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Maternal Inflammation and Neurodevelopmental Programming: A Review of Preclinical Outcomes and Implications for Translational Psychiatry

Gumusoglu, Serena B., Stevens, Hanna E.·2019·Biological Psychiatry
DOI 10.1016/j.biopsych.2018.08.008
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Research works printed but not linked: 116

  1. Barker, 1986, Childhood respiratory infection and adult chronic bronchitis in England and Wales, Br Med J (Clin Res Ed), 293, 1271, 10.1136/bmj.293.6557.1271 · DOI
  2. Barker, 1986, Infant mortality, childhood nutrition, and ischaemic heart disease in England and Wales, Lancet, 1, 1077, 10.1016/S0140-6736(86)91340-1 · DOI · Paper page
  3. Barker, 1993, Fetal origins of coronary heart disease, Br Heart J, 69, 195, 10.1136/hrt.69.3.195 · DOI
  4. Stevens, 2015, How animal models inform child and adolescent psychiatry, J Am Acad Child Adolesc Psychiatry, 54, 352, 10.1016/j.jaac.2015.01.019 · DOI
  5. Hirabayashi, 2005, Stage-dependent fate determination of neural precursor cells in mouse forebrain, Neurosci Res, 51, 331, 10.1016/j.neures.2005.01.004 · DOI
  6. Tau, 2010, Normal development of brain circuits, Neuropsychopharmacology, 35, 147, 10.1038/npp.2009.115 · DOI · Paper page
  7. Lind, 2007, The use of pigs in neuroscience: Modeling brain disorders, Neurosci Biobehav Rev, 31, 728, 10.1016/j.neubiorev.2007.02.003 · DOI
  8. Hodyl, 2007, Modelling prenatal bacterial infection: Functional consequences of altered hypothalamic pituitary adrenal axis development, Behav Brain Res, 178, 108, 10.1016/j.bbr.2006.12.008 · DOI
  9. Krishnan, 2013, From mice to women: The conundrum of immunity to infection during pregnancy, J Reprod Immunol, 97, 62, 10.1016/j.jri.2012.10.015 · DOI
  10. Nemzek, 2008, Modeling sepsis in the laboratory: Merging sound science with animal well-being, Comp Med, 58, 120
  11. Seok, 2013, Genomic responses in mouse models poorly mimic human inflammatory diseases, Proc Natl Acad Sci U S A, 110, 3507, 10.1073/pnas.1222878110 · DOI · Paper page
  12. Beckman, 1990, Experimental manipulation of the rodent visceral yolk sac, Teratology, 41, 395, 10.1002/tera.1420410405 · DOI
  13. Carter, 2007, Animal models of human placentation—A review, Placenta, 28, S41, 10.1016/j.placenta.2006.11.002 · DOI
  14. Than, 2009, A primate subfamily of galectins expressed at the maternal-fetal interface that promote immune cell death, Proc Natl Acad Sci U S A, 106, 9731, 10.1073/pnas.0903568106 · DOI
  15. Hsiao, 2012, Placental regulation of maternal-fetal interactions and brain development, Dev Neurobiol, 72, 1317, 10.1002/dneu.22045 · DOI
  16. Meyer, 2009, In-vivo rodent models for the experimental investigation of prenatal immune activation effects in neurodevelopmental brain disorders, Neurosci Biobehav Rev, 33, 1061, 10.1016/j.neubiorev.2009.05.001 · DOI
  17. Alexander, 2001, Bacterial lipopolysaccharides and innate immunity, J Endotoxin Res, 7, 167
  18. Homan, 1972, Studies on poly I:C toxicity in experimental animals, Toxicol Appl Pharmacol, 23, 579, 10.1016/0041-008X(72)90098-1 · DOI
  19. Reisinger, 2015, The poly(I:C)-induced maternal immune activation model in preclinical neuropsychiatric drug discovery, Pharmacol Ther, 149, 213, 10.1016/j.pharmthera.2015.01.001 · DOI
  20. Zuckerman, 2003, Immune activation during pregnancy in rats leads to a postpubertal emergence of disrupted latent inhibition, dopaminergic hyperfunction, and altered limbic morphology in the offspring: A novel neurodevelopmental model of schizophrenia, Neuropsychopharmacology, 28, 1778, 10.1038/sj.npp.1300248 · DOI
  21. Triantafilou, 2002, Lipopolysaccharide recognition: CD14, TLRs and the LPS-activation cluster, Trends Immunol, 23, 301, 10.1016/S1471-4906(02)02233-0 · DOI
  22. Triantafilou, 2002, Mediators of innate immune recognition of bacteria concentrate in lipid rafts and facilitate lipopolysaccharide-induced cell activation, J Cell Sci, 115, 2603, 10.1242/jcs.115.12.2603 · DOI
  23. Lin, 2012, Prenatal lipopolysaccharide exposure increases anxiety-like behaviors and enhances stress-induced corticosterone responses in adult rats, Brain Behav Immun, 26, 459, 10.1016/j.bbi.2011.12.003 · DOI
  24. Arsenault, 2014, The different effects of LPS and poly I:C prenatal immune challenges on the behavior, development and inflammatory responses in pregnant mice and their offspring, Brain Behav Immun, 38, 77, 10.1016/j.bbi.2013.12.016 · DOI · Paper page
  25. Schwartzer, 2013, Maternal immune activation and strain specific interactions in the development of autism-like behaviors in mice, Transl Psychiatry, 3, e240, 10.1038/tp.2013.16 · DOI
  26. Nakanishi, 2007, Microglia-derived interleukin-6 and leukaemia inhibitory factor promote astrocytic differentiation of neural stem/progenitor cells, Eur J Neurosci, 25, 649, 10.1111/j.1460-9568.2007.05309.x · DOI
  27. Brown, 2017, Exposure to intrauterine inflammation alters metabolomic profiles in the amniotic fluid, fetal and neonatal brain in the mouse, PLoS One, 12, e0186656, 10.1371/journal.pone.0186656 · DOI
  28. Gao, 2016, New perspective on impact of folic acid supplementation during pregnancy on neurodevelopment/autism in the offspring children—A systematic review, PLoS One, 11, e0165626, 10.1371/journal.pone.0165626 · DOI
  29. Taylor, 2017, Effects of nutritional interventions during pregnancy on infant and child cognitive outcomes: A systematic review and meta-analysis, Nutrients, 9, E1265, 10.3390/nu9111265 · DOI
  30. Frick, 2013, Microglial dysregulation in psychiatric disease, Clin Dev Immunol, 2013, 608654, 10.1155/2013/608654 · DOI · Paper page
  31. Sacco, 2015, Head circumference and brain size in autism spectrum disorder: A systematic review and meta-analysis, Psychiatry Res, 234, 239, 10.1016/j.pscychresns.2015.08.016 · DOI · Paper page
  32. Harrison, 2004, The hippocampus in schizophrenia: A review of the neuropathological evidence and its pathophysiological implications, Psychopharmacology (Berl), 174, 151, 10.1007/s00213-003-1761-y · DOI · Paper page
  33. Hercher, 2009, Through the looking glass: Examining neuroanatomical evidence for cellular alterations in major depression, J Psychiatr Res, 43, 947, 10.1016/j.jpsychires.2009.01.006 · DOI
  34. Coley, 2018, PSD95: A synaptic protein implicated in schizophrenia or autism?, Prog Neuropsychopharmacol Biol Psychiatry, 82, 187, 10.1016/j.pnpbp.2017.11.016 · DOI
  35. Schmidt-Hieber, 2017, Synaptic integrative mechanisms for spatial cognition, Nat Neurosci, 20, 1483, 10.1038/nn.4652 · DOI
  36. Teffer, 2012, Human prefrontal cortex: Evolution, development, and pathology, Prog Brain Res, 195, 191, 10.1016/B978-0-444-53860-4.00009-X · DOI
  37. Olson, 2004, Microglia initiate central nervous system innate and adaptive immune responses through multiple TLRs, J Immunol, 173, 3916, 10.4049/jimmunol.173.6.3916 · DOI · Paper page
  38. Czeh, 2011, The yin and yang of microglia, Dev Neurosci, 33, 199, 10.1159/000328989 · DOI
  39. Cuadros, 1998, The origin and differentiation of microglial cells during development, Prog Neurobiol, 56, 173, 10.1016/S0301-0082(98)00035-5 · DOI
  40. Paolicelli, 2017, Function and dysfunction of microglia during brain development: Consequences for synapses and neural circuits, Front Synaptic Neurosci, 9, 9, 10.3389/fnsyn.2017.00009 · DOI
  41. Dean, 2011, Delayed cortical impairment following lipopolysaccharide exposure in preterm fetal sheep, Ann Neurol, 70, 846, 10.1002/ana.22480 · DOI
  42. Hutton, 2008, Microglial activation, macrophage infiltration, and evidence of cell death in the fetal brain after uteroplacental administration of lipopolysaccharide in sheep in late gestation, Am J Obstet Gynecol, 198, 10.1016/j.ajog.2007.06.035 · DOI
  43. Ling, 2006, Progressive dopamine neuron loss following supra-nigral lipopolysaccharide (LPS) infusion into rats exposed to LPS prenatally, Exp Neurol, 199, 499, 10.1016/j.expneurol.2006.01.010 · DOI
  44. Girard, 2010, IL-1 receptor antagonist protects against placental and neurodevelopmental defects induced by maternal inflammation, J Immunol, 184, 3997, 10.4049/jimmunol.0903349 · DOI
  45. Van den Eynde, 2014, Hypolocomotive behaviour associated with increased microglia in a prenatal immune activation model with relevance to schizophrenia, Behav Brain Res, 258, 179, 10.1016/j.bbr.2013.10.005 · DOI
  46. Ratnayake, 2012, Behaviour and hippocampus-specific changes in spiny mouse neonates after treatment of the mother with the viral-mimetic Poly I:C at mid-pregnancy, Brain Behav Immun, 26, 1288, 10.1016/j.bbi.2012.08.011 · DOI · Paper page
  47. Cunningham, 2013, Microglia regulate the number of neural precursor cells in the developing cerebral cortex, J Neurosci, 33, 4216, 10.1523/JNEUROSCI.3441-12.2013 · DOI · Paper page
  48. Paolicelli, 2011, Microglia in development: Linking brain wiring to brain environment, Neuron Glia Biol, 7, 77, 10.1017/S1740925X12000105 · DOI
  49. Welberg, 2014, Synaptic plasticity: A synaptic role for microglia, Nat Rev Neurosci, 15, 69, 10.1038/nrn3678 · DOI
  50. Levin, 2017, Modulating effect of cytokines on mechanisms of synaptic plasticity in the brain, Biochemistry (Mosc), 82, 264, 10.1134/S000629791703004X · DOI
  51. Cao, 2015, Fetal microglial phenotype in vitro carries memory of prior in vivo exposure to inflammation, Front Cell Neurosci, 9, 294, 10.3389/fncel.2015.00294 · DOI
  52. Schaafsma, 2017, Maternal inflammation induces immune activation of fetal microglia and leads to disrupted microglia immune responses, behavior, and learning performance in adulthood, Neurobiol Dis, 106, 291, 10.1016/j.nbd.2017.07.017 · DOI
  53. Zager, 2015, Maternal immune activation in late gestation increases neuroinflammation and aggravates experimental autoimmune encephalomyelitis in the offspring, Brain Behav Immun, 43, 159, 10.1016/j.bbi.2014.07.021 · DOI
  54. Schwarz, 2012, Sex differences in microglial colonization of the developing rat brain, J Neurochem, 120, 948, 10.1111/j.1471-4159.2011.07630.x · DOI · Paper page
  55. Manitz, 2016, Flow cytometric characterization of microglia in the offspring of PolyI:C treated mice, Brain Res, 1636, 172, 10.1016/j.brainres.2016.02.004 · DOI
  56. Nelson, 2017, The immune system as a novel regulator of sex differences in brain and behavioral development, J Neurosci Res, 95, 447, 10.1002/jnr.23821 · DOI
  57. Kalisch-Smith, 2017, Sex differences in rat placental development: From pre-implantation to late gestation, Biol Sex Differ, 8, 17, 10.1186/s13293-017-0138-6 · DOI
  58. Wolstenholme, 2013, Sexual differentiation in the developing mouse brain: Contributions of sex chromosome genes, Genes Brain Behav, 12, 166, 10.1111/gbb.12010 · DOI
  59. Bittle, 2018, The role of glucocorticoid, interleukin-1β, and antioxidants in prenatal stress effects on embryonic microglia, J Neuroinflammation, 15, 44, 10.1186/s12974-018-1079-7 · DOI
  60. Diz-Chaves, 2012, Prenatal stress causes alterations in the morphology of microglia and the inflammatory response of the hippocampus of adult female mice, J Neuroinflammation, 9, 71, 10.1186/1742-2094-9-71 · DOI
  61. Diz-Chaves, 2013, Prenatal stress increases the expression of proinflammatory cytokines and exacerbates the inflammatory response to LPS in the hippocampal formation of adult male mice, Brain Behav Immun, 28, 196, 10.1016/j.bbi.2012.11.013 · DOI
  62. Smolders, 2015, Maternal immune activation evoked by polyinosinic:polycytidylic acid does not evoke microglial cell activation in the embryo, Front Cell Neurosci, 9, 301, 10.3389/fncel.2015.00301 · DOI
  63. Garay, 2013, Maternal immune activation causes age- and region-specific changes in brain cytokines in offspring throughout development, Brain Behav Immun, 31, 54, 10.1016/j.bbi.2012.07.008 · DOI · Paper page
  64. Giovanoli, 2015, Late prenatal immune activation causes hippocampal deficits in the absence of persistent inflammation across aging, J Neuroinflammation, 12, 221, 10.1186/s12974-015-0437-y · DOI · Paper page
  65. Giovanoli, 2016, Prenatal immune activation causes hippocampal synaptic deficits in the absence of overt microglia anomalies, Brain Behav Immun, 55, 25, 10.1016/j.bbi.2015.09.015 · DOI
  66. Antonson, 2017, Maternal viral infection during pregnancy elicits anti-social behavior in neonatal piglet offspring independent of postnatal microglial cell activation, Brain Behav Immun, 59, 300, 10.1016/j.bbi.2016.09.019 · DOI
  67. Bhattacharya, 2017, Role of Neuro-Immunological Factors in the Pathophysiology of Mood Disorders: Implications for Novel Therapeutics for Treatment Resistant Depression, Curr Top Behav Neurosci, 31, 339, 10.1007/7854_2016_43 · DOI
  68. Tong, 2016, Role of microglia in embryonic neurogenesis, Exp Biol Med (Maywood), 241, 1669, 10.1177/1535370216664430 · DOI
  69. Fatemi, 2008, Maternal infection leads to abnormal gene regulation and brain atrophy in mouse offspring: Implications for genesis of neurodevelopmental disorders, Schizophr Res, 99, 56, 10.1016/j.schres.2007.11.018 · DOI · Paper page
  70. Le Belle, 2014, Maternal inflammation contributes to brain overgrowth and autism-associated behaviors through altered redox signaling in stem and progenitor cells, Stem Cell Reports, 3, 725, 10.1016/j.stemcr.2014.09.004 · DOI · Paper page
  71. Piontkewitz, 2011, Abnormal trajectories of neurodevelopment and behavior following in utero insult in the rat, Biol Psychiatry, 70, 842, 10.1016/j.biopsych.2011.06.007 · DOI
  72. Kriegstein, 2006, Patterns of neural stem and progenitor cell division may underlie evolutionary cortical expansion, Nat Rev Neurosci, 7, 883, 10.1038/nrn2008 · DOI · Paper page
  73. Chen, 2017, Developmental neurogenetics and multimodal neuroimaging of sex differences in autism, Brain Imaging Behav, 11, 38, 10.1007/s11682-015-9504-3 · DOI
  74. Liu, 2013, Effects of maternal immune activation on adult neurogenesis in the subventricular zone-olfactory bulb pathway and olfactory discrimination, Schizophr Res, 151, 1, 10.1016/j.schres.2013.09.007 · DOI
  75. Khan, 2014, Long-term effects of maternal immune activation on depression-like behavior in the mouse, Transl Psychiatry, 4, e363, 10.1038/tp.2013.132 · DOI
  76. Aavani, 2015, Maternal immune activation produces cerebellar hyperplasia and alterations in motor and social behaviors in male and female mice, Cerebellum, 14, 491, 10.1007/s12311-015-0669-5 · DOI
  77. Wallace, 2010, Prenatal infection decreases calbindin, decreases Purkinje cell volume and density and produces long-term motor deficits in Sprague-Dawley rats, Dev Neurosci, 32, 302, 10.1159/000319506 · DOI
  78. Wischhof, 2015, Prenatal LPS-exposure—a neurodevelopmental rat model of schizophrenia—differentially affects cognitive functions, myelination and parvalbumin expression in male and female offspring, Prog Neuropsychopharmacol Biol Psychiatry, 57, 17, 10.1016/j.pnpbp.2014.10.004 · DOI
  79. Rousset, 2006, Maternal exposure to LPS induces hypomyelination in the internal capsule and programmed cell death in the deep gray matter in newborn rats, Pediatr Res, 59, 428, 10.1203/01.pdr.0000199905.08848.55 · DOI
  80. Marx, 2001, Cytokine effects on cortical neuron MAP-2 immunoreactivity: Implications for schizophrenia, Biol Psychiatry, 50, 743, 10.1016/S0006-3223(01)01209-4 · DOI
  81. Fatemi, 1999, Defective corticogenesis and reduction in Reelin immunoreactivity in cortex and hippocampus of prenatally infected neonatal mice, Mol Psychiatry, 4, 145, 10.1038/sj.mp.4000520 · DOI
  82. Corradini, 2018, Maternal immune activation delays excitatory-to-inhibitory gamma-aminobutyric acid switch in offspring, Biol Psychiatry, 83, 680, 10.1016/j.biopsych.2017.09.030 · DOI
  83. Cassella, 2016, Maternal immune activation alters glutamic acid decarboxylase-67 expression in the brains of adult rat offspring, Schizophr Res, 171, 195, 10.1016/j.schres.2016.01.041 · DOI
  84. Paylor, 2016, Developmental disruption of perineuronal nets in the medial prefrontal cortex after maternal immune activation, Sci Rep, 6, 37580, 10.1038/srep37580 · DOI
  85. Mauney, 2013, Developmental pattern of perineuronal nets in the human prefrontal cortex and their deficit in schizophrenia, Biol Psychiatry, 74, 427, 10.1016/j.biopsych.2013.05.007 · DOI · Paper page
  86. Connor, 2012, Maternal immune activation alters behavior in adult offspring, with subtle changes in the cortical transcriptome and epigenome, Schizophr Res, 140, 175, 10.1016/j.schres.2012.06.037 · DOI
  87. Richetto, 2017, Genome-wide DNA methylation changes in a mouse model of infection-mediated neurodevelopmental disorders, Biol Psychiatry, 81, 265, 10.1016/j.biopsych.2016.08.010 · DOI · Paper page
  88. Pendyala, 2017, Maternal immune activation causes behavioral impairments and altered cerebellar cytokine and synaptic protein expression, Neuropsychopharmacology, 42, 1435, 10.1038/npp.2017.7 · DOI
  89. Elmer, 2013, MHCI requires MEF2 transcription factors to negatively regulate synapse density during development and in disease, J Neurosci, 33, 13791, 10.1523/JNEUROSCI.2366-13.2013 · DOI · Paper page
  90. Fernandez de Cossio, 2017, Prenatal infection leads to ASD-like behavior and altered synaptic pruning in the mouse offspring, Brain Behav Immun, 63, 88, 10.1016/j.bbi.2016.09.028 · DOI
  91. Gilmore, 2004, Prenatal infection and risk for schizophrenia: IL-1beta, IL-6, and TNFalpha inhibit cortical neuron dendrite development, Neuropsychopharmacology, 29, 1221, 10.1038/sj.npp.1300446 · DOI
  92. Stumm, 2007, CXC chemokine receptor 4 regulates neuronal migration and axonal pathfinding in the developing nervous system: Implications for neuronal regeneration in the adult brain, J Mol Endocrinol, 38, 377, 10.1677/JME-06-0032 · DOI
  93. Escobar, 2011, Early, time-dependent disturbances of hippocampal synaptic transmission and plasticity after in utero immune challenge, Biol Psychiatry, 70, 992, 10.1016/j.biopsych.2011.01.009 · DOI
  94. Ito, 2010, Maternal immune activation alters nonspatial information processing in the hippocampus of the adult offspring, Brain Behav Immun, 24, 930, 10.1016/j.bbi.2010.03.004 · DOI
  95. Patrich, 2016, Maturation- and sex-sensitive depression of hippocampal excitatory transmission in a rat schizophrenia model, Brain Behav Immun, 51, 240, 10.1016/j.bbi.2015.08.021 · DOI
  96. Ronovsky, 2017, Maternal immune activation transgenerationally modulates maternal care and offspring depression-like behavior, Brain Behav Immun, 63, 127, 10.1016/j.bbi.2016.10.016 · DOI
  97. Ronovsky, 2016, Animal models of maternal immune activation in depression research, Curr Neuropharmacol, 14, 688, 10.2174/1570159X14666151215095359 · DOI
  98. Depino, 2015, Early prenatal exposure to LPS results in anxiety- and depression-related behaviors in adulthood, Neuroscience, 299, 56, 10.1016/j.neuroscience.2015.04.065 · DOI · Paper page
  99. Majidi-Zolbanin, 2015, Prenatal maternal immune activation increases anxiety- and depressive-like behaviors in offspring with experimental autoimmune encephalomyelitis, Neuroscience, 294, 69, 10.1016/j.neuroscience.2015.03.016 · DOI
  100. Zhang, 2015, Maternal immune activation differentially impacts mature and adult-born hippocampal neurons in male mice, Brain Behav Immun, 45, 60, 10.1016/j.bbi.2014.10.010 · DOI
  101. Babri, 2014, Strain-dependent effects of prenatal maternal immune activation on anxiety- and depression-like behaviors in offspring, Brain Behav Immun, 37, 164, 10.1016/j.bbi.2013.12.003 · DOI
  102. Lin, 2014, Prenatal lipopolysaccharide exposure increases depression-like behaviors and reduces hippocampal neurogenesis in adult rats, Behav Brain Res, 259, 24, 10.1016/j.bbr.2013.10.034 · DOI
  103. Smith, 2007, Maternal immune activation alters fetal brain development through interleukin-6, J Neurosci, 27, 10695, 10.1523/JNEUROSCI.2178-07.2007 · DOI · Paper page
  104. Mena, 2016, Reduced prepulse inhibition as a biomarker of schizophrenia, Front Behav Neurosci, 10, 202, 10.3389/fnbeh.2016.00202 · DOI
  105. Borrell, 2002, Prenatal immune challenge disrupts sensorimotor gating in adult rats. Implications for the etiopathogenesis of schizophrenia, Neuropsychopharmacology, 26, 204, 10.1016/S0893-133X(01)00360-8 · DOI
  106. Meehan, 2017, Effects of immune activation during early or late gestation on schizophrenia-related behaviour in adult rat offspring, Brain Behav Immun, 63, 8, 10.1016/j.bbi.2016.07.144 · DOI
  107. Careaga, 2017, Maternal immune activation and autism spectrum disorder: From rodents to nonhuman and human primates, Biol Psychiatry, 81, 391, 10.1016/j.biopsych.2016.10.020 · DOI · Paper page
  108. Malkova, 2012, Maternal immune activation yields offspring displaying mouse versions of the three core symptoms of autism, Brain Behav Immun, 26, 607, 10.1016/j.bbi.2012.01.011 · DOI · Paper page
  109. Xuan, 2014, Gender-dependent effects of maternal immune activation on the behavior of mouse offspring, PLoS One, 9, e104433, 10.1371/journal.pone.0104433 · DOI
  110. Ehninger, 2012, Gestational immune activation and Tsc2 haploinsufficiency cooperate to disrupt fetal survival and may perturb social behavior in adult mice, Mol Psychiatry, 17, 62, 10.1038/mp.2010.115 · DOI · Paper page
  111. Bauman, 2014, Activation of the maternal immune system during pregnancy alters behavioral development of rhesus monkey offspring, Biol Psychiatry, 75, 332, 10.1016/j.biopsych.2013.06.025 · DOI · Paper page
  112. Parker-Athill, 2010, Maternal immune activation and autism spectrum disorder: Interleukin-6 signaling as a key mechanistic pathway, Neurosignals, 18, 113, 10.1159/000319828 · DOI · Paper page
  113. Layeghifard, 2017, Disentangling interactions in the microbiome: A network perspective, Trends Microbiol, 25, 217, 10.1016/j.tim.2016.11.008 · DOI
  114. McCarroll, 2013, Progress in the genetics of polygenic brain disorders: Significant new challenges for neurobiology, Neuron, 80, 578, 10.1016/j.neuron.2013.10.046 · DOI
  115. Iossifov, 2012, De novo gene disruptions in children on the autistic spectrum, Neuron, 74, 285, 10.1016/j.neuron.2012.04.009 · DOI · Paper page
  116. Ortutay, 2006, Immunome: A reference set of genes and proteins for systems biology of the human immune system, Cell Immunol, 244, 87, 10.1016/j.cellimm.2007.01.012 · DOI

Cited by

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Metadata

Authors
Gumusoglu, S. B., & Stevens, H. E.
Venue
Biological Psychiatry
Publisher
Elsevier BV
Published
2019-01
Volume
85
Issue
2
Pages
107-121
ISSN
0006-3223
DOI
10.1016/j.biopsych.2018.08.008
Cited by
220
References
33
Language
en
Licence
Funders
  • Roy J. Carver Charitable Trust
  • Graduate College, University of Iowa

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