Zobrazeno 1 - 10
of 119
pro vyhledávání: '"Ziarih Hawi"'
Publikováno v:
Ibn Al-Haitham Journal for Pure and Applied Sciences, Vol 37, Iss 2 (2024)
Although not uncommon worldwide, consanguinity has been a part of Arab culture and tradition as a means to strengthen tribal blood relations. However, this type of union has been linked to inherited diseases, particularly those of a recessive nature
Externí odkaz:
https://doaj.org/article/daf800b3b35e46e6befcbb14fde8ea7b
Autor:
Kealan Pugsley, Atefeh Namipashaki, Katerina Vlahos, Kirsten Furley, Alison Graham, Beth P Johnson, Kathryn Kallady, Jia Yi Kuah, Vishnu Priya Mohanakumar Sindhu, Annabelle Suter, Ziarih Hawi, Mark A Bellgrove
Publikováno v:
Stem Cell Research, Vol 71, Iss , Pp 103170- (2023)
Uncovering the molecular mechanisms of autism spectrum disorder (autism) necessitates development of relevant experimental models that are capable of recapitulating features of the clinical phenotype. Using non-integrative episomal vectors, periphera
Externí odkaz:
https://doaj.org/article/5fb273b2e3334ac79a48fa92eda49925
Autor:
Rachael Knott, Beth P. Johnson, Jeggan Tiego, Olivia Mellahn, Amy Finlay, Kathryn Kallady, Maria Kouspos, Vishnu Priya Mohanakumar Sindhu, Ziarih Hawi, Aurina Arnatkeviciute, Tracey Chau, Dalia Maron, Emily-Clare Mercieca, Kirsten Furley, Katrina Harris, Katrina Williams, Alexandra Ure, Alex Fornito, Kylie Gray, David Coghill, Ann Nicholson, Dinh Phung, Eva Loth, Luke Mason, Declan Murphy, Jan Buitelaar, Mark A. Bellgrove
Publikováno v:
Molecular Autism, Vol 12, Iss 1, Pp 1-24 (2021)
Abstract Background ASD and ADHD are prevalent neurodevelopmental disorders that frequently co-occur and have strong evidence for a degree of shared genetic aetiology. Behavioural and neurocognitive heterogeneity in ASD and ADHD has hampered attempts
Externí odkaz:
https://doaj.org/article/40602d2099c14f7cbb70a6e3e590465b
Autor:
Aurina Arnatkeviciute, Ben D. Fulcher, Stuart Oldham, Jeggan Tiego, Casey Paquola, Zachary Gerring, Kevin Aquino, Ziarih Hawi, Beth Johnson, Gareth Ball, Marieke Klein, Gustavo Deco, Barbara Franke, Mark A. Bellgrove, Alex Fornito
Publikováno v:
Nature Communications, Vol 12, Iss 1, Pp 1-14 (2021)
How genes sculpt the complex architecture of the human connectome remains unclear. Here, the authors show that genes preferentially influence the strength of connectivity between functionally valuable, metabolically costly connections between brain n
Externí odkaz:
https://doaj.org/article/d2ca80b7dfdb42b8bba8ca8fcfa0dbfb
Autor:
Nathália G. Souza-Silva, Eduardo S. Nicolau, Kate Hoy, Ziarih Hawi, Mark A. Bellgrove, Débora M. Miranda, Marco A. Romano-Silva, Paul B. Fitzgerald
Publikováno v:
Brain Stimulation, Vol 13, Iss 4, Pp 1091-1093 (2020)
Externí odkaz:
https://doaj.org/article/5ca7be63449c4f8ea6ddc0f829f8690a
Autor:
Janette Tong, Kyung Min Lee, Xiaodong Liu, Christian M. Nefzger, Prasidhee Vijayakumar, Ziarih Hawi, Ken C. Pang, Clare L. Parish, Jose M. Polo, Mark A. Bellgrove
Publikováno v:
Stem Cell Research, Vol 34, Iss , Pp - (2019)
Peripheral blood mononuclear cells were donated by a male teenager with clinically diagnosed attention deficit hyperactivity disorder (ADHD) under the Diagnostic and Statistical Manual of Mental Disorders IV criteria and his unaffected male sibling.
Externí odkaz:
https://doaj.org/article/3b99aa8f183c40f99a35f88233584ab9
Autor:
Ziarih Hawi, Natasha Matthews, Joseph Wagner, Robyn H Wallace, Tim J Butler, Alasdair Vance, Lindsey Kent, Michael Gill, Mark A Bellgrove
Publikováno v:
PLoS ONE, Vol 8, Iss 4, p e60274 (2013)
The Coloboma mouse carries a ∼2 cM deletion encompassing the SNAP25 gene and has a hyperactive phenotype similar to that of ADHD. Such mice are 3 fold more active compared to their control littermates. Genetic association studies support a role for
Externí odkaz:
https://doaj.org/article/7ac12c9c90b74b60be6fa60c3863327c
Autor:
Jeggan Tiego, Kate Thompson, Aurina Arnatkeviciute, Ziarih Hawi, Amy Finlay, Kristina Sabaroedin, Beth Johnson, Mark A Bellgrove, Alex Fornito
Publikováno v:
Schizophrenia Bulletin.
Schizotypy is a multidimensional construct that captures a continuum of risk for developing schizophrenia-spectrum psychopathology. Existing 3-factor models of schizotypy, consisting of positive, negative, and disorganized dimensions have yielded mix
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::86df5d3d91356cd73f054fef6b2b6f6d
https://doi.org/10.1093/schbul/sbac016
https://doi.org/10.1093/schbul/sbac016
Autor:
Aurina Arnatkeviciute, Mathieu Lemire, Claire Morrison, Michael Mooney, Peter Ryabinin, Nicole Roslin, Molly Nikolas, James Coxon, Jeggan Tiego, Ziarih Hawi, Alex Fornito, Walter Henrik, Jean-Luc Martinot, Marie-Laure Paillère Martinot, Eric Artiges, Hugh Garavan, Joel Nigg, Naomi Friedman, Christie Burton, Russell Schachar, Jennifer Crosbie, Mark A. Bellgrove
Deficits in effective executive function, including inhibitory control are associated with risk for a number of psychiatric disorders and significantly impact everyday functioning. These complex traits have been proposed to serve as endophenotypes, h
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::27c48578ba131e7e283e6f29a9f7479a
https://doi.org/10.1101/2022.10.13.22281074
https://doi.org/10.1101/2022.10.13.22281074
Publikováno v:
Molecular Psychiatry. 27:710-730
Although the full aetiology of autism spectrum disorder (ASD) is unknown, familial and twin studies demonstrate high heritability of 60–90%, indicating a predominant role of genetics in the development of the disorder. The genetic architecture of A
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::d8dc1a6d7fa9b9e83c7197b88b4fda30
https://doi.org/10.1038/s41380-021-01142-w
https://doi.org/10.1038/s41380-021-01142-w