Guiqing Cai

Schizophrenia-associated somatic copy-number variants from 12,834 cases reveal recurrent NRXN1 and ABCB11 disruptions

Interaction Testing and Polygenic Risk Scoring to Estimate the Association of Common Genetic Variants With Treatment Resistance in Schizophrenia

A Comparison of Ten Polygenic Score Methods for Psychiatric Disorders Applied Across Multiple Cohorts

Sex-Dependent Shared and Nonshared Genetic Architecture Across Mood and Psychotic Disorders

Age at first birth in women is genetically associated with increased risk of schizophrenia

Genomic dissection of bipolar disorder and schizophrenia including 28 subphenotypes

Contribution of copy number variants to schizophrenia from a genome-wide study of 41,321 subjects

<i>ABCA7</i> frameshift deletion associated with Alzheimer disease in African Americans

A contribution of novel CNVs to schizophrenia from a genome-wide study of 41,321 subjects: CNV Analysis Group and the Schizophrenia Working Group of the Psychiatric Genomics Consortium

Modeling Linkage Disequilibrium Increases Accuracy of Polygenic Risk Scores

Two knockdown models of the autism genes SYNGAP1 and SHANK3 in zebrafish produce similar behavioral phenotypes associated with embryonic disruptions of brain morphogenesis

Convergence of Genes and Cellular Pathways Dysregulated in Autism Spectrum Disorders

Partitioning Heritability of Regulatory and Cell-Type-Specific Variants across 11 Common Diseases

De novo SCN2A splice site mutation in a boy with Autism spectrum disorder

Prospective investigation of autism and genotype-phenotype correlations in 22q13 deletion syndrome and SHANK3 deficiency

Whole exome sequencing reveals minimal differences between cell line and whole blood derived DNA

Patterns and rates of exonic de novo mutations in autism spectrum disorders

A common X-linked inborn error of carnitine biosynthesis may be a risk factor for nondysmorphic autism

Next-Generation Sequencing For Gene and Pathway Discovery and Analysis in Autism Spectrum Disorders