Gut microbiome approaches to treat obesity in humans

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 · see citing works

Untitled work

Hill (2014) · doi:10.1038/nrgastro.2014.66 · Cited by 9,592 · see citing works

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 · see citing works

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 · see citing works

Expert consensus document: The International Scientific Association for Probiotics and Prebiotics (ISAPP) consensus statement on the definition and scope of prebiotics

Gibson, G. R., Hutkins, R., Sanders, M. E., Prescott, S. L., Reimer, R. A., Salminen, S. J., Scott, K., Stanton, C., Swanson, K. S., Cani, P. D., et al. (2017) · Nature Reviews Gastroenterology & Hepatology · doi:10.1038/nrgastro.2017.75 · Cited by 5,634 · see citing works

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 · see citing works

Gut Microbiota from Twins Discordant for Obesity Modulate Metabolism in Mice

Ridaura, V. K., Faith, J. J., Rey, F. E., Cheng, J., Duncan, A. E., Kau, A. L., Griffin, N. W., Lombard, V., Henrissat, B., Bain, J. R., et al. (2013) · Science · doi:10.1126/science.1241214 · Cited by 3,788 · see citing works

Exercise as medicine - evidence for prescribing exercise as therapy in 26 different chronic diseases

Pedersen, B. K., & Saltin, B. (2015) · Scandinavian Journal of Medicine & Science in Sports · doi:10.1111/sms.12581 · Cited by 3,514 · see citing works

Transfer of intestinal microbiota from lean donors increases insulin sensitivity in individuals with metabolic syndrome

Vrieze, A., Van Nood, E., Holleman, F., Salojärvi, J., Kootte, R. S., Bartelsman, J. F. W. M., Dallinga–Thie, G. M., Ackermans, M. T., Serlie, M. J., Oozeer, R., et al. (2012) · Gastroenterology · doi:10.1053/j.gastro.2012.06.031 · Cited by 2,913 · see citing works

The gut-brain axis: interactions between enteric microbiota, central and enteric nervous systems.

(2015) · PubMed Central · Cited by 2,540 · see citing works

Microbiota and SCFA in lean and overweight healthy subjects

Schwiertz, A., Taras, D., Schäfer, K., Beijer, S., Bos, N. A., Donus, C., & Hardt, P. D. (2010) · Obesity · doi:10.1038/oby.2009.167 · Cited by 2,457 · see citing works

Short-chain fatty acids in control of body weight and insulin sensitivity

Canfora, E. E., Jocken, J. W., & Blaak, E. E. (2015) · Nature Reviews Endocrinology · doi:10.1038/nrendo.2015.128 · Cited by 2,298 · see citing works

Intestinal Short Chain Fatty Acids and their Link with Diet and Human Health

Ríos-Covián, D., Ruas‐Madiedo, P., Margollés, A., Gueimonde, M., Reyes‐Gavilán, C. G. D. L., & Salazar, N. (2016) · Frontiers in Microbiology · doi:10.3389/fmicb.2016.00185 · Cited by 2,215 · see citing works

Defining feasibility and pilot studies in preparation for randomised controlled trials: development of a conceptual framework

Eldridge, S. M., Lancaster, G. A., Campbell, M. J., Thabane, L., Hopewell, S., Coleman, C. L., & Bond, C. M. (2016) · PLOS ONE · doi:10.1371/journal.pone.0150205 · Cited by 1,581 · see citing works

The two mucus layers of colon are organized by the MUC2 mucin, whereas the outer layer is a legislator of host–microbial interactions

Johansson, M., Larsson, J. M. H., & Hansson, G. C. (2010) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1006451107 · Cited by 1,459 · see citing works

Exercise and associated dietary extremes impact on gut microbial diversity

Clarke, S. F., Murphy, E. F., O'Sullivan, O., Lucey, A. J., Humphreys, M., Hogan, A., Hayes, P., O'Reilly, M., Jeffery, I. B., Wood-Martin, R., et al. (2014) · Gut · doi:10.1136/gutjnl-2013-306541 · Cited by 1,439 · see citing works

Human colonic microbiota associated with diet, obesity and weight loss

Duncan, S. H., Lobley, G. E., Holtrop, G., Ince, J., Johnstone, A. M., Louis, P., & Flint, H. J. (2008) · International Journal of Obesity · doi:10.1038/ijo.2008.155 · Cited by 1,222 · see citing works

European consensus conference on faecal microbiota transplantation in clinical practice

Cammarota, G., Ianiro, G., Tilg, H., Rajilić-Stojanović, M., Kump, P., Satokari, R., Sokol, H., Arkkila, P., Pintus, C., Hart, A., et al. (2017) · Gut · doi:10.1136/gutjnl-2016-313017 · Cited by 1,207 · see citing works

Revisiting the STEC Testing Approach: Using espK and espV to Make Enterohemorrhagic Escherichia coli (EHEC) Detection More Reliable in Beef

Delannoy, S., Chaves, B. D., Ison, S. A., Webb, H. E., Beutin, L., Delaval, J., Billet, I., & Fach, P. (2016) · Frontiers in Microbiology · doi:10.3389/fmicb.2016.00001 · Cited by 1,186 · see citing works

Improvement of insulin sensitivity after lean donor feces in metabolic syndrome is driven by baseline intestinal microbiota composition

Kootte, R. S., Levin, E., Salojärvi, J., Smits, L. P., Hartstra, A. V., Udayappan, S. D., Hermes, G., Bouter, K. E., Koopen, A. M., Holst, J. J., et al. (2017) · Cell Metabolism · doi:10.1016/j.cmet.2017.09.008 · Cited by 1,039 · see citing works

Association between body mass index and Firmicutes/Bacteroidetes ratio in an adult Ukrainian population

Koliada, A., Syzenko, G., Moseiko, V., Budovska, L., Puchkov, K., Perederiy, V., Gavalko, Y., Dorofeyev, A., Romanenko, M., Tkach, S., et al. (2017) · BMC Microbiology · doi:10.1186/s12866-017-1027-1 · Cited by 1,000 · see citing works

Targeting the microbiota-gut-brain axis: prebiotics have anxiolytic and antidepressant-like effects and reverse the impact of chronic stress in mice

Burokas, A., Arboleya, S., Moloney, R. D., Peterson, V. L., Murphy, K., Clarke, G., Stanton, C., Dinan, T. G., & Cryan, J. F. (2017) · Biological Psychiatry · doi:10.1016/j.biopsych.2016.12.031 · Cited by 952 · see citing works

Do Altmetrics Work? Twitter and Ten Other Social Web Services

Thelwall, M., Haustein, S., Larivière, V., & Sugimoto, C. R. (2013) · PLoS ONE · doi:10.1371/journal.pone.0064841 · Cited by 907 · see citing works

Akkermansia muciniphila inversely correlates with the onset of inflammation, altered adipose tissue metabolism and metabolic disorders during obesity in mice

Schneeberger, M., Everard, A., Gómez-Valadés, A. G., Matamoros, S., Ramírez, S., Delzenne, N. M., Gomis, R., Claret, M., & Cani, P. D. (2015) · Scientific Reports · doi:10.1038/srep16643 · Cited by 798 · see citing works

Diversity of human colonic butyrate‐producing bacteria revealed by analysis of the butyryl‐CoA:acetate CoA‐transferase gene

Louis, P., Young, P., Holtrop, G., & Flint, H. J. (2009) · Environmental Microbiology · doi:10.1111/j.1462-2920.2009.02066.x · Cited by 783 · see citing works

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

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

Dietary Polyphenols Promote Growth of the Gut Bacterium <i>Akkermansia muciniphila</i> and Attenuate High-Fat Diet–Induced Metabolic Syndrome

Roopchand, D. E., Carmody, R. N., Kuhn, P., Moskal, K., Rojas-Silva, P., Turnbaugh, P. J., & Raskin, I. (2015) · Diabetes · doi:10.2337/db14-1916 · Cited by 678 · see citing works

Exercise Modifies the Gut Microbiota with Positive Health Effects

Monda, V., Villano, I., Messina, A., Valenzano, A., Esposito, T., Moscatelli, F., Viggiano, A., Cibelli, G., Chieffi, S., Monda, M., et al. (2017) · Oxidative Medicine and Cellular Longevity · doi:10.1155/2017/3831972 · Cited by 654 · see citing works

Exercise Prevents Weight Gain and Alters the Gut Microbiota in a Mouse Model of High Fat Diet-Induced Obesity

Evans, C. C., LePard, K. J., Kwak, J. W., Stancukas, M. C., Laskowski, S., Dougherty, J., Moulton, L., Glawe, A., Wang, Y., Leone, V., et al. (2014) · PLoS ONE · doi:10.1371/journal.pone.0092193 · Cited by 587 · see citing works

Comparison of the gut microbiota composition between obese and non-obese individuals in a Japanese population, as analyzed by terminal restriction fragment length polymorphism and next-generation sequencing

Kasai, C., Sugimoto, K., Moritani, I., Tanaka, J., Oya, Y., Inoue, H., Tameda, M., Shiraki, K., Ito, M., Takei, Y., et al. (2015) · BMC Gastroenterology · doi:10.1186/s12876-015-0330-2 · Cited by 581 · see citing works

Vagal pathways for microbiome-brain-gut axis communication

Forsythe, P., Bienenstock, J., & Kunze, W. A. (2014) · Advances in Experimental Medicine and Biology · doi:10.1007/978-1-4939-0897-4_5 · Cited by 576 · see citing works

Prebiotics Reduce Body Fat and Alter Intestinal Microbiota in Children Who Are Overweight or With Obesity

Nicolucci, A. C., Hume, M. P., Martínez, I., Mayengbam, S., Walter, J., & Reimer, R. A. (2017) · Gastroenterology · doi:10.1053/j.gastro.2017.05.055 · Cited by 517 · see citing works

Differences in gut microbiota profile between women with active lifestyle and sedentary women

Bressa, C., Bailén-Andrino, M., Pérez-Santiago, J., González-Soltero, R., Pérez, M., Montalvo-Lominchar, M. G., Maté-Muñoz, J. L., Domínguez, R., Moreno, D., & Larrosa, M. (2017) · PLOS ONE · doi:10.1371/journal.pone.0171352 · Cited by 501 · see citing works

Gut Microbiota Composition in Male Rat Models under Different Nutritional Status and Physical Activity and Its Association with Serum Leptin and Ghrelin Levels

Queipo-Ortuño, M. I., Seoane, L. M., Murri, M., Pardo, M., Gomez-Zumaquero, J. M., Cardona, F., Casanueva, F., & Tinahones, F. J. (2013) · PLoS ONE · doi:10.1371/journal.pone.0065465 · Cited by 497 · see citing works

Species–function relationships shape ecological properties of the human gut microbiome

Vieira‐Silva, S., Falony, G., Darzi, Y., Lima‐Mendez, G., Yunta, R. G., Okuda, S., Vandeputte, D., Valles‐Colomer, M., Hildebrand, F., Chaffron, S., et al. (2016) · Nature Microbiology · doi:10.1038/nmicrobiol.2016.88 · Cited by 487 · see citing works

Cardiorespiratory fitness as a predictor of intestinal microbial diversity and distinct metagenomic functions

Estaki, M., Pither, J., Baumeister, P., Little, J. P., Gill, S. K., Ghosh, S., Ahmadi-Vand, Z., Marsden, K. R., & Gibson, D. L. (2016) · Microbiome · doi:10.1186/s40168-016-0189-7 · Cited by 476 · see citing works

Differences in gut microbiota composition between obese and lean children: a cross-sectional study

Bervoets, L., Hoorenbeeck, K. V., Kortleven, I., Noten, C. V., Hens, N., Vael, C., Goossens, H., Desager, K., & Vankerckhoven, V. (2013) · Gut Pathogens · doi:10.1186/1757-4749-5-10 · Cited by 452 · see citing works

Inferring Social Status and Rich Club Effects in Enterprise Communication Networks

Dong, Y., Tang, J., Chawla, N. V., Lou, T., Yang, Y., & Wang, B. (2015) · PLoS ONE · doi:10.1371/journal.pone.0119446 · Cited by 439 · see citing works

Role of the Gut Microbiome in the Pathogenesis of Obesity and Obesity-Related Metabolic Dysfunction

Bouter, K. E. C., van Raalte, D. H., Groen, A. K., & Nieuwdorp, M. (2017) · Gastroenterology · doi:10.1053/j.gastro.2016.12.048 · Cited by 433 · see citing works

Total fecal microbiota transplantation alleviates high-fat diet-induced steatohepatitis in mice via beneficial regulation of gut microbiota

Zhou, D., Pan, Q., Shen, F., Cao, H.-X., Ding, W.-J., Chen, Y.-W., & Fan, J.-G. (2017) · Scientific Reports · doi:10.1038/s41598-017-01751-y · Cited by 421 · see citing works

Correction: Corrigendum: Application of a novel phosphinothricin N-acetyltransferase (RePAT) gene in developing glufosinate-resistant rice

Cui, Y., Liu, Z., Li, Y., Zhou, F., Chen, H., & Lin, Y. (2018) · Scientific Reports · doi:10.1038/srep46937 · Cited by 418 · see citing works

Responses of gut microbiota to diet composition and weight loss in lean and obese mice

Ravussin, Y., Koren, O., Spor, A., LeDuc, C., Gutman, R., Stombaugh, J., Knight, R., Ley, R. E., & Leibel, R. L. (2012) · Obesity · doi:10.1038/oby.2011.111 · Cited by 406 · see citing works

Microbiota conservation and BMI signatures in adult monozygotic twins

Tims, S., Derom, C., Jonkers, D. M., Vlietinck, R., Saris, W. H., Kleerebezem, M., de Vos, W. M., & Zoetendal, E. G. (2013) · The ISME Journal · doi:10.1038/ismej.2012.146 · Cited by 367 · see citing works

Gut Microbiota Modulation and Its Relationship with Obesity Using Prebiotic Fibers and Probiotics: A Review

Dahiya, D. K., Renuka, Puniya, M., Shandilya, U. K., Dhewa, T., Kumar, N., Kumar, S., Puniya, A. K., & Shukla, P. (2017) · Frontiers in Microbiology · doi:10.3389/fmicb.2017.00563 · Cited by 357 · see citing works

Voluntary Running Exercise Alters Microbiota Composition and Increases n-Butyrate Concentration in the Rat Cecum

MATSUMOTO, M., INOUE, R., TSUKAHARA, T., USHIDA, K., CHIJI, H., MATSUBARA, N., & HARA, H. (2008) · Bioscience, Biotechnology, and Biochemistry · doi:10.1271/bbb.70474 · Cited by 352 · see citing works

Enhanced translocation of bacteria across metabolically stressed epithelia is reduced by butyrate†

Lewis, K. J., Lutgendorff, F., Phan, V., Söderholm, J. D., Sherman, P. M., & McKay, D. M. (2009) · Inflammatory Bowel Diseases · doi:10.1002/ibd.21177 · Cited by 338 · see citing works

Diet and exercise orthogonally alter the gut microbiome and reveal independent associations with anxiety and cognition

Kang, S. S., Jeraldo, P., Kurti, A., Miller, M. E. B., Cook, M. D., Whitlock, K. G., Goldenfeld, N. D., Woods, J. A., White, B. A., Chia, N., et al. (2014) · Molecular Neurodegeneration · doi:10.1186/1750-1326-9-36 · Cited by 322 · see citing works

A taxonomic signature of obesity in a large study of American adults

Peters, B. A., Shapiro, J. A., Church, T. R., Miller, G., Trinh‐Shevrin, C., Yuen, E., Friedlander, C., Hayes, R. B., & Ahn, J. (2018) · Scientific Reports · doi:10.1038/s41598-018-28126-1 · Cited by 319 · see citing works

The direct and indirect costs of both overweight and obesity: a systematic review

Dee, A., Kearns, K., O’Neill, C., Sharp, L., Staines, A. S., O’Dwyer, V., Fitzgerald, S., & Perry, I. J. (2014) · BMC Research Notes · doi:10.1186/1756-0500-7-242 · Cited by 311 · see citing works

Blueberry polyphenols extract as a potential prebiotic with anti-obesity effects on C57BL/6 J mice by modulating the gut microbiota

Jiao, X., Wang, Y., Lin, Y., Lang, Y., Li, E., Zhang, X., Zhang, Q., Feng, Y., Meng, X., & Li, B. (2018) · The Journal of Nutritional Biochemistry · doi:10.1016/j.jnutbio.2018.07.008 · Cited by 310 · see citing works

Prebiotic potential of pectins and pectic oligosaccharides derived from lemon peel wastes and sugar beet pulp: A comparative evaluation

Gómez, B., Gullón, B., Yáñez, R., Schols, H. A., & Alonsó, J. L. (2015) · Journal of Functional Foods · doi:10.1016/j.jff.2015.10.029 · Cited by 307 · see citing works

Exercise induction of gut microbiota modifications in obese, non-obese and hypertensive rats

Petriz, B. A., Castro, A. P., Almeida, J. A., Gomes, C. P., Fernandes, G. R., Kruger, R. H., Pereira, R. W., & Franco, O. L. (2014) · BMC Genomics · doi:10.1186/1471-2164-15-511 · Cited by 293 · see citing works

An NMR Study of Biomimetic Fluorapatite – Gelatine Mesocrystals

Vyalikh, A., Simon, P., Владимировна, Р. Е., Buder, J., Scheler, U., & Kniep, R. (2015) · Scientific Reports · doi:10.1038/srep15797 · Cited by 278 · see citing works

Correction: Corrigendum: Genomic inference of the metabolism of cosmopolitan subsurface Archaea, Hadesarchaea

Baker, B. J., Saw, J. H. W., Lind, A. E., Lazar, C. S., Hinrichs, K., Teske, A., & Ettema, T. J. G. (2016) · Nature Microbiology · doi:10.1038/nmicrobiol.2016.32 · Cited by 277 · see citing works

Hemorrhagic Fever with Renal Syndrome: Pathogenesis and Clinical Picture

Jiang, H. X., Du, H., Wang, L. M., Wang, P. Z., & Bai, X. (2016) · Frontiers in Cellular and Infection Microbiology · doi:10.3389/fcimb.2016.00001 · Cited by 275 · see citing works

Frequency of Firmicutes and Bacteroidetes in gut microbiota in obese and normal weight Egyptian children and adults

Ismail, N. A., Ragab, S. H., ElBaky, A. A., Shoeib, A. R. S., Alhosary, Y., & Fekry, D. (2011) · Archives of Medical Science · doi:10.5114/aoms.2011.23418 · Cited by 268 · see citing works

The effect of diet and exercise on intestinal integrity and microbial diversity in mice

Campbell, S. C., Wisniewski, P. J., Noji, M., McGuinness, L. R., Häggblom, M. M., Lightfoot, S. A., Joseph, L. B., & Kerkhof, L. J. (2016) · PLOS ONE · doi:10.1371/journal.pone.0150502 · Cited by 268 · see citing works

High-intensity exercise training increases the diversity and metabolic capacity of the mouse distal gut microbiota during diet-induced obesity

Denou, E., Marcinko, K., Surette, M. G., Steinberg, G. R., & Schertzer, J. D. (2016) · American Journal of Physiology-Endocrinology and Metabolism · doi:10.1152/ajpendo.00537.2015 · Cited by 260 · see citing works

Connection Between BMI-Related Plasma Metabolite Profile and Gut Microbiota

Ottosson, F. A., Brunkwall, L., Ericson, U., Nilsson, P. M., Almgren, P., Fernandez, C., Melander, O., & Orho‐Melander, M. (2018) · The Journal of Clinical Endocrinology & Metabolism · doi:10.1210/jc.2017-02114 · Cited by 246 · see citing works

The obesity paradox: Understanding the effect of obesity on mortality among individuals with cardiovascular disease

Banack, H. R., & Kaufman, J. S. (2014) · Preventive Medicine · doi:10.1016/j.ypmed.2014.02.003 · Cited by 233 · see citing works

A proliferative probiotic Bifidobacterium strain in the gut ameliorates progression of metabolic disorders via microbiota modulation and acetate elevation

Aoki, R., Kamikado, K., Suda, W., Takii, H., Mikami, Y., Suganuma, N., Hattori, M., & Koga, Y. (2017) · Scientific Reports · doi:10.1038/srep43522 · Cited by 225 · see citing works

Apple-Derived Pectin Modulates Gut Microbiota, Improves Gut Barrier Function, and Attenuates Metabolic Endotoxemia in Rats with Diet-Induced Obesity

Jiang, T., Gao, X., Wu, C., Tian, F., Lei, Q., Bi, J., Xie, B., Wang, H., Chen, D., & Wang, X. (2016) · Nutrients · doi:10.3390/nu8030126 · Cited by 223 · see citing works

Exercise training modifies gut microbiota in normal and diabetic mice

Lambert, J. E., Myslicki, J. P., Bomhof, M. R., Belke, D. D., Shearer, J., & Reimer, R. A. (2015) · Applied Physiology, Nutrition, and Metabolism · doi:10.1139/apnm-2014-0452 · Cited by 214 · see citing works

Microbial Endocrinology: The Microbiota-Gut-Brain Axis in Health and Disease

Lyte, M., & Cryan, J. (2014) · Advances in Experimental Medicine and Biology · doi:10.1007/978-1-4939-0897-4 · Cited by 212 · see citing works

Functional and phylogenetic assembly of microbial communities in the human microbiome

Shafquat, A., Cordy, R. J., Simmons, S. L., & Huttenhower, C. (2014) · Trends in Microbiology · doi:10.1016/j.tim.2014.01.011 · Cited by 212 · see citing works

Quantitative differences in intestinal Faecalibacterium prausnitzii in obese Indian children

Ramadass, B., George, G., Kabeerdoss, J., Hepsiba, J., Chandragunasekaran, A. M. S., & Ramakrishna, B. (2009) · British Journal Of Nutrition · doi:10.1017/s0007114509992182 · Cited by 209 · see citing works

Pre-treatment microbial Prevotella-to-Bacteroides ratio, determines body fat loss success during a 6-month randomized controlled diet intervention

Hjorth, M. F., Roager, H. M., Larsen, T. M., Poulsen, S. K., Licht, T. R., Bahl, M. I., Zohar, Y., & Astrup, A. V. (2017) · International Journal of Obesity · doi:10.1038/ijo.2017.220 · Cited by 207 · see citing works

Correlation between body mass index and faecal microbiota from children

Ignácio, A., Fernandes, M. R., Rodrigues, V. A. A., Groppo, F. C., Cardoso, A. L., Ávila-Campos, M. J., & Nakano, V. (2015) · Clinical Microbiology and Infection · doi:10.1016/j.cmi.2015.10.031 · Cited by 204 · see citing works

Alterations in the Porcine Colon Microbiota Induced by the Gastrointestinal Nematode Trichuris suis

Li, R. W., Wu, S., Li, W., Navarro, K., Couch, R. D., Hill, D. E., & Urban, J. F. (2012) · Infection and Immunity · doi:10.1128/iai.00141-12 · Cited by 203 · see citing works

Axonal BACE1 dynamics and targeting in hippocampal neurons: a role for Rab11 GTPase

Buggia-Prévot, V., Fernandez, C., Riordan, S. M., Vetrivel, K. S., Roseman, J., Waters, J., Bindokas, V. P., Vassar, R. J., & Thinakaran, G. (2014) · Molecular Neurodegeneration · doi:10.1186/1750-1326-9-1 · Cited by 201 · see citing works

Exercise Is More Effective at Altering Gut Microbial Composition and Producing Stable Changes in Lean Mass in Juvenile versus Adult Male F344 Rats

Mika, A., Van Treuren, W., González, A., Herrera, J. J., Knight, R., & Fleshner, M. (2015) · PLOS ONE · doi:10.1371/journal.pone.0125889 · Cited by 197 · see citing works

Lactate- and acetate-based cross-feeding interactions between selected strains of lactobacilli, bifidobacteria and colon bacteria in the presence of inulin-type fructans

Moens, F., Verce, M., & Vuyst, L. D. (2016) · International Journal of Food Microbiology · doi:10.1016/j.ijfoodmicro.2016.10.019 · Cited by 191 · see citing works

Microbial enterotypes in personalized nutrition and obesity management

Christensen, L. H., Roager, H. M., Astrup, A. V., & Hjorth, M. F. (2018) · American Journal of Clinical Nutrition · doi:10.1093/ajcn/nqy175 · Cited by 191 · see citing works

Beneficial metabolic effects of selected probiotics on diet‐induced obesity and insulin resistance in mice are associated with improvement of dysbiotic gut microbiota

Alard, J., Lehrter, V., Rhimi, M., Mangin, I., Peucelle, V., Abraham, A., Mariadassou, M., Maguin, E., Waligora‐Dupriet, A., Pot, B., et al. (2015) · Environmental Microbiology · doi:10.1111/1462-2920.13181 · Cited by 190 · see citing works

Kefir alleviates obesity and hepatic steatosis in high-fat diet-fed mice by modulation of gut microbiota and mycobiota: Targeted and untargeted community analysis with correlation of biomarkers

Kim, D.-H., Kim, H., Jeong, D., Kang, I.-B., Chon, J.-W., Kim, H.-S., Song, K.-Y., & Seo, K.-H. (2017) · The Journal of Nutritional Biochemistry · doi:10.1016/j.jnutbio.2017.02.014 · Cited by 179 · see citing works

Probiotics: interaction with gut microbiome and antiobesity potential.

Arora, T., Singh, S., & Sharma, R. K. (2013) · Nutrition · doi:10.1016/j.nut.2012.07.017 · Cited by 176 · see citing works

Obesity Alters the Microbial Community Profile in Korean Adolescents

Hu, H., Park, S.-G., Jang, H. B., Choi, M.-G., Park, K., Kang, J., Park, S. I., Lee, H.-J., & Cho, S.-H. (2015) · PLoS ONE · doi:10.1371/journal.pone.0134333 · Cited by 169 · see citing works

Effects of Weight Loss on Lean Mass, Strength, Bone, and Aerobic Capacity

WEISS, E. P., JORDAN, R. C., FRESE, E. M., ALBERT, S. G., & VILLAREAL, D. T. (2017) · Medicine &amp; Science in Sports &amp; Exercise · doi:10.1249/mss.0000000000001074 · Cited by 169 · see citing works

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

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

Screening and monitoring microbial xenobiotics’ biodegradation via rapid, inexpensive and easy to perform microplate

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