Zobrazeno 1 - 10
of 22
pro vyhledávání: '"Judith S Miller"'
Autor:
Kate E Wallis, Whitney Guthrie, Amanda E Bennett, Marsha Gerdes, Susan E Levy, David S Mandell, Judith S Miller
Publikováno v:
PLoS ONE, Vol 15, Iss 5, p e0232335 (2020)
OBJECTIVES:Although the American Academy of Pediatrics recommends screening for autism spectrum disorder (ASD) for all young children, disparities in ASD diagnosis and intervention in minority children persist. One potential contributor to disparitie
Externí odkaz:
https://doaj.org/article/41f6a351f6164559847c05452d99e3ce
Autor:
Rebecca P Thomas, Leah A L Wang, Whitney Guthrie, Meredith Cola, Joseph P McCleery, Juhi Pandey, Robert T Schultz, Judith S Miller
Publikováno v:
PLoS ONE, Vol 14, Iss 5, p e0216051 (2019)
The ability to selectively respond to one's own name is important for social and language development, and is disrupted in atypically developing populations (e.g., autism spectrum disorder). Research with typically developing samples using event-rela
Externí odkaz:
https://doaj.org/article/f6b90168455745338e91f7c3a6954d96
Autor:
Caitlin C. Clements, Tara L. Wenger, Alisa R. Zoltowski, Jennifer R. Bertollo, Judith S. Miller, Ashley B. de Marchena, Lauren M. Mitteer, John C. Carey, Benjamin E. Yerys, Elaine H. Zackai, Beverly S. Emanuel, Donna M. McDonald-McGinn, Robert T. Schultz
Publikováno v:
Molecular Autism, Vol 8, Iss 1, Pp 1-17 (2017)
Abstract Background Previous studies have reported no clear critical region for medical comorbidities in children with deletions or duplications of 22q11.2. The purpose of this study was to evaluate whether individuals with small nested deletions or
Externí odkaz:
https://doaj.org/article/e0920fdf03b84cc287869873723def41
Autor:
Seth L. Ness, Abigail Bangerter, Nikolay V. Manyakov, David Lewin, Matthew Boice, Andrew Skalkin, Shyla Jagannatha, Meenakshi Chatterjee, Geraldine Dawson, Matthew S. Goodwin, Robert Hendren, Bennett Leventhal, Frederick Shic, Jean A. Frazier, Yvette Janvier, Bryan H. King, Judith S. Miller, Christopher J. Smith, Russell H. Tobe, Gahan Pandina
Publikováno v:
Frontiers in Neuroscience, Vol 13 (2019)
Objective: The Janssen Autism Knowledge Engine (JAKE®) is a clinical research outcomes assessment system developed to more sensitively measure treatment outcomes and identify subpopulations in autism spectrum disorder (ASD). Here we describe JAKE an
Externí odkaz:
https://doaj.org/article/233046f661aa4d178f578093c00aae2b
Publikováno v:
Journal of Autism and Developmental Disorders.
Autor:
Julia Schuchard, Elizabeth A. Kaplan‐Kahn, Adam C. Carle, Laura Graham Holmes, Kiely Law, Judith S. Miller, Julia Parish‐Morris, Christopher B. Forrest
Publikováno v:
Autism research : official journal of the International Society for Autism ResearchREFERENCES. 15(12)
The objectives of this study were to (1) demonstrate the application of percentiles to advance the interpretation of patient-reported outcomes and (2) establish autism-specific percentiles for four Patient-Reported Outcomes Measurement Information Sy
Autor:
Kate E Wallis, Toore Adebajo, Amanda E Bennett, Madison Drye, Marsha Gerdes, Judith S Miller, Whitney Guthrie
Publikováno v:
Autism. :136236132211473
In this retrospective cohort study using data from an integrated primary care and subspecialty network, we examined medical records of children seen in primary care at eligible autism spectrum disorder (ASD) screening ages and followed through at lea
Autor:
Kate E. Wallis, Ekaterina Nekrasova, Amanda E. Bennett, Alexander G. Fiks, Marsha Gerdes, Brian P. Jenssen, Judith S. Miller, Di Shu, Whitney Guthrie
Publikováno v:
Academic pediatrics. 22(8)
To assess the impact of the COVID-19 pandemic on screening for autism spectrum disorder (ASD) and screening equity among eligible children presenting for well-child care in a large primary care pediatric network, we compared rates of ASD screening co
Autor:
Carrie E. Bearden, Marianne Bernadette van den Bree, Samuel J.R.A. Chawner, Leila Kushan, Louise Gallagher, Jeremy Hall, Wendy R. Kates, Kevin M. Antshel, Joanne L. Doherty, Judith S Miller, Caitlin C. Clements, Hayley Moss, Goran Cuturilo, A. Maillard, Raquel E. Gur, Sarah R Curran, LeeAnne Green-Snyder, Tara L. Wenger, Wendy K Chung, Michael J Owen, Richard Anney, Jacob Vorstman, Robert T. Schultz, Milica Pejovic-Milovancevic, Robin P. Goin-Kochel, Sébastien Jacquemont, Ellen Hanson, D M McDonald-McGinn, Raphael Bernier, Marina Mihaljevic, Ania M Fiksinski
Objective: Certain copy number variants (CNVs) greatly increase the risk of autism. The authors conducted a genetics-first study to investigate whether heterogeneity in the clinical presentation of autism is underpinned by specific genotype-phenotype
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b2a71567fba7bdaac36b3b97eefed4c8
Autor:
Whitney Guthrie, Kate Wallis, Amanda Bennett, Elizabeth Brooks, Jesse Dudley, Marsha Gerdes, Juhi Pandey, Susan E. Levy, Robert T. Schultz, Judith S. Miller
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::79dccab95d78b0b80839072e4bbc64f8
https://doi.org/10.1542/9781610024716-part03-ch007
https://doi.org/10.1542/9781610024716-part03-ch007