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  1. SINEUP RNA rescues molecular phenotypes associated with CHD8 suppression in autism spectrum disorder model systems

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  2. Sex differences in autism: Examining intrinsic and extrinsic factors in children and adolescents enrolled in a national ASD cohort.

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  3. GIGYF1 disruption associates with autism and impaired IGF-1R signaling.

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  4. The early start Denver model intervention and Mu rhythm attenuation in autism spectrum disorders.

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  5. Differences in the number of de novo mutations between individuals are due to small family-specific effects and stochasticity.

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  6. Sleep problems in children with ASD and gene disrupting mutations.

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  7. Recent ultra-rare inherited variants implicate new autism candidate risk genes.

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  8. A neurogenetic analysis of female autism.

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  9. Coding and noncoding variants in EBF3 are involved in HADDS and simplex autism.

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  10. Reflections on the genetics-first approach to advancements in molecular genetic and neurobiological research on neurodevelopmental disorders.

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  11. The CHD8 CHD7/Kismet family links blood-brain barrier glia and serotonin to ASD-associated sleep defects

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  12. Rare deleterious mutations of HNRNP genes result in shared neurodevelopmental disorders.

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  13. A genetics-first approach to dissecting the heterogeneity of autism: Phenotypic comparison of autism risk copy number variants.

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  14. Large-scale targeted sequencing identifies risk genes for neurodevelopmental disorders.

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  15. Language characterization in 16p11.2 deletion and duplication syndromes.

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  16. Evaluating heterogeneity in ASD symptomatology, cognitive ability, and adaptive functioning among 16p11.2 CNV carriers.

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  17. Insufficient evidence for “autism-specific” genes.

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  18. The human-specific BOLA2 duplication modifies iron homeostasis and anemia predisposition in chromosome 16p11.2 autism individuals.

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  19. Disruptive mutations in TANC2 define a neurodevelopmental syndrome associated with psychiatric disorders

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  20. Disruptive variants of CSDE1 associate with autism and interfere with neuronal development and synaptic transmission.

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  21. Habituation learning is a widely affected mechanism in Drosophila models of intellectual disability and autism spectrum disorders.

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  22. Linking social motivation with social skill: The role of emotion dysregulation in autism spectrum disorder.

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  23. Genome sequencing identifies multiple deleterious variants in autism patients with more severe phenotypes.

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  24. Clinical presentation of a complex neurodevelopmental disorder caused by mutations in ADNP.

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  25. Psychiatric disorders in children with 16p11.2 deletion and duplication.

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  26. Neurodevelopmental disease genes implicated by de novo mutation and copy number variation morbidity.

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  27. Inherited and multiple de novo mutations in autism/developmental delay risk genes suggest a multifactorial model.

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  28. Gastrointestinal and psychiatric symptoms among children and adolescents with autism spectrum disorder.

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  29. Progress in understanding and treating SCN2A-mediated disorders.

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  30. Child and family characteristics moderate agreement between caregiver and clinician report of autism symptoms.

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  31. A genotype-first approach identifies an intellectual disability-overweight syndrome caused by PHIP haploinsufficiency.

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  32. Longitudinal report of child with de novo 16p11.2 triplication.

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  33. Associations between familial rates of psychiatric disorders and de novo genetic mutations in autism.

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  34. Gene disrupting mutations associated with regression in autism spectrum disorder.

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  35. Interactive effects of prenatal antidepressant exposure and likely gene disrupting mutations on the severity of autism spectrum disorder

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  36. Clinical phenotype of ASD-associated DYRK1A haploinsufficiency.

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  37. Exonic mosaic mutations contribute risk for autism spectrum disorder.

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  38. Hotspots of missense mutation identify neurodevelopmental disorder genes and functional domains.

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  39. Developmental trajectories for young children with 16p11.2 copy number variation.

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  40. Exploring the heterogeneity of neural social indices for genetically distinct etiologies of autism.

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  41. Targeted sequencing identifies 91 neurodevelopmental-disorder risk genes with autism and developmental-disability biases.

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  42. Severity of ASD symptoms and their correlation with the presence of copy number variations and exposure to first trimester ultrasound.

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  43. Denovo-db: A compendium of human de novo variants.

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  44. Association of rare missense variants in the second intracellular loop of NaV1.7 sodium channels with familial autism.

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  45. Autism spectrum disorder, developmental and psychiatric features in 16p11.2 duplication.

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  46. The number of genomic copies at the 16p11.2 locus modulates language, verbal memory, and inhibition.

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  47. Clinical phenotype of the recurrent 1q21.1 copy-number variant.

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  48. Disruption of POGZ is associated with intellectual disability and autism spectrum disorders.

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