Zobrazeno 1 - 10
of 35
pro vyhledávání: '"Shafali Jeste"'
Autor:
Vidya Saravanapandian, Melika Madani, India Nichols, Scott Vincent, Mary Dover, Dante Dikeman, Benjamin D. Philpot, Toru Takumi, Christopher S. Colwell, Shafali Jeste, Ketema N. Paul, Peyman Golshani
Publikováno v:
Journal of Neurodevelopmental Disorders, Vol 16, Iss 1, Pp 1-16 (2024)
Abstract Background Sleep disturbances are a prevalent and complex comorbidity in neurodevelopmental disorders (NDDs). Dup15q syndrome (duplications of 15q11.2-13.1) is a genetic disorder highly penetrant for NDDs such as autism and intellectual disa
Externí odkaz:
https://doaj.org/article/7a9ff40a16224580afd1c0543e8114e0
Autor:
Vardan Arutiunian, Megha Santhosh, Emily Neuhaus, Heather Borland, Chris Tompkins, Raphael A. Bernier, Susan Y. Bookheimer, Mirella Dapretto, Abha R. Gupta, Allison Jack, Shafali Jeste, James C. McPartland, Adam Naples, John D. Van Horn, Kevin A. Pelphrey, Sara Jane Webb
Publikováno v:
Molecular Autism, Vol 15, Iss 1, Pp 1-16 (2024)
Abstract Background Most children with Autism Spectrum Disorder (ASD) have co-occurring language impairments and some of these autism-specific language difficulties are also present in their non-autistic first-degree relatives. One of the possible ne
Externí odkaz:
https://doaj.org/article/2a915911ffab4dd7894744918d7e1457
Autor:
Tawny Tsang, Shulamite A. Green, Janelle Liu, Katherine Lawrence, Shafali Jeste, Susan Y. Bookheimer, Mirella Dapretto
Publikováno v:
Communications Biology, Vol 7, Iss 1, Pp 1-10 (2024)
Abstract Converging evidence implicates disrupted brain connectivity in autism spectrum disorder (ASD); however, the mechanisms linking altered connectivity early in development to the emergence of ASD symptomatology remain poorly understood. Here we
Externí odkaz:
https://doaj.org/article/627e7a24f46d4b358fd6a1930240b5fe
Autor:
Kirsten Blanco, Melissa Gabriel, Ashley Mills, Christina Cook, Vandana Mehta, Shafali Jeste, Tena Rosser, Matthew Deardorff
Publikováno v:
Genetics in Medicine Open, Vol 2, Iss , Pp 101461- (2024)
Externí odkaz:
https://doaj.org/article/ccb23f4180bc4274bf5392d7ff50957f
Autor:
Jorrit Tjeertes, Carlos A. Bacino, Terry Jo Bichell, Lynne M. Bird, Mariana Bustamante, Rebecca Crean, Shafali Jeste, Robert W. Komorowski, Michelle L. Krishnan, Meghan T. Miller, David Nobbs, Cesar Ochoa-Lubinoff, Kimberly A. Parkerson, Alexander Rotenberg, Anjali Sadhwani, Mark D. Shen, Lisa Squassante, Wen-Hann Tan, Brenda Vincenzi, Anne C. Wheeler, Joerg F. Hipp, Elizabeth Berry-Kravis
Publikováno v:
Journal of Neurodevelopmental Disorders, Vol 15, Iss 1, Pp 1-21 (2023)
Abstract Background Angelman syndrome (AS) is a rare neurodevelopmental disorder characterized by the absence of a functional UBE3A gene, which causes developmental, behavioral, and medical challenges. While currently untreatable, comprehensive data
Externí odkaz:
https://doaj.org/article/ef450fe783de498baf723d4e7e4e74fb
Autor:
Juliana Simon, Carly Hyde, Vidya Saravanapandian, Rujuta Wilson, Benjamin Schneider, Charlotte Distefano, Aaron Besterman, Shafali Jeste
Publikováno v:
Journal of Neurodevelopmental Disorders, Vol 15, Iss 1, Pp 1-1 (2023)
Externí odkaz:
https://doaj.org/article/db1589af49d444e8ba6444b86b7b6f3f
Autor:
Juliana Simon, Carly Hyde, Vidya Saravanapandian, Rujuta Wilson, Charlotte Distefano, Aaron Besterman, Shafali Jeste
Publikováno v:
Journal of Neurodevelopmental Disorders, Vol 14, Iss 1, Pp 1-10 (2022)
Abstract Background The development of advanced genetic technologies has resulted in rapid identification of genetic etiologies of neurodevelopmental disorders (NDDs) and has transformed the classification and diagnosis of various NDDs. However, diag
Externí odkaz:
https://doaj.org/article/11991ecafe5e41e08270f4aa7185ed47
Autor:
Emily Neuhaus, Sarah J. Lowry, Megha Santhosh, Anna Kresse, Laura A. Edwards, Jack Keller, Erin J. Libsack, Veronica Y. Kang, Adam Naples, Allison Jack, Shafali Jeste, James C. McPartland, Elizabeth Aylward, Raphael Bernier, Susan Bookheimer, Mirella Dapretto, John D. Van Horn, Kevin Pelphrey, Sara Jane Webb, and the ACE GENDAAR Network
Publikováno v:
Journal of Neurodevelopmental Disorders, Vol 13, Iss 1, Pp 1-15 (2021)
Abstract Background Identification of ASD biomarkers is a key priority for understanding etiology, facilitating early diagnosis, monitoring developmental trajectories, and targeting treatment efforts. Efforts have included exploration of resting stat
Externí odkaz:
https://doaj.org/article/01d79f0ba74b4ad8aecd684ab6842835
Autor:
Zachary Jacokes, Allison Jack, Catherine A. W. Sullivan, Elizabeth Aylward, Susan Y. Bookheimer, Mirella Dapretto, Raphael A. Bernier, Daniel H. Geschwind, Denis G. Sukhodolsky, James C. McPartland, Sara J. Webb, Carinna M. Torgerson, Jeffrey Eilbott, Lauren Kenworthy, Kevin A. Pelphrey, John D. Van Horn, The GENDAAR Consortium, Katy Ankenman, Sarah Corrigan, Dianna Depedro-Mercier, Nadine Gaab, Desiree Guilford, Abha R. Gupta, Shafali Jeste, Cara M. Keifer, Anna Kresse, Erin Libsack, Jennifer K. Lowe, Erin MacDonnell, Nicole McDonald, Adam Naples, Charles A. Nelson, Emily Neuhaus, Pamela Ventola, Olivia Welker, Julie Wolf
Publikováno v:
Frontiers in Neuroscience, Vol 16 (2022)
Autism Spectrum Disorder (ASD) is a developmental condition characterized by social and communication differences. Recent research suggests ASD affects 1-in-44 children in the United States. ASD is diagnosed more commonly in males, though it is uncle
Externí odkaz:
https://doaj.org/article/a3606502e36d49e0aeac12bb452fd062
Autor:
Sara Jane Webb, Iris Emerman, Catherine Sugar, Damla Senturk, Adam J. Naples, Susan Faja, Jessica Benton, Heather Borland, Carter Carlos, April R. Levin, Takumi McAllister, Megha Santhosh, Raphael A. Bernier, Katarzyna Chawarska, Geraldine Dawson, James Dziura, Shafali Jeste, Natalia Kleinhans, Michael Murias, Maura Sabatos-DeVito, Frederick Shic, James C. McPartland, the Autism Biomarkers Consortium for Clinical Trials
Publikováno v:
Frontiers in Psychiatry, Vol 13 (2022)
Recent proposals have suggested the potential for neural biomarkers to improve clinical trial processes in neurodevelopmental conditions; however, few efforts have identified whether chronological age-based adjustments will be necessary (as used in s
Externí odkaz:
https://doaj.org/article/e7f4d293b33e4059a93a28c6f1373978