Anne S. Bassett

发表

Manuscript Word Count: Abstract: 193; Text, with citations, without references: 3921 Number of Tables: 2; Supplemental Files: Yes Whole-genome sequencing suggests schizophrenia risk mechanisms in humans with 22q11.2 deletion syndrome

Brendan J. Frey, Daniele Merico, Babak Alipanahi, 2015 .

Voxel-based morphometry and automated lobar volumetry: The trade-off between spatial scale and statistical correction

Anne S. Bassett, Adrian P. Crawley, David J. Mikulis, 2010, NeuroImage.

MicroRNA Dysregulation, Gene Networks, and Risk for Schizophrenia in 22q11.2 Deletion Syndrome

Daniele Merico, Gregory Costain, Lucas Ogura, 2014, Front. Neurol..

Functional outcomes of adults with 22q11.2 deletion syndrome

Gregory Costain, Nancy J. Butcher, Eva W.C. Chow, 2012, Genetics in Medicine.

miRNA-mediated risk for schizophrenia in 22q11.2 deletion syndrome

Anne S. Bassett, Linda M. Brzustowicz, A. Bassett, 2012, Front. Gene..

Increasing Genotype-Phenotype Model Determinism: Application to Bivariate Reading/Language Traits and Epistatic Interactions in Language-Impaired Families

Stephen A. Petrill, Christopher W. Bartlett, Laura M. Justice, 2010, Human Heredity.

Rare Copy Number Variations in Adults with Tetralogy of Fallot Implicate Novel Risk Gene Pathways

Daniele Merico, Christian R. Marshall, Tracy Yuen, 2012, PLoS genetics.

Delineating the 15q13.3 microdeletion phenotype: a case series and comprehensive review of the literature

Christian R. Marshall, Dimitri J. Stavropoulos, Gregory Costain, 2014, Genetics in Medicine.

Expression of autism spectrum and schizophrenia in patients with a 22q11.2 deletion

Anne S. Bassett, Eva W. C. Chow, A. Bassett, 2013, Schizophrenia Research.

22q11.2 deletion syndrome.

Peter J. Scambler, Lauren A. Bohm, Anne S. Bassett, 2015, Nature reviews. Disease primers.

The Personal Genome Project Canada: findings from whole genome sequences of the inaugural 56 participants

Daniele Merico, Marc Fiume, John Wei, 2018, Canadian Medical Association Journal.

Impact of IQ on the diagnostic yield of chromosomal microarray in a community sample of adults with schizophrenia

Daniele Merico, John Wei, Christian R. Marshall, 2017, Genome Medicine.

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

Christian R. Marshall, Eva W.C. Chow, Anne S. Bassett, 2008, Human molecular genetics.

Large-scale mapping of cortical alterations in 22q11.2 deletion syndrome: Convergence with idiopathic psychosis and effects of deletion size

Paul M. Thompson, Jessica A. Turner, Christopher R. K. Ching, 2018, Molecular Psychiatry.

Copy Number Variable MicroRNAs in Schizophrenia and Their Neurodevelopmental Gene Targets

Daniele Merico, John Wei, Christian R. Marshall, 2015, Biological Psychiatry.