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Author Details

Lauren A Weiss
2003
68
33
PMIDPaper TitleJournal TitlePublished Year
37267418Combinations of genes at the 16p11.2 and 22q11.2 CNVs contribute to neurobehavioral traits.2023
35868305Can the "female protective effect" liability threshold model explain sex differences in autism spectrum disorder?Neuron2022
35511767Sex-heterogeneous SNPs disproportionately influence gene expression and health.PLoS Genetics2022
34715901Integration of genetic, transcriptomic, and clinical data provides insight into 16p11.2 and 22q11.2 CNV genes.Genome Med2021
33736683A profile and review of findings from the Early Markers for Autism study: unique contributions from a population-based case-control study in California.Molecular Autism2021
33648717Examining Sex-Differentiated Genetic Effects Across Neuropsychiatric and Behavioral Traits.Biol Psychiatry2021
32815557Autism in neurofibromatosis type 1: misuse of covariance to dismiss autistic trait burden.Dev Med Child Neurol2021
32665711Publisher Correction: Rates, distribution and implications of postzygotic mosaic mutations in autism spectrum disorder.Nat Neurosci2020
32047095Genetic Contributions to Maternal and Neonatal Vitamin D Levels.Genetics2020
31367015Mapping cis-regulatory chromatin contacts in neural cells links neuropsychiatric disorder risk variants to target genes.Nat Genet2019
29575620Age and ASD symptoms in Costello syndrome.American Journal of Medical Genetics, Part A2018
28401798Most Frequently Reported Prescription Medications and Supplements in Couples Planning Pregnancy: The LIFE Study.Reproductive Sciences2018
29930110Analysis of shared heritability in common disorders of the brain.Science2018
30134952Cross-genetic determination of maternal and neonatal immune mediators during pregnancy.Genome Medicine2018
29659143RASopathies are associated with a distinct personality profile.American Journal of Medical Genetics, Part B: Neuropsychiatric Genetics2018
29158583Patient-derived iPSCs show premature neural differentiation and neuron type-specific phenotypes relevant to neurodevelopment.Molecular Psychiatry2018
29575775Recurrent reciprocal copy number variants: Roles and rules in neurodevelopmental disorders.Developmental Neurobiology2018
27974502Genetic Mechanisms Leading to Sex Differences Across Common Diseases and Anthropometric Traits.Genetics2017
28591140Correction: Pleiotropic Mechanisms Indicated for Sex Differences in Autism.PLoS Genet2017
28895873Prenatal 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 Perspectives2017
28714951Rates, distribution and implications of postzygotic mosaic mutations in autism spectrum disorder.Nat Neurosci2017
29212016Cellular Phenotypes in Human iPSC-Derived Neurons from a Genetic Model of Autism Spectrum Disorder.Cell Rep2017
28076348Reverse Pathway Genetic Approach Identifies Epistasis in Autism Spectrum Disorders.PLoS Genetics2017
28265118Risk alleles of genes with monoallelic expression are enriched in gain-of-function variants and depleted in loss-of-function variants for neurodevelopmental disorders.Molecular Psychiatry2017
28235828Independent Maternal and Fetal Genetic Effects on Midgestational Circulating Levels of Environmental Pollutants.G3: Genes, Genomes, Genetics2017
27751841If 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 Probes2016
26740656Human iPS Cell-Derived Neurons Uncover the Impact of Increased Ras Signaling in Costello Syndrome.Journal of Neuroscience2016
27093065Maternal mid-pregnancy C-reactive protein and risk of autism spectrum disorders: the early markers for autism study.Translational Psychiatry2016
27760236Disease Burden and Symptom Structure of Autism in Neurofibromatosis Type 1: A Study of the International NF1-ASD Consortium Team (INFACT).JAMA Psychiatry2016
27569062Autonomous and Non-autonomous Defects Underlie Hypertrophic Cardiomyopathy in BRAF-Mutant hiPSC-Derived Cardiomyocytes.Stem Cell Reports2016
27846226Pleiotropic Mechanisms Indicated for Sex Differences in Autism.PLoS Genet2016
25947161Dysregulation of astrocyte extracellular signaling in Costello syndrome.Sci Transl Med2015
25582617Increased female autosomal burden of rare copy number variants in human populations and in autism families.Molecular Psychiatry2015
24101678Autism traits in the RASopathies.Journal of Medical Genetics2014
25363760Synaptic, transcriptional and chromatin genes disrupted in autism.Nature2014
24413397Cell-autonomous correction of ring chromosomes in human induced pluripotent stem cells.Nature2014
23575222An eQTL mapping approach reveals that rare variants in the SEMA5A regulatory network impact autism risk.Human Molecular Genetics2013
22946697Craniofacial and dental development in cardio-facio-cutaneous syndrome: the importance of Ras signaling homeostasis.Clinical Genetics2013
24002087A rare WNT1 missense variant overrepresented in ASD leads to increased Wnt signal pathway activation.Transl Psychiatry2013
23906504Associations between multivitamin supplement use and alcohol consumption before pregnancy: Pregnancy Risk Assessment Monitoring System, 2004 to 2008.Alcoholism: Clinical and Experimental Research2013
24204716A genome-wide survey of transgenerational genetic effects in autism.PLoS ONE2013
23794282Altered lipid metabolism in gastroschisis: a novel hypothesis.American Journal of Medical Genetics, Part A2013
24090431SFARI Gene 2.0: a community-driven knowledgebase for the autism spectrum disorders (ASDs).Molecular Autism2013
22315197The omega-6 fatty acid linoleic acid is associated with risk of gastroschisis: a novel dietary risk factor.American Journal of Medical Genetics, Part A2012
22457638Age-dependent brain gene expression and copy number anomalies in autism suggest distinct pathological processes at young versus mature ages.PLoS Genet2012
18805830Microdeletion/duplication at 15q13.2q13.3 among individuals with features of autism and other neuropsychiatric disorders.J Med Genet2009
19435489New insights into genomic variation in health and disease.Genome Medicine2009
19429002Preliminary evidence of association between EFHC2, a gene implicated in fear recognition, and harm avoidance.Neurosci Lett2009
19276229Polymorphisms of the scavenger receptor class B member 1 are associated with insulin resistance with evidence of gene by sex interaction.J Clin Endocrinol Metab2009
19895225Autism genetics: emerging data from genome-wide copy-number and single nucleotide polymorphism scans.Expert Review of Molecular Diagnostics2009
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