S
Shafali S. Jeste
Researcher at University of California, Los Angeles
Publications - 137
Citations - 4647
Shafali S. Jeste is an academic researcher from University of California, Los Angeles. The author has contributed to research in topics: Autism & Autism spectrum disorder. The author has an hindex of 29, co-authored 111 publications receiving 3560 citations. Previous affiliations of Shafali S. Jeste include Harvard University & Children's Hospital Los Angeles.
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Journal ArticleDOI
Disentangling the heterogeneity of autism spectrum disorder through genetic findings.
TL;DR: How some of the latest advances in the genetics of ASD have facilitated parsing of the phenotypic heterogeneity of this disorder is discussed, and it is argued that only through such advances will the authors begin to define endophenotypes that can benefit from targeted, hypothesis-driven treatments.
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Clinical Genetic Testing for Patients With Autism Spectrum Disorders
Yiping Shen,Kira A. Dies,Ingrid A. Holm,Carolyn Bridgemohan,Magdi M. Sobeih,Elizabeth B. Caronna,Karen J. Miller,Jean A. Frazier,Iris Silverstein,Jonathan Picker,Laura Weissman,Peter Raffalli,Shafali S. Jeste,Laurie A. Demmer,Heather Peters,Stephanie J. Brewster,Sara J J Kowalczyk,Beth Rosen-Sheidley,Caroline McGowan,Andrew Walter Duda,Sharyn A. Lincoln,Kathryn R. Lowe,Alison Schonwald,Michael Robbins,Fuki M. Hisama,Robert Wolff,Ronald E. Becker,Ramzi Nasir,David K. Urion,Jeff M. Milunsky,Leonard Rappaport,James F. Gusella,Christopher A. Walsh,Bai-Lin Wu,David T. Miller +34 more
TL;DR: CMA had the highest detection rate among clinically available genetic tests for patients with autism spectrum disorders and should be considered as part of the initial diagnostic evaluation of patients with ASD.
Journal ArticleDOI
Deletions of NRXN1 (Neurexin-1) Predispose to a Wide Spectrum of Developmental Disorders
Michael S L Ching,Yiping Shen,Yiping Shen,Wen-Hann Tan,Wen-Hann Tan,Shafali S. Jeste,Shafali S. Jeste,Eric M. Morrow,Xiaoli Chen,Nahit Motavalli Mukaddes,Seung Yun Yoo,Ellen Hanson,Ellen Hanson,Rachel J. Hundley,Rachel J. Hundley,Christina A. Austin,Ronald E. Becker,Ronald E. Becker,Gerard T. Berry,Gerard T. Berry,Katherine Driscoll,Katherine Driscoll,Elizabeth C. Engle,Sandra L. Friedman,Sandra L. Friedman,James F. Gusella,Fuki M. Hisama,Fuki M. Hisama,Mira Irons,Mira Irons,Tina Lafiosca,Tina Lafiosca,Elaine LeClair,Elaine LeClair,David T. Miller,David T. Miller,Michael Neessen,Michael Neessen,Jonathan Picker,Jonathan Picker,Leonard Rappaport,Leonard Rappaport,Cynthia M. Rooney,Cynthia M. Rooney,Dean Sarco,Dean Sarco,Joan M. Stoler,Joan M. Stoler,Christopher A. Walsh,Robert Wolff,Robert Wolff,Ting Zhang,Ramzi Nasir,Ramzi Nasir,Bai-Lin Wu,Bai-Lin Wu,Bai-Lin Wu +56 more
TL;DR: The study indicates that deletions of NRXN1 predispose to a wide spectrum of developmental disorders, including autism spectrum disorders, mental retardation, language delays and hypotonia.
Journal ArticleDOI
Characterization of Autism in Young Children With Tuberous Sclerosis Complex.
TL;DR: The authors conclude that clinic-referred children with tuberous sclerosis complex and autism are at considerable risk for cognitive impairment and characteristics may help to guide more tailored services for these high-risk children.
Journal ArticleDOI
Changes in access to educational and healthcare services for individuals with intellectual and developmental disabilities during COVID-19 restrictions.
Shafali S. Jeste,Carly Hyde,Charlotte DiStefano,A. Halladay,A. Halladay,S. Ray,M. Porath,Rujuta B. Wilson,A. Thurm +8 more
TL;DR: Telehealth may provide opportunities for delivery of care and education in a sustainable way, not only as restrictions endure but also after they have been lifted.