{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2026,7,31]],"date-time":"2026-07-31T09:39:37Z","timestamp":1785490777641,"version":"3.56.0"},"reference-count":309,"publisher":"Frontiers Media SA","license":[{"start":{"date-parts":[[2018,10,23]],"date-time":"2018-10-23T00:00:00Z","timestamp":1540252800000},"content-version":"unspecified","delay-in-days":0,"URL":"https:\/\/creativecommons.org\/licenses\/by\/4.0\/"}],"funder":[{"DOI":"10.13039\/501100000269","name":"Economic and Social Research Council","doi-asserted-by":"publisher","award":["1474910"],"award-info":[{"award-number":["1474910"]}],"id":[{"id":"10.13039\/501100000269","id-type":"DOI","asserted-by":"publisher"}]},{"DOI":"10.13039\/501100003329","name":"Ministerio de Econom\u00eda y Competitividad","doi-asserted-by":"publisher","award":["FFI2014-61888-EXP"],"award-info":[{"award-number":["FFI2014-61888-EXP"]}],"id":[{"id":"10.13039\/501100003329","id-type":"DOI","asserted-by":"publisher"}]},{"DOI":"10.13039\/501100003329","name":"Ministerio de Econom\u00eda y Competitividad","doi-asserted-by":"publisher","award":["FFI-2013-43823-P"],"award-info":[{"award-number":["FFI-2013-43823-P"]}],"id":[{"id":"10.13039\/501100003329","id-type":"DOI","asserted-by":"publisher"}]},{"DOI":"10.13039\/501100003329","name":"Ministerio de Econom\u00eda y Competitividad","doi-asserted-by":"publisher","award":["FEDER"],"award-info":[{"award-number":["FEDER"]}],"id":[{"id":"10.13039\/501100003329","id-type":"DOI","asserted-by":"publisher"}]}],"content-domain":{"domain":["frontiersin.org"],"crossmark-restriction":true},"short-container-title":["Front. Psychol."],"DOI":"10.3389\/fpsyg.2018.01999","type":"journal-article","created":{"date-parts":[[2018,10,23]],"date-time":"2018-10-23T02:40:03Z","timestamp":1540262403000},"update-policy":"https:\/\/doi.org\/10.3389\/crossmark-policy","source":"Crossref","is-referenced-by-count":22,"title":["Toward the Language Oscillogenome"],"prefix":"10.3389","volume":"9","author":[{"given":"Elliot","family":"Murphy","sequence":"first","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Antonio","family":"Ben\u00edtez-Burraco","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]}],"member":"1965","published-online":{"date-parts":[[2018,10,23]]},"reference":[{"key":"B1","doi-asserted-by":"publisher","first-page":"842","DOI":"10.1002\/humu.22816","article-title":"Microdeletions of ELP4 are associated with language impairment, autism spectrum disorder, and mental retardation.","volume":"36","author":"Addis","year":"2015","journal-title":"Hum. Mutat."},{"key":"B2","doi-asserted-by":"publisher","first-page":"5880","DOI":"10.1523\/JNEUROSCI.5462-11.2012","article-title":"Pten deletion in adult hippocampal neural stem\/progenitor cells causes cellular abnormalities and alters neurogenesis.","volume":"32","author":"Amiri","year":"2012","journal-title":"J. Neurosci."},{"key":"B3","doi-asserted-by":"publisher","first-page":"18120","DOI":"10.1073\/pnas.1216398109","article-title":"Candidate autism gene screen identifies critical role for cell-adhesion molecule CASPR2 in dendritic arborization and spine development.","volume":"109","author":"Anderson","year":"2012","journal-title":"Proc. Natl. Acad. Sci. U.S.A."},{"key":"B4","doi-asserted-by":"publisher","DOI":"10.1017\/S0140525X15000631","article-title":"Pr\u00e9cis of after phrenology: neural reuse and the interactive brain.","volume":"39","author":"Anderson","year":"2016","journal-title":"Behav. Brain Sci."},{"key":"B5","doi-asserted-by":"publisher","DOI":"10.1186\/2040-2392-3-12","article-title":"Brain region-specific altered expression and association of mitochondria-related genes in autism.","volume":"3","author":"Anitha","year":"2012","journal-title":"Mol. Autism"},{"key":"B6","doi-asserted-by":"publisher","first-page":"241","DOI":"10.1016\/j.neuroimage.2016.05.066","article-title":"Language-related cerebral oscillatory changes are influenced equally by genetic and environmental factors.","volume":"142","author":"Araki","year":"2016","journal-title":"Neuroimage"},{"key":"B7","doi-asserted-by":"publisher","first-page":"4402","DOI":"10.1074\/jbc.M406440200","article-title":"S100B increases proliferation in PC12 neuronal cells and reduces their responsiveness to nerve growth factor via Akt activation.","volume":"280","author":"Arcuri","year":"2005","journal-title":"J. Biol. Chem."},{"key":"B8","doi-asserted-by":"publisher","first-page":"129","DOI":"10.1016\/j.expneurol.2009.10.011","article-title":"Hepatocyte growth factor (HGF) modulates GABAergic inhibition and seizure susceptibility.","volume":"221","author":"Bae","year":"2010","journal-title":"Exp. Neurol."},{"key":"B9","doi-asserted-by":"publisher","first-page":"230","DOI":"10.1002\/hipo.20887","article-title":"Akt1 deficiency in schizophrenia and impairment of hippocampal plasticity and function.","volume":"22","author":"Balu","year":"2012","journal-title":"Hippocampus"},{"key":"B10","doi-asserted-by":"publisher","first-page":"202","DOI":"10.1016\/j.nicl.2014.08.020","article-title":"Reduced beta band connectivity during number estimation in autism.","volume":"16","author":"Bangel","year":"2014","journal-title":"NeuroImage. Clin."},{"key":"B11","doi-asserted-by":"publisher","first-page":"15276","DOI":"10.1523\/JNEUROSCI.1834-15.2015","article-title":"Interneuron transcriptional dysregulation causes frequency-dependent alterations in the balance of inhibition and excitation in hippocampus.","volume":"35","author":"Bartley","year":"2015","journal-title":"J. Neurosci."},{"key":"B12","doi-asserted-by":"publisher","first-page":"211","DOI":"10.1016\/j.eplepsyres.2013.03.012","article-title":"Cognitive decline in Dravet syndrome: is there a cerebellar role?","volume":"106","author":"Battaglia","year":"2013","journal-title":"Epilepsy Res."},{"key":"B13","doi-asserted-by":"publisher","DOI":"10.1038\/tp.2012.62","article-title":"Evidence for the involvement of ZNF804A in cognitive processes of relevance to reading and spelling.","volume":"2","author":"Becker","year":"2012","journal-title":"Transl. Psychiatry"},{"key":"B14","doi-asserted-by":"publisher","first-page":"162","DOI":"10.1016\/j.ijpsycho.2005.12.013","article-title":"Genetics of human brain oscillations.","volume":"60","author":"Begleiter","year":"2006","journal-title":"Int. J. Psychophysiol."},{"key":"B15","doi-asserted-by":"publisher","first-page":"660","DOI":"10.1016\/j.ccr.2013.10.006","article-title":"Reduced H3K27me3 and DNA hypomethylation are major drivers of gene expression in K27M mutant pediatric high-grade gliomas.","volume":"24","author":"Bender","year":"2013","journal-title":"Cancer Cell"},{"key":"B16","doi-asserted-by":"publisher","DOI":"10.3389\/fpsyg.2015.00794","article-title":"Possible functional links among brain- and skull-related genes selected in modern humans.","volume":"6","author":"Ben\u00edtez-Burraco","year":"2015","journal-title":"Front. Psychol."},{"key":"B17","doi-asserted-by":"publisher","DOI":"10.3389\/fnhum.2016.00120","article-title":"The oscillopathic nature of language deficits in autism: from genes to language evolution.","volume":"10","author":"Ben\u00edtez-Burraco","year":"2016","journal-title":"Front. Hum. Neurosci."},{"key":"B18","first-page":"9","article-title":"\u201cForeword: A bird\u2019s-eye view of human language and evolution,\u201d in","author":"Berwick","year":"2015","journal-title":"Birdsong, Speech, and Language: Exploring the Evolution of Mind and Brain"},{"key":"B19","doi-asserted-by":"publisher","first-page":"89","DOI":"10.1016\/j.tics.2012.12.002","article-title":"Evolution, brain, and the nature of language.","volume":"17","author":"Berwick","year":"2013","journal-title":"Trends Cog. Sci."},{"key":"B20","doi-asserted-by":"publisher","first-page":"15578","DOI":"10.1523\/JNEUROSCI.2217-10.2010","article-title":"Lower-frequency event-related desynchronization: a signature of late mismatch responses to sounds, which is reduced or absent in children with specific language impairment.","volume":"30","author":"Bishop","year":"2010","journal-title":"J. Neurosci."},{"key":"B21","doi-asserted-by":"publisher","DOI":"10.3389\/fpsyg.2014.00282","article-title":"The shape of the human language-ready brain.","volume":"5","author":"Boeckx","year":"","journal-title":"Front. Psychol."},{"key":"B22","doi-asserted-by":"publisher","DOI":"10.3389\/fpsyg.2014.01324","article-title":"Globularity and language-readiness: Generating new predictions by expanding the set of genes of interest.","volume":"5","author":"Boeckx","year":"","journal-title":"Front. Psychol."},{"key":"B23","doi-asserted-by":"publisher","first-page":"1020","DOI":"10.1038\/nn.2371","article-title":"Balanced gene regulation by an embryonic brain ncRNA is critical for adult hippocampal GABA circuitry.","volume":"12","author":"Bond","year":"2009","journal-title":"Nat. Neurosci."},{"key":"B24","doi-asserted-by":"publisher","first-page":"1074","DOI":"10.1111\/ejn.12549","article-title":"Neurophysiological modification of CA1 pyramidal neurons in a transgenic mouse expressing a truncated form of disrupted-in-schizophrenia 1.","volume":"39","author":"Booth","year":"2014","journal-title":"Eur. J. Neurosci."},{"key":"B25","doi-asserted-by":"publisher","first-page":"13973","DOI":"10.1074\/jbc.270.23.13973","article-title":"Stimulation of cannabinoid receptor CB1 induces krox-24 expression in human astrocytoma cells.","volume":"270","author":"Bouaboula","year":"1995","journal-title":"J. Biol. Chem."},{"key":"B26","doi-asserted-by":"publisher","first-page":"1177","DOI":"10.1016\/j.cell.2017.05.038","article-title":"An expanded view of complex traits: from polygenic to omnigenic.","volume":"169","author":"Boyle","year":"2017","journal-title":"Cell"},{"key":"B27","doi-asserted-by":"publisher","first-page":"1026","DOI":"10.1111\/j.1460-9568.2008.06064.x","article-title":"Contextual integration the unusual way: a magnetoencephalographic study of responses to semantic violation in individuals with autism spectrum disorder.","volume":"27","author":"Braeutigam","year":"2008","journal-title":"Eur. J. Neurosci."},{"key":"B28","doi-asserted-by":"publisher","DOI":"10.1038\/tp.2014.136","article-title":"Association between SNAP-25 gene polymorphisms and cognition in autism: functional consequences and potential therapeutic strategies.","volume":"5","author":"Braida","year":"2015","journal-title":"Transl. Psychiatry"},{"key":"B29","doi-asserted-by":"publisher","first-page":"707","DOI":"10.1038\/nrn3120","article-title":"Linking neurodevelopmental and synaptic theories of mental illness through DISC1.","volume":"12","author":"Brandon","year":"2011","journal-title":"Nat. Rev. Neurosci."},{"key":"B30","doi-asserted-by":"publisher","DOI":"10.1186\/1471-2105-7-488","article-title":"Evaluation of clustering algorithms for protein-protein interaction networks.","volume":"7","author":"Broh\u00e9e","year":"2006","journal-title":"BMC Bioinformatics"},{"key":"B31","doi-asserted-by":"publisher","first-page":"210","DOI":"10.1016\/j.nbd.2013.11.001","article-title":"The role of cannabinoid 1 receptor expressing interneurons in behavior.","volume":"63","author":"Brown","year":"2014","journal-title":"Neurobiol. Dis."},{"key":"B32","doi-asserted-by":"publisher","first-page":"1914","DOI":"10.2174\/138161211796718198","article-title":"The role of the urokinase receptor in epilepsy, in disorders of language, cognition, communication and behavior, and in the central nervous system.","volume":"17","author":"Bruneau","year":"2011","journal-title":"Curr. Pharm. Des."},{"key":"B33","doi-asserted-by":"publisher","DOI":"10.3389\/fnhum.2013.00742","article-title":"Altered oscillation patterns and connectivity during picture naming in autism.","volume":"7","author":"Buard","year":"2013","journal-title":"Front. Hum. Neurosci."},{"key":"B34","doi-asserted-by":"publisher","first-page":"556","DOI":"10.1002\/ajhb.20516","article-title":"Apolipoprotein E polymorphism and neuronal plasticity.","volume":"18","author":"Bufill","year":"2006","journal-title":"Am. J. Human Biol."},{"key":"B35","doi-asserted-by":"publisher","first-page":"484","DOI":"10.1002\/ajmg.b.30493","article-title":"Mutation screening of the PTEN gene in patients with autism spectrum disorders and macrocephaly.","author":"Buxbaum","year":"2007","journal-title":"Am. J. Med. Genet. B Neuropsychiatr. Genet."},{"key":"B36","first-page":"359","article-title":"The pharmacology of human information processing.","volume":"20","author":"Callaway","year":"1983","journal-title":"Psychopharmacologia"},{"key":"B37","doi-asserted-by":"publisher","first-page":"705","DOI":"10.1111\/ejn.12453","article-title":"Neurosystems: brain rhythms and cognitive processing.","volume":"39","author":"Cannon","year":"2014","journal-title":"Eur. J. Neurosci."},{"key":"B38","doi-asserted-by":"publisher","DOI":"10.1371\/journal.pone.0046289","article-title":"Resting-state network disruption and APOE genotype in Alzheimer\u2019s disease: a lagged functional connectivity study.","volume":"7","author":"Canuet","year":"2012","journal-title":"PLoS One"},{"key":"B39","doi-asserted-by":"publisher","first-page":"1216","DOI":"10.1038\/ejhg.2010.96","article-title":"Chiari I malformation, delayed gross motor skills, severe speech delay, and epileptiform discharges in a child with FOXP1 haploinsufficiency.","volume":"18","author":"Carr","year":"2010","journal-title":"Eur. J. Hum. Genet."},{"key":"B40","doi-asserted-by":"publisher","first-page":"825","DOI":"10.1038\/ng.2646","article-title":"Targeted resequencing in epileptic encephalopathies identifies de novo mutations in CHD2 and SYNGAP1.","volume":"45","author":"Carvill","year":"2013","journal-title":"Nat. Genet."},{"key":"B41","doi-asserted-by":"publisher","first-page":"1944","DOI":"10.1111\/j.1460-9568.2006.04697.x","article-title":"Variations in the human cannabinoid receptor (CNR1) gene modulate striatal responses to happy faces.","volume":"23","author":"Chakrabarti","year":"2006","journal-title":"Eur. J. Neurosci."},{"key":"B42","doi-asserted-by":"publisher","DOI":"10.1038\/srep33095","article-title":"Akting up in the GABA hypothesis of schizophrenia: Akt1 deficiency modulates GABAergic functions and hippocampus-dependent functions.","volume":"6","author":"Chang","year":"2016","journal-title":"Sci. Rep."},{"key":"B43","doi-asserted-by":"publisher","first-page":"263","DOI":"10.1038\/nature09582","article-title":"Dysfunction in GABA signalling mediates autism-like stereotypies and Rett syndrome phenotypes.","volume":"468","author":"Chao","year":"2010","journal-title":"Nature"},{"key":"B44","doi-asserted-by":"publisher","first-page":"359","DOI":"10.1002\/ajmg.b.30818","article-title":"Association of single nucleotide polymorphisms in a glutamate receptor gene (GRM8) with theta power of event-related oscillations and alcohol dependence.","author":"Chen","year":"2009","journal-title":"Am. J. Med. Genet. B Neuropsychiatr. Genet."},{"key":"B45","doi-asserted-by":"publisher","DOI":"10.1186\/1471-2105-14-128","article-title":"Enrichr: interactive and collaborative HTML5 gene list enrichment analysis tool.","volume":"14","author":"Chen","year":"2013","journal-title":"BMC Bioinformatics"},{"key":"B46","doi-asserted-by":"publisher","first-page":"402","DOI":"10.1016\/j.cell.2014.09.021","article-title":"Identification of causal genetic drivers of human disease through systems-level analysis of regulatory networks.","volume":"159","author":"Chen","year":"2014","journal-title":"Cell"},{"key":"B47","doi-asserted-by":"publisher","DOI":"10.1038\/srep46105","article-title":"Next-generation sequencing identifies novel gene variants and pathways involved in specific language impairment.","volume":"7","author":"Chen","year":"2017","journal-title":"Sci. Rep."},{"key":"B48","doi-asserted-by":"publisher","first-page":"1332","DOI":"10.1016\/j.neuron.2015.02.019","article-title":"Gamma rhythms link prefrontal interneuron dysfunction with cognitive inflexibility in Dlx5\/6(+\/-) mice.","volume":"85","author":"Cho","year":"2015","journal-title":"Neuron"},{"key":"B49","doi-asserted-by":"publisher","first-page":"34","DOI":"10.1038\/nrg3575","article-title":"Systems genetics approaches to understand complex traits.","volume":"15","author":"Civelek","year":"2013","journal-title":"Nat. Rev. Genet."},{"key":"B50","doi-asserted-by":"publisher","first-page":"3490","DOI":"10.1093\/hmg\/ddu057","article-title":"Pten haploinsufficient mice show broad brain overgrowth but selective impairments in autism-relevant behavioral tests.","volume":"23","author":"Clipperton-Allen","year":"2014","journal-title":"Hum. Mol. Genet."},{"key":"B51","doi-asserted-by":"publisher","first-page":"82","DOI":"10.1093\/cercor\/bhk003","article-title":"Cellular patterns of transcription factor expression in developing cortical interneurons.","volume":"16","author":"Cobos","year":"2006","journal-title":"Cereb. Cortex"},{"key":"B52","doi-asserted-by":"publisher","first-page":"1063","DOI":"10.1038\/ng.3092","article-title":"Refining analyses of copy number variation identifies specific genes associated with developmental delay.","volume":"46","author":"Coe","year":"2014","journal-title":"Nat. Genet."},{"key":"B53","doi-asserted-by":"publisher","first-page":"137","DOI":"10.1016\/j.tics.2016.12.008","article-title":"Brain oscillations and the importance of waveform shape.","volume":"21","author":"Cole","year":"2017","journal-title":"Trends Cogn. Sci."},{"key":"B54","doi-asserted-by":"publisher","first-page":"1077","DOI":"10.1086\/301832","article-title":"Linkage-disequilibrium mapping of autistic disorder, with 15q11-13 markers.","volume":"62","author":"Cook","year":"1998","journal-title":"Am. J. Hum. Genet."},{"key":"B55","doi-asserted-by":"publisher","first-page":"364","DOI":"10.1093\/cercor\/bhs316","article-title":"Epileptiform activity and cognitive deficits in SNAP-25+\/- mice are normalized by antiepileptic drugs.","volume":"24","author":"Corradini","year":"2014","journal-title":"Cereb. Cortex"},{"key":"B56","doi-asserted-by":"publisher","first-page":"731","DOI":"10.1136\/jmedgenet-2012-101251","article-title":"The DYRK1A gene is a cause of syndromic intellectual disability with severe microcephaly and epilepsy.","volume":"49","author":"Courcet","year":"2012","journal-title":"J. Med. Genet."},{"key":"B57","doi-asserted-by":"publisher","first-page":"2387","DOI":"10.1002\/hbm.22778","article-title":"Modulation of hippocampal theta and hippocampal-prefrontal cortex function by a schizophrenia risk gene.","volume":"36","author":"Cousijn","year":"2015","journal-title":"Hum. Brain Mapp."},{"key":"B58","doi-asserted-by":"publisher","first-page":"551","DOI":"10.1016\/j.cell.2008.11.043","article-title":"Elongator controls the migration and differentiation of cortical neurons through acetylation of alpha-tubulin.","volume":"136","author":"Creppe","year":"2009","journal-title":"Cell"},{"key":"B59","doi-asserted-by":"publisher","first-page":"493","DOI":"10.3233\/JAD-141872","article-title":"Influence of the APOE \u03b54 allele and mild cognitive impairment diagnosis in the disruption of the MEG resting state functional connectivity in sources space.","volume":"44","author":"Cuesta","year":"2015","journal-title":"J. Alzheimers Dis."},{"key":"B60","doi-asserted-by":"publisher","first-page":"40","DOI":"10.1016\/j.neuroimage.2016.08.012","article-title":"Atypical right hemisphere response to slow temporal modulations in children with developmental dyslexia.","volume":"143","author":"Cutini","year":"2016","journal-title":"Neuroimage"},{"key":"B61","doi-asserted-by":"publisher","first-page":"110","DOI":"10.1007\/s10519-010-9413-6","article-title":"Association of a rare variant with mismatch negativity in a region between KIAA0319 and DCDC2 in Dyslexia.","volume":"41","author":"Czamara","year":"2011","journal-title":"Behav. Genet."},{"key":"B62","doi-asserted-by":"publisher","first-page":"1060","DOI":"10.1101\/gad.1189704","article-title":"Angiopoietin-1 modulates endothelial cell function and gene expression via the transcription factor FKHR (FOXO1).","volume":"18","author":"Daly","year":"2004","journal-title":"Genes Dev."},{"key":"B63","doi-asserted-by":"publisher","first-page":"1505","DOI":"10.1038\/ejhg.2015.21","article-title":"CACNA1A haploinsufficiency causes cognitive impairment, autism and epileptic encephalopathy with mild cerebellar symptoms.","volume":"23","author":"Damaj","year":"2015","journal-title":"Eur. J. Hum. Genet."},{"key":"B64","doi-asserted-by":"publisher","DOI":"10.1371\/journal.pone.0010350","article-title":"Upregulation of PTEN in glioma cells by cord blood mesenchymal stem cells inhibits migration via downregulation of the PI3K\/Akt pathway.","volume":"5","author":"Dasari","year":"2010","journal-title":"PLoS One"},{"key":"B65","doi-asserted-by":"publisher","first-page":"2712","DOI":"10.1523\/JNEUROSCI.3433-10.2011","article-title":"Dynamic causal modeling of subcortical connectivity of language.","volume":"31","author":"David","year":"2011","journal-title":"J. Neurosci."},{"key":"B66","doi-asserted-by":"publisher","first-page":"482","DOI":"10.1016\/j.jns.2016.10.052","article-title":"Hippocampal adult neurogenesis: Does the immune system matter?","volume":"372","author":"de Miranda","year":"2017","journal-title":"J. Neurol Sci."},{"key":"B67","doi-asserted-by":"publisher","first-page":"201","DOI":"10.1016\/j.tics.2010.03.003","article-title":"Towards a bottom-up perspective on animal and human cognition.","volume":"14","author":"de Waal","year":"2010","journal-title":"Trends Cogn. Sci."},{"key":"B68","doi-asserted-by":"publisher","first-page":"447","DOI":"10.1089\/brain.2011.0064","article-title":"Altered structural brain connectivity in healthy carriers of the autism risk gene, CNTNAP2.","volume":"1","author":"Dennis","year":"2011","journal-title":"Brain Connect."},{"key":"B69","doi-asserted-by":"publisher","first-page":"370","DOI":"10.1111\/epi.12502","article-title":"A subset of genomic alterations detected in rolandic epilepsies contains candidate or known epilepsy genes including GRIN2A and PRRT2.","volume":"55","author":"Dimassi","year":"2014","journal-title":"Epilepsia"},{"key":"B70","doi-asserted-by":"publisher","first-page":"158","DOI":"10.1038\/nn.4186","article-title":"Cortical tracking of hierarchical linguistic structures in connected speech.","volume":"19","author":"Ding","year":"2016","journal-title":"Nat. Neurosci."},{"key":"B71","doi-asserted-by":"publisher","first-page":"312","DOI":"10.1016\/j.jad.2010.04.007","article-title":"A genome-wide association study of bipolar disorder in Norwegian individuals, followed by replication in Icelandic sample.","volume":"126","author":"Djurovic","year":"2010","journal-title":"J. Affect. Disord."},{"key":"B72","doi-asserted-by":"publisher","DOI":"10.3389\/fnhum.2013.00785","article-title":"Reduced theta connectivity during set-shifting in children with autism.","volume":"7","author":"Doesburg","year":"2013","journal-title":"Front. Hum. Neurosci."},{"key":"B73","doi-asserted-by":"publisher","first-page":"116","DOI":"10.1016\/j.brainres.2009.07.065","article-title":"Neuregulin 1 transgenic mice display reduced mismatch negativity, contextual fear conditioning and social interactions.","volume":"1294","author":"Ehrlichman","year":"2009","journal-title":"Brain Res."},{"key":"B74","doi-asserted-by":"publisher","first-page":"33","DOI":"10.1097\/00041444-200303000-00006","article-title":"Genetic origins of anxiety in women: a role for a functional catechol-O-methyltransferase polymorphism.","volume":"13","author":"Enoch","year":"2003","journal-title":"Psychiatric Genet."},{"key":"B75","doi-asserted-by":"publisher","first-page":"4349","DOI":"10.1002\/hbm.23313","article-title":"Neural correlates of maintaining generated images in visual working memory.","volume":"37","author":"Ewerdwalbesloh","year":"2016","journal-title":"Hum. Brain Mapp."},{"key":"B76","doi-asserted-by":"publisher","first-page":"1635","DOI":"10.1002\/ar.21299","article-title":"Metabotropic glutamate receptor 5 upregulation in children with autism is associated with underexpression of both Fragile X mental retardation protein and GABAA receptor beta 3 in adults with autism.","volume":"294","author":"Fatemi","year":"2011","journal-title":"Anat. Rec."},{"key":"B77","doi-asserted-by":"publisher","first-page":"1376","DOI":"10.1038\/nature08928","article-title":"Control of cortical GABA circuitry development by Nrg1 and ErbB4 signalling.","volume":"464","author":"Fazzari","year":"2010","journal-title":"Nature"},{"key":"B78","doi-asserted-by":"publisher","first-page":"639","DOI":"10.1007\/s00213-013-2997-9","article-title":"Electrophysiological and behavioral responses to ketamine in mice with reduced Akt1 expression.","volume":"227","author":"Featherstone","year":"2013","journal-title":"Psychopharmacology"},{"key":"B79","doi-asserted-by":"publisher","first-page":"117","DOI":"10.1136\/jmg.2010.084582","article-title":"Reduced expression by SETBP1 haploinsufficiency causes developmental and expressive language delay indicating a phenotype distinct from Schinzel-Giedion syndrome.","volume":"48","author":"Filges","year":"2011","journal-title":"J. Med. Genet."},{"key":"B80","doi-asserted-by":"publisher","first-page":"598","DOI":"10.1016\/j.neuroimage.2008.11.033","article-title":"Lateralization of the serotonin-1A receptor distribution in language areas revealed by PET.","volume":"45","author":"Fink","year":"2009","journal-title":"Neuroimage"},{"key":"B81","doi-asserted-by":"publisher","first-page":"133","DOI":"10.1177\/002221949202500207","article-title":"Electrophysiological correlates of dyslexic subtypes.","volume":"25","author":"Flynn","year":"1992","journal-title":"J. Learn. Disabil."},{"key":"B82","doi-asserted-by":"publisher","DOI":"10.1186\/1744-9081-9-20","article-title":"Behavioral phenotype in five individuals with de novo mutations within the GRIN2B gene.","volume":"9","author":"Freunscht","year":"2013","journal-title":"Behav. Brain Funct."},{"key":"B83","doi-asserted-by":"publisher","first-page":"1105","DOI":"10.1038\/nature09271","article-title":"A novel pathway regulates memory and plasticity via SIRT1 and miR-134.","volume":"466","author":"Gao","year":"2010","journal-title":"Nature"},{"key":"B84","doi-asserted-by":"publisher","first-page":"633","DOI":"10.1016\/j.neuron.2013.10.045","article-title":"Cortical evolution: judge the brain by its cover.","volume":"80","author":"Geschwind","year":"2013","journal-title":"Neuron"},{"key":"B85","doi-asserted-by":"publisher","first-page":"415","DOI":"10.1016\/j.ydbio.2008.07.029","article-title":"Characterization of a distinct subpopulation of striatal projection neurons expressing the Dlx genes in the basal ganglia through the activity of the I56ii enhancer.","volume":"322","author":"Ghanem","year":"2008","journal-title":"Dev. Biol."},{"key":"B86","doi-asserted-by":"publisher","first-page":"1930","DOI":"10.1073\/pnas.0510410103","article-title":"The role of neuregulin-ErbB4 interactions on the proliferation and organization of cells in the subventricular zone.","volume":"103","author":"Ghashghaei","year":"2006","journal-title":"Proc. Natl. Acad. Sci. U.S.A."},{"key":"B87","doi-asserted-by":"publisher","first-page":"567","DOI":"10.1542\/peds.99.4.567","article-title":"The clinical phenotype of succinic semialdehyde dehydrogenase deficiency (4-hydroxybutyric aciduria): case reports of 23 new patients.","volume":"99","author":"Gibson","year":"1997","journal-title":"Pediatrics"},{"key":"B88","doi-asserted-by":"publisher","first-page":"99","DOI":"10.1016\/j.jns.2015.03.042","article-title":"Two families with novel missense mutations in COL4A1: when diagnosis can be missed.","volume":"352","author":"Giorgio","year":"2015","journal-title":"J. Neurol Sci."},{"key":"B89","doi-asserted-by":"publisher","first-page":"511","DOI":"10.1038\/nn.3063","article-title":"Cortical oscillations and speech processing: emerging computational principles and operations.","volume":"15","author":"Giraud","year":"2012","journal-title":"Nat. Neurosci."},{"key":"B90","doi-asserted-by":"publisher","first-page":"37","DOI":"10.1016\/j.conb.2012.09.003","article-title":"Neurogenetics and auditory processing in developmental dyslexia.","volume":"23","author":"Giraud","year":"2013","journal-title":"Curr. Opin. Neurobiol"},{"key":"B91","doi-asserted-by":"publisher","first-page":"804","DOI":"10.1038\/nn.3710","article-title":"Cellular origins of auditory event-related potential deficits in Rett syndrome.","volume":"17","author":"Goffin","year":"2014","journal-title":"Nat. Neurosci."},{"key":"B92","doi-asserted-by":"publisher","DOI":"10.1186\/1471-2350-8-66","article-title":"Exploring the functional role of the CHRM2 gene in human cognition: results from a dense genotyping and brain expression study.","volume":"8","author":"Gosso","year":"2007","journal-title":"BMC Med. Genet."},{"key":"B93","doi-asserted-by":"publisher","first-page":"1","DOI":"10.1016\/j.jml.2013.03.001","article-title":"Impaired perception of syllable stress in children with dyslexia: a longitudinal study.","volume":"69","author":"Goswami","year":"2013","journal-title":"J. Mem. Lang."},{"key":"B94","doi-asserted-by":"publisher","first-page":"213","DOI":"10.1016\/j.neubiorev.2017.01.036","article-title":"A revival of the homo loquens as a builder of labeled structures: neurocognitive considerations.","author":"Goucha","year":"2017","journal-title":"Neurosci. Biobehav. Rev."},{"key":"B95","doi-asserted-by":"publisher","first-page":"710","DOI":"10.1126\/science.1188021","article-title":"A draft sequence of the neandertal genome.","volume":"328","author":"Green","year":"2010","journal-title":"Science"},{"key":"B96","doi-asserted-by":"publisher","first-page":"190","DOI":"10.1016\/j.nbd.2012.01.007","article-title":"DYRK1A: a master regulatory protein controlling brain growth.","volume":"46","author":"Guedj","year":"2012","journal-title":"Neurobiol. Dis."},{"key":"B97","doi-asserted-by":"publisher","first-page":"13223","DOI":"10.1074\/jbc.M110.102574","article-title":"DYRK1A and DYRK3 promote cell survival through phosphorylation and activation of SIRT1.","volume":"285","author":"Guo","year":"2010","journal-title":"J. Biol. Chem."},{"key":"B98","doi-asserted-by":"publisher","first-page":"1075","DOI":"10.1016\/j.biopsych.2007.12.005","article-title":"Activation of cannabinoid-1 receptors disrupts sensory gating and neuronal oscillation: relevance to schizophrenia.","volume":"63","author":"Haj\u00f3s","year":"2008","journal-title":"Biol. Psychiatry"},{"key":"B99","doi-asserted-by":"publisher","first-page":"2952","DOI":"10.1016\/j.neuroimage.2011.09.075","article-title":"Reduced phase locking to slow amplitude modulation in adults with dyslexia: an MEG study.","volume":"59","author":"H\u00e4m\u00e4l\u00e4inen","year":"2012","journal-title":"NeuroImage"},{"key":"B100","doi-asserted-by":"publisher","first-page":"2277","DOI":"10.1046\/j.1460-9568.2003.02665.x","article-title":"Expression patterns and subcellular localization of the Down syndrome candidate protein MNB\/DYRK1A suggest a role in late neuronal differentiation.","volume":"17","author":"H\u00e4mmerle","year":"2003","journal-title":"Eur. J. Neurosci."},{"key":"B101","doi-asserted-by":"crossref","first-page":"1569","DOI":"10.1126\/science.298.5598.1569","article-title":"The Faculty of Language: What is it, who has it, and how did it evolve?","volume":"298","author":"Hauser","year":"2002","journal-title":"Science"},{"key":"B102","doi-asserted-by":"publisher","first-page":"14223","DOI":"10.1523\/JNEUROSCI.3157-11.2011","article-title":"Altered neocortical rhythmic activity states in Fmr1 KO mice are due to enhanced mGluR5 signaling and involve changes in excitatory circuitry.","volume":"31","author":"Hays","year":"2011","journal-title":"J. Neurosci."},{"key":"B103","doi-asserted-by":"publisher","DOI":"10.3389\/fncel.2010.00018","article-title":"GABAergic synapse properties may explain genetic variation in hippocampal network oscillations in mice.","volume":"4","author":"Heistek","year":"2010","journal-title":"Front. Cell. Neurosci."},{"key":"B104","doi-asserted-by":"publisher","DOI":"10.1371\/journal.pone.0132456","article-title":"The rat homolog of the schizophrenia susceptibility gene ZNF804A is highly expressed during brain development, particularly in growth cones.","volume":"10","author":"Hinna","year":"2015","journal-title":"PLoS One"},{"key":"B105","doi-asserted-by":"publisher","first-page":"1651","DOI":"10.1111\/epi.13506","article-title":"The spectrum of epilepsy and electroencephalographic abnormalities due to SHANK3 loss-of-function mutations.","volume":"57","author":"Holder","year":"2016","journal-title":"Epilepsia"},{"key":"B106","doi-asserted-by":"publisher","first-page":"4143","DOI":"10.1073\/pnas.94.8.4143","article-title":"Mice devoid of gamma-aminobutyrate type A receptor beta3 subunit have epilepsy, cleft palate, and hypersensitive behavior.","volume":"94","author":"Homanics","year":"1997","journal-title":"Proc. Natl. Acad. Sci. U.S.A."},{"key":"B107","doi-asserted-by":"publisher","first-page":"93","DOI":"10.1038\/79246","article-title":"Autosomal recessive lissencephaly with cerebellar hypoplasia is associated with human RELN mutations.","volume":"26","author":"Hong","year":"2000","journal-title":"Nat. Genet"},{"key":"B108","doi-asserted-by":"publisher","first-page":"107","DOI":"10.1016\/j.neuroscience.2013.12.040","article-title":"Neuregulin 1\/ErbB4 enhances synchronized oscillations of prefrontal cortex neurons via inhibitory synapses.","volume":"261","author":"Hou","year":"2014","journal-title":"Neuroscience"},{"key":"B109","doi-asserted-by":"publisher","first-page":"115","DOI":"10.1016\/j.jphs.2016.10.002","article-title":"Human GRIN2B variants in neurodevelopmental disorders.","volume":"132","author":"Hu","year":"2016","journal-title":"J. Pharmacol. Sci."},{"key":"B110","doi-asserted-by":"publisher","DOI":"10.3389\/fnbeh.2014.00455","article-title":"Investigation of gene effects and epistatic interactions between Akt1 and neuregulin 1 in the regulation of behavioral phenotypes and social functions in genetic mouse models of schizophrenia.","volume":"8","author":"Huang","year":"2015","journal-title":"Front. Behav. Neurosci."},{"key":"B111","doi-asserted-by":"publisher","first-page":"2479","DOI":"10.1242\/jcs.001222","article-title":"Dynamic FoxO transcription factors.","volume":"120","author":"Huang","year":"2007","journal-title":"J. Cell Sci."},{"key":"B112","doi-asserted-by":"publisher","first-page":"824","DOI":"10.1194\/jlr.R075481","article-title":"Apolipoprotein E and Alzheimer\u2019s disease: the influence of apolipoprotein E on amyloid-\u03b2 and other amyloidogenic proteins.","volume":"58","author":"Huynh","year":"2017","journal-title":"J. Lipid Res."},{"key":"B113","doi-asserted-by":"publisher","first-page":"2920","DOI":"10.1073\/pnas.0511197103","article-title":"Voltage-gated ion channels in the axon initial segment of human cortical pyramidal cells and their relationship with chandelier cells.","volume":"103","author":"Inda","year":"2006","journal-title":"Proc. Natl. Acad. Sci. U.S.A."},{"key":"B114","doi-asserted-by":"publisher","DOI":"10.1371\/journal.pone.0012278","article-title":"Altered ultrasonic vocalization and impaired learning and memory in Angelman syndrome mouse model with a large maternal deletion from Ube3a to Gabrb3.","volume":"5","author":"Jiang","year":"2010","journal-title":"PLoS One"},{"key":"B115","doi-asserted-by":"publisher","first-page":"84","DOI":"10.1016\/j.bbr.2017.03.048","article-title":"An oscillopathic approach to developmental dyslexia: from genes to speech processing.","volume":"329","author":"Jim\u00e9nez-Bravo","year":"2017","journal-title":"Behav. Brain Res."},{"key":"B116","doi-asserted-by":"publisher","DOI":"10.3389\/fnhum.2015.00171","article-title":"Atypical coordination of cortical oscillations in response to speech in autism.","volume":"9","author":"Jochaut","year":"2015","journal-title":"Front. Hum. Neurosci."},{"key":"B117","doi-asserted-by":"publisher","first-page":"4187","DOI":"10.1113\/jphysiol.2014.279083","article-title":"5-Hydroxytryptamine1A receptor-activation hyperpolarizes pyramidal cells and suppresses hippocampal gamma oscillations via Kir3 channel activation.","volume":"592","author":"Johnston","year":"2014","journal-title":"J. Physiol."},{"key":"B118","doi-asserted-by":"publisher","first-page":"75","DOI":"10.1016\/j.ijpsycho.2004.02.004","article-title":"Linkage and linkage disequilibrium of evoked EEG oscillations with CHRM2 receptor gene polymorphisms: implications for human brain dynamics and cognition.","volume":"53","author":"Jones","year":"2004","journal-title":"Int. J. Psychophysiol."},{"key":"B119","doi-asserted-by":"publisher","first-page":"2017","DOI":"10.1111\/epi.12839","article-title":"Aberrant expression of miR-218 and miR-204 in human mesial temporal lobe epilepsy and hippocampal sclerosis-Convergence on axonal guidance.","volume":"55","author":"Kaalund","year":"2014","journal-title":"Epilepsia"},{"key":"B120","doi-asserted-by":"publisher","first-page":"91","DOI":"10.1016\/j.ydbio.2011.07.016","article-title":"Hes1 regulates the number and anterior-posterior patterning of mesencephalic dopaminergic neurons at the mid\/hindbrain boundary (isthmus).","volume":"358","author":"Kameda","year":"2011","journal-title":"Dev. Biol."},{"key":"B121","doi-asserted-by":"publisher","first-page":"220","DOI":"10.1016\/j.neuroscience.2009.12.004","article-title":"Molecular characterization of the intercalated cell masses of the amygdala: implications for the relationship with the striatum.","volume":"166","author":"Kaoru","year":"2010","journal-title":"Neuroscience"},{"key":"B122","doi-asserted-by":"publisher","first-page":"1487","DOI":"10.1002\/ajmg.a.35911","article-title":"A new single gene deletion on 2q34: ERBB4 is associated with intellectual disability.","author":"Kasnauskiene","year":"2013","journal-title":"Am. J. Med. Genet. A"},{"key":"B123","doi-asserted-by":"publisher","first-page":"225","DOI":"10.1002\/ajmg.a.30229","article-title":"Autism spectrum disorder in fragile X syndrome: communication, social interaction, and specific behaviors.","volume":"129","author":"Kaufmann","year":"2004","journal-title":"Am. J. Med. Genet. A"},{"key":"B124","doi-asserted-by":"publisher","DOI":"10.1038\/tp.2017.20","article-title":"Ablation of neuropsin-neuregulin 1 signaling imbalances ErbB4 inhibitory networks and disrupts hippocampal gamma oscillation.","volume":"7","author":"Kawata","year":"2017","journal-title":"Transl. Psychiatry"},{"key":"B125","doi-asserted-by":"publisher","first-page":"601","DOI":"10.1016\/j.neubiorev.2016.10.002","article-title":"Brain oscillations and connectivity in autism spectrum disorders (ASD): new approaches to methodology, measurement and modelling.","volume":"71","author":"Kessler","year":"2016","journal-title":"Neurosci. Biobehav. Rev."},{"key":"B126","doi-asserted-by":"publisher","first-page":"3","DOI":"10.1016\/j.tins.2014.09.007","article-title":"Thalamic pathways underlying prefrontal cortex\u2013medial temporal lobe oscillatory interactions.","volume":"38","author":"Ketz","year":"2015","journal-title":"Trends Neurosci."},{"key":"B127","doi-asserted-by":"publisher","first-page":"394","DOI":"10.1016\/j.nicl.2013.03.003","article-title":"Altered brain connectivity in 3-to 7-year-old children with autism spectrum disorder.","volume":"2","author":"Kikuchi","year":"2013","journal-title":"NeuroImage. Clin."},{"key":"B128","doi-asserted-by":"publisher","DOI":"10.1371\/journal.pbio.2000219","article-title":"Sequence learning modulates neural responses and oscillatory coupling in human and monkey auditory cortex.","volume":"15","author":"Kikuchi","year":"2017","journal-title":"PLoS Biol."},{"key":"B129","doi-asserted-by":"publisher","first-page":"3406","DOI":"10.1002\/hbm.20761","article-title":"Genetic variation in the schizophrenia-risk gene neuregulin 1 correlates with brain activation and impaired speech production in a verbal fluency task in healthy individuals.","volume":"30","author":"Kircher","year":"2009","journal-title":"Hum. Brain Mapp."},{"key":"B130","doi-asserted-by":"publisher","DOI":"10.3389\/fnsys.2013.00032","article-title":"Functional roles of the thalamus for language capacities.","volume":"7","author":"Klostermann","year":"2013","journal-title":"Front. Syst. Neurosci."},{"key":"B131","doi-asserted-by":"publisher","first-page":"525","DOI":"10.1007\/s00381-013-2047-2","article-title":"Distinct neurological features in a patient with Schinzel-Giedion syndrome caused by a recurrent SETBP1 mutation.","volume":"29","author":"Ko","year":"2013","journal-title":"Childs Nerv. Syst"},{"key":"B132","doi-asserted-by":"publisher","first-page":"987","DOI":"10.1016\/j.biopsych.2011.10.002","article-title":"Differential role of NR2A and NR2B subunits in N-methyl-D-aspartate receptor antagonist-induced aberrant cortical gamma oscillations.","volume":"71","author":"Kocsis","year":"2012","journal-title":"Biol. Psychiatry"},{"key":"B133","doi-asserted-by":"publisher","first-page":"213","DOI":"10.1038\/nature08549","article-title":"Human-specific transcriptional regulation of CNS development genes by FOXP2.","volume":"462","author":"Konopka","year":"2009","journal-title":"Nature"},{"key":"B134","doi-asserted-by":"publisher","first-page":"652","DOI":"10.1038\/ejhg.2015.178","article-title":"The Koolen-de Vries syndrome: a phenotypic comparison of patients with a 17q21.31 microdeletion versus a KANSL1 sequence variant.","volume":"24","author":"Koolen","year":"2016","journal-title":"Eur. J. Hum. Genet."},{"key":"B135","doi-asserted-by":"publisher","first-page":"1319","DOI":"10.1016\/j.neuron.2014.08.016","article-title":"Beyond the connectome: the dynome.","volume":"83","author":"Kopell","year":"2014","journal-title":"Neuron"},{"key":"B136","doi-asserted-by":"publisher","DOI":"10.1542\/peds.2015-2469","article-title":"Genome-wide association and exome sequencing study of language disorder in an isolated population.","volume":"137","author":"Kornilov","year":"2016","journal-title":"Pediatrics"},{"key":"B137","doi-asserted-by":"publisher","DOI":"10.1371\/journal.pone.0046995","article-title":"CNTNAP2 and language processing in healthy individuals as measured with ERPs.","volume":"7","author":"Kos","year":"2012","journal-title":"PLoS One"},{"key":"B138","doi-asserted-by":"publisher","first-page":"690","DOI":"10.1016\/j.psychres.2012.12.022","article-title":"Decreased fragile X mental retardation protein (FMRP) is associated with lower IQ and earlier illness onset in patients with schizophrenia.","volume":"210","author":"Kov\u00e1cs","year":"2013","journal-title":"Psychiatry Res."},{"key":"B139","doi-asserted-by":"publisher","first-page":"198","DOI":"10.1016\/j.tics.2006.03.001","article-title":"Generalist genes: implications for cognitive sciences.","volume":"10","author":"Kovas","year":"2006","journal-title":"Trends Cogn. Sci."},{"key":"B140","doi-asserted-by":"publisher","first-page":"459","DOI":"10.1007\/s00406-009-0010-8","article-title":"The effect of the COMT val(158)met polymorphism on neural correlates of semantic verbal fluency.","volume":"259","author":"Krug","year":"2009","journal-title":"Eur. Arch. Psychiatry Clin. Neurosci."},{"key":"B141","doi-asserted-by":"publisher","first-page":"1831","DOI":"10.1016\/j.neuroimage.2009.09.028","article-title":"Effect of CACNA1C rs1006737 on neural correlates of verbal fluency in healthy individuals.","volume":"49","author":"Krug","year":"2010","journal-title":"Neuroimage"},{"key":"B142","doi-asserted-by":"publisher","DOI":"10.1371\/journal.pone.0083218","article-title":"Identification of putative target genes of the transcription factor RUNX2.","volume":"8","author":"Kuhlwilm","year":"2013","journal-title":"PLoS One"},{"key":"B143","doi-asserted-by":"publisher","first-page":"W90","DOI":"10.1093\/nar\/gkw377","article-title":"Enrichr: a comprehensive gene set enrichment analysis web server 2016 update.","volume":"44","author":"Kuleshov","year":"2016","journal-title":"Nucleic Acids Res."},{"key":"B144","doi-asserted-by":"publisher","first-page":"1371","DOI":"10.5665\/sleep.4972","article-title":"Cacna1c (Cav1.2) modulates electroencephalographic rhythm and rapid eye movement sleep recovery.","volume":"38","author":"Kumar","year":"2015","journal-title":"Sleep"},{"key":"B145","doi-asserted-by":"publisher","DOI":"10.1098\/rspb.2014.1000","article-title":"Representations of specific acoustic patterns in the auditory cortex and hippocampus.","volume":"281","author":"Kumar","year":"2014","journal-title":"Proc. R. Soc. B"},{"key":"B146","doi-asserted-by":"publisher","first-page":"966","DOI":"10.1523\/JNEUROSCI.4007-11.2012","article-title":"Human ROBO1 regulates interaural interaction in auditory pathways.","volume":"32","author":"Lamminm\u00e4ki","year":"2012","journal-title":"J. Neurosci."},{"key":"B147","doi-asserted-by":"publisher","first-page":"13","DOI":"10.1111\/j.1467-7687.2012.01180.x","article-title":"The COMT Val\/Met polymorphism is associated with reading-related skills and consistent patterns of functional neural activation.","volume":"16","author":"Landi","year":"2013","journal-title":"Dev. Sci."},{"key":"B148","doi-asserted-by":"publisher","DOI":"10.1186\/2040-2392-4-45","article-title":"Transcriptomic analysis of genetically defined autism candidate genes reveals common mechanisms of action.","volume":"4","author":"Lanz","year":"2013","journal-title":"Mol. Autism"},{"key":"B149","doi-asserted-by":"publisher","DOI":"10.3389\/fncel.2015.00094","article-title":"Shank3-mutant mice lacking exon 9 show altered excitation\/inhibition balance, enhanced rearing, and spatial memory deficit.","volume":"9","author":"Lee","year":"2015","journal-title":"Front. Cell Neurosci."},{"key":"B150","doi-asserted-by":"publisher","first-page":"1080","DOI":"10.1016\/j.neuron.2011.11.002","article-title":"Altered low-gamma sampling in auditory cortex accounts for the three main facets of dyslexia.","volume":"72","author":"Lehongre","year":"2011","journal-title":"Neuron"},{"key":"B151","doi-asserted-by":"publisher","first-page":"1061","DOI":"10.1038\/ng.2726","article-title":"GRIN2A mutations in acquired epileptic aphasia and related childhood focal epilepsies and encephalopathies with speech and language dysfunction.","volume":"45","author":"Lesca","year":"2013","journal-title":"Nat. Genet."},{"key":"B152","doi-asserted-by":"publisher","first-page":"1526","DOI":"10.1111\/j.1528-1167.2012.03559.x","article-title":"Epileptic encephalopathies of the Landau-Kleffner and continuous spike and waves during slow-wave sleep types: genomic dissection makes the link with autism.","volume":"53","author":"Lesca","year":"2012","journal-title":"Epilepsia"},{"key":"B153","doi-asserted-by":"publisher","first-page":"2224","DOI":"10.1038\/npp.2016.14","article-title":"Prefrontal white matter structure mediates the influence of GAD1 on working memory.","volume":"41","author":"Lett","year":"2016","journal-title":"Neuropsychopharmacology"},{"key":"B154","doi-asserted-by":"publisher","DOI":"10.1186\/1749-8104-7-10","article-title":"Neuregulin repellent signaling via ErbB4 restricts GABAergic interneurons to migratory paths from ganglionic eminence to cortical destinations.","volume":"7","author":"Li","year":"2012","journal-title":"Neural Dev."},{"key":"B155","doi-asserted-by":"publisher","first-page":"42","DOI":"10.1016\/j.neulet.2015.10.014","article-title":"Evaluating the relationship between reelin gene variants (rs7341475 and rs262355) and schizophrenia: a meta-analysis.","volume":"609","author":"Li","year":"2015","journal-title":"Neurosci. Lett."},{"key":"B156","doi-asserted-by":"publisher","first-page":"490","DOI":"10.1007\/s12035-013-8437-3","article-title":"Sirt1 promotes axonogenesis by deacetylation of Akt and inactivation of GSK3.","volume":"48","author":"Li","year":"2013","journal-title":"Mol. Neurobiol."},{"key":"B157","doi-asserted-by":"publisher","DOI":"10.1155\/2017\/9823501","article-title":"Frequency specific effects of ApoE \u03b54 allele on resting-state networks in nondemented elders.","volume":"2017","author":"Liang","year":"2017","journal-title":"Biomed. Res. Int."},{"key":"B158","doi-asserted-by":"publisher","first-page":"88","DOI":"10.1016\/j.nbd.2011.12.048","article-title":"MeCP2+\/- mouse model of RTT reproduces auditory phenotypes associated with Rett syndrome and replicate select EEG endophenotypes of autism spectrum disorder.","volume":"46","author":"Liao","year":"2012","journal-title":"Neurobiol. Dis."},{"key":"B159","doi-asserted-by":"publisher","first-page":"55","DOI":"10.1002\/evan.20154","article-title":"Speculations about the selective basis for modern human craniofacial form.","volume":"17","author":"Lieberman","year":"2008","journal-title":"Evol. Anthropol."},{"key":"B160","doi-asserted-by":"publisher","first-page":"13882","DOI":"10.1523\/JNEUROSCI.3083-07.2007","article-title":"Genetic contributions to long-range temporal correlations in ongoing oscillations.","volume":"27","author":"Linkenkaer-Hansen","year":"2007","journal-title":"J. Neurosci."},{"key":"B161","doi-asserted-by":"publisher","first-page":"1","DOI":"10.1016\/j.brainres.2013.07.020","article-title":"Genetically engineered bone marrow mesenchymal stem cells improve functional outcome in a rat model of epilepsy.","volume":"1532","author":"Long","year":"2013","journal-title":"Brain. Res."},{"key":"B162","doi-asserted-by":"publisher","first-page":"127","DOI":"10.1016\/j.cell.2006.01.042","article-title":"Tangential neuronal migration controls axon guidance: a role for neuregulin-1 in thalamocortical axon navigation.","volume":"125","author":"L\u00f3pez-Bendito","year":"2006","journal-title":"Cell"},{"key":"B163","doi-asserted-by":"publisher","first-page":"159","DOI":"10.1038\/mp.2015.173","article-title":"Micro-electrode array recordings reveal reductions in both excitation and inhibition in cultured cortical neuron networks lacking Shank3.","volume":"21","author":"Lu","year":"2016","journal-title":"Mol. Psychiatry"},{"key":"B164","doi-asserted-by":"publisher","first-page":"139","DOI":"10.1016\/j.neulet.2010.08.036","article-title":"Elevated plasma S100B concentration is associated with mesial temporal lobe epilepsy in Han Chinese: A case\u2013control study.","volume":"484","author":"Lu","year":"2010","journal-title":"Neurosci. Lett."},{"key":"B165","doi-asserted-by":"publisher","first-page":"193","DOI":"10.1016\/j.biopsycho.2010.11.008","article-title":"Whole genome association scan for genetic polymorphisms influencing information processing speed.","volume":"86","author":"Luciano","year":"2011","journal-title":"Biol. Psychol."},{"key":"B166","doi-asserted-by":"publisher","first-page":"599","DOI":"10.1016\/j.biopsych.2015.10.003","article-title":"Reduced sleep spindles in schizophrenia: a treatable endophenotype that links risk genes to impaired cognition?","volume":"80","author":"Manoach","year":"2015","journal-title":"Biol. Psychiatry"},{"key":"B167","doi-asserted-by":"publisher","DOI":"10.1186\/1471-2350-15-26","article-title":"Autism-epilepsy phenotype with macrocephaly suggests PTEN, but not GLIALCAM, genetic screening.","volume":"15","author":"Marchese","year":"2014","journal-title":"BMC Med. Genet."},{"key":"B168","doi-asserted-by":"publisher","first-page":"69","DOI":"10.1007\/s12017-015-8378-2","article-title":"Targeted gene resequencing (astrochip) to explore the tripartite synapse in autism-epilepsy phenotype with macrocephaly.","volume":"18","author":"Marchese","year":"2016","journal-title":"Neuromol. Med."},{"key":"B169","doi-asserted-by":"publisher","first-page":"216","DOI":"10.1016\/j.ejmg.2012.01.005","article-title":"372 kb microdeletion in 18q12.3 causing SETBP1 haploinsufficiency associated with mild mental retardation and expressive speech impairment.","volume":"55","author":"Marseglia","year":"2012","journal-title":"Eur. J. Med. Genet."},{"key":"B170","doi-asserted-by":"publisher","first-page":"477","DOI":"10.1016\/j.ajhg.2007.12.009","article-title":"Structural variation of chromosomes in autism spectrum disorder.","volume":"82","author":"Marshall","year":"2008","journal-title":"Am. J. Hum. Genet."},{"key":"B171","doi-asserted-by":"publisher","DOI":"10.1371\/journal.pone.0016234","article-title":"Suppression of osteosarcoma cell invasion by chemotherapy is mediated by urokinase plasminogen activator activity via up-regulation of EGR1.","volume":"6","author":"Matsunoshita","year":"2011","journal-title":"PLoS One"},{"key":"B172","doi-asserted-by":"publisher","DOI":"10.1371\/journal.pgen.1000962","article-title":"Genome-wide copy number variation in epilepsy: novel susceptibility loci in idiopathic generalized and focal epilepsies.","volume":"6","author":"Mefford","year":"2010","journal-title":"PLoS Genet."},{"key":"B173","doi-asserted-by":"publisher","DOI":"10.1111\/ejn.13748","article-title":"The neural oscillations of speech processing and language comprehension: state of the art and emerging mechanisms.","author":"Meyer","year":"2017","journal-title":"Eur. J. Neurosci."},{"key":"B174","doi-asserted-by":"publisher","first-page":"1","DOI":"10.1162\/jocn_a_01236","article-title":"Synchronization of electrophysiological responses with speech benefits syntactic information processing.","volume":"11","author":"Meyer","year":"2018","journal-title":"J. Cogn. Neurosci."},{"key":"B175","doi-asserted-by":"publisher","first-page":"932","DOI":"10.1177\/0883073814541468","article-title":"West syndrome in a patient with Schinzel-Giedion syndrome.","volume":"30","author":"Miyake","year":"2015","journal-title":"J. Child Neurol."},{"key":"B176","doi-asserted-by":"publisher","first-page":"1188","DOI":"10.1111\/j.1582-4934.2008.00377.x","article-title":"DLX5 expression is monoallelic and Dlx5 is up-regulated in the Mecp2-null frontal cortex.","volume":"12","author":"Miyano","year":"2008","journal-title":"J. Cell Mol. Med."},{"key":"B177","doi-asserted-by":"publisher","first-page":"2767","DOI":"10.1002\/hbm.23206","article-title":"Out-of-synchrony speech entrainment in developmental dyslexia.","volume":"37","author":"Molinaro","year":"2016","journal-title":"Hum. Brain Mapp."},{"key":"B178","doi-asserted-by":"publisher","first-page":"659","DOI":"10.1093\/schbul\/sbr056","article-title":"High vs low frequency neural oscillations in schizophrenia.","volume":"37","author":"Moran","year":"2011","journal-title":"Schizophr. Bull."},{"key":"B179","doi-asserted-by":"publisher","first-page":"748","DOI":"10.1038\/sj.jcbfm.9600063","article-title":"Modulation of astrocytic activation by arundic acid (ONO-2506) mitigates detrimental effects of the apolipoprotein E4 isoform after permanent focal ischemia in apolipoprotein E knock-in mice.","volume":"25","author":"Mori","year":"2005","journal-title":"J. Cereb. Blood Flow Metab."},{"key":"B180","doi-asserted-by":"publisher","first-page":"125","DOI":"10.1016\/j.ijpsycho.2016.06.001","article-title":"Genetic influences on phase synchrony of brain oscillations supporting response inhibition.","volume":"115","author":"M\u00fcller","year":"2017","journal-title":"Int. J. Psychophysiol."},{"key":"B181","doi-asserted-by":"publisher","DOI":"10.3389\/fpsyg.2015.00715","article-title":"Labels, cognomes and cyclic computation: an ethological perspective.","volume":"6","author":"Murphy","year":"","journal-title":"Front. Psychol."},{"key":"B182","doi-asserted-by":"publisher","DOI":"10.3389\/fpsyg.2015.01515","article-title":"The brain dynamics of linguistic computation.","volume":"6","author":"Murphy","year":"","journal-title":"Front. Psychol."},{"key":"B183","doi-asserted-by":"crossref","first-page":"6","DOI":"10.5964\/bioling.9061","article-title":"The human oscillome and its explanatory potential.","volume":"10","author":"Murphy","year":"","journal-title":"Biolinguistics"},{"key":"B184","first-page":"1","article-title":"A theta-gamma neural code for feature set composition with phase-entrained delta nestings.","volume":"28","author":"Murphy","year":"","journal-title":"UCL Work. Pap. Linguist."},{"key":"B185","doi-asserted-by":"publisher","first-page":"335","DOI":"10.12775\/3991-1.081","article-title":"\u201cA domesticated code: on the emergence of the oscillatory basis of phrase structure,\u201d in","author":"Murphy","year":"","journal-title":"The Evolution of Language: Proceedings of the 12th International Conference (Evolang 12)"},{"key":"B186","article-title":"\u201cInterfaces (travelling oscillations) + recursion (delta-theta code) = language,\u201d in","author":"Murphy","year":"","journal-title":"The Talking Species: Perspectives on the Evolutionary, Neuronal and Cultural Foundations of Language"},{"key":"B187","doi-asserted-by":"publisher","DOI":"10.3389\/fnhum.2016.00422","article-title":"Bridging the gap between genes and language deficits in schizophrenia: an oscillopathic approach.","volume":"10","author":"Murphy","year":"","journal-title":"Front. Hum. Neurosci."},{"key":"B188","doi-asserted-by":"publisher","first-page":"742","DOI":"10.1016\/j.neubiorev.2016.07.029","article-title":"Language deficits in schizophrenia and autism as related oscillatory connectomophathies: an evolutionary account.","volume":"83","author":"Murphy","year":"","journal-title":"Neurosci. Biobehav. Rev."},{"key":"B189","doi-asserted-by":"publisher","first-page":"343","DOI":"10.1038\/ejhg.2012.157","article-title":"Detection of copy-number variation in AUTS2 gene by targeted exonic array CGH in patients with developmental delay and autistic spectrum disorders.","volume":"21","author":"Nagamani","year":"2013","journal-title":"Eur. J. Hum. Genet."},{"key":"B190","doi-asserted-by":"publisher","first-page":"945","DOI":"10.1016\/j.neuron.2012.10.012","article-title":"Molecular motor KIF5A is essential for GABAA receptor transport, and KIF5A deletion causes epilepsy.","volume":"76","author":"Nakajima","year":"2012","journal-title":"Neuron"},{"key":"B191","doi-asserted-by":"publisher","DOI":"10.1371\/journal.pone.0119258","article-title":"Relationships among parvalbumin-immunoreactive neuron density, phase-locked gamma oscillations, and autistic\/schizophrenic symptoms in PDGFR-\u03b2 knock-out and control mice.","volume":"10","author":"Nakamura","year":"2015","journal-title":"PLoS One"},{"key":"B192","doi-asserted-by":"publisher","first-page":"99","DOI":"10.1080\/10799890701357855","article-title":"Involvement of p38alpha in kainate-induced seizure and neuronal cell damage.","volume":"27","author":"Namiki","year":"2007","journal-title":"J. Recept. Signal. Transduct. Res."},{"key":"B193","doi-asserted-by":"publisher","first-page":"149","DOI":"10.1002\/1096-8628(20000911)94:2<149::AID-AJMG7>3.0.CO;2-","article-title":"Cole-Hughes macrocephaly syndrome and associated autistic manifestations.","volume":"94","author":"Naqvi","year":"2000","journal-title":"Am. J. Med. Genet"},{"key":"B194","doi-asserted-by":"publisher","first-page":"670","DOI":"10.1016\/j.neuroscience.2013.06.037","article-title":"A neuregulin. 1 transmembrane domain mutation causes imbalanced glutamatergic and dopaminergic receptor expression in mice.","volume":"248","author":"Newell","year":"2013","journal-title":"Neuroscience"},{"key":"B195","doi-asserted-by":"publisher","DOI":"10.1371\/journal.pone.0018004","article-title":"Cognitive and socio-emotional deficits in platelet-derived growth factor receptor-\u03b2 gene knockout mice.","volume":"6","author":"Nguyen","year":"2011","journal-title":"PLoS One"},{"key":"B196","doi-asserted-by":"publisher","first-page":"182","DOI":"10.1016\/j.cortex.2013.12.004","article-title":"Category fluency, latent semantic analysis and schizophrenia: a candidate gene approach.","volume":"55","author":"Nicodemus","year":"2014","journal-title":"Cortex"},{"key":"B197","doi-asserted-by":"publisher","first-page":"112","DOI":"10.1016\/j.brainres.2007.06.074","article-title":"A seizure-prone phenotype is associated with altered free-running rhythm in Pten mutant mice.","volume":"1168","author":"Ogawa","year":"2007","journal-title":"Brain Res."},{"key":"B198","doi-asserted-by":"publisher","first-page":"123","DOI":"10.1016\/j.bbrc.2016.06.031","article-title":"Akt isoform-dependent regulation of ATP-Binding cassette A1 expression by apolipoprotein E.","volume":"477","author":"Okoro","year":"2016","journal-title":"Biochem. Biophys. Res. Commun."},{"key":"B199","doi-asserted-by":"publisher","first-page":"600","DOI":"10.1016\/j.tig.2013.08.001","article-title":"The role of AUTS2 in neurodevelopment and human evolution.","volume":"29","author":"Oksenberg","year":"2013","journal-title":"Trends Genet."},{"key":"B200","doi-asserted-by":"publisher","DOI":"10.1038\/tp.2014.78","article-title":"Genome-wide distribution of Auts2 binding localizes with active neurodevelopmental genes.","volume":"4","author":"Oksenberg","year":"2014","journal-title":"Transl. Psychiatry"},{"key":"B201","doi-asserted-by":"publisher","DOI":"10.1371\/journal.pgen.1003221","article-title":"Function and regulation of AUTS2, a gene implicated in autism and human evolution.","volume":"9","author":"Oksenberg","year":"2013","journal-title":"PLoS Genet."},{"key":"B202","doi-asserted-by":"publisher","first-page":"585","DOI":"10.1038\/ng.835","article-title":"Exome sequencing in sporadic autism spectrum disorders identifies severe de novo mutations.","volume":"43","author":"O\u2019Roak","year":"2011","journal-title":"Nat. Genet."},{"key":"B203","doi-asserted-by":"publisher","first-page":"1865","DOI":"10.1002\/ajmg.a.34081","article-title":"Genetic and functional analyses identify DISC1 as a novel callosal agenesis candidate gene.","author":"Osbun","year":"2011","journal-title":"Am. J. Med. Genet. A"},{"key":"B204","doi-asserted-by":"publisher","first-page":"1989","DOI":"10.1073\/pnas.0804428106","article-title":"Haploinsufficiency for Pten and serotonin transporter cooperatively influences brain size and social behavior.","volume":"106","author":"Page","year":"2009","journal-title":"Proc. Natl. Acad. Sci. U.S.A."},{"key":"B205","doi-asserted-by":"publisher","first-page":"1004","DOI":"10.1111\/j.1601-183X.2010.00648.x","article-title":"Pleiotropic effects of the 11p13 locus on developmental verbal dyspraxia and EEG centrotemporal sharp waves.","volume":"9","author":"Pal","year":"2010","journal-title":"Genes Brain Behav."},{"key":"B206","doi-asserted-by":"publisher","first-page":"2517","DOI":"10.1093\/hmg\/ddm207","article-title":"Association of distinct allelic haplotypes of DISC1 with psychotic and bipolar spectrum disorders and with underlying cognitive impairments.","volume":"16","author":"Palo","year":"2007","journal-title":"Hum. Mol. Genet."},{"key":"B207","doi-asserted-by":"publisher","first-page":"2264","DOI":"10.1152\/jn.00421.2011","article-title":"Impaired inhibitory control of cortical synchronization in fragile X syndrome.","volume":"106","author":"Paluszkiewicz","year":"2011","journal-title":"J. Neurophysiol."},{"key":"B208","doi-asserted-by":"publisher","first-page":"53","DOI":"10.1016\/bs.adgen.2016.08.003","article-title":"\u201cAdvances in dyslexia genetics\u2014new insights into the role of brain asymmetries,\u201d in","author":"Paracchini","year":"2016","journal-title":"Advances in Genetics"},{"key":"B209","doi-asserted-by":"publisher","first-page":"441","DOI":"10.1038\/nrg3934","article-title":"Systems biology and gene networks in neurodevelopmental and neurodegenerative disorders.","volume":"16","author":"Parikshak","year":"2015","journal-title":"Nat. Rev. Genet."},{"key":"B210","doi-asserted-by":"publisher","first-page":"S73","DOI":"10.1212\/01.WNL.0000059549.70717.80","article-title":"Succinic semialdehyde dehydrogenase deficiency in children and adults.","author":"Pearl","year":"2003","journal-title":"Ann. Neurol."},{"key":"B211","doi-asserted-by":"publisher","first-page":"437","DOI":"10.1038\/nature09965","article-title":"Shank3 mutant mice display autistic-like behaviours and striatal dysfunction.","volume":"472","author":"Pe\u00e7a","year":"2011","journal-title":"Nature"},{"key":"B212","first-page":"131","article-title":"Issues in the acquisition of binding, control and raising in high-functioning children with autism.","volume":"25","author":"Perovic","year":"2013","journal-title":"UCL Work. Pap. Linguist."},{"key":"B213","article-title":"Knowledge of c-command and A-movement in children and adolescents with autism and with Asperger syndrome.","author":"Perovic","year":"2007","journal-title":"Paper Presented at GALA 2007: Generative Approaches to Language Acquisition"},{"key":"B214","doi-asserted-by":"publisher","first-page":"145","DOI":"10.1177\/0883073814530503","article-title":"Induced gamma oscillations differentiate familiar and novel voices in children with MECP2 duplication and Rett syndromes.","volume":"30","author":"Peters","year":"2015","journal-title":"J. Child Neurol."},{"key":"B215","doi-asserted-by":"publisher","DOI":"10.1186\/s11689-016-9157-6","article-title":"Further evidence for a parent-of-origin effect at the NOP9 locus on language-related phenotypes.","volume":"8","author":"Pettigrew","year":"2016","journal-title":"J. Neurodev. Disord."},{"key":"B216","doi-asserted-by":"publisher","first-page":"11366","DOI":"10.1073\/pnas.1603312113","article-title":"Direct brain recordings reveal hippocampal rhythm underpinnings of language processing.","volume":"113","author":"Piai","year":"2016","journal-title":"Proc. Natl. Acad. Sci. U.S.A."},{"key":"B217","doi-asserted-by":"publisher","first-page":"683","DOI":"10.1002\/ajmg.b.30890","article-title":"Association of AKT1 with verbal learning, verbal memory, and regional cortical gray matter density in twins.","author":"Pietil\u00e4inen","year":"2009","journal-title":"Am. J. Med. Genet. B Neuropsychiatr. Genet."},{"key":"B218","doi-asserted-by":"publisher","first-page":"81","DOI":"10.1016\/j.jphysparis.2011.09.007","article-title":"Neural circuits underlying the generation of theta oscillations.","volume":"106","author":"Pignatelli","year":"2012","journal-title":"J. Physiol. Paris"},{"key":"B219","doi-asserted-by":"publisher","first-page":"727","DOI":"10.1016\/S0896-6273(00)00149-5","article-title":"Cell migration from the ganglionic eminences is required for the development of hippocampal GABAergic interneurons.","volume":"28","author":"Pleasure","year":"2000","journal-title":"Neuron"},{"key":"B220","doi-asserted-by":"publisher","first-page":"592","DOI":"10.1037\/0033-2909.131.4.592","article-title":"Generalist genes and learning disabilities.","volume":"131","author":"Plomin","year":"2005","journal-title":"Psychol. Bull."},{"key":"B221","doi-asserted-by":"publisher","first-page":"365","DOI":"10.1038\/mp.2010.105","article-title":"A theoretical molecular network for dyslexia: integrating available genetic findings.","volume":"16","author":"Poelmans","year":"2011","journal-title":"Mol. Psychiatry"},{"key":"B222","doi-asserted-by":"publisher","first-page":"34","DOI":"10.1080\/02643294.2012.710600","article-title":"The maps problem and the mapping problem: Two challenges for a cognitive neuroscience of speech and language.","volume":"29","author":"Poeppel","year":"2012","journal-title":"Cogn. Neuropsychol."},{"key":"B223","doi-asserted-by":"publisher","first-page":"3089","DOI":"10.1242\/dev.051052","article-title":"An SNP in an ultraconserved regulatory element affects Dlx5\/Dlx6 regulation in the forebrain.","volume":"137","author":"Poitras","year":"2010","journal-title":"Development"},{"key":"B224","doi-asserted-by":"publisher","first-page":"27","DOI":"10.1016\/j.ejmg.2008.11.002","article-title":"Three de novo losses and one insertion within a pericentric inversion of chromosome 6 in a patient with complete absence of expressive speech and reduced pain perception.","volume":"52","author":"Poot","year":"2009","journal-title":"Med. Genet."},{"key":"B225","doi-asserted-by":"publisher","first-page":"3729","DOI":"10.1073\/pnas.052716399","article-title":"Linkage disequilibrium between the beta frequency of the human EEG and a GABAA receptor gene locus.","volume":"99","author":"Porjesz","year":"2002","journal-title":"Proc. Natl. Acad. Sci. U.S.A."},{"key":"B226","doi-asserted-by":"publisher","first-page":"1101","DOI":"10.1097\/WNR.0000000000000477","article-title":"Hippocampal dysregulation of FMRP\/mGluR5 signaling in engrailed-2 knockout mice: a model of autism spectrum disorders.","volume":"26","author":"Provenzano","year":"2015","journal-title":"Neuroreport"},{"key":"B227","doi-asserted-by":"publisher","first-page":"1022","DOI":"10.1016\/j.neuron.2012.08.002","article-title":"Excessive activation of mTOR in postnatally generated granule cells is sufficient to cause epilepsy.","volume":"75","author":"Pun","year":"2012","journal-title":"Neuron"},{"key":"B228","doi-asserted-by":"publisher","first-page":"125","DOI":"10.1016\/j.nbd.2016.01.003","article-title":"Impaired cognitive discrimination and discoordination of coupled theta-gamma oscillations in Fmr1 knockout mice.","volume":"88","author":"Radwan","year":"2016","journal-title":"Neurobiol. Dis."},{"key":"B229","doi-asserted-by":"publisher","first-page":"86","DOI":"10.1111\/j.1528-1167.2007.01294.x","article-title":"Activity-dependent gene expression correlates with interictal spiking in human neocortical epilepsy.","author":"Rakhade","year":"2007","journal-title":"Epilepsia"},{"key":"B230","doi-asserted-by":"publisher","first-page":"724","DOI":"10.1038\/nrn2719","article-title":"Evolution of the neocortex: a perspective from developmental biology.","volume":"10","author":"Rakic","year":"2009","journal-title":"Nat. Rev. Neurosci."},{"key":"B231","doi-asserted-by":"publisher","first-page":"135","DOI":"10.1016\/j.bandl.2013.02.004","article-title":"Are there susceptibility factors for primary progressive aphasia?","volume":"127","author":"Rogalski","year":"2013","journal-title":"Brain Lang."},{"key":"B232","doi-asserted-by":"publisher","first-page":"16241","DOI":"10.1523\/JNEUROSCI.3667-11.2011","article-title":"CX3CR1 deficiency leads to impairment of hippocampal cognitive function and synaptic plasticity.","volume":"31","author":"Rogers","year":"2011","journal-title":"J. Neurosci."},{"key":"B233","doi-asserted-by":"publisher","DOI":"10.1186\/1471-244X-8-66","article-title":"Reduced neural synchronization of gamma-band MEG oscillations in first-degree relatives of children with autism.","volume":"8","author":"Rojas","year":"2008","journal-title":"BMC Psychiatry"},{"key":"B234","doi-asserted-by":"publisher","first-page":"1195","DOI":"10.1093\/hmg\/ddl035","article-title":"SRPX2 mutations in disorders of language cortex and cognition.","volume":"15","author":"Roll","year":"2006","journal-title":"Hum. Mol. Genet."},{"key":"B235","doi-asserted-by":"publisher","first-page":"4848","DOI":"10.1093\/hmg\/ddq415","article-title":"Molecular networks implicated in speech-related disorders: FOXP2 regulates the SRPX2\/uPAR complex.","volume":"19","author":"Roll","year":"2010","journal-title":"Hum. Mol. Genet."},{"key":"B236","doi-asserted-by":"publisher","first-page":"859","DOI":"10.1111\/bdi.12347","article-title":"Polymorphisms of dopamine pathway genes NRG1 and LMX1A are associated with cognitive performance in bipolar disorder.","volume":"17","author":"Rolstad","year":"2015","journal-title":"Bipolar Disord."},{"key":"B237","doi-asserted-by":"publisher","first-page":"666","DOI":"10.1021\/acschemneuro.5b00002","article-title":"Targeting human central nervous system protein kinases: An isoform selective p38\u03b1MAPK inhibitor that attenuates disease progression in Alzheimer\u2019s disease mouse models.","volume":"6","author":"Roy","year":"2015","journal-title":"ACS Chem. Neurosci."},{"key":"B238","doi-asserted-by":"publisher","first-page":"3617","DOI":"10.1093\/hmg\/ddn256","article-title":"Epileptic and developmental disorders of the speech cortex: ligand\/receptor interaction of wild-type and mutant SRPX2 with the plasminogen activator receptor uPAR.","volume":"17","author":"Royer-Zemmour","year":"2008","journal-title":"Hum. Mol. Genet."},{"key":"B239","doi-asserted-by":"publisher","first-page":"753","DOI":"10.1126\/science.1223082","article-title":"The pulvinar regulates information transmission between cortical areas based on attention demands.","volume":"337","author":"Saalmann","year":"2012","journal-title":"Science"},{"key":"B240","doi-asserted-by":"publisher","first-page":"642","DOI":"10.1002\/jnr.23199","article-title":"SIRT1 regulates the neurogenic potential of neural precursors in the adult subventricular zone and hippocampus.","volume":"91","author":"Saharan","year":"2013","journal-title":"J. Neurosci. Res."},{"key":"B241","doi-asserted-by":"publisher","first-page":"3583","DOI":"10.1242\/jcs.03080","article-title":"Mechanism of polarized protrusion formation on neuronal precursors migrating in the developing chicken cerebellum.","volume":"119","author":"Sakakibara","year":"2006","journal-title":"J. Cell Sci."},{"key":"B242","doi-asserted-by":"publisher","first-page":"10928","DOI":"10.1523\/JNEUROSCI.3693-08.2008","article-title":"Neural-activity-dependent release of s100b from astrocytes enhances kainate-induced gamma oscillations in vivo.","volume":"28","author":"Sakatani","year":"2008","journal-title":"J. Neurosci."},{"key":"B243","doi-asserted-by":"publisher","first-page":"439","DOI":"10.1111\/gbb.12131","article-title":"Glutamic acid decarboxylase 67 haplodeficiency impairs social behavior in mice.","volume":"13","author":"Sandhu","year":"2014","journal-title":"Genes Brain Behav."},{"key":"B244","doi-asserted-by":"publisher","first-page":"1755","DOI":"10.1152\/jn.00824.2015","article-title":"Model systems for studying cellular mechanisms of SCN1A-related epilepsy.","volume":"115","author":"Schutte","year":"2016","journal-title":"J. Neurophysiol."},{"key":"B245","doi-asserted-by":"publisher","DOI":"10.1126\/scitranslmed.3001344","article-title":"Altered functional connectivity in frontal lobe circuits is associated with variation in the autism risk gene CNTNAP2.","volume":"2","author":"Scott-Van Zeeland","year":"2010","journal-title":"Sci. Transl. Med."},{"key":"B246","doi-asserted-by":"publisher","DOI":"10.1038\/ncomms10118","article-title":"Interneuronal DISC1 regulates NRG1-ErbB4 signalling and excitatory-inhibitory synapse formation in the mature cortex.","volume":"6","author":"Seshadri","year":"2015","journal-title":"Nat. Commun."},{"key":"B247","doi-asserted-by":"publisher","first-page":"5622","DOI":"10.1073\/pnas.0909284107","article-title":"Disrupted-in-Schizophrenia-1 expression is regulated by beta-site amyloid precursor protein cleaving enzyme-1-neuregulin cascade.","volume":"107","author":"Seshadri","year":"2010","journal-title":"Proc. Natl. Acad. Sci. U.S.A."},{"key":"B248","doi-asserted-by":"publisher","first-page":"539","DOI":"10.1086\/367846","article-title":"Fine mapping of autistic disorder to chromosome 15q11-q13 by use of phenotypic subtypes.","volume":"72","author":"Shao","year":"2003","journal-title":"Am. J. Hum. Genet."},{"key":"B249","doi-asserted-by":"publisher","DOI":"10.1371\/journal.pbio.1001427","article-title":"Human-specific histone methylation signatures at transcription start sites in prefrontal neurons.","volume":"10","author":"Shulha","year":"2012","journal-title":"PLoS Biol."},{"key":"B250","doi-asserted-by":"publisher","first-page":"616","DOI":"10.1016\/j.tics.2013.09.006","article-title":"Cortical dynamics revisited.","volume":"17","author":"Singer","year":"2013","journal-title":"Trends Cogn. Sci."},{"key":"B251","doi-asserted-by":"publisher","first-page":"304","DOI":"10.1002\/bdra.23488","article-title":"Novel COL4A1 mutation in an infant with severe dysmorphic syndrome with schizencephaly, periventricular calcifications, and cataract resembling congenital infection.","volume":"106","author":"Smigiel","year":"2016","journal-title":"Birth Defects Res. A Clin. Mol. Teratol."},{"key":"B252","doi-asserted-by":"publisher","first-page":"1","DOI":"10.1352\/1944-7558-117.1.1","article-title":"Behavioral phenotype of fragile X syndrome in adolescence and adulthood.","volume":"117","author":"Smith","year":"2012","journal-title":"Am. J. Intellect. Dev. Disabil."},{"key":"B253","doi-asserted-by":"publisher","first-page":"820","DOI":"10.1136\/jmedgenet-2016-103880","article-title":"Eight further individuals with intellectual disability and epilepsy carrying bi-allelic CNTNAP2 aberrations allow delineation of the mutational and phenotypic spectrum.","volume":"53","author":"Smogavec","year":"2016","journal-title":"J. Med. Genet."},{"key":"B254","doi-asserted-by":"publisher","first-page":"837","DOI":"10.3892\/mmr.2013.1564","article-title":"Gender effects of the COMT Val 158 Met genotype on verbal fluency in healthy adults.","volume":"8","author":"Soeiro-De-Souza","year":"2013","journal-title":"Mol. Med. Rep."},{"key":"B255","doi-asserted-by":"publisher","DOI":"10.1371\/journal.pone.0076608","article-title":"Differential entrainment of neuroelectric delta oscillations in developmental dyslexia.","volume":"8","author":"Solt\u00e9sz","year":"2013","journal-title":"PLoS One"},{"key":"B256","doi-asserted-by":"publisher","DOI":"10.1186\/2040-2392-4-18","article-title":"Prospective investigation of autism and genotype-phenotype correlations in 22q13 deletion syndrome and SHANK3 deficiency.","volume":"4","author":"Soorya","year":"2013","journal-title":"Mol. Autism"},{"key":"B257","doi-asserted-by":"publisher","first-page":"65","DOI":"10.1016\/j.nbd.2014.04.016","article-title":"Excitation\/inhibition balance and learning are modified by Dyrk1a gene dosage.","volume":"69","author":"Souchet","year":"2014","journal-title":"Neurobiol. Dis."},{"key":"B258","doi-asserted-by":"publisher","first-page":"1370","DOI":"10.1056\/NEJMoa052773","article-title":"Recessive symptomatic focal epilepsy and mutant contactin-associated protein-like 2.","volume":"354","author":"Strauss","year":"2006","journal-title":"N. Engl. J. Med."},{"key":"B259","author":"Striedter","year":"2005","journal-title":"Principles of Brain Evolution."},{"key":"B260","doi-asserted-by":"publisher","first-page":"1171","DOI":"10.1038\/ejhg.2008.267","article-title":"Centrotemporal sharp wave EEG trait in rolandic epilepsy maps to Elongator Protein Complex 4 (ELP4).","volume":"17","author":"Strug","year":"2009","journal-title":"Eur. J. Hum. Genet."},{"key":"B261","doi-asserted-by":"publisher","first-page":"112","DOI":"10.1016\/j.pscychresns.2015.05.005","article-title":"Brain structural and clinical changes after first episode psychosis: focus on cannabinoid receptor 1 polymorphisms.","volume":"233","author":"Su\u00e1rez-Pinilla","year":"2015","journal-title":"Psychiatry Res."},{"key":"B262","doi-asserted-by":"publisher","first-page":"104","DOI":"10.1093\/cercor\/bhw371","article-title":"Age-dependent effects of Catechol-O-Methyltransferase (COMT) gene Val158Met polymorphism on language function in developing children.","volume":"27","author":"Sugiura","year":"2017","journal-title":"Cereb. Cortex"},{"key":"B263","doi-asserted-by":"publisher","first-page":"4275","DOI":"10.1091\/mbc.E10-04-0332","article-title":"Cell death or survival promoted by alternative isoforms of ErbB4.","volume":"21","author":"Sundvall","year":"2010","journal-title":"Mol. Biol. Cell"},{"key":"B264","doi-asserted-by":"publisher","first-page":"D447","DOI":"10.1093\/nar\/gku1003","article-title":"STRING v10: protein-protein interaction networks, integrated over the tree of life.","volume":"43","author":"Szklarczyk","year":"2015","journal-title":"Nucleic Acids Res."},{"key":"B265","doi-asserted-by":"publisher","first-page":"551","DOI":"10.1016\/j.ajhg.2011.09.011","article-title":"Assessment of 2q23.1 microdeletion syndrome implicates MBD5 as a single causal locus of intellectual disability, epilepsy, and autism spectrum disorder.","volume":"89","author":"Talkowski","year":"2011","journal-title":"Am. J. Hum. Genet."},{"key":"B266","doi-asserted-by":"publisher","first-page":"1030","DOI":"10.1016\/j.neuroimage.2010.02.018","article-title":"Normal variation in fronto-occipital circuitry and cerebellar structure with an autism-associated polymorphism of CNTNAP2.","volume":"53","author":"Tan","year":"2010","journal-title":"Neuroimage"},{"key":"B267","doi-asserted-by":"publisher","first-page":"1007","DOI":"10.1038\/mp.2011.91","article-title":"Epistatic interactions of AKT1 on human medial temporal lobe biology and pharmacogenetic implications.","volume":"17","author":"Tan","year":"","journal-title":"Mol. Psychiatry"},{"key":"B268","doi-asserted-by":"publisher","first-page":"1436","DOI":"10.1093\/brain\/aws068","article-title":"Effective connectivity of AKT1-mediated dopaminergic working memory networks and pharmacogenetics of anti-dopaminergic treatment.","volume":"135","author":"Tan","year":"","journal-title":"Brain"},{"key":"B269","doi-asserted-by":"publisher","first-page":"84","DOI":"10.1038\/nn.2449","article-title":"The corticothalamocortical circuit drives higher-order cortex in the mouse.","volume":"13","author":"Theyel","year":"2009","journal-title":"Nat. Neurosci."},{"key":"B270","doi-asserted-by":"publisher","DOI":"10.1093\/sleep\/zsw026","article-title":"CNTNAP2 knockout rats and mice exhibit epileptiform activity and abnormal sleep-wake physiology.","volume":"40","author":"Thomas","year":"2017","journal-title":"Sleep"},{"key":"B271","doi-asserted-by":"publisher","first-page":"668","DOI":"10.1038\/mp.2013.68","article-title":"708 common and 2010 rare DISC1 locus variants identified in 1542 subjects: analysis for association with psychiatric disorder and cognitive traits.","volume":"19","author":"Thomson","year":"2014","journal-title":"Mol. Psychiatry"},{"key":"B272","doi-asserted-by":"publisher","first-page":"609","DOI":"10.1007\/s13311-015-0356-8","article-title":"Balancing proliferation and connectivity in PTEN-associated autism spectrum disorder.","volume":"12","author":"Tilot","year":"2015","journal-title":"Neurotherapeutics"},{"key":"B273","doi-asserted-by":"publisher","first-page":"119","DOI":"10.1159\/000330584","article-title":"Is neuregulin 1 involved in determining cerebral volumes in schizophrenia? Preliminary results showing a decrease in superior temporal gyrus volume.","volume":"65","author":"Tosato","year":"2012","journal-title":"Neuropsychobiology"},{"key":"B274","doi-asserted-by":"publisher","first-page":"743","DOI":"10.1212\/WNL.0000000000003635","article-title":"Dysarthria and broader motor speech deficits in Dravet syndrome.","volume":"88","author":"Turner","year":"2017","journal-title":"Neurology"},{"key":"B275","doi-asserted-by":"publisher","first-page":"586","DOI":"10.1212\/WNL.0000000000001228","article-title":"GRIN2A: an aptly named gene for speech dysfunction.","volume":"84","author":"Turner","year":"2015","journal-title":"Neurology"},{"key":"B276","doi-asserted-by":"publisher","first-page":"S233","DOI":"10.1016\/S0387-7604(01)00367-9","article-title":"Development of language in Rett syndrome.","volume":"23","author":"Uchino","year":"2001","journal-title":"Brain Dev."},{"key":"B277","doi-asserted-by":"publisher","first-page":"927","DOI":"10.1093\/schbul\/sbn062","article-title":"The role of oscillations and synchrony in cortical networks and their putative relevance for the pathophysiology of schizophrenia.","volume":"34","author":"Uhlhaas","year":"2008","journal-title":"Schizophr. Bull."},{"key":"B278","doi-asserted-by":"publisher","first-page":"997","DOI":"10.1016\/j.neuron.2013.02.033","article-title":"Thalamocortical synchronization and cognition: implications for schizophrenia?","volume":"77","author":"Uhlhaas","year":"2013","journal-title":"Neuron"},{"key":"B279","doi-asserted-by":"publisher","first-page":"2533","DOI":"10.1093\/hmg\/ddl174","article-title":"A GABRB3 promoter haplotype associated with childhood absence epilepsy impairs transcriptional activity.","volume":"15","author":"Urak","year":"2006","journal-title":"Hum. Mol. Genet."},{"key":"B280","first-page":"562","article-title":"Heritability of human brain functioning as assessed by electroencephalography.","volume":"58","author":"Van Beijsterveldt","year":"1996","journal-title":"Am. J. Hum. Genet."},{"key":"B281","doi-asserted-by":"publisher","first-page":"400","DOI":"10.1038\/ejhg.2010.211","article-title":"The phenotype. of. recurrent. 10q22q23 deletions and duplications.","volume":"19","author":"Van Bon","year":"2011","journal-title":"Eur. J. Hum. Genet."},{"key":"B282","doi-asserted-by":"publisher","first-page":"819","DOI":"10.1038\/sj.mp.4001505","article-title":"Molecular genetics of autism spectrum disorder.","volume":"9","author":"Veenstra-VanderWeele","year":"2004","journal-title":"Mol. Psychiatry"},{"key":"B283","doi-asserted-by":"publisher","first-page":"392","DOI":"10.1002\/ajmg.b.32042","article-title":"Impact of the Reelin signaling cascade (ligands-receptors-adaptor complex) on cognition in schizophrenia.","author":"Verbrugghe","year":"2012","journal-title":"Am. J. Med. Genet B Neuropsychiatr. Genet."},{"key":"B284","doi-asserted-by":"publisher","DOI":"10.1371\/journal.pgen.1002145","article-title":"Foxp2 regulates gene networks implicated in neurite outgrowth in the developing brain.","volume":"7","author":"Vernes","year":"2011","journal-title":"PLoS Genet."},{"key":"B285","first-page":"893","article-title":"Brainstem-diencephalo-septohippocampal systems controlling the theta rhythm of the hippocampus.","volume":"81","author":"Vertes","year":"1997","journal-title":"Neuroscience"},{"key":"B286","doi-asserted-by":"publisher","first-page":"89","DOI":"10.1016\/B978-0-12-420170-5.00004-0","article-title":"The transcription factor Zif268\/Egr1, brain plasticity, and memory.","volume":"122","author":"Veyrac","year":"2014","journal-title":"Prog. Mol. Biol. Transl. Sci."},{"key":"B287","doi-asserted-by":"publisher","DOI":"10.3389\/fnhum.2015.00257","article-title":"Increase in short-term memory capacity induced by down-regulating individual theta frequency via transcranial alternating current stimulation.","volume":"9","author":"Vosskuhl","year":"2015","journal-title":"Front. Hum. Neurosci."},{"key":"B288","author":"Wada","year":"2015","journal-title":"Clinician Recasts and Production of Complex Syntax by Children with and without Specific Language Impairment."},{"key":"B289","doi-asserted-by":"publisher","first-page":"695","DOI":"10.1016\/j.neuron.2008.07.011","article-title":"The human thalamus processes syntactic and semantic language violations.","volume":"59","author":"Wahl","year":"2008","journal-title":"Neuron"},{"key":"B290","doi-asserted-by":"publisher","first-page":"2862","DOI":"10.1093\/hmg\/dds111","article-title":"The DISC1 promoter: characterization and regulation by FOXP2.","volume":"21","author":"Walker","year":"2012","journal-title":"Hum. Mol. Genet."},{"key":"B291","doi-asserted-by":"publisher","first-page":"706","DOI":"10.1111\/epi.13348","article-title":"Targeting of microRNA-199a-5p protects against pilocarpine-induced status epilepticus and seizure damage via SIRT1-p53 cascade.","volume":"57","author":"Wang","year":"2016","journal-title":"Epilepsia"},{"key":"B292","doi-asserted-by":"publisher","DOI":"10.1155\/2014\/925350","article-title":"FOXO transcription factors: their clinical significance and regulation.","volume":"2014","author":"Wang","year":"2014","journal-title":"Biomed Res. Int."},{"key":"B293","doi-asserted-by":"publisher","first-page":"186","DOI":"10.1038\/sj.mp.4001241","article-title":"Sodium channels SCN1A, SCN2A and SCN3A in familial autism.","volume":"8","author":"Weiss","year":"2003","journal-title":"Mol. Psychiatry"},{"key":"B294","doi-asserted-by":"publisher","first-page":"941","DOI":"10.1002\/ajmg.b.31241","article-title":"Genetic variation in CNTNAP2 alters brain function during linguistic processing in healthy individuals.","author":"Whalley","year":"2011","journal-title":"Am. J. Med. Genet. B Neuropsychiatr. Genet."},{"key":"B295","doi-asserted-by":"publisher","first-page":"451","DOI":"10.1111\/j.1601-183X.2011.00684.x","article-title":"CNTNAP2 variants affect early language development in the general population.","volume":"10","author":"Whitehouse","year":"2011","journal-title":"Genes Brain Behav."},{"key":"B296","doi-asserted-by":"publisher","DOI":"10.3389\/fnhum.2013.00080","article-title":"Patterns of cortical oscillations organize neural activity into whole-brain functional networks evident in the fMRI BOLD signal.","volume":"7","author":"Whitman","year":"2013","journal-title":"Front. Hum. Neurosci."},{"key":"B297","first-page":"1","article-title":"Joint interventions in autism spectrum disorder: relating oscillopathies and syntactic deficits.","volume":"28","author":"Wilkinson","year":"2016","journal-title":"UCL Work. Pap. Linguist."},{"key":"B298","doi-asserted-by":"publisher","first-page":"436","DOI":"10.1038\/ejhg.2009.199","article-title":"Haploinsufficiency of MBD5 associated with a syndrome involving microcephaly, intellectual disabilities, severe speech impairment, and seizures.","volume":"18","author":"Williams","year":"2010","journal-title":"Eur. J. Hum. Genet."},{"key":"B299","doi-asserted-by":"publisher","first-page":"1938","DOI":"10.1093\/cercor\/bhu004","article-title":"Alpha oscillatory dynamics index temporal expectation benefits in working memory.","volume":"25","author":"Wilsch","year":"2015","journal-title":"Cereb. Cortex"},{"key":"B300","doi-asserted-by":"publisher","DOI":"10.1111\/ejn.13429","article-title":"The rhythm of the executive gate of speech: subthalamic low-frequency oscillations increase during verbal generation.","author":"Wojtecki","year":"2016","journal-title":"Eur. J. Neurosci."},{"key":"B301","doi-asserted-by":"publisher","first-page":"1458","DOI":"10.1523\/JNEUROSCI.3250-14.2015","article-title":"Neural alpha dynamics in younger and older listeners reflect acoustic challenges and predictive benefits.","volume":"35","author":"W\u00f6stmann","year":"2015","journal-title":"J. Neurosci."},{"key":"B302","doi-asserted-by":"publisher","first-page":"8","DOI":"10.1016\/j.exger.2013.12.006","article-title":"SIRT1 expression in the cochlea and auditory cortex of a mouse model of age-related hearing loss.","volume":"51","author":"Xiong","year":"2014","journal-title":"Exp. Gerontol."},{"key":"B303","doi-asserted-by":"publisher","first-page":"4923","DOI":"10.1109\/EMBC.2012.6347098","article-title":"Selection of abnormal neural oscillation patterns associated with sentence-level language disorder in schizophrenia.","volume":"2012","author":"Xu","year":"2012","journal-title":"Conf. Proc. IEEE Eng. Med. Biol. Soc."},{"key":"B304","doi-asserted-by":"publisher","first-page":"135","DOI":"10.1177\/1550059412465078","article-title":"Multidimensional analysis of the abnormal neural oscillations associated with lexical processing in schizophrenia.","volume":"44","author":"Xu","year":"2013","journal-title":"Clin. EEG Neurosci."},{"key":"B305","doi-asserted-by":"publisher","first-page":"186","DOI":"10.1097\/JCP.0b013e318283925e","article-title":"CNR1 gene and risk of the metabolic syndrome in patients with schizophrenia.","volume":"33","author":"Yu","year":"2013","journal-title":"J. Clin. Psycopharmacol."},{"key":"B306","doi-asserted-by":"publisher","first-page":"554","DOI":"10.1016\/j.neuroscience.2015.05.063","article-title":"Theta frequency prefrontal-hippocampal driving relationship during free exploration in mice.","volume":"300","author":"Zhan","year":"2015","journal-title":"Neuroscience"},{"key":"B307","doi-asserted-by":"publisher","first-page":"400","DOI":"10.1038\/nn.3641","article-title":"Deficient neuron-microglia signaling results in impaired functional brain connectivity and social behavior.","volume":"17","author":"Zhan","year":"2014","journal-title":"Nat. Neurosci."},{"key":"B308","doi-asserted-by":"publisher","first-page":"2302","DOI":"10.1242\/jcs.167056","article-title":"GABAB receptor promotes its own surface expression by recruiting a Rap1-dependent signaling cascade.","volume":"128","author":"Zhang","year":"2015","journal-title":"J. Cell Sci."},{"key":"B309","doi-asserted-by":"publisher","first-page":"72","DOI":"10.1016\/j.expneurol.2006.07.020","article-title":"Neuroprotection by estradiol: a role of aromatase against spine synapse loss after blockade of GABAA receptors.","volume":"203","author":"Zhou","year":"2007","journal-title":"Exp. Neurol."}],"container-title":["Frontiers in Psychology"],"original-title":[],"link":[{"URL":"https:\/\/www.frontiersin.org\/article\/10.3389\/fpsyg.2018.01999\/full","content-type":"unspecified","content-version":"vor","intended-application":"similarity-checking"}],"deposited":{"date-parts":[[2022,9,4]],"date-time":"2022-09-04T09:27:19Z","timestamp":1662283639000},"score":1,"resource":{"primary":{"URL":"https:\/\/www.frontiersin.org\/article\/10.3389\/fpsyg.2018.01999\/full"}},"subtitle":[],"short-title":[],"issued":{"date-parts":[[2018,10,23]]},"references-count":309,"alternative-id":["10.3389\/fpsyg.2018.01999"],"URL":"https:\/\/doi.org\/10.3389\/fpsyg.2018.01999","relation":{"has-preprint":[{"id-type":"doi","id":"10.1101\/114033","asserted-by":"object"}]},"ISSN":["1664-1078"],"issn-type":[{"value":"1664-1078","type":"electronic"}],"subject":[],"published":{"date-parts":[[2018,10,23]]},"article-number":"1999"}}