M., Zhang, L., Ding, J., & Lu, J. (2018) · Chinese Medicine · doi:10.1186/s13020-018-0192-y · Cited by 102 · see citing works
The gut microbiota–brain axis in neurological disorders
You, M., Chen, N., Yang, Y., Cheng, L., He, H., Cai, Y., Liu, Y., Liu, H., & Hong, G. (2024) · MedComm · doi:10.1002/mco2.656 · Cited by 107 · see citing works
Natural genetic variation drives microbiome selection in the Caenorhabditis elegans gut
Zhang, F., Weckhorst, J. L., Assié, A., Hosea, C. N., Ayoub, C. A., Khodakova, A. S., Cabrera, M. L., Vidal, D., Félix, M., & Samuel, B. S. (2021) · Current Biology · doi:10.1016/j.cub.2021.04.046 · Cited by 88 · see citing works
Murray, E. R., Kemp, M., & Nguyen, T. T. (2022) · Archives of Clinical Neuropsychology · doi:10.1093/arclin/acac008 · Cited by 98 · see citing works
An update on vitamin B12-related gene polymorphisms and B12 status
Surendran, S., Adaikalakoteswari, A., Saravanan, P., Shatwaan, I. A., Lovegrove, J. A., & Vimaleswaran, K. S. (2018) · Genes & Nutrition · doi:10.1186/s12263-018-0591-9 · Cited by 93 · see citing works
Interactions Between Food and Gut Microbiota: Impact on Human Health
Wu, Y., Wan, J., Choe, U., Pham, Q., Schoene, N. W., He, Q., Li, B., Yu, L. L., & Wang, T. T. Y. (2019) · Annual Review of Food Science and Technology · doi:10.1146/annurev-food-032818-121303 · Cited by 93 · see citing works
Zhu, X., Hu, J., Deng, S., Tan, Y., Qiu, C., Zhang, M., Ni, X., Lu, H., Wang, Z., Li, L., et al. (2021) · Frontiers in Psychiatry · doi:10.3389/fpsyt.2020.587670 · Cited by 92 · see citing works
The honey bee gut microbiota: strategies for study and characterization
Romero, S., Nastasa, A., Chapman, A., Kwong, W. K., & Foster, L. J. (2019) · Insect Molecular Biology · doi:10.1111/imb.12567 · Cited by 88 · see citing works
Zaramela, L. S., Martino, C., Alisson‐Silva, F., Rees, S. D., Diaz, S. L., Chuzel, L., Ganatra, M. B., Taron, C. H., Secrest, P., Zúñiga, C., et al. (2019) · Nature Microbiology · doi:10.1038/s41564-019-0564-9 · Cited by 87 · see citing works
Diet and gut microbiome in gastrointestinal disease
Trakman, G., Fehily, S. R., Basnayake, C., Hamilton, A. L., Russell, E., Wilson-O'Brien, A. L., & Kamm, M. A. (2021) · Journal of Gastroenterology and Hepatology · doi:10.1111/jgh.15728 · Cited by 88 · see citing works
Microbiome epidemiology and association studies in human health
VanEvery, H., Franzosa, E. A., Nguyen, L. H., & Huttenhower, C. (2022) · Nature Reviews Genetics · doi:10.1038/s41576-022-00529-x · Cited by 85 · see citing works
Noble, A. J., Nowak, J. K., Adams, A. T., Uhlig, H. H., & Satsangi, J. J. (2023) · Gastroenterology · doi:10.1053/j.gastro.2023.03.238 · Cited by 88 · see citing works
Alferink, L. J. M., Radjabzadeh, D., Erler, N. S., Vojinović, D., Medina‐Gómez, C., Uitterlinden, A. G., de Knegt, R. J., Amin, N., Ikram, M. A., Janssen, H. L. A., et al. (2020) · Hepatology · doi:10.1002/hep.31417 · Cited by 87 · see citing works
Rezaie, A. R., Heimanson, Z., McCallum, R. W., & Pimentel, M. (2019) · The American Journal of Gastroenterology · doi:10.14309/ajg.0000000000000444 · Cited by 84 · see citing works
Gut, oral and skin microbiome of Indian patrilineal families reveal perceptible association with age
Chaudhari, D. S., Dhotre, D. P., Agarwal, D. M., Gaike, A. H., Bhalerao, D., Jadhav, P., Mongad, D., Lubree, H., Sinkar, V. P., Patil, U. K., et al. (2020) · Scientific Reports · doi:10.1038/s41598-020-62195-5 · Cited by 81 · see citing works
Ma, Y., Zhang, Y., Jiang, H., Xiang, S., Zhao, Y., Xiao, M., Du, F., Ji, H., Kaboli, P. J., Wu, X., et al. (2021) · Frontiers in Cellular and Infection Microbiology · doi:10.3389/fcimb.2021.599734 · Cited by 84 · see citing works
Antigen discovery and specification of immunodominance hierarchies for MHCII-restricted epitopes
Graham, D. B., Luo, C., O’Connell, D. J., Lefkovith, A. J., Brown, E., Yassour, M., Varma, M., Abelin, J. G., Conway, K. L., Jasso, G. J., et al. (2018) · Nature Medicine · doi:10.1038/s41591-018-0203-7 · Cited by 79 · see citing works
Self-citationBreuninger, T. A., Wawro, N., Breuninger, J., Reitmeier, S., Clavel, T., Six-Merker, J., Pestoni, G., Rohrmann, S., Rathmann, W., Peters, A., et al. (2021) · Microbiome · doi:10.1186/s40168-020-00969-9 · Cited by 81 · see citing works
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Aykur, M., Malatyalı, E., Demirel, F., Koçak, B. C., Gentekaki, E., Tsaousis, A. D., & Al, F. D. (2024) · Microorganisms · doi:10.3390/microorganisms12030461 · Cited by 79 · see citing works
Guidelines for Transparency on Gut Microbiome Studies in Essential and Experimental Hypertension
Marques, F. Z., Jama, H. A., Tsyganov, K., Gill, P. A., Rhys-Jones, D. R., Muralitharan, R. R., Muir, J. G., Holmes, A. J., & Mackay, C. R. (2019) · Hypertension · doi:10.1161/hypertensionaha.119.13079 · Cited by 77 · see citing works
The intestinal microbiome and Alzheimer's disease: A review
Li, Z., Zhu, H., Zhang, L., & Qin, C. (2018) · Animal Models and Experimental Medicine · doi:10.1002/ame2.12033 · Cited by 75 · see citing works
Sun, Y., Cui, X., Duan, M., Ai, C., Song, S., & Chen, X. (2019) · Journal of Functional Foods · doi:10.1016/j.jff.2019.05.036 · Cited by 73 · see citing works
Role of Carbon Monoxide in Host–Gut Microbiome Communication
Hopper, C., Cruz, L. K. D. L., Lyles, K. V. M., Wareham, L. K., Gilbert, J. A., Eichenbaum, Z., Magierowski, M., Poole, R. K., Wollborn, J., & Wang, B. (2020) · Chemical Reviews · doi:10.1021/acs.chemrev.0c00586 · Cited by 72 · see citing works
Yadav, M., Lomash, A., Kapoor, S., Pandey, R., & Chauhan, N. S. (2021) · Scientific Reports · doi:10.1038/s41598-021-84964-6 · Cited by 73 · see citing works
Gubert, C., Choo, J. M., Love, C. J., Kodikara, S., Masson, B. A., Liew, J. J. M., Wang, Y., Kong, G., Narayana, V. K., Renoir, T., et al. (2022) · Brain Communications · doi:10.1093/braincomms/fcac205 · Cited by 71 · see citing works
Plant Genetic Networks Shaping Phyllosphere Microbial Community
Shakir, S., Zaidi, S. S., de Vries, F. T., & Mansoor, S. (2020) · Trends in Genetics · doi:10.1016/j.tig.2020.09.010 · Cited by 71 · see citing works
Approaches and advances in the genetic causes of autoimmune disease and their implications
Inshaw, J. R. J., Cutler, A. J., Burren, O. S., Stefana, M. I., & Todd, J. A. (2018) · Nature Immunology · doi:10.1038/s41590-018-0129-8 · Cited by 70 · see citing works
The Prenatal Microbiome: A New Player for Human Health
D’Argenio, V. (2018) · Microarrays · doi:10.3390/ht7040038 · Cited by 65 · see citing works
Impact of host genetics on gut microbiome: Take‐home lessons from human and mouse studies
Cahana, I., & Iraqi, F. A. (2020) · Animal Models and Experimental Medicine · doi:10.1002/ame2.12134 · Cited by 61 · see citing works
Gut microbiome and metabolites, the future direction of diagnosis and treatment of atherosclerosis?
Cao, H., Zhu, Y., Hu, G., Zhang, Q., & Zheng, L. (2022) · Pharmacological Research · doi:10.1016/j.phrs.2022.106586 · Cited by 63 · see citing works
Nutrition, Bioenergetics, and Metabolic Syndrome
García‐García, F. J., Monistrol-Mula, A., Cardellach, F., & Garrabou, G. (2020) · Nutrients · doi:10.3390/nu12092785 · Cited by 66 · see citing works
Crosstalk between sIgA-Coated Bacteria in Infant Gut and Early-Life Health
Ding, M., Yang, B. K., Ross, R. P., Stanton, C., Zhao, J., Zhang, H., & Chen, W. (2021) · Trends in Microbiology · doi:10.1016/j.tim.2021.01.012 · Cited by 61 · see citing works
Causality of gut microbiome and hypertension: A bidirectional mendelian randomization study
Li, Y., Fu, R., Li, R., Zeng, J., Liu, T., Li, X., & Jiang, W. (2023) · Frontiers in Cardiovascular Medicine · doi:10.3389/fcvm.2023.1167346 · Cited by 61 · see citing works
Probiotic Effects against Virus Infections: New Weapons for an Old War
López-Santamarina, A., Lamas, A., Mondragón, A. D. C., Cardelle‐Cobas, A., Regal, P., Rodríguez, J. A., Miranda, J. M., Franco, C. M., & Cepeda, A. (2021) · Foods · doi:10.3390/foods10010130 · Cited by 60 · see citing works
Human Gut Microbiota Plasticity throughout the Life Course
Thriene, K., & Michels, K. B. (2023) · International Journal of Environmental Research and Public Health · doi:10.3390/ijerph20021463 · Cited by 61 · see citing works
Kamath, S., Stringer, A. M., Prestidge, C. A., & Joyce, P. (2023) · Expert Opinion on Drug Delivery · doi:10.1080/17425247.2023.2233900 · Cited by 58 · see citing works
NLR and Intestinal Dysbiosis-Associated Inflammatory Illness: Drivers or Dampers?
Elias‐Oliveira, J., Leite, J. A., Pereira, Í. S., Guimarães, J. B., Manso, G. M. D. C., Silva, J. S., Tostes, R. C., & Carlos, D. (2020) · Frontiers in Immunology · doi:10.3389/fimmu.2020.01810 · Cited by 58 · see citing works
The gut microbiome as a biomarker of differential susceptibility to SARS-CoV-2
Sarkar, A., Harty, S., Moeller, A. H., Klein, S. L., Erdman, S. E., Friston, K. J., & Carmody, R. N. (2021) · Trends in Molecular Medicine · doi:10.1016/j.molmed.2021.09.009 · Cited by 55 · see citing works
Sex-Specific Linkages Between Taxonomic and Functional Profiles of Tick Gut Microbiomes
Obregón, D., Bard, É., Abrial, D., Estrada‐Peña, A., & Cabezas‐Cruz, A. (2019) · Frontiers in Cellular and Infection Microbiology · doi:10.3389/fcimb.2019.00298 · Cited by 53 · see citing works
Whole exome sequencing analyses reveal gene–microbiota interactions in the context of IBD
Hu, S., Vila, A. V., Gaćeša, R., Collij, V., Stevens, C. R., Fu, J. M., Wong, I., Talkowski, M. E., Rivas, M. A., Imhann, F., et al. (2020) · Gut · doi:10.1136/gutjnl-2019-319706 · Cited by 58 · see citing works
Self-citation
- Authors
- Hall, A. B., Tolonen, A. C., & Xavier, R. J.
- Affiliations
- Broad Institute (US)
- Corresponding author
- Hall, Andrew Brantley
- Xavier, Ramnik J.
- Venue
- Nature Reviews Genetics
- Published
- 2017-08-21
- Volume
- 18
- Issue
- 11
- Pages
- 690-699
- ISSN
- 1471-0056 (ISSN-L)
- 1471-0064
- OpenAlex
- W2749822530
- Cited by
- 517
- References
- 113
- Citations by year
- 2026: 35 · 2025: 42 · 2024: 63 · 2023: 63 · 2022: 62 · 2021: 61 · 2020: 66 · 2019: 60 · 2018: 58 · 2017: 5
- FWCI
- 4.84
- Type
- journal article
- Language
- en
- Open access
- closed
- Licence
- www.springer.com/tdm (tdm)
- Locations
- Nature Reviews Genetics (publishedVersion)
- PubMed (publishedVersion)
- Funders
- National Institute of Diabetes and Digestive and Kidney Diseases (R01DK092405, P30DK043351)
- National Institute of Dental and Craniofacial Research (U54DE023798)
- Topics
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Gut microbiota and health
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Genetics › Genetic Associations and Epidemiology
- Health Sciences › Dentistry › Periodontics › Oral microbiology and periodontitis research
- Keywords
- gut microbiota, host genetic variation, dysbiosis, metabolic disorders, host-microbe interactions, microbial community composition
- MeSH terms
- Gastrointestinal Microbiome, Humans, Genetic Variation, Dysbiosis
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