Autism Spectrum Disorders

Displaying 1 - 27 of 27CSV
Domingo-Espiñeira, J., Fraile-Martínez, Ó., García Montero, C., Lara Abelenda, F. J., Porta-Etessam, J., Baras Pastor, L., Muñoz-Manchado, L. I., Arrieta, M., Saeidi, M., Ortega, M. A., Alvarez De Mon, M., & Alvarez-Mon, M. A. (2024). Analyzing public discourse of dementia from Spanish and English tweets: a comparative analysis with other neurological disorders. Frontiers in Neurology, 15. https://doi.org/10.3389/fneur.2024.1459578
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Santana Almansa, A., Snyder, L. G., Chung, W. K., Bain, J. M., & Srivastava, S. (2024). Motor phenotypes associated with genetic neurodevelopmental disorders. Annals of Clinical and Translational Neurology. Portico. https://doi.org/10.1002/acn3.52231
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Firestein, M. R., Manessis, A., Warmingham, J. M., Xu, R., Hu, Y., Finkel, M. A., Kyle, M., Hussain, M., Ahmed, I., Lavallée, A., Solis, A., Chaves, V., Rodriguez, C., Goldman, S., Muhle, R. A., Lee, S., Austin, J., Silver, W. G., O’Reilly, K. C., … Dumitriu, D. (2024). Positive Autism Screening Rates in Toddlers Born During the COVID-19 Pandemic. JAMA Network Open, 7(9), e2435005. https://doi.org/10.1001/jamanetworkopen.2024.35005
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Sudnawa, K. K., Pini, N., Li, W., Kanner, C. H., Ryu, J., Calamia, S., Bain, J. M., Goldman, S., Montes, J., Shen, Y., & Chung, W. K. (2024). Clinical characteristics, longitudinal adaptive functioning, and association with electroencephalogram activity in PPP2R5D‐related neurodevelopmental disorder. Clinical Genetics. Portico. https://doi.org/10.1111/cge.14612
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Cook, L., Verbrugge, J., Schwantes-An, T.-H., Schulze, J., Foroud, T., Hall, A., Marder, K. S., Mata, I. F., Mencacci, N. E., Nance, M. A., Schwarzschild, M. A., Simuni, T., Bressman, S., Wills, A.-M., Fernandez, H. H., Litvan, I., Lyons, K. E., Shill, H. A., Singer, C., … Alcalay, R. N. (2024). Parkinson’s disease variant detection and disclosure: PD GENEration, a North American study. Brain, 147(8), 2668–2679. https://doi.org/10.1093/brain/awae142
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Wright, J. R., Astrovskaya, I., Barns, S. D., Goler, A., Zhou, X., Shu, C., Snyder, L. G., Han, B., Aarrestad, A., Abbeduto, L., Aberbach, G., Aberle, S., Adegbite, A., Adeniji, D., Aguilar, M., Ahlers, K., Albright, C., Alessandri, M., Algaze, Z., … Chung, W. K. (2024). Return of genetic research results in 21,532 individuals with autism. Genetics in Medicine, 101202. https://doi.org/10.1016/j.gim.2024.101202
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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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Irani, D., Blinderman, C. D., Levenson, J., Nash, S. S., Callahan, M., Shapiro, P., & Shalev, D. (2024). Promoting Collaborative CL Psychiatry and Palliative Care Education via Combined Fellow-focused Case Conferences. Journal of Pain and Symptom Management, 67(5), e615. https://doi.org/10.1016/j.jpainsymman.2024.02.040
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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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McLaughlin, N. C. R., Magnotti, J. F., Banks, G. P., Nanda, P., Hoexter, M. Q., Lopes, A. C., Batistuzzo, M. C., Asaad, W. F., Stewart, C., Paulo, D., Noren, G., Greenberg, B. D., Malloy, P., Salloway, S., Correia, S., Pathak, Y., Sheehan, J., Marsland, R., Gorgulho, A., … Sheth, S. A. (2023). Gamma knife capsulotomy for intractable OCD: Neuroimage analysis of lesion size, location, and clinical response. Translational Psychiatry, 13(1). https://doi.org/10.1038/s41398-023-02425-2
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Lachiewicz, A. M., Stackhouse, T. M., Burgess, K., Burgess, D., Andrews, H. F., Choo, T.-H., Kaufmann, W. E., & Kidd, S. A. (2023). Sensory Symptoms and Signs of Hyperarousal in Individuals with Fragile X Syndrome: Findings from the FORWARD Registry and Database Multisite Study. Journal of Autism and Developmental Disorders. https://doi.org/10.1007/s10803-023-06135-y
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Pal, G., Cook, L., Schulze, J., Verbrugge, J., Alcalay, R. N., Merello, M., Sue, C. M., Bardien, S., Bonifati, V., Chung, S. J., Foroud, T., Gatto, E., Hall, A., Hattori, N., Lynch, T., Marder, K., Mascalzoni, D., Novaković, I., Thaler, A., … Klein, C. (2023). Genetic Testing in Parkinson’s Disease. Movement Disorders, 38(8), 1384–1396. Portico. https://doi.org/10.1002/mds.29500
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Pagliaccio, D., Wengler, K., Durham, K., Fontaine, M., Rueppel, M., Becker, H., Bilek, E., Pieper, S., Risdon, C., Horga, G., Fitzgerald, K. D., & Marsh, R. (2023). Probing midbrain dopamine function in pediatric obsessive-compulsive disorder via neuromelanin-sensitive magnetic resonance imaging. Molecular Psychiatry, 28(7), 3075–3082. https://doi.org/10.1038/s41380-023-02105-z
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Johnson, J., Fernandez, K. K., Barker, M. S., Hernandez, M., Soto, E., Gu, Y., Stern, Y., & Cosentino, S. (2023). Phonemic Fluency in pathologically confirmed Alzheimer’s disease (AD) versus AD with Lewy Bodies. Alzheimer’s & Dementia, 19(S4). Portico. https://doi.org/10.1002/alz.067429
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Leuchter, J. D., Kook, M., Geller, D. A., Hertz, A. G., Garcia, J., Trent, E. S., Dibbs, T., Onyeka, O., Goodman, W. K., Guzick, A. G., Wiese, A. D., Palo, A. D., Small, B. J., Simpson, H. B., Havel, L. K., Nibras, S. A., Saxena, K., & Storch, E. A. (2023). Promoting OCD WEllness and resilience (POWER) study: Rationale, design, and methods. Psychiatry Research Communications, 3(2), 100111. https://doi.org/10.1016/j.psycom.2023.100111
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Frankel, E., Podder, A., Sharifi, M., Pillai, R., Belnap, N., Ramsey, K., Dodson, J., Venugopal, P., Brzezinski, M., Llaci, L., Gerald, B., Mills, G., Sanchez-Castillo, M., Balak, C. D., Szelinger, S., Jepsen, W. M., Siniard, A. L., Richholt, R., Naymik, M., … Rangasamy, S. (2023). Genetic and Protein Network Underlying the Convergence of Rett-Syndrome-like (RTT-L) Phenotype in Neurodevelopmental Disorders. Cells, 12(10), 1437. https://doi.org/10.3390/cells12101437
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Ferhat, A.-T., Verpy, E., Biton, A., Forget, B., De Chaumont, F., Mueller, F., Le Sourd, A.-M., Coqueran, S., Schmitt, J., Rochefort, C., Rondi-Reig, L., Leboucher, A., Boland, A., Fin, B., Deleuze, J.-F., Boeckers, T. M., Ey, E., & Bourgeron, T. (2023). Excessive self-grooming, gene dysregulation and imbalance between the striosome and matrix compartments in the striatum of Shank3 mutant mice. Frontiers in Molecular Neuroscience, 16. https://doi.org/10.3389/fnmol.2023.1139118
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Cook, L., Schulze, J., Uhlmann, W. R., Verbrugge, J., Marder, K., Lee, A. J., Wang, Y., Alcalay, R. N., Nance, M., & Beck, J. C. (2022). Tools for communicating risk for Parkinson’s disease. Npj Parkinson’s Disease, 8(1). https://doi.org/10.1038/s41531-022-00432-6
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Kayumi, S., Pérez-Jurado, L. A., Palomares, M., Rangu, S., Sheppard, S. E., Chung, W. K., Kruer, M. C., Kharbanda, M., Amor, D. J., McGillivray, G., Cohen, J. S., García-Miñaúr, S., van Eyk, C. L., Harper, K., Jolly, L. A., Webber, D. L., Barnett, C. P., Santos-Simarro, F., Pacio-Míguez, M., … Corbett, M. A. (2022). Genomic and phenotypic characterization of 404 individuals with neurodevelopmental disorders caused by CTNNB1 variants. Genetics in Medicine, 24(11), 2351–2366. https://doi.org/10.1016/j.gim.2022.08.006
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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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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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Wright, J., Barns, S., Goler, A., Hall, J., Han, B., Astrovskaya, I., Marchenko, O., Ganesan, S., Volfovsky, N., Feliciano, P., & Chung, W. (2022). eP287: Return of individual genetic results in the largest recontactable cohort of individuals with autism. Genetics in Medicine, 24(3), S181–S182. https://doi.org/10.1016/j.gim.2022.01.322
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Revah-Politi, A., Kushary, S. (Tina), Vena, N., May, H., Lippa, N., Bier, L., Goldman, J., Alkelai, A., Baugh, E., Zoghbi, A., Kayser, R., Goldstein, D., & Simpson, H. B. (2022). eP435: Issues in interpreting results in research genomic testing for common disorders: an example within an OCD cohort. Genetics in Medicine, 24(3), S272–S273. https://doi.org/10.1016/j.gim.2022.01.469
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