Zobrazeno 1 - 10
of 115
pro vyhledávání: '"Jennifer M. Phillips"'
Autor:
Michael S. Breen, Xuanjia Fan, Tess Levy, Rebecca M. Pollak, Brett Collins, Aya Osman, Anna S. Tocheva, Mustafa Sahin, Elizabeth Berry-Kravis, Latha Soorya, Audrey Thurm, Craig M. Powell, Jonathan A. Bernstein, Alexander Kolevzon, Joseph D. Buxbaum, Simon K. Warfield, Benoit Scherrer, Rajna Filip-Dhima, Kira Dies, Paige Siper, Ellen Hanson, Jennifer M. Phillips
Publikováno v:
HGG Advances, Vol 4, Iss 1, Pp 100145- (2023)
Summary: Phelan-McDermid syndrome (PMS) is a rare neurodevelopmental disorder caused at least in part by haploinsufficiency of the SHANK3 gene, due to sequence variants in SHANK3 or subtelomeric 22q13.3 deletions. Phenotypic differences have been rep
Externí odkaz:
https://doaj.org/article/3468f77f03d1418b9e1044467e8fe3e3
Autor:
Mirko Uljarević, Nicholas T. Bott, Robin A. Libove, Jennifer M. Phillips, Karen J. Parker, Antonio Y. Hardan
Publikováno v:
Frontiers in Psychology, Vol 12 (2022)
Emotion recognition skills and the ability to understand the mental states of others are crucial for normal social functioning. Conversely, delays and impairments in these processes can have a profound impact on capability to engage in, maintain, and
Externí odkaz:
https://doaj.org/article/0337e9540708435293feb3327e0f6f19
Autor:
Jennifer M. Phillips, Mirko Uljarević, Rachel K. Schuck, Salena Schapp, Elizabeth M. Solomon, Emma Salzman, Lauren Allerhand, Robin A. Libove, Thomas W. Frazier, Antonio Y. Hardan
Publikováno v:
Molecular Autism, Vol 10, Iss 1, Pp 1-16 (2019)
Abstract Background The aim of this paper was to provide an initial validation of a newly developed parent questionnaire—the Stanford Social Dimensions Scale (SSDS), designed to capture individual differences across several key social dimensions in
Externí odkaz:
https://doaj.org/article/ac6ed10ac05141b8a0f4e5cbe58ac1c0
Autor:
Morgan Steele, Mirko Uljarević, Gaëlle Rached, Thomas W. Frazier, Jennifer M. Phillips, Robin A. Libove, Robyn M. Busch, Patricia Klaas, Julian A. Martinez-Agosto, Siddharth Srivastava, Charis Eng, Mustafa Sahin, Antonio Y. Hardan
Publikováno v:
Frontiers in Psychiatry, Vol 12 (2021)
Germline heterozygous PTEN mutations have been associated with high prevalence of autism spectrum disorder (ASD) and elevated rates and severity of broadly defined behavioral problems. However, limited progress has been made toward understanding whet
Externí odkaz:
https://doaj.org/article/d3ba4bd56d2946178a59d34f216b9559
Publikováno v:
Biological Psychiatry: Cognitive Neuroscience and Neuroimaging. 8:531-541
Publikováno v:
Frontiers in Psychiatry, Vol 12 (2021)
Emotion regulation is theorized to be a transdiagnostic process and has been empirically shown to be associated with various mental health and neurodevelopmental conditions. However, the relationship between emotion regulation and internalizing and e
Externí odkaz:
https://doaj.org/article/4989e79f7365477a9a1fe18ccaceee4d
Autor:
Mirko Uljarević, Thomas W. Frazier, Booil Jo, Jennifer M. Phillips, Wesley Billingham, Matthew N. Cooper, Antonio Y. Hardan
Publikováno v:
Frontiers in Neuroscience, Vol 15 (2021)
Impairment in social motivation (SM) has been suggested as a key mechanism underlying social communication deficits observed in autism spectrum disorder (ASD). However, the factors accounting for variability in SM remain poorly described and understo
Externí odkaz:
https://doaj.org/article/e2cf0d7508194c11b1fb97aaa02dae86
Autor:
Debra S. Karhson, Karolina M. Krasinska, Jamie Ahloy Dallaire, Robin A. Libove, Jennifer M. Phillips, Allis S. Chien, Joseph P. Garner, Antonio Y. Hardan, Karen J. Parker
Publikováno v:
Molecular Autism, Vol 9, Iss 1, Pp 1-6 (2018)
Abstract Background Autism spectrum disorder (ASD) is a neurodevelopmental disorder characterized by restricted, stereotyped behaviors and impairments in social communication. Although the underlying biological mechanisms of ASD remain poorly underst
Externí odkaz:
https://doaj.org/article/e635a6af861a48de8e09f824ab0efc5e
Autor:
Sandra Tong, Pamela Ventola, Christina H. Frater, Jenna Klotz, Jennifer M. Phillips, Srikanth Muppidi, Selina S. Dwight, William F. Mueller, Brendan J. Beahm, Matt Wilsey, Kevin J. Lee
N-glycanase 1 (NGLY1) Deficiency is a debilitating, ultra-rare autosomal recessive disorder caused by loss of function of NGLY1, a cytosolic enzyme that deglycosylates other proteins. It is characterized by severe global developmental delay and/or in
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::99b5aaae221e3690d926f49815c1d09f
https://doi.org/10.1101/2023.05.10.23289581
https://doi.org/10.1101/2023.05.10.23289581
Autor:
Daniel Arthur Abrams, Aarthi Padmanabhan, Tianwen Chen, Paola Odriozola, Amanda E Baker, John Kochalka, Jennifer M Phillips, Vinod Menon
Publikováno v:
eLife, Vol 8 (2019)
Engaging with vocal sounds is critical for children’s social-emotional learning, and children with autism spectrum disorder (ASD) often ‘tune out’ voices in their environment. Little is known regarding the neurobiological basis of voice process
Externí odkaz:
https://doaj.org/article/0eb126f986364139a3bf353edf9777ae