L. Ogura

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 .

Genome-wide rare copy number variations contribute to genetic risk for transposition of the great arteries.

S. Scherer, A. C. Lionel, C. Marshall, 2016, International journal of cardiology.

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

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

Whole-genome sequencing suggests mechanisms for 22q11.2 deletion-associated Parkinson’s disease

S. Scherer, D. Merico, C. Marshall, 2017, PloS one.

Whole-Genome Sequencing Suggests Schizophrenia Risk Mechanisms in Humans with 22q11.2 Deletion Syndrome

Daniele Merico, Christian R Marshall, Babak Alipanahi, 2015, G3: Genes, Genomes, Genetics.

Fetal growth and gestational factors as predictors of schizophrenia in 22q11.2 deletion syndrome

A. Bassett, N. Butcher, G. Costain, 2015, Genetics in Medicine.

Reproductive Health Issues for Adults with a Common Genomic Disorder: 22q11.2 Deletion Syndrome

A. Bassett, C. Silversides, G. Costain, 2015, Journal of Genetic Counseling.