Sex Differences in the Gut-Brain Axis: Implications for Mental Health

Diagnostic and Statistical Manual of Mental Disorders

American Psychiatric Association (2013) · doi:10.1176/appi.books.9780890425596 · Cited by 116,369 · see citing works

Prevalence of Autism Spectrum Disorder Among Children Aged 8 Years — Autism and Developmental Disabilities Monitoring Network, 11 Sites, United States, 2014

Baio, J., Wiggins, L., Christensen, D. L., Maenner, M. J., Daniels, J., Warren, Z., Kurzius-Spencer, M., Zahorodny, W., Robinson, C., Rosenberg, et al. (2018) · MMWR. Surveillance Summaries · doi:10.15585/mmwr.ss6706a1 · Cited by 6,078 · see citing works

Increasing Incidence and Prevalence of the Inflammatory Bowel Diseases With Time, Based on Systematic Review

Molodecky, N. A., Soon, I. S., Rabi, D. M., Ghali, W. A., Ferris, M., Chernoff, G., Benchimol, E. I., Panaccione, R., Ghosh, S., Barkema, H. W., et al. (2012) · Gastroenterology · doi:10.1053/j.gastro.2011.10.001 · Cited by 4,833 · see citing works

Metagenomic Analysis of the Human Distal Gut Microbiome

Gill, S. R., Pop, M., DeBoy, R. T., Eckburg, P. B., Turnbaugh, P. J., Samuel, B. S., Gordon, J. I., Relman, D. A., Fraser-Liggett, C. M., & Nelson, K. E. (2006) · Science · doi:10.1126/science.1124234 · Cited by 4,699 · see citing works

Prevalence of Autism Spectrum Disorder Among Children Aged 8 Years — Autism and Developmental Disabilities Monitoring Network, 11 Sites, United States, 2016

Maenner, M. J., Shaw, K. A., Baio, J., EdS1, Washington, A., Patrick, M., DiRienzo, M., Christensen, D. L., Wiggins, L. D., Pettygrove, S., et al. (2020) · MMWR. Surveillance Summaries · doi:10.15585/mmwr.ss6904a1 · Cited by 3,780 · see citing works

Twelve‐month and lifetime prevalence and lifetime morbid risk of anxiety and mood disorders in the United States

Kessler, R. C., Petukhova, M., Sampson, N. A., Zaslavsky, A. M., & Wittchen, H. (2012) · International Journal of Methods in Psychiatric Research · doi:10.1002/mpr.1359 · Cited by 2,947 · 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

Gut–brain axis: How the microbiome influences anxiety and depression

Foster, J. A., & McVey Neufeld, K.-A. (2013) · Trends in Neurosciences · doi:10.1016/j.tins.2013.01.005 · Cited by 2,460 · see citing works

Epidemiology of Parkinson’s disease

Tysnes, O., & Storstein, A. M. (2017) · Journal of Neural Transmission · doi:10.1007/s00702-017-1686-y · Cited by 2,437 · see citing works

Schizophrenia: A Concise Overview of Incidence, Prevalence, and Mortality

McGrath, J., Saha, S., Chant, D., & Welham, J. (2008) · Epidemiologic Reviews · doi:10.1093/epirev/mxn001 · Cited by 2,280 · see citing works

Altered fecal microbiota composition in patients with major depressive disorder

Jiang, H., Ling, Z., Zhang, Y., Mao, H., Ma, Z., Yin, Y., Wang, W., Tang, W., Tan, Z., Shi, J., et al. (2015) · Brain, Behavior, and Immunity · doi:10.1016/j.bbi.2015.03.016 · Cited by 2,275 · see citing works

Inflammatory bowel disease: cause and immunobiology

Baumgart, D. C., & Carding, S. R. (2007) · The Lancet · doi:10.1016/s0140-6736(07)60750-8 · Cited by 2,147 · see citing works

Gut microbiome alterations in Alzheimer’s disease

Vogt, N. M., Kerby, R. L., Dill-McFarland, K. A., Harding, S. J., Merluzzi, A. P., Johnson, S. C., Carlsson, C. M., Asthana, S., Zetterberg, H., Blennow, K., et al. (2017) · Scientific Reports · doi:10.1038/s41598-017-13601-y · Cited by 2,137 · see citing works

Gut microbiota are related to Parkinson's disease and clinical phenotype

Scheperjans, F., Aho, V., Pereira, P. A. B., Koskinen, K., Paulin, L., Pekkonen, E., Haapaniemi, E., Kaakkola, S., Eerola‐Rautio, J., Pohja, M., et al. (2015) · Movement Disorders · doi:10.1002/mds.26069 · Cited by 1,968 · see citing works

Inflammatory bowel disease: clinical aspects and established and evolving therapies

Baumgart, D. C., & Sandborn, W. J. (2007) · The Lancet · doi:10.1016/s0140-6736(07)60751-x · Cited by 1,921 · see citing works

Assessment of psychotropic-like properties of a probiotic formulation ( <i>Lactobacillus helveticus</i> R0052 and <i>Bifidobacterium longum</i> R0175) in rats and human subjects

Messaoudi, M., Lalonde, R., Violle, N., Javelot, H., Desor, D., Nejdi, A., Bisson, J.-F., Rougeot, C., Pichelin, M., Cazaubiel, M., et al. (2011) · British Journal of Nutrition · doi:10.1017/s0007114510004319 · Cited by 1,324 · see citing works

Psychobiotics: A novel class of psychotropic

Dinan, T. G., Stanton, C., & Cryan, J. F. (2013) · Biological Psychiatry · doi:10.1016/j.biopsych.2013.05.001 · Cited by 1,287 · see citing works

Global variation in the prevalence and incidence of major depressive disorder: a systematic review of the epidemiological literature

Ferrari, A. J., Somerville, A. J., Baxter, A. J., Norman, R., Patten, S. B., Vos, T., & Whiteford, H. A. (2013) · Psychological Medicine · doi:10.1017/s0033291712001511 · Cited by 1,230 · see citing works

Microbiota and neurodevelopmental windows: implications for brain disorders

Borre, Y. E., O’Keeffe, G. W., Clarke, G., Stanton, C., Dinan, T. G., & Cryan, J. F. (2014) · Trends in Molecular Medicine · doi:10.1016/j.molmed.2014.05.002 · Cited by 1,089 · see citing works

Correlation between the human fecal microbiota and depression

Naseribafrouei, A., Hestad, K., Avershina, E., Sekelja, M., Linløkken, A., Wilson, R., & Rudi, K. (2014) · Neurogastroenterology &amp; Motility · doi:10.1111/nmo.12378 · Cited by 1,044 · see citing works

Estrogen–gut microbiome axis: Physiological and clinical implications

Baker, J. M., Al‐Nakkash, L., & Herbst‐Kralovetz, M. M. (2017) · Maturitas · doi:10.1016/j.maturitas.2017.06.025 · Cited by 1,024 · see citing works

Clinical epidemiology of Alzheimer&amp;rsquo;s disease: assessing sex and gender differences

Mielke, M., Vemuri, P., & Rocca, W. (2014) · Clinical Epidemiology · doi:10.2147/clep.s37929 · Cited by 1,021 · see citing works

Benefaction of probiotics for human health: A review

George Kerry, R., Patra, J. K., Gouda, S., Park, Y., Shin, H.-S., & Das, G. (2018) · Journal of Food and Drug Analysis · doi:10.1016/j.jfda.2018.01.002 · Cited by 898 · see citing works

Parkinson's disease and Parkinson's disease medications have distinct signatures of the gut microbiome

Hill‐Burns, E. M., Debelius, J. W., Morton, J. T., Wissemann, W. T., Lewis, M. R., Wallen, Z. D., Peddada, S. D., Factor, S. A., Molho, E., Zabetian, C. P., et al. (2017) · Movement Disorders · doi:10.1002/mds.26942 · Cited by 874 · see citing works

Brain-Gut-Microbiota Axis in Alzheimer’s Disease

Kowalski, K., & Mulak, A. (2019) · Journal of Neurogastroenterology and Motility · doi:10.5056/jnm18087 · Cited by 826 · see citing works

The Incidence of Parkinson's Disease: A Systematic Review and Meta-Analysis

Hirsch, L., Jetté, N., Frolkis, A. D., Steeves, T. D. L., & Pringsheim, T. M. (2016) · Neuroepidemiology · doi:10.1159/000445751 · Cited by 683 · see citing works

Maternal immune activation yields offspring displaying mouse versions of the three core symptoms of autism

Malkova, N. V., Yu, C. Z., Hsiao, E. Y., Moore, M. J., & Patterson, P. H. (2012) · Brain, Behavior, and Immunity · doi:10.1016/j.bbi.2012.01.011 · Cited by 662 · see citing works

Antibiotic-induced perturbations in gut microbial diversity influences neuro-inflammation and amyloidosis in a murine model of Alzheimer’s disease

Minter, M. R., Zhang, C., Leone, V., Ringus, D. L., Zhang, X., Oyler-Castrillo, P., Musch, M. W., Liao, F., Ward, J. F., Holtzman, D. M., et al. (2016) · Scientific Reports · doi:10.1038/srep30028 · Cited by 655 · see citing works

Fecal microbial determinants of fecal and systemic estrogens and estrogen metabolites: a cross-sectional study

Flores, R., Shi, J., Fuhrman, B., Xu, X., Veenstra, T. D., Gail, M. H., Gajer, P., Ravel, J., & Goedert, J. J. (2012) · Journal of Translational Medicine · doi:10.1186/1479-5876-10-253 · Cited by 615 · see citing works

Gut Microbiota’s Effect on Mental Health: The Gut-Brain Axis

Clapp, M., Aurora, N., Herrera, L., Bhatia, M., Wilen, E., & Wakefield, S. (2017) · Clinics and Practice · doi:10.4081/cp.2017.987 · Cited by 608 · see citing works

The gut-brain barrier in major depression: intestinal mucosal dysfunction with an increased translocation of LPS from gram negative enterobacteria (leaky gut) plays a role in the inflammatory pathophysiology of depression.

Maes, M. H. J., Kubera, M., & Leunis, J. (2008) · PubMed · Cited by 607 · see citing works

Controversies Revisited: A Systematic Review of the Comorbidity of Depression and Anxiety with Inflammatory Bowel Diseases

Mikocka-Walus, A., Knowles, S. R., Keefer, L., & Graff, L. (2016) · Inflammatory Bowel Diseases · doi:10.1097/mib.0000000000000620 · Cited by 567 · see citing works

Depression and anxiety in patients with Inflammatory Bowel Disease: a systematic review

Neuendorf, R., Harding, A., Stello, N., Hanes, D., & Wahbeh, H. (2016) · Journal of Psychosomatic Research · doi:10.1016/j.jpsychores.2016.06.001 · Cited by 561 · see citing works

Gut microbiota-brain axis

Wang, H.-X., & Wang, Y.-P. (2016) · Chinese Medical Journal · doi:10.4103/0366-6999.190667 · Cited by 546 · see citing works

Gut bacterial tyrosine decarboxylases restrict levels of levodopa in the treatment of Parkinson’s disease

van Kessel, S. P., Frye, A. K., El-Gendy, A. O., Castejon, M., Keshavarzian, A., van Dijk, G., & El Aidy, S. (2019) · Nature Communications · doi:10.1038/s41467-019-08294-y · Cited by 521 · see citing works

Gender and incidence of dementia in the Framingham Heart Study from mid‐adult life

Chêne, G., Beiser, A., Au, R., Preis, S. R., Wolf, P. A., Dufouil, C., & Seshadri, S. (2015) · Alzheimer's &amp; Dementia · doi:10.1016/j.jalz.2013.10.005 · Cited by 499 · see citing works

Neurobiological effects of intraventricular propionic acid in rats: Possible role of short chain fatty acids on the pathogenesis and characteristics of autism spectrum disorders

MACFABE, D., CAIN, D., RODRIGUEZCAPOTE, K., FRANKLIN, A., HOFFMAN, J., BOON, F., TAYLOR, A., KAVALIERS, M., & OSSENKOPP, K. (2007) · Behavioural Brain Research · doi:10.1016/j.bbr.2006.07.025 · Cited by 497 · see citing works

Analysis of Gut Microbiota in Patients with Parkinson’s Disease

Petrov, V. A., Saltykova, I. V., Zhukova, I. A., Alifirova, V. M., Zhukova, N. G., Dorofeeva, Y. B., Tyakht, A. V., Kovarsky, B. A., Alekseev, D. G., Kostryukova, E. S., et al. (2017) · Bulletin of Experimental Biology and Medicine · doi:10.1007/s10517-017-3700-7 · Cited by 487 · see citing works

Incidence and Prevalence of Crohn’s Disease and Ulcerative Colitis in Olmsted County, Minnesota From 1970 Through 2010

Shivashankar, R., Tremaine, W. J., Harmsen, W. S., & Loftus, E. V. (2017) · Clinical Gastroenterology and Hepatology · doi:10.1016/j.cgh.2016.10.039 · Cited by 455 · see citing works

Altered gut microbiota profile in patients with generalized anxiety disorder

Jiang, H., Zhang, X., Yu, Z., Zhang, Z., Deng, M., Zhao, J., & Ruan, B. (2018) · Journal of Psychiatric Research · doi:10.1016/j.jpsychires.2018.07.007 · Cited by 411 · see citing works

Bacterial Translocation from the Gastrointestinal Tract

Berg, R. D. (1999) · Advances in experimental medicine and biology · doi:10.1007/978-1-4615-4143-1_2 · Cited by 407 · see citing works

Sex Differences in the Association of Global Amyloid and Regional Tau Deposition Measured by Positron Emission Tomography in Clinically Normal Older Adults

Buckley, R. F., Mormino, E. C., Rabin, J. S., Hohman, T. J., Landau, S., Hanseeuw, B. J., Jacobs, H. I. L., Papp, K. V., Amariglio, R. E., Properzi, M. J., et al. (2019) · JAMA Neurology · doi:10.1001/jamaneurol.2018.4693 · Cited by 373 · see citing works

Gender differences in mental health.

Afifi, M. (2007) · PubMed · Cited by 367 · see citing works

Symptoms of depression and anxiety are independently associated with clinical recurrence of inflammatory bowel disease

Mikocka-Walus, A., Pittet, V., Rossel, J.-B., von Känel, R., Anderegg, C., Bauerfeind, P., Beglinger, C., Begré, S., Belli, D., Bengoa, J. M., et al. (2016) · Clinical Gastroenterology and Hepatology · doi:10.1016/j.cgh.2015.12.045 · Cited by 348 · see citing works

Results from the 2006 National Survey on Drug Use and Health

(2007) · PsycEXTRA Dataset · doi:10.1037/e723702007-017 · Cited by 338 · see citing works

Analysis of microbiota in first episode psychosis identifies preliminary associations with symptom severity and treatment response

Schwarz, E., Maukonen, J., Hyytiäinen, T., Kieseppä, T., Orešič, M., Sabunciyan, S., Mantere, O., Saarela, M., Yolken, R., & Suvisaari, J. (2018) · Schizophrenia Research · doi:10.1016/j.schres.2017.04.017 · Cited by 333 · see citing works

[Epidemiology of Parkinson disease].

Domínguez Carmona, M. (1989) · PubMed · Cited by 329 · see citing works

Brain-Gut-Microbiota Axis and Mental Health

Dinan, T. G., & Cryan, J. F. (2017) · Psychosomatic Medicine · doi:10.1097/psy.0000000000000519 · Cited by 325 · see citing works

Changes of colonic bacterial composition in Parkinson's disease and other neurodegenerative diseases

Gerhardt, S., & Mohajeri, M. H. (2018) · Nutrients · doi:10.3390/nu10060708 · Cited by 298 · see citing works

Sex differences in the gut microbiome–brain axis across the lifespan

Jašarević, E., Morrison, K. E., & Bale, T. L. (2016) · Philosophical Transactions of the Royal Society B Biological Sciences · doi:10.1098/rstb.2015.0122 · Cited by 295 · see citing works

Depression and inflammatory bowel disease: findings from two nationally representative Canadian surveys.

Fuller-Thomson, E., & Sulman, J. (2006) · Inflammatory Bowel Diseases · doi:10.1097/00054725-200608000-00005 · Cited by 292 · see citing works

Antibiotic-induced perturbations in microbial diversity during post-natal development alters amyloid pathology in an aged APPSWE/PS1ΔE9 murine model of Alzheimer’s disease

Minter, M. R., Hinterleitner, R., Meisel, M., Zhang, C., Leone, V., Zhang, X., Oyler-Castrillo, P., Zhang, X., Musch, M. W., Shen, X., et al. (2017) · Scientific Reports · doi:10.1038/s41598-017-11047-w · Cited by 292 · see citing works

International incidence of psychotic disorders, 2002–17: a systematic review and meta-analysis

Jongsma, H. E., Turner, C., Kirkbride, J. B., & Jones, P. B. (2019) · The Lancet Public Health · doi:10.1016/s2468-2667(19)30056-8 · Cited by 289 · see citing works

Sex-Based Differences in Incidence of Inflammatory Bowel Diseases—Pooled Analysis of Population-Based Studies From Western Countries

Shah, S. C., Khalili, H., Gower-Rousseau, C., Olen, O., Benchimol, E. I., Lynge, E., Nielsen, K. R., Brassard, P., Vutcovici, M., Bitton, A., et al. (2018) · Gastroenterology · doi:10.1053/j.gastro.2018.06.043 · Cited by 286 · see citing works

Early identification of autism spectrum disorder among children aged 4 years—Early Autism and Developmental Disabilities Monitoring Network, six sites, United States, 2016.

Shaw, K. A., Maenner, M. J., Baio, J., EdS1, Washington, A., Christensen, D. L., Wiggins, L. D., Pettygrove, S., Andrews, J. G., White, T., et al. (2020) · MMWR. Surveillance Summaries · doi:10.15585/mmwr.ss6903a1 · Cited by 286 · see citing works

Concurrent medical conditions and health care use and needs among children with learning and behavioral developmental disabilities, National Health Interview Survey, 2006–2010

Schieve, L. A., Gonzalez, V., Boulet, S. L., Visser, S. N., Rice, C. E., Braun, K. V. N., & Boyle, C. A. (2012) · Research in Developmental Disabilities · doi:10.1016/j.ridd.2011.10.008 · Cited by 273 · see citing works

Sex differences in gut microbiota in patients with major depressive disorder

Chen, J.-J., Zheng, P., Liu, Y.-Y., Zhong, X.-G., Wang, H.-Y., Guo, Y.-J., & Xie, P. (2018) · Neuropsychiatric Disease and Treatment · doi:10.2147/ndt.s159322 · Cited by 272 · see citing works

Composition, taxonomy and functional diversity of the oropharynx microbiome in individuals with schizophrenia and controls

Castro‐Nallar, E., Bendall, M. L., Pérez‐Losada, M., Sabunciyan, S., Severance, E. G., Dickerson, F., Schroeder, J. R., Yolken, R. H., & Crandall, K. A. (2015) · PeerJ · doi:10.7717/peerj.1140 · Cited by 269 · see citing works

The microbiome, immunity, and schizophrenia and bipolar disorder.

Dickerson, F., Severance, E., & Yolken, R. (2017) · Brain, Behavior, and Immunity · doi:10.1016/j.bbi.2016.12.010 · Cited by 268 · see citing works

Interaction Between Atypical Antipsychotics and the Gut Microbiome in a Bipolar Disease Cohort

Flowers, S. A., Evans, S. J., Ward, K. M., McInnis, M. G., & Ellingrod, V. L. (2017) · Pharmacotherapy: The Journal of Human Pharmacology and Drug Therapy · doi:10.1002/phar.1890 · Cited by 235 · see citing works

Sex differences in neurodevelopmental disorders

May, T., Adesina, I., McGillivray, J., & Rinehart, N. J. (2019) · Current Opinion in Neurology · doi:10.1097/wco.0000000000000714 · Cited by 235 · see citing works

Gender differences in mental health

Tansella, M. (1998) · Cited by 213 · see citing works

Overview and systematic review of studies of microbiome in schizophrenia and bipolar disorder

Nguyen, T. T., Kościółek, T., Eyler, L. T., Knight, R. D., & Jeste, D. V. (2018) · Journal of Psychiatric Research · doi:10.1016/j.jpsychires.2018.01.013 · Cited by 210 · see citing works

Sex: A Significant Risk Factor for Neurodevelopmental and Neurodegenerative Disorders

Pinares-Garcia, P., Stratikopoulos, M., Zagato, A., Loke, H., & Lee, J. (2018) · Brain Sciences · doi:10.3390/brainsci8080154 · Cited by 200 · see citing works

You’ve got male: Sex and the microbiota-gut-brain axis across the lifespan

Jaggar, M., Rea, K., Spichak, S., Dinan, T. G., & Cryan, J. F. (2020) · Frontiers in Neuroendocrinology · doi:10.1016/j.yfrne.2019.100815 · Cited by 200 · cited 1× · see citing works

Involvement of gut microbiome in human health and disease: brief overview, knowledge gaps and research opportunities

Liang, D., Leung, R. K., Guan, W., & Au, W. W. (2018) · Gut Pathogens · doi:10.1186/s13099-018-0230-4 · Cited by 198 · see citing works

Gastroenterology Issues in Schizophrenia: Why the Gut Matters

Severance, E. G., Prandovszky, E., Castiglione, J., & Yolken, R. H. (2015) · Current Psychiatry Reports · doi:10.1007/s11920-015-0574-0 · Cited by 196 · see citing works

Gut microbiome composition is associated with temperament during early childhood

Christian, L. M., Galley, J. D., Hade, E. M., Schoppe-Sullivan, S., Kamp Dush, C., & Bailey, M. T. (2015) · Brain, Behavior, and Immunity · doi:10.1016/j.bbi.2014.10.018 · Cited by 191 · see citing works

Peripheral and central inflammation in autism spectrum disorders

Depino, A. M. (2013) · Molecular and Cellular Neuroscience · doi:10.1016/j.mcn.2012.10.003 · Cited by 189 · see citing works

Probiotic normalization of Candida albicans in schizophrenia: A randomized, placebo-controlled, longitudinal pilot study

Severance, E. G., Gressitt, K. L., Stallings, C. R., Katsafanas, E., Schweinfurth, L. A. B., Savage, C. L. G., Adamos, M. B., Sweeney, K., Origoni, A. E., Khushalani, S., et al. (2016) · Brain Behavior and Immunity · doi:10.1016/j.bbi.2016.11.019 · Cited by 178 · see citing works

Does Parkinson’s disease start in the gut?

Lionnet, A., Leclair‐Visonneau, L., Neunlist, M., Murayama, S., Takao, M., Adler, C. H., Derkinderen, P., & Beach, T. G. (2017) · Acta Neuropathologica · doi:10.1007/s00401-017-1777-8 · Cited by 177 · see citing works

Parkinson’s Disease Psychosis: Presentation, Diagnosis and Management

Schneider, R. B., Iourinets, J., & Richard, I. H. (2017) · Neurodegenerative Disease Management · doi:10.2217/nmt-2017-0028 · Cited by 177 · see citing works

Sex-related alterations of gut microbiota composition in the BTBR mouse model of autism spectrum disorder

Coretti, L., Cristiano, C., Florio, E., Scala, G., Lama, A., Keller, S., Cuomo, M., Russo, R., Pero, R., Paciello, O., et al. (2017) · Scientific Reports · doi:10.1038/srep45356 · Cited by 175 · see citing works

The incidence and risk factors for developing depression after being diagnosed with inflammatory bowel disease: a cohort study

Panara, A. J., Yarur, A. J., Rieders, B., Proksell, S., Deshpande, A. R., Abreu, M. T., & Sussman, D. A. (2014) · Alimentary Pharmacology &amp; Therapeutics · doi:10.1111/apt.12669 · Cited by 168 · see citing works

Effects of maternal immune activation on gene expression patterns in the fetal brain

Garbett, K. A., Hsiao, E. Y., Kalman, J. L., Patterson, P. H., & Mirnics, K. (2012) · Translational Psychiatry · doi:10.1038/tp.2012.24 · Cited by 163 · see citing works

Oestradiol decreases colonic permeability through oestrogen receptor β‐mediated up‐regulation of occludin and junctional adhesion molecule‐A in epithelial cells

Braniste, V., Leveque, M., Buisson‐Brenac, C., Bueno, L. P., Fioramonti, J., & Houdeau, É. (2009) · The Journal of Physiology · doi:10.1113/jphysiol.2009.169300 · Cited by 161 · see citing works

Gut microbiota composition in patients with newly diagnosed bipolar disorder and their unaffected first-degree relatives

Coello, K., Hansen, T. H., Sørensen, N., Munkholm, K., Kessing, L. V., Pedersen, O. B., & Vinberg, M. (2018) · Brain Behavior and Immunity · doi:10.1016/j.bbi.2018.09.026 · Cited by 154 · see citing works

Modulation of the microbiota-gut-brain axis by probiotics in a murine model of inflammatory bowel disease

Emge, J. R., Huynh, K., Miller, E. N., Kaur, M., Reardon, C., Barrett, K. E., & Gareau, M. G. (2016) · American Journal of Physiology-Gastrointestinal and Liver Physiology · doi:10.1152/ajpgi.00086.2016 · Cited by 152 · see citing works

Gut microbiota changes in children with autism spectrum disorder: a systematic review

Ho, L. K. H., Tong, V. J. W., Syn, N., Nagarajan, N., Tham, E. H., Tay, S. K., Shorey, S., Tambyah, P. A., & Law, E. C. N. (2020) · Gut Pathogens · doi:10.1186/s13099-020-0346-1 · Cited by 149 · see citing works

Health-related quality of life in Crohn's disease: a prospective longitudinal study in 231 patients.

Blondel-Kucharski, F., Chircop, C., Marquis, P., Cortot, A., Baron, F., Jp, G., & Colombel, J. (2001) · PubMed · doi:10.1111/j.1572-0241.2001.4681_b.x · Cited by 134 · see citing works

Candida albicans exposures, sex specificity and cognitive deficits in schizophrenia and bipolar disorder

Severance, E. G., Gressitt, K. L., Stallings, C. R., Katsafanas, E., Schweinfurth, L. A. B., Savage, C. L. G., Adamos, M. B., Sweeney, K., Origoni, A. E., Khushalani, S., et al. (2016) · Schizophrenia · doi:10.1038/npjschz.2016.18 · Cited by 127 · see citing works

Health-related quality of life in Crohn’s disease: a prospective longitudinal study in 231 patients

Blondel-Kucharski, F., Chircop, C., Marquis, P., Cortot, A., Baron, F., Gendre, J.-P., Colombel, J.-F., & (GETAID), T. G. D. T. D. A. I. D. (2001) · The American Journal of Gastroenterology · doi:10.1111/j.1572-0241.2001.04681.x · Cited by 120 · see citing works

Sexually dimorphic effects of prenatal exposure to propionic acid and lipopolysaccharide on social behavior in neonatal, adolescent, and adult rats: Implications for autism spectrum disorders

Foley, K. A., MacFabe, D. F., Vaz, A., Ossenkopp, K., & Kavaliers, M. (2014) · International Journal of Developmental Neuroscience · doi:10.1016/j.ijdevneu.2014.04.001 · Cited by 116 · see citing works

Sex-related differences in oxidative stress and neurodegeneration

Tenkorang, M. A. A., Snyder, B., & Cunningham, R. L. (2017) · Steroids · doi:10.1016/j.steroids.2017.12.010 · Cited by 116 · see citing works

Gut Vibes in Parkinson's Disease: The Microbiota‐Gut‐Brain Axis

Bullich‐Vilarrubias, C., Keshavarzian, A., Garssen, J., Kraneveld, A. D., & Perez‐Pardo, P. (2019) · Movement Disorders Clinical Practice · doi:10.1002/mdc3.12840 · Cited by 116 · see citing works

A Novel Rodent Model of Autism: Intraventricular Infusions of Propionic Acid Increase Locomotor Activity and Induce Neuroinflammation and Oxidative Stress in Discrete Regions of Adult Rat Brain

MacFabe, D. F., Rodríguez-Capote, K., Hoffman, J. E., Franklin, A. E., Mohammad-A, Y., Taylor, A. R., Boon, F. H., Cain, D. P., Kavaliers, M., Possmayer, F., et al. (2008) · American journal of biochemistry & biotechnology/American journal of biochemistry and biotechnology · doi:10.3844/ajbbsp.2008.146.166 · Cited by 114 · see citing works

Health-Related Quality of Life in Patients with Ulcerative Colitis After a 10-year Disease Course: Results from the IBSEN Study

Høivik, M. L., Moum, B. A., Solberg, I. C., Cvancarova, M., Høie, O., Vatn, M. H., & Bernklev, T. (2011) · Inflammatory Bowel Diseases · doi:10.1002/ibd.21863 · Cited by 114 · see citing works

Sex-specific effects of docosahexaenoic acid (DHA) on the microbiome and behavior of socially-isolated mice

Davis, D. J., Hecht, P. M., Jasarevic, E., Beversdorf, D. Q., Will, M. J., Fritsche, K., & Gillespie, C. H. (2017) · Brain, Behavior, and Immunity · doi:10.1016/j.bbi.2016.09.003 · Cited by 112 · see citing works

Psychological stress and depression: risk factors for IBD

Bernstein, C. N. (2016) · Digestive Diseases · doi:10.1159/000442929 · Cited by 107 · see citing works

The gut-brain relationship: investigating the effect of multispecies probiotics on anxiety in a randomized placebo-controlled trial of healthy young adults

Tran, N., Zhebrak, M., Yacoub, C., Pelletier, J., & Hawley, D. (2019) · Journal of Affective Disorders · doi:10.1016/j.jad.2019.04.043 · Cited by 104 · see citing works

Systematic review: psychological morbidity in young people with inflammatory bowel disease - risk factors and impacts

Brooks, A. J., Rowse, G., Ryder, A., Peach, E. J., Corfe, B. M., & Lobo, A. J. (2016) · Alimentary Pharmacology &amp; Therapeutics · doi:10.1111/apt.13645 · Cited by 98 · see citing works

Association of rigid-compulsive behavior with functional constipation in autism spectrum disorder

Marler, S., Ferguson, B. J., Lee, E. B., Peters, B., Williams, K. C., McDonnell, E., Macklin, E. A., Levitt, P., Margolis, K. G., Beversdorf, D. Q., et al. (2017) · Journal of Autism and Developmental Disorders · doi:10.1007/s10803-017-3084-6 · Cited by 94 · see citing works

Estrogen and Alzheimer's disease: Still an attractive topic despite disappointment from early clinical results

Merlo, S., Spampinato, S. F., & Sortino, M. A. (2017) · European Journal of Pharmacology · doi:10.1016/j.ejphar.2017.05.059 · Cited by 90 · see citing works

Ovarian progesterone suppresses depression and anxiety-like behaviors by increasing the Lactobacillus population of gut microbiota in ovariectomized mice

Watcharin, S., Sovijit, W., Pu, S., Usuda, K., Inoüe, R., Watanabe, G., Yamaguchi, H., & Nagaoka, K. (2019) · Neuroscience Research · doi:10.1016/j.neures.2019.04.005 · Cited by 89 · see citing works

Stress-induced disturbances along the gut microbiota-immune-brain axis and implications for mental health: Does sex matter?

Audet, M. (2019) · Frontiers in Neuroendocrinology · doi:10.1016/j.yfrne.2019.100772 · Cited by 79 · see citing works

Alteration of gut microbiota-associated epitopes in children with autism spectrum disorders

Wang, M., Zhou, J., He, F., Cai, C., Wang, H., Wang, Y., Lin, Y., Rong, H., Cheng, G., Xu, R., et al. (2019) · Brain, Behavior, and Immunity · doi:10.1016/j.bbi.2018.10.006 · Cited by 77 · see citing works

Influence of Estrogen Modulation on Glia Activation in a Murine Model of Parkinson's Disease

Siani, F., Greco, R., Levandis, G., Ghezzi, C., Daviddi, F., Demartini, C., Vegeto, E., Armentero, M., & Blandini, F. (2017) · Frontiers in Neuroscience · doi:10.3389/fnins.2017.00306 · Cited by 75 · see citing works

Prenatal exposure to bacterial endotoxin reduces the number of GAD67- and reelin-immunoreactive neurons in the hippocampus of rat offspring

Nouel, D., Burt, M., Zhang, Y., Harvey, L., & Boksa, P. (2011) · European Neuropsychopharmacology · doi:10.1016/j.euroneuro.2011.08.001 · Cited by 70 · see citing works

Estrogen receptor-α is localized to neurofibrillary tangles in Alzheimer’s disease

Wang, C., Zhang, F., Jiang, S., Siedlak, S. L., Shen, L. H., Perry, G. L., Wang, X., Tang, B., & Zhu, X. (2016) · Scientific Reports · doi:10.1038/srep20352 · Cited by 69 · see citing works

A not entirely benign procedure: progression of Parkinson’s disease

Tredici, K. D., & Braak, H. (2008) · Acta Neuropathologica · doi:10.1007/s00401-008-0355-5 · Cited by 67 · see citing works

Meta-Analysis of Parkinson's Disease Transcriptome Data Using TRAM Software: Whole Substantia Nigra Tissue and Single Dopamine Neuron Differential Gene Expression

Mariani, E., Frabetti, F., Tarozzi, A., Pelleri, M. C., Pizzetti, F., & Casadei, R. (2016) · PLoS ONE · doi:10.1371/journal.pone.0161567 · Cited by 65 · see citing works

Transient Gastric Irritation in the Neonatal Rats Leads to Changes in Hypothalamic CRF Expression, Depression- and Anxiety-Like Behavior as Adults

Liu, L., Li, Q., Sapolsky, R. M., Liao, M., Mehta, K. R., Bhargava, A., & Pasricha, P. J. (2011) · PLoS ONE · doi:10.1371/journal.pone.0019498 · Cited by 55 · see citing works

Early‐life stress leads to sex‐dependent changes in pubertal timing in rats that are reversed by a probiotic formulation

Cowan, C. S. M., & Richardson, R. (2019) · Developmental Psychobiology · doi:10.1002/dev.21765 · Cited by 52 · see citing works

Randomized controlled trial of a gluten-free diet in patients with schizophrenia positive for antigliadin antibodies (AGA IgG): a pilot feasibility study

Kelly, D. L., Demyanovich, H. K., Rodriguez, K. M., Čiháková, D., Talor, M. V., McMahon, R. P., Richardson, C. M., Vyas, G. R., Adams, H. A., August, S. M., et al. (2019) · Journal of Psychiatry and Neuroscience · doi:10.1503/jpn.180174 · Cited by 48 · see citing works

The sex-specific interaction of the microbiome in neurodegenerative diseases

Cox, L. M., Abou‐El‐Hassan, H., Maghzi, A. H., Vincentini, J., & Weiner, H. L. (2019) · Brain Research · doi:10.1016/j.brainres.2019.146385 · Cited by 42 · see citing works

Experimental gastritis leads to anxiety- and depression-like behaviors in female but not male rats

Luo, J., Wang, T., Liang, S., Hu, X., Li, W., & Jin, F. (2013) · Behavioral and Brain Functions · doi:10.1186/1744-9081-9-46 · Cited by 41 · see citing works

Gender related differences in quality of life and affective status in patients with inflammatory bowel disease.

Hauser, G., Tkalčić, M., Štimac, D., Milić, S., & Sinčić, B. M. (2011) · PubMed · Cited by 39 · see citing works

Gluten sensitivity and relationship to psychiatric symptoms in people with schizophrenia

Jackson, J. R., Eaton, W. W., Cascella, N. G., Fasano, A., Santora, D., Sullivan, K. M., Feldman, S. M., Raley, H., McMahon, R. P., Carpenter, W. T., et al. (2014) · Schizophrenia Research · doi:10.1016/j.schres.2014.09.023 · Cited by 38 · see citing works

Association between gastrointestinal symptoms and affectivity in patients with bipolar disorder

Karling, P., Maripuu, M., Wikgren, M., Adolfsson, R., & Norrback, K. (2016) · World Journal of Gastroenterology · doi:10.3748/wjg.v22.i38.8540 · Cited by 37 · see citing works

Integrating sex and gender into neurodegeneration research: A six‐component strategy

Tierney, M. C., Curtis, A. F., Chertkow, H. M., & Rylett, R. J. (2017) · Alzheimer s & Dementia Translational Research & Clinical Interventions · doi:10.1016/j.trci.2017.10.006 · Cited by 36 · see citing works

Complete genome sequence of Lactobacillus pentosus SLC13, isolated from mustard pickles, a potential probiotic strain with antimicrobial activity against foodborne pathogenic microorganisms

Huang, M.-L., Huang, J.-Y., Kao, C., & Fang, T. J. (2018) · Gut Pathogens · doi:10.1186/s13099-018-0228-y · Cited by 33 · see citing works

Sex-Specific Transcriptome Differences in Substantia Nigra Tissue: A Meta-Analysis of Parkinson’s Disease Data

Mariani, E., Lombardini, L., Facchin, F., Pizzetti, F., Frabetti, F., Tarozzi, A., & Casadei, R. (2018) · Genes · doi:10.3390/genes9060275 · Cited by 25 · see citing works

Gliadin-related antibodies in schizophrenia

Čiháková, D., Eaton, W. W., Talor, M. V., Harkus, U. H., Demyanovich, H. K., Rodriguez, K. M., Feldman, S. M., & Kelly, D. L. (2017) · Schizophrenia Research · doi:10.1016/j.schres.2017.08.051 · Cited by 24 · see citing works

Gut bacterial tyrosine decarboxylases restrict the bioavailability of levodopa, the primary treatment in Parkinson’s diseasePreprint

van Kessel, S. P., Frye, A. K., EL-Gendy, A. O., et al. (2018) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/356246 · Cited by 10 · see citing works

Factors associated with gender and sex differences in anxiety prevalence and comorbidity: A systematic review

Farhane-Medina, N. Z., Luque, B., Tabernero, C., & Castillo-Mayén, R. (2022) · Science Progress · doi:10.1177/00368504221135469 · Cited by 409 · see citing works

Sex and gender in neurodevelopmental conditions

Bölte, S., Neufeld, J., Marschik, P. B., Williams, Z. J., Gallagher, L., & Lai, M.-C. (2023) · Nature Reviews Neurology · doi:10.1038/s41582-023-00774-6 · Cited by 249 · see citing works

The Crosstalk between Gut Microbiota and Nervous System: A Bidirectional Interaction between Microorganisms and Metabolome

Montagnani, M., Bottalico, L., Potenza, M. A., Charitos, I. A., Topi, S., Colella, M., & Santacroce, L. (2023) · International Journal of Molecular Sciences · doi:10.3390/ijms241210322 · Cited by 106 · see citing works

Gastrointestinal involvement of autism spectrum disorder: focus on gut microbiota

Settanni, C. R., Bibbò, S., Ianiro, G., Rinninella, E., Cintoni, M., Mele, M. C., Cammarota, G., & Gasbarrini, A. (2021) · Expert Review of Gastroenterology &amp; Hepatology · doi:10.1080/17474124.2021.1869938 · Cited by 98 · see citing works

Sexual Dimorphism in the Expression of Cytochrome P450 Enzymes in Rat Heart, Liver, Kidney, Lung, Brain, and Small Intestine

Gerges, S. H., & El‐Kadi, A. O. S. (2022) · Drug Metabolism and Disposition · doi:10.1124/dmd.122.000915 · Cited by 67 · see citing works

Sialic acid, the secret gift for the brain

Fan, L., Simpson, A. B., D’Costa, E., Bunn, F. S., & van Leeuwen, S. S. (2022) · Critical Reviews in Food Science and Nutrition · doi:10.1080/10408398.2022.2072270 · Cited by 65 · see citing works

Role of gut microbiota in neuropathy and neuropathic pain states: A systematic preclinical review

Pane, K., Boccella, S., Guida, F., Franzese, M., Maione, S., & Salvatore, M. (2022) · Neurobiology of Disease · doi:10.1016/j.nbd.2022.105773 · Cited by 52 · see citing works

Public awareness, specific knowledge, and worry about mpox (monkeypox): A preliminary community-based study in Shenzhen, China

Ren, F., Liu, J., Miao, J., Xu, Y., Zhang, R., Fan, J., & Lin, W. (2023) · Frontiers in Public Health · doi:10.3389/fpubh.2023.1077564 · Cited by 48 · see citing works

Gene-environment-gut interactions in Huntington's disease mice are associated with environmental modulation of the gut microbiome

Gubert, C., Love, C. J., Kodikara, S., Mei Liew, J. J., Renoir, T., Lê Cao, K.-A., & Hannan, A. J. (2022) · iScience · doi:10.1016/j.isci.2021.103687 · Cited by 41 · see citing works

Self‐efficacy matters: Influence of students’ perceived self‐efficacy on statistics anxiety

Kaufmann, L., Ninaus, M., Weiss, E. M., Gruber, W. R., & Wood, G. M. D. O. (2022) · Annals of the New York Academy of Sciences · doi:10.1111/nyas.14797 · Cited by 40 · see citing works

Precision Psychobiotics for Gut–Brain Axis Health: Advancing the Discovery Pipelines to Deliver Mechanistic Pathways and Proven Health Efficacy

Slykerman, R. F., Davies, N., Vlčková, K., O’Riordan, K. J., Bassett, S. A., Dekker, J., Schellekens, H., Hyland, N. P., Clarke, G. A., & Patterson, E. (2025) · Microbial Biotechnology · doi:10.1111/1751-7915.70079 · Cited by 43 · see citing works

Gut-brain axis: gut dysbiosis and psychiatric disorders in Alzheimer’s and Parkinson’s disease

Denman, C. R., Park, S. M., & Jo, J. (2023) · Frontiers in Neuroscience · doi:10.3389/fnins.2023.1268419 · Cited by 43 · see citing works

Gut microbiome effects on neuronal excitability & activity: Implications for epilepsy

Darch, H., & McCafferty, C. P. (2022) · Neurobiology of Disease · doi:10.1016/j.nbd.2022.105629 · Cited by 38 · see citing works

Gut microbiome-brain axis and inflammation in temperament, personality and psychopathology

Sumich, A. L., Heym, N., Lenzoni, S., & Hunter, K. A. (2022) · Current Opinion in Behavioral Sciences · doi:10.1016/j.cobeha.2022.101101 · Cited by 35 · see citing works

Depressive and Anxiety Disorders in Patients with Inflammatory Bowel Diseases: Are There Any Gender Differences?

Fracas, E., Costantino, A., Vecchi, M. L., & Buoli, M. (2023) · International Journal of Environmental Research and Public Health · doi:10.3390/ijerph20136255 · Cited by 33 · see citing works

The Role of Gut Microbiota in Neuropsychiatric Diseases – Creation of An Atlas-Based on Quantified Evidence

Bonnechère, B., Amin, N., & van Duijn, C. M. (2022) · Frontiers in Cellular and Infection Microbiology · doi:10.3389/fcimb.2022.831666 · Cited by 31 · see citing works

Assessment of the impact of intravenous antibiotics treatment on gut microbiota in patients: Clinical data from pre-and post-cardiac surgery

Xue, L., Ding, Y., Qin, Q., Liu, L., Ding, X., Zhou, Y., Liu, K., Singla, R. K., Shen, K., Din, A. U., et al. (2023) · Frontiers in Cellular and Infection Microbiology · doi:10.3389/fcimb.2022.1043971 · Cited by 25 · see citing works

Impact of micronutrients and nutraceuticals on cognitive function and performance in Alzheimer's disease.

Guarnieri, L., Bosco, F., Leo, A., Citraro, R., Palma, E., Sarro, G. D., & Mollace, V. (2024) · Ageing Research Reviews · doi:10.1016/j.arr.2024.102210 · Cited by 23 · see citing works

Changes in the rodent gut microbiome following chronic restraint stress and low-intensity rTMS

Seewoo, B. J., Chua, E. G., Arena-Foster, Y., Hennessy, L. A., Gorecki, A. M., Anderton, R. S., & Rodger, J. (2022) · Neurobiology of Stress · doi:10.1016/j.ynstr.2022.100430 · Cited by 26 · see citing works

Bisphenol S exposure induces intestinal inflammation: An integrated metabolomic and transcriptomic study

Ao, J., Liu, Y., Tang, W., & Zhang, J. (2021) · Chemosphere · doi:10.1016/j.chemosphere.2021.133510 · Cited by 24 · see citing works

Sexual dimorphism in neurobehavioural phenotype and gut microbial composition upon long-term exposure to structural analogues of bisphenol-A

Singh, D. P., Kumar, A., Prajapati, J., Bijalwan, V., Kumar, J., Amin, P., Kandoriya, D., Vidhani, H., Patil, G. P., Bishnoi, M., et al. (2024) · Journal of Hazardous Materials · doi:10.1016/j.jhazmat.2024.135178 · Cited by 19 · see citing works

Effect of parental absence during infancy and early childhood on cognition and depression in later life: A national household longitudinal study

Yang, J., Zhang, Q., Li, J., Guan, S., Wang, K., Xu, H., & Liu, Z. (2022) · Journal of Affective Disorders · doi:10.1016/j.jad.2022.09.113 · Cited by 14 · see citing works

Sex and gender as critical and distinct contributors to the human brain-gut-microbiome axis

Gancz, N. N., Levinson, J. A., & Callaghan, B. L. (2023) · Brain Research Bulletin · doi:10.1016/j.brainresbull.2023.110665 · Cited by 14 · see citing works

Dietary total anti-oxidant capacity is inversely related to the prevalence of depression in adolescent girls

Zohrabi, T., Ziaee, A., Salehi‐Abargouei, A., Ferns, G. A., Ghayour‐Mobarhan, M., & Khayyatzadeh, S. S. (2022) · BMC Pediatrics · doi:10.1186/s12887-022-03589-4 · Cited by 13 · see citing works

Neonatal immune challenge influences the microbiota and behaviour in a sexually dimorphic manner

Cuskelly, A., Hoedt, E. C., Harms, L. R., Talley, N. J., Tadros, M. A., Keely, S., & Hodgson, D. M. (2022) · Brain Behavior and Immunity · doi:10.1016/j.bbi.2022.04.023 · Cited by 13 · see citing works

The aging gut–glia–immune axis in alzheimer’s disease: microbiome-derived mediators of neuroinflammation and therapeutic innovation

Mir, P. A., Kumar, N. G., Bhutia, G. T., Chaudhary, P., Kaur, G., & Gupta, S. K. (2026) · GeroScience · doi:10.1007/s11357-025-02062-1 · Cited by 13 · see citing works

Recommendations for the Application of Sex and Gender Medicine in Preclinical, Epidemiological and Clinical Research

Cattaneo, A., Bellenghi, M., Ferroni, E., Mangia, C., Marconi, M., Rizza, P., Borghini, A., Martini, L., Luciani, M. N., Ortona, E., et al. (2024) · Journal of Personalized Medicine · doi:10.3390/jpm14090908 · Cited by 15 · see citing works

Combined oral contraceptives and mental health: Are adolescence and the gut-brain axis the missing links?

Kheloui, S., Smith, A. M., & Ismail, N. (2022) · Frontiers in neuroendocrinology (Print) · doi:10.1016/j.yfrne.2022.101041 · Cited by 13 · see citing works

Application of sex/gender-specific medicine in healthcare

Kim, N. (2023) · Korean journal of women health nursing/Yeoseong geon'gang ganho hag'hoeji/Yeoseong geon-gang ganho hakoeji · doi:10.4069/kjwhn.2023.03.13 · Cited by 12 · see citing works

The enteric metabolite, propionic acid, impairs social behavior and increases anxiety in a rodent ASD model: Examining sex differences and the influence of the estrous cycle

Benitah, K. C., Kavaliers, M., & Ossenkopp, K. (2023) · Pharmacology Biochemistry and Behavior · doi:10.1016/j.pbb.2023.173630 · Cited by 11 · see citing works

Perceived household financial decline and physical/mental health among adolescents during the COVID-19 crisis: Focusing on gender differences

Yoo, N., & Jang, S. H. (2023) · Preventive Medicine Reports · doi:10.1016/j.pmedr.2023.102119 · Cited by 11 · see citing works

The Role of Gut Microbiota in Inflammatory Bowel Disease-Current State of the Art

Safarpour, A. R., Askari, H., Shojaei‐Zarghani, S., Raeis-Abdollahi, E., Jahromi, H. K., Raise‐Abdullahi, P., Daliri, K., Tajbakhsh, A., & Rahmati, L. (2022) · Mini-Reviews in Medicinal Chemistry · doi:10.2174/1389557522666220914093331 · Cited by 10 · see citing works

Sex/Gender Differences in Depression and Anxiety Disorders

Park, H. Y. (2024) · Springer eBooks · doi:10.1007/978-981-97-0130-8_21 · Cited by 10 · see citing works

Molecular pathways linking the serotonin transporters (SERT) to depressive disorder: from mechanisms to treatments

Murthy, M. K. (2025) · Neuroscience · doi:10.1016/j.neuroscience.2025.08.009 · Cited by 10 · see citing works

Sex‐ and gender‐related differences in the prevalence and burden of disorders of gut‐brain interaction in Poland

Mulak, A., Freud, T., Waluga, M., Bangdiwala, S. I., Palsson, O. S., & Sperber, A. D. (2023) · Neurogastroenterology & Motility · doi:10.1111/nmo.14568 · Cited by 9 · see citing works

Animal Age Affects the Gut Microbiota and Immune System in Captive Koalas ( Phascolarctos cinereus )

Chen, J., Lv, W., Zhang, X., Zhang, T., Dong, J., Wang, Z., Liu, T., Zhang, P., Pyne, M. J., Dong, G., et al. (2023) · Microbiology Spectrum · doi:10.1128/spectrum.04101-22 · Cited by 9 · see citing works

Sex differences in gastrointestinal dysfunction among patients with Parkinson’s disease

Chang, H. J., Shin, C.-M., Cho, J. W., Koh, S., Yang, Y., Kim, H.-T., Kim, J., & Lee, J. (2023) · Neurological Sciences · doi:10.1007/s10072-023-06710-2 · Cited by 8 · see citing works

A potential role of gut microbiota in stroke: mechanisms, therapeutic strategies and future prospective

Kaur, M., Aran, K. R., & Paswan, R. (2024) · Psychopharmacology · doi:10.1007/s00213-024-06708-4 · Cited by 8 · see citing works

Effects of fecal microbiota transplantation from patients with generalized anxiety on anxiety-like behaviors: The role of the gut-microbiota-endocannabinoid-brain Axis

Cai, M., Xue, S., Zhou, C., Feng, Y., Liu, J., Liu, R., Wang, P., Wang, H., & Peng, Z. (2025) · Journal of Affective Disorders · doi:10.1016/j.jad.2025.04.018 · Cited by 8 · see citing works

Alternate-day fasting ameliorates α-synuclein pathology and suppresses inflammation via the gut-brain axis in an MPTP-induced subacute mouse model of Parkinson’s disease

Wang, Z., Cui, Y., Li, D., Yan, L., Zhu, S., Ma, X., Lu, Z., Li, C., Feng, J., Yuan, W., et al. (2025) · npj Biofilms and Microbiomes · doi:10.1038/s41522-025-00855-y · Cited by 8 · see citing works

Evaluation of the Effects of Instant Cascara Beverage on the Brain-Gut Axis of Healthy Male and Female Rats

Gallego-Barceló, P., Bagüés, A., Benítez-Álvarez, D., López‐Tofiño, Y., Gálvez-Robleño, C., López‐Gómez, L., del Castillo, M. D., & Abalo, R. (2023) · Nutrients · doi:10.3390/nu16010065 · Cited by 8 · see citing works

Influences of the Immune System and Microbiome on the Etiology of ASD and GI Symptomology of Autistic Individuals

Kim, A. J. H., Zisman, C. R., & Holingue, C. (2022) · Current topics in behavioral neurosciences · doi:10.1007/7854_2022_371 · Cited by 7 · see citing works

Electroacupuncture alleviates cognitive impairments in APP/PS1 mice via gastric vagal afferent-mediated activation of the nucleus tractus solitarius‒locus coeruleus noradrenergic circuit

Yu, C.-C., Li, M., Shen, F., Gao, S., Wang, J., He, C., Wang, L., Wu, Y., & Du, Y. (2025) · Chinese Medicine · doi:10.1186/s13020-025-01230-x · Cited by 7 · see citing works

Sex hormones, the gut microbiome, and neurodegenerative diseases: Lifespan perspective

Stahlke, S., & Theiß, C. (2025) · Neural Regeneration Research · doi:10.4103/nrr.nrr-d-25-00932 · Cited by 7 · see citing works

Microbiota–gut–brain axis and related therapeutics in Alzheimer’s disease: prospects for multitherapy and inflammation control

Li, J., Zhang, F., Zhao, L., & Dong, C. (2023) · Reviews in the Neurosciences · doi:10.1515/revneuro-2023-0006 · Cited by 6 · see citing works

Microbiota and social behavior alterations in a mouse model of down syndrome: Modulation by a synbiotic treatment

González-Parra, J. A., Barrera-Conde, M., Kossatz, E., Veza-Estévez, E., de la Torre, R., Busquets-García, A., Robledo, P., & Pizarro, N. (2024) · Progress in Neuro-Psychopharmacology and Biological Psychiatry · doi:10.1016/j.pnpbp.2024.111200 · Cited by 5 · see citing works

Microbiome affects mice metabolic homeostasis via differential regulation of gene expression in the brain and gut

Milhouse, W., Organski, A. C., Sun, X., Ai, D., Zhou, B., Cross, T.-W., & Ren, H. (2025) · Physiological Reports · doi:10.14814/phy2.70373 · Cited by 5 · see citing works

The colonic interleukin-19 aggravates the dextran sodium sulfate/stress-induced comorbidities due to colitis and anxiety

Li, Q., Meng, F., Ma, X., Sun, Z., Dai, J., Liu, J., Li, D., Cong, P., Xu, R., Zhao, D., et al. (2023) · Frontiers in Immunology · doi:10.3389/fimmu.2023.1153344 · Cited by 6 · see citing works

Special Section: Metabolic Psychiatry

Barch, D. M. (2023) · Biological Psychiatry Global Open Science · doi:10.1016/j.bpsgos.2023.08.017 · Cited by 5 · see citing works

The association between energy-adjusted dietary inflammatory index and physical activity with sleep quality: a cross-sectional study

Zare, M., Masoumi, S. J., & Zare, M. (2024) · BMC Nutrition · doi:10.1186/s40795-024-00834-0 · Cited by 5 · see citing works

Consumption of a Probiotic Blend with Vitamin D Improves Immunity, Redox, and Inflammatory State, Decreasing the Rate of Aging—A Pilot Study

Félix, J., Baca, A., Taboada, L., Álvarez-Calatayud, G., & la Fuente, M. D. (2024) · Biomolecules · doi:10.3390/biom14111360 · Cited by 5 · see citing works

Unravelling sex differences in the genetic architecture of anxiety

Hu, J., Lupton, M. K., Byrne, E. M., Martin, N. G., Whiteman, D. C., Olsen, C. M., Thomas, J. T., Medland, S. E., Grasby, K. L., & Mitchell, B. L. (2026) · Psychological Medicine · doi:10.1017/s0033291726104760 · Cited by 4 · see citing works

Factors associated with adverse mental health outcomes during the COVID-19 pandemic

Choi, S. H., & Kim, S. (2023) · Public Health in Practice · doi:10.1016/j.puhip.2023.100360 · Cited by 4 · see citing works

Sex Differences in Neurodevelopment and Its Disorders

Brown, R. E. (2023) · Springer eBooks · doi:10.1007/978-3-031-20792-1_11 · Cited by 4 · see citing works

Proportion, Correlates and the Associations of Meeting 24‐h Movement Guidelines With Mental Well‐Being and Psychological Distress: A Cross‐Sectional Study of 10 589 Chinese Students

Zhang, H., Sheng, J., Yue, X., Lou, H., Ban, X., Wu, W., Li, R., Gao, G., Wang, C., Lou, X., et al. (2024) · Child Care Health and Development · doi:10.1111/cch.13329 · Cited by 4 · see citing works

Intersection of Sex and Depression: Pathogenesis, Presentation, and Treatments

Frohman, D. F. T., Nnah, K., & Tsirka, S. E. (2023) · Handbook of experimental pharmacology · doi:10.1007/164_2023_670 · Cited by 3 · see citing works

Gut Microbiome Dysbiosis as a Potential Risk Factor for Idiopathic Toe-Walking in Children: A Review

Kononova, S., Kashparov, M., Xue, W., Бобкова, Н. В., Leonov, S. V., & Zagorodny, N. (2023) · International Journal of Molecular Sciences · doi:10.3390/ijms241713204 · Cited by 3 · see citing works

Has the COVID-19 Pandemic Worsened Health-Related Quality of Life of Patients with Inflammatory Bowel Disease? A Longitudinal Disease Activity-Controlled Study

Rosa, I., Conti, C. M., Zito, L., Efthymakis, K., Neri, M., & Porcelli, P. (2023) · International Journal of Environmental Research and Public Health · doi:10.3390/ijerph20021103 · Cited by 2 · see citing works

The Association between Change in Lifestyle Behaviors and Mental Health Indicators in Immunosuppressed Individuals during the COVID-19 Pandemic

Zeitoun, T., Plante, A., Sabiston, C. M., Dieudé, M., & Doré, I. (2023) · International Journal of Environmental Research and Public Health · doi:10.3390/ijerph20032099 · Cited by 3 · see citing works

Sex differences in the relationship between depression and Alzheimer’s disease—mechanisms, genetics, and therapeutic opportunities

Chen, Y., Wang, Z., Liu, X., Xu, J., & Mao, Z. (2024) · Frontiers in Aging Neuroscience · doi:10.3389/fnagi.2024.1301854 · Cited by 3 · see citing works

Vivaria housing conditions expose sex differences in brain oxidation, microglial activation, and immune system states in aged hAPOE4 mice

Reyes‐Reyes, E. M., Brown, J. A., Trial, M., Chinnasamy, D., Wiegand, J., Bradford, D. R., Brinton, R. D., & Rodgers, K. E. (2024) · Experimental Brain Research · doi:10.1007/s00221-023-06763-x · Cited by 2 · see citing works

Health disturbances stemming from overcrowding and inadequate housing among indigenous peoples within Canada

Anisman, H., Bombay, A., & Matheson, K. (2025) · Frontiers in Environmental Health · doi:10.3389/fenvh.2025.1720326 · Cited by 4 · see citing works

Childhood dietary factors are associated with maternal characteristics and sex-specific changes in neuropsychological deficits: A criminological assessment

Gibbs, W. J., & Beaver, K. M. (2026) · Journal of Criminal Justice · doi:10.1016/j.jcrimjus.2026.102613 · Cited by 3 · see citing works

Sex-specific microbial and tryptophan signatures of depression implicate archaeal methanogens and indole-3-acetic acid only in women

Motger‐Albertí, A., Gallardo‐Nuell, L., Rosell-Díaz, M., Stefoglo, M., Pons, J., Garre‐Olmo, J., Pérez‐Brocal, V., Moya, A., Puig, J., Ramos, R., et al. (2026) · npj Biofilms and Microbiomes · doi:10.1038/s41522-026-00983-z · Cited by 2 · see citing works

The dual-sensitive period gut-brain crosstalk, neuroinflammation, and the biological roots of adolescent depression

Shi, Y., & Ma, Q. (2026) · Frontiers in Immunology · doi:10.3389/fimmu.2026.1821502 · Cited by 3 · see citing works

Breast may not always be best: moderation of effects of postnatal depression by breastfeeding and infant sex

Braithwaite, E., Sharp, H. M., Pickles, A. R., Hill, J., & Wright, N. (2021) · Biology of Sex Differences · doi:10.1186/s13293-021-00403-1 · Cited by 2 · see citing works

Homeostatic regulation of neuronal excitability by probiotics in male germ‐free mice

Kim, J., Kim, D. W., Lee, A. C., Mason, M., Jouroukhin, Y., Woo, H., Yolken, R. H., & Pletnikov, M. V. (2021) · Journal of Neuroscience Research · doi:10.1002/jnr.24999 · Cited by 2 · see citing works

Evaluating the Relationship Between Acute Pain Perception and Gut Microbiota Among Female University Students in Japan: A Prospective Cohort Study

Shiro, Y., Arai, Y.-C. P., Ikemoto, T., & Ushida, T. (2022) · Anesthesiology and Pain Medicine · doi:10.5812/aapm-122489 · Cited by 2 · see citing works

A Sexually Dimorphic Role for Intestinal Cannabinoid Receptor Subtype-1 in the Behavioral Expression of Anxiety

Wood, C. P., Avalos, B., Alvarez, C., & DiPatrizio, N. V. (2023) · Cannabis and Cannabinoid Research · doi:10.1089/can.2023.0150 · Cited by 2 · see citing works

Effect of flavonoids on neurodegenerative diseases caused by acrylamide: Based on the perspective of intestinal flora

Ge, X., Cai, Y., Dai, H., Jiang, Y., Luo, S., Zhang, X., & Zhu, Y. (2025) · Journal of Future Foods · doi:10.1016/j.jfutfo.2024.09.003 · Cited by 1 · see citing works

Ulcerative colitis model triggers gut α-Synuclein aggregation without brain involvement or neuronal loss in female rats

Espinosa‐Oliva, A. M., Vázquez‐Carretero, M. D., Ruiz, R., Roca-Ceballos, M. A., García-Miranda, P., Peral, M. J., Soto, M. S., Herrera, A. J., Venero, J. L., & de Pablos, R. M. (2026) · Frontiers in Immunology · doi:10.3389/fimmu.2025.1637548 · Cited by 1 · see citing works

Short-chain fatty acid-producing commensals: Key modulators of AD neuroinflammation via the microbiota-gut-brain axis

Ling, Z., Huang, S., Cheng, Y., Liu, X., Xu, X., Chen, Y., Hu, P., Wu, L., & Cai, G. (2026) · Current Research in Microbial Sciences · doi:10.1016/j.crmicr.2026.100660 · Cited by 1 · see citing works

The Role of Emotion Regulation, Family Function, and Sex Differences in Early Adulthood Anxiety

Salimah, M. R., & Nuryanti, L. (2021) · IIUM JOURNAL OF HUMAN SCIENCES · doi:10.31436/ijohs.v3i2.213 · Cited by 1 · see citing works

Bacteria, Viruses, and the Microbiome

Anisman, H., Hayley, S. P., & Kusnecov, A. W. (2024) · Elsevier eBooks · doi:10.1016/b978-0-443-23565-8.00020-x

Gene-Environment-Gut Interactions in Huntington's Disease Mice Are Associated with Environmental Modulation of the Gut MicrobiomePreprint

Gubert, C., Love, C. J., Kodikara, S., Liew, J. J. M., Renoir, T., Cao, K. L., & Hannan, A. J. (2021) · SSRN Electronic Journal · doi:10.2139/ssrn.3904352

Disorders of Thought and Mood: Connectivity, Transmission, and Modulation as Trinity of Biological Psychiatry

Walter, G. F. (2022) · Neuroscience and Neurological Surgery · doi:10.31579/2578-8868/235

Has COVID-19 pandemic worsened quality of life of patients with Inflammatory Bowel Disease? A longitudinal disease activity-controlled studyPreprint

Rosa, I., Conti, C. M., Zito, L., & Porcelli, P. (2022) · Research Square · doi:10.21203/rs.3.rs-1853454/v1

Gastrointestinale Erkrankungen

Kapfhammer, H. (2022) · Springer eBooks · doi:10.1007/978-3-662-65873-4_6

References

(2024) · Elsevier eBooks · doi:10.1016/b978-0-443-23565-8.09996-8

Multiple Pathways Linked to Mental Health and Illness

Anisman, H., Hayley, S. P., & Kusnecov, A. W. (2024) · Elsevier eBooks · doi:10.1016/b978-0-443-23565-8.00014-4

Stressor Processes and Effects on Neurobiological Functioning

Anisman, H., Hayley, S. P., & Kusnecov, A. (2024) · Elsevier eBooks · doi:10.1016/b978-0-443-23565-8.00018-1

Interactions between sex hormones and the gut microbiome

Freeman, L. R. (2025) · Brain Behavior and Immunity · doi:10.1016/j.bbi.2025.02.025

Microanatomy of the enteric neurons and glia; expression patterns of the PGP9.5, S100b proteins, RET and SOX10 genes in the human fetal gut wall

Bhattarai, C., Poudel, P. P., Ghosh, A., Pradhan, S. M., Panthi, N., Joshi, D. S., Khadka, S., Kumari, S., Kalthur, G., Vani Lakshmi, R., et al. (2025) · Translational Research in Anatomy · doi:10.1016/j.tria.2025.100413

Common mental disorders in middle-aged and older women

Rabelo, D. F., da Silva, J., Ferreira, H. G., Ribeiro, F. S., & Leist, A. K. (2025) · Psico · doi:10.15448/1980-8623.2025.1.47066

Sotagliflozin pretreatment attenuates acute LPS-induced depression-like behavioral abnormalities and modulates the gut microbiota–immune–brain axis

Zeng, J., Zhou, L., Liao, L., Wu, D., Yang, R., Zhang, C., Bai, Z., Fan, X., Zhou, X., Zhang, C., et al. (2026) · Psychopharmacology · doi:10.1007/s00213-026-07127-3

Shedding light on biological sex differences and microbiota–gut–brain axis: a comprehensive review of its roles in neuropsychiatric disorders

Shobeiri, P., Kalantari, A., Teixeira, A. L., & Rezaei, N. (2022) · Biology of Sex Differences · doi:10.1186/s13293-022-00422-6 · Cited by 105 · see citing works

You’ve got male: Sex and the microbiota-gut-brain axis across the lifespan

Jaggar, M., Rea, K., Spichak, S., Dinan, T. G., & Cryan, J. F. (2020) · Frontiers in Neuroendocrinology · doi:10.1016/j.yfrne.2019.100815 · Cited by 200 · see citing works

Stress-induced disturbances along the gut microbiota-immune-brain axis and implications for mental health: Does sex matter?

Audet, M. (2019) · Frontiers in Neuroendocrinology · doi:10.1016/j.yfrne.2019.100772 · Cited by 79 · see citing works

Sex-related patterns of the gut-microbiota-brain axis in the neuropsychiatric conditions

Manosso, L. M., Lin, J. H. X., Carlessi, A. S., Recco, K. C. C., Quevedo, J., Gonçalves, C. L., & Réus, G. Z. (2021) · Brain Research Bulletin · doi:10.1016/j.brainresbull.2021.04.001 · Cited by 23 · see citing works

Sex shapes gut–microbiota–brain communication and disease

Hokanson, K. C., Hernández, C., Deitzler, G. E., Gaston, W. J., & David, M. M. (2023) · Trends in Microbiology · doi:10.1016/j.tim.2023.08.013 · Cited by 56 · see citing works