Christian R. Marshall

发表

Best practices for the analytical validation of clinical whole-genome sequencing intended for the diagnosis of germline disease

Christian R. Marshall, Shimul Chowdhury, Ryan J. Taft, 2020, npj Genomic Medicine.

transmembrane segments temperature dependence: NH2-terminal Determinants of cardiac Na+/Ca2+ exchanger

Glen F. Tibbits, Christian R. Marshall, Larry V. Hryshko, 2008 .

Using extended pedigrees to identify novel autism spectrum disorder (ASD) candidate genes

Daniele Merico, Joseph Piven, Veronica J. Vieland, 2014, Human Genetics.

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.

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.

Network Topologies and Convergent Aetiologies Arising from Deletions and Duplications Observed in Individuals with Autism

Caleb Webber, Chris P. Ponting, Christian R. Marshall, 2013, PLoS genetics.

Mutations in the SHANK2 synaptic scaffolding gene in autism spectrum disorder and mental retardation

Ute Moog, Volker Endris, Christian R. Marshall, 2010, Nature Genetics.

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.

Copy Number Variable MicroRNAs in Schizophrenia and Their Neurodevelopmental Gene Targets

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

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

Margaret A. Pericak-Vance, Kathryn Roeder, Thomas Bourgeron, 2010, Human molecular genetics.

Genome-Wide Analysis of Copy Number Variants in Attention Deficit Hyperactivity Disorder: The Role of Rare Variants and Duplications at 15q13.3

Susanne Walitza, Herbert Roeyers, Peter Holmans, 2012, The American journal of psychiatry.