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Marshall, Christian R

Department of Paediatric Laboratory Medicine, Division of Genome Diagnostics, The Hospital for Sick Children, Toronto, Ontario, Canada.

TitleYearPMID
Shared genetic risk between eating disorder- and substance-use-related phenotypes: Evidence from genome-wide association studies. 2021 32064741
Genome-wide analysis of copy number variants in attention deficit hyperactivity disorder: the role of rare variants and duplications at 15q13.3. 2012 22420048
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
Phenotypic spectrum associated with de novo and inherited deletions and duplications at 16p11.2 in individuals ascertained for diagnosis of autism spectrum disorder. 2010 19755429
Structural variation of chromosomes in autism spectrum disorder. 2008 18252227
Contribution of SHANK3 mutations to autism spectrum disorder. 2007 17999366
Mapping autism risk loci using genetic linkage and chromosomal rearrangements. 2007 17322880
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