Janet L. Sobell
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View article: Whole-genome sequence-based association analysis of African American individuals with bipolar disorder and schizophrenia
Whole-genome sequence-based association analysis of African American individuals with bipolar disorder and schizophrenia Open
View article: Whole genome sequence-based association analysis of African American individuals with bipolar disorder and schizophrenia
Whole genome sequence-based association analysis of African American individuals with bipolar disorder and schizophrenia Open
In studies of individuals of primarily European genetic ancestry, common and low-frequency variants and rare coding variants have been found to be associated with the risk of bipolar disorder (BD) and schizophrenia (SZ). However, less is k…
View article: Rare coding variants in ten genes confer substantial risk for schizophrenia
Rare coding variants in ten genes confer substantial risk for schizophrenia Open
View article: Genome-wide association study identifies new locus associated with OCD
Genome-wide association study identifies new locus associated with OCD Open
Obsessive-compulsive disorder (OCD) is a heritable disorder, but no definitive, replicated OCD susceptibility loci have yet been identified by any genome-wide association study (GWAS). Here, we report results from a GWAS in the largest OCD…
View article: Correction: Investigating rare pathogenic/likely pathogenic exonic variation in bipolar disorder
Correction: Investigating rare pathogenic/likely pathogenic exonic variation in bipolar disorder Open
View article: Investigating rare pathogenic/likely pathogenic exonic variation in bipolar disorder
Investigating rare pathogenic/likely pathogenic exonic variation in bipolar disorder Open
Bipolar disorder (BD) is a serious mental illness with substantial common variant heritability. However, the role of rare coding variation in BD is not well established. We examined the protein-coding (exonic) sequences of 3,987 unrelated …
View article: Contribution of rare copy number variants to bipolar disorder risk is limited to schizoaffective cases
Contribution of rare copy number variants to bipolar disorder risk is limited to schizoaffective cases Open
Background Genetic risk for bipolar disorder (BD) is conferred through many common alleles, while a role for rare copy number variants (CNVs) is less clear. BD subtypes schizoaffective disorder bipolar type (SAB), bipolar I disorder (BD I)…
View article: Evidence for genetic heterogeneity between clinical subtypes of bipolar disorder
Evidence for genetic heterogeneity between clinical subtypes of bipolar disorder Open
View article: Cover Image, Volume 171B, Number 4, June 2016
Cover Image, Volume 171B, Number 4, June 2016 Open
The cover image, by Fabio Macciardi et al., is based on the Research Article LINE1 insertions as a genomic risk factor for schizophrenia: Preliminary evidence from an affected family, DOI: 10.1002/ajmg.b.32437.
View article: Association of DNA Methylation Differences With Schizophrenia in an Epigenome-Wide Association Study
Association of DNA Methylation Differences With Schizophrenia in an Epigenome-Wide Association Study Open
IMPORTANCE: DNA methylation may play an important role in schizophrenia (SZ), either directly as a mechanism of pathogenesis or as a biomarker of risk. OBJECTIVE: To scan genome-wide DNA methylation data to identify differentially methylat…