Ethnicity can predict GLRA1 genotypes in hyperekplexia von Thomas, R H, Drew, C J G, Wood, S E, Hammond, C L, Chung, S K, Rees, M I

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Functional variants of antioxidant genes in smokers with COPD and in those with normal lung function von Young, R P, Hopkins, R, Black, P N, Eddy, C, Wu, L, Gamble, G D, Mills, G D, Garrett, J E, Eaton, T E, Rees, M I

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Flow-induced ATP release in patient-specific arterial geometries - a comparative study of computational models von Boileau, E., Bevan, R. L. T., Sazonov, I., Rees, M. I., Nithiarasu, P.

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Identifying and prioritising epilepsy treatment uncertainties von Thomas, R H, Hammond, C L, Bodger, O G, Rees, M I, Smith, P E M

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Near-miss SIDS due to Brugada syndrome von Skinner, J R, Chung, S-K, Montgomery, D, McCulley, C H, Crawford, J, French, J, Rees, M I

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Differential localization of γ-aminobutyric acid type a and glycine receptor subunits and gephyrin in the human pons, medulla oblongata and uppermost cervical segment of the spinal... von Waldvogel, H.J., Baer, K., Eady, E., Allen, K.L., Gilbert, R.T., Mohler, H., Rees, M.I., Nicholson, L.F.B., Faull, R.L.M.

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A Two-Stage Genome Scan for Schizophrenia Susceptibility Genes in 196 Affected Sibling Pairs von Williams, N. M., Rees, M. I., Holmans, P., Norton, N., Cardno, A. G., Jones, L. A., Murphy, K. C., Sanders, R. D., McCarthy, G., Gray, M. Y., Fenton, I., McGuffin, P., Owen, M. J.

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Genetic epilepsy with febrile seizures plus: definite and borderline phenotypes von Thomas, R H, Johnston, J A, Hammond, C L, Bagguley, S, White, C, Smith, P E, Rees, M I

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Pathophysiological mechanisms of dominant and recessive GLRA1 mutations in hyperekplexia von Chung, Seo-Kyung, Vanbellinghen, Jean-François, Mullins, Jonathan G L, Robinson, Angela, Hantke, Janina, Hammond, Carrie L, Gilbert, Daniel F, Freilinger, Michael, Ryan, Monique, Kruer, Michael C, Masri, Amira, Gurses, Candan, Ferrie, Colin, Harvey, Kirsten, Shiang, Rita, Christodoulou, John, Andermann, Frederick, Andermann, Eva, Thomas, Rhys H, Harvey, Robert J, Lynch, Joseph W, Rees, Mark I

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Association of gephyrin and glycine receptors in the human brainstem and spinal cord: an immunohistochemical analysis von Baer, K, Waldvogel, H.J, During, M.J, Snell, R.G, Faull, R.L.M, Rees, M.I

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Harris syndrome – a geographic perspective von NAINA, H. V. K., NAIR, S. C., HARRIS, S., WOODFIELD, G., REES, M. I.

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Further evidence of autosomal dominant congenital zonular pulverulent cataracts linked to 13q11 (CZP3) and a novel mutation in connexin 46 (GJA3) von REES, M. I, WATTS, P, FENTON, I, CLARKE, A, SNELL, R. G, OWEN, M. J, GRAY, J

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Characterisation, mutation detection, and association analysis of alternative promoters and 5' UTRs of the human dopamine D3 receptor gene in schizophrenia von ANNEY, R. J, REES, M. I, JONES, G, HOOGENDOORN, B, SMITH, K, HAMSHERE, M. L, COLEMAN, S, GUY, C, O'DONOVAN, M. C, OWEN, M. J, BUCKLAND, P. R, BRYAN, E, SPURLOCK, G, WILLIAMS, N, NORTON, N, WILLIAMS, H, CARDNO, A, ZAMMIT, S, JONES, S

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Posthumous diagnosis of long QT syndrome from neonatal screening cards von Gladding, P.A., MBCHB, Evans, C.-A., MSc (Med), Crawford, J., NZCS, Chung, S.K., BSc (Hons), Vaughan, A., BMLS, Webster, D., PhD, Neas, K., FRACP, Love, D.R., PhD, Rees, M.I., PhD, Shelling, A.N., PhD, Skinner, J.R., MD

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GABAA receptor subunit and gephyrin protein changes differ in the globus pallidus in Huntington's diseased brain von THOMPSON-VEST, N. M, WALDVOGEL, H. J, REES, M. I, FAULL, R. L. M

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Genotype-phenotype correlations in hyperekplexia: apnoeas, learning difficulties and speech delay von THOMAS, Rhys H, CHUNG, Seo-Kyung, WOOD, Sian E, CUSHION, Thomas D, DREW, Cheney J. G, HAMMOND, Carrie L, VANBELLINGHEN, Jean-Francois, MULLINS, Jonathan G. L, REES, Mark I

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Distribution of gephyrin in the human brain: an immunohistochemical analysis von Waldvogel, H.J., Baer, K., Snell, R.G., During, M.J., Faull, R.L.M., Rees, M.I.

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Differential localization of GABAA receptor subunits within the substantia nigra of the human brain: An immunohistochemical study von Waldvogel, H.J., Baer, K., Gai, W.-P., Gilbert, R.T., Rees, M.I., Mohler, H., Faull, R.L.M.

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PO.04 Ethnic variation in GLRA1 genotype in hyperekplexia von Thomas, R, Chung, S K, Hammond, C L, Robinson, A, Rees, M I

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Chromosome 2 interstitial deletion (del(2)(q14.1q21)) associated with connective tissue laxity and an attention deficit disorder von Baker, K L, Rees, M I, Thompson, P W, Howell, R T, Cole, T R, Hughes, H E, Upadhyaya, M, Ravine, D

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