Halliday GM - Search Results

1

A blood-based marker of mitochondrial DNA damage in Parkinson's disease.

Qi R, Sammler E, Gonzalez-Hunt CP, Barraza I, Pena N, Rouanet JP, Naaldijk Y, Goodson S, Fuzzati M, Blandini F, Erickson KI, Weinstein AM, Lutz MW, Kwok JB, Halliday GM, Dzamko N, Padmanabhan S, Alcalay RN, Waters C, Hogarth P, Simuni T, Smith D, Marras C, Tonelli F, Alessi DR, West AB, Shiva S, Hilfiker S, Sanders LH. Qi R, et al. Among authors: halliday gm. Sci Transl Med. 2023 Aug 30;15(711):eabo1557. doi: 10.1126/scitranslmed.abo1557. Epub 2023 Aug 30. Sci Transl Med. 2023. PMID: 37647388

2

GSK3B polymorphisms alter transcription and splicing in Parkinson's disease.

Kwok JB, Hallupp M, Loy CT, Chan DK, Woo J, Mellick GD, Buchanan DD, Silburn PA, Halliday GM, Schofield PR. Kwok JB, et al. Among authors: halliday gm. Ann Neurol. 2005 Dec;58(6):829-39. doi: 10.1002/ana.20691. Ann Neurol. 2005. PMID: 16315267

3

Prevalence and clinical features of common LRRK2 mutations in Australians with Parkinson's disease.

Huang Y, Halliday GM, Vandebona H, Mellick GD, Mastaglia F, Stevens J, Kwok J, Garlepp M, Silburn PA, Horne MK, Kotschet K, Venn A, Rowe DB, Rubio JP, Sue CM. Huang Y, et al. Among authors: halliday gm. Mov Disord. 2007 May 15;22(7):982-9. doi: 10.1002/mds.21477. Mov Disord. 2007. PMID: 17427941

4

Low serum progranulin predicts the presence of mutations: a prospective study.

Schofield EC, Halliday GM, Kwok J, Loy C, Double KL, Hodges JR. Schofield EC, et al. Among authors: halliday gm. J Alzheimers Dis. 2010;22(3):981-4. doi: 10.3233/JAD-2010-101032. J Alzheimers Dis. 2010. PMID: 20858962

5

Sigma nonopioid intracellular receptor 1 mutations cause frontotemporal lobar degeneration-motor neuron disease.

Luty AA, Kwok JB, Dobson-Stone C, Loy CT, Coupland KG, Karlström H, Sobow T, Tchorzewska J, Maruszak A, Barcikowska M, Panegyres PK, Zekanowski C, Brooks WS, Williams KL, Blair IP, Mather KA, Sachdev PS, Halliday GM, Schofield PR. Luty AA, et al. Among authors: halliday gm. Ann Neurol. 2010 Nov;68(5):639-49. doi: 10.1002/ana.22274. Ann Neurol. 2010. PMID: 21031579

6

Leucine-rich repeat kinase 2 and alternative splicing in Parkinson's disease.

Elliott DA, Kim WS, Gorissen S, Halliday GM, Kwok JB. Elliott DA, et al. Among authors: halliday gm. Mov Disord. 2012 Jul;27(8):1004-11. doi: 10.1002/mds.25005. Epub 2012 Apr 23. Mov Disord. 2012. PMID: 22528366

7

Srp20 regulates TrkB pre-mRNA splicing to generate TrkB-Shc transcripts with implications for Alzheimer's disease.

Wong J, Garner B, Halliday GM, Kwok JB. Wong J, et al. Among authors: halliday gm. J Neurochem. 2012 Oct;123(1):159-71. doi: 10.1111/j.1471-4159.2012.07873.x. Epub 2012 Aug 16. J Neurochem. 2012. PMID: 22788679 Free article.

8

C9ORF72 repeat expansion in clinical and neuropathologic frontotemporal dementia cohorts.

Dobson-Stone C, Hallupp M, Bartley L, Shepherd CE, Halliday GM, Schofield PR, Hodges JR, Kwok JB. Dobson-Stone C, et al. Among authors: halliday gm. Neurology. 2012 Sep 4;79(10):995-1001. doi: 10.1212/WNL.0b013e3182684634. Epub 2012 Aug 8. Neurology. 2012. PMID: 22875086 Free PMC article.

9

An emerging role for LRRK2 in the immune system.

Dzamko N, Halliday GM. Dzamko N, et al. Among authors: halliday gm. Biochem Soc Trans. 2012 Oct;40(5):1134-9. doi: 10.1042/BST20120119. Biochem Soc Trans. 2012. PMID: 22988878 Review.

10

Measurement of LRRK2 and Ser910/935 phosphorylated LRRK2 in peripheral blood mononuclear cells from idiopathic Parkinson's disease patients.

Dzamko N, Chua G, Ranola M, Rowe DB, Halliday GM. Dzamko N, et al. Among authors: halliday gm. J Parkinsons Dis. 2013;3(2):145-52. doi: 10.3233/JPD-130174. J Parkinsons Dis. 2013. PMID: 23938344

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