Bipolar disorder (BD) is a heritable mental illness with complex etiology. While the largest
published genome-wide association study identified 64 BD risk loci, the causal SNPs and …

Background Genome-wide association studies (GWASs) have identified multiple risk loci for
bipolar disorder (BD). However, pinpointing functional (or causal) variants in the reported …

Genome-wide association studies (GWASs) have identified numerous single nucleotide
polymorphisms (SNPs) associated with bipolar disorder (BD), but what the causal variants …

Background Bipolar disorder (BD) is a common and highly heritable disorder of mood.
Genome-wide association studies (GWAS) have identified several independent …

Since the bipolar disorder (BD) signals identified by genome-wide association study
(GWAS) often reside in the non-coding regions, understanding the biological relevance of …

Bipolar disorder (BD) is a common and highly heritable mental illness and genome-wide
association studies (GWAS) have robustly identified the first common genetic variants …

Background Genome‐wide association studies (GWASs) are used to identify genetic
variants for association with bipolar disorder (BD) risk; however, each GWAS can only reveal …

Bipolar disorder (BD) affects the quality of life of approximately 1% of the population and
represents a major public health concern. It is known to be highly heritable but large-scale …

Bipolar disorder (BD) is a leading contributor to the global burden of disease. Despite high
heritability (60-80%), the majority of the underlying genetic determinants remain unknown …

Bipolar disorder (BD) presents a significant challenge due to its chronic and relapsing
nature, with its underlying pathogenesis remaining elusive. This study employs Mendelian …