Evidence of a Recessively Inherited CCN3 Mutation as a Rare Cause of Early-Onset Parkinsonism von Bentley, Steven R., Khan, Suliman, Öchsner, Marco, Premarathne, Susitha, Aslam, Zain, Fowdar, Javed Y., Iqbal, Jamila, Naeem, Muhammad, Love, Christopher A., Wood, Stephen A., Mellick, George D., Sykes, Alex M.

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Investigation of Homocysteine-Pathway-Related Variants in Essential Hypertension von Lea, Rodney A., Lason, Marta V., Szvetko, Attila L., Griffiths, Lyn R., Fowdar, Javed Y.

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A genome-wide association study of essential hypertension in an Australian population using a DNA pooling approach von Fowdar, Javed Y., Grealy, Rebecca, Lu, Yi, Griffiths, Lyn R.

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Pipeline to gene discovery - Analysing familial Parkinsonism in the Queensland Parkinson's Project von Bentley, Steven R., Bortnick, Stephanie, Guella, Ilaria, Fowdar, Javed Y., Silburn, Peter A., Wood, Stephen A., Farrer, Matthew J., Mellick, George D.

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Hunting for Familial Parkinson's Disease Mutations in the Post Genome Era von Bentley, Steven R, Guella, Ilaria, Sherman, Holly E, Neuendorf, Hannah M, Sykes, Alex M, Fowdar, Javed Y, Silburn, Peter A, Wood, Stephen A, Farrer, Matthew J, Mellick, George D

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