{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2026,1,10]],"date-time":"2026-01-10T07:08:30Z","timestamp":1768028910943,"version":"3.49.0"},"reference-count":70,"publisher":"Public Library of Science (PLoS)","issue":"10","license":[{"start":{"date-parts":[[2010,10,28]],"date-time":"2010-10-28T00:00:00Z","timestamp":1288224000000},"content-version":"unspecified","delay-in-days":0,"URL":"http:\/\/creativecommons.org\/licenses\/by\/4.0\/"}],"content-domain":{"domain":["www.plosone.org"],"crossmark-restriction":false},"short-container-title":["PLoS ONE"],"DOI":"10.1371\/journal.pone.0013712","type":"journal-article","created":{"date-parts":[[2010,10,28]],"date-time":"2010-10-28T15:45:00Z","timestamp":1288280700000},"page":"e13712","update-policy":"https:\/\/doi.org\/10.1371\/journal.pone.corrections_policy","source":"Crossref","is-referenced-by-count":31,"title":["Identification of Candidate Genes for Dyslexia Susceptibility on Chromosome 18"],"prefix":"10.1371","volume":"5","author":[{"given":"Thomas S.","family":"Scerri","sequence":"first","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Silvia","family":"Paracchini","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Andrew","family":"Morris","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"I. Laurence","family":"MacPhie","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Joel","family":"Talcott","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"John","family":"Stein","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Shelley D.","family":"Smith","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Bruce F.","family":"Pennington","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Richard K.","family":"Olson","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"John C.","family":"DeFries","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Anthony P.","family":"Monaco","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]}],"member":"340","published-online":{"date-parts":[[2010,10,28]]},"reference":[{"key":"ref1","doi-asserted-by":"crossref","first-page":"2373","DOI":"10.1093\/brain\/123.12.2373","article-title":"The neurological basis of developmental dyslexia: an overview and working hypothesis.","volume":"123 Pt 12","author":"M Habib","year":"2000","journal-title":"Brain"},{"key":"ref2","doi-asserted-by":"crossref","first-page":"57","DOI":"10.1146\/annurev.genom.8.080706.092312","article-title":"The genetic lexicon of dyslexia.","volume":"8","author":"S Paracchini","year":"2007","journal-title":"Annu Rev Genomics Hum Genet"},{"key":"ref3","doi-asserted-by":"crossref","first-page":"289","DOI":"10.1136\/jmg.2006.046516","article-title":"Genetics of dyslexia: the evolving landscape.","volume":"44","author":"J Schumacher","year":"2007","journal-title":"J Med Genet"},{"key":"ref4","doi-asserted-by":"crossref","first-page":"307","DOI":"10.1056\/NEJM199801293380507","article-title":"Dyslexia.","volume":"338","author":"SE Shaywitz","year":"1998","journal-title":"N Engl J Med"},{"key":"ref5","doi-asserted-by":"crossref","first-page":"681","DOI":"10.1038\/sj.ejhg.5201575","article-title":"The genetics of developmental dyslexia.","volume":"14","author":"J Williams","year":"2006","journal-title":"Eur J Hum Genet"},{"key":"ref6","article-title":"The ICD-10 classification of mental and behavioural disorders: diagnostic criteria for research.","volume":"xii, 248","year":"1993"},{"key":"ref7","article-title":"Congenital \u201cword-blindness\u201d and its treatment.","volume":"3","author":"CJ Thomas","year":"1905","journal-title":"Ophthalmoscope"},{"key":"ref8","first-page":"608","article-title":"Four cases of congenital word-blindness affecting three generations of one family.","volume":"1","author":"J Hinshelwood","year":"1907","journal-title":"British Medical Journal"},{"key":"ref9","first-page":"482","article-title":"Six cases of congenital word-blindness affecting three generations of one family.","volume":"5","author":"S Stephenson","year":"1907","journal-title":"Ophthalmoscope"},{"key":"ref10","first-page":"1","article-title":"Specific dyslexia (congenital word-blindness); a clinical and genetic study.","volume":"Neurol","author":"B Hallgren","year":"1950","journal-title":"Acta Psychiatr"},{"key":"ref11","doi-asserted-by":"crossref","first-page":"184","DOI":"10.1111\/j.1469-8749.1973.tb15158.x","article-title":"Reading disability in twins.","volume":"15","author":"H Bakwin","year":"1973","journal-title":"Dev Med Child Neurol"},{"key":"ref12","doi-asserted-by":"crossref","first-page":"39","DOI":"10.1002\/(SICI)1098-2779(1996)2:1<39::AID-MRDD7>3.0.CO;2-S","article-title":"Genetics of specifc reading disability.","volume":"2","author":"JC DeFries","year":"1996","journal-title":"Mental Retardation and Developmental Disabilities: Reseach Reviews"},{"key":"ref13","doi-asserted-by":"crossref","first-page":"537","DOI":"10.1038\/329537a0","article-title":"Evidence for a genetic aetiology in reading disability of twins.","volume":"329","author":"JC DeFries","year":"1987","journal-title":"Nature"},{"key":"ref14","doi-asserted-by":"crossref","first-page":"229","DOI":"10.1111\/j.1469-7610.1987.tb00207.x","article-title":"A twin study of genetic influences on reading and spelling ability and disability.","volume":"28","author":"J Stevenson","year":"1987","journal-title":"J Child Psychol Psychiatry"},{"key":"ref15","doi-asserted-by":"crossref","first-page":"483","DOI":"10.1207\/S15326942DN2002_3","article-title":"Genetic and environmental influences on orthographic and phonological skills in children with reading disabilities.","volume":"20","author":"J Gayan","year":"2001","journal-title":"Dev Neuropsychol"},{"key":"ref16","doi-asserted-by":"crossref","first-page":"73","DOI":"10.1006\/jecp.1998.2482","article-title":"Varieties of developmental reading disorder: genetic and environmental influences.","volume":"72","author":"A Castles","year":"1999","journal-title":"J Exp Child Psychol"},{"key":"ref17","doi-asserted-by":"crossref","first-page":"11553","DOI":"10.1073\/pnas.1833911100","article-title":"A candidate gene for developmental dyslexia encodes a nuclear tetratricopeptide repeat domain protein dynamically regulated in brain.","volume":"100","author":"M Taipale","year":"2003","journal-title":"Proc Natl Acad Sci U S A"},{"key":"ref18","doi-asserted-by":"crossref","first-page":"17053","DOI":"10.1073\/pnas.0508591102","article-title":"DCDC2 is associated with reading disability and modulates neuronal development in the brain.","volume":"102","author":"H Meng","year":"2005","journal-title":"Proc Natl Acad Sci U S A"},{"key":"ref19","doi-asserted-by":"crossref","first-page":"1659","DOI":"10.1093\/hmg\/ddl089","article-title":"The chromosome 6p22 haplotype associated with dyslexia reduces the expression of KIAA0319, a novel gene involved in neuronal migration.","volume":"15","author":"S Paracchini","year":"2006","journal-title":"Hum Mol Genet"},{"key":"ref20","doi-asserted-by":"crossref","first-page":"e1000436","DOI":"10.1371\/journal.pgen.1000436","article-title":"A common variant associated with dyslexia reduces expression of the KIAA0319 gene.","volume":"5","author":"MY Dennis","year":"2009","journal-title":"PLoS Genet"},{"key":"ref21","doi-asserted-by":"crossref","first-page":"667","DOI":"10.1093\/hmg\/ddm009","article-title":"A locus on 2p12 containing the co-regulated MRPL19 and C2ORF3 genes is associated to dyslexia.","volume":"16","author":"H Anthoni","year":"2007","journal-title":"Hum Mol Genet"},{"key":"ref22","doi-asserted-by":"crossref","first-page":"e50","DOI":"10.1371\/journal.pgen.0010050","article-title":"The axon guidance receptor gene ROBO1 is a candidate gene for developmental dyslexia.","volume":"1","author":"K Hannula-Jouppi","year":"2005","journal-title":"PLoS Genet"},{"key":"ref23","doi-asserted-by":"crossref","first-page":"86","DOI":"10.1038\/ng792","article-title":"Independent genome-wide scans identify a chromosome 18 quantitative-trait locus influencing dyslexia.","volume":"30","author":"SE Fisher","year":"2002","journal-title":"Nat Genet"},{"key":"ref24","doi-asserted-by":"crossref","first-page":"561","DOI":"10.1086\/368201","article-title":"Use of multivariate linkage analysis for dissection of a complex cognitive trait.","volume":"72","author":"AJ Marlow","year":"2003","journal-title":"Am J Hum Genet"},{"key":"ref25","doi-asserted-by":"crossref","first-page":"658","DOI":"10.1136\/jmg.38.10.658","article-title":"A dominant gene for developmental dyslexia on chromosome 3.","volume":"38","author":"J Nopola-Hemmi","year":"2001","journal-title":"J Med Genet"},{"key":"ref26","doi-asserted-by":"crossref","first-page":"340","DOI":"10.1136\/jmg.40.5.340","article-title":"A genome scan for developmental dyslexia confirms linkage to chromosome 2p11 and suggests a new locus on 7q32.","volume":"40","author":"N Kaminen","year":"2003","journal-title":"J Med Genet"},{"key":"ref27","doi-asserted-by":"crossref","first-page":"652","DOI":"10.1136\/jmg.2003.012294","article-title":"Genomewide scan identifies susceptibility locus for dyslexia on Xq27 in an extended Dutch family.","volume":"41","author":"CG de Kovel","year":"2004","journal-title":"J Med Genet"},{"key":"ref28","doi-asserted-by":"crossref","first-page":"699","DOI":"10.1038\/sj.mp.4001657","article-title":"A genome scan in multigenerational families with dyslexia: Identification of a novel locus on chromosome 2q that contributes to phonological decoding efficiency.","volume":"10","author":"WH Raskind","year":"2005","journal-title":"Mol Psychiatry"},{"key":"ref29","doi-asserted-by":"crossref","first-page":"15","DOI":"10.1002\/ajmg.b.30245","article-title":"Genomewide scan for real-word reading subphenotypes of dyslexia: novel chromosome 13 locus and genetic complexity.","volume":"141B","author":"RP Igo Jr","year":"2006","journal-title":"Am J Med Genet B Neuropsychiatr Genet"},{"key":"ref30","first-page":"556","article-title":"Suggestive evidence of linkage with reading disability in a large Norwegian family.","volume":"96","author":"N Norton","year":"2000","journal-title":"Am J Med Genet"},{"key":"ref31","doi-asserted-by":"crossref","first-page":"67","DOI":"10.1002\/ajmg.b.30018","article-title":"Linkage analyses of four regions previously implicated in dyslexia: confirmation of a locus on chromosome 15q.","volume":"131B","author":"NH Chapman","year":"2004","journal-title":"Am J Med Genet B Neuropsychiatr Genet"},{"key":"ref32","doi-asserted-by":"crossref","first-page":"417","DOI":"10.1007\/s00702-005-0336-y","article-title":"Linkage analyses of chromosomal region 18p11-q12 in dyslexia.","volume":"113","author":"J Schumacher","year":"2006","journal-title":"J Neural Transm"},{"key":"ref33","doi-asserted-by":"crossref","first-page":"294","DOI":"10.1002\/ajmg.b.30598","article-title":"Confirmation of dyslexia susceptibility loci on chromosomes 1p and 2p, but not 6p in a Dutch sib-pair collection.","volume":"147","author":"CG de Kovel","year":"2008","journal-title":"Am J Med Genet B Neuropsychiatr Genet"},{"key":"ref34","doi-asserted-by":"crossref","first-page":"194","DOI":"10.1038\/sj.ejhg.5201739","article-title":"Replication of reported linkages for dyslexia and spelling and suggestive evidence for novel regions on chromosomes 4 and 17.","volume":"15","author":"TC Bates","year":"2007","journal-title":"Eur J Hum Genet"},{"key":"ref35","doi-asserted-by":"crossref","first-page":"S15","DOI":"10.1186\/1471-2350-8-S1-S15","article-title":"Genetic correlates of brain aging on MRI and cognitive test measures: a genome-wide association and linkage analysis in the Framingham Study.","volume":"8","author":"S Seshadri","year":"2007","journal-title":"BMC Med Genet"},{"key":"ref36","doi-asserted-by":"crossref","first-page":"69","DOI":"10.1101\/sqb.2003.68.69","article-title":"Highly parallel SNP genotyping.","volume":"68","author":"JB Fan","year":"2003","journal-title":"Cold Spring Harb Symp Quant Biol"},{"key":"ref37","first-page":"241","article-title":"MALDI-TOF mass spectrometry-based SNP genotyping.","volume":"212","author":"N Storm","year":"2003","journal-title":"Methods Mol Biol"},{"key":"ref38","doi-asserted-by":"crossref","first-page":"37","DOI":"10.1016\/S1387-3806(02)00980-6","article-title":"Single nucleotide polymorphism analyses by MALDI-TOF MS.","volume":"226","author":"K Tang","year":"2003","journal-title":"International Journal of Mass Spectrometry"},{"key":"ref39","doi-asserted-by":"crossref","first-page":"263","DOI":"10.1093\/bioinformatics\/bth457","article-title":"Haploview: analysis and visualization of LD and haplotype maps.","volume":"21","author":"JC Barrett","year":"2005","journal-title":"Bioinformatics"},{"key":"ref40","doi-asserted-by":"crossref","first-page":"2225","DOI":"10.1126\/science.1069424","article-title":"The structure of haplotype blocks in the human genome.","volume":"296","author":"SB Gabriel","year":"2002","journal-title":"Science"},{"key":"ref41","doi-asserted-by":"crossref","first-page":"210","DOI":"10.1186\/1471-2105-7-210","article-title":"An integrated system for genetic analysis.","volume":"7","author":"S Fiddy","year":"2006","journal-title":"BMC Bioinformatics"},{"key":"ref42","doi-asserted-by":"crossref","first-page":"97","DOI":"10.1038\/ng786","article-title":"Merlin\u2014rapid analysis of dense genetic maps using sparse gene flow trees.","volume":"30","author":"GR Abecasis","year":"2002","journal-title":"Nat Genet"},{"key":"ref43","doi-asserted-by":"crossref","first-page":"3445","DOI":"10.1093\/bioinformatics\/bti529","article-title":"PEDSTATS: descriptive statistics, graphics and quality assessment for gene mapping data.","volume":"21","author":"JE Wigginton","year":"2005","journal-title":"Bioinformatics"},{"key":"ref44","doi-asserted-by":"crossref","first-page":"1567","DOI":"10.1093\/genetics\/164.4.1567","article-title":"Inference of population structure using multilocus genotype data: linked loci and correlated allele frequencies.","volume":"164","author":"D Falush","year":"2003","journal-title":"Genetics"},{"key":"ref45","doi-asserted-by":"crossref","first-page":"945","DOI":"10.1093\/genetics\/155.2.945","article-title":"Inference of population structure using multilocus genotype data.","volume":"155","author":"JK Pritchard","year":"2000","journal-title":"Genetics"},{"key":"ref46","first-page":"1347","article-title":"Parametric and nonparametric linkage analysis: a unified multipoint approach.","volume":"58","author":"L Kruglyak","year":"1996","journal-title":"Am J Hum Genet"},{"key":"ref47","doi-asserted-by":"crossref","first-page":"3","DOI":"10.1007\/BF01066731","article-title":"The investigation of linkage between a quantitative trait and a marker locus.","volume":"2","author":"JK Haseman","year":"1972","journal-title":"Behav Genet"},{"key":"ref48","doi-asserted-by":"crossref","first-page":"299","DOI":"10.1007\/BF00354964","article-title":"Multiple regression analysis of sib-pair data on reading to detect quantitative trait loci.","volume":"3","author":"DW Fulker","year":"2004","journal-title":"Reading and Writing"},{"key":"ref49","doi-asserted-by":"crossref","first-page":"371","DOI":"10.1093\/bioinformatics\/17.4.371","article-title":"DeFries-Fulker multiple regression analysis of sibship QTL data: a SAS macro.","volume":"17","author":"JM Lessem","year":"2001","journal-title":"Bioinformatics"},{"key":"ref50","doi-asserted-by":"crossref","first-page":"279","DOI":"10.1086\/302698","article-title":"A general test of association for quantitative traits in nuclear families.","volume":"66","author":"GR Abecasis","year":"2000","journal-title":"Am J Hum Genet"},{"key":"ref51","doi-asserted-by":"crossref","first-page":"545","DOI":"10.1038\/sj.ejhg.5200494","article-title":"Pedigree tests of transmission disequilibrium.","volume":"8","author":"GR Abecasis","year":"2000","journal-title":"Eur J Hum Genet"},{"key":"ref52","doi-asserted-by":"crossref","first-page":"559","DOI":"10.1086\/519795","article-title":"PLINK: a tool set for whole-genome association and population-based linkage analyses.","volume":"81","author":"S Purcell","year":"2007","journal-title":"Am J Hum Genet"},{"key":"ref53","doi-asserted-by":"crossref","first-page":"1214","DOI":"10.1006\/bbrc.1994.1580","article-title":"Molecular cloning, expression, and characterization of a fifth melanocortin receptor.","volume":"200","author":"I Gantz","year":"1994","journal-title":"Biochem Biophys Res Commun"},{"key":"ref54","doi-asserted-by":"crossref","first-page":"63","DOI":"10.1016\/0031-9384(77)90095-6","article-title":"Influence of neonatal injections of alpha-MSH on learning, memory and attention in rats.","volume":"18","author":"BE Beckwith","year":"1977","journal-title":"Physiol Behav"},{"key":"ref55","doi-asserted-by":"crossref","first-page":"445","DOI":"10.1097\/00004714-200008000-00009","article-title":"Event-related brain potentials and working memory function in healthy humans after single-dose and prolonged intranasal administration of adrenocorticotropin 4-10 and desacetyl-alpha-melanocyte stimulating hormone.","volume":"20","author":"R Smolnik","year":"2000","journal-title":"J Clin Psychopharmacol"},{"key":"ref56","doi-asserted-by":"crossref","first-page":"1","DOI":"10.1124\/pr.56.1.1","article-title":"Targeting melanocortin receptors as a novel strategy to control inflammation.","volume":"56","author":"A Catania","year":"2004","journal-title":"Pharmacol Rev"},{"key":"ref57","doi-asserted-by":"crossref","first-page":"43","DOI":"10.1016\/0031-9384(78)90201-9","article-title":"Effects of MSH\/ACTH 4\u201310 on memory, attention and endogenous hormone levels in women.","volume":"20","author":"JL Veith","year":"1978","journal-title":"Physiol Behav"},{"key":"ref58","doi-asserted-by":"crossref","first-page":"669","DOI":"10.1016\/0031-9384(79)90228-2","article-title":"MSH\/ACTH 4-10 in men and women: effects upon performance of an attention and memory task.","volume":"22","author":"MM Ward","year":"1979","journal-title":"Physiol Behav"},{"key":"ref59","doi-asserted-by":"crossref","first-page":"33","DOI":"10.1016\/0306-4530(85)90037-X","article-title":"The relationship of endogenous ACTH levels to visual-attentional functioning in patients with congenital adrenal hyperplasia.","volume":"10","author":"JL Veith","year":"1985","journal-title":"Psychoneuroendocrinology"},{"key":"ref60","doi-asserted-by":"crossref","first-page":"45","DOI":"10.3109\/00207459209003277","article-title":"Testosterone, estradiol, ACTH and musical, spatial and verbal performance.","volume":"65","author":"M Hassler","year":"1992","journal-title":"Int J Neurosci"},{"key":"ref61","doi-asserted-by":"crossref","first-page":"419","DOI":"10.1086\/346176","article-title":"Mental retardation and abnormal skeletal development (Dyggve-Melchior-Clausen dysplasia) due to mutations in a novel, evolutionarily conserved gene.","volume":"72","author":"DH Cohn","year":"2003","journal-title":"Am J Hum Genet"},{"key":"ref62","doi-asserted-by":"crossref","first-page":"8597","DOI":"10.1074\/jbc.C000906200","article-title":"The Nedd4-like protein KIAA0439 is a potential regulator of the epithelial sodium channel.","volume":"276","author":"KF Harvey","year":"2001","journal-title":"J Biol Chem"},{"key":"ref63","doi-asserted-by":"crossref","first-page":"1345","DOI":"10.1002\/ajmg.b.30867","article-title":"Genome-wide association scan of quantitative traits for attention deficit hyperactivity disorder identifies novel associations and confirms candidate gene associations.","volume":"147B","author":"J Lasky-Su","year":"2008","journal-title":"Am J Med Genet B Neuropsychiatr Genet"},{"key":"ref64","doi-asserted-by":"crossref","first-page":"672","DOI":"10.1016\/j.amjhyper.2004.12.004","article-title":"Further evidence of a quantitative trait locus on chromosome 18 influencing postural change in systolic blood pressure: the Hypertension Genetic Epidemiology Network (HyperGEN) Study.","volume":"18","author":"JS Pankow","year":"2005","journal-title":"Am J Hypertens"},{"key":"ref65","doi-asserted-by":"crossref","first-page":"488","DOI":"10.1161\/01.HYP.0000178594.63193.c0","article-title":"Association of NEDD4L ubiquitin ligase with essential hypertension.","volume":"46","author":"CJ Russo","year":"2005","journal-title":"Hypertension"},{"key":"ref66","doi-asserted-by":"crossref","first-page":"562","DOI":"10.1038\/sj.ki.5001590","article-title":"24-h ambulatory blood pressure is linked to chromosome 18q21-22 and genetic variation of NEDD4L associates with cross-sectional and longitudinal blood pressure in Swedes.","volume":"70","author":"C Fava","year":"2006","journal-title":"Kidney Int"},{"key":"ref67","doi-asserted-by":"crossref","first-page":"87","DOI":"10.1080\/10641960801949909","article-title":"Two polymorphisms in NEDD4L gene and essential hypertension in Chinese Hans - a population-based case-control study.","volume":"30","author":"H Wen","year":"2008","journal-title":"Clin Exp Hypertens"},{"key":"ref68","doi-asserted-by":"crossref","first-page":"179","DOI":"10.1177\/002221940003300206","article-title":"Comorbidity of reading disability and attention-deficit\/hyperactivity disorder: differences by gender and subtype.","volume":"33","author":"EG Willcutt","year":"2000","journal-title":"J Learn Disabil"},{"key":"ref69","doi-asserted-by":"crossref","first-page":"30","DOI":"10.1136\/adc.86.1.30","article-title":"Dyslexia and familial high blood pressure: an observational pilot study.","volume":"86","author":"K Taylor","year":"2002","journal-title":"Arch Dis Child"},{"key":"ref70","doi-asserted-by":"crossref","first-page":"33","DOI":"10.1159\/000106060","article-title":"Haplotype diversity in four genes (CLCNKA, CLCNKB, BSND, NEDD4L) involved in renal salt reabsorption.","volume":"65","author":"S Sile","year":"2008","journal-title":"Hum Hered"}],"updated-by":[{"DOI":"10.1371\/annotation\/2294a38b-878d-42f0-9faf-0822db4a0248","type":"correction","label":"Correction","source":"publisher","updated":{"date-parts":[[2010,12,15]],"date-time":"2010-12-15T00:00:00Z","timestamp":1292371200000}}],"container-title":["PLoS ONE"],"original-title":[],"language":"en","link":[{"URL":"http:\/\/dx.plos.org\/10.1371\/journal.pone.0013712","content-type":"unspecified","content-version":"vor","intended-application":"similarity-checking"}],"deposited":{"date-parts":[[2021,11,12]],"date-time":"2021-11-12T15:47:56Z","timestamp":1636732076000},"score":1,"resource":{"primary":{"URL":"https:\/\/dx.plos.org\/10.1371\/journal.pone.0013712"}},"subtitle":[],"editor":[{"given":"Michael","family":"Hendricks","sequence":"first","affiliation":[],"role":[{"role":"editor","vocabulary":"crossref"}]}],"short-title":[],"issued":{"date-parts":[[2010,10,28]]},"references-count":70,"journal-issue":{"issue":"10","published-online":{"date-parts":[[2010,10,28]]}},"URL":"https:\/\/doi.org\/10.1371\/journal.pone.0013712","relation":{"correction":[{"id-type":"doi","id":"10.1371\/annotation\/2294a38b-878d-42f0-9faf-0822db4a0248","asserted-by":"object"}]},"ISSN":["1932-6203"],"issn-type":[{"value":"1932-6203","type":"electronic"}],"subject":[],"published":{"date-parts":[[2010,10,28]]}}}