Ion torrent high throughput mitochondrial genome sequencing (HTMGS) von Harvey, N R, Albury, C L, Stuart, S, Benton, M C, Eccles, D A, Connell, J R, Sutherland, H G, Allcock, R J N, Lea, R A, Haupt, L M, Griffiths, L R

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possible role for mitochondrial dysfunction in migraine von Stuart, S, Griffiths, L. R

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Pedigree derived mutation rate across the entire mitochondrial genome of the Norfolk Island population von Connell, J. R., Benton, M. C., Lea, R. A., Sutherland, H. G., Chaseling, J., Haupt, L. M., Wright, K. M., Griffiths, L. R.

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Investigation of Mitochondrial Related Variants in a Cerebral Small Vessel Disease Cohort von Dunn, P. J., Harvey, N. R., Maksemous, N., Smith, R. A., Sutherland, H. G., Haupt, L. M., Griffiths, L. R.

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Investigating diagnostic sequencing techniques for CADASIL diagnosis von Dunn, P J, Maksemous, N, Smith, R A, Sutherland, H G, Haupt, L M, Griffiths, L R

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Current perspectives in bladder cancer management von Griffiths, T. R. L.

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Developing Healthcare Team Observations for Patient Safety (HTOPS): senior medical students capture everyday clinical moments von Anderson, E S, Griffiths, T R L, Forey, T, Wobi, F, Norman, R I, Martin, G

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Common polygenic variation contributes to risk of migraine in the Norfolk Island population von Rodriguez-Acevedo, A. J., Ferreira, M. A., Benton, Miles C., Carless, Melanie A., Goring, Harald H., Curran, Joanne E., Blangero, John, Lea, R. A., Griffiths, L. R.

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CALIBER: a phase II randomized feasibility trial of chemoablation with mitomycin‐C vs surgical management in low‐risk non‐muscle‐invasive bladder cancer von Mostafid, A. Hugh, Porta, Nuria, Cresswell, Joanne, Griffiths, Thomas R.L., Kelly, John D., Penegar, Steven R., Davenport, Kim, McGrath, John S., Campain, Nicholas, Cooke, Peter, Masood, Shikohe, Knowles, Margaret A., Feber, Andrew, Knight, Allen, Catto, James W.F., Lewis, Rebecca, Hall, Emma

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Association study of calcitonin gene-related polypeptide-alpha (CALCA) gene polymorphism with migraine von Menon, S, Buteri, J, Roy, B, Murrell, M, Quinlan, S, MacMillan, J.C, Lea, R.A, Haupt, L.M, Griffiths, L.R

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Serum bilirubin concentration is modified by UGT1A1 haplotypes and influences risk of type-2 diabetes in the Norfolk Island genetic isolate von Benton, M C, Lea, R A, Macartney-Coxson, D, Bellis, C, Carless, M A, Curran, J E, Hanna, M, Eccles, D, Chambers, G K, Blangero, J, Griffiths, L R

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A molecular genetic approach for forensic animal species identification von Bellis, C., Ashton, K.J., Freney, L., Blair, B., Griffiths, L.R.

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Association between a 19 bp deletion polymorphism at the dopamine beta-hydroxylase (DBH) locus and migraine with aura von Fernandez, F., Lea, R.A., Colson, N.J., Bellis, C., Quinlan, S., Griffiths, L.R.

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Association between migraine and a functional polymorphism at the dopamine β-hydroxylase locus von Fernandez, F., Colson, N., Quinlan, S., MacMillan, J., Lea, R. A., Griffiths, L. R.

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Polymorphisms of the VDR gene are associated with presence of solar keratoses on the skin von Carless, M.A., Kraska, T., Lintell, N., Neale, R.E., Green, A.C., Griffiths, L.R.

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Distribution of conjunctival ultraviolet autoflourescence in a population-based study: the Norfolk Island Eye Study von Sherwin, J C, Hewitt, A W, Kearns, L S, Coroneo, M T, Griffiths, L R, Mackey, D A

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β-Actin—an unsuitable internal control for RT-PCR von Selvey, S., Thompson, E.W., Matthaei, K., Lea, R.A., Irving, M.G., Griffiths, L.R.

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search for migraine genes: an overview of current knowledge von Colson, N. J, Fernandez, F, Lea, R. A, Griffiths, L. R

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Familial typical migraine : linkage to chromosome 19p13 and evidence for genetic heterogeneity von NYHOLT, D. R, LEA, R. A, GOADSBY, P. J, BRIMAGE, P. J, GRIFFITHS, L. R

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Clinical and genetic spectrum of SCN2A-associated episodic ataxia von Schwarz, N., Bast, T., Gaily, E., Golla, G., Gorman, K.M., Griffiths, L.R., Hahn, A., Hukin, J., King, M., Korff, C., Miranda, M.J., Møller, R.S., Neubauer, B., Smith, R.A., Smol, T., Striano, P., Stroud, B., Vaccarezza, M., Kluger, G., Lerche, H., Fazeli, W.

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