Use of Estonian Biobank Data and Participant Recall to Improve Wilson’s Disease Management
Classification of Schizophrenia, Bipolar Disorder and Major Depressive Disorder with Comorbid Traits and Deep Learning Algorithms
Polygenic scores stratify ND-CNV carrier cognitive outcomes in the UK Biobank
Pan-cancer copy number variant analysis identifies optimized size thresholds and co-occurrence models for individualized risk-stratification
Divergent transcriptomic profiles in depressed individuals with hyper- and hypophagia implicating inflammatory status
A clustering approach to improve our understanding of the genetic and phenotypic complexity of chronic kidney disease
Evaluating the association between placenta DNA methylation and cognitive functions in the offspring
Redefining counting of copy number variations and single-nucleotide polymorphisms by applying a novel concept based on the STexS and STexS II method
Detection of distant relatedness in biobanks for identification of undiagnosed carriers of a Mendelian disease variant: application to Long QT Syndrome
Actionability and Familial Uptake Following Opportunistic Genomic Screening in a Pediatric Cancer Cohort