Zobrazeno 1 - 10
of 14
pro vyhledávání: '"Zoë Hawks"'
Autor:
Adam T. Eggebrecht, Ally Dworetsky, Zoë Hawks, Rebecca Coalson, Babatunde Adeyemo, Savannah Davis, Daniel Gray, Alana McMichael, Steven E. Petersen, John N. Constantino, John R. Pruett
Publikováno v:
Molecular Autism, Vol 11, Iss 1, Pp 1-13 (2020)
Abstract Background Autism spectrum disorder (ASD) is characterized by high population-level heritability and a three-to-one male-to-female ratio that occurs independent of sex linkage. Prior research in a mixed-sex pediatric sample identified neural
Externí odkaz:
https://doaj.org/article/ab226822651e42168636ef07dd0de54b
Autor:
Zoë Hawks, Joshua Shimony, Jerrel Rutlin, Dorothy K. Grange, Shawn E. Christ, Desirée A. White
Publikováno v:
Molecular Genetics and Metabolism Reports, Vol 12, Iss C, Pp 8-13 (2017)
Sapropterin dihydrochloride (BH4) reduces phenylalanine (Phe) levels and improves white matter integrity in a subset of individuals with phenylketonuria (PKU) known as “responders.” Although prior research has identified biochemical and genotypic
Externí odkaz:
https://doaj.org/article/ab8317c1c00a4f3c88ab34c6b0b96482
Autor:
Zoë Hawks, Anna M. Hood, Dov B. Lerman-Sinkoff, Joshua S. Shimony, Jerrel Rutlin, Daniel Lagoni, Dorothy K. Grange, Desirée A. White
Publikováno v:
NeuroImage: Clinical, Vol 23, Iss , Pp - (2019)
Phenylketonuria (PKU) is a recessive disorder characterized by disruption in the metabolism of the amino acid phenylalanine (Phe). Prior research indicates that individuals with PKU have substantial white matter (WM) compromise. Much less is known ab
Externí odkaz:
https://doaj.org/article/4a0004033ef044bc95ce911cd45509c2
Autor:
Jessica B, Girault, Kevin, Donovan, Zoë, Hawks, Muhamed, Talovic, Elizabeth, Forsen, Jed T, Elison, Mark D, Shen, Meghan R, Swanson, Jason J, Wolff, Sun Hyung, Kim, Tomoyuki, Nishino, Savannah, Davis, Abraham Z, Snyder, Kelly N, Botteron, Annette M, Estes, Stephen R, Dager, Heather C, Hazlett, Guido, Gerig, Robert, McKinstry, Juhi, Pandey, Robert T, Schultz, Tanya, St John, Lonnie, Zwaigenbaum, Alexandre, Todorov, Young, Truong, Martin, Styner, John R, Pruett, John N, Constantino, Joseph, Piven
Publikováno v:
The American journal of psychiatry. 179(8)
Autism spectrum disorder (ASD) is heritable, and younger siblings of ASD probands are at higher likelihood of developing ASD themselves. Prospective MRI studies of siblings report that atypical brain development precedes ASD diagnosis, although the l
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3eddbdf5517e8f44d34eb0c442d8a025
https://pubmed.ncbi.nlm.nih.gov/35921396
https://pubmed.ncbi.nlm.nih.gov/35921396
Autor:
Natasha Marrus, Kelly N. Botteron, Zoë Hawks, John R. Pruett, Jed T. Elison, Joshua J. Jackson, Lori Markson, Adam T. Eggebrecht, Catherine A. Burrows, Lonnie Zwaigenbaum, Stephen R. Dager, Annette M. Estes, Heather Cody Hazlett, Robert T. Schultz, Joseph Piven, John N. Constantino
Publikováno v:
Development and psychopathology.
Pre-diagnostic deficits in social motivation are hypothesized to contribute to autism spectrum disorder (ASD), a heritable neurodevelopmental condition. We evaluated psychometric properties of a social motivation index (SMI) using parent-report item-
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::cde9961ad0f8823f5a4a5f6b2cf770ce
https://pubmed.ncbi.nlm.nih.gov/36189644
https://pubmed.ncbi.nlm.nih.gov/36189644
Autor:
John N. Constantino, Savannah Davis, Zoë Hawks, Rebecca S. Coalson, John R. Pruett, Daniel Gray, Alana McMichael, Ally Dworetsky, Steven E. Petersen, Adam T. Eggebrecht, Babatunde Adeyemo
Publikováno v:
Molecular Autism, Vol 11, Iss 1, Pp 1-13 (2020)
Molecular Autism
Molecular Autism
Background Autism spectrum disorder (ASD) is characterized by high population-level heritability and a three-to-one male-to-female ratio that occurs independent of sex linkage. Prior research in a mixed-sex pediatric sample identified neural signatur
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6c9d1e21752f8e203330e933528a16ba
http://link.springer.com/article/10.1186/s13229-020-00381-y
http://link.springer.com/article/10.1186/s13229-020-00381-y
Autor:
John N. Constantino, Zoë Hawks
Publikováno v:
J Am Acad Child Adolesc Psychiatry
Behavioral comorbidity is the rule rather than the exception in autism spectrum disorder (ASD), and the co-occurrence of autistic traits with subclinical manifestations of other psychiatric syndromes (e.g. anxiety, developmental coordination disorder
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2e23e8d32a81dfb1aa237a7c5386fcbd
https://doi.org/10.1016/j.jaac.2019.07.008
https://doi.org/10.1016/j.jaac.2019.07.008
Publikováno v:
Molecular genetics and metabolism. 132(1)
Even with early and continuous treatment, individuals with phenylketonuria (PKU) may exhibit abnormalities of cortical white matter (WM). The present study utilizes a new analysis approach called Automated Fiber-Tract Quantification (AFQ) to advance
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::776fd6882a02e90188ba0285e0bd8bfe
https://pubmed.ncbi.nlm.nih.gov/33334682
https://pubmed.ncbi.nlm.nih.gov/33334682
Publikováno v:
Journal of Abnormal Child Psychology
Previous research has suggested that behavioral comorbidity is the rule rather than the exception in autism. The present study aimed to trace the respective origins of autistic and general psychopathologic traits—and their association—to infancy.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::841cb7f26a2f2a56d2f9014ec945e00a
http://europepmc.org/articles/PMC6139282
http://europepmc.org/articles/PMC6139282
Publikováno v:
Developmental Neuropsychology. 43:207-218
Phenylketonuria (PKU) is a hereditary disorder characterized by disrupted phenylalanine metabolism and cognitive impairment. However, the precise nature and developmental trajectory of this cognitive impairment remains unclear. The present study used
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a446695381ee7e7380715c45ee326d6f
https://doi.org/10.1080/87565641.2018.1438439
https://doi.org/10.1080/87565641.2018.1438439