New variant and expression studies provide further insight into the genotype-phenotype correlation in YAP1-related developmental eye disorders von Holt, R., Ceroni, F., Bax, D. A., Broadgate, S., Diaz, D. Gold, Santos, C., Gerrelli, D., Ragge, N. K.

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Identification and functional characterisation of genetic variants in OLFM2 in children with developmental eye disorders von Holt, R., Ugur Iseri, S. A., Wyatt, A. W., Bax, D. A., Gold Diaz, D., Santos, C., Broadgate, S., Dunn, R., Bruty, J., Wallis, Y., McMullan, D., Ogilvie, C., Gerrelli, D., Zhang, Y., Ragge, Nicola

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FOXP2 expression during brain development coincides with adult sites of pathology in a severe speech and language disorder von Lai, Cecilia S. L., Gerrelli, Dianne, Monaco, Anthony P., Fisher, Simon E., Copp, Andrew J.

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Rare familial 16q21 microdeletions under a linkage peak implicate cadherin 8 (CDH8) in susceptibility to autism and learning disability von Pagnamenta, Alistair T, Khan, Hameed, Walker, Susan, Gerrelli, Dianne, Wing, Kirsty, Bonaglia, Maria Clara, Giorda, Roberto, Berney, Tom, Mani, Elisa, Molteni, Massimo, Pinto, Dalila, Le Couteur, Ann, Hallmayer, Joachim, Sutcliffe, James S, Szatmari, Peter, Paterson, Andrew D, Scherer, Stephen W, Vieland, Veronica J, Monaco, Anthony P

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Novel mutations in LHX3 are associated with hypopituitarism and sensorineural hearing loss von Rajab, Anna, Kelberman, Daniel, de Castro, Sandra C.P., Biebermann, Heike, Shaikh, Hala, Pearce, Kerra, Hall, Catherine M., Shaikh, Guftar, Gerrelli, Dianne, Grueters, Annette, Krude, Heiko, Dattani, Mehul T.

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Sonic hedgehog and the molecular regulation of mouse neural tube closure von Ybot-Gonzalez, Patricia, Cogram, Patricia, Gerrelli, Dianne, Copp, Andrew J

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Mutations in CPAMD8 cause a unique form of autosomal-recessive anterior segment dysgenesis von Cheong, S-S, Hentschel, L, Davidson, AE, Gerrelli, D, Davie, R, Rizzo, R, Pontikos, N, Plagnol, V, Moore, AT, Sowden, JC, Michaelides, M, Snead, M, Tuft, SJ, Hardcastle, AJ

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Heterozygous Mutations of OTX2 Cause Severe Ocular Malformations von Ragge, Nicola K., Brown, Alison G., Poloschek, Charlotte M., Lorenz, Birgit, Henderson, R. Alex, Clarke, Michael P., Russell-Eggitt, Isabelle, Fielder, Alistair, Gerrelli, Dianne, Martinez-Barbera, Juan Pedro, Ruddle, Piers, Hurst, Jane, Collin, J. Richard O., Salt, Alison, Cooper, Simon T., Thompson, Pamela J., Sisodiya, Sanjay M., Williamson, Kathleen A., FitzPatrick, David R., Heyningen, Veronica van, Hanson, Isabel M.

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Cordon-bleu is a conserved gene involved in neural tube formation von Carroll, Elizabeth A, Gerrelli, Dianne, Gasca, Stéphan, Berg, Elizabeth, Beier, David R, Copp, Andrew J, Klingensmith, John

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Antagonistic Effects of Retinoic Acid and Thyroid Hormone on the Expression of the Tissue-specific Splicing Protein SmN in a Clonal Cell Line Derived from Rat Heart von Gerrelli, D., Huntriss, J.D., Latchman, D.S.

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Genetic enhancement of cognition in a kindred with cone–rod dystrophy due to RIMS1 mutation von Sisodiya, Sanjay M, Thompson, Pamela J, Need, Anna, Harris, Sarah E, Weale, Michael E, Wilkie, Susan E, Michaelides, Michel, Free, Samantha L, Walley, Nicole, Gumbs, Curtis, Gerrelli, Dianne, Ruddle, Piers, Whalley, Lawrence J, Starr, John M, Hunt, David M, Goldstein, David B, Deary, Ian J, Moore, Anthony T

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Cardiovascular Defects Associated With Abnormalities in Midline Development in the Loop-tail Mouse Mutant von Henderson, Deborah J, Conway, Simon J, Greene, Nicholas D.E, Gerrelli, Dianne, Murdoch, Jennifer N, Anderson, Robert H, Copp, Andrew J

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Ostertagia ostertagi infection in the calf: effects of a trickle challenge on appetite, digestibility, rate of passage of digesta and liveweight gain von FOX, M.T., GERRELLI, D., PITT, S.R., JACOBS, D.E., GILL, M., GALE, D.L.

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Effect of omeprazole treatment on feed intake and blood gastrin and pepsinogen levels in the calf von FOX, M.T., GERRELLI, D., SHIVALKAR, P., JACOBS, D.E.

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Endocrine effects of a single infection with Ostertagia ostertagi in the calf von Fox, M.T., Gerrelli, D., Pitt, S.R., Jacobs, D.E., Hart, I.C., Simmonds, A.D.

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Genomic organization and embryonic expression of igsf8, an immunoglobulin superfamily member implicated in development of the nervous system and organ epithelia von Murdoch, Jennifer N, Doudney, Kit, Gerrelli, Dianne, Wortham, Noel, Paternotte, Caroline, Stanier, Philip, Copp, Andrew J

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Ostertagia ostertagi infection in the calf: effects of a trickle challenge on the hormonal control of digestive and metabolic function von FOX, M.T., GERRELLI, D., PITT, S.R., JACOBS, D.E., GILL, M., SIMMONDS, A.D.

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Enabling research with human embryonic and fetal tissue resources von Gerrelli, D, Lisgo, S, Copp, AJ, Lindsay, S

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Mechanisms of normal and abnormal neurulation: evidence from embryo culture studies von Fleming, A, Gerrelli, D, Greene, N D, Copp, A J

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The relationship between appetite and plasma non-esterified fatty acid levels in housed calves von Fox, M.T. (Royal Veterinary Coll., London (United Kingdom). Dept. of Veterinary Pathology), Gerrelli, D, Pitt, S.R, Jacobs, D.E

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