{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2026,7,20]],"date-time":"2026-07-20T15:23:07Z","timestamp":1784560987898,"version":"3.55.0"},"reference-count":69,"publisher":"Elsevier BV","issue":"1","license":[{"start":{"date-parts":[[2024,1,1]],"date-time":"2024-01-01T00:00:00Z","timestamp":1704067200000},"content-version":"tdm","delay-in-days":0,"URL":"https:\/\/www.elsevier.com\/tdm\/userlicense\/1.0\/"},{"start":{"date-parts":[[2024,1,1]],"date-time":"2024-01-01T00:00:00Z","timestamp":1704067200000},"content-version":"tdm","delay-in-days":0,"URL":"https:\/\/www.elsevier.com\/legal\/tdmrep-license"},{"start":{"date-parts":[[2025,1,3]],"date-time":"2025-01-03T00:00:00Z","timestamp":1735862400000},"content-version":"vor","delay-in-days":368,"URL":"http:\/\/creativecommons.org\/licenses\/by-nc-nd\/4.0\/"}],"content-domain":{"domain":["elsevier.com","sciencedirect.com"],"crossmark-restriction":true},"short-container-title":["Global Medical Genetics"],"published-print":{"date-parts":[[2024]]},"DOI":"10.1055\/s-0044-1781456","type":"journal-article","created":{"date-parts":[[2024,2,27]],"date-time":"2024-02-27T19:56:38Z","timestamp":1709063798000},"page":"76-85","update-policy":"https:\/\/doi.org\/10.1016\/elsevier_cm_policy","source":"Crossref","is-referenced-by-count":4,"title":["Genetic Modifications of Developmental Dyslexia and Its Representation Using In Vivo, In Vitro Model"],"prefix":"10.1016","volume":"11","author":[{"given":"Zakiyyah M.M.","family":"Zaki","sequence":"first","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Siti A.","family":"Ali","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Mazira M.","family":"Ghazali","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Faidruz A.","family":"Jam","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]}],"member":"78","reference":[{"issue":"02","key":"10.1055\/s-0044-1781456_bib1","doi-asserted-by":"crossref","first-page":"285","DOI":"10.1002\/rrq.477","article-title":"Forty years of reading intervention research for elementary students with or at risk for dyslexia: a systematic review and meta-analysis","volume":"58","author":"Hall","year":"2022","journal-title":"Read Res Q"},{"issue":"03","key":"10.1055\/s-0044-1781456_bib2","doi-asserted-by":"crossref","first-page":"415","DOI":"10.1037\/0022-0663.91.3.415","article-title":"The double-deficit hypothesis for the development dyslexias","volume":"91","author":"Wolf","year":"1999","journal-title":"J Educ Psychol"},{"issue":"02","key":"10.1055\/s-0044-1781456_bib3","doi-asserted-by":"crossref","first-page":"208","DOI":"10.3390\/brainsci13020208","article-title":"Theories about developmental dyslexia","volume":"13","author":"Stein","year":"2023","journal-title":"Brain Sci"},{"issue":"Pt 1","key":"10.1055\/s-0044-1781456_bib4","doi-asserted-by":"crossref","first-page":"71","DOI":"10.1093\/brain\/awn300","article-title":"The neural basis of surface dyslexia in semantic dementia","volume":"132","author":"Wilson","year":"2009","journal-title":"Brain"},{"issue":"9419","key":"10.1055\/s-0044-1781456_bib5","doi-asserted-by":"crossref","first-page":"1451","DOI":"10.1016\/S0140-6736(04)16106-0","article-title":"Developmental dyslexia","volume":"363","author":"D\u00e9monet","year":"2004","journal-title":"Lancet"},{"key":"10.1055\/s-0044-1781456_bib6","doi-asserted-by":"crossref","first-page":"814","DOI":"10.1016\/j.nicl.2018.03.012","article-title":"Abnormal age-related cortical folding and neurite morphology in children with developmental dyslexia","volume":"18","author":"Caverzasi","year":"2018","journal-title":"Neuroimage Clin"},{"issue":"02","key":"10.1055\/s-0044-1781456_bib7","doi-asserted-by":"crossref","first-page":"94","DOI":"10.1002\/ana.410060203","article-title":"Cytoarchitectonic abnormalities in developmental dyslexia: a case study","volume":"6","author":"Galaburda","year":"1979","journal-title":"Ann Neurol"},{"key":"10.1055\/s-0044-1781456_bib8","doi-asserted-by":"crossref","first-page":"66","DOI":"10.1016\/j.neuropsychologia.2018.03.022","article-title":"The current status of the magnocellular theory of developmental dyslexia","volume":"130","author":"Stein","year":"2019","journal-title":"Neuropsychologia"},{"issue":"04","key":"10.1055\/s-0044-1781456_bib9","doi-asserted-by":"crossref","first-page":"355","DOI":"10.1111\/j.1467-9450.1995.tb00993.x","article-title":"Immune disorders and handedness in dyslexic boys and their relatives","volume":"36","author":"Jariabkov\u00e1","year":"1995","journal-title":"Scand J Psychol"},{"issue":"01","key":"10.1055\/s-0044-1781456_bib10","doi-asserted-by":"crossref","first-page":"44","DOI":"10.1007\/BF02928173","article-title":"Familial dyslexia: genetic and medical findings in eleven three-generation families","volume":"43","author":"Lubs","year":"1993","journal-title":"Ann Dyslexia"},{"issue":"03","key":"10.1055\/s-0044-1781456_bib11","doi-asserted-by":"crossref","first-page":"143","DOI":"10.1002\/dys.228","article-title":"Dyslexia: nature and nurture","volume":"8","author":"Olson","year":"2002","journal-title":"Dyslexia"},{"issue":"05","key":"10.1055\/s-0044-1781456_bib12","doi-asserted-by":"crossref","first-page":"289","DOI":"10.1136\/jmg.2006.046516","article-title":"Genetics of dyslexia: the evolving landscape","volume":"44","author":"Schumacher","year":"2007","journal-title":"J Med Genet"},{"issue":"05","key":"10.1055\/s-0044-1781456_bib13","doi-asserted-by":"crossref","first-page":"498","DOI":"10.1037\/bul0000037","article-title":"Oral language deficits in familial dyslexia: a meta-analysis and review","volume":"142","author":"Snowling","year":"2016","journal-title":"Psychol Bull"},{"issue":"03","key":"10.1055\/s-0044-1781456_bib14","doi-asserted-by":"crossref","first-page":"742","DOI":"10.1016\/j.neuroimage.2010.09.055","article-title":"Structural brain alterations associated with dyslexia predate reading onset","volume":"57","author":"Raschle","year":"2011","journal-title":"Neuroimage"},{"issue":"01","key":"10.1055\/s-0044-1781456_bib15","doi-asserted-by":"crossref","first-page":"84","DOI":"10.1002\/dys.1604","article-title":"N1 lateralization and dyslexia: an event-related potential study in children with a familial risk of dyslexia","volume":"25","author":"van Setten","year":"2019","journal-title":"Dyslexia"},{"issue":"09","key":"10.1055\/s-0044-1781456_bib16","doi-asserted-by":"crossref","first-page":"2489","DOI":"10.1093\/cercor\/bht104","article-title":"Altered neuronal response during rapid auditory processing and its relation to phonological processing in prereading children at familial risk for dyslexia","volume":"24","author":"Raschle","year":"2014","journal-title":"Cereb Cortex"},{"issue":"10","key":"10.1055\/s-0044-1781456_bib17","doi-asserted-by":"crossref","DOI":"10.1001\/jamanetworkopen.2022.36102","article-title":"Patterns of neural functional connectivity in infants at familial risk of developmental dyslexia","volume":"5","author":"Yu","year":"2022","journal-title":"JAMA Netw Open"},{"key":"10.1055\/s-0044-1781456_bib18","doi-asserted-by":"crossref","DOI":"10.1016\/j.ynstr.2020.100223","article-title":"Dyslexia as an adaptation to cortico-limbic stress system reactivity","volume":"12","author":"Kershner","year":"2020","journal-title":"Neurobiol Stress"},{"issue":"06","key":"10.1055\/s-0044-1781456_bib19","doi-asserted-by":"crossref","first-page":"782","DOI":"10.3390\/brainsci11060782","article-title":"Developmental dyslexia: environment matters","volume":"11","author":"Theodoridou","year":"2021","journal-title":"Brain Sci"},{"issue":"03","key":"10.1055\/s-0044-1781456_bib20","doi-asserted-by":"crossref","DOI":"10.1111\/desc.12764","article-title":"Parents\u2019 early book reading to children: Relation to children's later language and literacy outcomes controlling for other parent language input","volume":"22","author":"Ece Demir-Lira","year":"2019","journal-title":"Dev Sci"},{"key":"10.1055\/s-0044-1781456_bib21","doi-asserted-by":"crossref","DOI":"10.1016\/j.jecp.2021.105314","article-title":"Long-term effects of the home literacy environment on reading development: familial risk for dyslexia as a moderator","volume":"215","author":"Torppa","year":"2022","journal-title":"J Exp Child Psychol"},{"issue":"7-8","key":"10.1055\/s-0044-1781456_bib22","doi-asserted-by":"crossref","first-page":"423","DOI":"10.1080\/87565641.2017.1374960","article-title":"Genetic and environmental risk factors for developmental dyslexia in children: systematic review of the last decade","volume":"42","author":"Becker","year":"2017","journal-title":"Dev Neuropsychol"},{"key":"10.1055\/s-0044-1781456_bib23","article-title":"Descriptive epidemiology of prenatal and perinatal risk factors in a Chinese population with reading disorder","volume":"6","author":"Liu","year":"2016","journal-title":"Sci Rep"},{"issue":"03","key":"10.1055\/s-0044-1781456_bib24","doi-asserted-by":"crossref","first-page":"901","DOI":"10.1523\/JNEUROSCI.2092-13.2013","article-title":"An investigation into the origin of anatomical differences in dyslexia","volume":"34","author":"Krafnick","year":"2014","journal-title":"J Neurosci"},{"key":"10.1055\/s-0044-1781456_bib25","author":"Kujala"},{"issue":"01","key":"10.1055\/s-0044-1781456_bib26","doi-asserted-by":"crossref","DOI":"10.1038\/s41598-021-89317-x","article-title":"Voxel and surface based whole brain analysis shows reading skill associated grey matter abnormalities in dyslexia","volume":"11","author":"Kujala","year":"2021","journal-title":"Sci Rep"},{"issue":"01","key":"10.1055\/s-0044-1781456_bib27","doi-asserted-by":"crossref","first-page":"37","DOI":"10.1186\/s11689-018-9251-z","article-title":"Applying a network framework to the neurobiology of reading and dyslexia","volume":"10","author":"Bailey","year":"2018","journal-title":"J Neurodev Disord"},{"issue":"06","key":"10.1055\/s-0044-1781456_bib28","doi-asserted-by":"crossref","DOI":"10.1111\/gbb.12808","article-title":"Rapid auditory processing and medial geniculate nucleus anomalies in Kiaa0319 knockout mice","volume":"21","author":"Perrino","year":"2022","journal-title":"Genes Brain Behav"},{"key":"10.1055\/s-0044-1781456_bib29","doi-asserted-by":"crossref","DOI":"10.1016\/j.dcn.2020.100869","article-title":"Auditory brainstem measures and genotyping boost the prediction of literacy: a longitudinal study on early markers of dyslexia","volume":"46","author":"Liebig","year":"2020","journal-title":"Dev Cogn Neurosci"},{"issue":"02","key":"10.1055\/s-0044-1781456_bib30","doi-asserted-by":"crossref","first-page":"83","DOI":"10.1016\/j.molmed.2013.10.008","article-title":"The genetic relationship between handedness and neurodevelopmental disorders","volume":"20","author":"Brandler","year":"2014","journal-title":"Trends Mol Med"},{"issue":"03","key":"10.1055\/s-0044-1781456_bib31","doi-asserted-by":"crossref","first-page":"817","DOI":"10.1523\/JNEUROSCI.5996-10.2012","article-title":"Genetic variants of FOXP2 and KIAA0319\/TTRAP\/THEM2 locus are associated with altered brain activation in distinct language-related regions","volume":"32","author":"Pinel","year":"2012","journal-title":"J Neurosci"},{"key":"10.1055\/s-0044-1781456_bib32","doi-asserted-by":"crossref","first-page":"1","DOI":"10.1016\/j.bbr.2017.09.035","article-title":"KIAA0319 promoter DNA methylation predicts dichotic listening performance in forced-attention conditions","volume":"337","author":"Schmitz","year":"2018","journal-title":"Behav Brain Res"},{"issue":"01","key":"10.1055\/s-0044-1781456_bib33","doi-asserted-by":"crossref","first-page":"75","DOI":"10.1111\/jcpp.12612","article-title":"Complex effects of dyslexia risk factors account for ADHD traits: evidence from two independent samples","volume":"58","author":"Mascheretti","year":"2017","journal-title":"J Child Psychol Psychiatry"},{"issue":"10","key":"10.1055\/s-0044-1781456_bib34","doi-asserted-by":"crossref","first-page":"767","DOI":"10.1038\/nrn936","article-title":"Developmental dyslexia: genetic dissection of a complex cognitive trait","volume":"3","author":"Fisher","year":"2002","journal-title":"Nat Rev Neurosci"},{"issue":"07","key":"10.1055\/s-0044-1781456_bib35","doi-asserted-by":"crossref","first-page":"333","DOI":"10.1016\/j.molmed.2006.05.007","article-title":"Breakthroughs in the search for dyslexia candidate genes","volume":"12","author":"McGrath","year":"2006","journal-title":"Trends Mol Med"},{"issue":"04","key":"10.1055\/s-0044-1781456_bib36","doi-asserted-by":"crossref","first-page":"441","DOI":"10.1002\/wcs.138","article-title":"Molecular genetics and molecular biology of dyslexia","volume":"2","author":"Kere","year":"2011","journal-title":"Wiley Interdiscip Rev Cogn Sci"},{"key":"10.1055\/s-0044-1781456_bib37","doi-asserted-by":"crossref","first-page":"283","DOI":"10.1146\/annurev-clinpsy-032814-112842","article-title":"Developmental dyslexia","volume":"11","author":"Peterson","year":"2015","journal-title":"Annu Rev Clin Psychol"},{"issue":"11","key":"10.1055\/s-0044-1781456_bib38","doi-asserted-by":"crossref","first-page":"1621","DOI":"10.1038\/s41588-022-01192-y","article-title":"Discovery of 42 genome-wide significant loci associated with dyslexia","volume":"54","author":"Doust","year":"2022","journal-title":"Nat Genet"},{"key":"10.1055\/s-0044-1781456_bib39","doi-asserted-by":"crossref","DOI":"10.3389\/fnins.2022.981801","article-title":"Animal models of developmental dyslexia","volume":"16","author":"Galaburda","year":"2022","journal-title":"Front Neurosci"},{"issue":"12","key":"10.1055\/s-0044-1781456_bib40","doi-asserted-by":"crossref","first-page":"5831","DOI":"10.1093\/cercor\/bhx269","article-title":"Knockout mice for dyslexia susceptibility gene homologs KIAA0319 and KIAA0319L have unaffected neuronal migration but display abnormal auditory processing","volume":"27","author":"Guidi","year":"2017","journal-title":"Cereb Cortex"},{"issue":"08","key":"10.1055\/s-0044-1781456_bib41","doi-asserted-by":"crossref","first-page":"868","DOI":"10.1111\/j.1601-183X.2011.00727.x","article-title":"Mutation of the dyslexia-associated gene Dcdc2 impairs LTM and visuo-spatial performance in mice","volume":"10","author":"Gabel","year":"2011","journal-title":"Genes Brain Behav"},{"issue":"02","key":"10.1055\/s-0044-1781456_bib42","doi-asserted-by":"crossref","first-page":"116","DOI":"10.1159\/000516667","article-title":"Identifying dyslexia: link between maze learning and dyslexia susceptibility gene, DCDC2, in young children","volume":"43","author":"Gabel","year":"2021","journal-title":"Dev Neurosci"},{"issue":"11","key":"10.1055\/s-0044-1781456_bib43","doi-asserted-by":"crossref","first-page":"2243","DOI":"10.1242\/dev.02379","article-title":"Robo1 regulates the development of major axon tracts and interneuron migration in the forebrain","volume":"133","author":"Andrews","year":"2006","journal-title":"Development"},{"issue":"01","key":"10.1055\/s-0044-1781456_bib44","doi-asserted-by":"crossref","first-page":"495","DOI":"10.1038\/s41398-022-02250-z","article-title":"Hypothesis-driven genome-wide association studies provide novel insights into genetics of reading disabilities","volume":"12","author":"Price","year":"2022","journal-title":"Transl Psychiatry"},{"issue":"1710","key":"10.1055\/s-0044-1781456_bib45","doi-asserted-by":"crossref","DOI":"10.1098\/rstb.2015.0410","article-title":"Cilia in vertebrate left-right patterning","volume":"371","author":"Dasgupta","year":"2016","journal-title":"Philos Trans R Soc Lond B Biol Sci"},{"issue":"01","key":"10.1055\/s-0044-1781456_bib46","doi-asserted-by":"crossref","first-page":"3","DOI":"10.3758\/s13423-017-1236-5","article-title":"Empirical approaches to the study of language evolution","volume":"24","author":"Fitch","year":"2017","journal-title":"Psychon Bull Rev"},{"issue":"01","key":"10.1055\/s-0044-1781456_bib47","doi-asserted-by":"crossref","first-page":"118","DOI":"10.3758\/s13423-016-1166-7","article-title":"Culture and biology in the origins of linguistic structure","volume":"24","author":"Kirby","year":"2017","journal-title":"Psychon Bull Rev"},{"key":"10.1055\/s-0044-1781456_bib48","doi-asserted-by":"crossref","DOI":"10.3389\/fcell.2022.967147","article-title":"Dyslexia associated gene KIAA0319 regulates cell cycle during human neuroepithelial cell development","volume":"10","author":"Paniagua","year":"2022","journal-title":"Front Cell Dev Biol"},{"issue":"01","key":"10.1055\/s-0044-1781456_bib49","doi-asserted-by":"crossref","first-page":"722","DOI":"10.1038\/s41598-021-04539-3","article-title":"KIAA0319 influences cilia length, cell migration and mechanical cell-substrate interaction","volume":"12","author":"Diaz","year":"2022","journal-title":"Sci Rep"},{"issue":"01","key":"10.1055\/s-0044-1781456_bib50","doi-asserted-by":"crossref","first-page":"C160","DOI":"10.1152\/ajpcell.00630.2008","article-title":"The dyslexia-associated protein KIAA0319 interacts with adaptor protein 2 and follows the classical clathrin-mediated endocytosis pathway","volume":"297","author":"Levecque","year":"2009","journal-title":"Am J Physiol Cell Physiol"},{"issue":"10","key":"10.1055\/s-0044-1781456_bib51","doi-asserted-by":"crossref","first-page":"3578","DOI":"10.1096\/fj.201500124RR","article-title":"Ciliary dyslexia candidate genes DYX1C1 and DCDC2 are regulated by regulatory factor X (RFX) transcription factors through X-box promoter motifs","volume":"30","author":"Tammimies","year":"2016","journal-title":"FASEB J"},{"issue":"07","key":"10.1055\/s-0044-1781456_bib52","doi-asserted-by":"crossref","first-page":"2944","DOI":"10.1007\/s12035-020-01905-6","article-title":"Dyslexia candidate gene and ciliary gene expression dynamics during human neuronal differentiation","volume":"57","author":"Bieder","year":"2020","journal-title":"Mol Neurobiol"},{"issue":"08","key":"10.1055\/s-0044-1781456_bib53","doi-asserted-by":"crossref","first-page":"3001","DOI":"10.1096\/fj.07-104455","article-title":"The complex of TFII-I, PARP1, and SFPQ proteins regulates the DYX1C1 gene implicated in neuronal migration and dyslexia","volume":"22","author":"Tapia-P\u00e1ez","year":"2008","journal-title":"FASEB J"},{"issue":"06","key":"10.1055\/s-0044-1781456_bib54","doi-asserted-by":"crossref","DOI":"10.1371\/journal.pone.0020580","article-title":"Increased expression of the dyslexia candidate gene DCDC2 affects length and signaling of primary cilia in neurons","volume":"6","author":"Massinen","year":"2011","journal-title":"PLoS One"},{"key":"10.1055\/s-0044-1781456_bib55","doi-asserted-by":"crossref","first-page":"577","DOI":"10.3389\/fncel.2019.00577","article-title":"Two autism\/dyslexia linked variations of DOCK4 disrupt the gene function on Rac1\/Rap1 activation, neurite outgrowth, and synapse development","volume":"13","author":"Huang","year":"2020","journal-title":"Front Cell Neurosci"},{"key":"10.1055\/s-0044-1781456_bib56","doi-asserted-by":"crossref","first-page":"4","DOI":"10.1186\/s11689-016-9136-y","article-title":"Genomic sequencing of a dyslexia susceptibility haplotype encompassing ROBO1","volume":"8","author":"Massinen","year":"2016","journal-title":"J Neuro-dev Disord"},{"issue":"07","key":"10.1055\/s-0044-1781456_bib57","doi-asserted-by":"crossref","first-page":"622","DOI":"10.1016\/j.biopsych.2023.01.012","article-title":"Stem cell-based organoid models of neurodevelopmental disorders","volume":"93","author":"Wang","year":"2023","journal-title":"Biol Psychiatry"},{"issue":"35","key":"10.1055\/s-0044-1781456_bib58","doi-asserted-by":"crossref","DOI":"10.1073\/pnas.2202764119","article-title":"Genome-wide analyses of individual differences in quantitatively assessed reading- and language-related skills in up to 34,000 people","volume":"119","author":"Eising","year":"2022","journal-title":"Proc Natl Acad Sci U S A"},{"issue":"01","key":"10.1055\/s-0044-1781456_bib59","doi-asserted-by":"crossref","first-page":"10","DOI":"10.1097\/YPG.0000000000000009","article-title":"Association of SNPs of DYX1C1 with developmental dyslexia in an Indian population","volume":"24","author":"Venkatesh","year":"2014","journal-title":"Psychiatr Genet"},{"issue":"07","key":"10.1055\/s-0044-1781456_bib60","doi-asserted-by":"crossref","first-page":"3004","DOI":"10.1038\/s41380-020-00898-x","article-title":"Genome-wide association study reveals new insights into the heritability and genetic correlates of developmental dyslexia","volume":"26","author":"Gialluisi","year":"2021","journal-title":"Mol Psychiatry"},{"issue":"05","key":"10.1055\/s-0044-1781456_bib61","doi-asserted-by":"crossref","first-page":"2616","DOI":"10.1002\/hbm.23546","article-title":"ROBO1 polymorphisms, callosal connectivity, and reading skills","volume":"38","author":"Sun","year":"2017","journal-title":"Hum Brain Mapp"},{"issue":"02","key":"10.1055\/s-0044-1781456_bib62","doi-asserted-by":"crossref","first-page":"158","DOI":"10.1111\/j.1601-183X.2010.00651.x","article-title":"Analysis of dyslexia candidate genes in the Raine cohort representing the general Australian population","volume":"10","author":"Paracchini","year":"2011","journal-title":"Genes Brain Behav"},{"issue":"15","key":"10.1055\/s-0044-1781456_bib63","doi-asserted-by":"crossref","first-page":"2802","DOI":"10.1093\/hmg\/ddp215","article-title":"Functional interaction of DYX1C1 with estrogen receptors suggests involvement of hormonal pathways in dyslexia","volume":"18","author":"Massinen","year":"2009","journal-title":"Hum Mol Genet"},{"issue":"09","key":"10.1055\/s-0044-1781456_bib64","doi-asserted-by":"crossref","first-page":"995","DOI":"10.1038\/ng.2707","article-title":"DYX1C1 is required for axonemal dynein assembly and ciliary motility","volume":"45","author":"Tarkar","year":"2013","journal-title":"Nat Genet"},{"issue":"06","key":"10.1055\/s-0044-1781456_bib65","doi-asserted-by":"crossref","first-page":"1495","DOI":"10.1093\/cercor\/bhs141","article-title":"Robo1 regulates the migration and laminar distribution of upper-layer pyramidal neurons of the cerebral cortex","volume":"23","author":"Gonda","year":"2013","journal-title":"Cereb Cortex"},{"key":"10.1055\/s-0044-1781456_bib66","doi-asserted-by":"crossref","DOI":"10.3389\/fcell.2020.607415","article-title":"Beyond axon guidance: roles of slit-robo signaling in neocortical formation","volume":"8","author":"Gonda","year":"2020","journal-title":"Front Cell Dev Biol"},{"issue":"03","key":"10.1055\/s-0044-1781456_bib67","doi-asserted-by":"crossref","first-page":"723","DOI":"10.1016\/j.neuroscience.2008.01.020","article-title":"Postnatal analysis of the effect of embryonic knockdown and overexpression of candidate dyslexia susceptibility gene homolog Dcdc2 in the rat","volume":"152","author":"Burbridge","year":"2008","journal-title":"Neuroscience"},{"issue":"08","key":"10.1055\/s-0044-1781456_bib68","doi-asserted-by":"crossref","first-page":"671","DOI":"10.1016\/j.biopsych.2012.05.008","article-title":"Three dyslexia susceptibility genes, DYX1C1, DCDC2, and KIAA0319, affect temporo-parietal white matter structure","volume":"72","author":"Darki","year":"2012","journal-title":"Biol Psychiatry"},{"issue":"16","key":"10.1055\/s-0044-1781456_bib69","doi-asserted-by":"crossref","first-page":"2634","DOI":"10.1002\/cne.24696","article-title":"The dyslexia susceptibility KIAA0319 gene shows a specific expression pattern during zebrafish development supporting a role beyond neuronal migration","volume":"527","author":"Gostic","year":"2019","journal-title":"J Comp Neurol"}],"container-title":["Global Medical Genetics"],"original-title":[],"language":"en","link":[{"URL":"https:\/\/api.elsevier.com\/content\/article\/PII:S2699940425000141?httpAccept=text\/xml","content-type":"text\/xml","content-version":"vor","intended-application":"text-mining"},{"URL":"https:\/\/api.elsevier.com\/content\/article\/PII:S2699940425000141?httpAccept=text\/plain","content-type":"text\/plain","content-version":"vor","intended-application":"text-mining"},{"URL":"http:\/\/www.thieme-connect.de\/products\/ejournals\/pdf\/10.1055\/s-0044-1781456.pdf","content-type":"unspecified","content-version":"vor","intended-application":"similarity-checking"}],"deposited":{"date-parts":[[2025,10,23]],"date-time":"2025-10-23T07:36:11Z","timestamp":1761204971000},"score":1,"resource":{"primary":{"URL":"https:\/\/linkinghub.elsevier.com\/retrieve\/pii\/S2699940425000141"}},"subtitle":[],"short-title":[],"issued":{"date-parts":[[2024]]},"references-count":69,"journal-issue":{"issue":"1","published-print":{"date-parts":[[2024]]}},"alternative-id":["S2699940425000141"],"URL":"https:\/\/doi.org\/10.1055\/s-0044-1781456","relation":{},"ISSN":["2699-9404"],"issn-type":[{"value":"2699-9404","type":"print"}],"subject":[],"published":{"date-parts":[[2024]]},"assertion":[{"value":"Elsevier","name":"publisher","label":"This article is maintained by"},{"value":"Genetic Modifications of Developmental Dyslexia and Its Representation Using In Vivo, In Vitro Model","name":"articletitle","label":"Article Title"},{"value":"Global Medical Genetics","name":"journaltitle","label":"Journal Title"},{"value":"https:\/\/doi.org\/10.1055\/s-0044-1781456","name":"articlelink","label":"CrossRef DOI link to publisher maintained version"},{"value":"article","name":"content_type","label":"Content Type"},{"value":"Copyright \u00a9 2024 International Knowledge Direct Medical Associations. Publishing services by Elsevier B.V. on behalf of KeAi Communications Co. Ltd. Published by Elsevier B.V.","name":"copyright","label":"Copyright"}]}}