Anath C. Lionel
Anath C. Lionel
Department of Medicine, University of Toronto
Verified email at mail.utoronto.ca
Title
Cited by
Cited by
Year
Functional impact of global rare copy number variation in autism spectrum disorders
D Pinto, AT Pagnamenta, L Klei, R Anney, D Merico, R Regan, J Conroy, ...
Nature 466 (7304), 368-372, 2010
19912010
Structural variation of chromosomes in autism spectrum disorder
CR Marshall, A Noor, JB Vincent, AC Lionel, L Feuk, J Skaug, M Shago, ...
The American Journal of Human Genetics 82 (2), 477-488, 2008
18392008
Subgroup-specific structural variation across 1,000 medulloblastoma genomes
PA Northcott, DJH Shih, J Peacock, L Garzia, AS Morrissy, T Zichner, ...
Nature 488 (7409), 49-56, 2012
7322012
A genome-wide scan for common alleles affecting risk for autism
R Anney, L Klei, D Pinto, R Regan, J Conroy, TR Magalhaes, C Correia, ...
Human molecular genetics 19 (20), 4072-4082, 2010
6082010
Comprehensive assessment of array-based platforms and calling algorithms for detection of copy number variants
D Pinto, K Darvishi, X Shi, D Rajan, D Rigler, T Fitzgerald, AC Lionel, ...
Nature biotechnology 29 (6), 512-520, 2011
4172011
Rare copy number variation discovery and cross-disorder comparisons identify risk genes for ADHD
AC Lionel, J Crosbie, N Barbosa, T Goodale, B Thiruvahindrapuram, ...
Science translational medicine 3 (95), 95ra75-95ra75, 2011
3292011
SHANK1 deletions in males with autism spectrum disorder
D Sato, AC Lionel, CS Leblond, A Prasad, D Pinto, S Walker, I O'Connor, ...
The American Journal of Human Genetics 90 (5), 879-887, 2012
3002012
Single cell-derived clonal analysis of human glioblastoma links functional and genomic heterogeneity
M Meyer, J Reimand, X Lan, R Head, X Zhu, M Kushida, J Bayani, ...
Proceedings of the National Academy of Sciences 112 (3), 851-856, 2015
2922015
Genome-wide analysis of copy number variants in attention deficit hyperactivity disorder: the role of rare variants and duplications at 15q13. 3
NM Williams, B Franke, E Mick, RJL Anney, CM Freitag, M Gill, A Thapar, ...
American Journal of Psychiatry 169 (2), 195-204, 2012
2922012
Molecular diagnostic yield of chromosomal microarray analysis and whole-exome sequencing in children with autism spectrum disorder
K Tammimies, CR Marshall, S Walker, G Kaur, B Thiruvahindrapuram, ...
Jama 314 (9), 895-903, 2015
2882015
Improved diagnostic yield compared with targeted gene sequencing panels suggests a role for whole-genome sequencing as a first-tier genetic test
AC Lionel, G Costain, N Monfared, S Walker, MS Reuter, SM Hosseini, ...
Genetics in Medicine 20 (4), 435-443, 2018
2482018
Rare deletions at the neurexin 3 locus in autism spectrum disorder
AK Vaags, AC Lionel, D Sato, MK Goodenberger, QP Stein, S Curran, ...
The American Journal of Human Genetics 90 (1), 133-141, 2012
2052012
Disruption at the PTCHD1 Locus on Xp22. 11 in Autism spectrum disorder and intellectual disability
A Noor, A Whibley, CR Marshall, PJ Gianakopoulos, A Piton, AR Carson, ...
Science translational medicine 2 (49), 49ra68-49ra68, 2010
2052010
Copy number variations and risk for schizophrenia in 22q11. 2 deletion syndrome
AS Bassett, CR Marshall, AC Lionel, EWC Chow, SW Scherer
Human molecular genetics 17 (24), 4045-4053, 2008
1942008
A discovery resource of rare copy number variations in individuals with autism spectrum disorder
A Prasad, D Merico, B Thiruvahindrapuram, J Wei, AC Lionel, D Sato, ...
G3: Genes| Genomes| Genetics 2 (12), 1665-1685, 2012
1692012
Rare copy number variations in adults with tetralogy of Fallot implicate novel risk gene pathways
CK Silversides, AC Lionel, G Costain, D Merico, O Migita, B Liu, T Yuen, ...
Public Library of Science 8 (8), e1002843, 2012
1632012
Rare exonic deletions implicate the synaptic organizer Gephyrin (GPHN) in risk for autism, schizophrenia and seizures
AC Lionel, AK Vaags, D Sato, MJ Gazzellone, EB Mitchell, HY Chen, ...
Human molecular genetics 22 (10), 2055-2066, 2013
1422013
Rare copy number variants contribute to congenital left-sided heart disease
MP Hitz, LP Lemieux-Perreault, C Marshall, Y Feroz-Zada, R Davies, ...
Public Library of Science 8 (9), e1002903, 2012
1412012
Exonic deletions in AUTS2 cause a syndromic form of intellectual disability and suggest a critical role for the C terminus
G Beunders, E Voorhoeve, C Golzio, LM Pardo, JA Rosenfeld, ...
The American Journal of Human Genetics 92 (2), 210-220, 2013
1342013
Disruption of the ASTN2/TRIM32 locus at 9q33.1 is a risk factor in males for autism spectrum disorders, ADHD and other neurodevelopmental phenotypes
AC Lionel, K Tammimies, AK Vaags, JA Rosenfeld, JW Ahn, D Merico, ...
Human molecular genetics 23 (10), 2752-2768, 2014
1182014
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