Autism Spectrum Disorder

Displaying 1 - 45 of 45CSV
Nutor, C., Dickerson, A. S., Hsu, T., Al‐Jadiri, A., Camargo, C. A., Schweitzer, J. B., Shuster, C. L., Karagas, M. R., Madan, J. C., Restrepo, B., Schmidt, R. J., Lugo‐Candelas, C., Neiderhiser, J., Sathyanarayana, S., Dunlop, A. L., & Brennan, P. A. (2024). Examining the association between prenatal cannabis exposure and child autism traits: A multi‐cohort investigation in the environmental influences on child health outcome program. Autism Research, 17(8), 1651–1664. Portico. https://doi.org/10.1002/aur.3185
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Havdahl, A., Farmer, C., Surén, P., Øyen, A., Magnus, P., Susser, E., Lipkin, W. I., Reichborn‐Kjennerud, T., Stoltenberg, C., Bishop, S., & Thurm, A. (2023). Attainment and loss of early social‐communication skills across neurodevelopmental conditions in the Norwegian Mother, Father and Child Cohort Study. Journal of Child Psychology and Psychiatry, 65(5), 610–619. Portico. https://doi.org/10.1111/jcpp.13792
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Ratanatharathorn, A., Quan, L., Koenen, K. C., Chibnik, L. B., Weisskopf, M. G., Slopen, N., & Roberts, A. L. (2024). Polygenic risk for major depression, attention deficit hyperactivity disorder, neuroticism, and schizophrenia are correlated with experience of intimate partner violence. Translational Psychiatry, 14(1). https://doi.org/10.1038/s41398-024-02814-1
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Feldman, J. I., Garla, V., Dunham, K., Markfeld, J. E., Bowman, S. M., Golden, A. J., Daly, C., Kaiser, S., Mailapur, N., Raj, S., Santapuram, P., Suzman, E., Augustine, A. E., Muhumuza, A., Cascio, C. J., Williams, K. L., Kirby, A. V., Keceli-Kaysili, B., & Woynaroski, T. G. (2022). Longitudinal Relations Between Early Sensory Responsiveness and Later Communication in Infants with Autistic and Non-autistic Siblings. Journal of Autism and Developmental Disorders, 54(2), 594–606. https://doi.org/10.1007/s10803-022-05817-3
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Tener, S. J., Lin, Z., Park, S. J., Oraedu, K., Ulgherait, M., Van Beek, E., Martínez-Muñiz, A., Pantalia, M., Gatto, J. A., Volpi, J., Stavropoulos, N., Ja, W. W., Canman, J. C., & Shirasu-Hiza, M. (2024). Neuronal knockdown of Cullin3 as a Drosophila model of autism spectrum disorder. Scientific Reports, 14(1). https://doi.org/10.1038/s41598-024-51657-9
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Campi, E., Choi, E., Chen, Y.-J., Holland, C. M., Bristol, S., Sideris, J., Crais, E. R., Watson, L. R., & Baranek, G. T. (2022). Sensory Reactivity of Infants at Elevated Likelihood of Autism and Associations with Caregiver Responsiveness. Journal of Autism and Developmental Disorders, 54(1), 270–279. https://doi.org/10.1007/s10803-022-05764-z
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Neuhaus, E., Santhosh, M., Kresse, A., Aylward, E., Bernier, R., Bookheimer, S., Jeste, S., Jack, A., McPartland, J. C., Naples, A., Van Horn, J. D., Pelphrey, K., & Webb, S. J. (2023). Frontal EEG alpha asymmetry in youth with autism: Sex differences and social–emotional correlates. Autism Research, 16(12), 2364–2377. Portico. https://doi.org/10.1002/aur.3032
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Columbia Affiliation
Nuske, H. J., Young, A. V., Khan, F. Y., Palermo, E. H., Ajanaku, B., Pellecchia, M., Vivanti, G., Mazefsky, C. A., Brookman-Frazee, L., McPartland, J. C., Goodwin, M. S., & Mandell, D. S. (2023). Systematic review: emotion dysregulation and challenging behavior interventions for children and adolescents on the autism spectrum with graded key evidence-based strategy recommendations. European Child & Adolescent Psychiatry, 33(6), 1963–1976. https://doi.org/10.1007/s00787-023-02298-2
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Lowther, C., Valkanas, E., Giordano, J. L., Wang, H. Z., Currall, B. B., O’Keefe, K., Pierce-Hoffman, E., Kurtas, N. E., Whelan, C. W., Hao, S. P., Weisburd, B., Jalili, V., Fu, J., Wong, I., Collins, R. L., Zhao, X., Austin-Tse, C. A., Evangelista, E., Lemire, G., … Talkowski, M. E. (2023). Systematic evaluation of genome sequencing for the diagnostic assessment of autism spectrum disorder and fetal structural anomalies. The American Journal of Human Genetics, 110(9), 1454–1469. https://doi.org/10.1016/j.ajhg.2023.07.010
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Ming, N. R., Noble, D., Chussid, S., Ziegler, A., & Chung, W. K. (2023). Caregiver‐reported dental manifestations in individuals with genetic neurodevelopmental disorders. International Journal of Paediatric Dentistry, 34(2), 145–152. Portico. https://doi.org/10.1111/ipd.13116
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Avalos, L. A., Chandran, A., Churchill, M. L., Gao, X., Ames, J. L., Nozadi, S. S., Roubinov, D., Brennan, P. A., Bush, N. R., Camargo, C. A., Carroll, K. N., Cioffi, C. C., Ferrara, A., Goldson, B., Hedderson, M. M., Hipwell, A. E., Kerver, J. M., O’Connor, T. G., … Porucznik, C. A. (2023). Prenatal depression and risk of child autism‐related traits among participants in the Environmental influences on Child Health Outcomes program. Autism Research, 16(9), 1825–1835. Portico. https://doi.org/10.1002/aur.2988
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Albers, J., Kraja, G., Eller, D., Eck, K., McBrian, D., & Bain, J. M. (2023). Assessing the feasibility of using the ketogenic diet in autism spectrum disorder. Journal of Human Nutrition and Dietetics, 36(4), 1303–1315. Portico. https://doi.org/10.1111/jhn.13115
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Rolland, T., Cliquet, F., Anney, R. J. L., Moreau, C., Traut, N., Mathieu, A., Huguet, G., Duan, J., Warrier, V., Portalier, S., Dry, L., Leblond, C. S., Douard, E., Amsellem, F., Malesys, S., Maruani, A., Toro, R., Børglum, A. D., Grove, J., … Bourgeron, T. (2023). Phenotypic effects of genetic variants associated with autism. Nature Medicine, 29(7), 1671–1680. https://doi.org/10.1038/s41591-023-02408-2
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Schmid, C. M., Gregor, A., Costain, G., Morel, C. F., Massingham, L., Schwab, J., Quélin, C., Faoucher, M., Kaplan, J., Procopio, R., Saunders, C. J., Cohen, A. S. A., Lemire, G., Sacharow, S., O’Donnell-Luria, A., Segal, R. J., Kianmahd Shamshoni, J., Schweitzer, D., Ebrahimi-Fakhari, D., … Zweier, C. (2023). LHX2 haploinsufficiency causes a variable neurodevelopmental disorder. Genetics in Medicine, 25(7), 100839. https://doi.org/10.1016/j.gim.2023.100839
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Che, X., Roy, A., Bresnahan, M., Mjaaland, S., Reichborn-Kjennerud, T., Magnus, P., Stoltenberg, C., Shang, Y., Zhang, K., Susser, E., Fiehn, O., & Lipkin, W. I. (2023). Metabolomic analysis of maternal mid-gestation plasma and cord blood in autism spectrum disorders. Molecular Psychiatry, 28(6), 2355–2369. https://doi.org/10.1038/s41380-023-02051-w
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Sourander, A., Silwal, S., Surcel, H.-M., Hinkka-Yli-Salomäki, S., Upadhyaya, S., McKeague, I. W., Cheslack-Postava, K., & Brown, A. S. (2023). Maternal Serum Vitamin B12 during Pregnancy and Offspring Autism Spectrum Disorder. Nutrients, 15(8), 2009. https://doi.org/10.3390/nu15082009
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Vandana, P., Simkin, D. R., Hendren, R. L., & Arnold, L. E. (2023). Autism Spectrum Disorder and Complementary-Integrative Medicine. Child and Adolescent Psychiatric Clinics of North America, 32(2), 469–494. https://doi.org/10.1016/j.chc.2022.08.004
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Hong, S.-J., Mottron, L., Park, B., Benkarim, O., Valk, S. L., Paquola, C., Larivière, S., Vos de Wael, R., Degré-Pelletier, J., Soulieres, I., Ramphal, B., Margolis, A., Milham, M., Di Martino, A., & Bernhardt, B. C. (2022). A convergent structure–function substrate of cognitive imbalances in autism. Cerebral Cortex, 33(5), 1566–1580. https://doi.org/10.1093/cercor/bhac156
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Moog, N. K., Cummings, P. D., Jackson, K. L., Aschner, J. L., Barrett, E. S., Bastain, T. M., Blackwell, C. K., Bosquet Enlow, M., Breton, C. V., Bush, N. R., Deoni, S. C. L., Duarte, C. S., Ferrara, A., Grant, T. L., Hipwell, A. E., Jones, K., Leve, L. D., Lovinsky-Desir, S., Miller, R. K., … Buss, C. (2023). Intergenerational transmission of the effects of maternal exposure to childhood maltreatment in the USA: a retrospective cohort study. The Lancet Public Health, 8(3), e226–e237. https://doi.org/10.1016/s2468-2667(23)00025-7
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McGee, S. R., Rajamanickam, S., Adhikari, S., Falayi, O. C., Wilson, T. A., Shayota, B. J., Cooley Coleman, J. A., Skinner, C., Caylor, R. C., Stevenson, R. E., Quaio, C. R. D. A. C., Wilke, B. C., Bain, J. M., Anyane-Yeboa, K., Brown, K., Greally, J. M., Bijlsma, E. K., Ruivenkamp, C. A. L., Politi, K., … Jensik, P. J. (2022). Expansion and mechanistic insights into de novo DEAF1 variants in DEAF1-associated neurodevelopmental disorders. Human Molecular Genetics, 32(3), 386–401. https://doi.org/10.1093/hmg/ddac200
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Baker, B. H., Rafikian, E. E., Hamblin, P. B., Strait, M. D., Yang, M., & Pearson, B. L. (2023). Sex-specific neurobehavioral and prefrontal cortex gene expression alterations following developmental acetaminophen exposure in mice. Neurobiology of Disease, 177, 105970. https://doi.org/10.1016/j.nbd.2022.105970
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Morton, S. U., Norris-Brilliant, A., Cunningham, S., King, E., Goldmuntz, E., Brueckner, M., Miller, T. A., Thomas, N. H., Liu, C., Adams, H. R., Bellinger, D. C., Cleveland, J., Cnota, J. F., Dale, A. M., Frommelt, M., Gelb, B. D., Grant, P. E., Goldberg, C. S., Huang, H., … Newburger, J. W. (2023). Association of Potentially Damaging De Novo Gene Variants With Neurologic Outcomes in Congenital Heart Disease. JAMA Network Open, 6(1), e2253191. https://doi.org/10.1001/jamanetworkopen.2022.53191
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Lipman, A. R., Fan, X., Shen, Y., & Chung, W. K. (2022). Clinical and genetic characterization of CACNA1A‐related disease. Clinical Genetics, 102(4), 288–295. Portico. https://doi.org/10.1111/cge.14180
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Firestein, M. R., Romeo, R. D., Winstead, H., Goldman, D. A., Grobman, W. A., Haas, D. M., Parry, S., Reddy, U. M., Silver, R. M., Wapner, R. J., & Champagne, F. A. (2022). Hypertensive disorders during pregnancy and polycystic ovary syndrome are associated with child communication and social skills in a sex-specific and androgen-dependent manner. Frontiers in Endocrinology, 13. https://doi.org/10.3389/fendo.2022.1000732
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Riggs, E. R., Bingaman, T. I., Barry, C.-A., Behlmann, A., Bluske, K., Bostwick, B., Bright, A., Chen, C.-A., Clause, A. R., Dharmadhikari, A. V., Ganapathi, M., Gonzaga-Jauregui, C., Grant, A. R., Hughes, M. Y., Kim, S. R., Krause, A., Liao, J., Lumaka, A., Mah, M., … Schaaf, C. P. (2022). Clinical validity assessment of genes frequently tested on intellectual disability/autism sequencing panels. Genetics in Medicine, 24(9), 1899–1908. https://doi.org/10.1016/j.gim.2022.05.001
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O’Grady, L., Schrier Vergano, S. A., Hoffman, T. L., Sarco, D., Cherny, S., Bryant, E., Schultz‐Rogers, L., Chung, W. K., Sacharow, S., Immken, L. L., Holder, S., Blackwell, R. R., Buchanan, C., Yusupov, R., Lecoquierre, F., Guerrot, A., Rodan, L., de Vries, B. B. A., Kamsteeg, E. J., … Gold, N. B. (2022). Heterozygous variants in PRPF8 are associated with neurodevelopmental disorders. American Journal of Medical Genetics Part A, 188(9), 2750–2759. Portico. https://doi.org/10.1002/ajmg.a.62772
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Zuniga-Kennedy, M., Davoren, M., Shuffrey, L. C., Luna, R. A., Savidge, T., Prasad, V., Anderson, G. M., Veenstra-VanderWeele, J., & Williams, K. C. (2022). Intestinal Predictors of Whole Blood Serotonin Levels in Children With or Without Autism. Journal of Autism and Developmental Disorders, 52(9), 3780–3789. https://doi.org/10.1007/s10803-022-05597-w
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Temkin, A. B., Beaumont, R., Wkya, K., Hariton, J. R., Flye, B. L., Sheridan, E., Miranda, A., Vela, J., Zendegui, E., Schild, J., Gasparro, S., Loubriel, D., Damianides, A., Weisman, J., Silvestre, A., Yadegar, M., Catarozoli, C., & Bennett, S. M. (2022). Secret Agent Society: A Randomized Controlled Trial of a Transdiagnostic Youth Social Skills Group Treatment. Research on Child and Adolescent Psychopathology, 50(9), 1107–1119. https://doi.org/10.1007/s10802-022-00919-z
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Zhou, X., Feliciano, P., Shu, C., Wang, T., Astrovskaya, I., Hall, J. B., Obiajulu, J. U., Wright, J. R., Murali, S. C., Xu, S. X., Brueggeman, L., Thomas, T. R., Marchenko, O., Fleisch, C., Barns, S. D., Snyder, L. G., Han, B., Chang, T. S., Turner, T. N., … Chung, W. K. (2022). Integrating de novo and inherited variants in 42,607 autism cases identifies mutations in new moderate-risk genes. Nature Genetics, 54(9), 1305–1319. https://doi.org/10.1038/s41588-022-01148-2
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Villamor, E., Susser, E. S., & Cnattingius, S. (2022). Defective placentation syndromes and autism spectrum disorder in the offspring: population-based cohort and sibling-controlled studies. European Journal of Epidemiology, 37(8), 827–836. https://doi.org/10.1007/s10654-022-00884-3
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Fenster, R., Ziegler, A., Kentros, C., Geltzeiler, A., Green Snyder, L., Brooks, E., & Chung, W. K. (2022). Characterization of phenotypic range in DYRK1A haploinsufficiency syndrome using standardized behavioral measures. American Journal of Medical Genetics Part A, 188(7), 1954–1963. Portico. https://doi.org/10.1002/ajmg.a.62721
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Zhang, A., Sokolova, I., Domissy, A., Davis, J., Rao, L., Hana Utami, K., Wang, Y., Hagerman, R. J., Pouladi, M. A., Sanna, P., Boland, M. J., & Loring, J. F. (2022). Maturation Delay of Human GABAergic Neurogenesis in Fragile X Syndrome Pluripotent Stem Cells. Stem Cells Translational Medicine, 11(6), 613–629. https://doi.org/10.1093/stcltm/szac022
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Castaldelli-Maia, J. M., & Bhugra, D. (2022). Analysis of global prevalence of mental and substance use disorders within countries: focus on sociodemographic characteristics and income levels. International Review of Psychiatry, 34(1), 6–15. https://doi.org/10.1080/09540261.2022.2040450
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Shuffrey, L. C., Pini, N., Potter, M., Springer, P., Lucchini, M., Rayport, Y., Sania, A., Firestein, M., Brink, L., Isler, J. R., Odendaal, H., & Fifer, W. P. (2022). Aperiodic electrophysiological activity in preterm infants is linked to subsequent autism risk. Developmental Psychobiology, 64(4). Portico. https://doi.org/10.1002/dev.22271
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Budimirovic, D. B., Protic, D. D., Delahunty, C. M., Andrews, H. F., Choo, T., Xu, Q., Berry‐Kravis, E., & Kaufmann, W. E. (2021). Sleep problems in fragile X syndrome: Cross‐sectional analysis of a large clinic‐based cohort. American Journal of Medical Genetics Part A, 188(4), 1029–1039. Portico. https://doi.org/10.1002/ajmg.a.62601
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Firestein, M. R., Romeo, R. D., Winstead, H., Goldman, D. A., Grobman, W. A., Haas, D., Mercer, B., Parker, C., Parry, S., Reddy, U., Silver, R., Simhan, H., Wapner, R. J., & Champagne, F. A. (2022). Elevated prenatal maternal sex hormones, but not placental aromatase, are associated with child neurodevelopment. Hormones and Behavior, 140, 105125. https://doi.org/10.1016/j.yhbeh.2022.105125
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Che, X., Hornig, M., Bresnahan, M., Stoltenberg, C., Magnus, P., Surén, P., Mjaaland, S., Reichborn-Kjennerud, T., Susser, E., & Lipkin, W. I. (2022). Maternal mid-gestational and child cord blood immune signatures are strongly associated with offspring risk of ASD. Molecular Psychiatry, 27(3), 1527–1541. https://doi.org/10.1038/s41380-021-01415-4
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Kumble, S., Levy, A. M., Punetha, J., Gao, H., Ah Mew, N., Anyane‐Yeboa, K., Benke, P. J., Berger, S. M., Bjerglund, L., Campos‐Xavier, B., Ciliberto, M., Cohen, J. S., Comi, A. M., Curry, C., Damaj, L., Denommé‐Pichon, A., Emrick, L., Faivre, L., Fasano, M. B., … Tümer, Z. (2021). The clinical and molecular spectrum of QRICH1 associated neurodevelopmental disorder. Human Mutation, 43(2), 266–282. Portico. https://doi.org/10.1002/humu.24308
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Hickman, R. A., O’Shea, S. A., Mehler, M. F., & Chung, W. K. (2022). Neurogenetic disorders across the lifespan: from aberrant development to degeneration. Nature Reviews Neurology, 18(2), 117–124. https://doi.org/10.1038/s41582-021-00595-5
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