The impact of serotonin transporter genotype on default network connectivity in children and adolescents with autism spectrum disorders

NeuroImage: Clinical

Volumn 2, Issue 1, 2013, Pages 17-24

  Wiggins, Jillian Lee ^a   Peltier, Scott J ^a   Bedoyan, Jirair K ^b   Carrasco, Melisa ^b   Welsh, Robert C ^b,c   Martin, Donna M ^b   Lord, Catherine ^d   Monk, Christopher S ^a,b,c  

^a UNIVERSITY OF MICHIGAN   (United States)

^b UNIVERSITY OF MICHIGAN MEDICAL SCHOOL   (United States)

^c UNIVERSITY OF MICHIGAN HEALTH SYSTEM   (United States)

^d WEILL CORNELL MEDICAL COLLEGE   (United States)

Author keywords

Autism; Default network; Development; Functional MRI; Resting connectivity; Serotonin transporter gene

Indexed keywords

SEROTONIN TRANSPORTER;

ADOLESCENCE; ADOLESCENT; ALLELE; ARTICLE; AUTISM; BRAIN FUNCTION; CHILD; CLINICAL ARTICLE; CONTROLLED STUDY; FEMALE; FUNCTIONAL MAGNETIC RESONANCE IMAGING; GENE SEQUENCE; GENETIC VARIABILITY; GENOTYPE; HUMAN; MALE; NERVE CELL NETWORK; POLYMERASE CHAIN REACTION; PRIORITY JOURNAL; SOCIAL ASPECT;

EID: 84870515556     PISSN: None     EISSN: 22131582     Source Type: Journal    
DOI: 10.1016/j.nicl.2012.10.008     Document Type: Article

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