| Autism genome-wide copy number variation reveals ubiquitin and neuronal genes. |
2009 |
19404257 |
| Common genetic variants on 5p14.1 associate with autism spectrum disorders. |
2009 |
19404256 |
| Adjustment of genomic waves in signal intensities from whole-genome SNP genotyping platforms. |
2008 |
18784189 |
| Mapping autism risk loci using genetic linkage and chromosomal rearrangements. |
2007 |
17322880 |
| Pathway-based approaches for analysis of genomewide association studies. |
2007 |
17966091 |
| PennCNV: an integrated hidden Markov model designed for high-resolution copy number variation detection in whole-genome SNP genotyping data. |
2007 |
17921354 |