Dysbiosis of the gut microbiota in disease

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

A human gut microbial gene catalogue established by metagenomic sequencing

MetaHIT Consortium, Qin, J., Li, R., Raes, J., Arumugam, M., Burgdorf, K. S., Manichanh, C., Nielsen, T., Pons, N., Levenez, F., et al. (2010) · Nature · doi:10.1038/nature08821 · Cited by 11,624

Human gut microbes associated with obesity

Ley, R. E., Turnbaugh, P. J., Klein, S., & Gordon, J. I. (2006) · Nature · doi:10.1038/4441022a · Cited by 8,785

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

A metagenome-wide association study of gut microbiota in type 2 diabetes

Qin, J., Li, Y., Cai, Z., Li, S., Zhu, J., Zhang, F., Liang, S., Zhang, W., Guan, Y., Shen, D., et al. (2012) · Nature · doi:10.1038/nature11450 · Cited by 6,762

Obesity alters gut microbial ecology

Ley, R. E., Bäckhed, F., Turnbaugh, P., Lozupone, C. A., Knight, R. D., & Gordon, J. I. (2005) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0504978102 · Cited by 6,176

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

The role of short-chain fatty acids in the interplay between diet, gut microbiota, and host energy metabolism

den Besten, G., van Eunen, K., Groen, A. K., Venema, K., Reijngoud, D.-J., & Bakker, B. M. (2013) · Journal of Lipid Research · doi:10.1194/jlr.r036012 · Cited by 5,048

Changes in gut microbiota control metabolic endotoxemia-induced inflammation in high-fat diet-induced obesity and diabetes in mice

Cani, P. D., Bibiloni, R., Knauf, C., Waget, A., Neyrinck, A. M., Delzenne, N. M., & Burcelin, R. (2008) · Diabetes · doi:10.2337/db07-1403 · Cited by 4,819

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

Association of Constipation with risk of end-stage renal disease in patients with chronic kidney disease

Lu, C., Chen, Y.-C., Lu, Y.-W., Muo, C., & Chang, R. (2019) · BMC Nephrology · doi:10.1186/s12882-019-1481-0 · Cited by 25

Electrochemical assays for microbial analysis: how far they are from solving microbiota and microbiome challenges

Ferapontova, E. E. (2020) · Current Opinion in Electrochemistry · doi:10.1016/j.coelec.2019.12.005 · Cited by 26

Exploring the connection between the gut microbiome and parkinson's disease symptom progression and pathology: implications for supplementary treatment options

Chan, D. G., Ventura, K., Villeneuve, A., Du Bois, P., & Holahan, M. R. (2022) · Journal of Parkinson's Disease · doi:10.3233/jpd-223461 · Cited by 24

Bibliometric analysis of intestinal microbiota and lung diseases

Sun, W., Zhou, T., Ding, P., Guo, L., Zhou, X., & Long, K. (2024) · Frontiers in Cellular and Infection Microbiology · doi:10.3389/fcimb.2024.1347110 · Cited by 26

Effect of Lacticaseibacillus rhamnosus IDCC 3201 on irritable bowel syndrome with constipation: a randomized, double-blind, and placebo-controlled trial

Kwon, H., Nam, E. H., Kim, H., Jo, H.-N., Bang, W. Y., Lee, M., Shin, H., Kim, D., Kim, J. H., Kim, H.-J., et al. (2024) · Scientific Reports · doi:10.1038/s41598-024-72887-x · Cited by 32

Computational Metagenomics: State of the Art

Pita-Galeana, M. A., Ruhle, M., López-Vázquez, L., de Anda‐Jáuregui, G., & Lemus, E. H. (2025) · International Journal of Molecular Sciences · doi:10.3390/ijms26189206 · Cited by 28

Methods and Strategies to Examine the Human Breastmilk Microbiome

LeMay‐Nedjelski, L., Copeland, J. K., Wang, P. W., Butcher, J., Unger, S. L., Stintzi, A., & O’Connor, D. L. (2018) · Methods in molecular biology · doi:10.1007/978-1-4939-8728-3_5 · Cited by 22

High-throughput sequencing of 16S rRNA amplicons characterizes gut microbiota shift of juvenile sea cucumber Apostichopus japonicus feeding with three antibiotics

Zhao, Y., Wang, Q., Liu, H., Li, B., & Zhang, H. (2018) · Journal of Oceanology and Limnology · doi:10.1007/s00343-019-8308-5 · Cited by 24

Intestinal Microbial Dysbiosis in Beagles Naturally Infected with Canine Parvovirus

Park, J., Guevarra, R. B., Kim, B.-R., Lee, J. H., Lee, S. H., Cho, J. H., Kim, H., Cho, J. H., Song, M., Lee, J.-H., et al. (2019) · Journal of Microbiology and Biotechnology · doi:10.4014/jmb.1901.01047 · Cited by 24

Gut Microbiota Interactions With Obesity

Falalyeyeva, T. M., Chornenka, N., Cherkasova, L., Tsyryuk, O., Molchek, N., Kovalchuk, O. I., Kyriachenko, Y., Остапченко, Л. І., & Kobyliak, N. M. (2021) · Elsevier eBooks · doi:10.1016/b978-0-12-819265-8.00030-9 · Cited by 24

Potential Role of Probiotics for Inflammaging: A Narrative Review

Peladic, N. J., Dell’Aquila, G., Carrieri, B., Maggio, M. G., Cherubini, A., & Orlandoni, P. (2021) · Nutrients · doi:10.3390/nu13092919 · Cited by 27

The impact of maternal exposure to antibiotics on the development of child gut microbiome

Miyoshi, J., & Hisamatsu, T. (2021) · Immunological Medicine · doi:10.1080/25785826.2021.1963189 · Cited by 26

Commercial microbiota test revealed differences in the composition of intestinal microorganisms between children with autism spectrum disorders and neurotypical peers

Jendraszak, M., Gałęcka, M., Kotwicka, M., Regdos, A., Pazgrat-Patan, M., & Andrusiewicz, M. (2021) · Scientific Reports · doi:10.1038/s41598-021-03794-8 · Cited by 25

Implication of Paraprobiotics in Age-Associated Gut Dysbiosis and Neurodegenerative Diseases

Rahman, Z., & Dandekar, M. P. (2022) · NeuroMolecular Medicine · doi:10.1007/s12017-022-08722-1 · Cited by 25

Gut microbiome diversity and composition is associated with exploratory behavior in a wild-caught songbird

Florkowski, M. R., & Yorzinski, J. L. (2023) · Animal Microbiome · doi:10.1186/s42523-023-00227-x · Cited by 28

Association between Gut Microbiota and Breast Cancer: Diet as a Potential Modulating Factor

Dindar, D. A., Chun, B., Palma, A., Cheney, J., Krieger, M., Kasschau, K. D., Stagaman, K., Mitri, Z. I., Goodyear, S. M., Shannon, J., et al. (2023) · Nutrients · doi:10.3390/nu15214628 · Cited by 24

Inbred Mouse Populations Exhibit Intergenerational Changes in Intestinal Microbiota Composition and Function Following Introduction to a Facility

Choo, J. M., Trim, P. J., Leong, L. E. X., Abell, G. C. J., Brune, C., Jeffries, N., Wesselingh, S. L., Dear, T. N., Snel, M. F., & Rogers, G. B. (2017) · Frontiers in Microbiology · doi:10.3389/fmicb.2017.00608 · Cited by 26

Inflammation in gastrointestinal disorders: prevalent socioeconomic factors

Ribaldone, D. G., Pellicano, R., & Actis, G. C. (2019) · Clinical and Experimental Gastroenterology · doi:10.2147/ceg.s210844 · Cited by 25

Systems to model the personalized aspects of microbiome health and gut dysbiosis

Matthewman, C., Narin, A., Huston, H., & Hopkins, C. E. (2023) · Molecular Aspects of Medicine · doi:10.1016/j.mam.2022.101115 · Cited by 23

Metagenomic analysis of ecological niche overlap and community collapse in microbiome dynamics

Fujita, H., Ushio, M., Suzuki, K. T., Abe, M., Yamamichi, M., Okazaki, Y., Canarini, A., Hayashi, I., Fukushima, K., Fukuda, S., et al. (2023) · Frontiers in Microbiology · doi:10.3389/fmicb.2023.1261137 · Cited by 23

Next-generation prebiotics: Maillard-conjugates of 2′-fucosyllactose and lactoferrin hydrolysates beneficially modulate gut microbiome composition and health promoting activity in a murine model

Peled, S., Freilich, S., Hanani, H., Kashi, Y., & Livney, Y. D. (2023) · Food Research International · doi:10.1016/j.foodres.2023.113830 · Cited by 24

Comparative analysis of endometrial, vaginal, and gut microbiota in patients with and without adenomyosis

Valdés‐Bango, M., Gràcia, M., Rubio-García, E., Vergara, A., Casals‐Pascual, C., Ros, C., Rius, M., Martínez‐Zamora, M. Á., Mensión, E., Quintas, L., et al. (2024) · Acta Obstetricia Et Gynecologica Scandinavica · doi:10.1111/aogs.14847 · Cited by 23

Effects of Heat-Treated Lactobacillus helveticus CP790-Fermented Milk on Gastrointestinal Health in Healthy Adults: A Randomized Double-Blind Placebo-Controlled Trial

Tanihiro, R., Yuki, M., Sakano, K., Sasai, M., Sawada, D., Ebihara, S., & Hirota, T. (2024) · Nutrients · doi:10.3390/nu16142191 · Cited by 29

Antibiotic-mediated dysbiosis leads to activation of inflammatory pathways

Taitz, J., Tan, J., Ni, D., Potier‐Villette, C., Grau, G. E., Nanan, R. K. H., & Macia, L. (2025) · Frontiers in Immunology · doi:10.3389/fimmu.2024.1493991 · Cited by 26

The infiltration of microplastics in human systems: Gastrointestinal accumulation and pathogenic impacts

Sinha, P., Saini, V., Varshney, N., Pandey, R. K., & Jha, H. C. (2025) · Heliyon · doi:10.1016/j.heliyon.2025.e42606 · Cited by 25

Gut dysbiosis in cancer immunotherapy: microbiota-mediated resistance and emerging treatments

Eiman, L., Moazzam, K., Anjum, S., Kausar, H., Sharif, E. A. M., & Ibrahim, W. N. (2025) · Frontiers in Immunology · doi:10.3389/fimmu.2025.1575452 · Cited by 28

Polymeric Films for the Encapsulation, Storage, and Tunable Release of Therapeutic Microbes

Qiu, K., Young, I. C., Woodburn, B. M. D., Huang, Y., & Anselmo, A. C. (2020) · Advanced Healthcare Materials · doi:10.1002/adhm.201901643 · Cited by 26

The Impact of Intraspecies and Interspecies Bacterial Interactions on Disease Outcome

Baishya, J., Bisht, K., Rimbey, J. N., Yihunie, K. D., Islam, S., Mahmud, H. A., Waller, J., & Wakeman, C. A. (2021) · Pathogens · doi:10.3390/pathogens10020096 · Cited by 25

Postbiotic Gamma-Aminobutyric Acid and Camel Milk Intervention as Innovative Trends Against Hyperglycemia and Hyperlipidemia in Streptozotocin-Induced C57BL/6J Diabetic Mice

Abdelazez, A., Alshehry, G. A., Algarni, E. H. A., Aljumayi, H., Abdel-Motaal, H., & Meng, X. (2022) · Frontiers in Microbiology · doi:10.3389/fmicb.2022.943930 · Cited by 23

Deferiprone has less benefits on gut microbiota and metabolites in high iron-diet induced iron overload thalassemic mice than in iron overload wild-type mice: A preclinical study

Sriwichaiin, S., Thiennimitr, P., Thonusin, C., Sarichai, P., Buddhasiri, S., Kumfu, S., Nawara, W., Kittichotirat, W., Fucharoen, S., Chattipakorn, N., et al. (2022) · Life Sciences · doi:10.1016/j.lfs.2022.120871 · Cited by 25

An anti-inflammatory and low fermentable oligo, di, and monosaccharides and polyols diet improved patient reported outcomes in fibromyalgia: A randomized controlled trial

Silva, A. R., Bernardo, A., de Mesquita, M. F., Patto, J. V., Moreira, P. A. M., Silva, M. L., & Padrão, P. (2022) · Frontiers in Nutrition · doi:10.3389/fnut.2022.856216 · Cited by 26

A review on Impact of dietary interventions, drugs, and traditional herbal supplements on the gut microbiome

Karim, M. R., Iqbal, S., Mohammad, S., Lee, J. H., Jung, D.-H., Mathiyalagan, R., Yang, D., Yang, D. U., & Yang, D. U. (2023) · Microbiological Research · doi:10.1016/j.micres.2023.127346 · Cited by 27

Dietary supplementation with Lactiplantibacillus plantarum P-8 improves the growth performance and gut microbiota of weaned piglets

Yu, J. Z., Zuo, B., Li, Q., Zhao, F., Wang, J., Huang, W., Sun, Z., & Chen, Y. (2024) · Microbiology Spectrum · doi:10.1128/spectrum.02345-22 · Cited by 23

The Many Faces of Metabolic Dysfunction-Associated Fatty Liver Disease Treatment: From the Mediterranean Diet to Fecal Microbiota Transplantation

Abenavoli, L., Gambardella, M. L., Scarlata, G. G. M., Lenci, I., Baiocchi, L., & Luzza, F. (2024) · Medicina · doi:10.3390/medicina60040563 · Cited by 22

Adipose tissue microbiota in humans: an open issue

Zulian, A., Cancello, R., Cesana, E., Rizzi, E., Consolandi, C., Severgnini, M., Panizzo, V., Blasio, A. M. D., Micheletto, G., & Invitti, C. (2016) · International Journal of Obesity · doi:10.1038/ijo.2016.111 · Cited by 23

Correlations between intestinal innate immune genes and cecal microbiota highlight potential for probiotic development for immune modulation in poultry

Willson, N.-L., Nattrass, G. S., Hughes, R., Moore, R. J., Stanley, D., Hynd, P., & Forder, R. E. A. (2018) · Applied Microbiology and Biotechnology · doi:10.1007/s00253-018-9281-1 · Cited by 24

High‐Salt Diet‐Induced Gastritis in C57BL/6 Mice is Associated with Microbial Dysbiosis and Alleviated by a Buckwheat Diet

Li, Y., Li, W., Wang, X., Ding, C., Liu, J., Li, Y., Li, W., & Sun, Y. (2020) · Molecular Nutrition & Food Research · doi:10.1002/mnfr.201900965 · Cited by 25

An Integrated Multi-Disciplinary Perspective for Addressing Challenges of the Human Gut Microbiome

Shah, R., McKenzie, E. J., Rosin, M., Jadhav, S. R., Gondalia, S. V., Rosendale, D., & Beale, D. J. (2020) · Metabolites · doi:10.3390/metabo10030094 · Cited by 25

High-Throughput Stool Metaproteomics: Method and Application to Human Specimens

Gonzalez, C. G., Wastyk, H. C., Topf, M. A., Gardner, C. D., Sonnenburg, J. L., & Elias, J. E. (2020) · mSystems · doi:10.1128/msystems.00200-20 · Cited by 26

Propolis ethanolic extract has double-face in vitro effect on the planktonic growth and biofilm formation of some commercial probiotics

Alfarrayeh, I., Fekete, C., Gazdag, Z., & Papp, G. (2020) · Saudi Journal of Biological Sciences · doi:10.1016/j.sjbs.2020.11.047 · Cited by 24

Modulating Gut Microbiota: An Emerging Approach in the Prevention and Treatment of Multiple Sclerosis

Ullah, H., Товчига, О. В., Daglia, M., & Khan, H. Z. (2021) · Current Neuropharmacology · doi:10.2174/1570159x19666210217084827 · Cited by 25

Potent health-promoting effects of a synbiotic formulation prepared from Lactobacillus acidophilus NCDC15 fermented milk and Cichorium intybus root powder in Labrador dogs

Kumar, S., Pattanaik, A. K., & Jadhav, S. E. (2021) · Current Research in Biotechnology · doi:10.1016/j.crbiot.2021.06.001 · Cited by 23

Reconstruction of intestinal microecology of type 2 diabetes by fecal microbiota transplantation: Why and how

Hou, K., Zhang, S., Wu, Z., Zhu, D., Chen, F., Lei, Z.-N., Liu, W., Xiao, C., & Chen, Z.-S. (2021) · Biomolecules and Biomedicine · doi:10.17305/bjbms.2021.6323 · Cited by 24

Classical methods and perspectives for manipulating the human gut microbial ecosystem

Avalos, J. A. J., Arrevillaga-Boni, G., González‐López, L., García-Carvajal, Z. Y., & González‐Ávila, M. (2020) · Critical Reviews in Food Science and Nutrition · doi:10.1080/10408398.2020.1724075 · Cited by 23

Effects of metformin on the glucose regulation, lipid levels and gut microbiota in high-fat diet with streptozotocin induced type 2 diabetes mellitus rats

Zhou, X., Zhou, J., Ban, Q., Zhang, M., & Ban, B. (2024) · Endocrine · doi:10.1007/s12020-024-03843-y · Cited by 27

Crosstalk between butyrate oxidation in colonocyte and butyrate-producing bacteria

Park, B., Kim, J. Y., Riffey, O. F., Walsh, T. J., Johnson, J., & Donohoe, D. R. (2024) · iScience · doi:10.1016/j.isci.2024.110853 · Cited by 25

Pathogen- and Microbial- Associated Molecular Patterns (PAMPs/MAMPs) and the Innate Immune Response in Crohn’s Disease

Schaefer, A. K., Melnyk, J. E., He, Z., del Rosario, J. F., & Grimes, C. L. (2017) · Elsevier eBooks · doi:10.1016/b978-0-12-805417-8.00014-7 · Cited by 22

Electrochemical Immuno- and Aptamer-Based Assays for Bacteria: Pros and Cons over Traditional Detection Schemes

Jamal, R. B., Shipovskov, S., & Ferapontova, E. E. (2020) · Sensors · doi:10.3390/s20195561 · Cited by 22

Preparation and Evaluation of Colon-Targeted Prodrugs of the Microbial Metabolite 3-Indolepropionic Acid as an Anticolitic Agent

Lee, H., Park, S., Ju, S., Kim, S., Yoo, J., Yoon, I., Min, D. S., & Jung, Y. (2021) · Molecular Pharmaceutics · doi:10.1021/acs.molpharmaceut.0c01228 · Cited by 22

Oxalobacter formigenes: A new hope as a live biotherapeutic agent in the management of calcium oxalate renal stones

Hiremath, S. S., & Viswanathan, P. (2022) · Anaerobe · doi:10.1016/j.anaerobe.2022.102572 · Cited by 23

Ameliorative effect of tuna elastin peptides on AIA mice by regulating the composition of intestinal microorganisms and SCFAs

Zhang, Z., Wan, H., Han, J., Sun, X., Yu, R., Liu, B., Lu, C., Zhou, J., & Su, X. (2022) · Journal of Functional Foods · doi:10.1016/j.jff.2022.105076 · Cited by 22

Effects of adherence to the Mediterranean diet in children and adolescents with irritable bowel syndrome

Al‐Beltagi, M., Amrousy, D. M. E., Ashry, H. E., Maher, S., Mohammed, M., & Hasan, S. (2022) · World Journal of Clinical Pediatrics · doi:10.5409/wjcp.v11.i4.330 · Cited by 22

Enhancing the prebiotic and antioxidant effects of exopolysaccharides derived from Cordyceps militaris by enzyme-digestion

Kang, J. Y., Lee, B., Kim, C. H., Choi, J. H., & Kim, M. (2022) · LWT · doi:10.1016/j.lwt.2022.113830 · Cited by 22

Efficacy of Triphala extracts on the changes of obese fecal microbiome and metabolome in the human gut model

Kwandee, P., Somnuk, S., Wanikorn, B., Nakphaichit, M., & Tunsagool, P. (2023) · Journal of Traditional and Complementary Medicine · doi:10.1016/j.jtcme.2023.02.011 · Cited by 23

Gut Microbiota and Inflammation Modulation in a Rat Model for Ulcerative Colitis after the Intraperitoneal Administration of Apigenin, Luteolin, and Xanthohumol

Magadán‐Corpas, P., Pérez‐Valero, Á., Ye, S., Sordon, S., Huszcza, E., Popłoński, J., Villar, C. J., & Lombó, F. (2024) · International Journal of Molecular Sciences · doi:10.3390/ijms25063236 · Cited by 22

Specific dietary fibers prevent heavy metal disruption of the human gut microbiota in vitro

Román-Ochoa, Y., Cantu-Jungles, T. M., Delgado, G. T. C., Bulut, N., Tejada-Purizaca, T. R., Yucra-Condori, H. R., Duran, A. E., & Hamaker, B. R. (2023) · Food Research International · doi:10.1016/j.foodres.2023.113858 · Cited by 21

Navigating the complex relationship between human gut microbiota and breast cancer: Physiopathological, prognostic and therapeutic implications

Schettini, F., Gattazzo, F., Nucera, S., Rubio-García, E., López-Aladid, R., Morelli, L., Fontana, A., Vigneri, P. G., Casals‐Pascual, C., Iebba, V., et al. (2024) · Cancer Treatment Reviews · doi:10.1016/j.ctrv.2024.102816 · Cited by 22

Unveiling the complex interplay between gut microbiota and polycystic ovary syndrome: A narrative review

Gautam, R., Maan, P., Patel, A. K., Vasudevan, S., & Arora, T. K. (2024) · Clinical Nutrition · doi:10.1016/j.clnu.2024.10.028 · Cited by 25

Connect and Conquer: Collectivized Behavior of Mitochondria and Bacteria

Williams, C. F., & George, C. H. (2019) · Frontiers in Physiology · doi:10.3389/fphys.2019.00340 · Cited by 21

Changes in gut microbial flora after Roux-en-Y gastric bypass and sleeve gastrectomy and their effects on post-operative weight loss

Karami, R., Kermansaravi, M., Pishgahroudsari, M., Talebi, M., Mohammadzadeh, N., & Pazouki, A. (2020) · Updates in Surgery · doi:10.1007/s13304-020-00900-9 · Cited by 21

Role of HCA2 in Regulating Intestinal Homeostasis and Suppressing Colon Carcinogenesis

Li, Z., MCCAFFERTY, K. J., & Judd, R. L. (2021) · Frontiers in Immunology · doi:10.3389/fimmu.2021.606384 · Cited by 21

Characterization of the consensus mucosal microbiome of colorectal cancer

Zhao, L., Grimes, S. M., Greer, S., Kubit, M. A., Lee, H., Nadauld, L. D., & Ji, H. P. (2021) · NAR Cancer · doi:10.1093/narcan/zcab049 · Cited by 20

Gut microbiota signatures and modulation in irritable bowel syndrome

Marasco, G., Cremon, C., Barbaro, M. R., Stanghellini, V., & Barbara, G. (2022) · Microbiome Research Reports · doi:10.20517/mrr.2021.12 · Cited by 22

Host lung microbiota promotes malaria-associated acute respiratory distress syndrome

Mukherjee, D., Chora, Â. F., Lone, J., Ramiro, R. S., Blankenhaus, B., Serre, K., Ramirez, M., Gordo, I., Veldhoen, M., Varga‐Weisz, P., et al. (2022) · Nature Communications · doi:10.1038/s41467-022-31301-8 · Cited by 21

Brief overview of dietary intake, some types of gut microbiota, metabolic markers and research opportunities in sample of Egyptian women

Hassan, N. E., Shebini, S. M. E., El-Masry, S. A., Ahmed, N. H., Kamal, A. N., Ismail, A. S., Alian, K. M., Mostafa, M. I., Selim, M. K., & Afify, M. A. S. (2022) · Scientific Reports · doi:10.1038/s41598-022-21056-z · Cited by 21

Geography and elevation as drivers of cloacal microbiome assemblages of a passerine bird distributed across Sulawesi, Indonesia

Joakim, R. L., Irham, M., Haryoko, T., Rowe, K. M. C., Dalimunthe, Y., Anita, S., Achmadi, A. S., McGuire, J. A., Perkins, S. L., & Bowie, R. C. K. (2023) · Animal Microbiome · doi:10.1186/s42523-022-00219-3 · Cited by 20

Intestinal microbiome diversity of diabetic and non-diabetic kidney disease: Current status and future perspective

Das, S., & Ramanathan, G. (2023) · Life Sciences · doi:10.1016/j.lfs.2023.121414 · Cited by 21

Gut Microbiota, LADA, and Type 1 Diabetes Mellitus: An Evolving Relationship

Piccioni, A., Rosa, F., Mannucci, S., Manca, F., Merra, G., Chiloiro, S., Candelli, M., Covino, M., Gasbarrini, A., & Franceschi, F. (2023) · Biomedicines · doi:10.3390/biomedicines11030707 · Cited by 21

Food additives and their implication in inflammatory bowel disease and metabolic syndrome

Besedin, D. A., Shah, R. N., Brennan, C. S., Panzeri, E., Van, T. T. H., & Eri, R. D. (2024) · Clinical Nutrition ESPEN · doi:10.1016/j.clnesp.2024.10.171 · Cited by 22

Irritable bowel syndrome and active inflammatory bowel disease diagnosed by faecal gas analysis

Aggio, R. B. M., White, P., Jayasena, H., Costello, B. D. L., Ratcliffe, N. M., & Probert, C. S. (2016) · Alimentary Pharmacology & Therapeutics · doi:10.1111/apt.13822 · Cited by 21

Time‐, Sex‐, and Dose‐Dependent Alterations of the Gut Microbiota by Consumption of Dietary Daikenchuto (TU‐100)

Miyoshi, J., Nobutani, K., Musch, M. W., Ringus, D. L., Hubert, N. A., Yamamoto, M., Kase, Y., Nishiyama, M., & Chang, E. B. (2018) · Evidence-based Complementary and Alternative Medicine · doi:10.1155/2018/7415975 · Cited by 21

Neuroimmunomodulation of tissue injury and disease: an expanding view of the inflammatory reflex pathway

Tanaka, S., HAMMOND, B. F., Rosin, D. L., & Okusa, M. D. (2019) · Bioelectronic Medicine · doi:10.1186/s42234-019-0029-8 · Cited by 22

Tofacitinib for the treatment of active ankylosing spondylitis in adults

Mohanakrishnan, R., Beier, S., & Deodhar, A. (2022) · Expert Review of Clinical Immunology · doi:10.1080/1744666x.2022.2038134 · Cited by 21

Postbiotic Administration Ameliorates Colitis and Inflammation in Rats Possibly through Gut Microbiota Modulation

Feng, C., Peng, C., Zhang, W., Zhang, T., He, Q., Kwok, L., & Zhang, H. (2024) · Journal of Agricultural and Food Chemistry · doi:10.1021/acs.jafc.3c03901 · Cited by 23

Compendium of Bifidobacterium-based probiotics: characteristics and therapeutic impact on human diseases

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