Search

What are you looking for?

  1. Polygenic and developmental profiles of autism differ by age at diagnosis.

    Publication

  2. Molecular cascades and cell-type specific signatures in ASD revealed by single cell genomics.

    Publication

  3. The contributions of rare inherited and polygenic risk to ASD in multiplex families.

    Publication

  4. Broad transcriptomic dysregulation occurs across the cerebral cortex in ASD.

    Publication

  5. Integrating de novo and inherited variants in 42,607 autism cases identifies mutations in new moderate-risk genes.

    Publication

  6. Genetic correlates of phenotypic heterogeneity in autism.

    Publication

  7. Association between resting-state functional brain connectivity and gene expression is altered in autism spectrum disorder.

    Publication

  8. The contributions of rare inherited and polygenic risk to ASD in multiplex families.

    Publication

  9. Oxytocin normalizes altered circuit connectivity for social rescue of the Cntnap2 knockout mouse.

    Publication

  10. Coexpression network architecture reveals the brain-wide and multiregional basis of disease susceptibility.

    Publication

  11. A neurogenetic analysis of female autism.

    Publication

  12. Polygenic profiles define aspects of clinical heterogeneity in ADHD.

    Publication

  13. Polygenicity in psychiatry-like it or not, we have to understand it.

    Publication

  14. Integrative genomics identifies a convergent molecular subtype that links epigenomic with transcriptomic differences in autism.

    Publication

  15. Profiling allele-specific gene expression in brains from individuals with autism spectrum disorder reveals preferential minor allele usage.

    Publication

  16. Inherited and de novo genetic risk for autism impacts shared networks.

    Publication

  17. Genome-wide DNA methylation profiling identifies convergent molecular signatures associated with idiopathic and syndromic autism in post-mortem human brain tissue.

    Publication

  18. Human gut microbiota from autism spectrum disorder promote behavioral symptoms in mice.

    Publication

  19. Reduced prefrontal synaptic connectivity and disturbed oscillatory population dynamics in the CNTNAP2 model of autism.

    Publication

  20. Identification of common genetic risk variants for autism spectrum disorder.

    Publication

  21. A genome-wide association study of shared risk across psychiatric disorders implicates gene regulation during fetal neurodevelopment.

    Publication

  22. Integrative functional genomic analysis of human brain development and neuropsychiatric risks.

    Publication

  23. Transcriptome-wide isoform-level dysregulation in ASD, schizophrenia, and bipolar disorder.

    Publication

  24. Autism-like phenotype and risk gene mRNA deadenylation by CPEB4 mis-splicing.

    Publication

  25. Strong correlation of downregulated genes related to synaptic transmission and mitochondria in post-mortem autism cerebral cortex.

    Publication

  26. Shared molecular neuropathology across major psychiatric disorders parallels polygenic overlap.

    Publication

  27. Whole genome sequencing in psychiatric disorders: the WGSPD consortium.

    Publication

  28. Genome-wide changes in lncRNA, splicing, and regional gene expression patterns in autism.

    Publication

  29. Histone acetylome-wide association study of autism spectrum disorder.

    Publication

  30. The central nervous system and the gut microbiome.

    Publication

  31. The genetics-driven revival in neuropsychiatric drug development.

    Publication

  32. Correspondence between resting-state activity and brain gene expression.

    Publication

  33. Insights into autism spectrum disorder genomic architecture and biology from 71 risk loci.

    Publication

  34. Systems biology and gene networks in neurodevelopmental and neurodegenerative disorders.

    Publication

  35. Cerebellar associative sensory learning defects in five mouse autism models.

    Publication

  36. A genome-wide association study of autism using the Simons Simplex Collection: Does reducing phenotypic heterogeneity in autism increase genetic homogeneity?

    Publication

  37. Clustering autism: Using neuroanatomical differences in 26 mouse models to gain insight into the heterogeneity.

    Publication

  38. Exogenous and evoked oxytocin restores social behavior in the CNTNAP2 mouse model of autism.

    Publication

  39. A highly conserved program of neuronal microexons is misregulated in autistic brains.

    Publication

  40. Modest impact on risk for autism spectrum disorder of rare copy number variants at 15q11.2, specifically breakpoints 1 to 2.

    Publication

  41. Genes for endosomal NHE6 and NHE9 are misregulated in autism brains.

    Publication

  42. Integrative functional genomic analyses implicate specific molecular pathways and circuits in autism.

    Publication

  43. Cortical evolution: Judge the brain by its cover.

    Publication

  44. Adjusting head circumference for covariates in autism: clinical correlates of a highly heritable continuous trait.

    Publication

  45. Using large clinical datasets to infer pathogenicity for rare copy number variants in autism cohorts.

    Publication

  46. Intellectual disability is associated with increased runs of homozygosity in simplex autism.

    Publication

  47. The disruption of CELF6, a gene identified by translational profiling of serotonergic neurons, results in autism-related behaviors.

    Publication

  48. Common genetic variants, acting additively, are a major source of risk for autism.

    Publication