Niamh L. O’Brien
Publications by Year
Research Areas
Genetic Associations and Epidemiology, Genetics and Neurodevelopmental Disorders, Epigenetics and DNA Methylation, Genomics and Rare Diseases, Bipolar Disorder and Treatment
Most-Cited Works
- → Rare coding variants in ten genes confer substantial risk for schizophrenia(2022)840 cited
- → Sensitivity to reward and punishment in eating disorders(2010)232 cited
- → Patient-specific Alzheimer-like pathology in trisomy 21 cerebral organoids reveals BACE2 as a gene dose-sensitive AD suppressor in human brain(2020)120 cited
- → A Rare Functional Noncoding Variant at the GWAS-Implicated MIR137/MIR2682 Locus Might Confer Risk to Schizophrenia and Bipolar Disorder(2014)109 cited
- → CACNA1C hypermethylation is associated with bipolar disorder(2016)58 cited
- → Analysis of ANK3 and CACNA1C variants identified in bipolar disorder whole genome sequence data(2014)57 cited
- → The functional GRM3 Kozak sequence variant rs148754219 affects the risk of schizophrenia and alcohol dependence as well as bipolar disorder(2014)45 cited
- → Whole-exome sequencing of individuals from an isolated population implicates rare risk variants in bipolar disorder(2017)28 cited
- → Hypomethylation of FAM63B in bipolar disorder patients(2016)26 cited
- → “Patient-specific Alzheimer-like pathology in trisomy 21 cerebral organoids reveals BACE2 as a gene-dose-sensitive AD-suppressor in human brain”(2020)26 cited