Common EIF4E variants modulate risk for autism spectrum disorders in the high-functioning range

Journal of Neural Transmission

Volumn 121, Issue 9, 2014, Pages 1107-1116

  Waltes, Regina ^a   Gfesser, Johannes ^a   Haslinger, Denise ^a   Schneider Momm, Katja ^b   Biscaldi, Monica ^b   Voran, Anette ^c   Freitag, Christine M ^a   Chiocchetti, Andreas G ^a  

^a GOETHE UNIVERSITY   (Germany)

^b UNIVERSITY OF FREIBURG   (Germany)

^c SAARLAND UNIVERSITY   (Germany)

Author keywords

Association analysis; Common variant; High functioning autism; Repetitive behaviour; Transmission disequilibrium testing

Indexed keywords

INITIATION FACTOR 4E; EIF4ENIF1 PROTEIN, HUMAN; NUCLEOCYTOPLASMIC TRANSPORT PROTEIN;

ALLELE; ARTICLE; ASPERGER SYNDROME; AUTISM; CHILD; COHORT ANALYSIS; COMPULSION; COMPUTER MODEL; CONTROLLED STUDY; FEMALE; GENE FREQUENCY; GENETIC ASSOCIATION; GENETIC RISK; GENETIC VARIABILITY; GENOTYPE; GESTURE; HUMAN; MAJOR CLINICAL STUDY; MALE; PRIORITY JOURNAL; SINGLE NUCLEOTIDE POLYMORPHISM; STEREOTYPY; STRICT AUTISM; GENETIC PREDISPOSITION; GENETICS; GENOTYPING TECHNIQUE; PSYCHOLOGICAL RATING SCALE; STATISTICAL MODEL;

CHILD; CHILD DEVELOPMENT DISORDERS, PERVASIVE; COHORT STUDIES; FEMALE; GENETIC PREDISPOSITION TO DISEASE; GENOTYPING TECHNIQUES; HUMANS; LOGISTIC MODELS; MALE; NUCLEOCYTOPLASMIC TRANSPORT PROTEINS; POLYMORPHISM, SINGLE NUCLEOTIDE; PSYCHIATRIC STATUS RATING SCALES;

EID: 84907597997     PISSN: 03009564     EISSN: 14351463     Source Type: Journal    
DOI: 10.1007/s00702-014-1230-2     Document Type: Article

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