A. C. Lionel

A genome-wide scan for common alleles affecting risk for autism

Richard Anney, Lambertus Klei, Dalila Pinto et al. · Human Molecular Genetics · 2010 · 588 citations · Full text

Life Sciences, Genetics, Molecular Genetics +13

Disruption of the ASTN2/TRIM32 locus at 9q33.1 is a risk factor in males for autism spectrum disorders, ADHD and other neurodevelopmental phenotypes

A. C. Lionel, Kristiina Tammimies, Andrea K. Vaags et al. · Human Molecular Genetics · 2013 · 175 citations · Full text

Life Sciences, Genetics, Neuroscience +17

Pathogenic rare copy number variants in community-based schizophrenia suggest a potential role for clinical microarrays

Gregory Costain, A. C. Lionel, Daniele Merico et al. · Human Molecular Genetics · 2013 · 136 citations · Full text

Life Sciences, Genetics, Molecular Genetics +17

Copy number variations and risk for schizophrenia in 22q11.2 deletion syndrome

A. S. Bassett, C. R. Marshall, A. C. Lionel et al. · Human Molecular Genetics · 2009 · 15 citations · Full text

Life Sciences, Genetics, Molecular Genetics +14

Disruption at the PTCHD1 Locus on Xp22.11 in Autism Spectrum Disorder and Intellectual Disability

P. J. Gianakopoulos, G. Dawson, A. R. Carson et al. · 2020 · 13 citations · Full text

Medicine, Genetics, Molecular Genetics +16