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11. Somatic Mutations in Cerebral Cortical Malformations

12. Copy number variation plays an important role in clinical epilepsy

13. Disruption of the ASTN2/TRIM32 locus at 9q33.1 is a risk factor in males for autism spectrum disorders, ADHD and other neurodevelopmental phenotypes

22. Highly Penetrant Alterations of a Critical Region Including BDNF in Human Psychopathology and Obesity

26. The adult galactosemic phenotype

28. Mirror extreme BMI phenotypes associated with gene dosage at the chromosome 16p11.2 locus

48. Association between Microdeletion and Microduplication at 16p11.2 and Autism

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