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Items: 8

1.

Analysis of DNA methylation associates the cystine-glutamate antiporter SLC7A11 with risk of Parkinson's disease.

Vallerga CL, Zhang F, Fowdar J, McRae AF, Qi T, Nabais MF, Zhang Q, Kassam I, Henders AK, Wallace L, Montgomery G, Chuang YH, Horvath S, Ritz B, Halliday G, Hickie I, Kwok JB, Pearson J, Pitcher T, Kennedy M, Bentley SR, Silburn PA, Yang J, Wray NR, Lewis SJG, Anderson T, Dalrymple-Alford J, Mellick GD, Visscher PM, Gratten J.

Nat Commun. 2020 Mar 6;11(1):1238. doi: 10.1038/s41467-020-15065-7.

2.

Improved precision of epigenetic clock estimates across tissues and its implication for biological ageing.

Zhang Q, Vallerga CL, Walker RM, Lin T, Henders AK, Montgomery GW, He J, Fan D, Fowdar J, Kennedy M, Pitcher T, Pearson J, Halliday G, Kwok JB, Hickie I, Lewis S, Anderson T, Silburn PA, Mellick GD, Harris SE, Redmond P, Murray AD, Porteous DJ, Haley CS, Evans KL, McIntosh AM, Yang J, Gratten J, Marioni RE, Wray NR, Deary IJ, McRae AF, Visscher PM.

Genome Med. 2019 Aug 23;11(1):54. doi: 10.1186/s13073-019-0667-1.

3.

Association of Schizophrenia Risk With Disordered Niacin Metabolism in an Indian Genome-wide Association Study.

Periyasamy S, John S, Padmavati R, Rajendren P, Thirunavukkarasu P, Gratten J, Vinkhuyzen A, McRae A, Holliday EG, Nyholt DR, Nancarrow D, Bakshi A, Hemani G, Nertney D, Smith H, Filippich C, Patel K, Fowdar J, McLean D, Tirupati S, Nagasundaram A, Gundugurti PR, Selvaraj K, Jegadeesan J, Jorde LB, Wray NR, Brown MA, Suetani R, Giacomotto J, Thara R, Mowry BJ.

JAMA Psychiatry. 2019 Jul 3. doi: 10.1001/jamapsychiatry.2019.1335. [Epub ahead of print]

PMID:
31268507
4.

Pipeline to gene discovery - Analysing familial Parkinsonism in the Queensland Parkinson's Project.

Bentley SR, Bortnick S, Guella I, Fowdar JY, Silburn PA, Wood SA, Farrer MJ, Mellick GD.

Parkinsonism Relat Disord. 2018 Apr;49:34-41. doi: 10.1016/j.parkreldis.2017.12.033. Epub 2018 Jan 3.

PMID:
29329938
5.

A genome-wide association study of essential hypertension in an Australian population using a DNA pooling approach.

Fowdar JY, Grealy R, Lu Y, Griffiths LR.

Mol Genet Genomics. 2017 Apr;292(2):307-324. doi: 10.1007/s00438-016-1274-0. Epub 2016 Nov 19.

PMID:
27866268
6.

Investigation of homocysteine-pathway-related variants in essential hypertension.

Fowdar JY, Lason MV, Szvetko AL, Lea RA, Griffiths LR.

Int J Hypertens. 2012;2012:190923. doi: 10.1155/2012/190923. Epub 2012 Oct 23.

7.

Investigation of the role of the GABRG2 gene variant in migraine.

Chen T, Murrell M, Fowdar J, Roy B, Grealy R, Griffiths LR.

J Neurol Sci. 2012 Jul 15;318(1-2):112-4. doi: 10.1016/j.jns.2012.03.014. Epub 2012 May 7.

PMID:
22572707
8.

No association between MTHFR A1298C and MTRR A66G polymorphisms, and MS in an Australian cohort.

Szvetko AL, Fowdar J, Nelson J, Colson N, Tajouri L, Csurhes PA, Pender MP, Griffiths LR.

J Neurol Sci. 2007 Jan 15;252(1):49-52. Epub 2006 Nov 20.

PMID:
17113603

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