Zobrazeno 1 - 10
of 827
pro vyhledávání: '"Raphael Bernier"'
Autor:
Alexander J. M. Dingemans, Kim M. G. Truijen, Sam van de Ven, Raphael Bernier, Ernie M. H. F. Bongers, Arjan Bouman, Laura de Graaff – Herder, Evan E. Eichler, Erica H. Gerkes, Christa M. De Geus, Johanna M. van Hagen, Philip R. Jansen, Jennifer Kerkhof, Anneke J. A. Kievit, Tjitske Kleefstra, Saskia M. Maas, Stella A. de Man, Haley McConkey, Wesley G. Patterson, Amy T. Dobson, Eloise J. Prijoles, Bekim Sadikovic, Raissa Relator, Roger E. Stevenson, Connie T. R. M. Stumpel, Malou Heijligers, Kyra E. Stuurman, Katharina Löhner, Shimriet Zeidler, Jennifer A. Lee, Amanda Lindy, Fanggeng Zou, Matthew L. Tedder, Lisenka E. L. M. Vissers, Bert B. A. de Vries
Publikováno v:
Translational Psychiatry, Vol 12, Iss 1, Pp 1-11 (2022)
Abstract CHD8, a major autism gene, functions in chromatin remodelling and has various roles involving several biological pathways. Therefore, unsurprisingly, previous studies have shown that intellectual developmental disorder with autism and macroc
Externí odkaz:
https://doaj.org/article/7ea31eb997db422aa3beb7b35aae7a11
Autor:
Frederick Shic, Adam J. Naples, Erin C. Barney, Shou An Chang, Beibin Li, Takumi McAllister, Minah Kim, Kelsey J. Dommer, Simone Hasselmo, Adham Atyabi, Quan Wang, Gerhard Helleman, April R. Levin, Helen Seow, Raphael Bernier, Katarzyna Charwaska, Geraldine Dawson, James Dziura, Susan Faja, Shafali Spurling Jeste, Scott P. Johnson, Michael Murias, Charles A. Nelson, Maura Sabatos-DeVito, Damla Senturk, Catherine A. Sugar, Sara J. Webb, James C. McPartland
Publikováno v:
Molecular Autism, Vol 13, Iss 1, Pp 1-17 (2022)
Abstract Background Eye tracking (ET) is a powerful methodology for studying attentional processes through quantification of eye movements. The precision, usability, and cost-effectiveness of ET render it a promising platform for developing biomarker
Externí odkaz:
https://doaj.org/article/88ee9597126347c68f7211e9f79fbd76
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:
Santhosh Girirajan, Zoran Brkanac, Bradley P Coe, Carl Baker, Laura Vives, Tiffany H Vu, Neil Shafer, Raphael Bernier, Giovanni B Ferrero, Margherita Silengo, Stephen T Warren, Carlos S Moreno, Marco Fichera, Corrado Romano, Wendy H Raskind, Evan E Eichler
Publikováno v:
PLoS Genetics, Vol 7, Iss 11, p e1002334 (2011)
While numerous studies have implicated copy number variants (CNVs) in a range of neurological phenotypes, the impact relative to disease severity has been difficult to ascertain due to small sample sizes, lack of phenotypic details, and heterogeneity
Externí odkaz:
https://doaj.org/article/4f4f7583269c46e28b71e81346b44b8d
Autor:
Jennifer Gerdts, Raphael Bernier
Publikováno v:
Autism Research and Treatment, Vol 2011 (2011)
The presence of autism-related traits has been well documented in undiagnosed family members of individuals with autism spectrum disorder (ASD). The most common finding is mild impairments in social and communication skills that are similar to those
Externí odkaz:
https://doaj.org/article/a69ac597bcda474b8c60f2b9cb4eea29
Akademický článek
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Autor:
Sara Jane Webb, Adam J. Naples, April R. Levin, Gerhard Hellemann, Heather Borland, Jessica Benton, Carter Carlos, Takumi McAllister, Megha Santhosh, Helen Seow, Adham Atyabi, Raphael Bernier, Katarzyna Chawarska, Geraldine Dawson, James Dziura, Susan Faja, Shafali Jeste, Michael Murias, Charles A. Nelson, Maura Sabatos-DeVito, Damla Senturk, Frederick Shic, Catherine A. Sugar, James C. McPartland
Publikováno v:
American Journal of Psychiatry. 180:41-49
Numerous candidate EEG biomarkers have been put forward for use in clinical research on autism spectrum disorder (ASD), but biomarker development has been hindered by limited attention to the psychometric properties of derived variables, inconsistent
Autor:
Aksheya Sridhar, Jocelyn Kuhn, Susan Faja, Maura Sabatos-DeVito, Julia I. Nikolaeva, Geraldine Dawson, Charles A. Nelson, Sara J. Webb, Raphael Bernier, Shafali Jeste, Katarzyna Chawarska, Catherine A. Sugar, Frederick Shic, Adam Naples, James Dziura, James C. McPartland, null the ABC-CT Consortium
Publikováno v:
Res Autism Spectr Disord
When designing and interpreting results from clinical trials evaluating treatments for children on the autism spectrum, a complicating factor is that most children receive a range of concurrent treatments. Thus, it is important to better understand t
Autor:
Emily F, Dillon, Stephen, Kanne, Rebecca J, Landa, Robert, Annett, Raphael, Bernier, Catherine, Bradley, Laura, Carpenter, So Hyun, Kim, Julia, Parish-Morris, Robert, Schultz, Ericka L, Wodka
Publikováno v:
Journal of Autism and Developmental Disorders. 53:1305-1318
Discernment of possible sex-based variations in presentations of autism spectrum disorder (ASD) symptoms is limited by smaller female samples with ASD and confounds with ASD ascertainment. A large national cohort of individuals with autism, SPARK, al
Autor:
Cheryl Klaiman, Stormi White, Shana Richardson, Emma McQueen, Hasse Walum, Christa Aoki, Christopher Smith, Mendy Minjarez, Raphael Bernier, Ernest Pedapati, Somer Bishop, Whitney Ence, Allison Wainer, Jennifer Moriuchi, Sew-Wah Tay, Yiming Deng, Warren Jones, Scott Gillespie, Ami Klin
Publikováno v:
Journal of autism and developmental disorders.
Differential diagnosis of young children with suspected autism spectrum disorder (ASD) is challenging, and clinician uncertainty about a child's diagnosis may contribute to misdiagnosis and subsequent delays in access to early treatment. The current