Imaging-genetics in dyslexia: Connecting risk genetic variants to brain neuroimaging and ultimately to reading impairments

Molecular Genetics and Metabolism

Volumn 110, Issue 3, 2013, Pages 201-212

  Eicher, John D ^a   Gruen, Jeffrey R ^a  

^a YALE UNIVERSITY SCHOOL OF MEDICINE   (United States)

Author keywords

Dyslexia; Genetics; Imaging genetics; Neuroimaging

Indexed keywords

ARTICLE; BRAIN REGION; C2ORF3 GENE; CNTNAP2 GENE; CYP19A1 GENE; DCDC2 GENE; DRD2 GENE; DRD4 GENE; DYSLEXIA; DYX1C1 GENE; FOXP2 GENE; FRACTIONAL ANISOTROPY; FUNCTIONAL MAGNETIC RESONANCE IMAGING; GENE LOCUS; GENETIC RISK; GENETIC VARIABILITY; HUMAN; IN VIVO STUDY; KIAA0319 GENE; KIAA0319L GENE; MRPL19 GENE; NEUROIMAGING; NONHUMAN; NUCLEAR MAGNETIC RESONANCE IMAGING; PHENOTYPE; POSITRON EMISSION TOMOGRAPHY; PRIORITY JOURNAL; READING; ROBO1 GENE; THEM2 GENE; TTRAP GENE;

ANIMALIA;

DYSLEXIA; GENETICS; IMAGING-GENETICS; NEUROIMAGING;

BRAIN; DYSLEXIA; GENETIC PREDISPOSITION TO DISEASE; GENETIC VARIATION; HUMANS; NEUROIMAGING;

EID: 84885421684     PISSN: 10967192     EISSN: 10967206     Source Type: Journal    
DOI: 10.1016/j.ymgme.2013.07.001     Document Type: Review

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