Rare Risk Variants Identification by Identity-by-Descent Mapping and Whole-Exome Sequencing Implicates Neuronal Development Pathways in Schizophrenia and Bipolar Disorder - Salvoro, C.; Bortoluzzi, S.; Coppe, A.; Valle, G.; Feltrin, E.; Mostacciuolo, M. L.; Vazza, G. (Molecular neurobiology, 2018)
Keywords: Alleles; Axon guidance; Biomedical and Life Sciences; Biomedicine; Bipolar disorder; Bipolar Disorder - genetics; Calcium channels; Calcium channels (voltage-gated); Cell Biology; Etiology; Extracellular matrix; Fragile X syndrome; Gene mapping; Gene Regulatory Networks; Genetic Predisposition to Disease; Genetic Variation; Haplotypes; Heritability; Humans; Intellectual disabilities; Neural networks; Neurobiology; Neurology; Neurons - metabolism; Neurons - pathology; Neurosciences; Risk Factors; Schizophrenia; Schizophrenia - genetics; Synaptic density; Whole Exome Sequencing; rare variants; development of neuronal connectivity; bipolar disorder; schizophrenia; whole-exome sequencing; identity-by-descent