A systematic variant annotation approach for ranking genes associated with autism spectrum disorders

Molecular Autism

Volumn 7, Issue 1, 2016, Pages

  Larsen, Eric ^a   Menashe, Idan ^b   Ziats, Mark N ^c   Pereanu, Wayne ^a   Packer, Alan ^d   Banerjee Basu, Sharmila ^a  

^a MindSpec McLean   (United States)

^b BEN GURION UNIVERSITY OF THE NEGEV   (Israel)

^c EUNICE KENNEDY SHRIVER NATIONAL INSTITUTE OF CHILD HEALTH AND HUMAN DEVELOPMENT   (United States)

^d FLATIRON INSTITUTE   (United States)

Author keywords

Autistic disorder; Autosomal recessive; Common variants; Genetic variation; Rare variants

Indexed keywords

SCATTER FACTOR RECEPTOR; ADNP PROTEIN, HUMAN; CHD8 PROTEIN, HUMAN; DNA BINDING PROTEIN; HOMEODOMAIN PROTEIN; NERVE PROTEIN; SHANK3 PROTEIN, HUMAN; TRANSCRIPTION FACTOR;

ADNP GENE; ALGORITHM; ARTICLE; AUTISM; CHD8 GENE; CLASSIFICATION; CNTNAP2 GENE; CORRELATIONAL STUDY; GENE; GENE RANKING; GENETIC ASSOCIATION; GENETIC VARIABILITY; MET GENE; MSNP1AS GENE; PREDICTOR VARIABLE; PRIORITY JOURNAL; SHANK3 GENE; GENE EXPRESSION; GENETIC DATABASE; GENETIC PREDISPOSITION; GENETIC VARIATION; GENETICS; HUMAN; INFORMATION PROCESSING; METHODOLOGY; MOLECULAR GENETICS; PATHOPHYSIOLOGY;

ALGORITHMS; AUTISM SPECTRUM DISORDER; DATABASES, GENETIC; DATASETS AS TOPIC; DNA-BINDING PROTEINS; GENE EXPRESSION; GENETIC PREDISPOSITION TO DISEASE; GENETIC VARIATION; HOMEODOMAIN PROTEINS; HUMANS; MOLECULAR SEQUENCE ANNOTATION; NERVE TISSUE PROTEINS; RESEARCH DESIGN; TRANSCRIPTION FACTORS;

EID: 84992147507     PISSN: None     EISSN: 20402392     Source Type: Journal    
DOI: 10.1186/s13229-016-0103-y     Document Type: Article

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