The microbiome and innate immunity

An obesity-associated gut microbiome with increased capacity for energy harvest

Turnbaugh, P. J., Ley, R. E., Mahowald, M. A., Magrini, V., Mardis, E. R., & Gordon, J. I. (2006) · Nature · doi:10.1038/nature05414 · Cited by 12,444

Diversity of the Human Intestinal Microbial Flora

Eckburg, P. B., Bik, E. M., Bernstein, C. N., Purdom, E., Dethlefsen, L., Sargent, M., Gill, S. R., Nelson, K. E., & Relman, D. A. (2005) · Science · doi:10.1126/science.1110591 · Cited by 7,913

Gut flora metabolism of phosphatidylcholine promotes cardiovascular disease

Wang, Z., Klipfell, E., Bennett, B. J., Koeth, R., Levison, B. S., DuGar, B., Feldstein, A. E., Britt, E. B., Fu, X., Chung, Y.-M., et al. (2011) · Nature · doi:10.1038/nature09922 · Cited by 5,597

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

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

Richness of human gut microbiome correlates with metabolic markers

Le Chatelier, E., Nielsen, T., Qin, J., Prifti, E., Hildebrand, F., Falony, G., Almeida, M., Arumugam, M., Batto, J.-M., Kennedy, S., et al. (2013) · Nature · doi:10.1038/nature12506 · Cited by 4,662

Intestinal microbiota metabolism of l-carnitine, a nutrient in red meat, promotes atherosclerosis

Koeth, R. A., Wang, Z., Levison, B. S., Buffa, J. A., Org, E., Sheehy, B. T., Britt, E. B., Fu, X., Wu, Y., Li, L., et al. (2013) · Nature Medicine · doi:10.1038/nm.3145 · Cited by 4,386

Recognition of Commensal Microflora by Toll-Like Receptors Is Required for Intestinal Homeostasis

Rakoff-Nahoum, S., Paglino, J., Eslami-Varzaneh, F., Edberg, S., & Medzhitov, R. (2004) · Cell · doi:10.1016/j.cell.2004.07.002 · Cited by 4,251

Commensal Bifidobacterium promotes antitumor immunity and facilitates anti–PD-L1 efficacy

Sivan, A., Corrales, L., Hubert, N., Williams, J. B., Aquino-Michaels, K., Earley, Z. M., Benyamin, F. W., Man Lei, Y., Jabri, B., Alegre, M.-L., et al. (2015) · Science · doi:10.1126/science.aac4255 · Cited by 3,888

Type 2 diabetes as an inflammatory disease

Donath, M. Y., & Shoelson, S. E. (2011) · Nature Reviews Immunology · doi:10.1038/nri2925 · Cited by 3,737

Fecal microbiota transplantation from warthog to pig confirms the influence of the gut microbiota on African swine fever susceptibility

Zhang, J., Rodrı́guez, F., Navas, M. J., Costa-Hurtado, M., Almagro, V., Bosch-Camós, L., López, E., Cuadrado‐Matías, R., Accensi, F., Pina-Pedrero, S., et al. (2020) · Scientific Reports · doi:10.1038/s41598-020-74651-3 · Cited by 36

The Mammalian Metaorganism: A Holistic View on How Microbes of All Kingdoms and Niches Shape Local and Systemic Immunity

Runge, S., & Rosshart, S. P. (2021) · Frontiers in Immunology · doi:10.3389/fimmu.2021.702378 · Cited by 36

Dysbiosis of human microbiome and infectious diseases

Gupta, A., Singh, V., & Mani, I. (2022) · Progress in molecular biology and translational science · doi:10.1016/bs.pmbts.2022.06.016 · Cited by 36

Gastrointestinal Manifestations of SARS-CoV-2: Transmission, Pathogenesis, Immunomodulation, Microflora Dysbiosis, and Clinical Implications

Durairajan, S. S. K., Singh, A. K., Saravanan, U. B., Namachivayam, M., Radhakrishnan, M., Huang, J., Dhodapkar, R., & Zhang, H. (2023) · Viruses · doi:10.3390/v15061231 · Cited by 37

Roles of Toll-Like Receptors in Radiotherapy- and Chemotherapy-Induced Oral Mucositis: A Concise Review

Ji, L., Hao, S., Wang, J., Zou, J., & Wang, Y. (2022) · Frontiers in Cellular and Infection Microbiology · doi:10.3389/fcimb.2022.831387 · Cited by 38

Gut Microbiome in Sepsis

Klingensmith, N. J., & Coopersmith, C. M. (2023) · Surgical Infections · doi:10.1089/sur.2022.420 · Cited by 35

Astragaloside IV Alleviates Depression in Rats by Modulating Intestinal Microbiota, T-Immune Balance, and Metabolome

Liu, X., Wang, S., Wu, X., Zhao, Z., Chen, J., Li, M., & Qin, X. (2023) · Journal of Agricultural and Food Chemistry · doi:10.1021/acs.jafc.3c04063 · Cited by 35

Polyethylene terephthalate microplastics affect gut microbiota distribution and intestinal damage in mice

Sun, X., Zhuang, Y., Wang, Y., Zhang, Z., An, L., & Xu, Q. (2025) · Ecotoxicology and Environmental Safety · doi:10.1016/j.ecoenv.2025.118119 · Cited by 36

Gut microbiota in rheumatoid arthritis: Mechanistic insights, clinical biomarkers, and translational perspectives

Qi, X., Liu, M., Jiang, X., Gao, T., Xu, G., Zhang, H., Su, Q. Y., Du, Y., Luo, J., & Zhang, S. (2025) · Autoimmunity Reviews · doi:10.1016/j.autrev.2025.103912 · Cited by 35

Strategies to increase the efficacy of using gut microbiota for the modulation of obesity

Li, J., Rajoka, M. S. R., Shao, D., Jiang, C., Jin, M., Huang, Q., Yang, H., & Shi, J. (2017) · Obesity Reviews · doi:10.1111/obr.12590 · Cited by 37

Particle size determines the anti-inflammatory effect of wheat bran in a model of fructose over-consumption: Implication of the gut microbiota

Suriano, F., Neyrinck, A. M., Verspreet, J., Olivares, M., Leclercq, S., de Wiele, T. V., Courtin, C. M., Cani, P. D., Bindels, L. B., & Delzenne, N. M. (2017) · Journal of Functional Foods · doi:10.1016/j.jff.2017.12.035 · Cited by 37

Impact of the Use and Type of Antibiotics on Acute Graft-versus-Host Disease

Nishi, K., Kanda, J., Hishizawa, M., Kitano, T., Kondo, T., Yamashita, K., & Takaori‐Kondo, A. (2018) · Transplantation and Cellular Therapy · doi:10.1016/j.bbmt.2018.06.031 · Cited by 35

Fecal Microbiota Transplantation for the Critically Ill Patient

Limketkai, B. N., Hendler, S., Ting, P., & Parian, A. M. (2018) · Nutrition in Clinical Practice · doi:10.1002/ncp.10228 · Cited by 36

The efficacy of lactic acid bacteria usage in turbot Scophthalmus maximus on intestinal microbiota and expression of the immune related genes

Guo, G., Li, C., Xia, B., Jiang, S., Zhou, S., Men, X., & Ren, Y. (2020) · Fish & Shellfish Immunology · doi:10.1016/j.fsi.2020.03.003 · Cited by 35

Circulation of gut-preactivated naïve CD8 + T cells enhances antitumor immunity in B cell-defective mice

Akrami, M., Menzies, R. J., Chamoto, K., Miyajima, M., Suzuki, R., Sato, H., Nishii, A., Tomura, M., Fagarasan, S., & Honjo, T. (2020) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.2010981117 · Cited by 35

Immune Gene Expression Covaries with Gut Microbiome Composition in Stickleback

Fuess, L. E., den Haan, S., Ling, F., Weber, J. N., Steinel, N. C., & Bolnick, D. I. (2021) · mBio · doi:10.1128/mbio.00145-21 · Cited by 36

Consistent Alterations of Human Fecal Microbes After Transplantation into Germ-Free Mice

Li, Y., Cao, W., Gao, N., Zhao, X., & Chen, W. (2021) · Genomics Proteomics & Bioinformatics · doi:10.1016/j.gpb.2020.06.024 · Cited by 35

Immune Response to Enterococcus gallinarum in Lupus Patients Is Associated With a Subset of Lupus-Associated Autoantibodies

Bagavant, H., Araszkiewicz, A. M., Ingram, J. K., Cizio, K., Merrill, J. T., Arriens, C., Guthridge, J. M., James, J. A., & Deshmukh, U. S. (2021) · Frontiers in Immunology · doi:10.3389/fimmu.2021.635072 · Cited by 35

Ferroptosis: A mixed blessing for infectious diseases

Xiao, L.-Y., Huang, H., Fan, S., Zheng, B., Wu, J., Zhang, J., Pi, J., & Xu, J.-F. (2022) · Frontiers in Pharmacology · doi:10.3389/fphar.2022.992734 · Cited by 37

Colitis-associated intestinal microbiota regulates brain glycine and host behavior in mice

Morozova, M. V., Borisova, M. A., Snytnikova, O. A., Achasova, K. M., Litvinova, E. A., Tsentalovich, Y. P., & Kozhevnikova, E. N. (2022) · Scientific Reports · doi:10.1038/s41598-022-19219-z · Cited by 36

Dynamic network modeling of gut microbiota during Alzheimer’s disease progression in mice

Li, Y., Chen, Y., Fan, Y., Chen, Y., & Chen, Y. (2023) · Gut Microbes · doi:10.1080/19490976.2023.2172672 · Cited by 35

Pattern-recognition receptors (PRRs) in SARS-CoV-2

Isazadeh, A., Heris, J. A., Shahabi, P., Mohammadinasab, R., Shomali, N., Nasiri, H., Valedkarimi, Z., Khosroshahi, A. J., Hajazimian, S., Akbari, M., et al. (2023) · Life Sciences · doi:10.1016/j.lfs.2023.121940 · Cited by 37

The Human Gut Microbiome in Liver Diseases

Davis, B., & Bajaj, J. (2017) · Seminars in Liver Disease · doi:10.1055/s-0037-1602763 · Cited by 34

Living Probiotics - Loaded Hydrogel Microspheres with Gastric Acid Resistance and ROS Triggered Release for Potential Therapy of Inflammatory Bowel Disease

Zhu, Y. N., Wang, Q., Chen, Y., Xie, Y., Han, G., Liu, S., Song, Y., Lu, W., & Guo, Y. (2022) · ACS Applied Polymer Materials · doi:10.1021/acsapm.2c01893 · Cited by 34

Disruption of the early-life microbiota alters Peyer’s patch development and germinal center formation in gastrointestinal-associated lymphoid tissue

Borbet, T. C., Pawline, M. B., Li, J., Ho, M. L., Yin, Y. S., Zhang, X., Novikova, E., Jackson, K., Mullins, B. J., Ruiz, V. E., et al. (2023) · iScience · doi:10.1016/j.isci.2023.106810 · Cited by 34

Gut microbiome-derived bacterial extracellular vesicles in patients with solid tumours

Mishra, S., Tejesvi, M. V., Hekkala, J., Turunen, J., Unnisa, N. K. F., Kaisanlahti, A., Suokas, M., Leppä, S., Vihinen, P., Kuitunen, H. K., et al. (2024) · Journal of Advanced Research · doi:10.1016/j.jare.2024.03.003 · Cited by 34

Unraveling the Microbiome–Human Body Axis: A Comprehensive Examination of Therapeutic Strategies, Interactions and Implications

Olteanu, G., Pană, M.-A., Busnatu, Ș., Lupuliasa, D., Neacșu, S. M., Mititelu, M., Musuc, A. M., Ioniță-Mîndrican, C.-B., & Boroghină, S. C. (2024) · International Journal of Molecular Sciences · doi:10.3390/ijms25105561 · Cited by 36

Gut microbiota and their metabolites in the immune response of rheumatoid arthritis: Therapeutic potential and future directions

Cai, X. T., Ren, F., & Yao, Y. (2025) · International Immunopharmacology · doi:10.1016/j.intimp.2025.114034 · Cited by 34

Codevelopment of Microbiota and Innate Immunity and the Risk for Group B Streptococcal Disease

Kolter, J., & Henneke, P. (2017) · Frontiers in Immunology · doi:10.3389/fimmu.2017.01497 · Cited by 37

Morphine Potentiates Dysbiotic Microbial and Metabolic Shifts in Acute SIV Infection

Sindberg, G. M., Callen, S. E., Banerjee, S., Meng, J., Hale, V. L., Hegde, R., Cheney, P. D., Villinger, F. J., Roy, S., & Buch, S. J. (2018) · Journal of Neuroimmune Pharmacology · doi:10.1007/s11481-018-9805-6 · Cited by 34

Comparative analysis of the fecal microbiota from different species of domesticated and wild suids

Correa‐Fiz, F., Blanco-Fuertes, M., Navas, M. J., Lacasta, A., Bishop, R. P., Githaka, N., Onzere, C., Potier, M. L., Almagro, V., Martínez, J., et al. (2019) · Scientific Reports · doi:10.1038/s41598-019-49897-1 · Cited by 34

The gut microbiota of brood parasite and host nestlings reared within the same environment: disentangling genetic and environmental effects

Lee, C. Y., Peralta‐Sánchez, J. M., Martínez‐Bueno, M., Møller, A. P., Rabelo-Ruiz, M., Zamora‐Muñoz, C., & Soler, J. J. (2020) · The ISME Journal · doi:10.1038/s41396-020-0719-y · Cited by 35

Alterations in the gut virome in patients with ankylosing spondylitis

Li, C., Zhang, Y., Yan, Q., Guo, R., Chen, C., Li, S., Zhang, Y., Meng, J., Ma, J., You, W., et al. (2023) · Frontiers in Immunology · doi:10.3389/fimmu.2023.1154380 · Cited by 34

Corrigendum: Inflammatory and Microbiota-Related Regulation of the Intestinal Epithelial Barrier

Barbara, G., Barbaro, M. R., Fuschi, D., Palombo, M., Falangone, F., Cremon, C., Marasco, G., & Stanghellini, V. (2021) · Frontiers in Nutrition · doi:10.3389/fnut.2021.790387 · Cited by 41

Gut microbiota dysbiosis is associated with altered tryptophan metabolism and dysregulated inflammatory response in COVID-19

Essex, M., Pascual-Leone, B. M., Löber, U., Kuhring, M., Zhang, B., Brüning, U., Fritsche‐Guenther, R., Krzanowski, M., Vernengo, F. F., Brumhard, S., et al. (2024) · npj Biofilms and Microbiomes · doi:10.1038/s41522-024-00538-0 · Cited by 34

Lactobacillus gasseri attenuates allergic airway inflammation through PPARγ activation in dendritic cells

Hsieh, M.-H., Jan, R.-L., Wu, L. S.-H., Chen, P., Kao, H.-F., Kuo, W., & Wang, J. (2017) · Journal of Molecular Medicine · doi:10.1007/s00109-017-1598-1 · Cited by 34

16S rRNA gene sequencing reveals an altered composition of the gut microbiota in chickens infected with a nephropathogenic infectious bronchitis virus

Xu, P., Shi, Y., Liu, P., Yang, Y., Zhou, C., Li, G., Luo, J., Zhang, C., Cao, H., Hu, G., et al. (2020) · Scientific Reports · doi:10.1038/s41598-020-60564-8 · Cited by 33

Effects of ploidy and salmonid alphavirus infection on the skin and gill microbiome of Atlantic salmon (Salmo salar)

Brown, R., Moore, L. J., Mani, A., Patel, S., & Salinas, I. (2021) · PLoS ONE · doi:10.1371/journal.pone.0243684 · Cited by 33

Bidirectional communication between mast cells and the gut-brain axis in neurodegenerative diseases: Avenues for therapeutic intervention

Bhuiyan, P., Chen, Y., Karim, M., Dong, H., & Qian, Y. (2021) · Brain Research Bulletin · doi:10.1016/j.brainresbull.2021.04.010 · Cited by 33

Intestinal microbiota: A potential target for enhancing the antitumor efficacy and reducing the toxicity of immune checkpoint inhibitors

Luo, B., Zhang, Y., Zhang, C., Liu, X., & Shi, C. (2021) · Cancer Letters · doi:10.1016/j.canlet.2021.04.001 · Cited by 33

The interplay between fasting, gut microbiota, and lipid profile

Mohammadzadeh, A., Roshanravan, N., Alamdari, N. M., Safaiyan, A., Mosharkesh, E., Hadi, A., Barati, M., & Ostadrahimi, A. (2021) · International Journal of Clinical Practice · doi:10.1111/ijcp.14591 · Cited by 35

Host Genetics and Gut Microbiome: Perspectives for Multiple Sclerosis

Maglione, A., Zuccalà, M., Tosi, M., Clerico, M., & Rolla, S. (2021) · Genes · doi:10.3390/genes12081181 · Cited by 34

Protective effects of dietary supplementation of probiotic Bacillus licheniformis Dahb1 against ammonia induced immunotoxicity and oxidative stress in Oreochromis mossambicus

Gopi, N., Iswarya, A., Vijayakumar, S., Jayanthi, S., Nor, S. A. M., Velusamy, P., & Vaseeharan, B. (2022) · Comparative Biochemistry and Physiology Part C Toxicology & Pharmacology · doi:10.1016/j.cbpc.2022.109379 · Cited by 33

Therapeutic approaches to colorectal cancer via strategies based on modulation of gut microbiota

Chen, M., Lin, W., Li, N., Wang, Q., Zhu, S., Zeng, A., & Song, L. (2022) · Frontiers in Microbiology · doi:10.3389/fmicb.2022.945533 · Cited by 33

Does the Gut Microbial Metabolome Really Matter? The Connection between GUT Metabolome and Neurological Disorders

Marć, M. A., Jastrząb, R., & Mytych, J. (2022) · Nutrients · doi:10.3390/nu14193967 · Cited by 33

Curcumin alleviates LPS-induced intestinal homeostatic imbalance through reshaping gut microbiota structure and regulating group 3 innate lymphoid cells in chickens

Ruan, D., Wu, S., Fouad, A. M., Zhu, Y., Huang, W., Chen, Z., Gou, Z., Wang, Y., Yongquan, H., Yan, S., et al. (2022) · Food & Function · doi:10.1039/d2fo02598a · Cited by 33

Host–microbiota interaction induces bi-phasic inflammation and glucose intolerance in mice

Molinaro, A., Caesar, R., Mannerås-Holm, L., Tremaroli, V., Cani, P. D., & Bäckhed, F. (2017) · Molecular Metabolism · doi:10.1016/j.molmet.2017.08.016 · Cited by 33

CARD9 Signaling in Intestinal Immune Homeostasis and Oncogenesis

Hartjes, L., & Ruland, J. (2019) · Frontiers in Immunology · doi:10.3389/fimmu.2019.00419 · Cited by 35

Shifting Climates, Foods, and Diseases: The Human Microbiome through Evolution

Amato, K. R., Jeyakumar, T., Poinar, H. N., & Gros, P. (2019) · BioEssays · doi:10.1002/bies.201900034 · Cited by 36

Bacterial modification of the host glycosaminoglycan heparan sulfate modulates SARS-CoV-2 infectivityPreprint

Martino, C., Kellman, B. P., Sandoval, D. R., Clausen, T. M., Marotz, C. A., Song, S. J., Wandro, S., Zaramela, L. S., Benítez, R. A. S., Zhu, Q., et al. (2020) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2020.08.17.238444 · Cited by 33

The microbiome-metabolome crosstalk in the pathogenesis of respiratory fungal diseases

Gonçalves, S. M., Lagrou, K., Duarte-Oliveira, C., Maertens, J. A., Cunha, C., & Carvalho, A. (2017) · Virulence · doi:10.1080/21505594.2016.1257458 · Cited by 32

Gut microbiota: A double-edged sword in immune checkpoint blockade immunotherapy against tumors

Wang, J., Zhu, N., Su, L., & Yang, R. (2023) · Cancer Letters · doi:10.1016/j.canlet.2023.216582 · Cited by 35

Modulation of gut microbiota by probiotics to improve the efficacy of immunotherapy in hepatocellular carcinoma

Chen, P., Yang, C., Ren, K., Xu, M., Pan, C., Ye, X., & Li, L. (2024) · Frontiers in Immunology · doi:10.3389/fimmu.2024.1504948 · Cited by 33

The Inducible Response of the Nematode Caenorhabditis elegans to Members of Its Natural Microbiota Across Development and Adult Life

Yang, W., Petersen, C., Pees, B., Zimmermann, J., Waschina, S., Dirksen, P., Rosenstiel, P. C., Tholey, A., Leippe, M., Dierking, K., et al. (2019) · Frontiers in Microbiology · doi:10.3389/fmicb.2019.01793 · Cited by 33

How gut microbiome interactions affect nutritional traits of Drosophila melanogaster

McMullen, J. G., Peters-Schulze, G., Cai, J., Patterson, A. D., & Douglas, A. E. (2020) · Journal of Experimental Biology · doi:10.1242/jeb.227843 · Cited by 36

Gut microbiota-derived metabolites and colorectal cancer: New insights and updates

Mohseni, A. H., Taghinezhad‐S, S., & Fu, X. (2020) · Microbial Pathogenesis · doi:10.1016/j.micpath.2020.104569 · Cited by 32

The anti-obesity effects exerted by different fractions of Artemisia sphaerocephala Krasch polysaccharide in diet-induced obese mice

Li, J., Han, J., Yan, X., Shao, D., Hu, X., & Shi, J. (2021) · International Journal of Biological Macromolecules · doi:10.1016/j.ijbiomac.2021.04.070 · Cited by 32

Seaweed Dietary Fiber Sodium Alginate Suppresses the Migration of Colonic Inflammatory Monocytes and Diet-Induced Metabolic Syndrome via the Gut Microbiota

Ejima, R., Akiyama, M., Sato, H., Tomioka, S., Yakabe, K., Kimizuka, T., Seki, N., Fujimura, Y., Hirayama, A., Fukuda, S., et al. (2021) · Nutrients · doi:10.3390/nu13082812 · Cited by 32

Immunoregulatory Intestinal Microbiota and COVID-19 in Patients with Type Two Diabetes: A Double-Edged Sword

Petakh, P., Kamyshna, I. I., Nykyforuk, A., Yao, R., Imbery, J. F., Oksenych, V., Korda, M. M., & Kamyshnyi, O. (2022) · Viruses · doi:10.3390/v14030477 · Cited by 33

Effects of the maternal gut microbiome and gut-placental axis on melatonin efficacy in alleviating cadmium-induced fetal growth restriction

Zhang, H., Liu, X., Zheng, Y., Zha, X., Elsabagh, M., Zhang, Y., Ma, Y., Loor, J. J., Wang, M., & Wang, H. (2022) · Ecotoxicology and Environmental Safety · doi:10.1016/j.ecoenv.2022.113550 · Cited by 32

Gut microbiota plasticity in insular lizards under reversed island syndrome

Buglione, M., Ricca, E., Petrelli, S., Baccigalupi, L., Troiano, C., Saggese, A., Rivieccio, E., & Fulgione, D. (2022) · Scientific Reports · doi:10.1038/s41598-022-16955-0 · Cited by 32

A Review of the Role of Oral Microbiome in the Development, Detection, and Management of Head and Neck Squamous Cell Cancers

Burcher, K. M., Burcher, J. T., Inscore, L., Bloomer, C. H., Furdui, C. M., & Porosnicu, M. (2022) · Cancers · doi:10.3390/cancers14174116 · Cited by 34

Digestive properties and prebiotic activity of garlic saccharides with different-molecular-weight obtained by acidolysis

Zhao, R., Qiu, Z., Bai, X., Lu, X., Qiao, Y., & Lu, X. (2022) · Current Research in Food Science · doi:10.1016/j.crfs.2022.10.022 · Cited by 33

Mast Cell Cytokines in Acute and Chronic Gingival Tissue Inflammation: Role of IL-33 and IL-37

Trimarchi, M., Lauritano, D., Ronconi, G., Caraffa, A., Gallenga, C. E., Frydas, I., Kritas, S. K., Calvisi, V., & Conti, P. (2022) · International Journal of Molecular Sciences · doi:10.3390/ijms232113242 · Cited by 33

Emerging epigenetic dynamics in gut-microglia brain axis: experimental and clinical implications for accelerated brain aging in schizophrenia

Ben‐Azu, B., del Re, E. C., VanderZwaag, J., Carrier, M., Keshavan, M. S., Khakpour, M., & Tremblay, M. (2023) · Frontiers in Cellular Neuroscience · doi:10.3389/fncel.2023.1139357 · Cited by 32

Can Consideration of the Microbiome Improve Antimicrobial Utilization and Treatment Outcomes in the Oncology Patient?

Galloway-Peña, J., Jenq, R. R., & Shelburne, S. A. (2017) · Clinical Cancer Research · doi:10.1158/1078-0432.ccr-16-3173 · Cited by 32

The protective effect of protopanaxatriol-type saponin on intestinal health in antibiotic-treated mice

Zhang, M., Zhao, J., Deng, J., Duan, Z., Zhu, C., & Fan, D. (2019) · Food & Function · doi:10.1039/c9fo00242a · Cited by 32

Gut microbiota, immunity, and bile acid metabolism: decoding metabolic disease interactions

Zhao, Q., Wu, J., Ding, Y., Pang, Y., & Jiang, C. (2023) · Life Metabolism · doi:10.1093/lifemeta/load032 · Cited by 31

Shattering the Amyloid Illusion: The Microbial Enigma of Alzheimer’s Disease Pathogenesis—From Gut Microbiota and Viruses to Brain Biofilms

Onisiforou, A., Charalambous, E. G., & Zanos, P. (2025) · Microorganisms · doi:10.3390/microorganisms13010090 · Cited by 32

Mass Azithromycin Distribution and Community Microbiome: A Cluster-Randomized Trial

Doan, T. A., Hinterwirth, A. J., Arzika, A. M., Cotter, S. Y., Ray, K. J., O’Brien, K. S., Zhong, L., Chow, E. D., Zhou, Z., Cummings, M. E., et al. (2018) · Open Forum Infectious Diseases · doi:10.1093/ofid/ofy182 · Cited by 31

Gut Microbiota of Great Spotted Cuckoo Nestlings is a Mixture of Those of Their Foster Magpie Siblings and of Cuckoo Adults

Ruiz‐Rodríguez, M., Martín‐Vivaldi, M., Martínez‐Bueno, M., & Soler, J. J. (2018) · Genes · doi:10.3390/genes9080381 · Cited by 31

The Fecal Metagenomics of Malayan Pangolins Identifies an Extensive Adaptation to Myrmecophagy

Ma, J., Jiang, H., Li, L., Zhang, X., Li, G.-Y., Li, H., Jin, X.-J., & Chen, J. (2018) · Frontiers in Microbiology · doi:10.3389/fmicb.2018.02793 · Cited by 31

Organ transplantation and gut microbiota: current reviews and future challenges.

Xiao, J., Peng, Z., Liao, Y., Sun, H., Chen, W., Chen, X., Wei, Z., Yang, C., Nussler, A. K., Liu, J., et al. (2018) · Europe PMC (PubMed Central) · Cited by 31

Food ingredients in human health: Ecological and metabolic perspectives implicating gut microbiota function

Wu, Q., Chen, T., El-Nezami, H. S., & Savidge, T. (2020) · Trends in Food Science & Technology · doi:10.1016/j.tifs.2020.04.007 · Cited by 31

The Microbiome and Its Implications in Cancer Immunotherapy

Choudhry, H. (2021) · Molecules · doi:10.3390/molecules26010206 · Cited by 31

Interplay of Microbiota and Citrullination in the Immunopathogenesis of Rheumatoid Arthritis

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