Rare variant analyses in ancestrally diverse cohorts reveal novel ADHD risk genes. Jung S., Caballero M., Olfson E., Newcorn J.H., Fernandez T., Mahjani B.

Primary complex motor stereotypies are associated with de novo damaging DNA coding mutations that identify KDM5B as a risk gene. Fernandez T., Williams Z., Kline T., Rajendran S., Augustine F., Wright N., Sullivan C.A.W., Olfson E., Abdallah S.B., Liu W., Hoffman E., Gupta A., Singer H.S.

De novo damaging DNA coding mutations are associated with obsessive-compulsive disorder and overlap with Tourette’s disorder and autism. Cappi C., Oliphant M.E., Péter Z., Zai G., do Rosário M.C., Sullivan C.A.W., Gupta A., Hoffman E., Virdee M., Olfson E., Abdallah S.B., Willsey A. J., Shavitt R.G., Miguel E.C., Kennedy J.L., Richter M.A., Fernandez T.