Vysotskiy M, Consortium AWorking Gr, Consortium BDisorder W, Consortium SWorking Gr, Weiss LA.  2023.  Combinations of genes at the 16p11.2 and 22q11.2 CNVs contribute to neurobehavioral traits.. PLoS genetics. 19:e1010780.

Dougherty JD, Marrus N, Maloney SE, Yip B, Sandin S, Turner TN, Selmanovic D, Kroll KL, Gutmann DH, Constantino JN et al..  2022.  Can the "female protective effect" liability threshold model explain sex differences in autism spectrum disorder? Neuron. 110:3243-3262.

Traglia M, Bout M, Weiss LA.  2022.  Sex-heterogeneous SNPs disproportionately influence gene expression and health.. PLoS genetics. 18:e1010147.

Vysotskiy M, Zhong X, Miller-Fleming TW, Zhou D, Consortium^ AWorking Gr, Consortium^ BDisorder W, Consortium^ SWorking Gr, Cox NJ, Weiss LA.  2021.  Integration of genetic, transcriptomic, and clinical data provides insight into 16p11.2 and 22q11.2 CNV genes.. Genome medicine. 13:172.

Lyall K, Ames JL, Pearl M, Traglia M, Weiss LA, Windham GC, Kharrazi M, Yoshida CK, Yolken R, Volk HE et al..  2021.  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. 12:24.

Traglia M, Windham GC, Pearl M, Poon V, Eyles D, Jones KL, Lyall K, Kharrazi M, Croen LA, Weiss LA.  2020.  Genetic Contributions to Maternal and Neonatal Vitamin D Levels.. Genetics. 214:1091-1102.

Traglia M, Croen LA, Jones KL, Heuer LS, Yolken R, Kharrazi M, DeLorenze GN, Ashwood P, Van de Water J, Weiss LA.  2018.  Cross-genetic determination of maternal and neonatal immune mediators during pregnancy.. Genome medicine. 10:67.

Bizaoui V, Gage J, Brar R, Rauen KA, Weiss LA.  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.

Deshpande A, Weiss LA.  2018.  Recurrent reciprocal copy number variants: Roles and rules in neurodevelopmental disorders.. Developmental neurobiology. 78:519-530.

Wang H, Zhang D, Bolm C.  2018.  Sulfoximidations of Benzylic C-H bonds by Photocatalysis.. Angewandte Chemie (International ed. in English). 57:5863-5866.

Deshpande A, Yadav S, Dao DQ, Wu Z-Y, Hokanson KC, Cahill MK, Wiita AP, Jan Y-N, Ullian EM, Weiss LA.  2017.  Cellular Phenotypes in Human iPSC-Derived Neurons from a Genetic Model of Autism Spectrum Disorder.. Cell reports. 21:2678-2687.

Traglia M, Bseiso D, Gusev A, Adviento B, Park DS, Mefford JA, Zaitlen N, Weiss LA.  2017.  Genetic Mechanisms Leading to Sex Differences Across Common Diseases and Anthropometric Traits.. Genetics. 205:979-992.

Traglia M, Croen LA, Lyall K, Windham GC, Kharrazi M, DeLorenze GN, Torres AR, Weiss LA.  2017.  Independent Maternal and Fetal Genetic Effects on Midgestational Circulating Levels of Environmental Pollutants.. G3 (Bethesda, Md.). 7:1287-1299.

Mitra I, Lavillaureix A, Yeh E, Traglia M, Tsang K, Bearden CE, Rauen KA, Weiss LA.  2017.  Reverse Pathway Genetic Approach Identifies Epistasis in Autism Spectrum Disorders.. PLoS genetics. 13:e1006516.

Savova V, Vinogradova S, Pruss D, Gimelbrant AA, Weiss LA.  2017.  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. 22:1785-1794.

Rooney GE, Goodwin AF, Depeille P, Sharir A, Schofield CM, Yeh E, Roose JP, Klein OD, Rauen KA, Weiss LA et al..  2016.  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.

Yeh E, Weiss LA.  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.

Zerbo O, Traglia M, Yoshida C, Heuer LS, Ashwood P, Delorenze GN, Hansen RL, Kharrazi M, Van de Water J, Yolken RH et al..  2016.  Maternal mid-pregnancy C-reactive protein and risk of autism spectrum disorders: the early markers for autism study.. Translational psychiatry. 6:e783.

Mitra I, Tsang K, Ladd-Acosta C, Croen LA, Aldinger KA, Hendren RL, Traglia M, Lavillaureix A, Zaitlen N, Oldham MC et al..  2016.  Pleiotropic Mechanisms Indicated for Sex Differences in Autism.. PLoS genetics. 12:e1006425.

Krencik R, Hokanson KC, Narayan AR, Dvornik J, Rooney GE, Rauen KA, Weiss LA, Rowitch DH, Ullian EM.  2015.  Dysregulation of astrocyte extracellular signaling in Costello syndrome.. Science translational medicine. 7:286ra66.

Desachy G, Croen LA, Torres AR, Kharrazi M, Delorenze GN, Windham GC, Yoshida CK, Weiss LA.  2015.  Increased female autosomal burden of rare copy number variants in human populations and in autism families.. Molecular psychiatry. 20:170-5.

Maier R, Moser G, Chen G-B, Ripke S, Consortium C-DWorking Gr, Coryell W, Potash JB, Scheftner WA, Shi J, Weissman MM et al..  2015.  Joint analysis of psychiatric disorders increases accuracy of risk prediction for schizophrenia, bipolar disorder, and major depressive disorder.. American journal of human genetics. 96:283-94.

Network, Consortium PAnalysis S.  2015.  Psychiatric genome-wide association study analyses implicate neuronal, immune and histone pathways.. Nature neuroscience. 18:199-209.

Adviento B, Corbin IL, Widjaja F, Desachy G, Enrique N, Rosser T, Risi S, Marco EJ, Hendren RL, Bearden CE et al..  2014.  Autism traits in the RASopathies.. Journal of medical genetics. 51:10-20.

Bershteyn M, Hayashi Y, Desachy G, Hsiao EC, Sami S, Tsang KM, Weiss LA, Kriegstein AR, Yamanaka S, Wynshaw-Boris A.  2014.  Cell-autonomous correction of ring chromosomes in human induced pluripotent stem cells.. Nature. 507:99-103.