Olena Korvatska

Common genetic variants on 5p14.1 associate with autism spectrum disorders

Robert T. Schultz, Margaret A. Pericak-Vance, Takeshi Sakurai, 2009, Nature.

Altered splicing of ATP6AP2 causes X-linked parkinsonism with spasticity (XPDS).

Deborah A Nickerson, James B Leverenz, Evan E Eichler, 2013, Human molecular genetics.

Autism genome-wide copy number variation reveals ubiquitin and neuronal genes

Robert T. Schultz, Takeshi Sakurai, Joseph Piven, 2009, Nature.

A genome-wide scan for common alleles affecting risk for autism

Margaret A. Pericak-Vance, Kathryn Roeder, Thomas Bourgeron, 2010, Human molecular genetics.

Support for the N-methyl-D-aspartate receptor hypofunction hypothesis of schizophrenia from exome sequencing in multiplex families.

Carl Baker, Santhosh Girirajan, Michael O Dorschner, 2013, JAMA psychiatry.