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STRUCTURED, SPARSE REGRESSION WITH APPLICATION TO HIV DRUG RESISTANCE.
Functional impact of global rare copy number variation in autism spectrum disorders
Common genetic variants, acting additively, are a major source of risk for autism
On the use of general control samples for genome-wide association studies: genetic matching highlights causal variants
Multiple Recurrent De Novo CNVs, Including Duplications of the 7q11.23 Williams Syndrome Region, Are Strongly Associated with Autism
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Disequilibrium Mapping: Composite Likelihood for Pairwise Disequilibrium
Large-Scale Exome Sequencing Study Implicates Both Developmental and Functional Changes in the Neurobiology of Autism
Refining the role of de novo protein-truncating variants in neurodevelopmental disorders by using population reference samples
The heritability of IQ