| 37267418 | Combinations of genes at the 16p11.2 and 22q11.2 CNVs contribute to neurobehavioral traits. | | 2023 |
| 35868305 | Can the "female protective effect" liability threshold model explain sex differences in autism spectrum disorder? | Neuron | 2022 |
| 35511767 | Sex-heterogeneous SNPs disproportionately influence gene expression and health. | PLoS Genetics | 2022 |
| 34715901 | Integration of genetic, transcriptomic, and clinical data provides insight into 16p11.2 and 22q11.2 CNV genes. | Genome Med | 2021 |
| 33736683 | A profile and review of findings from the Early Markers for Autism study: unique contributions from a population-based case-control study in California. | Molecular Autism | 2021 |
| 33648717 | Examining Sex-Differentiated Genetic Effects Across Neuropsychiatric and Behavioral Traits. | Biol Psychiatry | 2021 |
| 32815557 | Autism in neurofibromatosis type 1: misuse of covariance to dismiss autistic trait burden. | Dev Med Child Neurol | 2021 |
| 32665711 | Publisher Correction: Rates, distribution and implications of postzygotic mosaic mutations in autism spectrum disorder. | Nat Neurosci | 2020 |
| 32047095 | Genetic Contributions to Maternal and Neonatal Vitamin D Levels. | Genetics | 2020 |
| 31367015 | Mapping cis-regulatory chromatin contacts in neural cells links neuropsychiatric disorder risk variants to target genes. | Nat Genet | 2019 |
| 29575620 | Age and ASD symptoms in Costello syndrome. | American Journal of Medical Genetics, Part A | 2018 |
| 28401798 | Most Frequently Reported Prescription Medications and Supplements in Couples Planning Pregnancy: The LIFE Study. | Reproductive Sciences | 2018 |
| 29930110 | Analysis of shared heritability in common disorders of the brain. | Science | 2018 |
| 30134952 | Cross-genetic determination of maternal and neonatal immune mediators during pregnancy. | Genome Medicine | 2018 |
| 29659143 | RASopathies are associated with a distinct personality profile. | American Journal of Medical Genetics, Part B: Neuropsychiatric Genetics | 2018 |
| 29158583 | Patient-derived iPSCs show premature neural differentiation and neuron type-specific phenotypes relevant to neurodevelopment. | Molecular Psychiatry | 2018 |
| 29575775 | Recurrent reciprocal copy number variants: Roles and rules in neurodevelopmental disorders. | Developmental Neurobiology | 2018 |
| 27974502 | Genetic Mechanisms Leading to Sex Differences Across Common Diseases and Anthropometric Traits. | Genetics | 2017 |
| 28591140 | Correction: Pleiotropic Mechanisms Indicated for Sex Differences in Autism. | PLoS Genet | 2017 |
| 28895873 | Prenatal Serum Concentrations of Brominated Flame Retardants and Autism Spectrum Disorder and Intellectual Disability in the Early Markers of Autism Study: A Population-Based Case-Control Study in California. | Environmental Health Perspectives | 2017 |
| 28714951 | Rates, distribution and implications of postzygotic mosaic mutations in autism spectrum disorder. | Nat Neurosci | 2017 |
| 29212016 | Cellular Phenotypes in Human iPSC-Derived Neurons from a Genetic Model of Autism Spectrum Disorder. | Cell Rep | 2017 |
| 28076348 | Reverse Pathway Genetic Approach Identifies Epistasis in Autism Spectrum Disorders. | PLoS Genetics | 2017 |
| 28265118 | Risk alleles of genes with monoallelic expression are enriched in gain-of-function variants and depleted in loss-of-function variants for neurodevelopmental disorders. | Molecular Psychiatry | 2017 |
| 28235828 | Independent Maternal and Fetal Genetic Effects on Midgestational Circulating Levels of Environmental Pollutants. | G3: Genes, Genomes, Genetics | 2017 |
| 27751841 | If genetic variation could talk: What genomic data may teach us about the importance of gene expression regulation in the genetics of autism. | Molecular and Cellular Probes | 2016 |
| 26740656 | Human iPS Cell-Derived Neurons Uncover the Impact of Increased Ras Signaling in Costello Syndrome. | Journal of Neuroscience | 2016 |
| 27093065 | Maternal mid-pregnancy C-reactive protein and risk of autism spectrum disorders: the early markers for autism study. | Translational Psychiatry | 2016 |
| 27760236 | Disease Burden and Symptom Structure of Autism in Neurofibromatosis Type 1: A Study of the International NF1-ASD Consortium Team (INFACT). | JAMA Psychiatry | 2016 |
| 27569062 | Autonomous and Non-autonomous Defects Underlie Hypertrophic Cardiomyopathy in BRAF-Mutant hiPSC-Derived Cardiomyocytes. | Stem Cell Reports | 2016 |
| 27846226 | Pleiotropic Mechanisms Indicated for Sex Differences in Autism. | PLoS Genet | 2016 |
| 25947161 | Dysregulation of astrocyte extracellular signaling in Costello syndrome. | Sci Transl Med | 2015 |
| 25582617 | Increased female autosomal burden of rare copy number variants in human populations and in autism families. | Molecular Psychiatry | 2015 |
| 24101678 | Autism traits in the RASopathies. | Journal of Medical Genetics | 2014 |
| 25363760 | Synaptic, transcriptional and chromatin genes disrupted in autism. | Nature | 2014 |
| 24413397 | Cell-autonomous correction of ring chromosomes in human induced pluripotent stem cells. | Nature | 2014 |
| 23575222 | An eQTL mapping approach reveals that rare variants in the SEMA5A regulatory network impact autism risk. | Human Molecular Genetics | 2013 |
| 22946697 | Craniofacial and dental development in cardio-facio-cutaneous syndrome: the importance of Ras signaling homeostasis. | Clinical Genetics | 2013 |
| 24002087 | A rare WNT1 missense variant overrepresented in ASD leads to increased Wnt signal pathway activation. | Transl Psychiatry | 2013 |
| 23906504 | Associations between multivitamin supplement use and alcohol consumption before pregnancy: Pregnancy Risk Assessment Monitoring System, 2004 to 2008. | Alcoholism: Clinical and Experimental Research | 2013 |
| 24204716 | A genome-wide survey of transgenerational genetic effects in autism. | PLoS ONE | 2013 |
| 23794282 | Altered lipid metabolism in gastroschisis: a novel hypothesis. | American Journal of Medical Genetics, Part A | 2013 |
| 24090431 | SFARI Gene 2.0: a community-driven knowledgebase for the autism spectrum disorders (ASDs). | Molecular Autism | 2013 |
| 22315197 | The omega-6 fatty acid linoleic acid is associated with risk of gastroschisis: a novel dietary risk factor. | American Journal of Medical Genetics, Part A | 2012 |
| 22457638 | Age-dependent brain gene expression and copy number anomalies in autism suggest distinct pathological processes at young versus mature ages. | PLoS Genet | 2012 |
| 18805830 | Microdeletion/duplication at 15q13.2q13.3 among individuals with features of autism and other neuropsychiatric disorders. | J Med Genet | 2009 |
| 19435489 | New insights into genomic variation in health and disease. | Genome Medicine | 2009 |
| 19429002 | Preliminary evidence of association between EFHC2, a gene implicated in fear recognition, and harm avoidance. | Neurosci Lett | 2009 |
| 19276229 | Polymorphisms of the scavenger receptor class B member 1 are associated with insulin resistance with evidence of gene by sex interaction. | J Clin Endocrinol Metab | 2009 |
| 19895225 | Autism genetics: emerging data from genome-wide copy-number and single nucleotide polymorphism scans. | Expert Review of Molecular Diagnostics | 2009 |