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Hayley Cullen

Ms

  • The University of Western Australia (M519), 35 Stirling Highway,

    6009 Perth

    Australia

  • 39 Citations
  • 4 h-Index
20162019
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Fingerprint Dive into the research topics where Hayley Cullen is active. These topic labels come from the works of this person. Together they form a unique fingerprint.

  • 3 Similar Profiles
Cerebral Cortex Medicine & Life Sciences
Neurons Medicine & Life Sciences
Neurogenesis Medicine & Life Sciences
Congenital, Hereditary, and Neonatal Diseases and Abnormalities Medicine & Life Sciences
Dendritic Spines Medicine & Life Sciences
Brain Diseases Medicine & Life Sciences
Protein Biosynthesis Medicine & Life Sciences
Down Syndrome Medicine & Life Sciences

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Research Output 2016 2019

  • 39 Citations
  • 4 h-Index
  • 5 Article

Disease-associated missense variants in ZBTB18 disrupt DNA binding and impair the development of neurons within the embryonic cerebral cortex

Hemming, I. A., Clément, O., Gladwyn-Ng, I. E., Cullen, H. D., Ng, H. L., See, H. B., Ngo, L., Ulgiati, D., Pfleger, K. D. G., Agostino, M. & Heng, J. I. T., 21 May 2019, In : Human Mutation. 15 p.

Research output: Contribution to journalArticle

Cerebral Cortex
Neurons
DNA
Zinc Fingers
Brain Diseases
10 Citations (Scopus)
255 Downloads (Pure)

Bacurd1/Kctd13 and Bacurd2/Tnfaip1 are interacting partners to Rnd proteins which influence the long-term positioning and dendritic maturation of cerebral cortical neurons

Gladwyn-Ng, I., Huang, L., Ngo, L., Li, S. S., Qu, Z., Vanyai, H., Cullen, H., Davis, J. M. & Heng, J., 11 Mar 2016, In : Neural Development. 11, p. 1-8 7.

Research output: Contribution to journalArticle

Open Access
File
Neurons
Cerebral Cortex
Dendritic Spines
Proteins
Electroporation
13 Citations (Scopus)

De Novo Mutations in DENR Disrupt Neuronal Development and Link Congenital Neurological Disorders to Faulty mRNA Translation Re-initiation

Haas, M. A., Ngo, L., Li, S. S., Schleich, S., Qu, Z., Vanyai, H. K., Cullen, H. D., Cardona-Alberich, A., Gladwyn-Ng, I. E., Pagnamenta, A. T., Taylor, J. C., Stewart, H., Kini, U., Duncan, K. E., Teleman, A. A., Keays, D. A. & Heng, J. I. T., 2016, In : Cell Reports. 15, 10, p. 2251-2265 15 p.

Research output: Contribution to journalArticle

Open Access
Congenital, Hereditary, and Neonatal Diseases and Abnormalities
Protein Biosynthesis
Nervous System Diseases
Neurons
Messenger RNA
11 Citations (Scopus)

Infantile neurodegenerative disorder associated with mutations in TBCD, an essential gene in the tubulin heterodimer assembly pathway

Edvardson, S., Tian, G., Cullen, H., Vanyai, H., Ngo, L., Bhat, S., Aran, A., Daana, M., Da'amseh, N., Abu-Libdeh, B., Cowan, N. J. J., Heng, J. I. T. & Elpeleg, O., 2016, In : Human Molecular Genetics. 25, 21, p. 4635-4648 14 p.

Research output: Contribution to journalArticle

5 Citations (Scopus)

The HSA21 gene EURL/C21ORF91 controls neurogenesis within the cerebral cortex and is implicated in the pathogenesis of Down Syndrome

Li, S. S., Qu, Z., Haas, M., Ngo, L., Heo, Y. J., Kang, H. J., Britto, J. M., Cullen, H., Vanyai, H., Tan, S. S., Chan-Ling, T., Gunnersen, J. M. & Heng, J., 11 Jul 2016, In : Scientific Reports. 6, p. 1-14 14 p., 29514.

Research output: Contribution to journalArticle

Open Access
Neurogenesis
Down Syndrome
Cerebral Cortex
Catenins
Genes