FOXP2 expression during brain development coincides with adult sites of pathology in a severe speech and language disorder. by Lai, C, Gerrelli, D, Monaco, A, Fisher, S, Copp, A

Neuronal function of Tbx20 conserved from nematodes to vertebrates. by Pocock, R, Mione, M, Hussain, S, Maxwell, S, Pontecorvi, M, Aslam, S, Gerrelli, D, Sowden, J, Woollard, A

The Meckel-Gruber Syndrome proteins MKS1 and meckelin interact and are required for primary cilium formation. by Dawe, H, Smith, U, Cullinane, A, Gerrelli, D, Cox, P, Badano, J, Blair-Reid, S, Sriram, N, Katsanis, N, Attie-Bitach, T, Afford, S, Copp, A, Kelly, D, Gull, K, Johnson, C

Frontorhiny, a distinctive presentation of frontonasal dysplasia caused by recessive mutations in the ALX3 homeobox gene. by Twigg, SR, Versnel, S, Nürnberg, G, Lees, M, Bhat, M, Hammond, P, Hennekam, R, Hoogeboom, A, Hurst, J, Johnson, D, Robinson, A, Scambler, P, Gerrelli, D, Nürnberg, P, Mathijssen, I, Wilkie, A

Rare familial 16q21 microdeletions under a linkage peak implicate cadherin 8 (CDH8) in susceptibility to autism and learning disability. by Pagnamenta, A, Khan, H, Walker, S, Gerrelli, D, Wing, K, Bonaglia, M, Giorda, R, Berney, T, Mani, E, Molteni, M, Pinto, D, Le Couteur, A, Hallmayer, J, Sutcliffe, J, Szatmari, P, Paterson, A, Scherer, S, Vieland, V, Monaco, A

Rare familial 16q21 microdeletions under a linkage peak implicate cadherin 8 (CDH8) in susceptibility to autism and learning disability by Pagnamenta, A, Khan, H, Walker, S, Gerrelli, D, Wing, K, Bonaglia, M, Giorda, R, Berney, T, Mani, E, Molteni, M, Pinto, D, Le Couteur, A, Hallmayer, J, Sutcliffe, J, Szatmari, P, Paterson, A, Scherer, S, Vieland, V, Monaco, A

Mutations in BMP4 cause eye, brain, and digit developmental anomalies: overlap between the BMP4 and hedgehog signaling pathways. by Bakrania, P, Efthymiou, M, Klein, J, Salt, A, Bunyan, D, Wyatt, A, Ponting, C, Martin, A, Williams, S, Lindley, V, Gilmore, J, Restori, M, Robson, A, Neveu, M, Holder, G, Collin, JR, Robinson, DO, Farndon, P, Johansen-Berg, H, Gerrelli, D, Ragge, N