Development of the gut microbiota in infancy and its impact on health in later life

Human gut microbiome viewed across age and geography

Yatsunenko, T., Rey, F. E., Manary, M. J., Trehan, I., Dominguez-Bello, M. G., Contreras, M., Magris, M., Hidalgo, G., Baldassano, R. N., Anokhin, A. P., et al. (2012) · Nature · doi:10.1038/nature11053 · Cited by 7,815 · see citing works

Enterotypes of the human gut microbiome

MetaHIT Consortium (additional members), Arumugam, M., Raes, J., Pelletier, E., Le Paslier, D., Yamada, T., Mende, D. R., Fernandes, G. R., Tap, J., Bruls, T., et al. (2011) · Nature · doi:10.1038/nature09944 · Cited by 7,548 · see citing works

Commensal microbe-derived butyrate induces the differentiation of colonic regulatory T cells

Furusawa, Y., Obata, Y., Fukuda, S., Endo, T. A., Nakato, G., Takahashi, D., Nakanishi, Y., Uetake, C., Kato, K., Kato, T., et al. (2013) · Nature · doi:10.1038/nature12721 · Cited by 5,549 · see citing works

Role of the microbiota in immunity and inflammation.

Belkaid, Y., & Hand, T. W. (2014) · Cell · doi:10.1016/j.cell.2014.03.011 · Cited by 5,385 · see citing works

Host-Bacterial Mutualism in the Human Intestine

Bäckhed, F., Ley, R. E., Sonnenburg, J. L., Peterson, D. A., & Gordon, J. I. (2005) · Science · doi:10.1126/science.1104816 · Cited by 5,277 · see citing works

The gut microbiota shapes intestinal immune responses during health and disease

Round, J. L., & Mazmanian, S. K. (2009) · Nature Reviews Immunology · doi:10.1038/nri2515 · Cited by 5,029 · see citing works

Delivery mode shapes the acquisition and structure of the initial microbiota across multiple body habitats in newborns

Dominguez-Bello, M. G., Costello, E. K., Contreras, M., Magris, M., Hidalgo, G., Fierer, N., & Knight, R. (2010) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1002601107 · Cited by 4,774 · see citing works

Host-gut microbiota metabolic interactions

Nicholson, J. K., Holmes, E., Kinross, J., Burcelin, R., Gibson, G., Jia, W., & Pettersson, S. (2012) · Science · doi:10.1126/science.1223813 · Cited by 4,760 · see citing works

Induction of Colonic Regulatory T Cells by Indigenous <i>Clostridium</i> Species

Atarashi, K., Tanoue, T., Shima, T., Imaoka, A., Kuwahara, T., Momose, Y., Cheng, G., Yamasaki, S., Saito, T., Ohba, Y., et al. (2011) · Science · doi:10.1126/science.1198469 · Cited by 3,752 · see citing works

The impact of the gut microbiota on human health: an integrative view

Clemente, J. C., Ursell, L. K., Parfrey, L. W., & Knight, R. (2012) · Cell · doi:10.1016/j.cell.2012.01.035 · Cited by 3,710 · see citing works

A CD4+T-cell subset inhibits antigen-specific T-cell responses and prevents colitis

Groux, H., O’Garra, A., Bigler, M., Rouleau, M., Antonenko, S. V., de Vries, J. E., & Roncarolo, M. G. (1997) · Nature · doi:10.1038/39614 · Cited by 3,588 · see citing works

Dynamics and Stabilization of the Human Gut Microbiome during the First Year of Life

Bäckhed, F., Roswall, J., Peng, Y., Feng, Q., Jia, H., Kovatcheva-Datchary, P., Li, Y., Xia, Y., Xie, H., Zhong, H., et al. (2015) · Cell Host &amp; Microbe · doi:10.1016/j.chom.2015.04.004 · Cited by 3,315 · see citing works

The Effect of Diet on the Human Gut Microbiome: A Metagenomic Analysis in Humanized Gnotobiotic Mice

Turnbaugh, P. J., Ridaura, V. K., Faith, J. J., Rey, F. E., Knight, R., & Gordon, J. I. (2009) · Science Translational Medicine · doi:10.1126/scitranslmed.3000322 · Cited by 3,058 · see citing works

Development of the Human Infant Intestinal Microbiota

Palmer, C., Bik, E. M., DiGiulio, D. B., Relman, D. A., & Brown, P. O. (2007) · PLoS Biology · doi:10.1371/journal.pbio.0050177 · Cited by 2,877 · see citing works

The Placenta Harbors a Unique Microbiome

Aagaard, K., Ma, J., Antony, K. M., Ganu, R., Petrosino, J., & Versalovic, J. (2014) · Science Translational Medicine · doi:10.1126/scitranslmed.3008599 · Cited by 2,494 · see citing works

Inducible Foxp3 ⁺ regulatory T-cell development by a commensal bacterium of the intestinal microbiota

Round, J. L., & Mazmanian, S. K. (2010) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0909122107 · Cited by 2,233 · see citing works

Factors influencing the composition of the intestinal microbiota in early infancy

Penders, J., Thijs, C., Vink, C., Stelma, F. F., Snijders, B., Kummeling, I., van den Brandt, P. A., & Stobberingh, E. E. (2006) · PEDIATRICS · doi:10.1542/peds.2005-2824 · Cited by 2,232 · see citing works

Early infancy microbial and metabolic alterations affect risk of childhood asthma

Arrieta, M., Stiemsma, L. T., Dimitriu, P. A., Thorson, L., Russell, S., Yurist‐Doutsch, S., Kuzeljevic, B., Gold, M. J., Britton, H. M., Lefebvre, D. L., et al. (2015) · Science Translational Medicine · doi:10.1126/scitranslmed.aab2271 · Cited by 1,783 · see citing works

Interactions between commensal intestinal bacteria and the immune system

Macpherson, A. J., & Harris, N. L. (2004) · Nature reviews. Immunology · doi:10.1038/nri1373 · Cited by 1,607 · see citing works

Immune adaptations that maintain homeostasis with the intestinal microbiota

Hooper, L. V., & Macpherson, A. J. (2010) · Nature reviews. Immunology · doi:10.1038/nri2710 · Cited by 1,455 · see citing works

Variation in Microbiome LPS Immunogenicity Contributes to Autoimmunity in Humans

Vatanen, T., Kostic, A. D., d’Hennezel, E., Siljander, H., Franzosa, E. A., Yassour, M., Kolde, R., Vlamakis, H., Arthur, T. D., Hämäläinen, A.-M., et al. (2016) · Cell · doi:10.1016/j.cell.2016.04.007 · Cited by 1,289 · see citing works

Distinct patterns of neonatal gut microflora in infants in whom atopy was and was not developing

Kalliomäki, M., Kirjavainen, P., Eerola, E., Kero, P., Salminen, S., & Isolauri, E. (2001) · Journal of Allergy and Clinical Immunology · doi:10.1067/mai.2001.111237 · Cited by 1,255 · see citing works

Allergy development and the intestinal microflora during the first year of life

Björkstén, B., Sepp, E., Julge, K., Voor, T., & Mikelsaar, M. (2001) · Journal of Allergy and Clinical Immunology · doi:10.1067/mai.2001.118130 · Cited by 1,203 · see citing works

Neonatal gut microbiota associates with childhood multisensitized atopy and T cell differentiation

Fujimura, K. E., Sitarik, A. R., Havstad, S. L., Lin, D. L., Levan, S., Fadrosh, D. W., Panzer, A. R., LaMere, B. J., Rackaityte, E., Lukacs, N. W., et al. (2016) · Nature Medicine · doi:10.1038/nm.4176 · Cited by 1,168 · see citing works

ATP drives lamina propria TH17 cell differentiation

Atarashi, K., Nishimura, J., Shima, T., Umesaki, Y., Yamamoto, M., Onoue, M., Yagita, H., Ishii, N., Evans, R., Honda, K., et al. (2008) · Nature · doi:10.1038/nature07240 · Cited by 1,089 · see citing works

Th17 cell induction by adhesion of microbes to intestinal epithelial cells

Atarashi, K., Tanoue, T., Ando, M., Kamada, N., Nagano, Y., Narushima, S., Suda, W., Imaoka, A., Setoyama, H., Nagamori, T., et al. (2015) · Cell · doi:10.1016/j.cell.2015.08.058 · Cited by 1,071 · see citing works

The requirement of intestinal bacterial flora for the development of an IgE production system fully susceptible to oral tolerance induction

Sudo, N., Sawamura, S., Tanaka, K., Aiba, Y., Kubo, C., & Koga, Y. (1997) · The Journal of Immunology · doi:10.4049/jimmunol.159.4.1739 · Cited by 1,070 · see citing works

Gut microbiota of healthy Canadian infants: profiles by mode of delivery and infant diet at 4 months

Azad, M. B., Konya, T., Maughan, H., Guttman, D. S., Field, C. J., Chari, R. S., Sears, M. R., Becker, A. B., Scott, J. A., & Kozyrskyj, A. L. (2013) · Canadian Medical Association Journal · doi:10.1503/cmaj.121189 · Cited by 953 · see citing works

Is meconium from healthy newborns actually sterile?

Jiménez, E., Marín, M. L., Martı́n, R., Odriozola, J. M., Olivares, M. M., Xaus, J., Fernández, L., & Rodríguez, J. M. (2008) · Research in Microbiology · doi:10.1016/j.resmic.2007.12.007 · Cited by 944 · see citing works

The effects of antibiotics on the microbiome throughout development and alternative approaches for therapeutic modulation

Langdon, A. E., Crook, N., & Dantas, G. A. (2016) · Genome Medicine · doi:10.1186/s13073-016-0294-z · Cited by 917 · see citing works

The human milk microbiome changes over lactation and is shaped by maternal weight and mode of delivery

Cabrera-Rubio, R., Collado, M. C., Laitinen, K., Salminen, S., Isolauri, E., & Mira, A. (2012) · The American Journal of Clinical Nutrition · doi:10.3945/ajcn.112.037382 · Cited by 886 · see citing works

Intestinal Bacterial Colonization Induces Mutualistic Regulatory T Cell Responses

Geuking, M. B., Cahenzli, J., Lawson, M. A. E., Ng, D. C. K., Slack, E., Hapfelmeier, S., McCoy, K. D., & Macpherson, A. J. (2011) · Immunity · doi:10.1016/j.immuni.2011.03.021 · Cited by 840 · see citing works

Extrathymically generated regulatory T cells control mucosal TH2 inflammation

Josefowicz, S. Z., Niec, R. E., Kim, H. Y., Treuting, P. M., Chinen, T., Zheng, Y., Umetsu, D. T., & Rudensky, A. Y. (2012) · Nature · doi:10.1038/nature10772 · Cited by 823 · see citing works

Low diversity of the gut microbiota in infants with atopic eczema

Abrahamsson, T., Jakobsson, H. E., Andersson, A. F., Björkstén, B., Engstrand, L. G., & Jenmalm, M. C. (2011) · Journal of Allergy and Clinical Immunology · doi:10.1016/j.jaci.2011.10.025 · Cited by 816 · see citing works

The role of microbiome in central nervous system disorders

Wang, Y., & Kasper, L. H. (2014) · Brain Behavior and Immunity · doi:10.1016/j.bbi.2013.12.015 · Cited by 803 · see citing works

Microbial Prevalence, Diversity and Abundance in Amniotic Fluid During Preterm Labor: A Molecular and Culture-Based Investigation

DiGiulio, D. B., Romero, R. J., Amogan, H., Kusanovic, J. P., Bik, E. M., Gotsch, F., Kim, C. J., Erez, O., Edwin, S. S., & Relman, D. A. (2008) · PLoS ONE · doi:10.1371/journal.pone.0003056 · Cited by 798 · see citing works

Reduced diversity of the intestinal microbiota during infancy is associated with increased risk of allergic disease at school age

Bisgaard, H., Li, N., Bonnelykke, K., Chawes, B. L. K., Skov, T., Paludan-Müller, G., Stokholm, J., Smith, B., & Krogfelt, K. A. (2011) · Journal of Allergy and Clinical Immunology · doi:10.1016/j.jaci.2011.04.060 · Cited by 786 · see citing works

Xanthomonas citri MinC Oscillates from Pole to Pole to Ensure Proper Cell Division and Shape

Lorenzoni, A. S. G., Dantas, G. C., Bergsma, T., Ferreira, H., & Scheffers, D. (2017) · Frontiers in Microbiology · doi:10.3389/fmicb.2017.01352 · Cited by 727 · 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

Regulation of abdominal adiposity by probiotics (Lactobacillus gasseri SBT2055) in adults with obese tendencies in a randomized controlled trial

Kadooka, Y., Sato, M., Imaizumi, K., Ogawa, A., Ikuyama, K., Akai, Y., Okano, M., Kagoshima, M., & Tsuchida, T. (2010) · European Journal of Clinical Nutrition · doi:10.1038/ejcn.2010.19 · Cited by 700 · see citing works

Isolation of Commensal Bacteria from Umbilical Cord Blood of Healthy Neonates Born by Cesarean Section

Jiménez, E., Fernández, L., Marín, M. L., Martı́n, R., Odriozola, J. M., Nueno‐Palop, C., Narbad, A., Olivares, M. M., Xaus, J., & Rodríguez, J. M. (2005) · Current Microbiology · doi:10.1007/s00284-005-0020-3 · Cited by 681 · see citing works

The gut microbiota: a major player in the toxicity of environmental pollutants?

Claus, S. P., Guillou, H., & Ellero-Simatos, S. (2016) · npj Biofilms and Microbiomes · doi:10.1038/npjbiofilms.2016.3 · Cited by 678 · see citing works

A global survey of changing patterns of food allergy burden in children

Prescott, S. L., Pawankar, R., Allen, K. J., Campbell, D. E., Sinn, J. K. H., Fiocchi, A. G., Ebisawa, M., Sampson, H. A., Beyer, K., & Lee, B. W. (2013) · World Allergy Organization Journal · doi:10.1186/1939-4551-6-21 · Cited by 606 · see citing works

Critical Roles of Activation-Induced Cytidine Deaminase in the Homeostasis of Gut Flora

Fagarasan, S., Muramatsu, M., Suzuki, K., Nagaoka, H., Hiai, H., & Honjo, T. (2002) · Science · doi:10.1126/science.1077336 · Cited by 590 · see citing works

Exposure to endotoxin or other bacterial components might protect against the development of atopy

Mutius, V., Braun‐Fahrländer, Schierl, Riedler, Ehlermann, Maisch, Waser, & Nowak (2000) · Clinical & Experimental Allergy · doi:10.1046/j.1365-2222.2000.00959.x · Cited by 579 · see citing works

Bacteroides in the infant gut consume milk oligosaccharides via mucus-utilization pathways

Marcobal, A., Barboza, M., Sonnenburg, E. D., Pudlo, N., Martens, E. C., Desai, P., Lebrilla, C. B., Weimer, B. C., Mills, D. A., German, J. B., et al. (2011) · Cell Host &amp; Microbe · doi:10.1016/j.chom.2011.10.007 · Cited by 574 · see citing works

Consumption of human milk oligosaccharides by gut-related microbes

Marcobal, A., Barboza, M., Froehlich, J. W., Block, D. E., German, J. B., Lebrilla, C. B., & Mills, D. A. (2010) · Journal of Agricultural and Food Chemistry · doi:10.1021/jf9044205 · Cited by 568 · see citing works

Innate and Adaptive Humoral Responses Coat Distinct Commensal Bacteria with Immunoglobulin A

Bunker, J. J., Flynn, T. M., Koval, J., Shaw, D. G., Meisel, M., McDonald, B. D., Ishizuka, I. E., Dent, A. L., Wilson, P. C., Jabrì, B., et al. (2015) · Immunity · doi:10.1016/j.immuni.2015.08.007 · Cited by 557 · see citing works

The Immunological Components of Human Milk and Their Effect on Immune Development in Infants ,

Field, C. J. (2005) · Journal of Nutrition · doi:10.1093/jn/135.1.1 · Cited by 555 · see citing works

Establishment of intestinal microbiota during early life: a longitudinal, explorative study of a large cohort of Danish infants

Bergström, A., Skov, T. H., Bahl, M. I., Roager, H. M., Christensen, L. B., Ejlerskov, K. T., Mølgaard, C., Michaelsen, K. F., & Licht, T. R. (2014) · Applied and Environmental Microbiology · doi:10.1128/aem.00342-14 · Cited by 532 · see citing works

The subgingival microbial flora during pregnancy

Kornman, K. S., & Loesche, W. J. (1980) · Journal of Periodontal Research · doi:10.1111/j.1600-0765.1980.tb00265.x · Cited by 504 · see citing works

Inhibition of Staphylococcus aureus by the commensal bacteria of human milk

Heikkilä, M., & Saris, P. E. J. (2003) · Journal of Applied Microbiology · doi:10.1046/j.1365-2672.2003.02002.x · Cited by 501 · see citing works

Infant gut microbiota and food sensitization: associations in the first year of life

Azad, M. B., Konya, T., Guttman, D. S., Field, C. J., Sears, M. R., HayGlass, K. T., Mandhane, P. J., Turvey, S. E., Subbarao, P., Becker, A. B., et al. (2015) · Clinical & Experimental Allergy · doi:10.1111/cea.12487 · Cited by 500 · see citing works

High-Throughput Sequencing Reveals the Incomplete, Short-Term Recovery of Infant Gut Microbiota following Parenteral Antibiotic Treatment with Ampicillin and Gentamicin

Fouhy, F., Guinane, C. M., Hussey, S., Wall, R., Ryan, C. A., Dempsey, E. M., Murphy, B. P., Ross, R. P., Fitzgerald, G. F., Stanton, C., et al. (2012) · Antimicrobial Agents and Chemotherapy · doi:10.1128/aac.00789-12 · Cited by 499 · see citing works

Prevalence and Diversity of Microbes in the Amniotic Fluid, the Fetal Inflammatory Response, and Pregnancy Outcome in Women with Preterm Pre‐Labor Rupture of Membranes

DiGiulio, D. B., Romero, R. J., Kusanovic, J. P., Gómez, R., Kim, C. J., Seok, K. S., Gotsch, F., Mazaki‐Tovi, S., Vaisbuch, E., Sanders, K. M., et al. (2010) · American Journal of Reproductive Immunology · doi:10.1111/j.1600-0897.2010.00830.x · Cited by 459 · see citing works

Cesarean Delivery May Affect the Early Biodiversity of Intestinal Bacteria1,

Biasucci, G., Benenati, B., Morelli, L., Bessi, E., & Boehm, G. (2008) · The Journal of Nutrition · doi:10.1093/jn/138.9.1796s · Cited by 458 · see citing works

Early-life gut microbiome composition and milk allergy resolution

Bunyavanich, S., Shen, N., Grishin, A. V., Wood, R. A., Burks, W. A., Dawson, P. M., Jones, S. M., Leung, D. Y. M., Sampson, H. A., Sicherer, S. H., et al. (2016) · Journal of Allergy and Clinical Immunology · doi:10.1016/j.jaci.2016.03.041 · Cited by 432 · see citing works

Early Empiric Antibiotic Use in Preterm Infants Is Associated with Lower Bacterial Diversity and Higher Relative Abundance of Enterobacter

Greenwood, C., Morrow, A. L., Lagomarcino, A. J., Altaye, M., Taft, D. H., Yu, Z., Newburg, D. S., Ward, D. V., & Schibler, K. R. (2014) · The Journal of Pediatrics · doi:10.1016/j.jpeds.2014.01.010 · Cited by 410 · see citing works

Breast-<i>v.</i>formula-feeding: impacts on the digestive tract and immediate and long-term health effects

Le Huërou-Luron, I., Blat, S., & Boudry, G. (2010) · Nutrition Research Reviews · doi:10.1017/s0954422410000065 · Cited by 407 · see citing works

Regulation of the T cell response

Romagnani, S. (2006) · Clinical & Experimental Allergy · doi:10.1111/j.1365-2222.2006.02606.x · Cited by 402 · see citing works

Influence of antibiotic exposure in the early postnatal period on the development of intestinal microbiota

Tanaka, S., Kobayashi, T., Songjinda, P., Tateyama, A., Tsubouchi, M., Kiyohara, C., Shirakawa, T., Sonomoto, K., & Nakayama, J. (2009) · FEMS Immunology & Medical Microbiology · doi:10.1111/j.1574-695x.2009.00553.x · Cited by 396 · see citing works

Determinants of the human infant intestinal microbiota after the introduction of first complementary foods in infant samples from five European centres

Fallani, M., Amarri, S., Uusijärvi, A., Adam, R., Khanna, S., Aguilera, J., Gil, Á., Vieites, J. M., Norin, E. L., Young, D., et al. (2011) · Microbiology · doi:10.1099/mic.0.042143-0 · Cited by 393 · see citing works

Meconium microbiota types dominated by lactic acid or enteric bacteria are differentially associated with maternal eczema and respiratory problems in infants

Gosalbes, M. J., Llop, S., Vallès, Y., Moyá, A., Ballester, F., & Francino, M. P. (2012) · Clinical & Experimental Allergy · doi:10.1111/cea.12063 · Cited by 382 · see citing works

Bacterial Diversity in Meconium of Preterm Neonates and Evolution of Their Fecal Microbiota during the First Month of Life

Moles, L., Gómez, M., Heilig, H. G. H. J., Bustos, G., Fuentes, S., de Vos, W. M., Fernández, L., Rodríguez, J. M., & Jiménez, E. (2013) · PLoS ONE · doi:10.1371/journal.pone.0066986 · Cited by 378 · see citing works

Altered Fecal Microbiota Composition Associated with Food Allergy in Infants

Ling, Z., Li, Z., Liu, X., Cheng, Y., Luo, Y., Tong, X., Li, Y., Wang, Y., Sun, J., Li, L., et al. (2014) · Applied and Environmental Microbiology · doi:10.1128/aem.00003-14 · Cited by 375 · see citing works

A key genetic factor for fucosyllactose utilization affects infant gut microbiota development

Matsuki, T., Yahagi, K., Mori, H., Matsumoto, H., Hara, T., Tajima, S., Ogawa, E., Kodama, H., Yamamoto, K., Yamada, T., et al. (2016) · Nature Communications · doi:10.1038/ncomms11939 · Cited by 375 · see citing works

Assessment of bacterial diversity in breast milk using culture-dependent and culture-independent approaches

Jost, T., Lacroix, C., Braegger, C., & Chassard, C. (2013) · British Journal Of Nutrition · doi:10.1017/s0007114513000597 · Cited by 356 · see citing works

Human milk: a source of more life than we imagine

Jeurink, P. V., van Bergenhenegouwen, J., Jiménez, E., Knippels, L. M. J., Fernández, L., Garssen, J., Knol, J., Rodríguez, J. M., & Martín, R. (2013) · Beneficial Microbes · doi:10.3920/bm2012.0040 · Cited by 354 · see citing works

Dynamics of Infant Gut Microbiota Are Influenced by Delivery Mode and Gestational Duration and Are Associated with Subsequent Adiposity

Dogra, S. K., Sakwińska, O., Soh, S., Ngom‐Bru, C., Brück, W. M., Berger, B. W., Brüssow, H., Lee, Y. S., Yap, F. K. P., Chong, Y. S., et al. (2015) · mBio · doi:10.1128/mbio.02419-14 · Cited by 350 · see citing works

Caesarean section delivery and the risk of allergic disorders in childhood

Renz‐Polster, H., David, M., Buist, A. S., Vollmer, W. M., O’Connor, E., Frazier, E. A., & Wall, M. A. (2005) · Clinical & Experimental Allergy · doi:10.1111/j.1365-2222.2005.02356.x · Cited by 339 · see citing works

Influence of early gut microbiota on the maturation of childhood mucosal and systemic immune responses: Gut microbiota and immune responses

Sjögren, Y. M., Tomicic, S., Lundberg, A., Böttcher, M. F., Björkstén, B., Sverremark‐Ekström, E., & Jenmalm, M. C. (2009) · Clinical &amp; Experimental Allergy · doi:10.1111/j.1365-2222.2009.03326.x · Cited by 337 · see citing works

Mucosal immunity: integration between mother and the breast-fed infant

Brandtzaeg, P. (2003) · Vaccine · doi:10.1016/s0264-410x(03)00338-4 · Cited by 320 · see citing works

Distinct distal gut microbiome diversity and composition in healthy children from Bangladesh and the United States

Lin, A., Bik, E. M., Costello, E. K., Dethlefsen, L., Haque, R., Relman, D. A., & Singh, U. (2013) · PLoS ONE · doi:10.1371/journal.pone.0053838 · Cited by 314 · see citing works

Suppressive effect of Lactobacillus gasseri OLL 2716 (LG21) on Helicobacter pylori infection in humans

Sakamoto, I., Igarashi, M., Kimura, K., Takagi, A., Miwa, T., & Koga, Y. (2001) · Journal of Antimicrobial Chemotherapy · doi:10.1093/jac/47.5.709 · Cited by 304 · see citing works

The role of intestinal microbiota and the immune system.

Purchiaroni, F., Tortora, A., Gabrielli, M., Bertucci, F., Gigante, G. E., Ianiro, G., Ojetti, V., Scarpellini, E., & Gasbarrini, A. (2013) · PubMed · Cited by 297 · see citing works

Diversity in gut bacterial community of school-age children in Asia

Nakayama, J., Watanabe, K., Jiang, J., Matsuda, K., Chao, S.-H., Haryono, P., La-ongkham, O., Sarwoko, M.-A., Sujaya, I. N., Zhao, L., et al. (2015) · Scientific Reports · doi:10.1038/srep08397 · Cited by 287 · see citing works

Extensive Modulation of the Fecal Metagenome in Children With Crohn’s Disease During Exclusive Enteral Nutrition

Quince, C., Ijaz, U. Z., Loman, N. J., Eren, A. M., Saulnier, D. M. A., Russell, J. A., Haig, S., Calus, S., Quick, J., Barclay, A. R., et al. (2015) · The American Journal of Gastroenterology · doi:10.1038/ajg.2015.357 · Cited by 285 · see citing works

Bifidobacteria isolated from infants and cultured on human milk oligosaccharides affect intestinal epithelial function

Chichlowski, M., De Lartigue, G., German, J. B., Raybould, H. E., & Mills, D. A. (2012) · Journal of Pediatric Gastroenterology and Nutrition · doi:10.1097/mpg.0b013e31824fb899 · Cited by 276 · see citing works

Distinct Patterns in Human Milk Microbiota and Fatty Acid Profiles Across Specific Geographic Locations

Kumar, H., du Toit, E., Kulkarni, A., Aakko, J., Linderborg, K. M., Zhang, Y., Nicol, M. P., Isolauri, E., Yang, B., Collado, M. C., et al. (2016) · Frontiers in Microbiology · doi:10.3389/fmicb.2016.01619 · Cited by 271 · see citing works

Immunology of breast milk

Palmeira, P., & Carneiro-Sampaio, M. M. S. (2016) · Revista da Associação Médica Brasileira · doi:10.1590/1806-9282.62.06.584 · Cited by 257 · see citing works

Lactobacilli and Bifidobacteria in Human Breast Milk

Soto, A., Martín, V., Jiménez, E., Mader, I., Rodríguez, J. M., & Fernández, L. (2014) · Journal of Pediatric Gastroenterology and Nutrition · doi:10.1097/mpg.0000000000000347 · Cited by 252 · see citing works

A Molecular Analysis of Fecal and Mucosal Bacterial Communities in Irritable Bowel Syndrome

Codling, C., O’Mahony, L., Shanahan, F., Quigley, E. M. M., & Marchesi, J. R. (2010) · Digestive Diseases and Sciences · doi:10.1007/s10620-009-0934-x · Cited by 243 · see citing works

Comparative Metagenomics and Population Dynamics of the Gut Microbiota in Mother and Infant

Vaishampayan, P., Kuehl, J. V., Froula, J. L., Morgan, J. L., Ochman, H., & Francino, M. P. (2010) · Genome Biology and Evolution · doi:10.1093/gbe/evp057 · Cited by 236 · see citing works

Influence of maternal breast milk ingestion on acquisition of the intestinal microbiome in preterm infants

Gregory, K. E., Samuel, B. S., Houghteling, P. D., Shan, G., Ausubel, F. M., Sadreyev, R. I., & Walker, W. A. (2016) · Microbiome · doi:10.1186/s40168-016-0214-x · Cited by 234 · see citing works

Clinical chorioamnionitis at term I: microbiology of the amniotic cavity using cultivation and molecular techniques

Romero, R. J., Miranda, J., Kusanovic, J. P., Chaiworapongsa, T., Chaemsaithong, P., Martinez, A., Gotsch, F., Dong, Z., Ahmed, A. I., Shaman, M., et al. (2015) · Journal of Perinatal Medicine · doi:10.1515/jpm-2014-0249 · Cited by 232 · see citing works

Anti-Obesity Effect of Lactobacillus gasseri BNR17 in High-Sucrose Diet-Induced Obese Mice

Kang, J.-H., Yun, S.-I., Park, M.-H., Park, J.-H., Jeong, S.-Y., & Park, H.-O. (2013) · PLoS ONE · doi:10.1371/journal.pone.0054617 · Cited by 230 · see citing works

Early Development of the Gut Microbiota and Immune Health

Francino, M. P. (2014) · Pathogens · doi:10.3390/pathogens3030769 · Cited by 220 · see citing works

Comparison of mucosal adhesion and species identification of bifidobacteria isolated from healthy and allergic infants

He, F., Ouwehand, A. C., Isolauri, E., Hashimoto, H., Benno, Y., & Salminen, S. (2001) · FEMS Immunology &amp; Medical Microbiology · doi:10.1111/j.1574-695x.2001.tb01548.x · Cited by 220 · see citing works

Lactobacillus rhamnosusCNCM I-3690 and the commensal bacteriumFaecalibacterium prausnitziiA2-165 exhibit similar protective effects to induced barrier hyper-permeability in mice

Laval, L., Martín, R., Natividad, J. M., Chain, F., Miquel, S., de Maredsous, C. D., Capronnier, S., Sokol, H., Verdu, E. F., Vlieg, J. E. T. V. H., et al. (2014) · Gut Microbes · doi:10.4161/19490976.2014.990784 · Cited by 215 · see citing works

Microbial Succession in the Gut: Directional Trends of Taxonomic and Functional Change in a Birth Cohort of Spanish Infants

Vallès, Y., Artacho, A., Pascual‐García, A., Ferrús, M. L., Gosalbes, M. J., Abellan, J. J., & Francino, M. P. (2014) · PLoS Genetics · doi:10.1371/journal.pgen.1004406 · Cited by 202 · see citing works

Advances in Quantitative Hepcidin Measurements by Time-of-Flight Mass Spectrometry

Swinkels, D. W., Girelli, D., Laarakkers, C. M., Kroot, J. J., Campostrini, N., Kemna, E., & Tjalsma, H. (2008) · PLoS ONE · doi:10.1371/journal.pone.0002706 · Cited by 202 · see citing works

Alterations in the gut microbiotas of children with food sensitization in early life

Chen, C., Chen, K., Kong, M., Chang, H., & Huang, J. (2015) · Pediatric Allergy and Immunology · doi:10.1111/pai.12522 · Cited by 189 · see citing works

Characterizing the composition of intestinal microflora as a prospective treatment target in infant allergic disease

Kirjavainen, P. V., Apostolou, E., Arvola, T., Salminen, S., Gibson, G. R., & Isolauri, E. (2001) · FEMS Immunology & Medical Microbiology · doi:10.1111/j.1574-695x.2001.tb00526.x · Cited by 185 · see citing works

Asthma and the microbiome: defining the critical window in early life

Stiemsma, L. T., & Turvey, S. E. (2017) · Allergy Asthma and Clinical Immunology · doi:10.1186/s13223-016-0173-6 · Cited by 185 · see citing works

Healthy immune response to allergens: T regulatory cells and more

Akdis, M. (2006) · Current Opinion in Immunology · doi:10.1016/j.coi.2006.06.003 · Cited by 174 · see citing works

Physiological and bifidogenic effects of prebiotic supplements in infant formulae

Veereman‐Wauters, G., Staelens, S., Van de Broek, H., Plaskie, K., Wesling, F., Roger, L., McCartney, A., & Assam, P. (2011) · Journal of Pediatric Gastroenterology and Nutrition · doi:10.1097/mpg.0b013e3182139f39 · Cited by 171 · see citing works

Impact of Westernized Diet on Gut Microbiota in Children on Leyte Island

Nakayama, J., Yamamoto, A., Conde, L. A., Higashi, K., Sonomoto, K., Tan, J. D., & Lee, Y. K. (2017) · Frontiers in Microbiology · doi:10.3389/fmicb.2017.00197 · Cited by 163 · see citing works

Risk Factors for Late-Life Cognitive Decline and Variation with Age and Sex in the Sydney Memory and Ageing Study

Lipnicki, D. M., Sachdev, P. S., Crawford, J., Reppermund, S., Kochan, N. A., Trollor, J. N., Draper, B., Slavin, M. J., Kang, K., Lux, O., et al. (2013) · PLoS ONE · doi:10.1371/journal.pone.0065841 · Cited by 149 · see citing works

Prevalence of allergy, patterns of allergic sensitization and allergy risk factors in rural and urban children

Majkowska–Wojciechowska, B., Pełka, J., Korzon, L., Kozłowska, A., Kaczała, M., Jarzębska, M., Gwardys, T., & Kowalski, M. L. (2007) · Allergy · doi:10.1111/j.1398-9995.2007.01457.x · Cited by 148 · see citing works

Anti-obesity effect of Lactobacillus gasseri SBT2055 accompanied by inhibition of pro-inflammatory gene expression in the visceral adipose tissue in diet-induced obese mice

Miyoshi, M., Ogawa, A., Higurashi, S., & Kadooka, Y. (2013) · European Journal of Nutrition · doi:10.1007/s00394-013-0568-9 · Cited by 145 · see citing works

Breast Milk Fatty Acids, Eicosanoids, and Cytokines in Mothers with and without Allergic Disease

Laiho, K., Lampi, A., Hämäläinen, M., Moilanen, E., Piironen, V. I., Arvola, T., Syrjänen, S., & Isolauri, E. (2003) · Pediatric Research · doi:10.1203/01.pdr.0000055778.58807.c8 · Cited by 124 · see citing works

Breast-feeding, infant formulas, and the immune system

Hanson, L. Å., Korotkova, M., & Telemo, E. (2003) · Annals of Allergy Asthma & Immunology · doi:10.1016/s1081-1206(10)61662-6 · Cited by 120 · see citing works

Mucosal macrophages and the regulation of immune responses in the intestine

Platt, A. M., & Mowat, A. M. (2008) · Immunology Letters · doi:10.1016/j.imlet.2008.05.009 · Cited by 117 · see citing works

Development of Functional Foods

MITSUOKA, T. (2014) · Bioscience of Microbiota Food and Health · doi:10.12938/bmfh.33.117 · Cited by 111 · see citing works

Gut resistome development in healthy twin pairs in the first year of life

Moore, A. M., Ahmadi, S., Patel, S., Gibson, M. K., Wang, B., Ndao, I. M., Deych, E., Shannon, W., Tarr, P. I., Warner, B. B., et al. (2015) · Microbiome · doi:10.1186/s40168-015-0090-9 · Cited by 109 · see citing works

Lacto-N-biosidase Encoded by a Novel Gene of Bifidobacterium longum Subspecies longum Shows Unique Substrate Specificity and Requires a Designated Chaperone for Its Active Expression

Sakurama, H., Kiyohara, M., Wada, J., Honda, Y., Yamaguchi, M., Fukiya, S., Yokota, A., Ashida, H., Kumagai, H., Kitaoka, M., et al. (2013) · Journal of Biological Chemistry · doi:10.1074/jbc.m113.484733 · Cited by 104 · see citing works

The anti-obesity effects ofLactobacillus caseistrain Shirota versus Orlistat on high fat diet-induced obese rats

Karimi, G., Sabran, M. R., Jamaluddin, R., Parvaneh, K., Mohtarrudin, N., Ahmad, Z., Khaza’ai, H., & Khodavandi, A. (2015) · Food & Nutrition Research · doi:10.3402/fnr.v59.29273 · Cited by 103 · see citing works

Microbial Community of Healthy Thai Vegetarians and Non-Vegetarians, Their Core Gut Microbiota, and Pathogen Risk

Ruengsomwong, S., La-ongkham, O., Jiang, J., Wannissorn, B., Nakayama, J., & Nitisinprasert, S. (2016) · Journal of Microbiology and Biotechnology · doi:10.4014/jmb.1603.03057 · Cited by 102 · see citing works

Distinct Pattern of Commensal Gut Microbiota in Toddlers with Eczema

Mah, K. W., Björkstén, B., Lee, B. W., Bever, H. P. V., Shek, L. P., Tan, T. N., Lee, Y. K., & Chua, K. Y. (2006) · International Archives of Allergy and Immunology · doi:10.1159/000092555 · Cited by 101 · see citing works

Cesarean delivery is associated with celiac disease but not inflammatory bowel disease in children

Decker, E., Hornef, M. W., & Stockinger, S. (2011) · Gut Microbes · doi:10.4161/gmic.2.2.15414 · Cited by 95 · see citing works

Rate of establishing the gut microbiota in infancy has consequences for future health

Dogra, S. K., Sakwińska, O., Soh, S., Ngom‐Bru, C., Brück, W. M., Berger, B. W., Brüssow, H., Karnani, N., Lee, Y. S., Yap, F. K. P., et al. (2015) · Gut Microbes · doi:10.1080/19490976.2015.1078051 · Cited by 93 · see citing works

The microbiome and development of allergic disease

Lynch, S. V., & Boushey, H. A. (2016) · Current Opinion in Allergy &amp; Clinical Immunology · doi:10.1097/aci.0000000000000255 · Cited by 92 · see citing works

Faecal short chain fatty acid pattern and allergy in early childhood

Sandin, A., Bråbäck, L., Norin, E. L., & Björkstén, B. (2009) · Acta Paediatrica · doi:10.1111/j.1651-2227.2008.01215.x · Cited by 90 · see citing works

Microbiome and food allergy

Blázquez, A. B., & Berin, M. C. (2016) · Translational research · doi:10.1016/j.trsl.2016.09.003 · Cited by 90 · see citing works

Aberrant structures of fecal bacterial community in allergic infants profiled by 16S rRNA gene pyrosequencing

Nakayama, J., Kobayashi, T., Tanaka, S., Korenori, Y., Tateyama, A., Sakamoto, N., Kiyohara, C., Shirakawa, T., & Sonomoto, K. (2011) · FEMS Immunology & Medical Microbiology · doi:10.1111/j.1574-695x.2011.00872.x · Cited by 87 · see citing works

Clostridia isolated from the feces of infants during the first year of life

Stark, P. L., & Lee, A. (1982) · The Journal of Pediatrics · doi:10.1016/s0022-3476(82)80430-7 · Cited by 80 · see citing works

The allergy‐protective properties of Acinetobacter lwoffii F78 are imparted by its lipopolysaccharide

Debarry, J., Hanuszkiewicz, A., Stein, K., Holst, O., & Heine, H. (2009) · Allergy · doi:10.1111/j.1398-9995.2009.02253.x · Cited by 77 · see citing works

Immune Factors in Breast Milk and the Development of Atopic Disease

Iyengar, S. R., & Walker, W. A. (2012) · Journal of Pediatric Gastroenterology and Nutrition · doi:10.1097/mpg.0b013e3182617a9d · Cited by 69 · see citing works

Signatures in the gut microbiota of Japanese infants who developed food allergies in early childhood

Tanaka, M., Korenori, Y., Washio, M., Kobayashi, T., Momoda, R., Kiyohara, C., Kuroda, A., Saito, Y., Sonomoto, K., & Nakayama, J. (2017) · FEMS Microbiology Ecology · doi:10.1093/femsec/fix099 · Cited by 66 · see citing works

The Impact of the Gut Microbiota on Humoral Immunity to Pathogens and Vaccination in Early Infancy

Nguyen, Q. N., Himes, J. E., Martinez, D. R., & Permar, S. R. (2016) · PLoS Pathogens · doi:10.1371/journal.ppat.1005997 · Cited by 64 · see citing works

Early gut colonization by Bifidobacterium breve and B. catenulatum differentially modulates eczema risk in children at high risk of developing allergic disease

Ismail, I. H., Boyle, R. J., Licciardi, P. V., Oppedisano, F., Lahtinen, S. J., Robins-Browne, R. M., & Tang, M. L. K. (2016) · Pediatric Allergy and Immunology · doi:10.1111/pai.12646 · Cited by 58 · see citing works

Prevention of food allergy – Early dietary interventions

Toit, G. D., Foong, R.-X. M., & Lack, G. (2016) · Allergology International · doi:10.1016/j.alit.2016.08.001 · Cited by 51 · see citing works

The role of IL-10 in microbiome-associated immune modulation and disease tolerance

Levast, B., Li, Z., & Madrenas, J. (2014) · Cytokine · doi:10.1016/j.cyto.2014.11.027 · Cited by 42 · see citing works

Mouse Models for Assessing the Protective Efficacy ofLactobacillus gasseri SBT 2055 againstHelicobacter suisInfection Associated with the Development of Gastric Mucosa‐Associated Lymphoid Tissue Lymphoma

Matsui, H., Takahashi, T., Øverby, A., Murayama, S. Y., Yoshida, H., Yamamoto, Y., Nishiyama, K., Seto, Y., Takahashi, T., Mukai, T., et al. (2015) · Helicobacter · doi:10.1111/hel.12203 · Cited by 29 · see citing works

Use of gnotobiotic mice to identify and characterize key microbes responsible for the development of the intestinal immune system

Umesaki, Y. (2014) · Proceedings of the Japan Academy Series B · doi:10.2183/pjab.90.313 · Cited by 28 · see citing works

Microbiome/microbiota and allergies

Inoue, Y., & Shimojo, N. (2014) · Seminars in Immunopathology · doi:10.1007/s00281-014-0453-5 · Cited by 23 · see citing works

Transcriptomic and Metabolomic Analysis Revealed Multifaceted Effects of Phage Protein Gp70.1 on Pseudomonas aeruginosa

Zhao, X., Chen, C., Jiang, X., Shen, W., Huang, G., Le, S., Lu, S., Zou, L., Ni, Q., Li, M., et al. (2016) · Frontiers in Microbiology · doi:10.3389/fmicb.2016.01519 · Cited by 22 · see citing works

Canadian Society of Allergy and Clinical Immunology annual scientific meeting 2016

and the Canadian Healthy Infant Longitudinal Development Study Investigators, Alsayegh, M. A., Alshamali, H., Khadada, M., Ciccolini, A., Ellis, A. K., Quint, D. J., Powley, W. M., Lee, L. A., Fiteih, Y., et al. (2017) · Allergy Asthma and Clinical Immunology · doi:10.1186/s13223-017-0192-y · Cited by 8 · see citing works

Effects of Probiotics on the Immune System and Allergic Diseases

Shimojo, N., Suzuki, S., Campos‐Alberto, E., & Kohno, Y. (2005) · Allergology International · doi:10.2332/allergolint.54.515 · Cited by 4 · see citing works

What is the Healthy Gut Microbiota Composition? A Changing Ecosystem across Age, Environment, Diet, and Diseases

Rinninella, E., Raoul, P., Cintoni, M., Franceschi, F., Miggiano, G. A. D., Gasbarrini, A., & Mele, M. C. (2019) · Microorganisms · doi:10.3390/microorganisms7010014 · Cited by 3,462 · see citing works

The gut microbiota in anxiety and depression—A systematic review

Simpson, C. A., Diaz-Arteche, C., Eliby, D., Schwartz, O. S., Simmons, J. G., & Cowan, C. S. M. (2021) · Clinical Psychology Review · doi:10.1016/j.cpr.2020.101943 · Cited by 912 · see citing works

Effect of Diet on the Gut Microbiota: Rethinking Intervention Duration

Leeming, E. R., Johnson, A. J., Spector, T. D., & Le Roy, C. I. (2019) · Nutrients · doi:10.3390/nu11122862 · Cited by 817 · see citing works

Gut Microbiota and Obesity: A Role for Probiotics

Abenavoli, L., Scarpellini, E., Colica, C., Boccuto, L., Salehi, B., Sharifi-Rad, J., Aiello, V., Romano, B., De Lorenzo, A., Izzo, A. A., et al. (2019) · Nutrients · doi:10.3390/nu11112690 · Cited by 615 · see citing works

Impact of gut microbiome on skin health: gut-skin axis observed through the lenses of therapeutics and skin diseases

Mahmud, M. R., Akter, S., Tamanna, S. K., Mazumder, L., Esti, I. Z., Banerjee, S., Akter, S., Hasan, M. R., Acharjee, M., Hossain, M. S., et al. (2022) · Gut Microbes · doi:10.1080/19490976.2022.2096995 · Cited by 498 · see citing works

Beneficial Effects of Dietary Polyphenols on Gut Microbiota and Strategies to Improve Delivery Efficiency

Singh, A. K., Cabral, C., Kumar, R., Ganguly, R., Rana, H. K., Gupta, A., Lauro, M. R., Carbone, C., Reis, F., & Pandey, A. K. (2019) · Nutrients · doi:10.3390/nu11092216 · Cited by 444 · see citing works

Precision Nutrition and the Microbiome, Part I: Current State of the Science

Mills, S., Stanton, C., Lane, J. A., Smith, G., & Ross, R. P. (2019) · Nutrients · doi:10.3390/nu11040923 · Cited by 406 · see citing works

Interaction of the microbiota with the human body in health and diseases

Altveş, S., Yıldız, H. K., & Vural, H. C. (2019) · Bioscience of Microbiota Food and Health · doi:10.12938/bmfh.19-023 · Cited by 389 · see citing works

Pathogenesis of allergic diseases and implications for therapeutic interventions

Wang, J., Zhou, Y., Zhang, H., Hu, L., Liu, J., Wang, L., Wang, T., Zhang, H., Cong, L., & Wang, Q. (2023) · Signal Transduction and Targeted Therapy · doi:10.1038/s41392-023-01344-4 · Cited by 415 · see citing works

The mutual interplay of gut microbiota, diet and human disease

Illiano, P., Brambilla, R., & Parolini, C. (2020) · FEBS Journal · doi:10.1111/febs.15217 · Cited by 331 · see citing works

Exploring the emerging role of the microbiome in cancer immunotherapy

Fessler, J. L., Matson, V. Z., & Gajewski, T. F. (2019) · Journal for ImmunoTherapy of Cancer · doi:10.1186/s40425-019-0574-4 · Cited by 318 · see citing works

Microbiome of the Skin and Gut in Atopic Dermatitis (AD): Understanding the Pathophysiology and Finding Novel Management Strategies

Kim, J. E., & Kim, H. S. (2019) · Journal of Clinical Medicine · doi:10.3390/jcm8040444 · Cited by 244 · see citing works

Vitamin A and vitamin D regulate the microbial complexity, barrier function, and the mucosal immune responses to ensure intestinal homeostasis

Cantorna, M. T., Snyder, L. M., & Arora, J. (2019) · Critical Reviews in Biochemistry and Molecular Biology · doi:10.1080/10409238.2019.1611734 · Cited by 241 · see citing works

Thinking bigger: how early-life environmental exposures shape the gut microbiome and influence the development of asthma and allergic disease

Sbihi, H., Boutin, R. C., Cutler, C., Suen, M., Finlay, B. B., & Turvey, S. E. (2019) · Allergy · doi:10.1111/all.13812 · Cited by 199 · see citing works

Maternal exposures and the infant gut microbiome: a systematic review with meta-analysis

Grech, A. M., Collins, C. E., Holmes, A. J., Lal, R., Duncanson, K., Taylor, R., & Gordon, A. (2021) · Gut Microbes · doi:10.1080/19490976.2021.1897210 · Cited by 189 · see citing works

Beneficial Effects of Phenolic Compounds on Gut Microbiota and Metabolic Syndrome

Kasprzak‐Drozd, K., Oniszczuk, T., Stasiak, M., & Oniszczuk, A. (2021) · International Journal of Molecular Sciences · doi:10.3390/ijms22073715 · Cited by 193 · see citing works

Postbiotics: From emerging concept to application

Aggarwal, S., Sabharwal, V., Kaushik, P., Joshi, A., Aayushi, A., & Suri, M. (2022) · Frontiers in Sustainable Food Systems · doi:10.3389/fsufs.2022.887642 · Cited by 181 · see citing works

Circular bioeconomy and integrated biorefinery in the production of xylooligosaccharides from lignocellulosic biomass: A review

Pinales‐Márquez, C. D., Rodríguez‐Jasso, R. M., Araújo, R. G., Loredo‐Treviño, A., Nabarlatz, D., Gullón, B., & Ruíz, H. A. (2021) · Industrial Crops and Products · doi:10.1016/j.indcrop.2021.113274 · Cited by 169 · see citing works

The Prebiotic and Probiotic Properties of Human Milk: Implications for Infant Immune Development and Pediatric Asthma

Moossavi, S., Miliku, K., Sepehri, S., Khafipour, E., & Azad, M. B. (2018) · Frontiers in Pediatrics · doi:10.3389/fped.2018.00197 · Cited by 154 · see citing works

Breastfeeding Contributes to Physiological Immune Programming in the Newborn

Camacho‐Morales, A., Caba, M., García‐Juárez, M., Caba‐Flores, M. D., Viveros-Contreras, R., & Valenzuela, C. (2021) · Frontiers in Pediatrics · doi:10.3389/fped.2021.744104 · Cited by 156 · see citing works

Effects of Fish n-3 PUFAs on Intestinal Microbiota and Immune System

Parolini, C. (2019) · Marine Drugs · doi:10.3390/md17060374 · Cited by 154 · see citing works

The role of microbiome in rheumatoid arthritis treatment

Bodkhe, R., Balakrishnan, B., & Taneja, V. (2019) · Therapeutic Advances in Musculoskeletal Disease · doi:10.1177/1759720x19844632 · Cited by 146 · see citing works

The microbiome: An emerging key player in aging and longevity

Kim, M., & Benayoun, B. A. (2020) · Translational Medicine of Aging · doi:10.1016/j.tma.2020.07.004 · Cited by 142 · see citing works

Factors influencing the gut microbiome in children: from infancy to childhood

Kumbhare, S. V., Patangia, D. V., Patil, R. H., Shouche, Y. S., & Patil, N. P. (2019) · Journal of Biosciences · doi:10.1007/s12038-019-9860-z · Cited by 143 · see citing works

Host/microbiota interactions in health and diseases—Time for mucosal microbiology!

Daniel, N., Lécuyer, E., & Chassaing, B. (2021) · Mucosal Immunology · doi:10.1038/s41385-021-00383-w · Cited by 141 · see citing works

Postbiotics: Functional Food Materials and Therapeutic Agents for Cancer, Diabetes, and Inflammatory Diseases

Gurunathan, S., Pratheep, T., & Kim, J. (2023) · Foods · doi:10.3390/foods13010089 · Cited by 139 · see citing works

The meconium microbiota shares more features with the amniotic fluid microbiota than the maternal fecal and vaginal microbiota

He, Q., Kwok, L., Xi, X., Zhong, Z., Ma, T., Xu, H., Meng, H., Zhao, F., & Zhang, H. (2020) · Gut Microbes · doi:10.1080/19490976.2020.1794266 · Cited by 134 · see citing works

Widespread sex dimorphism in aging and age-related diseases

Sampathkumar, N. K., Bravo, J. I., Chen, Y., Danthi, P. S., Donahue, E. K., Lai, R. W., Lu, R. J., Randall, L. T., Vinson, N. M., & Benayoun, B. A. (2019) · Human Genetics · doi:10.1007/s00439-019-02082-w · Cited by 127 · see citing works

The microbial ecology of Escherichia coli in the vertebrate gut

Foster-Nyarko, E., & Pallen, M. J. (2022) · FEMS Microbiology Reviews · doi:10.1093/femsre/fuac008 · Cited by 146 · see citing works

Colonization and development of the gut microbiome in calves

Du, Y., Gao, Y., Hu, M., Hou, J., Yang, L., Wang, X., Du, W., Liu, J., & Xu, Q. (2023) · Journal of Animal Science and Biotechnology/Journal of animal science and biotechnology · doi:10.1186/s40104-023-00856-x · Cited by 129 · see citing works

Gut Microbiota and Mucosal Immunity in the Neonate

Dzidic, M., Boix-Amorós, A., Selma‐Royo, M., Mira, Á., & Collado, M. C. (2018) · Medical Sciences · doi:10.3390/medsci6030056 · Cited by 130 · see citing works

Engineering the microbiome for animal health and conservation

Song, S. J., Woodhams, D. C., Martino, C., Allaband, C., Mu, A., Javorschi-Miller-Montgomery, S., Suchodolski, J. S., & Knight, R. D. (2019) · Experimental Biology and Medicine · doi:10.1177/1535370219830075 · Cited by 127 · see citing works

Specific class of intrapartum antibiotics relates to maturation of the infant gut microbiota: a prospective cohort study

Coker, M. O., Hoen, A., Dade, E. F., Lundgren, S., Li, Z., Wong, A., Zens, M. S., Palys, T. J., Morrison, H., Sogin, M., et al. (2019) · BJOG An International Journal of Obstetrics & Gynaecology · doi:10.1111/1471-0528.15799 · Cited by 123 · see citing works

The role of the gut microbiota in health and cardiovascular diseases

Wang, L., Wang, S., Zhang, Q., He, C., Fu, C., & Wei, Q. (2022) · Molecular Biomedicine · doi:10.1186/s43556-022-00091-2 · Cited by 124 · see citing works

Polyphenols: Secondary Metabolites with a Biological Impression

Bolat, E., Sarıtaş, S., Duman, H., Eker, F., Akdaşçi, E., Karav, S., & Witkowska, A. M. (2024) · Nutrients · doi:10.3390/nu16152550 · Cited by 127 · see citing works

Emergence and significance of carbohydrate-specific antibodies

Kappler, K., & Hennet, T. (2020) · Genes and Immunity · doi:10.1038/s41435-020-0105-9 · Cited by 113 · see citing works

Role of mucosal immunity and epithelial–vascular barrier in modulating gut homeostasis

Sabatino, A. D., Santacroce, G., Rossi, C. M., Broglio, G., & Lenti, M. V. (2023) · Internal and Emergency Medicine · doi:10.1007/s11739-023-03329-1 · Cited by 116 · see citing works

Bioactive Compounds in Infant Formula and Their Effects on Infant Nutrition and Health: A Systematic Literature Review

de Almeida, C. C., Pereira, B. F. D. M., Leandro, K. C., da Costa, M. P., Spisso, B. F., & Conte‐Júnior, C. A. (2021) · International Journal of Food Science · doi:10.1155/2021/8850080 · Cited by 113 · see citing works

Short-Chain Fatty Acids Augment Differentiation and Function of Human Induced Regulatory T Cells

Hu, M., Alhamwe, B. A., Santner‐Nanan, B., Miethe, S., Harb, H., Renz, H. E., Potaczek, D. P., & Nanan, R. K. H. (2022) · International Journal of Molecular Sciences · doi:10.3390/ijms23105740 · Cited by 106 · see citing works

A complete guide to human microbiomes: Body niches, transmission, development, dysbiosis, and restoration

Reynoso-García, J., Miranda-Santiago, A. E., Meléndez-Vázquez, N. M., Acosta-Pagán, K. T., Rosado, M. R. S., Díaz-Rivera, J., Rosado-Quiñones, A. M., Acevedo-Márquez, L., Cruz-Roldán, L., Tosado-Rodríguez, E. L., et al. (2022) · Frontiers in Systems Biology · doi:10.3389/fsysb.2022.951403 · Cited by 106 · see citing works

Impact of outdoor nature-related activities on gut microbiota, fecal serotonin, and perceived stress in preschool children: the Play&Grow randomized controlled trial

Sobko, T., Liang, S., Cheng, W. H. G., & Tun, H. M. (2020) · Scientific Reports · doi:10.1038/s41598-020-78642-2 · Cited by 102 · see citing works

The Human Gut Phageome: Origins and Roles in the Human Gut Microbiome

Townsend, E. M., Kelly, L., Muscatt, G., Box, J. D., Hargraves, N., Lilley, D., & Jameson, E. (2021) · Frontiers in Cellular and Infection Microbiology · doi:10.3389/fcimb.2021.643214 · Cited by 102 · see citing works

Maternal and Perinatal Factors Associated with the Human Milk Microbiome

Demmelmair, H., Jiménez, E., Collado, M. C., Salminen, S., & McGuire, M. K. (2020) · Current Developments in Nutrition · doi:10.1093/cdn/nzaa027 · Cited by 99 · see citing works

The Importance of Lactose in the Human Diet: Outcomes of a Mexican Consensus Meeting

Romero‐Velarde, E., Delgado‐Franco, D., García-Gutiérrez, M., Gurrola‐Díaz, C. M., Larrosa‐Haro, A., Montijo-Barrios, É., Muskiet, F. A. J., Vargas‐Guerrero, B., & Geurts, J. M. W. (2019) · Nutrients · doi:10.3390/nu11112737 · Cited by 100 · see citing works

Epigenetics in depression and gut-brain axis: A molecular crosstalk

Begum, N., Mandhare, A., Tryphena, K. P., Srivastava, S., Shaikh, M. F., Singh, S. B., & Khatri, D. K. (2022) · Frontiers in Aging Neuroscience · doi:10.3389/fnagi.2022.1048333 · Cited by 99 · see citing works

An updated overview on the relationship between human gut microbiome dysbiosis and psychiatric and psychological disorders

Borrego-Ruiz, A., & Borrego, J. J. (2023) · Progress in Neuro-Psychopharmacology and Biological Psychiatry · doi:10.1016/j.pnpbp.2023.110861 · Cited by 106 · see citing works

The Role of Diet and Nutritional Interventions for the Infant Gut Microbiome

Catassi, G. N., Aloi, M., Giorgio, V., Gasbarrini, A., Cammarota, G., & Ianiro, G. (2024) · Nutrients · doi:10.3390/nu16030400 · Cited by 88 · see citing works

The Interplay between Immune System and Microbiota in Inflammatory Bowel Disease: A Narrative Review

Aldars‐García, L., Marín, A. C., Chaparro, M., & Gisbert, J. P. (2021) · International Journal of Molecular Sciences · doi:10.3390/ijms22063076 · Cited by 89 · see citing works

The Brain-Gut-Microbiome System: Pathways and Implications for Autism Spectrum Disorder

Chernikova, M. A., Flores, G. D., Kilroy, E., Labus, J. S., Mayer, E. A., & Aziz‐Zadeh, L. (2021) · Nutrients · doi:10.3390/nu13124497 · Cited by 86 · see citing works

Metabolomics Signatures of Aging: Recent Advances

Adav, S. S., & Wang, Y. (2021) · Aging and Disease · doi:10.14336/ad.2020.0909 · Cited by 85 · see citing works

Biology of human milk oligosaccharides: From basic science to clinical evidence

Sprenger, N., Tytgat, H. L. P., Binia, A., Austin, S., & Singhal, A. (2022) · Journal of Human Nutrition and Dietetics · doi:10.1111/jhn.12990 · Cited by 89 · see citing works

Lactation as a programming window for metabolic syndrome

Picó, C., Reis, F., Egas, C., Mathias, P. C. D. F., & Matafome, P. N. (2020) · European Journal of Clinical Investigation · doi:10.1111/eci.13482 · Cited by 83 · see citing works

Dietary polyphenols and human health: sources, biological activities, nutritional and immunological aspects, and bioavailability– a comprehensive review

Saad, A. M., Mohammed, D. M., Alkafaas, S. S., Ghosh, S. B., Negm, S. H., Salem, H. M., Fahmy, M. A., Semary, H. E., Ibrahim, E. H., AbuQamar, S. F., et al. (2025) · Frontiers in Immunology · doi:10.3389/fimmu.2025.1653378 · Cited by 97 · see citing works

Gut microbiomes from Gambian infants reveal the development of a non-industrialized Prevotella-based trophic network

de Goffau, M. C., Jallow, A. T., Sanyang, C., Prentice, A. M., Meagher, N., Price, D. J., Revill, P. A., Parkhill, J., Pereira, D. I. A., & Wagner, J. (2021) · Nature Microbiology · doi:10.1038/s41564-021-01023-6 · Cited by 82 · see citing works

Gut dysbiosis and age-related neurological diseases; an innovative approach for therapeutic interventions

Holmes, A., Finger, C. E., Morales‐Scheihing, D., Lee, J., & McCullough, L. D. (2020) · Translational research · doi:10.1016/j.trsl.2020.07.012 · Cited by 87 · see citing works

Lactobacillus reuteri Stimulates Intestinal Epithelial Proliferation and Induces Differentiation into Goblet Cells in Young Chickens

Xie, S., Zhao, S., Jiang, L., Lu, L., Yang, Q., & Yu, Q. (2019) · Journal of Agricultural and Food Chemistry · doi:10.1021/acs.jafc.9b06256 · Cited by 81 · see citing works

Associations between habitual diet, metabolic disease, and the gut microbiota using latent Dirichlet allocation

Breuninger, 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

Infant gut microbiome is enriched with Bifidobacterium longum ssp. infantis in Old Order Mennonites with traditional farming lifestyle

Seppo, A., Bu, K., Jumabaeva, M., Thakar, J., Choudhury, R. A., Yonemitsu, C., Bode, L., Martina, C. A., Allen, M., Tamburini, S., et al. (2021) · Allergy · doi:10.1111/all.14877 · Cited by 80 · see citing works

Beneficial microbiota. Probiotics and pharmaceutical products in functional nutrition and medicine

Novik, G. I., & Savich, V. V. (2019) · Microbes and Infection · doi:10.1016/j.micinf.2019.06.004 · Cited by 77 · see citing works

Metagenomic insights of the infant microbiome community structure and function across multiple sites in the United States

Casaburi, G., Duar, R. M., Brown, H. K., Mitchell, R. D., Kazi, S., Chew, S., Cagney, O., Flannery, R. L., Sylvester, K. G., Frese, S. A., et al. (2021) · Scientific Reports · doi:10.1038/s41598-020-80583-9 · Cited by 75 · see citing works

Dynamic distribution of gut microbiota during embryonic development in chicken

Akinyemi, F. T., Ding, J., Zhou, H., Xu, K., He, C., Han, C., Zheng, Y., Luo, H., Yang, K., Gu, C., et al. (2020) · Poultry Science · doi:10.1016/j.psj.2020.06.016 · Cited by 75 · see citing works

Comparative Analysis of the Microbiome across the Gut–Skin Axis in Atopic Dermatitis

Park, D. H., Kim, J. W., Park, H., & Hahm, D. (2021) · International Journal of Molecular Sciences · doi:10.3390/ijms22084228 · Cited by 76 · see citing works

The role of antimicrobial treatment during pregnancy on the neonatal gut microbiome and the development of atopy, asthma, allergy and obesity in childhood

Milliken, S., Allen, R. M., & Lamont, R. (2019) · Expert Opinion on Drug Safety · doi:10.1080/14740338.2019.1579795 · Cited by 74 · see citing works

The Nidobiome: A Framework for Understanding Microbiome Assembly in Neonates

Campos-Cerda, F., & Bohannan, B. J. M. (2020) · Trends in Ecology & Evolution · doi:10.1016/j.tree.2020.03.007 · Cited by 72 · see citing works

The Role of the Microbiome in Food Allergy: A Review

Nance, C. L., Deniskin, R., Diaz, V. C., Paul, M., Anvari, S., & Anagnostou, A. (2020) · Children · doi:10.3390/children7060050 · Cited by 71 · see citing works

Prospective views for whey protein and/or resistance training against age-related sarcopenia

Liao, Y., Peng, Z., Chen, L., Zhang, Y., Cheng, Q., Nüssler, A. K., Bao, W., Liu, L., & Yang, W. (2019) · Aging and Disease · doi:10.14336/ad.2018.0325 · Cited by 68 · see citing works

Potential Impacts of Prebiotics and Probiotics on Cancer Prevention

Samanta, S. (2020) · Anti-Cancer Agents in Medicinal Chemistry · doi:10.2174/1871520621999201210220442 · Cited by 72 · see citing works

The gut microbiota is associated with the small intestinal paracellular permeability and the development of the immune system in healthy children during the first two years of life

Kaczmarczyk, M., Löber, U., Adamek, K., Węgrzyn, D., Skonieczna‐Żydecka, K., Malinowski, D., Łoniewski, I., Markó, L., Ulas, T., Forslund, S. K., et al. (2021) · Journal of Translational Medicine · doi:10.1186/s12967-021-02839-w · Cited by 68 · see citing works

Early alterations in a mouse model of Rett syndrome: the GABA developmental shift is abolished at birth

Lozovaya, N., Nardou, R., Tyzio, R., Chiesa, M., Pons-Bennaceur, A., Eftekhari, S., Bui, T.-T., Billon-Grand, M., Rasero, J., Bonifazi, P., et al. (2019) · Scientific Reports · doi:10.1038/s41598-019-45635-9 · Cited by 68 · see citing works

Ruminococcus gnavus ameliorates atopic dermatitis by enhancing Treg cell and metabolites in BALB/c mice

Ahn, J.-W., Lee, S., Kim, B., Nam, M. H., Ahn, Y. G., Park, Y. M., Jeong, S., Park, M. J., Song, K. B., Lee, S., et al. (2021) · Pediatric Allergy and Immunology · doi:10.1111/pai.13678 · Cited by 68 · see citing works

Risk Factors for Infant Colonization by Hypervirulent CC17 Group B Streptococcus: Toward the Understanding of Late-onset Disease

Tazi, A., Plainvert, C., Anselem, O., Ballon, M., Marcou, V., Seco, A., Alaoui, F. E., Joubrel, C., Helali, N. E., Falloukh, E., et al. (2019) · Clinical Infectious Diseases · doi:10.1093/cid/ciz033 · Cited by 67 · see citing works

Effect of Probiotics on Respiratory Tract Allergic Disease and Gut Microbiota

Huang, J., Zhang, J., Wang, X., Jin, Z., Zhang, P., Su, H., & Sun, X. (2022) · Frontiers in Nutrition · doi:10.3389/fnut.2022.821900 · Cited by 74 · see citing works

Disordered development of gut microbiome interferes with the establishment of the gut ecosystem during early childhood with atopic dermatitis

Lee, M.-J., Park, Y. M., Kim, B., Tae, I. H., Kim, N.-E., Pranata, M., Kim, T., Won, S., Kang, N. J., Lee, D., et al. (2022) · Gut Microbes · doi:10.1080/19490976.2022.2068366 · Cited by 66 · see citing works

The edible plant microbiome: evidence for the occurrence of fruit and vegetable bacteria in the human gut

Wicaksono, W. A., Cernava, T., Wassermann, B., Abdelfattah, A., Soto-Girón, M. J., Toledo, G. V., Virtanen, S. M., Knip, M., Hyöty, H., & Berg, G. (2023) · Gut Microbes · doi:10.1080/19490976.2023.2258565 · Cited by 66 · see citing works

Infant Complementary Feeding of Prebiotics for the Microbiome and Immunity

McKeen, S., Young, W., Mullaney, J. A., Fraser, K., McNabb, W. C., & Roy, N. C. (2019) · Nutrients · doi:10.3390/nu11020364 · Cited by 65 · see citing works

Mucosal immunity to poliovirus

Connor, R. I., Brickley, E. B., Wieland‐Alter, W., Ackerman, M. E., Weiner, J. A., Modlin, J. F., Bandyopadhyay, A. S., & Wright, P. F. (2021) · Mucosal Immunology · doi:10.1038/s41385-021-00428-0 · Cited by 66 · see citing works

Revealing the importance of prenatal gut microbiome in offspring neurodevelopment in humans

Sun, Z., Lee‐Sarwar, K. A., Kelly, R. S., Lasky-Su, J. A., Litonjua, A. A., Weiss, S. T., & Liu, Y. (2023) · EBioMedicine · doi:10.1016/j.ebiom.2023.104491 · Cited by 67 · see citing works

Understanding the Chemical Exposome During Fetal Development and Early Childhood: A Review

Krausová, M., Braun, D., Buerki-Thurnherr, T., Gundacker, C., Schernhammer, E., Wisgrill, L., & Warth, B. (2023) · Annual Review of Pharmacology and Toxicology · doi:10.1146/annurev-pharmtox-051922-113350 · Cited by 61 · see citing works

Human milk microbiota associated with early colonization of the neonatal gut in Mexican newborns

Corona-Cervantes, K., García‐González, I., Villalobos-Flores, L. E., Hernández-Quiroz, F., Piña-Escobedo, A., Hoyo‐Vadillo, C., Rangel-Calvillo, M. N., & Garcı́a-Mena, J. (2020) · PeerJ · doi:10.7717/peerj.9205 · Cited by 62 · see citing works

Impact of Toll-Like Receptor 4 Signaling in Necrotizing Enterocolitis

Mihi, B., & Good, M. L. (2018) · Clinics in Perinatology · doi:10.1016/j.clp.2018.09.007 · Cited by 62 · see citing works

Utilizing the fecal microbiota to understand foal gut transitions from birth to weaning

Torre, U. D. L., Henderson, J., Furtado, K. L., Pedroja, M., Elenamarie, O., Mora, A., Pechanec, M. Y., Maga, E. A., & Mienaltowski, M. J. (2019) · PLoS ONE · doi:10.1371/journal.pone.0216211 · Cited by 62 · see citing works

Maternal Emulsifier P80 Intake Induces Gut Dysbiosis in Offspring and Increases Their Susceptibility to Colitis in Adulthood

Jin, G., Tang, Q., Ma, J., Liu, X., Zhou, B., Sun, Y., Pang, X., Guo, Z., Xie, R., Liu, T., et al. (2021) · mSystems · doi:10.1128/msystems.01337-20 · Cited by 61 · see citing works

Psoriasis: Interplay between dysbiosis and host immune system

Kapoor, B., Gulati, M., Rani, P., & Gupta, R. (2022) · Autoimmunity Reviews · doi:10.1016/j.autrev.2022.103169 · Cited by 61 · see citing works

Dynamic construction of gut microbiota may influence allergic diseases of infants in Southwest China

Shen, X. P., Wang, M., Zhang, X., He, M., Li, M., Cheng, G., Wan, C., & He, F. (2019) · BMC Microbiology · doi:10.1186/s12866-019-1489-4 · Cited by 60 · see citing works

Examining the Complex Relationship Between Tuberculosis and Other Infectious Diseases in Children

Whittaker, E., López‐Varela, E., Broderick, C. M., & Seddon, J. A. (2019) · Frontiers in Pediatrics · doi:10.3389/fped.2019.00233 · Cited by 63 · see citing works

The potential of outdoor environments to supply beneficial butyrate-producing bacteria to humans

Brame, J. E., Liddicoat, C., Abbott, C. A., & Breed, M. F. (2021) · The Science of The Total Environment · doi:10.1016/j.scitotenv.2021.146063 · Cited by 59 · see citing works

Personalized Diets based on the Gut Microbiome as a Target for Health Maintenance: from Current Evidence to Future Possibilities

Song, E., & Shin, J. (2022) · Journal of Microbiology and Biotechnology · doi:10.4014/jmb.2209.09050 · Cited by 59 · see citing works

A standardized gnotobiotic mouse model harboring a minimal 15-member mouse gut microbiota recapitulates SOPF/SPF phenotypes

Darnaud, M., Vadder, F. D., Bogeat, P., Boucinha, L., Bulteau, A., Bunescu, A., Couturier, C., Delgado, A., Dugua, H., Elie, C., et al. (2021) · Nature Communications · doi:10.1038/s41467-021-26963-9 · Cited by 54 · see citing works

Babies, Bugs, and Barriers: Dietary Modulation of Intestinal Barrier Function in Early Life

Wells, J. M., Gao, Y., de Groot, N., Vonk, M. M., Ulfman, L. H., & van Neerven, R. J. J. (2022) · Annual Review of Nutrition · doi:10.1146/annurev-nutr-122221-103916 · Cited by 58 · see citing works

Bacterial analysis in the early developmental stages of the black tiger shrimp (Penaeus monodon)

Angthong, P., Uengwetwanit, T., Arayamethakorn, S., Chaitongsakul, P., Karoonuthaisiri, N., & Rungrassamee, W. (2020) · Scientific Reports · doi:10.1038/s41598-020-61559-1 · Cited by 58 · see citing works

Breast milk: more than just nutrition!

Nuzzi, G., Trambusti, I., Cicco, M. D., & Peroni, D. G. (2021) · Minerva Pediatrics · doi:10.23736/s2724-5276.21.06223-x · Cited by 57 · see citing works

Risk Factors for Gut Dysbiosis in Early Life

Parkin, K., Christophersen, C. T., Verhasselt, V., Cooper, M. N., & Martino, D. (2021) · Microorganisms · doi:10.3390/microorganisms9102066 · Cited by 58 · see citing works

Vitamin D Regulates the Microbiota to Control the Numbers of RORγt/FoxP3+ Regulatory T Cells in the Colon

Cantorna, M. T., Lin, Y., Arora, J., Bora, S. A., Tian, Y., Nichols, R. G., & Patterson, A. D. (2019) · Frontiers in Immunology · doi:10.3389/fimmu.2019.01772 · Cited by 56 · see citing works

A Review on Probiotic Microencapsulation and Recent Advances of their Application in Bakery Products

Arepally, D., Reddy, R. S., Goswami, T. K., & Coorey, R. (2022) · Food and Bioprocess Technology · doi:10.1007/s11947-022-02796-2 · Cited by 55 · see citing works

Mucus, Microbiomes and Pulmonary Disease

Meldrum, O. W., & Chotirmall, S. H. (2021) · Biomedicines · doi:10.3390/biomedicines9060675 · Cited by 53 · see citing works

When a pandemic and an epidemic collide: COVID-19, gut microbiota, and the double burden of malnutrition

Littlejohn, P. T., & Finlay, B. B. (2021) · BMC Medicine · doi:10.1186/s12916-021-01910-z · Cited by 53 · see citing works

Can we modulate the breastfed infant gut microbiota through maternal diet?

Sindi, A. S., Geddes, D. T., Wlodek, M. E., Mühlhäusler, B. S., Payne, M. S., & Stinson, L. F. (2021) · FEMS Microbiology Reviews · doi:10.1093/femsre/fuab011 · Cited by 54 · see citing works

Impact of dietary fibers in infant formulas on gut microbiota and the intestinal immune barrier

Kong, C., Faas, M. M., de Vos, P., & Akkerman, R. (2020) · Food & Function · doi:10.1039/d0fo01700k · Cited by 51 · see citing works

Microbial modulation of the gut microbiome for treating autoimmune diseases

Balakrishnan, B., & Taneja, V. (2018) · Expert Review of Gastroenterology & Hepatology · doi:10.1080/17474124.2018.1517044 · Cited by 51 · see citing works

The association between gut microbiota development and maturation of intestinal bile acid metabolism in the first 3 y of healthy Japanese infants

Tanaka, M., Sanefuji, M., Morokuma, S., Yoden, M., Momoda, R., Sonomoto, K., Ogawa, M., Kato, K., & Nakayama, J. (2019) · Gut Microbes · doi:10.1080/19490976.2019.1650997 · Cited by 51 · see citing works

Early-life interactions between the microbiota and immune system: impact on immune system development and atopic disease

Donald, K., & Finlay, B. B. (2023) · Nature reviews. Immunology · doi:10.1038/s41577-023-00874-w · Cited by 362 · see citing works

The first thousand days - intestinal microbiology of early life: Establishing a symbiosis

Wopereis, H., Oozeer, R., Knipping, K., Belzer, C., & Knol, J. (2014) · Pediatric Allergy and Immunology · doi:10.1111/pai.12232 · Cited by 352 · see citing works

Development of systemic and mucosal immune responses against gut microbiota in early life and implications for the onset of allergies

Pirker, A.-L., & Vogl, T. J. (2024) · Frontiers in Allergy · doi:10.3389/falgy.2024.1439303 · Cited by 12 · see citing works

Correlation between early-life regulation of the immune system by microbiota and allergy development

Gensollen, T., & Blumberg, R. S. (2017) · Journal of Allergy and Clinical Immunology · doi:10.1016/j.jaci.2017.02.011 · Cited by 140 · see citing works

How the early life microbiome shapes immune programming in childhood asthma and allergies

Hoskinson, C., Petersen, C., & Turvey, S. E. (2024) · Mucosal Immunology · doi:10.1016/j.mucimm.2024.12.005 · Cited by 28 · see citing works