Hannah Suddull

Emailhannah.suddullmq.eduau, hannah.suddullhdr.mq.eduau

h-index

Research activity per year

If you made any changes in Pure these will be visible here soon.

Fingerprint

Dive into the research topics where Hannah Suddull is active. These topic labels come from the works of this person. Together they form a unique fingerprint.

1 Similar Profiles

3 Finished

Predicting Motor Neuron Disease (MND) Patient Status by Machine Learning
Lee, A., Liu, S. & Suddull, H.
24/01/21 → 31/12/22
Project: Research
Proteomic and molecular investigations into the diagnosis and progression of Motor Neuron Disease by the identification of biomarkers found in plasma
Suddull, H., Chung, R. & Lee, A.
1/07/19 → 30/06/22
Project: Research
Proteomic and Molecular Investigations into the Diagnosis and Progression of Motor Neuron Disease by the Identification of Biomarkers found in Plasma
Suddull, H. & Chung, R.
18/05/19 → 18/05/22
Project: Research

2 Article
1 Editorial

How can proteomics help solve the lack of biomarkers to aid in the early diagnosis of motor neuron disease (MND)?
Suddull, H. J., Rosa-Fernandes, L. & Lee, A., 24 Jul 2023, (E-pub ahead of print) In: Expert Review of Proteomics. 3 p.
Research output: Contribution to journal › Editorial › peer-review
Sodium valproate increases activity of the sirtuin pathway resulting in beneficial effects for spinocerebellar ataxia-3 in vivo
Watchon, M., Luu, L., Robinson, K. J., Yuan, K. C., De Luca, A., Suddull, H. J., Tym, M. C., Guillemin, G. J., Cole, N. J., Nicholson, G. A., Chung, R. S., Lee, A. & Laird, A. S., 20 Aug 2021, In: Molecular Brain. 14, 1, p. 1-16 16 p., 128.
Research output: Contribution to journal › Article › peer-review

Open Access
File
8 Citations (Scopus)

13 Downloads (Pure)
Unbiased label-free quantitative proteomics of cells expressing amyotrophic lateral sclerosis (ALS) mutations in CCNF reveals activation of the apoptosis pathway: a workflow to screen pathogenic gene mutations
Cheng, F., Luca, A. D., Hogan, A. L., Rayner, S. L., Davidson, J. M., Watchon, M., Stevens, C. H., Muñoz, S. S., Ooi, L., Yerbury, J. J., Don, E. K., Fifita, J. A., Villalva, M. D., Suddull, H., Chapman, T. R., Hedl, T. J., Walker, A. K., Yang, S., Morsch, M., Shi, B., & 4 othersBlair, I. P., Laird, A. S., Chung, R. S. & Lee, A., 27 Apr 2021, In: Frontiers in Molecular Neuroscience. 14, p. 1-18 18 p., 627740.
Research output: Contribution to journal › Article › peer-review

Open Access
File
12 Citations (Scopus)

26 Downloads (Pure)

Hannah Suddull

Fingerprint

Collaborations and top research areas from the last five years

Dive into details

Predicting Motor Neuron Disease (MND) Patient Status by Machine Learning

Proteomic and molecular investigations into the diagnosis and progression of Motor Neuron Disease by the identification of biomarkers found in plasma

Proteomic and Molecular Investigations into the Diagnosis and Progression of Motor Neuron Disease by the Identification of Biomarkers found in Plasma

How can proteomics help solve the lack of biomarkers to aid in the early diagnosis of motor neuron disease (MND)?

Sodium valproate increases activity of the sirtuin pathway resulting in beneficial effects for spinocerebellar ataxia-3 in vivo

Unbiased label-free quantitative proteomics of cells expressing amyotrophic lateral sclerosis (ALS) mutations in CCNF reveals activation of the apoptosis pathway: a workflow to screen pathogenic gene mutations

Hannah Suddull

Fingerprint

Collaborations and top research areas from the last five years

Projects

Predicting Motor Neuron Disease (MND) Patient Status by Machine Learning

Proteomic and molecular investigations into the diagnosis and progression of Motor Neuron Disease by the identification of biomarkers found in plasma

Proteomic and Molecular Investigations into the Diagnosis and Progression of Motor Neuron Disease by the Identification of Biomarkers found in Plasma

Research Outputs

How can proteomics help solve the lack of biomarkers to aid in the early diagnosis of motor neuron disease (MND)?

Sodium valproate increases activity of the sirtuin pathway resulting in beneficial effects for spinocerebellar ataxia-3 in vivo

Unbiased label-free quantitative proteomics of cells expressing amyotrophic lateral sclerosis (ALS) mutations in CCNF reveals activation of the apoptosis pathway: a workflow to screen pathogenic gene mutations