The maternal vaginal microbiome partially mediates the effects of prenatal stress on offspring gut and hypothalamus

R: A Language and Environment for Statistical Computing

R Core Team (2000) · doi:10.32614/r.manuals · Cited by 355,706 · see citing works

limma powers differential expression analyses for RNA-sequencing and microarray studies

Ritchie, M. E., Phipson, B., Wu, D., Hu, Y., Law, C. W., Shi, W., & Smyth, G. K. (2015) · Nucleic Acids Research · doi:10.1093/nar/gkv007 · Cited by 40,458 · see citing works

QIIME allows analysis of high-throughput community sequencing data

Caporaso, J. G., Kuczynski, J., Stombaugh, J., Bittinger, K., Bushman, F. D., Costello, E. K., Fierer, N., Peña, A. G., Goodrich, J. K., Gordon, J. I., et al. (2010) · Nature Methods · doi:10.1038/nmeth.f.303 · Cited by 34,887 · see citing works

Analyzing real-time PCR data by the comparative CT method

Schmittgen, T. D., & Livak, K. J. (2008) · Nature Protocols · doi:10.1038/nprot.2008.73 · Cited by 26,190 · see citing works

Introducing mothur: Open-Source, Platform-Independent, Community-Supported Software for Describing and Comparing Microbial Communities

Schloss, P. D., Westcott, S. L., Ryabin, T., Hall, J. R., Hartmann, M., Hollister, E. B., Lesniewski, R. A., Oakley, B. B., Parks, D. H., Robinson, C. J., et al. (2009) · Applied and Environmental Microbiology · doi:10.1128/aem.01541-09 · Cited by 20,966 · see citing works

Near-optimal probabilistic RNA-seq quantification

Bray, N. L., Pimentel, H., Melsted, P., & Pachter, L. (2016) · Nature Biotechnology · doi:10.1038/nbt.3519 · Cited by 9,723 · see citing works

Toll-like receptor signalling

Akira, S., & Takeda, K. (2004) · Nature reviews. Immunology · doi:10.1038/nri1391 · Cited by 8,312 · see citing works

Human gut microbiome viewed across age and geography

Yatsunenko, T., Rey, F. E., Manary, M. J., Trehan, I., Dominguez-Bello, M. G., Contreras, M., Magris, M., Hidalgo, G., Baldassano, R. N., Anokhin, A. P., et al. (2012) · Nature · doi:10.1038/nature11053 · Cited by 7,815 · see citing works

Development of a Dual-Index Sequencing Strategy and Curation Pipeline for Analyzing Amplicon Sequence Data on the MiSeq Illumina Sequencing Platform

Kozich, J. J., Westcott, S. L., Baxter, N. T., Highlander, S. K., & Schloss, P. D. (2013) · Applied and Environmental Microbiology · doi:10.1128/aem.01043-13 · Cited by 7,004 · see citing works

voom: precision weights unlock linear model analysis tools for RNA-seq read counts

Law, C. W., Chen, Y., Shi, W., & Smyth, G. K. (2014) · Genome Biology · doi:10.1186/gb-2014-15-2-r29 · Cited by 6,155 · 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

Delivery mode shapes the acquisition and structure of the initial microbiota across multiple body habitats in newborns

Dominguez-Bello, M. G., Costello, E. K., Contreras, M., Magris, M., Hidalgo, G., Fierer, N., & Knight, R. (2010) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1002601107 · Cited by 4,774 · see citing works

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

Differential analyses for RNA-seq: transcript-level estimates improve gene-level inferences

Soneson, C., Love, M. I., & Robinson, M. D. (2015) · F1000Research · doi:10.12688/f1000research.7563.1 · Cited by 3,929 · see citing works

Ingestion of <i>Lactobacillus</i> strain regulates emotional behavior and central GABA receptor expression in a mouse via the vagus nerve

Bravo, J. A., Forsythe, P., Chew, M. V., Escaravage, E., Savignac, H. M., Dinan, T. G., Bienenstock, J., & Cryan, J. F. (2011) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1102999108 · Cited by 3,888 · see citing works

Differential abundance analysis for microbial marker-gene surveys

Paulson, J. N., Stine, O. C., Bravo, H. C., & Pop, M. (2013) · Nature Methods · doi:10.1038/nmeth.2658 · Cited by 2,393 · see citing works

Gut feelings: the emerging biology of gut-brain communication

Mayer, E. A. (2011) · Nature Reviews Neuroscience · doi:10.1038/nrn3071 · Cited by 1,726 · see citing works

Comparative genomics of the lactic acid bacteria.

Makarova, K., Slesarev, A., Wolf, Y., Sorokin, A., Mirkin, B., Koonin, E., Pavlov, A., Pavlova, N., Karamychev, V., Polouchine, N., et al. (2006) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0607117103 · Cited by 1,391 · see citing works

The maternal microbiota drives early postnatal innate immune development

Gomez de Agüero, M., Ganal-Vonarburg, S. C., Fuhrer, T., Rupp, S., Uchimura, Y., Li, H., Steinert, A., Heikenwalder, M., Hapfelmeier, S., Sauer, U., et al. (2016) · Science · doi:10.1126/science.aad2571 · Cited by 1,231 · see citing works

Microbial reconstitution reverses maternal diet-induced social and synaptic deficits in offspring

Buffington, S. A., Di Prisco, G. V., Auchtung, T. A., Ajami, N. J., Petrosino, J. F., & Costa-Mattioli, M. (2016) · Cell · doi:10.1016/j.cell.2016.06.001 · Cited by 1,163 · see citing works

Control of brain development, function, and behavior by the microbiome

Sampson, T. R., & Mazmanian, S. K. (2015) · Cell Host &amp; Microbe · doi:10.1016/j.chom.2015.04.011 · Cited by 1,093 · 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

Partial restoration of the microbiota of cesarean-born infants via vaginal microbial transfer

Dominguez-Bello, M. G., De Jesus-Laboy, K. M., Shen, N., Cox, L. M., Amir, A., Gonzalez, A., Bokulich, N. A., Song, S. J., Hoashi, M., Rivera-Vinas, J. I., et al. (2016) · Nature Medicine · doi:10.1038/nm.4039 · Cited by 1,014 · see citing works

Sex-Specific Programming of Offspring Emotionality after Stress Early in Pregnancy

Mueller, B. R., & Bale, T. L. (2008) · The Journal of Neuroscience · doi:10.1523/jneurosci.1424-08.2008 · Cited by 988 · see citing works

Reciprocal Gut Microbiota Transplants from Zebrafish and Mice to Germ-free Recipients Reveal Host Habitat Selection

Rawls, J. F., Mahowald, M. A., Ley, R. E., & Gordon, J. I. (2006) · Cell · doi:10.1016/j.cell.2006.08.043 · Cited by 962 · see citing works

Early Life Programming and Neurodevelopmental Disorders

Bale, T. L., Baram, T. Z., Brown, A. S., Goldstein, J. M., Insel, T. R., McCarthy, M. M., Nemeroff, C. B., Reyes, T. M., Simerly, R. B., Susser, E. S., et al. (2010) · Biological Psychiatry · doi:10.1016/j.biopsych.2010.05.028 · Cited by 961 · see citing works

Mice deficient for corticotropin-releasing hormone receptor-2 display anxiety-like behaviour and are hypersensitive to stress

Bale, T. L., Contarino, A., Smith, G. W., Chan, R. K. W., Gold, L. H., Sawchenko, P. E., Koob, G. F., Vale, W. W., & Lee, K. (2000) · Nature Genetics · doi:10.1038/74263 · Cited by 850 · see citing works

Paternal Stress Exposure Alters Sperm MicroRNA Content and Reprograms Offspring HPA Stress Axis Regulation

Rodgers, A. B., Morgan, C. P., Bronson, S. L., Revello, S., & Bale, T. L. (2013) · The Journal of Neuroscience · doi:10.1523/jneurosci.0914-13.2013 · Cited by 814 · see citing works

The neurobiology of stress and gastrointestinal disease

MAYER, E. A. (2000) · Gut · doi:10.1136/gut.47.6.861 · Cited by 666 · 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

The microbiota regulates neutrophil homeostasis and host resistance to Escherichia coli K1 sepsis in neonatal mice

Deshmukh, H. S., Liu, Y., Menkiti, O. R., Mei, J., Dai, N., O'Leary, C. E., Oliver, P. M., Kolls, J. K., Weiser, J. N., & Worthen, G. S. (2014) · Nature Medicine · doi:10.1038/nm.3542 · Cited by 579 · see citing works

Rank–rank hypergeometric overlap: identification of statistically significant overlap between gene-expression signatures

Plaisier, S. B., Taschereau, R., Wong, J. A., & Graeber, T. G. (2010) · Nucleic Acids Research · doi:10.1093/nar/gkq636 · Cited by 468 · see citing works

Maternal prenatal stress is associated with the infant intestinal microbiota

Zijlmans, M. A. C., Korpela, K., Riksen-Walraven, J. M., de Vos, W. M., & de Weerth, C. (2015) · Psychoneuroendocrinology · doi:10.1016/j.psyneuen.2015.01.006 · Cited by 438 · see citing works

Probiotic gut effect prevents the chronic psychological stress‐induced brain activity abnormality in mice

Ait‐Belgnaoui, A., Colom, A., Braniste, V., Ramalho, L., Marrot, A., Cartier, C., Houdeau, E., Theodorou, V., & Tompkins, T. (2014) · Neurogastroenterology &amp; Motility · doi:10.1111/nmo.12295 · Cited by 434 · see citing works

Immunomodulatory mechanisms of lactobacilli

Wells, J. M. (2011) · Microbial Cell Factories · doi:10.1186/1475-2859-10-s1-s17 · Cited by 431 · see citing works

Why Is Initial Bacterial Colonization of the Intestine Important to Infants' and Children's Health?

Houghteling, P. D., & Walker, W. A. (2014) · Journal of Pediatric Gastroenterology and Nutrition · doi:10.1097/mpg.0000000000000597 · Cited by 342 · see citing works

Prenatal Stress Alters Bacterial Colonization of the Gut in Infant Monkeys

Bailey, M. T., Lubach, G. R., & Coe, C. L. (2004) · Journal of Pediatric Gastroenterology and Nutrition · doi:10.1097/00005176-200404000-00009 · Cited by 339 · see citing works

Alterations in the Vaginal Microbiome by Maternal Stress Are Associated With Metabolic Reprogramming of the Offspring Gut and Brain

Jašarević, E., Howerton, C. L., Howard, C. D., & Bale, T. L. (2015) · Endocrinology · doi:10.1210/en.2015-1177 · Cited by 329 · see citing works

Distinct Commensals Induce Interleukin-1β via NLRP3 Inflammasome in Inflammatory Monocytes to Promote Intestinal Inflammation in Response to Injury

Seo, S.-U., Kamada, N., Muñoz-Planillo, R., Kim, Y.-G., Kim, D., Koizumi, Y., Hasegawa, M., Himpsl, S. D., Browne, H. P., Lawley, T. D., et al. (2015) · Immunity · doi:10.1016/j.immuni.2015.03.004 · Cited by 318 · see citing works

Prenatal Stress-Induced Increases in Placental Inflammation and Offspring Hyperactivity Are Male-Specific and Ameliorated by Maternal Antiinflammatory Treatment

Bronson, S. L., & Bale, T. L. (2014) · Endocrinology · doi:10.1210/en.2014-1040 · Cited by 299 · 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 294 · see citing works

Prenatal stress-induced alterations in major physiological systems correlate with gut microbiota composition in adulthood

Golubeva, A. V., Crampton, S., Desbonnet, L., Edge, D., O'Sullivan, O., Lomasney, K. W., Zhdanov, A. V., Crispie, F., Moloney, R. D., Borre, Y. E., et al. (2015) · Psychoneuroendocrinology · doi:10.1016/j.psyneuen.2015.06.002 · Cited by 283 · see citing works

Neurotrophic cross‐talk between the nervous and immune systems: Implications for neurological diseases

Kerschensteiner, M., Stadelmann, C., Dechant, G., Wekerle, H., & Hohlfeld, R. (2003) · Annals of Neurology · doi:10.1002/ana.10446 · Cited by 273 · see citing works

Stress during pregnancy alters temporal and spatial dynamics of the maternal and offspring microbiome in a sex-specific manner

Jašarević, E., Howard, C. D., Misic, A. M., Beiting, D. P., & Bale, T. L. (2017) · Scientific Reports · doi:10.1038/srep44182 · Cited by 262 · see citing works

Early prenatal stress impact on coping strategies and learning performance is sex dependent

Mueller, B. R., & Bale, T. L. (2007) · Physiology & Behavior · doi:10.1016/j.physbeh.2007.01.017 · Cited by 216 · see citing works

Prenatal stress affects placental cytokines and neurotrophins, commensal microbes, and anxiety-like behavior in adult female offspring

Gur, T. L., Shay, L., Palkar, A. V., Fisher, S., Varaljay, V. A., Dowd, S., & Bailey, M. T. (2017) · Brain, Behavior, and Immunity · doi:10.1016/j.bbi.2016.12.021 · Cited by 213 · see citing works

Impact of prenatal stress on long term body weight is dependent on timing and maternal sensitivity

MUELLER, B., & Bale, T. L. (2006) · Physiology & Behavior · doi:10.1016/j.physbeh.2006.05.019 · Cited by 162 · see citing works

Targeted placental deletion of OGT recapitulates the prenatal stress phenotype including hypothalamic mitochondrial dysfunction

Howerton, C. L., & Bale, T. L. (2014) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1401203111 · Cited by 159 · see citing works

Effect of Lactobacilli on Paracellular Permeability in the Gut

Ahrné, S., & Hagslätt, M.-L. J. (2011) · Nutrients · doi:10.3390/nu3010104 · Cited by 157 · see citing works

Intraluminal Containment of Commensal Outgrowth in the Gut during Infection-Induced Dysbiosis

Molloy, M. J., Grainger, J. R., Bouladoux, N. J., Hand, T. W., Koo, L. Y., Naik, S., Quiñones, M., Dzutsev, A., Gao, J., Trinchieri, G., et al. (2013) · Cell Host & Microbe · doi:10.1016/j.chom.2013.08.003 · Cited by 156 · see citing works

The ecological importance of the Staphylococcus sciuri species group as a reservoir for resistance and virulence genes

Nemeghaire, S., Argudín, M. Á., Feßler, A. T., Hauschild, T., Schwarz, Š., & Butaye, P. (2014) · Veterinary Microbiology · doi:10.1016/j.vetmic.2014.02.005 · Cited by 153 · see citing works

Manipulating the Gut Microbiota: Methods and Challenges: Figure 1

Ericsson, A. C., & Franklin, C. L. (2015) · ILAR Journal · doi:10.1093/ilar/ilv021 · Cited by 135 · see citing works

Analysis of gene–environment interactions in postnatal development of the mammalian intestine

Rakoff-Nahoum, S., Kong, Y., Kleinstein, S. H., Subramanian, S., Ahern, P. P., Gordon, J. I., & Medzhitov, R. M. (2015) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1424886112 · Cited by 108 · see citing works

Why related bacterial species bloom simultaneously in the gut: principles underlying the ‘Like will to like’ concept

Winter, S., & Bäumler, A. J. (2013) · Cellular Microbiology · doi:10.1111/cmi.12245 · Cited by 102 · see citing works

Prenatal stress programming of offspring feeding behavior and energy balance begins early in pregnancy

Pankevich, D. E., Mueller, B. R., Brockel, B. J., & Bale, T. L. (2009) · Physiology & Behavior · doi:10.1016/j.physbeh.2009.04.015 · Cited by 82 · see citing works

Influence of Sex and Corticotropin-Releasing Factor Pathways as Determinants in Serotonin Sensitivity

McEuen, J. G., Semsar, K., Lim, M. A., & Bale, T. L. (2009) · Endocrinology · doi:10.1210/en.2008-1721 · Cited by 36 · see citing works

Colonization of the Mouse Upper Gastrointestinal Tract by Lactobacillus murinus: A Histological, Immunocytochemical, and Ultrastructural Study

Almirón, M. A., Traglia, G. M., Rubio, A., & Sanjuan, N. A. (2013) · Current Microbiology · doi:10.1007/s00284-013-0367-9 · Cited by 16 · see citing works

Caesarean Section and FosteringPreprint

Nagy, A., Gertsenstein, M., Vintersten, K., & Behringer, R. R. (2006) · Cold Spring Harbor Protocols · doi:10.1101/pdb.prot4381 · Cited by 8 · see citing works

Caesarean Section and Fostering

Murphy, D. (2003) · Humana Press eBooks · doi:10.1385/0-89603-245-0:177 · Cited by 8 · see citing works

Untitled work

Bailey (1999) · doi:10.1002/(sici)1098-2302(199909)35:2

The Microbiota-Gut-Brain Axis

Cryan, J. F., O'Riordan, K. J., Cowan, C. S. M., Sandhu, K. V., Bastiaanssen, T. F. S., Boehme, M., Codagnone, M. G., Cussotto, S., Fulling, C., Golubeva, A. V., et al. (2019) · Physiological Reviews · doi:10.1152/physrev.00018.2018 · Cited by 5,286 · see citing works

The gut microbiota–brain axis in behaviour and brain disorders

Morais, L. H., Schreiber, H. L., & Mazmanian, S. K. (2021) · Nature Reviews Microbiology · doi:10.1038/s41579-020-00460-0 · Cited by 2,149 · see citing works

Maternal immune activation and neuroinflammation in human neurodevelopmental disorders

Han, V. X., Patel, S., Jones, H. F., & Dale, R. C. (2021) · Nature Reviews Neurology · doi:10.1038/s41582-021-00530-8 · Cited by 683 · see citing works

The maternal microbiome modulates fetal neurodevelopment in mice

Vuong, H. E., Pronovost, G. N., Williams, D. W., Coley, E. J. L., Siegler, E. L., Qiu, A., Kazantsev, M., Wilson, C. J., Rendon, T., & Hsiao, E. Y. (2020) · Nature · doi:10.1038/s41586-020-2745-3 · Cited by 564 · see citing works

The impact of the gut microbiota on the reproductive and metabolic endocrine system

Qi, X., Yun, C., Pang, Y., & Qiao, J. (2021) · Gut Microbes · doi:10.1080/19490976.2021.1894070 · Cited by 573 · see citing works

Signalling cognition: The gut microbiota and hypothalamic-pituitary-adrenal axis

Rusch, J. A., Layden, B. T., & Dugas, L. R. (2023) · Frontiers in Endocrinology · doi:10.3389/fendo.2023.1130689 · Cited by 415 · see citing works

Brain–gut–microbiome interactions in obesity and food addiction

Gupta, A., Osadchiy, V., & Mayer, E. A. (2020) · Nature Reviews Gastroenterology & Hepatology · doi:10.1038/s41575-020-0341-5 · Cited by 268 · see citing works

The microbiota and the hypothalamus-pituitary-adrenocortical (HPA) axis, implications for anxiety and stress disorders

Frankiensztajn, L. M., Elliott, E., & Koren, O. (2020) · Current Opinion in Neurobiology · doi:10.1016/j.conb.2019.12.003 · Cited by 248 · 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

Role of Gut Microbiome in Autism Spectrum Disorder and Its Therapeutic Regulation

Taniya, M. A., Chung, H.-J., Al Mamun, A., Alam, S., Aziz, M. A., Emon, N. U., Islam, M. M., Hong, S.-T. S., Podder, B. R., Ara Mimi, A., et al. (2022) · Frontiers in Cellular and Infection Microbiology · doi:10.3389/fcimb.2022.915701 · Cited by 207 · see citing works

Priming for Life: Early Life Nutrition and the Microbiota-Gut-Brain Axis

Ratsika, A., Codagnone, M. G., O’Mahony, S. M., Stanton, C., & Cryan, J. F. (2021) · Nutrients · doi:10.3390/nu13020423 · Cited by 184 · see citing works

The impact of acute and chronic stress on gastrointestinal physiology and function: a microbiota–gut–brain axis perspective

Leigh, S., Uhlig, F., Wilmes, L., Sánchez-Díaz, P., Gheorghe, C. E., Goodson, M. S., Kelley‐Loughnane, N., Hyland, N. P., Cryan, J. F., & Clarke, G. A. (2023) · The Journal of Physiology · doi:10.1113/jp281951 · Cited by 193 · see citing works

Probiotic consumption during puberty mitigates LPS-induced immune responses and protects against stress-induced depression- and anxiety-like behaviors in adulthood in a sex-specific manner

Murray, E., Sharma, R., Smith, K. B., Mar, K. D., Barve, R., Lukasik, M., Pirwani, A. F., Malette-Guyon, E., Lamba, S., Thomas, B. J., et al. (2019) · Brain Behavior and Immunity · doi:10.1016/j.bbi.2019.06.016 · Cited by 150 · see citing works

Perinatal Interactions between the Microbiome, Immunity, and Neurodevelopment

Pronovost, G. N., & Hsiao, E. Y. (2019) · Immunity · doi:10.1016/j.immuni.2018.11.016 · Cited by 146 · see citing works

Development of Gut Microbiota in the First 1000 Days after Birth and Potential Interventions

Pantazi, A. C., Bălașa, A. L., Mihai, C. M., Chisnoiu, T., Lupu, V. V., Kassim, M. A. K., Mihai, L., Frecuș, C. E., Chirila, S. I., Lupu, A., et al. (2023) · Nutrients · doi:10.3390/nu15163647 · Cited by 163 · see citing works

The role of the microbiome in the neurobiology of social behaviour

Sarkar, A., Harty, S., Johnson, K. V. ‐., Moeller, A. H., Carmody, R. N., Lehto, S. M., Erdman, S. E., Dunbar, R. I. M., & Burnet, P. W. J. (2020) · Biological Reviews · doi:10.1111/brv.12603 · Cited by 135 · see citing works

Prenatal and postnatal contributions of the maternal microbiome on offspring programming

Jašarević, E., & Bale, T. L. (2019) · Frontiers in Neuroendocrinology · doi:10.1016/j.yfrne.2019.100797 · Cited by 127 · see citing works

Microbiota-brain interactions: Moving toward mechanisms in model organisms

Nagpal, J. K., & Cryan, J. F. (2021) · Neuron · doi:10.1016/j.neuron.2021.09.036 · Cited by 107 · see citing works

Sperm microRNAs confer depression susceptibility to offspring

Wang, Y., Chen, Z., Hu, H., Lei, J., Zhou, Z., Yao, B., Chen, L., Liang, G., Zhan, S., Zhu, X., et al. (2021) · Science Advances · doi:10.1126/sciadv.abd7605 · Cited by 108 · see citing works

Enduring behavioral effects induced by birth by caesarean section in the mouse

Morais, L. H., Golubeva, A. V., Moloney, G. M., Moya-Pérez, A., Ventura-Silva, A. P., Arboleya, S., Bastiaanssen, T. F. S., O’Sullivan, O., Rea, K., Borre, Y., et al. (2020) · Current Biology · doi:10.1016/j.cub.2020.07.044 · Cited by 104 · see citing works

The Maternal–Fetal Gut Microbiota Axis: Physiological Changes, Dietary Influence, and Modulation Possibilities

Mikó, É., Csaszar, A., Bódis, J., & Kovács, K. A. (2022) · Life · doi:10.3390/life12030424 · Cited by 98 · see citing works

Autism Spectrum Disorders and the Gastrointestinal Tract: Insights into Mechanisms and Clinical Relevance

Hung, L. Y., & Margolis, K. G. (2024) · Nature Reviews Gastroenterology &amp; Hepatology · doi:10.1038/s41575-023-00857-1 · Cited by 96 · see citing works

Effects of Microbiota Imbalance in Anxiety and Eating Disorders: Probiotics as Novel Therapeutic Approaches

Navarro‐Tapia, E., Almeida-Toledano, L., Sebastiani, G., Serra-Delgado, M., García‐Algar, Ó., & Andreu-Férnández, V. (2021) · International Journal of Molecular Sciences · doi:10.3390/ijms22052351 · Cited by 91 · see citing works

The composition of human vaginal microbiota transferred at birth affects offspring health in a mouse model

Jašarević, E., Hill, E. M., Kane, P. J., Rutt, L., Gyles, T. M., Folts, L. M., Rock, K. D., Howard, C. D., Morrison, K. E., Ravel, J., et al. (2021) · Nature Communications · doi:10.1038/s41467-021-26634-9 · Cited by 83 · see citing works

Mouse models of neurodegeneration: Know your question, know your mouse

Fisher, E., & Bannerman, D. M. (2019) · Science Translational Medicine · doi:10.1126/scitranslmed.aaq1818 · Cited by 79 · see citing works

Maternal prenatal psychological distress and hair cortisol levels associate with infant fecal microbiota composition at 2.5 months of age

Aatsinki, A., Keskitalo, A., Laitinen, V., Munukka, E., Uusitupa, H., Lahti, L., Kortesluoma, S., Mustonen, P., Rodrigues, A. J., Coimbra, B., et al. (2020) · Psychoneuroendocrinology · doi:10.1016/j.psyneuen.2020.104754 · Cited by 81 · see citing works

Developmental responses to early‐life adversity: Evolutionary and mechanistic perspectives

Lu, A., Petrullo, L. A., Carrera, S. C., Feder, J. A., Schneider‐Crease, I. A., & Snyder‐Mackler, N. (2019) · Evolutionary Anthropology Issues News and Reviews · doi:10.1002/evan.21791 · Cited by 75 · see citing works

The Impact of Maternal Gut Microbiota during Pregnancy on Fetal Gut–Brain Axis Development and Life-Long Health Outcomes

Sajdel, E. M. (2023) · Microorganisms · doi:10.3390/microorganisms11092199 · Cited by 82 · see citing works

When a Neonate Is Born, So Is a Microbiota

Coscia, A., Bardanzellu, F., Caboni, E., Fanos, V., & Peroni, D. G. (2021) · Life · doi:10.3390/life11020148 · Cited by 76 · see citing works

Intrauterine Microbiota: Missing, or the Missing Link?

Chen, H. J., & Gur, T. (2019) · Trends in Neurosciences · doi:10.1016/j.tins.2019.03.008 · Cited by 70 · see citing works

Mood and Microbes

Kelly, J. R., Keane, V. O., Cryan, J. F., Clarke, G., & Dinan, T. G. (2019) · Gastroenterology Clinics of North America · doi:10.1016/j.gtc.2019.04.006 · Cited by 65 · see citing works

Revealing the importance of prenatal gut microbiome in offspring neurodevelopment in humans

Sun, Z., Lee‐Sarwar, K. A., Kelly, R. S., Lasky-Su, J. A., Litonjua, A. A., Weiss, S. T., & Liu, Y. (2023) · EBioMedicine · doi:10.1016/j.ebiom.2023.104491 · Cited by 67 · see citing works

Gut microbiota and neuropsychiatric disorders: Implications for neuroendocrine-immune regulation

Ge, T., Yao, X., Zhao, H., Yang, W., Zou, X., Peng, F., Li, B., & Cui, R. (2021) · Pharmacological Research · doi:10.1016/j.phrs.2021.105909 · Cited by 62 · see citing works

Antidepressant treatment with fluoxetine during pregnancy and lactation modulates the gut microbiome and metabolome in a rat model relevant to depression

Ramsteijn, A. S., Jašarević, E., Houwing, D. J., Bale, T. L., & Olivier, J. D. (2020) · Gut Microbes · doi:10.1080/19490976.2019.1705728 · Cited by 65 · see citing works

Placental CRH as a Signal of Pregnancy Adversity and Impact on Fetal Neurodevelopment

Kassotaki, I., Valsamakis, G., Mastorakos, G. P., & Grammatopoulos, D. K. (2021) · Frontiers in Endocrinology · doi:10.3389/fendo.2021.714214 · Cited by 62 · see citing works

Prenatal exposure to TiO2 nanoparticles in mice causes behavioral deficits with relevance to autism spectrum disorder and beyond

Notter, T., Aengenheister, L., Weber‐Stadlbauer, U., Naegeli, H., Wick, P., Meyer, U., & Buerki‐Thurnherr, T. (2018) · Translational Psychiatry · doi:10.1038/s41398-018-0251-2 · Cited by 59 · see citing works

At the crux of maternal immune activation: Viruses, microglia, microbes, and IL‐17A

Otero, A. M., & Antonson, A. M. (2022) · Immunological Reviews · doi:10.1111/imr.13125 · Cited by 55 · see citing works

The microbiome and gut endocannabinoid system in the regulation of stress responses and metabolism

Srivastava, R. K., Lutz, B., & Ruiz de Azua, I. (2022) · Frontiers in Cellular Neuroscience · doi:10.3389/fncel.2022.867267 · Cited by 56 · see citing works

The human microbiome in clinical translation: from bench to bedside

Bautista, J., Echeverría, C. E., Maldonado-Noboa, I., Ojeda-Mosquera, S., Hidalgo-Tinoco, C., & López-Cortés, A. (2025) · Frontiers in Microbiology · doi:10.3389/fmicb.2025.1632435 · Cited by 55 · see citing works

Evolutionary Significance of the Neuroendocrine Stress Axis on Vertebrate Immunity and the Influence of the Microbiome on Early-Life Stress Regulation and Health Outcomes

Ortega, V. A., Mercer, E. M., Giesbrecht, G. F., & Arrieta, M. (2021) · Frontiers in Microbiology · doi:10.3389/fmicb.2021.634539 · Cited by 51 · see citing works

Maternal separation in rodents: a journey from gut to brain and nutritional perspectives

Rincel, M., & Darnaudéry, M. (2019) · Proceedings of The Nutrition Society · doi:10.1017/s0029665119000958 · Cited by 50 · see citing works

Maternal effects in mammals: Broadening our understanding of offspring programming

Edwards, P. D., Lavergne, S. G., McCaw, L. K., Wijenayake, S., Boonstra, R., McGowan, P. O., & Holmes, M. M. (2021) · Frontiers in Neuroendocrinology · doi:10.1016/j.yfrne.2021.100924 · Cited by 47 · see citing works

Prenatal Maternal Stress Exacerbates Experimental Colitis of Offspring in Adulthood

Sun, Y., Xie, R., Lü, L., Jin, G., Zhou, B., Huang, H., Li, M., Yang, Y., Liu, X., Cao, X., et al. (2021) · Frontiers in Immunology · doi:10.3389/fimmu.2021.700995 · Cited by 47 · see citing works

Decoding the neurocircuitry of gut feelings: Region-specific microbiome-mediated brain alterations

Sharvin, B. L., Aburto, M. R., & Cryan, J. F. (2023) · Neurobiology of Disease · doi:10.1016/j.nbd.2023.106033 · Cited by 49 · see citing works

Unique maternal immune and functional microbial profiles during prenatal stress

Antonson, A. M., Evans, M. V., Galley, J. D., Chen, H. J., Rajasekera, T. A., Lammers, S. M., Hale, V. L., Bailey, M. T., & Gur, T. (2020) · Scientific Reports · doi:10.1038/s41598-020-77265-x · Cited by 47 · see citing works

Maternal Obesity and Gut Microbiota Are Associated with Fetal Brain Development

Basak, S., Das, R. K., Banerjee, A., Paul, S., Pathak, S., & Duttaroy, A. K. (2022) · Nutrients · doi:10.3390/nu14214515 · Cited by 50 · see citing works

An epigenetic, transgenerational model of increased mental health disorders in children, adolescents and young adults

Monaco, A. P. (2020) · European Journal of Human Genetics · doi:10.1038/s41431-020-00726-4 · Cited by 45 · see citing works

Emerging evidence linking the gut microbiome to neurologic disorders

Griffiths, J. A., & Mazmanian, S. K. (2018) · Genome Medicine · doi:10.1186/s13073-018-0609-3 · Cited by 44 · see citing works

Identification of bacterial lipopeptides as key players in IBS

Petitfils, C., Maurel, S., Payros, G., Hueber, A., Agaiz, B., Gazzo, G., Marrocco, R., Auvray, F., Langevin, G., Motta, J., et al. (2022) · Gut · doi:10.1136/gutjnl-2022-328084 · Cited by 43 · see citing works

Extracellular vesicles are dynamic regulators of maternal glucose homeostasis during pregnancy

Zierden, H. C., Marx-Rattner, R., Rock, K. D., Montgomery, K. R., Anastasiadis, P., Folts, L. M., & Bale, T. L. (2023) · Scientific Reports · doi:10.1038/s41598-023-31425-x · Cited by 42 · see citing works

The paraventricular thalamus mediates visceral pain and anxiety-like behaviors via two distinct pathways

Li, D., Li, Y., Zhu, Z.-Y., Zhang, F., Zhao, Q., Jiang, J.-H., Shen, B., Tang, Y., & Xu, G. (2025) · Neuron · doi:10.1016/j.neuron.2025.04.019 · Cited by 42 · see citing works

Malnutrition and the microbiome as modifiers of early neurodevelopment

Coley, E. J. L., & Hsiao, E. Y. (2021) · Trends in Neurosciences · doi:10.1016/j.tins.2021.06.004 · Cited by 40 · see citing works

Vaginal microbiota transplantation is a truly opulent and promising edge: fully grasp its potential

Meng, Y., Sun, J., & Zhang, G. (2024) · Frontiers in Cellular and Infection Microbiology · doi:10.3389/fcimb.2024.1280636 · Cited by 39 · see citing works

Maternal Distress and Offspring Neurodevelopment: Challenges and Opportunities for Pre-clinical Research Models

Fitzgerald, E., Parent, C. I., Kee, M. Z. L., & Meaney, M. J. (2021) · Frontiers in Human Neuroscience · doi:10.3389/fnhum.2021.635304 · Cited by 39 · see citing works

The Microbiome as a Maternal Effect: A Systematic Review on Vertical Transmission of Microbiota

Murphy, K., Le, S. M., Wilson, A. E., & Warner, D. A. (2023) · Integrative and Comparative Biology · doi:10.1093/icb/icad031 · Cited by 40 · see citing works

Deciphering microbiome and neuroactive immune gene interactions in schizophrenia

Severance, E. G., & Yolken, R. H. (2018) · Neurobiology of Disease · doi:10.1016/j.nbd.2018.11.016 · Cited by 39 · see citing works

Diet-induced dysbiosis of the maternal gut microbiome in early life programming of neurodevelopmental disorders

Gesù, C. M. D., Matz, L. M., & Buffington, S. A. (2021) · Neuroscience Research · doi:10.1016/j.neures.2021.05.003 · Cited by 46 · see citing works

One Giant Leap from Mouse to Man: The Microbiota–Gut–Brain Axis in Mood Disorders and Translational Challenges Moving towards Human Clinical Trials

Forssten, S. D., Ouwehand, A. C., Griffin, S. M., & Patterson, E. (2022) · Nutrients · doi:10.3390/nu14030568 · Cited by 39 · see citing works

A Review of the Impact of Maternal Prenatal Stress on Offspring Microbiota and Metabolites

Yeramilli, V. A., Cheddadi, R., Shah, J., Brawner, K. M., & Martin, C. A. (2023) · Metabolites · doi:10.3390/metabo13040535 · Cited by 35 · see citing works

The call of the wild: using non-model systems to investigate microbiome–behaviour relationships

Cusick, J. A., Wellman, C. L., & Demas, G. E. (2021) · Journal of Experimental Biology · doi:10.1242/jeb.224485 · Cited by 34 · see citing works

Pubertal probiotic blocks LPS-induced anxiety and the associated neurochemical and microbial outcomes, in a sex dependent manner

Murray, E., Smith, K. B., Stoby, K. S., Thomas, B. J., Swenson, M. J., Arber, L., Frenette, E., & Ismail, N. (2019) · Psychoneuroendocrinology · doi:10.1016/j.psyneuen.2019.104481 · Cited by 33 · see citing works

Disaster-related prenatal maternal stress, and childhood HPA-axis regulation and anxiety: The QF2011 Queensland Flood Study

McLean, M. A., Simcock, G. P., Elgbeili, G., Laplante, D. P., Kildea, S. V., Hurrion, E. M., Lequertier, B., Cobham, V. E., & King, S. (2020) · Psychoneuroendocrinology · doi:10.1016/j.psyneuen.2020.104716 · Cited by 35 · see citing works

Paternal Nongenetic Intergenerational Transmission of Metabolic Disease Risk

Su, L., & Patti, M. (2019) · Current Diabetes Reports · doi:10.1007/s11892-019-1163-0 · Cited by 34 · see citing works

Early Life Stress and the Development of the Infant Gut Microbiota: Implications for Mental Health and Neurocognitive Development

Vogel, S. C., Brito, N. H., & Callaghan, B. L. (2020) · Current Psychiatry Reports · doi:10.1007/s11920-020-01186-9 · Cited by 31 · see citing works

Prenatal stress effects on offspring brain and behavior: Mediators, alterations and dysregulated epigenetic mechanisms

Haq, S. U., Bhat, U. A., & Kumar, A. (2021) · Journal of Biosciences · doi:10.1007/s12038-021-00153-7 · Cited by 34 · see citing works

Altered gut microbiome and autism like behavior are associated with parental high salt diet in male mice

Afroz, K. F., Reyes, N., Young, K., Parikh, K., Misra, V., & Alviña, K. (2021) · Scientific Reports · doi:10.1038/s41598-021-87678-x · Cited by 32 · see citing works

Maternal microbiome disturbance induces deficits in the offspring’s behaviors: a systematic review and meta-analysis

Hassib, L., de Oliveira, C. L., Rouvier, G. A., Kanashiro, A., Guimarães, F. S., & Ferreira, F. R. (2023) · Gut Microbes · doi:10.1080/19490976.2023.2226282 · Cited by 33 · see citing works

The Adverse Effects of Prenatal METH Exposure on the Offspring: A Review

Li, J.-H., Liu, J.-L., Zhang, K.-K., Chen, L., Xu, J., & Xie, X. (2021) · Frontiers in Pharmacology · doi:10.3389/fphar.2021.715176 · Cited by 31 · see citing works

Prenatal stress increases IgA coating of offspring microbiota and exacerbates necrotizing enterocolitis-like injury in a sex-dependent manner

Brawner, K. M., Yeramilli, V. A., Kennedy, B. A., Patel, R. K., & Martin, C. A. (2020) · Brain Behavior and Immunity · doi:10.1016/j.bbi.2020.07.008 · Cited by 29 · see citing works

Vertical transmission of gut microbiota: Points of action of environmental factors influencing brain development

Tochitani, S. (2020) · Neuroscience Research · doi:10.1016/j.neures.2020.11.006 · Cited by 30 · see citing works

Perceived Stress and Molecular Bacterial Vaginosis in the National Institutes of Health Longitudinal Study of Vaginal Flora

Turpin, R., Slopen, N. B., Borgogna, J.-L. C., Yeoman, C. J., He, X., Miller, R. S., Klebanoff, M. A., Ravel, J., & Brotman, R. M. (2021) · American Journal of Epidemiology · doi:10.1093/aje/kwab147 · Cited by 32 · see citing works

Risk Factors for Chronic Stress in Sows Housed in Groups, and Associated Risks of Prenatal Stress in Their Offspring

Lagoda, M. E., Marchewka, J., O’Driscoll, K., & Boyle, L. A. (2022) · Frontiers in Veterinary Science · doi:10.3389/fvets.2022.883154 · Cited by 32 · see citing works

Ontogenetic rules for the molecular diversification of hypothalamic neurons

Benevento, M., Hökfelt, T. G. M., & Harkany, T. (2022) · Nature reviews. Neuroscience · doi:10.1038/s41583-022-00615-3 · Cited by 28 · see citing works

The microbiota–gut–brain axis: A novel nutritional therapeutic target for growth retardation

Qi, M., Tan, B., Wang, J., Liao, S., Deng, Y., Ji, P., Song, T., Zha, A., & Yin, Y. (2021) · Critical Reviews in Food Science and Nutrition · doi:10.1080/10408398.2021.1879004 · Cited by 26 · see citing works

Distribution characteristics of intestinal microbiota during pregnancy and postpartum in healthy women

Qin, S., Liu, Y., Wang, S., Ma, J., & Yang, H. (2021) · The Journal of Maternal-Fetal & Neonatal Medicine · doi:10.1080/14767058.2020.1812571 · Cited by 27 · see citing works

Heat stress affects fetal brain and intestinal function associated with the alterations of placental barrier in late pregnant mouse

Guo, H., Yang, Y., Qiao, Y., He, J., Yao, W., & Zheng, W. (2021) · Ecotoxicology and Environmental Safety · doi:10.1016/j.ecoenv.2021.112916 · Cited by 23 · see citing works

The Sexome ‐ A proof of concept study into microbial transfer between heterosexual couples after sexual intercourse

Dixon, R., Egan, S. L., Hughes-Stamm, S. R., & Chapman, B. (2023) · Forensic Science International · doi:10.1016/j.forsciint.2023.111711 · Cited by 24 · see citing works

Early-life gut microbiome development and its potential long-term impact on health outcomes

Borrego-Ruiz, A., & Borrego, J. J. (2025) · Microbiome Research Reports · doi:10.20517/mrr.2024.78 · Cited by 29 · see citing works

Considering the Microbiome in Stress-Related and Neurodevelopmental Trajectories to Schizophrenia

Hoffman, K. W., Lee, J. J., Corcoran, C. M., Kimhy, D., Kranz, T. M., & Malaspina, D. (2020) · Frontiers in Psychiatry · doi:10.3389/fpsyt.2020.00629 · Cited by 23 · see citing works

Wrapping Things Up: Recent Developments in Understanding the Role of the Microbiome in Regulating Myelination

Lynch, C. M. K., Nagpal, J. K., Clarke, G. A., & Cryan, J. F. (2021) · Current Opinion in Physiology · doi:10.1016/j.cophys.2021.100468 · Cited by 23 · see citing works

Pubertal adversity alters chromatin dynamics and stress circuitry in the pregnant brain

Morrison, K. E., Cole, A. B., Kane, P. J., Meadows, V. E., Thompson, S. M., & Bale, T. L. (2020) · Neuropsychopharmacology · doi:10.1038/s41386-020-0634-y · Cited by 23 · see citing works

Stress and the Gut-Brain Axis: Implications for Cancer, Inflammation and Sepsis

Moughnyeh, M., Brawner, K. M., Kennedy, B. A., Yeramilli, V. A., Udayakumar, N., Graham, J. A., & Martin, C. A. (2021) · Journal of Surgical Research · doi:10.1016/j.jss.2021.02.055 · Cited by 22 · see citing works

Decoding the Role of Gut-Microbiome in the Food Addiction Paradigm

Novelle, M. G. (2021) · International Journal of Environmental Research and Public Health · doi:10.3390/ijerph18136825 · Cited by 23 · see citing works

Should we modulate the neonatal microbiome and what should be the goal?

van Best, N., Domínguez-Bello, M. G., Hornef, M. W., Jašarević, E., Korpela, K., & Lawley, T. D. (2022) · Microbiome · doi:10.1186/s40168-022-01281-4 · Cited by 22 · see citing works

Vaginal Probiotic Lactobacillus crispatus Seems to Inhibit Sperm Activity and Subsequently Reduces Pregnancies in Rat

Li, P., Wei, K., He, X., Zhang, L., Liu, Z., Wei, J., Chen, X., Hong Kui, W. E. I., & Chen, T. (2021) · Frontiers in Cell and Developmental Biology · doi:10.3389/fcell.2021.705690 · Cited by 22 · see citing works

The microbiota extends the reproductive lifespan of mice by safeguarding the ovarian reserve

Munyoki, S. K., Goff, J. P., Reshke, A., Wilderoter, E., Mafarachisi, N., Kolobaric, A., Sheng, Y., Mullett, S. J., King, G. E., DeSchepper, J. D., et al. (2025) · Cell Host & Microbe · doi:10.1016/j.chom.2025.09.006 · Cited by 21 · see citing works

A role for the microbiome in mother–infant interaction and perinatal depression

Sanders, A., Rackers, H., & Kimmel, M. (2019) · International Review of Psychiatry · doi:10.1080/09540261.2018.1548431 · Cited by 21 · see citing works

Altered stress responses in adults born by Caesarean section

Dinan, T. G., Kennedy, P. J., Morais, L. H., Murphy, A., Long-Smith, C. M., Moloney, G. M., Bastiaanssen, T. F. S., Allen, A. P., Collery, A., Mullins, D., et al. (2021) · Neurobiology of Stress · doi:10.1016/j.ynstr.2021.100425 · Cited by 20 · see citing works

Exploring the effect of prenatal maternal stress on the microbiomes of mothers and infants: A systematic review

Mepham, J. R., Nelles‐McGee, T., Andrews, K., & González, A. (2023) · Developmental Psychobiology · doi:10.1002/dev.22424 · Cited by 20 · see citing works

Roles of the gut microbiota in human neurodevelopment and adult brain disorders

Mallick, R., Basak, S., Das, R. K., Banerjee, A., Paul, S., Pathak, S., & Duttaroy, A. K. (2024) · Frontiers in Neuroscience · doi:10.3389/fnins.2024.1446700 · Cited by 51 · see citing works

MeCP2 mediates transgenerational transmission of chronic pain

Tao, W., Chen, C., Wang, Y., Zhou, W., Jin, Y., Mao, Y., Wang, H., Wang, L., Xie, W. J., Zhang, X., et al. (2020) · Progress in Neurobiology · doi:10.1016/j.pneurobio.2020.101790 · Cited by 19 · see citing works

Gut microbiota features associated with Clostridioides difficile colonization in puppies

Berry, A. S. F., Barnhart, D., Kelly, B. J., Kelly, D. J., Beiting, D. P., Baldassano, R. N., & Redding, L. E. (2019) · PLoS ONE · doi:10.1371/journal.pone.0215497 · Cited by 19 · see citing works

Developmental opioid exposures: Neurobiological underpinnings, behavioral impacts, and policy implications

Goldfarb, S. S., Stanwood, G. D., Flynn, H. A., & Graham, D. L. (2019) · Experimental Biology and Medicine · doi:10.1177/1535370219883601 · Cited by 18 · see citing works

Animal models for assessing impact of C-section delivery on biological systems

Cabré, S., Ratsika, A., Rea, K., Stanton, C., & Cryan, J. F. (2022) · Neuroscience & Biobehavioral Reviews · doi:10.1016/j.neubiorev.2022.104555 · Cited by 17 · see citing works

Perinatal transmission of a probiotic Bifidobacterium strain protects against early life stress-induced mood and gastrointestinal motility disorders

Zhu, H., Tian, P., Qian, X., Gu, L., Zhao, J., Wang, G., & Chen, W. (2022) · Food & Function · doi:10.1039/d2fo01164f · Cited by 18 · see citing works

Multifactorial effects of probiotic Parasutterella excrementihominis on gestational inflammation, offspring behaviour and prenatal-stress induced disruptions in tryptophan metabolism

Galley, J. D., Rajasekera, T. A., Bennouna, D., Batabyal, A., Verosky, B. G., Woodke, S. T., Stokes, J., Brown, A. K., Murthy, S., Kopec, R. E., et al. (2024) · Beneficial Microbes · doi:10.1163/18762891-bja00047 · Cited by 17 · see citing works

Context‐dependent effects of glucocorticoids on the lizard gut microbiome

MacLeod, K. J., Kohl, K. D., Trevelline, B. K., & Langkilde, T. L. (2021) · Molecular Ecology · doi:10.1111/mec.16229 · Cited by 16 · see citing works

Gut microbiota – host interactions now also brain-immune axis

Hajjo, H., & Geva‐Zatorsky, N. (2019) · Current Opinion in Neurobiology · doi:10.1016/j.conb.2019.10.009 · Cited by 16 · see citing works

Cinnamaldehyde prevents intergenerational effect of paternal depression in mice via regulating GR/miR-190b/BDNF pathway

Gao, Z.-Y., Chen, T.-Y., Yu, T.-T., Zhang, L.-P., Zhao, S.-J., Gu, X.-Y., Pan, Y., & Kong, L.-D. (2022) · Acta Pharmacologica Sinica · doi:10.1038/s41401-021-00831-0 · Cited by 18 · see citing works

Maternal stress and the maternal microbiome have sex-specific effects on offspring development and aggressive behavior in Siberian hamsters (Phodopus sungorus)

Cusick, J. A., Wellman, C. L., & Demas, G. E. (2022) · Hormones and Behavior · doi:10.1016/j.yhbeh.2022.105146 · Cited by 16 · see citing works

38. Stress Alterations to the Maternal Microbiome Mediate Sex-Specific Neuroimmune Development

Jašarević, E., Howard, C. D., & Bale, T. L. (2019) · Biological Psychiatry · doi:10.1016/j.biopsych.2019.03.052

356 Microbial origins in the developmental programming of offspring health

Jašarević, E. (2020) · Journal of Animal Science · doi:10.1093/jas/skaa278.170

Alterations in the Vaginal Microbiome by Maternal Stress Are Associated With Metabolic Reprogramming of the Offspring Gut and Brain

Jašarević, E., Howerton, C. L., Howard, C. D., & Bale, T. L. (2015) · Endocrinology · doi:10.1210/en.2015-1177 · Cited by 329 · see citing works

Stress during pregnancy alters temporal and spatial dynamics of the maternal and offspring microbiome in a sex-specific manner

Jašarević, E., Howard, C. D., Misic, A. M., Beiting, D. P., & Bale, T. L. (2017) · Scientific Reports · doi:10.1038/srep44182 · Cited by 262 · see citing works

A novel role for maternal stress and microbial transmission in early life programming and neurodevelopment

Jašarević, E., Rodgers, A. B., & Bale, T. L. (2014) · Neurobiology of Stress · doi:10.1016/j.ynstr.2014.10.005 · Cited by 147 · see citing works