Analysis of the function of two circadian‐regulated CONSTANS‐LIKE genes by Ledger, Susan, Strayer, Carl, Ashton, Fern, Kay, Steve A., Putterill, Jo

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Implications of a Chr7q21.11 Microdeletion and the Role of the PCLO Gene in Developmental Delay by Love , Donald R, Aftimos , Salim, Mazzaschi , Roberto L, Ashton , Fern, George , Alice M

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Microduplication of 3p26.3 Implicated in Cognitive Development by Te Weehi, Leah, Maikoo, Raj, Mc Cormack, Adrian, Mazzaschi, Roberto L. P., Ashton, Fern, Zhang, Liangtao, George, Alice M., Love, Donald R.

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A Novel 2.3 Mb Microduplication of 9q34.3 Inserted into 19q13.4 in a Patient with Learning Disabilities by Singh, Shalinder, Ashton, Fern, Marquis-Nicholson, Renate, Love, Jennifer M., Lan, Chuan-Ching, Aftimos, Salim, George, Alice M., Love, Donald R.

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Amino-Terminal Microdeletion within the CNTNAP2 Gene Associated with Variable Expressivity of Speech Delay by Ashton, Fern, George, Alice M., al-Murrani, Amel, Love, Donald R., Aftimos, Salim

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The p.Ala510Val mutation in the SPG7 (paraplegin) gene is the most common mutation causing adult onset neurogenetic disease in patients of British ancestry by Roxburgh, Richard H., Marquis-Nicholson, Renate, Ashton, Fern, George, Alice M., Lea, Rod A., Eccles, David, Mossman, Stuart, Bird, Thomas, van Gassen, Koen L., Kamsteeg, Erik-Jan, Love, Donald R.

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Compound heterozygous SLC19A3 mutations further refine the critical promoter region for biotin-thiamine-responsive basal ganglia disease by Whitford, Whitney, Hawkins, Isobel, Glamuzina, Emma, Wilson, Francessa, Marshall, Andrew, Ashton, Fern, Love, Donald R, Taylor, Juliet, Hill, Rosamund, Lehnert, Klaus, Snell, Russell G, Jacobsen, Jessie C

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SNP analysis and whole exome sequencing: Their application in the analysis of a consanguineous pedigree segregating ataxia by Nickerson, Sarah L., Marquis-Nicholson, Renate, Claxton, Karen, Ashton, Fern, Leong, Ivone U.S., Prosser, Debra O., Love, Jennifer M., George, Alice M., Taylor, Graham, Wilson, Callum, McKinlay Gardner, R.J., Love, Donald R.

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The p.Ala510Val variant in the SPG7 gene: re-assessing the pathogenic significance of a ‘benign’ polymorphism by Marquis-Nicholson, Renate, Roxburgh, Richard H., Ashton, Fern, Love, Donald R.

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Microarray testing in clinical diagnosis: an analysis of 5,300 New Zealand patients by Mc Cormack, Adrian, Claxton, Karen, Ashton, Fern, Asquith, Philip, Atack, Edward, Mazzaschi, Roberto, Moverley, Paula, O'Connor, Rachel, Qorri, Methat, Sheath, Karen, Love, Donald R, George, Alice M

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Pseudotrisomy 13 syndrome: Use of homozygosity mapping to target candidate genes by Marquis-Nicholson, Renate, Aftimos, Salim, Ashton, Fern, Love, Jennifer M., Stone, Peter, McFarlane, Jeannette, George, Alice M., Love, Donald R.

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Mutations within the protein Z‐dependent protease inhibitor gene are associated with venous thromboembolic disease: a new form of thrombophilia by Water, Neil, Tan, Tina, Ashton, Fern, O'Grady, Anna, Day, Tony, Browett, Peter, Ockelford, Paul, Harper, Paul

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Implications of a Chr7q21.11 Microdeletion and the Role of the PCLO Gene in Developmental Delay = الأثار المترتبة على فقدان الخبن الصبغي الجزيئي و دور جين PCLO في صعوبات التعلم... by Mazzaschi, Roberto L., Ashton, Fern, Aftimos, Salim, George, Alice M., Love, Donald R.

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Mutations within the Protein Z-Dependent Protease Inhibitor (ZPI) Gene Are Associated with Venous Thromboembolic Disease: A New Form of Thrombophilia by Harper, Paul L., Van de Water, Neil S., Ashton, Fern, Tan, Tina, Grady, Anne O, Ockelford, Paul A., Browett, Peter

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SNP Analysis and Whole Exome Sequencing: Their Application in the Analysis of a Consanguineous Pedigree Segregating Ataxia by Nickerson, Sarah L, Marquis-Nicholson, Renate, Claxton, Karen, Ashton, Fern, Leong, Ivone U S, Prosser, Debra O, Love, Jennifer M, George, Alice M, Taylor, Graham, Wilson, Callum, Gardner, R J McKinlay, Love, Donald R

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SNP Analysis and Whole Exome Sequencing: Their Application in the Analysis of a Consanguineous Pedigree Segregating Ataxia by Nickerson, Sarah L, Marquis-Nicholson, Renate, Claxton, Karen, Ashton, Fern, Leong, Ivone U S, Prosser, Debra O, Love, Jennifer M, George, Alice M, Taylor, Graham, Wilson, Callum, Gardner, R J McKinlay, Love, Donald R

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Amino-Terminal Microdeletion within the CNTNAP2 Gene Associated with Variable Expressivity of Speech Delay by Al-Murrani, Amel, Ashton, Fern, Aftimos, Salim, George, Alice M, Love, Donald R

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Safety of Nonsteroidal Anti-inflammatory Drugs in Major Gastrointestinal Surgery: A Prospective, Multicenter Cohort Study by Abburu, S., Adams, R., Aidoo‐Micah, G. E., Amajuoyi, A., Ashwood, J., Bartlett, J., Bath, M. F., Botchey, S., Bullman, L. M., Burgess, A., Burke, J., Chan, N., Chaudhary, M., Chrastek, D., Chua, E. Y., Clesham, K., Coffin, J., Collier, H., Copley, H. C., Cundy, O. J., Daoub, A., Davies, J., Dhanji, A., Dinsmore, L., Dobson, J., Dunn, C. E., Elkawafi, M., Fautz, T., FitzPatrick, D., Greig, R. J., Griffin, E. J., Hameed, M., Harrison, P. L. M., Hayat, U., Heneghan, H., Holmes, C., Ingham, R., Iqbal, S., Johnston, A., Johnstone, M., Karia, M., Kelly, M., Kerai, A., Khan, T., Kisyov, I., Kumar, A. N., Kwan, M. L., Lalor, P., Lee, A. H. Y., Lim, S. J., Lotfallah, A., Lynne, S., Maclennan, D., Malys, M. K., Mastan, A., McAleer, S., McCance, E., McCrann, C., McKelvey, L. L., Meek, J., Momoh, Z., Murphy, L., Naqib, S., Navayogaarajah, V., O’Connor, A., O’Neill, S., O’Sullivan, K., Patel, N., Patel, B., Pericleous, A., Phan, P. N., Puan, L., Rajan, N., Rampal, R., Robertson, V., Robertson, D. T., Rothwell, L., Ryan, M., Sahathevan, A., Sandhu, S., Sethi, R. K., Shafiq, N. M., Sheldon, A., Shepherd, P., Simpson, A., Singh, R., Sirakaya, M., Smith, N., Sorah, T., Sukumar, S., Tahmina, A., Theodoropoulou, K., Tongo, F., Torrance, H. D., Turner, J., Whatling, E. A., Whewell, H., Wilkinson, D., Xiao, C., Ziff, O.

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