The autism susceptibility candidate 2 (AUTS2) gene is associated with multiple neurological
diseases, including autism, and has been implicated as an important gene in human …

Schizophrenia (SZ) and autism spectrum disorders (ASD) are characterised by marked
language deficits, but it is not clear how these arise from gene mutations associated with the …

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 …

Aging is the primary risk factor for cognitive decline, an emerging health threat to aging
societies worldwide. Whether anti-aging factors such as klotho can counteract cognitive …

This cohort profile describes the origins, tracing, recruitment, testing and follow-up of the
University of Edinburgh-based Lothian Birth Cohorts of 1921 (LBC1921; N= 550) and 1936 …

To identify common variants contributing to normal variation in two specific domains of
cognitive functioning, we conducted a genome-wide association study (GWAS) of executive …

Nucleotide changes in the AUTS2 locus, some of which affect only noncoding regions, are
associated with autism and other neurological disorders, including attention deficit …

The accumulation of toxic metals in the human body is influenced by exposure and
mechanisms involved in metabolism, some of which may be under genetic control. This is …

The joint modeling of brain imaging information and genetic data is a promising research
avenue to highlight the functional role of genes in determining the pathophysiological …

Background Category fluency is a widely used task that relies on multiple neurocognitive
processes and is a sensitive assay of cortical dysfunction, including in schizophrenia. The …