2016

, , , , Oliver, Christopher, , Smith, Maree, & (2016) The effect of 1 mg folic acid supplementation on clinical outcomes in female migraine with aura patients. The Journal of Headache and Pain, 17, Article number-60. (https://eprints.qut.edu.au/97578/)

, , Au, Anthony, , , Gan, Siew Hua, & (2016) Methylenetetrahydrofolate reductase CpG islands: Epigenotyping. Journal of Clinical Laboratory Analysis, 30(4), pp. 335-344. (https://eprints.qut.edu.au/94409/)

, , , & (2016) Next generation sequencing identifies novel CACNA1A gene mutations in Episodic Ataxia type 2. Molecular Genetics and Genomic Medicine, 4(2), pp. 211-222. (https://eprints.qut.edu.au/94391/)

, , , , Bellis, Claire, , , Chambers, Suzanne K., Youl, Philippa H., & (2016) Association of the microRNA-Single Nucleotide Polymorphism rs2910164 in miR146a with sporadic breast cancer susceptibility: A case control study. Gene, 576(1, Part 2), pp. 256-260. (https://eprints.qut.edu.au/94369/)

, , , , , & (2016) Cell surface heparan sulfate proteoglycans as novel markers of human neural stem cell fate determination. Stem Cell Research, 16(1), pp. 92-104. (https://eprints.qut.edu.au/94382/)

Gerring, Zachary, Rodriguez-Acevedo, Astrid J., Powell, Joseph E., Griffiths, Lyn R., Montgomery, Grant W., & (2016) Blood gene expression studies in migraine: Potential and caveats. Cephalalgia, 36(7), pp. 669-678. (https://eprints.qut.edu.au/91800/)

, , , & (2016) Data defining markers of human neural stem cell lineage potential. Data in Brief, 7, pp. 206-215. (https://eprints.qut.edu.au/103915/)

, , , & (2016) Dysregulated microRNA expression profiles and potential cellular, circulating and polymorphic biomarkers in Non-Hodgkin Lymphoma. Genes, 7(12), Article number-130. (https://eprints.qut.edu.au/105619/)

Gasparini, Claudia F., , & (2016) Genetic insights into migraine and glutamate: A protagonist driving the headache. Journal of the Neurological Sciences, 367, pp. 258-268. (https://eprints.qut.edu.au/105622/)

, , , & (2016) Targeted next generation sequencing identifies novel NOTCH3 gene mutations in CADASIL diagnostics patients. Human Genomics, 10, Article number-38. (https://eprints.qut.edu.au/105626/)