Zobrazeno 1 - 9
of 9
pro vyhledávání: '"Tanya Vick"'
Autor:
Greta Gillies, Keri Finlay, Hayley S. Mountford, Peter Hickey, Ingrid E. Scheffer, Vesna Lukic, Bradley P. Coe, Kiymet Bozaoglu, Melanie Bahlo, Haloom Rafehi, Audrey Rattray, Paul J. Lockhart, Natasha J Brown, Dana Alhuzaimi, Tanya Vick, Miriam Fanjul-Fernández, Cherie C Green, Sarah J. Wilson, Martin B. Delatycki, Savannah Young, Evan E. Eichler, Peter Diakumis
Publikováno v:
Hum Mutat
Autism spectrum disorders (ASD) are neurodevelopmental disorders with an estimated heritability of >60%. Family-based genetic studies of ASD have generally focused on multiple small kindreds, searching for de novo variants of major effect. We hypothe
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1061e3918e4b875e007635c67e625a48
https://europepmc.org/articles/PMC8720068/
https://europepmc.org/articles/PMC8720068/
Autor:
Paul J. Lockhart, Cherie C Green, Krysta J Trevis, Tarishi Desai, Martin B. Delatycki, Natasha J Brown, Sarah J. Wilson, Emmanuel Peng Kiat Pua, Melanie Bahlo, Ingrid E. Scheffer, Vicki Anderson, Tanya Vick
Publikováno v:
International Journal of Molecular Sciences
Volume 21
Issue 21
International Journal of Molecular Sciences, Vol 21, Iss 7965, p 7965 (2020)
Volume 21
Issue 21
International Journal of Molecular Sciences, Vol 21, Iss 7965, p 7965 (2020)
Families comprising many individuals with Autism Spectrum Disorders (ASD) may carry a dominant predisposing mutation. We implemented rigorous phenotyping of the &ldquo
Broader Autism Phenotype&rdquo
(BAP) in large multiplex ASD families usi
Broader Autism Phenotype&rdquo
(BAP) in large multiplex ASD families usi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::762a08553bb7f0cfd803a010ec4ce911
Autor:
Paul J. Lockhart, Greta Gillies, Martin B. Delatycki, Peter Hickey, Cherie C Green, Tarishi Desai, P Hewson, Sarah J. Wilson, Catherine J. Bromhead, Natasha J Brown, Tanya Vick, Vicki Anderson, Krysta J Trevis, Elizabeth A. Fitzpatrick, Hayley S. Mountford, Miriam Fanjul-Fernández, Lavinia Gordon, Ingrid E. Scheffer
Families comprising many individuals with Autism Spectrum Disorder (ASD) may carry a dominant predisposing mutation. Our aim was to use rigorous phenotyping of the ‘Broader Autism Phenotype’ (BAP) in large multiplex ASD families to identify endop
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c89b9f9100c3c994f40f8547fbcf9c17
Autor:
Olivia M Dean, Kylie Megan Gray, Bruce J. Tonge, Michael Berk, Seetal Dodd, Mohammadreza Mohebbi, Kristi-Ann Villagonzalo, Tanya Vick
Publikováno v:
Australian & New Zealand Journal of Psychiatry. 51:241-249
Objective: Oxidative stress, inflammation and heavy metals have been implicated in the aetiology of autistic disorder. N-acetyl cysteine has been shown to modulate these pathways, providing a rationale to trial N-acetyl cysteine for autistic disorder
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::fadf4a7313341868043bc6788f274eb0
https://doi.org/10.1177/0004867416652735
https://doi.org/10.1177/0004867416652735
Autor:
Kylie Megan Gray, Bruce J. Tonge, Michael Berk, Mohammadreza Mohebbi, Olivia M Dean, Kristi-Ann Villagonzalo, Seetal Dodd, Tanya Vick
Publikováno v:
Journal of Intellectual Disability Research. 59:787-799
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::77c94679bf5f5fdc7dc62a292b7ab318
https://doi.org/10.1111/jir.12212
https://doi.org/10.1111/jir.12212
Autor:
Horberg, Michael S, Eberhart, Lindsay MHS, Bhatia, Mamta MS, Jonas, Cabell, Cherico-Hsii, Sara, Tamrat, Yonas, Bhandari, Binamrata, Kadlecik, Peter, Gahunia, Mona K. DO, Horberg, Michael, Eberhart, Lindsay, Bhatia, Mamta, Gahunia, Mona K
Publikováno v:
Sexually Transmitted Diseases; Apr2022, Vol. 49 Issue 4, p268-273, 6p
Autor:
Green, Cherie C., Brown, Natasha J., Yap, Valerie M.Z., Scheffer, Ingrid E., Wilson, Sarah J.
Publikováno v:
Autism Research: Official Journal of the International Society for Autism Research; Jun2020, Vol. 13 Issue 6, p921-934, 14p
Autor:
Trevis, Krysta J.1,2 (AUTHOR) kjtrevis@gmail.com, Brown, Natasha J.3,4 (AUTHOR) cats-info@unimelb.edu.au, Green, Cherie C.1,2,5 (AUTHOR) c.green@latrobe.edu.au, Lockhart, Paul J.6,7 (AUTHOR) paul.lockhart@mcri.edu.au, Desai, Tarishi1,2 (AUTHOR) tdesai@unimelb.edu.au, Vick, Tanya4 (AUTHOR), Anderson, Vicki2,8,9 (AUTHOR), Pua, Emmanuel P. K.1 (AUTHOR) pk.pua@unimelb.edu.au, Bahlo, Melanie10,11 (AUTHOR) bahlo@wehi.edu.au, Delatycki, Martin B.3,6,7 (AUTHOR) martin.delatycki@vcgs.org.au, Scheffer, Ingrid E.1,3,9,12 (AUTHOR) i.scheffer@unimelb.edu.au, Wilson, Sarah J.1,2,12 (AUTHOR) sarahw@unimelb.edu.au
Publikováno v:
International Journal of Molecular Sciences. Nov2020, Vol. 21 Issue 21, p7965. 1p.
Publikováno v:
Human Mutation; Jan2022, Vol. 43 Issue 1, p1-2, 2p