Common variation near ROBO2 is associated with expressive vocabulary in infancy

Nature Communications

Volumn 5, Issue , 2014, Pages

  St Pourcain, Beate ^a   Cents, Rolieke A M ^b   Whitehouse, Andrew J O ^c   Haworth, Claire M A ^d,e   Davis, Oliver S P ^e,f   O'Reilly, Paul F ^e,g   Roulstone, Susan ^h   Wren, Yvonne ^h   Ang, Qi W ⁱ   Velders, Fleur P ^b   Evans, David M ^a,j   Kemp, John P ^a,j   Warrington, Nicole M ^i,j   Miller, Laura ^a   Timpson, Nicholas J ^a   Ring, Susan M ^a   Verhulst, Frank C ^b   Hofman, Albert ^b   Rivadeneira, Fernando ^b   Meaburn, Emma L ^k   Price, Thomas S ^l   Dale, Philip S ^m   Pillas, Demetris ^g   Yliherva, Anneli ⁿ   Rodriguez, Alina ^g,o   Golding, Jean ^a   Jaddoe, Vincent W V ^b   Jarvelin, Marjo Riitta ^g,n,p,q   Plomin, Robert ^e   Pennell, Craig E ⁱ   Tiemeier, Henning ^b   Smith, George Davey ^a   more..

^a UNIVERSITY OF BRISTOL   (United Kingdom)

^b ERASMUS MEDICAL CENTER   (Netherlands)

^c UNIVERSITY OF WESTERN AUSTRALIA   (Australia)

^d UNIVERSITY OF WARWICK   (United Kingdom)

^e KING'S COLLEGE LONDON   (United Kingdom)

^f UNIVERSITY COLLEGE LONDON   (United Kingdom)

^g PUBLIC HEALTH ENGLAND   (United Kingdom)

^h UNIVERSITY OF THE WEST OF ENGLAND   (United Kingdom)

ⁱ UNIVERSITY OF WESTERN AUSTRALIA   (Australia)

^j UNIVERSITY OF QUEENSLAND   (Australia)

^k UNIVERSITY OF LONDON   (United Kingdom)

^l UNIVERSITY OF PENNSYLVANIA   (United States)

^m UNIVERSITY OF NEW MEXICO   (United States)

ⁿ UNIVERSITY OF OULU   (Finland)

^o MID SWEDEN UNIVERSITY   (Sweden)

^p OULU UNIVERSITY HOSPITAL   (Finland)

^q NATIONAL PUBLIC HEALTH INSTITUTE   (Finland)

more..

Author keywords

[No Author keywords available]

Indexed keywords

ROUNDABOUT RECEPTOR; ROUNDABOUT RECEPTOR 2; UNCLASSIFIED DRUG; IMMUNOGLOBULIN RECEPTOR; ROBO2 PROTEIN, HUMAN;

CHILD HEALTH; GENE EXPRESSION; PROTEIN;

ARTICLE; AUTISM; CHILD; DIZYGOTIC TWINS; DYSLEXIA; EUROPEAN; FEMALE; FOLLOW UP; GENE LINKAGE DISEQUILIBRIUM; GENE LOCUS; GENETIC ANALYSIS; GENETIC ASSOCIATION; GENETIC LINKAGE; GENETIC SCREENING; GENETIC TRAIT; GENETIC VARIABILITY; HUMAN; INFANCY; LANGUAGE; LANGUAGE DEVELOPMENT; LINGUISTICS; MALE; MONOZYGOTIC TWINS; NERVE FIBER; PRESCHOOL CHILD; READING; RECEPTOR BINDING; SINGLE NUCLEOTIDE POLYMORPHISM; SPEECH SOUND DISORDER; TODDLER; CAUCASIAN; CHROMOSOME MAP; CLINICAL TRIAL; ETHNOLOGY; GENE EXPRESSION; GENETIC PREDISPOSITION; GENETICS; INFANT; LANGUAGE DISABILITY; MULTICENTER STUDY; PATHOPHYSIOLOGY; PHENOTYPE; PHYSIOLOGY; QUANTITATIVE TRAIT LOCUS; SPEECH;

AUTISTIC DISORDER; CHILD, PRESCHOOL; CHROMOSOME MAPPING; DYSLEXIA; EUROPEAN CONTINENTAL ANCESTRY GROUP; FEMALE; GENE EXPRESSION; GENETIC LINKAGE; GENETIC PREDISPOSITION TO DISEASE; GENOME-WIDE ASSOCIATION STUDY; HUMANS; INFANT; LANGUAGE; LANGUAGE DEVELOPMENT; LANGUAGE DISORDERS; MALE; PHENOTYPE; POLYMORPHISM, SINGLE NUCLEOTIDE; QUANTITATIVE TRAIT LOCI; RECEPTORS, IMMUNOLOGIC; SPEECH; SPEECH SOUND DISORDER; VOCABULARY;

EID: 84910107464     PISSN: None     EISSN: 20411723     Source Type: Journal    
DOI: 10.1038/ncomms5831     Document Type: Article

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