Author
University of WorcesterORCID 0000-0003-4083-1143Unclaimed ORCID profile · follow to get notified of new preprints
Mutual co-authors in cluster
7 papers
Recent·Most cited
Omar Shanta, Marieke Klein, Molly Sacks…·Annette M. Hartmann
The paper identifies novel CNV loci and dose-dependent gene effects across six psychiatric disorders using genome-wide analysis.
Worrawat Engchuan, Omar Shanta, Kuldeep Kumar…·Michael Foster Green
The paper identifies shared and divergent genetic mechanisms across psychiatric disorders using gene-set burden analysis of copy number variants.
Tracey van der Veen, Markos Tesfaye, Jessica Mei Kay Yang…·Melvin G. McInnis
This study identifies genetic risk loci and factors underlying clinical subtypes of bipolar disorder using GWAS and meta-analysis.
Niamh Mullins, Andreas J. Forstner, Kevin Sean O’Connell…·Janos L. Kalman
Meta-analysis of 41,917 European-ancestry bipolar disorder cases versus 371,549 controls yields 64 risk loci (33 novel), neuronal and synaptic gene enrichment, and 15 eQTL-prioritized genes.
Eli A. Stahl, Gerome D. Breen, Andreas J. Forstner…·Anders Juréus
This study identifies 30 genome-wide significant loci associated with bipolar disorder, including novel genes involved in ion channels, neurotransmitters, and synaptic components.
Katie Swaden Lewis, Alexander L. Richards, Ganna Leonenko…·Arianna Di Florio
This study finds that genetic risk scores for insomnia and sleep duration differ between bipolar I and II subtypes, suggesting distinct genetic liabilities.
Alexander W. Charney, Eli A. Stahl, Elaine Green…·Pamela B. Sklar
The study finds that rare copy number variants (CNVs) contribute to bipolar disorder risk primarily in schizoaffective disorder bipolar type cases, with differences in CNV burden and schizophrenia polygenic risk scores between subtypes.