Metagenomic Analysis of the Gut Microbiome Reveals Enrichment of Menaquinones (Vitamin K2) Pathway in Diabetes Mellitus

Trimmomatic: a flexible trimmer for Illumina sequence data

Bolger, A. M., Lohse, M., & Usadel, B. (2014) · Bioinformatics · doi:10.1093/bioinformatics/btu170 · Cited by 65,548 · see citing works

FLASH: fast length adjustment of short reads to improve genome assemblies

Magoč, T., & Salzberg, S. L. (2011) · Bioinformatics · doi:10.1093/bioinformatics/btr507 · Cited by 15,366 · see citing works

Predictive functional profiling of microbial communities using 16S rRNA marker gene sequences

Langille, M. G. I., Zaneveld, J., Caporaso, J. G., McDonald, D., Knights, D., Reyes, J. A., Clemente, J. C., Burkepile, D. E., Vega Thurber, R. L., Knight, R., et al. (2013) · Nature Biotechnology · doi:10.1038/nbt.2676 · Cited by 9,116 · see citing works

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

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 · see citing works

Functional interactions between the gut microbiota and host metabolism

Tremaroli, V., & Bäckhed, F. (2012) · Nature · doi:10.1038/nature11552 · Cited by 4,387 · see citing works

The MetaCyc database of metabolic pathways and enzymes and the BioCyc collection of pathway/genome databases

Caspi, R., Billington, R., Ferrer, L., Foerster, H., Fulcher, C. A., Keseler, I. M., Kothari, A., Krummenacker, M., Latendresse, M., Mueller, L. A., et al. (2016) · Nucleic Acids Research · doi:10.1093/nar/gkv1164 · Cited by 3,395 · see citing works

Gut microbiota composition correlates with diet and health in the elderly

Claesson, M. J., Jeffery, I. B., Conde, S., Power, S. E., O’Connor, E. M., Cusack, S., Harris, H. M. B., Coakley, M., Lakshminarayanan, B., O’Sullivan, O., et al. (2012) · Nature · doi:10.1038/nature11319 · Cited by 3,314 · see citing works

Gut Microbiota in Human Adults with Type 2 Diabetes Differs from Non-Diabetic Adults

Larsen, N., Vogensen, F. K., van den Berg, F. W. J., Nielsen, D. S., Andreasen, A. S., Pedersen, B. K., Al-Soud, W. A., Sørensen, S. J., Hansen, L. H., & Jakobsen, M. (2010) · PLoS ONE · doi:10.1371/journal.pone.0009085 · Cited by 2,952 · see citing works

MetaPhlAn2 for enhanced metagenomic taxonomic profiling

Truong, D. T., Franzosa, E. A., Tickle, T. L., Scholz, M., Weingart, G., Pasolli, E., Tett, A., Huttenhower, C., & Segata, N. (2015) · Nature Methods · doi:10.1038/nmeth.3589 · Cited by 2,185 · see citing works

Disentangling type 2 diabetes and metformin treatment signatures in the human gut microbiota

MetaHIT consortium, Forslund, K., Hildebrand, F., Nielsen, T., Falony, G., Le Chatelier, E., Sunagawa, S., Prifti, E., Vieira-Silva, S., Gudmundsdottir, V., et al. (2015) · Nature · doi:10.1038/nature15766 · Cited by 2,116 · see citing works

Human gut microbiota in obesity and after gastric bypass

Zhang, H., DiBaise, J. K., Zuccolo, A., Kudrna, D., Braidotti, M., Yu, Y., Parameswaran, P., Crowell, M. D., Wing, R., Rittmann, B. E., et al. (2009) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0812600106 · Cited by 1,880 · see citing works

Immunoglobulin A Coating Identifies Colitogenic Bacteria in Inflammatory Bowel Disease

Palm, N. W., de Zoete, M. R., Cullen, T. W., Barry, N. A., Stefanowski, J., Hao, L., Degnan, P. H., Hu, J., Peter, I., Zhang, W., et al. (2014) · Cell · doi:10.1016/j.cell.2014.08.006 · Cited by 1,286 · see citing works

Revealing the Bacterial Butyrate Synthesis Pathways by Analyzing (Meta)genomic Data

Vital, M., Howe, A. C., & Tiedje, J. M. (2014) · mBio · doi:10.1128/mbio.00889-14 · Cited by 1,189 · see citing works

Human Gut Microbiota Changes Reveal the Progression of Glucose Intolerance

Zhang, X., Shen, D., Fang, Z., Jie, Z., Qiu, X., Zhang, C., Chen, Y., & Ji, L. (2013) · PLoS ONE · doi:10.1371/journal.pone.0071108 · Cited by 946 · see citing works

Involvement of gut microbiota in the development of low-grade inflammation and type 2 diabetes associated with obesity

Cani, P. D., Osto, M., Geurts, L., & Everard, A. (2012) · Gut Microbes · doi:10.4161/gmic.19625 · Cited by 864 · see citing works

Microbiota and diabetes: an evolving relationship

Tilg, H., & Moschen, A. R. (2014) · Gut · doi:10.1136/gutjnl-2014-306928 · Cited by 853 · see citing works

Intestinal Microbiota, Microbial Translocation, and Systemic Inflammation in Chronic HIV Infection

Dinh, D. M., Volpe, G. E., Duffalo, C., Bhalchandra, S., Tai, A., Kane, A. V., WANKE, C. A., & Ward, H. (2014) · The Journal of Infectious Diseases · doi:10.1093/infdis/jiu409 · Cited by 531 · see citing works

Dysbiotic gut microbiota causes transmissible Crohn's disease-like ileitis independent of failure in antimicrobial defence

Schaubeck, M., Clavel, T., Calasan, J., Lagkouvardos, I., Haange, S. B., Jehmlich, N., Basic, M., Dupont, A., Hornef, M., Bergen, M. V., et al. (2016) · Gut · doi:10.1136/gutjnl-2015-309333 · Cited by 447 · see citing works

Metagenome-wide association studies: fine-mining the microbiome

Wang, J., & Jia, H. (2016) · Nature Reviews Microbiology · doi:10.1038/nrmicro.2016.83 · Cited by 429 · see citing works

Unlocking the potential of metagenomics through replicated experimental design

Knight, R. D., Jansson, J. K., Field, D., Fierer, N., Desai, N., Fuhrman, J. A., Hugenholtz, P., van der Lelie, D., Meyer, F., Stevens, R. L., et al. (2012) · Nature Biotechnology · doi:10.1038/nbt.2235 · Cited by 278 · see citing works

The impact of gut microbiota on gender-specific differences in immunity

Fransen, F., van Beek, A. A., Borghuis, T., Meijer, B., Hugenholtz, F., van der Gaast-de Jongh, C., Savelkoul, H. F., de Jonge, M. I., Faas, M. M., Boekschoten, M. V., et al. (2017) · Frontiers in Immunology · doi:10.3389/fimmu.2017.00754 · Cited by 266 · see citing works

Osteocalcin in Human Serum: A Circadian Rhythm*

Gundberg, C. M., MARKOWITZ, M. E., Mizruchi, M. S., & Rosen, J. F. (1985) · The Journal of Clinical Endocrinology & Metabolism · doi:10.1210/jcem-60-4-736 · Cited by 261 · see citing works

The Importance of Menaquinones in Human Nutrition

Suttie, J. W. (1995) · Annual Review of Nutrition · doi:10.1146/annurev.nu.15.070195.002151 · Cited by 231 · see citing works

Age-dependent changes in GI physiology and microbiota: time to reconsider?

An, R., Wilms, E., Masclee, A. A. M., Smidt, H., Zoetendal, E. G., & Jonkers, D. (2018) · Gut · doi:10.1136/gutjnl-2017-315542 · Cited by 209 · see citing works

Menaquinone-7 supplementation improves arterial stiffness in healthy postmenopausal women

Knapen, M. H. J., Braam, L. A. J. L. M., Drummen, N. E. A., Bekers, O., Hoeks, A. P. G., & Vermeer, C. (2015) · Thrombosis and Haemostasis · doi:10.1160/th14-08-0675 · Cited by 193 · see citing works

Effect of Vitamin K Supplementation on Insulin Resistance in Older Men and Women

Yoshida, M., Jacques, P. F., Meigs, J. B., Saltzman, E., Shea, M. K., Gundberg, C., Dawson-Hughes, B., Dallal, G., & Booth, S. L. (2008) · Diabetes Care · doi:10.2337/dc08-1204 · Cited by 177 · see citing works

Dietary Phylloquinone and Menaquinones Intakes and Risk of Type 2 Diabetes

Beulens, J. W. J., van der A, D. L., Grobbee, D. E., Sluijs, I., Spijkerman, A. M. W., & van der Schouw, Y. T. (2010) · Diabetes Care · doi:10.2337/dc09-2302 · Cited by 177 · see citing works

Gut Microbiota, Low-grade Inflammation, and Metabolic Syndrome

Chassaing, B., & Gewirtz, A. T. (2013) · Toxicologic Pathology · doi:10.1177/0192623313508481 · Cited by 174 · see citing works

Creatinine Metabolism in Humans with Decreased Renal Function: Creatinine Deficit

Jones, J. D., & Burnett, P. C. (1974) · Clinical Chemistry · doi:10.1093/clinchem/20.9.1204 · Cited by 166 · see citing works

Aging and the human gut microbiota—from correlation to causality

Saraswati, S., & Sitaraman, R. (2015) · Frontiers in Microbiology · doi:10.3389/fmicb.2014.00764 · Cited by 153 · see citing works

The production of menaquinones (vitamin K2) by intestinal bacteria and their role in maintaining coagulation homeostasis.

Conly, J. M., & Stein, K. (1993) · PubMed · Cited by 141 · see citing works

Association of Multiple Inflammatory Markers with Carotid Intimal Medial Thickness and Stenosis (from the Framingham Heart Study)

Thakore, A. H., Guo, C., Larson, M. G., Corey, D., Wang, T. J., Vasan, R. S., D’Agostino, R. B., Lipinska, I., Keaney, J. F., Benjamin, E. J., et al. (2007) · The American Journal of Cardiology · doi:10.1016/j.amjcard.2007.01.036 · Cited by 131 · see citing works

Glucose metabolism: Focus on gut microbiota, the endocannabinoid system and beyond

Cani, P. D., Geurts, L., Matamoros, S., Plovier, H., & Duparc, T. (2014) · Diabetes & Metabolism · doi:10.1016/j.diabet.2014.02.004 · Cited by 130 · see citing works

Vitamin K2 stimulates osteoblastogenesis and suppresses osteoclastogenesis by suppressing NF-κB activation

Yamaguchi, M. (2010) · International Journal of Molecular Medicine · doi:10.3892/ijmm.2010.562 · Cited by 115 · see citing works

Increased intestinal permeability to oral chromium ( 51 Cr) ‐ EDTA in human Type 2 diabetes

Horton, F., Wright, J., Smith, L., Hinton, P. J., & Robertson, M. D. (2013) · Diabetic Medicine · doi:10.1111/dme.12360 · Cited by 112 · see citing works

Vitamin K2 Supplementation Improves Insulin Sensitivity via Osteocalcin Metabolism: A Placebo-Controlled Trial

Choi, H. J., Yu, J., Choi, H., An, J. H., Kim, S. W., Park, K. S., Jang, H. C., Kim, S. Y., & Shin, C. S. (2011) · Diabetes Care · doi:10.2337/dc11-0551 · Cited by 106 · see citing works

Determining Microbial Products and Identifying Molecular Targets in the Human Microbiome

Cordy, R. J., Yasuda, K., Shafquat, A., Morgan, X. C., & Huttenhower, C. (2014) · Cell Metabolism · doi:10.1016/j.cmet.2014.10.003 · Cited by 100 · see citing works

Gas and the Microbiome

Pimentel, M., Mathur, R., & Chang, C. C.-C. (2013) · Current Gastroenterology Reports · doi:10.1007/s11894-013-0356-y · Cited by 88 · see citing works

Diabetes Induces Lysine Acetylation of Intermediary Metabolism Enzymes in the Kidney

Kosanam, H., Thai, K., Zhang, Y., Advani, A., Connelly, K. A., Diamandis, E. P., & Gilbert, R. E. (2014) · Diabetes · doi:10.2337/db12-1770 · Cited by 72 · see citing works

Possible effects of one week vitamin K (menaquinone-4) tablets intake on glucose tolerance in healthy young male volunteers with different descarboxy prothrombin levels

SAKAMOTO, N., Nishiike, T., Iguchi, H., & SAKAMOTO, K. (2000) · Clinical Nutrition · doi:10.1054/clnu.2000.0102 · Cited by 43 · see citing works

Validity and Reproducibility of a Habitual Dietary Fibre Intake Short Food Frequency Questionnaire

Healey, G. R., Brough, L., Murphy, R., HEDDERLEY, D. I., Butts, C. A., & Coad, J. (2016) · Nutrients · doi:10.3390/nu8090558 · Cited by 40 · see citing works

Metagenomic systems biology and metabolic modeling of the human microbiome

Levy, R., & Borenstein, E. (2014) · Gut Microbes · doi:10.4161/gmic.28261 · Cited by 39 · see citing works

Isolation of vitamin K2(35) from Nocardia restrictus and Corynebacterium simplex. A natural electron acceptor in microbial steroid ring A dehydrogenations.

Abul‐Hajj, Y. J. (1978) · Journal of Biological Chemistry · doi:10.1016/s0021-9258(17)38081-x · Cited by 34 · see citing works

Personalized microbiome-driven effects of non-nutritive sweeteners on human glucose tolerance

Suez, J., Cohen, Y., Valdés‐Mas, R., Mor, U., Dori-Bachash, M., Federici, S., Zmora, N., Leshem, A., Heinemann, M., Linevsky, R., et al. (2022) · Cell · doi:10.1016/j.cell.2022.07.016 · Cited by 431 · see citing works

Longitudinal gut microbiome changes in immune checkpoint blockade-treated advanced melanoma

Björk, J. R., Bolte, L. A., Maltez Thomas, A., Lee, K. A., Rossi, N., Wind, T. T., Smit, L. M., Armanini, F., Asnicar, F., Blanco-Miguez, A., et al. (2024) · Nature Medicine · doi:10.1038/s41591-024-02803-3 · Cited by 156 · see citing works

Unraveling metagenomics through long-read sequencing: a comprehensive review

Kim, C., Pongpanich, M., & Porntaveetus, T. (2024) · Journal of Translational Medicine · doi:10.1186/s12967-024-04917-1 · Cited by 129 · see citing works

Vitamin K2 Holds Promise for Alzheimer’s Prevention and Treatment

Popescu, A., & German, M. (2021) · Nutrients · doi:10.3390/nu13072206 · Cited by 55 · see citing works

Type 1 diabetes in pregnancy is associated with distinct changes in the composition and function of the gut microbiome

Roth‐Schulze, A. J., Penno, M. A. S., Ngui, K., Oakey, H., Bandala‐Sanchez, E., Smith, A. D., Allnutt, T. R., Thomson, R. L., Vuillermin, P., Craig, M. E., et al. (2021) · Microbiome · doi:10.1186/s40168-021-01104-y · Cited by 40 · see citing works

Uncovering the relationship between gut microbial dysbiosis, metabolomics, and dietary intake in type 2 diabetes mellitus and in healthy volunteers: a multi-omics analysis

Bataineh, M. T. A., Künstner, A., Dash, N. R., AlSafar, H. S., Ragab, M., Schmelter, F., Sina, C., Busch, H. S., & Ibrahim, S. M. (2023) · Scientific Reports · doi:10.1038/s41598-023-45066-7 · Cited by 41 · see citing works

Functional alterations and predictive capacity of gut microbiome in type 2 diabetes

Dash, N. R., Bataineh, M. T. A., Alili, R., Safar, H. A., Alkhayyal, N., Prifti, E., Zucker, J., Belda, E., & Clément, K. (2023) · Scientific Reports · doi:10.1038/s41598-023-49679-w · Cited by 40 · see citing works

The gut microbiota pathway mechanisms of diabetes

Bajinka, O., Tan, Y., Darboe, A., Ighaede-Edwards, I. G., & Abdelhalim, K. A. (2023) · AMB Express · doi:10.1186/s13568-023-01520-3 · Cited by 38 · see citing works

Adiposity is associated with expansion of the genus Dialister in rheumatoid arthritis patients

Vázquez, N. M., Ruiz‐Limón, P., Moreno‐Indias, I., Arija, S. M., Lisbona-Montañez, J. M., Rioja, J., Mucientes, A., Martín‐Núñez, G. M., Cano‐García, L., Tinahones, F. J., et al. (2023) · Biomedicine & Pharmacotherapy · doi:10.1016/j.biopha.2023.114388 · Cited by 26 · see citing works

The Effect of Polyphenol Extract from Rosa Roxburghii Fruit on Plasma Metabolome and Gut Microbiota in Type 2 Diabetic Mice

Wang, H., Chen, Z., Wang, M., Long, M., Ren, T., Chen, C., Dai, X., Yang, S., & Tan, S. (2022) · Foods · doi:10.3390/foods11121747 · Cited by 26 · see citing works

Effects of Non-Polar Dietary and Endogenous Lipids on Gut Microbiota Alterations: The Role of Lipidomics

Tsiantas, K., Konteles, S. J., Kritsi, E., Sinanoglou, V. J., Tsiaka, T., & Zoumpoulakis, P. G. (2022) · International Journal of Molecular Sciences · doi:10.3390/ijms23084070 · Cited by 25 · see citing works

Virulence Factors of the Gut Microbiome Are Associated with BMI and Metabolic Blood Parameters in Children with Obesity

Murga-Garrido, S. M., Ulloa‐Pérez, E., Díaz-Benítez, C. E., Orbe-Orihuela, Y. C., Cornejo‐Granados, F., Ochoa‐Leyva, A., Sánchez‐Flores, A., Cruz, M., Castañeda-Márquez, A. C., Plett-Torres, T., et al. (2023) · Microbiology Spectrum · doi:10.1128/spectrum.03382-22 · Cited by 23 · see citing works

Vitamin biosynthesis in the gut: interplay between mammalian host and its resident microbiota

Tarracchini, C., Lordan, C., Milani, C., Moreira, L. D. P. D., Alabedallat, Q. M., de LeBlanc, A. D. M., Turroni, F., Lugli, G. A., Mancabelli, L., Longhi, G., et al. (2025) · Microbiology and Molecular Biology Reviews · doi:10.1128/mmbr.00184-23 · Cited by 29 · see citing works

Schizophyllum commune-derived β-glucan improves intestinal health demonstrating protective effects against constipation and common metabolic disorders

Vu, V., Muthuramalingam, K., Singh, V., Choi, C., Kim, Y. M., Unno, T., & Cho, M. (2022) · Applied Biological Chemistry · doi:10.1186/s13765-022-00680-3 · Cited by 22 · see citing works

Microbial vitamin production mediates dietary effects on diabetic risk

Wang, D., Pham, V. T., Steinert, R. E., Zhernakova, A., & Fu, J. (2022) · Gut Microbes · doi:10.1080/19490976.2022.2154550 · Cited by 18 · see citing works

The microbiome in adolescents with irritable bowel syndrome and changes with percutaneous electrical nerve field stimulation

Castillo, D., Denson, L. A., Haslam, D. B., Hommel, K. A., Ollberding, N. J., Sahay, R. D., & Santucci, N. R. (2023) · Neurogastroenterology & Motility · doi:10.1111/nmo.14573 · Cited by 17 · see citing works

Recent Progress in the Diagnosis and Management of Type 2 Diabetes Mellitus in the Era of COVID-19 and Single Cell Multi-Omics Technologies

Kupai, K., Várkonyi, T. T., Török, S., Gáti, V., Czimmerer, Z., Puskás, L. G., & Szebeni, G. J. (2022) · Life · doi:10.3390/life12081205 · Cited by 16 · see citing works

From One-Size-Fits-All to Precision Medicine: The Promise of Personalized Probiotics

Montazeri‐Najafabady, N. (2025) · Probiotics and Antimicrobial Proteins · doi:10.1007/s12602-025-10815-9 · Cited by 14 · see citing works

Clinical benefits of β-glucan supplementation in children: a review

Bhoite, R., Satyavrat, V., & Sadananda, M. P. (2022) · Discover Food · doi:10.1007/s44187-022-00038-0 · Cited by 13 · see citing works

Vitamin K2 Enhances Fat Degradation to Improve the Survival of C. elegans

Qu, Z., Zhang, L., Huang, W. M., & Zheng, S. (2022) · Frontiers in Nutrition · doi:10.3389/fnut.2022.858481 · Cited by 13 · see citing works

Microbial Communities in Home-Made and Commercial Kefir and Their Hypoglycemic Properties

Yılmaz, B., Elibol, E., Shangpliang, H. N. J., Özoğul, F., & Tamang, J. P. (2022) · Fermentation · doi:10.3390/fermentation8110590 · Cited by 13 · see citing works

Untargeted Metabolomic Plasma Profiling of Emirati Dialysis Patients with Diabetes versus Non-Diabetic: A Pilot Study

Banimfreg, B. H., Alshraideh, H. A., Shamayleh, A., Guella, A., Semreen, M. H., Bataineh, M. T. A., & Soares, N. C. (2022) · Biomolecules · doi:10.3390/biom12070962 · Cited by 10 · see citing works

The Synergism of Human Lactobacillaceae and Inulin Decrease Hyperglycemia via Regulating the Composition of Gut Microbiota and Metabolic Profiles in db/db Mice

Li, P., Tong, T., Wu, Y., Zhou, X., Zhang, M., Liu, J., She, Y., Li, Z., & Li, Y. (2023) · Journal of Microbiology and Biotechnology · doi:10.4014/jmb.2304.04039 · Cited by 9 · see citing works

Integrative Metagenomic Analyses Reveal Gut Microbiota-Derived Multiple Hits Connected to Development of Diabetes Mellitus

Alarifi, S. N., Alyamani, E. J., Alarawi, M. S., Alquait, A. A., Alolayan, M. A., Aldossary, A. M., EL-Rahman, R. A. A., & Mir, R. (2024) · Metabolites · doi:10.3390/metabo14120720 · Cited by 7 · see citing works

The link between gut microbiome, nutraceuticals, diet, and diabetes mellitus: a bibliometric and visual analysis of research and emerging trends from 2012 to 2022

Sarkar, A., Khan, A. S., Kaul, R., Lee, S., Kamal, I., Paul, P., Laws, S., & Châari, A. (2024) · Discover Public Health · doi:10.1186/s12982-024-00213-x · Cited by 5 · see citing works

Chimonanthus nitens Oliv leaves essential oil alleviates colitis induced by sodium dextran sulfate in BALB/C mice via MAPK/NF-κB/Nrf2 signaling pathway

Zhang, Y., He, J., Chen, L., & Wang, W. (2024) · Journal of Functional Foods · doi:10.1016/j.jff.2024.106095 · Cited by 5 · see citing works

The Role of Flavonoids in Glycemic Control and Diabetic Complications: Current Evidence and Future Directions

Pathak, G., Mangla, S., Bhan, V., Ahlawat, Y. K., Sharma, N., Malik, A., Gautam, P., Verma, R., Gupta, S., & Bisht, K. (2026) · Phytotherapy Research · doi:10.1002/ptr.70213 · Cited by 5 · see citing works

Review of the Gut Microbiota Dynamics in Type-2 Diabetes Mellitus (T2DM): A Focus on Human-Based Studies

Oluwaloni, F. O., Yakubu, O. F., Adebayo, A. H., Koyejo, O. D., & Lawal, A. K. (2023) · Tropical Journal of Natural Product Research · doi:10.26538/tjnpr/v7i6.2 · Cited by 3 · see citing works

Micronutrients and the gut microbiome: a bidirectional interaction

Kodentsova, V. M., & Risnik, D. V. (2024) · Medical alphabet · doi:10.33667/2078-5631-2024-16-40-46 · Cited by 1 · see citing works

Vitamin K2 reprograms the multi-organ transcriptional landscape in mice with high-fat diet-induced obesity

Wang, X.-Y., Zhang, Y., Liu, L., Ma, H., Wei, C., Xu, X., Zhang, J., Pan, S.-J., Zhang, Y., Chen, J., et al. (2025) · Food & Function · doi:10.1039/d5fo01613d · Cited by 1 · see citing works

Biosynthesis and therapeutic applications of MK-7: A comprehensive review

Maneesha, M., & Devi, C. S. (2025) · Cogent Food & Agriculture · doi:10.1080/23311932.2025.2509677

Primary resistance to ICI-based regimens is associated with early longitudinal changes in the fecal microbiome and loss of microbial stabilityPreprint

Zhao, Y., Naidoo, J., Conroy, M. R., Ferri, J. T., Gills, J. J., Chen, K. Y., White, J. R., Glass, S., Assan, W. O., Peloza, K. E., et al. (2025) · medRxiv · doi:10.1101/2025.10.01.25336378

Additional file 2 of Type 1 diabetes in pregnancy is associated with distinct changes in the composition and function of the gut microbiome

Roth‐Schulze, A. J., Penno, M. A. S., Ngui, K., Oakey, H., Bandala‐Sanchez, E., Smith, A. D., Allnutt, T. R., Thomson, R. L., Vuillermin, P. J., Craig, M. E., et al. (2021) · Figshare · doi:10.6084/m9.figshare.15128280

Microbial Genomics: Unraveling the Healthomic Code

Sultana, M., Hossain, A., Noor-E-Meem, & Begum, A. (2026) · Interdisciplinary biotechnological advances · doi:10.1007/978-981-95-3612-2_2

Role of lipid metabolites in mediating causal effects of gut microbiota on type 2 diabetes mellitus

Li, L., Tang, S., Liu, F., & Yang, M. (2026) · Computational Biology and Chemistry · doi:10.1016/j.compbiolchem.2026.108955

Depletion of Blautia wexlerae and Parabacteroides distasonis in adiposity-related prehypertension

Luo, L., Cheng, K., Chen, B., Li, Y., Ruan, L., Li, Z., Zhu, S., Zhao, L., Zhang, C., Liu, Y., et al. (2026) · Frontiers in Microbiology · doi:10.3389/fmicb.2026.1873803

Pea and fava bean protein hydrolysates supplementation ameliorates metabolic dysfunction and reshapes gut microbiota in diet-induced obese mice

Uriz-Martínez, M., Ansorena, D., Astiasarán, I., Sáinź, N., Lópeź‐Yoldi, M., & Aranaz, P. (2026) · Future Foods · doi:10.1016/j.fufo.2026.101124

The Metabolic Functional Feature of Gut Microbiota in Mongolian Patients with Type 2 Diabetes

Liu, Y., Gao, Y., Zhao, L., Jiao, Y., Jiao, Y., & Wang, M. (2024) · Journal of Microbiology and Biotechnology · doi:10.4014/jmb.2402.02021 · Cited by 1 · see citing works

Gut Microbiota and Type 2 Diabetes Mellitus: A Review

Dr. Shivkumar S. Ladde*1, M. S. (2026) · Zenodo (CERN European Organization for Nuclear Research) · doi:10.5281/zenodo.18333789

A comparative study of microbial community and functions of type 2 diabetes mellitus patients with obesity and healthy people

Wang, T., Zhang, X., Chen, A., Zhang, J., Lv, B., Ma, M.-H., Lian, J., Wu, Y., Zhou, Y.-T., Ma, C., et al. (2020) · Applied Microbiology and Biotechnology · doi:10.1007/s00253-020-10689-7 · Cited by 75 · see citing works

Gut Microbiota Dysbiosis and Its Impact on Type 2 Diabetes: From Pathogenesis to Therapeutic Strategies

Yu, Y., Ding, Y., Wang, S., & Jiang, L. (2025) · Metabolites · doi:10.3390/metabo15060397 · Cited by 67 · see citing works

Determination of microbial metagenomic markers of Type 2 Diabetes Mellitus (T2DM) in patients visiting South C Health Centre in Nairobi Kenya

Kumar, B., Kinyua, J. D. M., & Kimotho, J. H. (2022) · Journal of Agriculture Science and Technology · doi:10.4314/jagst.v21i2.7 · Cited by 3 · see citing works