Biblio
Found 37 results
Filters: Author is Lauren A Weiss [Clear All Filters]
Combinations of genes at the 16p11.2 and 22q11.2 CNVs contribute to neurobehavioral traits.. PLoS genetics. 19:e1010780.
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2023. Can the "female protective effect" liability threshold model explain sex differences in autism spectrum disorder? Neuron. 110:3243-3262.
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2022. Sex-heterogeneous SNPs disproportionately influence gene expression and health.. PLoS genetics. 18:e1010147.
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Genetic Contributions to Maternal and Neonatal Vitamin D Levels.. Genetics. 214:1091-1102.
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2020. Cross-genetic determination of maternal and neonatal immune mediators during pregnancy.. Genome medicine. 10:67.
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2018. RASopathies are associated with a distinct personality profile.. American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics. 177:434-446.
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2018. Recurrent reciprocal copy number variants: Roles and rules in neurodevelopmental disorders.. Developmental neurobiology. 78:519-530.
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2018. Cellular Phenotypes in Human iPSC-Derived Neurons from a Genetic Model of Autism Spectrum Disorder.. Cell reports. 21:2678-2687.
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2017. Genetic Mechanisms Leading to Sex Differences Across Common Diseases and Anthropometric Traits.. Genetics. 205:979-992.
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2017. Independent Maternal and Fetal Genetic Effects on Midgestational Circulating Levels of Environmental Pollutants.. G3 (Bethesda, Md.). 7:1287-1299.
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2017. Reverse Pathway Genetic Approach Identifies Epistasis in Autism Spectrum Disorders.. PLoS genetics. 13:e1006516.
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2017. Human iPS Cell-Derived Neurons Uncover the Impact of Increased Ras Signaling in Costello Syndrome.. The Journal of neuroscience : the official journal of the Society for Neuroscience. 36:142-52.
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2016. 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. 30:346-356.
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2016. Pleiotropic Mechanisms Indicated for Sex Differences in Autism.. PLoS genetics. 12:e1006425.
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2016. Dysregulation of astrocyte extracellular signaling in Costello syndrome.. Science translational medicine. 7:286ra66.
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2015. Autism traits in the RASopathies.. Journal of medical genetics. 51:10-20.
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2014. Cell-autonomous correction of ring chromosomes in human induced pluripotent stem cells.. Nature. 507:99-103.
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2014. Synaptic, transcriptional and chromatin genes disrupted in autism.. Nature. 515:209-15.
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2014. A genome-wide survey of transgenerational genetic effects in autism.. PloS one. 8:e76978.
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2013. SFARI Gene 2.0: a community-driven knowledgebase for the autism spectrum disorders (ASDs).. Molecular autism. 4:36.
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2013. Autism genetics: emerging data from genome-wide copy-number and single nucleotide polymorphism scans.. Expert review of molecular diagnostics. 9:795-803.
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2009. A genome-wide linkage and association scan reveals novel loci for autism.. Nature. 461:802-8.
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2009. Preliminary evidence of association between EFHC2, a gene implicated in fear recognition, and harm avoidance.. Neuroscience letters. 452:84-6.
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