Wendy Anne Gold (Wendy A Gold, Wendy Gold)

Scopus Author ID ORCID

Publication Activity (10 Years)

Years Active: 2017-2023
Publications (10 Years): 9

Top Venues

International journal of molecular sciences

Human mutation

American journal of medical genetics. Part A

Clinical case reports

The University of Sydney

This page only lists publications with an associated author ORCID identifier.

Affiliation History

The University of Sydney

Australia

Coordinator AMED3888 & Dalyell Scholars Program :: Applied Medical Science, School of Medical Sciences

Publications

Artur Shvetcov, Shannon Thomson, Jessica Spathos, Ann-Na Cho, Heather M Wilkins, Shea J Andrews, Fabien Delerue, Timothy A Couttas, Jasmeen Kaur Issar, Finula Isik, Simranpreet Kaur, Eleanor Drummond, Carol Dobson-Stone, Shantel L Duffy, Natasha M Rogers, Daniel R Catchpoole, Wendy Anne Gold, Russell H Swerdlow, David A Brown, Caitlin A Finney
Blood-Based Transcriptomic Biomarkers Are Predictive of Neurodegeneration Rather Than Alzheimer's Disease. International journal of molecular sciences 24 (19) (2023)
Florencia Haase, Rachna Singh, Brian Gloss, Patrick P L Tam, Wendy Anne Gold
Meta-Analysis Identifies BDNF and Novel Common Genes Differently Altered in Cross-Species Models of Rett Syndrome. International journal of molecular sciences 23 (19) (2022)
Yilin Mao, Elizabeth E Evans, Vikas Mishra, Leslie Balch, Allison Eberhardt, Maurice Zauderer, Wendy Anne Gold
Anti-Semaphorin 4D Rescues Motor, Cognitive, and Respiratory Phenotypes in a Rett Syndrome Mouse Model. International journal of molecular sciences 22 (17) (2021)
Florencia Haase, Brian S Gloss, Patrick P L Tam, Wendy Anne Gold
WGCNA Identifies Translational and Proteasome-Ubiquitin Dysfunction in Rett Syndrome. International journal of molecular sciences 22 (18) (2021)
Simranpreet Kaur, Nicole J Van Bergen, Kristen J Verhey, Cameron J Nowell, Breane Budaitis, Yang Yue, Carolyn Jane Ellaway, Nicola Brunetti-Pierri, Gerarda Cappuccio, Irene Bruno, Lia Boyle, Vincenzo Nigro, Anna Laura Torella, Tony Roscioli, Mark J Cowley, Sean Massey, Rhea Sonawane, Matthew D Burton, Bitten Schönewolf-Greulich, Zeynep Tümer, Wendy K Chung, Wendy Anne Gold, John Chrisodoulou
Expansion of the phenotypic spectrum of de novo missense variants in kinesin family member 1A (KIF1A). Human mutation 41 (10) (2020)
Simranpreet Kaur, Nicole J Van Bergen, Wendy Anne Gold, Stefanie Eggers, Sebastian Lunke, Susan M White, Carolyn Ellaway, John Chrisodoulou
Whole exome sequencing reveals a de novo missense variant in EEF1A2 in a Rett syndrome-like patient. Clinical case reports 7 (12) (2019)
Rahul Krishnaraj, Florencia Haase, Bronte Coorey, Edward J Luca, Ingar Wong, Alexandra Boyling, Carolyn Ellaway, John Chrisodoulou, Wendy Anne Gold
Genome-wide transcriptomic and proteomic studies of Rett syndrome mouse models identify common signaling pathways and cellular functions as potential therapeutic targets. Human mutation 40 (12) (2019)
Wendy Anne Gold, Rahul Krishnarajy, Carolyn Ellaway, John Christodoulou
Rett Syndrome: A Genetic Update and Clinical Review Focusing on Comorbidities. ACS chemical neuroscience 9 (2) (2017)
Wendy Anne Gold, Nara Sobreira, Elsa Wiame, Alexandre Marbaix, Emile Van Schaftingen, Patricia Franzka, Lisa G Riley, Lisa Worgan, Christian A Hübner, John Christodoulou, Lesley C Adès
A novel mutation in GMPPA in siblings with apparent intellectual disability, epilepsy, dysmorphism, and autonomic dysfunction. American journal of medical genetics. Part A 173 (8) (2017)

Wendy Anne Gold.css-eqlu8i{font-size:small;padding-left:4px;} (Wendy A Gold, Wendy Gold)

Publication Activity (10 Years)

Top Topics

Top Venues

Wendy Anne Gold (Wendy A Gold, Wendy Gold)