| 37100590 | Direct additive genetics and maternal effect contribute to the risk of Tourette disorder. | J Neurol Neurosurg Psychiatry | 2023 |
| 36123423 | Comment on: What genes are differentially expressed in individuals with schizophrenia? A systematic review. | Mol Psychiatry | 2023 |
| 37595579 | Systematic evaluation of genome sequencing for the diagnostic assessment of autism spectrum disorder and fetal structural anomalies. | Am J Hum Genet | 2023 |
| 37986747 | Comparison of gene expression in living and postmortem human brain. | medRxiv | 2023 |
| 37790341 | Evaluating and Improving Health Equity and Fairness of Polygenic Scores. | | 2023 |
| 37773317 | Heritable Composite Phenotypes Defined by Combinations of Conduct Problem, Depression, and Temperament Features: Contributions to risk for Alcohol Problems. | | 2023 |
| 37128669 | Adapting Patient and Public Involvement processes in response to the Covid-19 pandemic. | | 2023 |
| 34789012 | The Genetic Architecture of Obsessive-Compulsive Disorder: Contribution of Liability to OCD From Alleles Across the Frequency Spectrum. | Am J Psychiatry | 2022 |
| 35987687 | Schizophrenia-associated differential DNA methylation in brain is distributed across the genome and annotated to MAD1L1, a locus at which DNA methylation and transcription phenotypes share genetic variation with schizophrenia risk. | Transl Psychiatry | 2022 |
| 36323256 | Spatiotemporal and genetic regulation of A-to-I editing throughout human brain development. | Cell Rep | 2022 |
| 35982160 | Rare coding variation provides insight into the genetic architecture and phenotypic context of autism. | Nat Genet | 2022 |
| 34154796 | Sex Differences in the Human Brain Transcriptome of Cases With Schizophrenia. | Biol Psychiatry | 2022 |
| 34615521 | How rare and common risk variation jointly affect liability for autism spectrum disorder. | Mol Autism | 2021 |
| 34112972 | Genome-wide association identifies the first risk loci for psychosis in Alzheimer disease. | Mol Psychiatry | 2021 |
| 33837133 | Bayesian estimation of cell type-specific gene expression with prior derived from single-cell data. | Genome Research | 2021 |
| 33723209 | Transcriptome alterations are enriched for synapse-associated genes in the striatum of subjects with obsessive-compulsive disorder. | Transl Psychiatry | 2021 |
| 33714545 | Investigating Shared Genetic Basis Across Tourette Syndrome and Comorbid Neurodevelopmental Disorders Along the Impulsivity-Compulsivity Spectrum. | Biol Psychiatry | 2021 |
| 33372276 | H-MAGMA, inheriting a shaky statistical foundation, yields excess false positives. | Annals of Human Genetics | 2021 |
| 34459489 | An approach to gene-based testing accounting for dependence of tests among nearby genes. | Briefings in Bioinformatics | 2021 |
| 34615535 | Prevalence and phenotypic impact of rare potentially damaging variants in autism spectrum disorder. | Mol Autism | 2021 |
| 31424081 | Resting-State Functional Network Organization Is Stable Across Adolescent Development for Typical and Psychosis Spectrum Youth. | Schizophrenia Bulletin | 2020 |
| 32268104 | Whole-Genome and RNA Sequencing Reveal Variation and Transcriptomic Coordination in the Developing Human Prefrontal Cortex. | Cell Rep | 2020 |
| 32199606 | Maternal Effects as Causes of Risk for Obsessive-Compulsive Disorder. | Biol Psychiatry | 2020 |
| 31907560 | Cohort profile: Epidemiology and Genetics of Obsessive-compulsive disorder and chronic tic disorders in Sweden (EGOS). | Soc Psychiatry Psychiatr Epidemiol | 2020 |
| 31928911 | Age dependent association of inbreeding with risk for schizophrenia in Egypt. | Schizophrenia Research | 2020 |
| 32652852 | Functional connectome fingerprinting accuracy in youths and adults is similar when examined on the same day and 1.5-years apart. | Human Brain Mapping | 2020 |
| 32648044 | Heterogeneous Trajectories of Problematic Alcohol Use, Depressive Symptoms, and their Co-Occurrence in Young Adults with and without Childhood ADHD. | Journal of Abnormal Child Psychology | 2020 |
| 33032641 | De novo missense variants disrupting protein-protein interactions affect risk for autism through gene co-expression and protein networks in neuronal cell types. | Mol Autism | 2020 |
| 32522875 | A selective inference approach for false discovery rate control using multiomics covariates yields insights into disease risk. | Proceedings of the National Academy of Sciences of the United States of America | 2020 |
| 32894416 | Correction to: Heterogeneous Trajectories of Problematic Alcohol Use, Depressive Symptoms, and their Co-Occurrence in Young Adults with and without Childhood ADHD. | Journal of Abnormal Child Psychology | 2020 |
| 33157004 | Not All Autism Genes Are Created Equal: A Response to Myers et al. | Am J Hum Genet | 2020 |
| 30862939 | Correction: Genetic risk for schizophrenia and psychosis in Alzheimer disease. | Mol Psychiatry | 2020 |
| 31400192 | Using multiple measurements of tissue to estimate subject- and cell-type-specific gene expression. | | 2020 |
| 31086353 | Publisher Correction: Gene expression imputation across multiple brain regions provides insights into schizophrenia risk. | Nat Genet | 2019 |
| 31551426 | CommonMind Consortium provides transcriptomic and epigenomic data for Schizophrenia and Bipolar Disorder. | Sci Data | 2019 |
| 30587579 | Semisoft clustering of single-cell data. | Proceedings of the National Academy of Sciences of the United States of America | 2019 |
| 29740122 | Differential activity of transcribed enhancers in the prefrontal cortex of 537 cases with schizophrenia and controls. | Mol Psychiatry | 2019 |
| 30983407 | Variations in Genes Related to Sleep Patterns in Children With Autism Spectrum Disorder. | Biol Res Nurs | 2019 |
| 29805045 | Landscape of Conditional eQTL in Dorsolateral Prefrontal Cortex and Co-localization with Schizophrenia GWAS. | Am J Hum Genet | 2018 |
| 28461698 | Genetic risk for schizophrenia and psychosis in Alzheimer disease. | Mol Psychiatry | 2018 |
| 30174778 | A UNIFIED STATISTICAL FRAMEWORK FOR SINGLE CELL AND BULK RNA SEQUENCING DATA. | Annals of Applied Statistics | 2018 |
| 29892012 | An interactome perturbation framework prioritizes damaging missense mutations for developmental disorders. | Nat Genet | 2018 |
| 30545852 | Genome-wide de novo risk score implicates promoter variation in autism spectrum disorder. | Science | 2018 |
| 29100626 | Heritable Variation, With Little or No Maternal Effect, Accounts for Recurrence Risk to Autism Spectrum Disorder in Sweden. | Biol Psychiatry | 2018 |
| 29306175 | Joint evaluation of serum C-Reactive Protein levels and polygenic risk scores as risk factors for schizophrenia. | Psychiatry Research | 2018 |
| 29700473 | An analytical framework for whole-genome sequence association studies and its implications for autism spectrum disorder. | Nat Genet | 2018 |
| 28191890 | Refining the role of de novo protein-truncating variants in neurodevelopmental disorders by using population reference samples. | Nat Genet | 2017 |
| 28504703 | Polygenic transmission disequilibrium confirms that common and rare variation act additively to create risk for autism spectrum disorders. | Nat Genet | 2017 |
| 28426285 | The Yin and Yang of Autism Genetics: How Rare De Novo and Common Variations Affect Liability. | Annual Review of Genomics and Human Genetics | 2017 |
| 28570395 | Runs of homozygosity, copy number variation, and risk for depression and suicidal behavior in an Arab Bedouin kindred. | Psychiatr Genet | 2017 |