The role of microbes and autoimmunity in the pathogenesis of neuropsychiatric illness

Mind-altering microorganisms: the impact of the gut microbiota on brain and behaviour

Cryan, J. F., & Dinan, T. G. (2012) · Nature Reviews Neuroscience · doi:10.1038/nrn3346 · Cited by 4,572 · see citing works

CYTOKINE TARGETS IN THE BRAIN: IMPACT ON NEUROTRANSMITTERS AND NEUROCIRCUITS: Review: Cytokine Targets in the Brain

Miller, A. H., Haroon, E., Raison, C. L., & Felger, J. C. (2013) · Depression and Anxiety · doi:10.1002/da.22084 · Cited by 892 · 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

Prevention of gut leakiness by a probiotic treatment leads to attenuated HPA response to an acute psychological stress in rats

Ait-Belgnaoui, A., Durand, H., Cartier, C., Chaumaz, G., Eutamene, H., Ferrier, L., Houdeau, E., Fioramonti, J., Bueno, L., & Theodorou, V. (2012) · Psychoneuroendocrinology · doi:10.1016/j.psyneuen.2012.03.024 · Cited by 612 · see citing works

Molecular Mimicry as a Mechanism of Autoimmune Disease

Cusick, M. F., Libbey, J. E., & Fujinami, R. S. (2011) · Clinical Reviews in Allergy & Immunology · doi:10.1007/s12016-011-8294-7 · Cited by 607 · see citing works

Autoimmune Diseases and Severe Infections as Risk Factors for Schizophrenia: A 30-Year Population-Based Register Study

Benros, M. E., Nielsen, P. R., Nordentoft, M., Eaton, W. W., Dalton, S. O., & Mortensen, P. B. (2011) · American Journal of Psychiatry · doi:10.1176/appi.ajp.2011.11030516 · Cited by 582 · see citing works

Impaired Carbohydrate Digestion and Transport and Mucosal Dysbiosis in the Intestines of Children with Autism and Gastrointestinal Disturbances

Williams, B. L., Hornig, M., Buie, T., Bauman, M. L., Cho Paik, M., Wick, I., Bennett, A., Jabado, O., Hirschberg, D. L., & Lipkin, W. I. (2011) · PLoS ONE · doi:10.1371/journal.pone.0024585 · Cited by 492 · see citing works

Immune–neural connections: how the immune system’s response to infectious agents influences behavior

McCusker, R. H., & Kelley, K. W. (2013) · Journal of Experimental Biology · doi:10.1242/jeb.073411 · Cited by 429 · see citing works

From Research Subgroup to Clinical Syndrome: Modifying the PANDAS Criteria to Describe PANS (Pediatric Acute-onset Neuropsychiatric Syndrome)

Swedo, S. E. (2012) · Pediatrics & Therapeutics · doi:10.4172/2161-0665.1000113 · Cited by 423 · see citing works

Epidemiologic studies of exposure to prenatal infection and risk of schizophrenia and autism

Brown, A. S. (2012) · Developmental Neurobiology · doi:10.1002/dneu.22024 · Cited by 420 · see citing works

Application of Novel PCR-Based Methods for Detection, Quantitation, and Phylogenetic Characterization of <i>Sutterella</i> Species in Intestinal Biopsy Samples from Children with Autism and Gastrointestinal Disturbances

Williams, B. L., Hornig, M., Parekh, T., & Lipkin, W. I. (2012) · mBio · doi:10.1128/mbio.00261-11 · Cited by 378 · see citing works

Modeling an autism risk factor in mice leads to permanent immune dysregulation

Hsiao, E. Y., McBride, S. W., Chow, J., Mazmanian, S. K., & Patterson, P. H. (2012) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1202556109 · Cited by 340 · see citing works

The microbiome is essential for normal gut intrinsic primary afferent neuron excitability in the mouse

McVey Neufeld, K. A., Mao, Y. K., Bienenstock, J., Foster, J. A., & Kunze, W. A. (2013) · Neurogastroenterology &amp; Motility · doi:10.1111/nmo.12049 · Cited by 299 · see citing works

Autoimmune diseases, bipolar disorder, and non-affective psychosis

Eaton, W. W., Pedersen, M. G., Nielsen, P. R., & Mortensen, P. B. (2010) · Bipolar Disorders · doi:10.1111/j.1399-5618.2010.00853.x · Cited by 262 · see citing works

Cerebral folate receptor autoantibodies in autism spectrum disorder

Frye, R. E., Sequeira, J. M., Quadros, E. V., James, S. J., & Rossignol, D. A. (2012) · Molecular Psychiatry · doi:10.1038/mp.2011.175 · Cited by 257 · see citing works

Maternal immune activation by LPS selectively alters specific gene expression profiles of interneuron migration and oxidative stress in the fetus without triggering a fetal immune response

Oskvig, D. B., Elkahloun, A. G., Johnson, K. R., Phillips, T. M., & Herkenham, M. (2012) · Brain, Behavior, and Immunity · doi:10.1016/j.bbi.2012.01.015 · Cited by 248 · see citing works

To poly(I:C) or not to poly(I:C): Advancing preclinical schizophrenia research through the use of prenatal immune activation models

Meyer, U., & Feldon, J. (2011) · Neuropharmacology · doi:10.1016/j.neuropharm.2011.01.009 · Cited by 247 · see citing works

Infectious agents associated with schizophrenia: A meta-analysis

Arias, I., Sorlózano, A., Villegas, E., Luna, J. D. D., McKenney, K., Cervilla, J. A., Gutiérrez, B., & Fernández, J. G. (2011) · Schizophrenia Research · doi:10.1016/j.schres.2011.10.026 · Cited by 235 · see citing works

Psychoactive bacteria <i>Lactobacillus rhamnosus</i> (JB-1) elicits rapid frequency facilitation in vagal afferents

Perez-Burgos, A., Wang, B., Mao, Y.-K., Mistry, B., Neufeld, K.-A. M., Bienenstock, J., & Kunze, W. (2013) · American Journal of Physiology-Gastrointestinal and Liver Physiology · doi:10.1152/ajpgi.00128.2012 · Cited by 235 · see citing works

Gastrointestinal inflammation and associated immune activation in schizophrenia

Severance, E. G., Alaedini, A., Yang, S., Halling, M., Gressitt, K. L., Stallings, C. R., Origoni, A. E., Vaughan, C., Khushalani, S., Leweke, F. M., et al. (2012) · Schizophrenia Research · doi:10.1016/j.schres.2012.02.025 · Cited by 226 · see citing works

Effect of Intestinal Microbial Ecology on the Developing Brain

Douglas‐Escobar, M., Elliott, E., & Neu, J. (2013) · Archives of Pediatrics and Adolescent Medicine · doi:10.1001/jamapediatrics.2013.497 · Cited by 207 · see citing works

Behavioral, pharmacological, and immunological abnormalities after streptococcal exposure: a novel rat model of Sydenham chorea and related neuropsychiatric disorders

Brimberg, L., Benhar, I., Mascaro-Blanco, A., Alvarez, K., Lotan, D., Winter, C., Klein, J., Moses, A. E., Somnier, F. E., Leckman, J. F., et al. (2012) · Neuropsychopharmacology · doi:10.1038/npp.2012.56 · Cited by 202 · see citing works

Autoimmune diseases and infections as risk factors for schizophrenia

Benros, M. E., Mortensen, P. B., & Eaton, W. W. (2012) · Annals of the New York Academy of Sciences · doi:10.1111/j.1749-6632.2012.06638.x · Cited by 190 · see citing works

Urinary p-cresol in autism spectrum disorder

Persico, A. M., & Napolioni, V. (2013) · Neurotoxicology and Teratology · doi:10.1016/j.ntt.2012.09.002 · Cited by 189 · see citing works

The Relationship Between Toxoplasma Gondii Infection and Mood Disorders in the Third National Health and Nutrition Survey

Pearce, B. D., Kruszon‐Moran, D., & Jones, J. L. (2012) · Biological Psychiatry · doi:10.1016/j.biopsych.2012.01.003 · Cited by 169 · see citing works

Parental Autoimmune Diseases Associated With Autism Spectrum Disorders in Offspring

Keil, A., Daniels, J. L., Forssen, U., Hultman, C., Cnattingius, S., Söderberg, K. C., Feychting, M., & Sparen, P. (2010) · Epidemiology · doi:10.1097/ede.0b013e3181f26e3f · 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

Autoimmunity versus horror autotoxicus: The struggle for recognition

Silverstein, A. M. (2001) · Nature Immunology · doi:10.1038/86280 · Cited by 151 · see citing works

Passive transfer of streptococcus-induced antibodies reproduces behavioral disturbances in a mouse model of pediatric autoimmune neuropsychiatric disorders associated with streptococcal infection

Yaddanapudi, K., Hornig, M., Serge, R., Miranda, J. D., Baghban, A. A., Villar, G., & Lipkin, W. I. (2009) · Molecular Psychiatry · doi:10.1038/mp.2009.77 · Cited by 149 · see citing works

Maternal immune activation by poly(I:C) induces expression of cytokines IL-1β and IL-13, chemokine MCP-1 and colony stimulating factor VEGF in fetal mouse brain

Arrode-Brusés, G., & Brusés, J. L. (2012) · Journal of Neuroinflammation · doi:10.1186/1742-2094-9-83 · Cited by 146 · see citing works

Clinical factors associated with pediatric autoimmune neuropsychiatric disorders associated with streptococcal infections

Murphy, T. K., Storch, E. A., Lewin, A. B., Edge, P. J., & Goodman, W. K. (2012) · The Journal of Pediatrics · doi:10.1016/j.jpeds.2011.07.012 · Cited by 138 · see citing works

On communication between gut microbes and the brain

Forsythe, P., Kunze, W. A., & Bienenstock, J. (2012) · Current Opinion in Gastroenterology · doi:10.1097/mog.0b013e3283572ffa · Cited by 137 · see citing works

Neonatal Behavioral Changes in Rats With Gestational Exposure to Lipopolysaccharide: A Prenatal Infection Model for Developmental Neuropsychiatric Disorders

Baharnoori, M., Bhardwaj, S. K., & Srivastava, L. K. (2010) · Schizophrenia Bulletin · doi:10.1093/schbul/sbq098 · Cited by 134 · see citing works

Prenatal inflammation and neurodevelopment in schizophrenia: A review of human studies

Miller, B. J., Culpepper, N. H., Rapaport, M. H., & Buckley, P. F. (2012) · Progress in Neuro-Psychopharmacology and Biological Psychiatry · doi:10.1016/j.pnpbp.2012.03.010 · Cited by 124 · see citing works

Maternal Autoantibodies in Autism

Braunschweig, D., & Van de Water, J. (2012) · Archives of Neurology · doi:10.1001/archneurol.2011.2506 · Cited by 122 · see citing works

IgM-mediated autoimmune responses directed against multiple neoepitopes in depression: New pathways that underpin the inflammatory and neuroprogressive pathophysiology

Maes, M. H. J., Mihaylova, I., Kubera, M., Leunis, J., & Geffard, M. (2011) · Journal of Affective Disorders · doi:10.1016/j.jad.2011.08.023 · Cited by 120 · see citing works

Brain-reactive autoantibodies are nearly ubiquitous in human sera and may be linked to pathology in the context of blood–brain barrier breakdown

Levin, E. C., Acharya, N. K., Han, M. C., Zavareh, S., Sedeyn, J. C., Venkataraman, V., & Nagele, R. G. (2010) · Brain Research · doi:10.1016/j.brainres.2010.05.038 · Cited by 113 · see citing works

A Danish National Birth Cohort study of maternal HSV-2 antibodies as a risk factor for schizophrenia in their offspring

Mortensen, P. B., Pedersen, C. B., HOUGAARD, D. M., Nørgaard‐Petersen, B., Mors, O. N., Børglum, A. D., & Yolken, R. H. (2010) · Schizophrenia Research · doi:10.1016/j.schres.2010.06.010 · Cited by 111 · see citing works

Induction of Toll-Like Receptor 3-Mediated Immunity during Gestation Inhibits Cortical Neurogenesis and Causes Behavioral Disturbances

Miranda, J. D., Yaddanapudi, K., Hornig, M., Villar, G., Serge, R., & Lipkin, W. I. (2010) · mBio · doi:10.1128/mbio.00176-10 · Cited by 102 · see citing works

Does the gut microbiota have a role in type 1 diabetes? Early evidence from humans and animal models of the disease

Atkinson, M. A., & Chervonsky, A. V. (2012) · Diabetologia · doi:10.1007/s00125-012-2672-4 · Cited by 90 · see citing works

Infectious and immune factors in the pathogenesis of neurodevelopmental disorders: Epidemiology, hypotheses, and animal models

Hornig, M., & Lipkin, W. I. (2001) · Mental Retardation and Developmental Disabilities Research Reviews · doi:10.1002/mrdd.1028 · Cited by 89 · see citing works

Mouse maternal systemic inflammation at the zygote stage causes blunted cytokine responsiveness in lipopolysaccharide-challenged adult offspring

Williams, C. L., Teeling, J. L., Perry, V. H., & Fleming, T. P. (2011) · BMC Biology · doi:10.1186/1741-7007-9-49 · Cited by 85 · see citing works

Absence of evidence for bornavirus infection in schizophrenia, bipolar disorder and major depressive disorder

Hornig, M., Briese, T., Licinio, J., KHABBAZ, R. F., Altshuler, L. L., Potkin, S. G., Schwemmle, M., Siemetzki, U., Mintz, J., Honkavuori, K. S., et al. (2012) · Molecular Psychiatry · doi:10.1038/mp.2011.179 · Cited by 85 · see citing works

The link of C4B null allele to autism and to a family history of autoimmunity in Egyptian autistic children

Mostafa, G. A., & Shehab, A. (2010) · Journal of Neuroimmunology · doi:10.1016/j.jneuroim.2010.03.025 · Cited by 84 · see citing works

Schizophrenia in patients with atopic disorders with particular emphasis on asthma: A Danish population-based study

Pedersen, M. S., Benros, M. E., Agerbo, E., Børglum, A. D., & Mortensen, P. B. (2012) · Schizophrenia Research · doi:10.1016/j.schres.2012.02.019 · Cited by 79 · see citing works

LPS elicits a much larger and broader inflammatory response than Escherichia coli infection within the hippocampus of neonatal rats

Schwarz, J. M., & Bilbo, S. D. (2011) · Neuroscience Letters · doi:10.1016/j.neulet.2011.04.042 · Cited by 74 · see citing works

Autoimmune Basal Ganglia Disorders

Dale, R. C., & Brilot, F. (2012) · Journal of Child Neurology · doi:10.1177/0883073812451327 · Cited by 71 · see citing works

Markers of gluten sensitivity and celiac disease in bipolar disorder

Dickerson, F., Stallings, C. R., Origoni, A. E., Vaughan, C., Khushalani, S., Alaedini, A., & Yolken, R. H. (2011) · Bipolar Disorders · doi:10.1111/j.1399-5618.2011.00894.x · Cited by 71 · 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

Magnesium sulfate reduces bacterial LPS-induced inflammation at the maternal–fetal interface

Dowling, O., Chatterjee, P. K., Gupta, M., Tam, H. B. T., Xue, X., Lewis, D., Rochelson, B. L., & Metz, C. N. (2012) · Placenta · doi:10.1016/j.placenta.2012.01.013 · Cited by 70 · see citing works

Toxoplasmosis and Polygenic Disease Susceptibility Genes: ExtensiveToxoplasma gondiiHost/Pathogen Interactome Enrichment in Nine Psychiatric or Neurological Disorders

Carter, C. (2013) · Journal of Pathogens · doi:10.1155/2013/965046 · Cited by 68 · see citing works

Presence of GAD65 autoantibodies in the serum of children with autism or ADHD

Rout, U. K., Mungan, N. K., & Dhossche, D. M. (2012) · European Child & Adolescent Psychiatry · doi:10.1007/s00787-012-0245-1 · Cited by 65 · see citing works

Maternal and fetal antibrain antibodies in development and disease

Fox, E., Amaral, D. G., & de Water, J. V. (2012) · Developmental Neurobiology · doi:10.1002/dneu.22052 · Cited by 63 · see citing works

Anti-Gluten Immune Response following Toxoplasma gondii Infection in Mice

Severance, E. G., Kannan, G., Gressitt, K. L., Xiao, J., Alaedini, A., Pletnikov, M. V., & Yolken, R. H. (2012) · PLoS ONE · doi:10.1371/journal.pone.0050991 · Cited by 56 · see citing works

Detection of plasma autoantibodies to brain tissue in young children with and without autism spectrum disorders

Rossi, C. C., de Water, J. V., Rogers, S. J., & Amaral, D. G. (2011) · Brain Behavior and Immunity · doi:10.1016/j.bbi.2011.02.011 · Cited by 56 · see citing works

Complement C1q formation of immune complexes with milk caseins and wheat glutens in schizophrenia

Severance, E. G., Gressitt, K. L., Halling, M., Stallings, C. R., Origoni, A. E., Vaughan, C., Khushalani, S., Alaedini, A., Dupont, D., Dickerson, F., et al. (2012) · Neurobiology of Disease · doi:10.1016/j.nbd.2012.07.005 · Cited by 53 · see citing works

IgM-mediated autoimmune responses directed against anchorage epitopes are greater in Myalgic encephalomyelitis/chronic fatigue syndrome (ME/CFS) than in major depression

Maes, M., Mihaylova, I., Kubera, M., Leunis, J.-C., Twisk, F. N. M., & Geffard, M. (2012) · Metabolic Brain Disease · doi:10.1007/s11011-012-9316-8 · Cited by 52 · see citing works

Immune Dysfunction in Tourette Syndrome

Elamin, I., Edwards, M. J., & Martino, D. (2013) · Behavioural Neurology · doi:10.1155/2013/329375 · Cited by 44 · see citing works

N-acetylcysteine attenuates the maternal and fetal proinflammatory response to intrauterine LPS injection in an animal model for preterm birth and brain injury

Chang, E., Zhang, J., SULLIVAN, S. A., Newman, R., & Singh, I. (2011) · The Journal of Maternal-Fetal & Neonatal Medicine · doi:10.3109/14767058.2010.528089 · Cited by 42 · see citing works

Role of Lactobacillus acidophilus loaded floating beads in chronic fatigue syndrome: behavioral and biochemical evidences

Singh, P. K., Chopra, K., Kuhad, A., & Kaur, I. P. (2012) · Neurogastroenterology & Motility · doi:10.1111/j.1365-2982.2011.01861.x · Cited by 32 · see citing works

Toll-like Receptor 3 Regulates Neural Stem Cell Proliferation by Modulating the Sonic Hedgehog Pathway

Yaddanapudi, K., Miranda, J. D., Hornig, M., & Lipkin, W. I. (2011) · PLoS ONE · doi:10.1371/journal.pone.0026766 · Cited by 31 · see citing works

Glutamic Acid Decarboxylase Autoantibody Syndrome Presenting as Schizophrenia

Najjar, S., Pearlman, D. M., Zagzag, D., Golfinos, J. G., & Devinsky, O. (2012) · The Neurologist · doi:10.1097/nrl.0b013e318247b87d · Cited by 30 · see citing works

Immune dysfunction in Tourette syndrome.

Elamin, I., Edwards, M. J., & Martino, D. (2013) · PubMed · doi:10.3233/ben-120295 · Cited by 28 · see citing works

Differential mRNA expression of neuroimmune markers in the hippocampus of infant mice following toluene exposure during brain developmental period

Win‐Shwe, T., Kunugita, N., Yoshida, Y., Nakajima, D., Tsukahara, S., & Fujimaki, H. (2011) · Journal of Applied Toxicology · doi:10.1002/jat.1643 · Cited by 27 · see citing works

Regulatory T‐cell abnormalities and the global epidemic of immuno‐inflammatory disease

Groth, B. F. D. S. (2012) · Immunology and Cell Biology · doi:10.1038/icb.2011.113 · Cited by 25 · see citing works

Autoimmune and proinflammatory activity of oxidized immunoglobulins

Omersel, J., Jurgec, I., Čučnik, S., Kveder, T., Rozman, B., Sodin‐Šemrl, S., & Božič, B. (2008) · Autoimmunity Reviews · doi:10.1016/j.autrev.2008.04.005 · Cited by 24 · see citing works

The Timing and Specificity of Prenatal Immune Risk Factors for Autism Modeled in the Mouse and Relevance to Schizophrenia

McAlonan, G. M., Li, Q., & Cheung, C. (2010) · Neurosignals · doi:10.1159/000321080 · Cited by 24 · see citing works

Antibodies to retroviruses in recent onset psychosis and multi-episode schizophrenia

Dickerson, F., Lillehoj, E. P., Stallings, C. R., Wiley, M., Origoni, A. E., Vaughan, C., Khushalani, S., Sabunciyan, S., & Yolken, R. H. (2012) · Schizophrenia Research · doi:10.1016/j.schres.2012.03.037 · Cited by 24 · see citing works

Prenatal and Postnatal Epigenetic Programming: Implications for GI, Immune, and Neuronal Function in Autism

Waly, M. I., Hornig, M., Trivedi, M. S., Hodgson, N., Kini, R., Ohta, A., & Deth, R. C. (2012) · Autism Research and Treatment · doi:10.1155/2012/190930 · Cited by 23 · see citing works

Anti-streptococcus IgM antibodies induce repetitive stereotyped movements: Cell activation and co-localization with Fcα/μ receptors in the striatum and motor cortex

Zhang, D., Patel, A., Zhu, Y., Siegel, A., & Zalcman, S. S. (2012) · Brain Behavior and Immunity · doi:10.1016/j.bbi.2012.01.005 · Cited by 22 · see citing works

Is Autism a Member of a Family of Diseases Resulting from Genetic/Cultural Mismatches? Implications for Treatment and Prevention

Bilbo, S. D., Jones, J. P., & Parker, W. (2012) · Autism Research and Treatment · doi:10.1155/2012/910946 · Cited by 21 · see citing works

Aretaeus the cappadocian on mental illness

Kotsopoulos, S. (1986) · Comprehensive Psychiatry · doi:10.1016/0010-440x(86)90026-x · Cited by 20 · see citing works

Wheat gliadin promotes the interleukin-4-induced IgE production by normal human peripheral mononuclear cells through a redox-dependent mechanism

Dugas, B., Dugas, N., Conti, M., Calenda, A., Pino, P., Thomas, Y., Mazier, D., & Vouldoukis, I. (2003) · Cytokine · doi:10.1016/s1043-4666(03)00100-5 · Cited by 17 · see citing works

Redox‐Reactive Autoantibodies in Cerebrospinal Fluids

McIntyre, J. A., Hamilton, R. L., & DeKosky, S. T. (2007) · Annals of the New York Academy of Sciences · doi:10.1196/annals.1398.035 · Cited by 12 · see citing works

Autoimmune reactivity of IgM acquired after oxidation

Omersel, J., Avberšek-Lužnik, I., Grabnar, P. A., Kveder, T., Rozman, B., & Božič, B. (2011) · Redox Report · doi:10.1179/174329211x13190184351680 · Cited by 9 · see citing works

Factors affecting the composition of the gut microbiota, and its modulation

Hasan, N., & Yang, H. (2019) · PeerJ · doi:10.7717/peerj.7502 · Cited by 763 · see citing works

The Gut Microbiome and the Brain

Galland, L. (2014) · Journal of Medicinal Food · doi:10.1089/jmf.2014.7000 · Cited by 648 · see citing works

Role of gut microbiota and nutrients in amyloid formation and pathogenesis of Alzheimer disease

Pistollato, F., Sumalla Cano, S., Elio, I., Masias Vergara, M., Giampieri, F., & Battino, M. (2016) · Nutrition Reviews · doi:10.1093/nutrit/nuw023 · Cited by 496 · see citing works

The microbiome: stress, health and disease

Moloney, R. D., Desbonnet, L., Clarke, G., Dinan, T. G., & Cryan, J. F. (2014) · Mammalian Genome · doi:10.1007/s00335-013-9488-5 · Cited by 430 · see citing works

The Possible Role of the Microbiota-Gut-Brain-Axis in Autism Spectrum Disorder

Srikantha, P., & Mohajeri, M. H. (2019) · International Journal of Molecular Sciences · doi:10.3390/ijms20092115 · Cited by 400 · see citing works

Systematic Review: Adverse Events of Fecal Microbiota Transplantation

Wang, S., Xu, M., Wang, W., Cao, X., Piao, M., Khan, S., Yan, F., Cao, H., & Wang, B. (2016) · PLoS ONE · doi:10.1371/journal.pone.0161174 · Cited by 410 · see citing works

Vagus nerve stimulation

Howland, R. H. (2014) · Current Behavioral Neuroscience Reports · doi:10.1007/s40473-014-0010-5 · Cited by 405 · see citing works

Clinical evaluation of youth with pediatric acute-onset neuropsychiatric syndrome (PANS): recommendations from the 2013 PANS Consensus Conference

Chang, K., Frankovich, J., Cooperstock, M., Cunningham, M. W., Latimer, M. E., Murphy, T. K., Pasternack, M., Thienemann, M., Williams, K., Walter, J., et al. (2015) · Journal of Child and Adolescent Psychopharmacology · doi:10.1089/cap.2014.0084 · Cited by 359 · see citing works

The gut-brain axis: the missing link in depression

Evrensel, A., & Ceylan, M. E. (2015) · Clinical Psychopharmacology and Neuroscience · doi:10.9758/cpn.2015.13.3.239 · Cited by 338 · see citing works

The Impact of Microbiota on Brain and Behavior: Mechanisms &amp; Therapeutic Potential

Borre, Y. E., Moloney, R. D., Clarke, G., Dinan, T. G., & Cryan, J. F. (2014) · Advances in Experimental Medicine and Biology · doi:10.1007/978-1-4939-0897-4_17 · Cited by 329 · see citing works

Microbiota-gut-brain axis and the central nervous system

Zhu, X., Han, Y., Du, J., Liu, R., Jin, K., & Yi, W. (2017) · Oncotarget · doi:10.18632/oncotarget.17754 · Cited by 308 · see citing works

Microbiota regulation of the mammalian gut-brain axis

Burokas, A., Moloney, R. D., Dinan, T. G., & Cryan, J. F. (2015) · Advances in applied microbiology · doi:10.1016/bs.aambs.2015.02.001 · Cited by 300 · see citing works

Development of the preterm infant gut microbiome: a research priority

Groer, M. W., Luciano, A. A., Dishaw, L. J., Ashmeade, T. L., Miller, E. M., & Gilbert, J. A. (2014) · Microbiome · doi:10.1186/2049-2618-2-38 · Cited by 285 · see citing works

Inflammation and the two-hit hypothesis of schizophrenia

Feigenson, K. A., Kusnecov, A., & Silverstein, S. M. (2013) · Neuroscience & Biobehavioral Reviews · doi:10.1016/j.neubiorev.2013.11.006 · Cited by 280 · see citing works

Environmental Chemical Exposures and Autism Spectrum Disorders: A Review of the Epidemiological Evidence

Kalkbrenner, A. E., Schmidt, R. J., & Penlesky, A. C. (2014) · Current Problems in Pediatric and Adolescent Health Care · doi:10.1016/j.cppeds.2014.06.001 · Cited by 268 · see citing works

Gut microbiota changes in the extreme decades of human life: a focus on centenarians

Santoro, A., Ostan, R., Candela, M., Biagi, E., Brigidi, P., Capri, M., & Franceschi, C. (2018) · Cellular and Molecular Life Sciences · doi:10.1007/s00018-017-2674-y · Cited by 250 · see citing works

Autoimmune diseases, gastrointestinal disorders and the microbiome in schizophrenia: more than a gut feeling

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Alzheimer's disease and the microbiome

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