Zobrazeno 1 - 10
of 145
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:
Abigail Dickinson, Madison Booth, Manjari Daniel, Alana Campbell, Neely Miller, Bonnie Lau, John Zempel, Sara Jane Webb, Jed Elison, Adrian K.C. Lee, Annette Estes, Stephen Dager, Heather Hazlett, Jason Wolff, Robert Schultz, Natasha Marrus, Alan Evans, Joseph Piven, John R. Pruett, Jr., Shafali Jeste
Publikováno v:
Developmental Cognitive Neuroscience, Vol 69, Iss , Pp 101425- (2024)
Brain differences linked to autism spectrum disorder (ASD) can manifest before observable symptoms. Studying these early neural precursors in larger and more diverse cohorts is crucial for advancing our understanding of developmental pathways and pot
Externí odkaz:
https://doaj.org/article/21fe3641585f437a87353d46df9f5d2f
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:
Eve Bender
Publikováno v:
Psychiatric News. 54
Autor:
Jeste, Shafali
Publikováno v:
New Scientist. 6/2/2018, Vol. 238 Issue 3180, p22-23. 2p.
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