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A novel hybrid yeast-human network analysis reveals an essential role for FNBP1L in antibacterial autophagy.
Identifying relationships among genomic disease regions: predicting genes at pathogenic SNP associations and rare deletions.
Accurately assessing the risk of schizophrenia conferred by rare copy-number variation affecting genes with brain function.
Rare complete knockouts in humans: population distribution and significant role in autism spectrum disorders.
Associations of CFHR1-CFHR3 deletion and a CFH SNP to age-related macular degeneration are not independent.
Identification of small exonic CNV from whole-exome sequence data and application to autism spectrum disorder.
Human knockouts and phenotypic analysis in a cohort with a high rate of consanguinity.