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Lionel, Anath C

The Centre for Applied Genomics, Hospital for Sick Children, Toronto, Ontario, Canada

TitleYearPMID
Genome-wide analysis of copy number variants in attention deficit hyperactivity disorder: the role of rare variants and duplications at 15q13.3. 2012 22420048
Comprehensive assessment of array-based platforms and calling algorithms for detection of copy number variants. 2011 21552272
Rare copy number variation discovery and cross-disorder comparisons identify risk genes for ADHD. 2011 21832240
A genome-wide scan for common alleles affecting risk for autism. 2010 20663923
Disruption at the PTCHD1 Locus on Xp22.11 in Autism spectrum disorder and intellectual disability. 2010 20844286
Functional impact of global rare copy number variation in autism spectrum disorders. 2010 20531469
Structural variation of chromosomes in autism spectrum disorder. 2008 18252227
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