Mellick GD - Search Results

1

Heterozygous PINK1 p.G411S increases risk of Parkinson's disease via a dominant-negative mechanism.

Puschmann A, Fiesel FC, Caulfield TR, Hudec R, Ando M, Truban D, Hou X, Ogaki K, Heckman MG, James ED, Swanberg M, Jimenez-Ferrer I, Hansson O, Opala G, Siuda J, Boczarska-Jedynak M, Friedman A, Koziorowski D, Rudzińska-Bar M, Aasly JO, Lynch T, Mellick GD, Mohan M, Silburn PA, Sanotsky Y, Vilariño-Güell C, Farrer MJ, Chen L, Dawson VL, Dawson TM, Wszolek ZK, Ross OA, Springer W. Puschmann A, et al. Among authors: mellick gd. Brain. 2017 Jan;140(1):98-117. doi: 10.1093/brain/aww261. Epub 2016 Nov 2. Brain. 2017. PMID: 27807026 Free PMC article.

2

The monoamine oxidase B gene GT repeat polymorphism and Parkinson's disease in a Chinese population.

Mellick GD, Buchanan DD, Silburn PA, Chan DK, Le Couteur DG, Law LK, Woo J, Pang CP. Mellick GD, et al. J Neurol. 2000 Jan;247(1):52-5. doi: 10.1007/s004150050010. J Neurol. 2000. PMID: 10701898

3

The serotonin transporter gene and Parkinson's disease.

McCann SJ, McManus ME, Johnson AG, Mellick GD, Le Couteur DG, Pond SM. McCann SJ, et al. Among authors: mellick gd. Eur Neurol. 2000;44(2):108-11. doi: 10.1159/000008206. Eur Neurol. 2000. PMID: 10965163

4

The ubiquitin carboxy-terminal hydrolase-L1 gene S18Y polymorphism does not confer protection against idiopathic Parkinson's disease.

Mellick GD, Silburn PA. Mellick GD, et al. Neurosci Lett. 2000 Oct 27;293(2):127-30. doi: 10.1016/s0304-3940(00)01510-x. Neurosci Lett. 2000. PMID: 11027850

5

The parkin gene S/N167 polymorphism in Australian Parkinson's disease patients and controls.

Mellick GD, Buchanan DD, Hattori N, Brookes AJ, Mizuno Y, Le Couteur DG, Silburn PA. Mellick GD, et al. Parkinsonism Relat Disord. 2001 Apr;7(2):89-91. doi: 10.1016/s1353-8020(00)00018-3. Parkinsonism Relat Disord. 2001. PMID: 11248588

6

The Cys282Tyr polymorphism in the HFE gene in Australian Parkinson's disease patients.

Buchanan DD, Silburn PA, Chalk JB, Le Couteur DG, Mellick GD. Buchanan DD, et al. Among authors: mellick gd. Neurosci Lett. 2002 Jul 19;327(2):91-4. doi: 10.1016/s0304-3940(02)00398-1. Neurosci Lett. 2002. PMID: 12098643

7

A novel screen for nuclear mitochondrial gene associations with Parkinson's disease.

Mellick GD, Silburn PA, Prince JA, Brookes AJ. Mellick GD, et al. J Neural Transm (Vienna). 2004 Feb;111(2):191-9. doi: 10.1007/s00702-003-0085-8. Epub 2003 Dec 12. J Neural Transm (Vienna). 2004. PMID: 14767722

8

Tau haplotypes regulate transcription and are associated with Parkinson's disease.

Kwok JB, Teber ET, Loy C, Hallupp M, Nicholson G, Mellick GD, Buchanan DD, Silburn PA, Schofield PR. Kwok JB, et al. Among authors: mellick gd. Ann Neurol. 2004 Mar;55(3):329-34. doi: 10.1002/ana.10826. Ann Neurol. 2004. PMID: 14991810

9

UCHL1 is a Parkinson's disease susceptibility gene.

Maraganore DM, Lesnick TG, Elbaz A, Chartier-Harlin MC, Gasser T, Krüger R, Hattori N, Mellick GD, Quattrone A, Satoh J, Toda T, Wang J, Ioannidis JP, de Andrade M, Rocca WA; UCHL1 Global Genetics Consortium. Maraganore DM, et al. Among authors: mellick gd. Ann Neurol. 2004 Apr;55(4):512-21. doi: 10.1002/ana.20017. Ann Neurol. 2004. PMID: 15048890

10

Sequence variation in the proximity of IDE may impact age at onset of both Parkinson disease and Alzheimer disease.

Blomqvist ME, Silburn PA, Buchanan DD, Andreasen N, Blennow K, Pedersen NL, Brookes AJ, Mellick GD, Prince JA. Blomqvist ME, et al. Among authors: mellick gd. Neurogenetics. 2004 Jun;5(2):115-9. doi: 10.1007/s10048-004-0173-4. Epub 2004 Apr 16. Neurogenetics. 2004. PMID: 15088150

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