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Works
6
Functional impact of global rare copy number variation in autism spectrum disorders
Mapping autism risk loci using genetic linkage and chromosomal rearrangements
Between a ROC and a hard place: decision making and making decisions about using the SCQ.
Individual common variants exert weak effects on the risk for autism spectrum disorders
Resilience to adult psychopathology following childhood maltreatment: evidence from a community sample
A novel approach of homozygous haplotype sharing identifies candidate genes in autism spectrum disorder
