Rare OCD Variants in NPY5R, DLGAP1, and MAPK8IP3 Segregate in Families
A 2026 whole-genome sequencing preprint found rare variant signals in 2 multiplex obsessive-compulsive disorder (OCD) families: an NPY5R missense variant in 10 of 15 affected people in 1 pedigree, plus DLGAP1 and MAPK8IP3 signals that tracked all 3 sequenced cases in a branch of a second pedigree.1 The finding is a candidate-gene result, not a …