Mechanisms and consequences of intestinal dysbiosis

The “Golden Age” of Probiotics: A Systematic Review and Meta-Analysis of Randomized and Observational Studies in Preterm Infants

Dermyshi, E., Wang, Y., Yan, C., Hong, W., Qiu, G., Gong, X., & Zhang, T. (2017) · Neonatology · doi:10.1159/000454668 · Cited by 24,586

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

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

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

Changes of Intestinal Functions in Liver Cirrhosis

Fukui, H., & Wiest, R. (2016) · Inflammatory Intestinal Diseases · doi:10.1159/000444436 · Cited by 6,820

Metabolic Endotoxemia Initiates Obesity and Insulin Resistance

Cani, P. D., Amar, J., Iglesias, M. A., Poggi, M., Knauf, C., Bastelica, D., Neyrinck, A. M., Fava, F., Tuohy, K. M., Chabo, C., et al. (2007) · Diabetes · doi:10.2337/db06-1491 · Cited by 6,638

Linking long-term dietary patterns with gut microbial enterotypes

Wu, G. D., Chen, J., Hoffmann, C., Bittinger, K., Chen, Y.-Y., Keilbaugh, S. A., Bewtra, M., Knights, D., Walters, W. A., Knight, R., et al. (2011) · Science · doi:10.1126/science.1208344 · Cited by 6,513

The gut microbiota as an environmental factor that regulates fat storage

Bäckhed, F., Ding, H., Wang, T., Hooper, L. V., Koh, G. Y., Nagy, A., Semenkovich, C. F., & Gordon, J. I. (2004) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0407076101 · Cited by 6,245

Foodomics-Based Approaches Shed Light on the Potential Protective Effects of Polyphenols in Inflammatory Bowel Disease

Pratelli, G., Tamburini, B., Carlisi, D., Blasio, A. D., D’Anneo, A., Emanuele, S., Notaro, A., Affranchi, F., Giuliano, M., Seidita, A., et al. (2023) · International Journal of Molecular Sciences · doi:10.3390/ijms241914619 · Cited by 14

Composition of gut microbiota and its correlations with neurological, intestinal, cardiovascular and metabolic diseases

Sciuto, M., & Catanzaro, R. (2023) · Acta Microbiologica et Immunologica Hungarica · doi:10.1556/030.2023.02134 · Cited by 15

Dysbiosis in inflammatory bowel diseases: egg, not chicken

Stange, E. F. (2024) · Frontiers in Medicine · doi:10.3389/fmed.2024.1395861 · Cited by 14

Gut microbiome features in pediatric food allergy: a scoping review

Farnetano, M., Carucci, L. R., Coppola, S., Oglio, F., Masino, A., Cozzolino, M., Nocerino, R., & Canani, R. B. (2024) · Frontiers in Allergy · doi:10.3389/falgy.2024.1438252 · Cited by 16

Gut Microbes and Neuropathology: Is There a Causal Nexus?

Dinan, K., & Dinan, T. G. (2022) · Pathogens · doi:10.3390/pathogens11070796 · Cited by 15

Stress and Immune Function

Castellazzi, A. M., Tagliacarne, S. C., Soldi, S., Perna, S., Ziviani, L., Milleri, S., Montagna, L., & Valsecchi, C. (2018) · Journal of Clinical Gastroenterology · doi:10.1097/mcg.0000000000001056 · Cited by 14

Experimental Cyclic Heat Stress on Intestinal Permeability, Bone Mineralization, Leukocyte Proportions and Meat Quality in Broiler Chickens

Rocchi, A. J., Ruff, J., Maynard, C. J., Forga, A. J., Señas-Cuesta, R., Greene, E. S., Latorre, J. D., Vuong, C. N., Graham, B. D., Hernández-Velasco, X., et al. (2022) · Animals · doi:10.3390/ani12101273 · Cited by 13

Intestinal changes associated with nitrite exposure in Bufo gargarizans larvae: Histological damage, immune response, and microbiota dysbiosis

Liu, Y., Wang, H., Wu, L., Han, J. Z., Sui, B., Meng, L., Xu, Y., Lu, S., Wang, H., & Peng, J. (2022) · Aquatic Toxicology · doi:10.1016/j.aquatox.2022.106228 · Cited by 13

Prebiotics and Probiotics: Effects on Dyslipidemia and NAFLD/NASH and the Associated Mechanisms of Action

Fernández‐Martínez, E., Rodríguez-Pastén, A., Pérez‐Hernández, N., Soria-Jasso, L. E., & Cariño‐Cortés, R. (2022) · Current Pharmaceutical Biotechnology · doi:10.2174/1389201023666220818145350 · Cited by 13

Evidence for proton-pump inhibitor (PPI)-associated dysbiosis in metabolically unhealthy obesity

Burmeister, M. A., Smith, T. E., Fincher, T. K., & Weldon, A. J. (2023) · Frontiers in Endocrinology · doi:10.3389/fendo.2023.1205490 · Cited by 14

Gut–Kidney–Heart: A Novel Trilogy

Caldarelli, M., Franza, L., Rio, P., Gasbarrini, A., Gambassi, G., & Cianci, R. (2023) · Biomedicines · doi:10.3390/biomedicines11113063 · Cited by 14

Recent progresses in gut microbiome mediates obstructive sleep apnea‐induced cardiovascular diseases

Zhang, X., Zhang, H., Li, S. C., Fang, F., Yin, Y., & Wang, Q. (2024) · FASEB BioAdvances · doi:10.1096/fba.2023-00153 · Cited by 13

Gut microbial dysbiosis and inflammation: Impact on periodontal health

Zhao, Y., Liu, Y. F., & Lü, J. (2024) · Journal of Periodontal Research · doi:10.1111/jre.13324 · Cited by 14

Vitis vinifera L. Leaf Extract, a Microbiota Green Ally against Infectious and Inflammatory Skin and Scalp Diseases: An In-Depth Update

Armari, M., Zavattaro, E., Trejo, C. F., Galeazzi, A., Grossetti, A., Veronese, F., Savoia, P., & Azzimonti, B. (2024) · Antibiotics · doi:10.3390/antibiotics13080697 · Cited by 13

The Role of Microbiome and Probiotics in Chemo‐Radiotherapy‐Induced Diarrhea: A Narrative Review of the Current Evidence

Khorashadizadeh, S., Abbasifar, S., Yousefi, M., Fayedeh, F., & Ghalibaf, A. M. (2024) · Cancer Reports · doi:10.1002/cnr2.70029 · Cited by 14

Disbiose Intestinal: Correlação com doenças crônicas da atualidade e intervenção nutricional

NeuHannig, C., Regis, C., Soika, J. H., Silva, L. A. D. S., Quintanilha, V. A. B., Bussolotto, L. T., Vicentini, M. S., & Bello, S. R. D. B. (2019) · Research Society and Development · doi:10.33448/rsd-v8i6.1054 · Cited by 13

Microbes as Drugs: The Potential of Pharmabiotics

LeBegue, C. E., Love, B. L., & Wyatt, M. D. (2019) · Pharmacotherapy The Journal of Human Pharmacology and Drug Therapy · doi:10.1002/phar.2357 · Cited by 13

The Gut Microbiota–Polyphenol–NLRP3 Inflammasome Axis: A Key Regulatory Network Linking Diet to Chronic Inflammation

Mosca, L., Pagano, C., Tafuri, M. G., Maio, G. D., Rejano-Gordillo, C. M., Marca, R. D., D’Angelo, S., Monda, M., Messina, G., Polito, R., et al. (2026) · Nutrients · doi:10.3390/nu18101483 · Cited by 13

The effect of microbiome composition on impulsive and violent behavior: A systematic review

Langmajerová, M., Roubalová, R., Šebela, A., & Vevera, J. (2022) · Behavioural Brain Research · doi:10.1016/j.bbr.2022.114266 · Cited by 15

Role of Gut Microbiota and Oxidative Stress in the Progression of Transplant-Related Complications following Hematopoietic Stem Cell Transplantation

Chi, M., Jiang, T., He, X., Peng, H., Li, Y., Zhang, J., Wang, L., Nian, Q., Ma, K., & Liu, C. (2023) · Oxidative Medicine and Cellular Longevity · doi:10.1155/2023/3532756 · Cited by 12

The possible role of gut microbiota dysbiosis in the pathophysiology of delirium in older persons

Ticinesi, A., Parise, A., Nouvenne, A., Cerundolo, N., Prati, B., & Meschi, T. (2023) · Microbiome Research Reports · doi:10.20517/mrr.2023.15 · Cited by 12

Alteration of intestinal microbiota is associated with diabetic retinopathy and its severity: Samples collected from southeast coast Chinese

Gu, X., Lu, C., Pan, J. G., Ye, J., & Zhu, Q. (2023) · World Journal of Diabetes · doi:10.4239/wjd.v14.i6.862 · Cited by 12

Mechanisms of Male Reproductive Sterility Triggered by Dysbiosis of Intestinal Microorganisms

Wei, M., Liu, H., Wang, Y., Sun, M., & Shang, P. (2024) · Life · doi:10.3390/life14060694 · Cited by 15

The Critical Role of Faecalibacterium prausnitzii in Cardiovascular Diseases

Zheng, T., Meng, C., Lv, Z., Wu, C., Zhou, X., & Mao, W. (2025) · Reviews in Cardiovascular Medicine · doi:10.31083/rcm26740 · Cited by 15

Human gut microbiome gene co-expression network reveals a loss in taxonomic and functional diversity in Parkinson’s disease

Villette, R., Novikova, P. V., Laczny, C. C., Mollenhauer, B., May, P., & Wilmes, P. (2025) · npj Biofilms and Microbiomes · doi:10.1038/s41522-025-00780-0 · Cited by 16

A Mechanistic Model of Gut–Brain Axis Perturbation and High-Fat Diet Pathways to Gut Microbiome Homeostatic Disruption, Systemic Inflammation, and Type 2 Diabetes

Lew, K. N., Starkweather, A. R., Cong, X. S., & Judge, M. P. (2019) · Biological Research For Nursing · doi:10.1177/1099800419849109 · Cited by 12

Kefir and the Gut–Skin Axis

Alves, E., Gregório, J., Rijo, P. M., Rosado, C., & Rodrigues, L. M. (2022) · International Journal of Environmental Research and Public Health · doi:10.3390/ijerph192113791 · Cited by 13

Clostridioides difficile Binary Toxin Binding Component Increases Virulence in a Hamster Model

Simpson, M. D., Bilverstone, T. W., Leslie, J. L., Donlan, A. N., Uddin, M. J., Petri, W. A., Marin, N., Schwan, C., Kuehne, S., Minton, N. P., et al. (2023) · Open Forum Infectious Diseases · doi:10.1093/ofid/ofad040 · Cited by 12

The Value of a Comparative Approach to Understand the Complex Interplay between Microbiota and Host Immunity

Morella, N. M., & Koskella, B. (2017) · Frontiers in Immunology · doi:10.3389/fimmu.2017.01114 · Cited by 12

Local Bacteriotherapy – a promising preventive tool in recurrent respiratory infections

Ciprandi, G., Mantia, I. L., Damiani, V., & Passàli, D. (2020) · Expert Review of Clinical Immunology · doi:10.1080/1744666x.2021.1833720 · Cited by 12

Shugan Hewei Decoction Alleviates Cecum Mucosal Injury and Improves Depressive- and Anxiety-Like Behaviors in Chronic Stress Model Rats by Regulating Cecal Microbiota and Inhibiting NLRP3 Inflammasome

Yue, Y., Chen, Y., Liu, H., Xu, L.-S., Zhou, X., Ming, H., Chen, X., Chen, M., Lin, Y., Liu, L., et al. (2021) · Frontiers in Pharmacology · doi:10.3389/fphar.2021.766474 · Cited by 12

Beneficial Role of Fruits, Their Juices, and Freeze-Dried Powders on Inflammatory Bowel Disease and Related Dysbiosis

Perri, M. R., Romano, C., Marrelli, M., Zicarelli, L., Toma, C.-C., Basta, D., Conforti, F., & Statti, G. A. (2021) · Plants · doi:10.3390/plants11010004 · Cited by 13

Dispersed Crude Oil Induces Dysbiosis in the Red Snapper Lutjanus campechanus External Microbiota

Tarnecki, A. M., Miller, C., Sherwood, T. A., Griffitt, R. J., Schloesser, R. W., & Wetzel, D. L. (2022) · Microbiology Spectrum · doi:10.1128/spectrum.00587-21 · Cited by 12

Intratumoral microbiome: the double-edged sword in remodeling cancer immunotherapy

Yan, D., Yu, Y., Liang, C., Cui, Z., Shi, L., Li, G., & Ren, C. (2026) · Molecular Cancer · doi:10.1186/s12943-025-02566-6 · Cited by 11

Impact of gut-peripheral nervous system axis on the development of diabetic neuropathy

Mázala-de-Oliveira, T., de Sá, Y. A. P. J., & Carvalho, V. F. (2023) · Memórias do Instituto Oswaldo Cruz · doi:10.1590/0074-02760220197 · Cited by 12

Dracocephalum moldavica L. extract alleviates experimental colitis in rats by modulating gut microbiome and inflammatory pathways

Gang, S., Bai, W., Yu, H., Gula, A., & Wang, Z. (2023) · Molecular Medicine Reports · doi:10.3892/mmr.2023.13115 · Cited by 11

The role of intestinal flora on tumor immunotherapy: recent progress and treatment implications

Zhou, Y., Liu, X., Gao, W., Luo, X., Lv, J., Wang, Y., & Liu, D. (2023) · Heliyon · doi:10.1016/j.heliyon.2023.e23919 · Cited by 11

Neutrophils in the Focus: Impact on Neuroimmune Dynamics and the Gut–Brain Axis

Kršek, A., & Batičić, L. (2024) · Gastrointestinal Disorders · doi:10.3390/gidisord6030039 · Cited by 13

Unveiling the Gut-Disc Axis: How Microbiome Dysbiosis Accelerates Intervertebral Disc Degeneration

Sun, Y., Li, Z., Duan, J., Liu, E., Sun, F., Yang, L., Chen, L., & Yang, S. (2024) · Journal of Inflammation Research · doi:10.2147/jir.s487936 · Cited by 11

The impact of gut microbiome on immune and metabolic homeostasis in type 1 diabetes: Clinical insights for prevention and treatment strategies

Li, J., Xie, Z., Yang, L., Guo, K., & Zhou, Z. (2025) · Journal of Autoimmunity · doi:10.1016/j.jaut.2025.103371 · Cited by 12

Linoleic acid, mitochondria, gut microbiome, and metabolic health: a mechanistic review

Mercola, J. M. (2025) · Advances in Redox Research · doi:10.1016/j.arres.2025.100128 · Cited by 11

Effects of dietary macronutrient profile on apparent total tract macronutrient digestibility and fecal microbiota, fermentative metabolites, and bile acids of female dogs after spay surgery

Phungviwatnikul, T., Alexander, C., Do, S., He, F., Suchodolski, J. S., de Godoy, M. R. C., & Swanson, K. S. (2021) · Journal of Animal Science · doi:10.1093/jas/skab225 · Cited by 17

Dynamic alterations of the mice gut virome after Coxsackievirus B3 infection

Bao, S., Wang, H., Li, W., Ji, L., Wang, X., Shen, Q., Yang, S., Zhou, C., & Zhang, W. (2022) · Journal of Medical Virology · doi:10.1002/jmv.27946 · Cited by 10

Gut–Lung Microbiota Interaction in COPD Patients: A Literature Review

Krūmiņa, A., Bogdanova, M., Gintere, S., & Vīksna, L. (2022) · Medicina · doi:10.3390/medicina58121760 · Cited by 12

Maturation state of colonization sites promotes symbiotic resiliency in the Euprymna scolopes-Vibrio fischeri partnership

Essock‐Burns, T., Lawhorn, S., Wu, L., McClosky, S., Moriano‐Gutierrez, S., Ruby, E. G., & McFall‐Ngai, M. (2023) · Microbiome · doi:10.1186/s40168-023-01509-x · Cited by 11

Effect of gut microbiome regulated Taohong Siwu Decoction metabolism on glioma cell phenotype

Feng, S., Wan, Q., Wu, W., Zhang, C., Lu, H., & Lu, X. (2023) · Frontiers in Cellular and Infection Microbiology · doi:10.3389/fcimb.2023.1192589 · Cited by 11

Moringa oleifera Leaves Protein Enhances Intestinal Permeability by Activating TLR4 Upstream Signaling and Disrupting Tight Junctions

Liu, X., Xi, C., Li, W., Su, H., Yang, H., Bai, Z., Tian, Y., & Song, S. (2023) · International Journal of Molecular Sciences · doi:10.3390/ijms242216425 · Cited by 11

Ileal Pouch–Anal Anastomosis and Pouchitis: The Role of the Microbiota in the Pathogenesis and Therapy

Gabbiadini, R., Buono, A. D., Correale, C., Spinelli, A., Repici, A., Armuzzi, A., & Roda, G. (2022) · Nutrients · doi:10.3390/nu14132610 · Cited by 11

Dynamics of the Gut Microbiome and Transcriptome in Korea Native Ricefish (Oryzias latipes) during Chronic Antibiotic Exposure

Yoon, J. B., Hwang, S., Yang, J. H., Lee, S., Bang, W. Y., & Moon, K. H. (2022) · Genes · doi:10.3390/genes13071243 · Cited by 11

Oral administration of RDP58 ameliorated DSS-induced colitis in intestinal microbiota dependent manner

Zheng, D., Ke, X., Cai, H., Yan, C., Chen, Y., Sun, J., & Chen, G. (2024) · International Immunopharmacology · doi:10.1016/j.intimp.2024.112325 · Cited by 10

Should We Treat SIBO Patients? Impact on Quality of Life and Response to Comprehensive Treatment: A Real-World Clinical Practice Study

Liebana, A. R., Redondo‐Cuevas, L., Nicolás, Á., Martín-Carbonell, V., Artero, L. S., Olivares, A., Grau, F., Ynfante, M., Colmenares, M., Molina, M. J. T., et al. (2025) · Nutrients · doi:10.3390/nu17071251 · Cited by 10

Exploring the gut microbiome’s influence on cancer-associated anemia: Mechanisms, clinical challenges, and innovative therapies

Bangolo, A., Amoozgar, B., Habibi, M., Simms, E., Nagesh, V. K., Wadhwani, S., Wadhwani, N., Auda, A., Eliáš, D., Mansour, C., et al. (2025) · World Journal of Gastrointestinal Pharmacology and Therapeutics · doi:10.4292/wjgpt.v16.i2.105375 · Cited by 10

Could modulating the esophageal microbiome be the answer for eosinophilic esophagitis treatment?

Facchin, S., Bonazzi, E., Tomasulo, A., Bertin, L., Lorenzon, G., Maniero, D., Zingone, F., Cardin, R., Barberio, B., Ghisa, M., et al. (2025) · Expert Review of Gastroenterology & Hepatology · doi:10.1080/17474124.2025.2530606 · Cited by 10

Gut Microbiota Changes in Metabolic Dysfunction-Associated Steatohepatitis and Inflammatory Bowel Disease: Common Pathogenic Features

Scarlata, G. G. M., Morano, D., Ismaiel, A., Spagnuolo, R., Luzza, F., Dumitrascu, D. L., & Abenavoli, L. (2025) · Current Issues in Molecular Biology · doi:10.3390/cimb47100847 · Cited by 12

Immunometabolism, Micronutrients, and Bariatric Surgery: The Use of Transcriptomics and Microbiota-Targeted Therapies

Galyean, S., Sawant, D., & Shin, A. C. (2020) · Mediators of Inflammation · doi:10.1155/2020/8862034 · Cited by 11

Immunonutrition and SARS-CoV-2 Infection in Children with Obesity

D’Auria, E., Calcaterra, V., Verduci, E., Ghezzi, M., Lamberti, R., Vizzuso, S., Baldassarre, P., Pendezza, E., Perico, V., Bosetti, A., et al. (2022) · Nutrients · doi:10.3390/nu14091701 · Cited by 10

Black corn (Zea mays L.) flour has the potential to improve the gut microbiota composition and goblet cell proliferation in mice fed a high-fat diet

Verediano, T. A., Ana, C. T. S., Grancieri, M., Tako, E., Paes, M. C. D., & Martino, H. S. D. (2022) · Nutrition Research · doi:10.1016/j.nutres.2022.10.005 · Cited by 10

Electroacupuncture Inhibits Atherosclerosis through Regulating Intestinal Flora and Host Metabolites in Rabbit

Shen, Y., Cheng, Z.-D., Yi-guo, C., sun, R., Ma, X., Hou, G., & Rui, W. (2020) · Evidence-based Complementary and Alternative Medicine · doi:10.1155/2020/5790275 · Cited by 10

Meta-analysis of metagenomes via machine learning and assembly graphs reveals strain switches in Crohn’s diseasePreprint

Reiter, T. E., Irber, L. C., Gingrich, A. A., Haynes, D., Pierce‐Ward, N. T., Brooks, P., Mizutani, Y., Moritz, D., Reidl, F., Willis, A. D., et al. (2022) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2022.06.30.498290 · Cited by 10

Intestinal Flora Imbalance Induced by Antibiotic Use in Rats

Tong, G., Qian, H., Li, D., Li, J., Chen, J., Li, X., & Tan, Z. (2024) · Journal of Inflammation Research · doi:10.2147/jir.s447098 · Cited by 9

Wheat germ supplementation has modest effects on gut health markers but improves glucose homeostasis markers in adults classified as overweight: A randomized controlled pilot study

Dotimas, L., Ojo, B. A., Kaur, A., Alake, S. E., Dixon, M. D., El-Rassi, G. D., Ice, J. A., Zhao, J., Emerson, S. R., Smith, B. J., et al. (2024) · Nutrition Research · doi:10.1016/j.nutres.2024.05.001 · Cited by 9

Advanced Lung Cancer Inflammation Index: A Novel Comprehensive Biomarker of Host Status for Patients with Metastatic Colorectal Cancer

Horino, T., Tokunaga, R., Miyamoto, Y., & Baba, H. (2024) · Journal of the Anus Rectum and Colon · doi:10.23922/jarc.2023-077 · Cited by 9

Epigallocatechin-3-Gallate, Quercetin, and Kaempferol for Treatment of Parkinson’s Disease Through Prevention of Gut Dysbiosis and Attenuation of Multiple Molecular Mechanisms of Pathogenesis

Kalu, A., & Ray, S. K. (2025) · Brain Sciences · doi:10.3390/brainsci15020144 · Cited by 11

Proline rich-39 (PR-39) antimicrobial protein alleviated lipopolysaccharide-induced intestinal barrier dysfunction in piglets by altering intestinal flora associated bile acid metabolism and in turn regulating TGR-5/NF-κB/MLCK/MLC pathway

Liu, Z., Qin, X., Zhang, B., Nong, K., Chen, W., Yang, Z., Wen, L., Liu, X., Li, L., Wang, X., et al. (2025) · International Journal of Biological Macromolecules · doi:10.1016/j.ijbiomac.2025.141930 · Cited by 9

Exploring bacteriophages to combat gut dysbiosis: A promising new frontier in microbiome therapy

Easwaran, M., Abdelrahman, F. I., El‐Shibiny, A., Venkidasamy, B., Thiruvengadam, M., Sivalingam, P., Ganapathy, D. M., Ahn, J., & Shin, H. (2025) · Microbial Pathogenesis · doi:10.1016/j.micpath.2025.108008 · Cited by 9

Regulation of Intestinal Permeability in Health and Disease: Possible Therapeutic Applications

Güemes-González, A. M., Arriaga‐Pizano, L., Chacón‐Salinas, R., Wong‐Baeza, I., & Ferat-Osorio, E. A. (2025) · Archives of Medical Research · doi:10.1016/j.arcmed.2025.103321 · Cited by 13

Alteration of Gut Microbiota by Ketogenic Diet as an Alternative Therapeutic Target for Drug-Resistant Epilepsy

Tang, M., Wang, W., Wang, J., & Wang, Y. (2025) · Microorganisms · doi:10.3390/microorganisms13112539 · Cited by 10

An integrated approach to assess exposure and early health effects in human populations exposed to micro- and nanoplastics

Catalán, J., Afanou, A. K., Arranz, J. A., Ballesteros, A., Banić, I., Dirven, H. A. A. M., Estrela‐Lopis, I., Hernández, A., Kanerva, T., Laforsch, C., et al. (2025) · NanoImpact · doi:10.1016/j.impact.2025.100600 · Cited by 9

A importância da microbiota intestinal e seus efeitos na obesidade

de Souza, C. S. C., de Souza, R. C., Evangelista, J. D. N., & Ferreira, J. C. D. S. (2021) · Research Society and Development · doi:10.33448/rsd-v10i6.16086 · Cited by 9

Effect of Administration of Azithromycin and/or Probiotic Bacteria on Bones of Estrogen-Deficient Rats

Cegieła, U., Londzin, P., Janas, A., Pytlik, M., & Folwarczna, J. (2022) · Pharmaceuticals · doi:10.3390/ph15080915 · Cited by 9

Effects of isolation and confinement on gastrointestinal microbiota–a systematic review

Klos, B., Steinbach, C., Ketel, J., Lambert, C., Penders, J., Dore, J. M., Enck, P., & Mack, I. (2023) · Frontiers in Nutrition · doi:10.3389/fnut.2023.1214016 · Cited by 10

Intestinal Microbiome in Dogs with Chronic Hepatobiliary Disease: Can We Talk about the Gut–Liver Axis?

Habermaass, V., Olivero, D., Gori, E., Mariti, C., Longhi, E., & Marchetti, V. (2023) · Animals · doi:10.3390/ani13203174 · Cited by 10

Summatory Effects of Anaerobic Exercise and a ‘Westernized Athletic Diet’ on Gut Dysbiosis and Chronic Low-Grade Metabolic Acidosis

Álvarez‐Herms, J. (2024) · Microorganisms · doi:10.3390/microorganisms12061138 · Cited by 9

Effects of the Cistanche tubulosa Aqueous Extract on the Gut Microbiota of Mice with Intestinal Disorders

Bao, X., Bai, D., Liu, X., Wang, Y., Zeng, L., Wei, C., & Jin, W. (2021) · Evidence-based Complementary and Alternative Medicine · doi:10.1155/2021/4936970 · Cited by 9

A Novel Approach toward Less Invasive Multiomics Gut Analyses: a Pilot Study

Berlinberg, A. J., Brar, A., Stahly, A., Gerich, M. E., Fennimore, B. P., Scott, F. I., & Kuhn, K. A. (2022) · Microbiology Spectrum · doi:10.1128/spectrum.02446-21 · Cited by 9

Nonextractable Polyphenols: A Relevant Group with Health Effects

Martínez‐Meza, Y., Reynoso‐Camacho, R., & Pérez‐Jiménez, J. (2020) · Wiley eBooks · doi:10.1002/9781119563754.ch2 · Cited by 9

Targeting Polyphosphate Kinases in the Fight against Pseudomonas aeruginosa

Baijal, K., & Downey, M. (2021) · mBio · doi:10.1128/mbio.01477-21 · Cited by 9

Abnormalities in microbial composition and function in infants with necrotizing enterocolitis: A single-center observational study

Huang, H., Peng, Q., Zhang, Y., Li, Y., Huang, N., Miao, D., & Huang, B. (2022) · Frontiers in Pediatrics · doi:10.3389/fped.2022.963345 · Cited by 8

Bowel dysfunctions after acquired brain injury: a scoping review

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