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    Number of items: 5.

    Gidziela, A. and Ahmadzadeh, Y.I. and Michelini, G. and Allegrini, A.G. and Agnew-Blais, J. and Lau, L.Y. and Duret, M. and Procopio, F. and Daly, E. and Ronald, Angelica and Rimfeld, K. and Malanchini, M. (2023) A meta-analysis of genetic effects on neurodevelopmental disorders and co-occurring conditions. Nature Human Behaviour , ISSN 2397-3374.

    Pote, I. and Wang, S. and Sethna, V. and Blasi, Anna and Daly, E. and Kuklisova-Murgasova, M. and Lloyd-Fox, Sarah and Mercure, E. and Busuulwa, P. and Stoencheva, V. and Charman, T. and Williams, S.C.R. and Johnson, Mark H. and Murphy, D.G.M. and McAlonan, G.M. (2019) Familial risk of autism alters subcortical and cerebellar brain anatomy in infants and predicts the emergence of repetitive behaviors in early childhood. Autism Research 12 (4), pp. 614-627. ISSN 1939-3792.

    Sethna, V. and Pote, I. and Wang, S. and Gudbrandsen, M. and Blasi, Anna and McCukser, C. and Daly, E. and Perry, E. and Adams, K.P.H. and Kuklisova-Murgasova, M. and Busuulwa, P. and Lloyd-Fox, Sarah and Murray, L. and Johnson, Mark H. and Williams, S.R.C. and Murphy, D.G.M. and Craig, M.C. and McAlonan, G.M. (2017) Mother-infant interactions and regional brain volumes in infancy: an MRI study. Brain Structure and Function 222 (5), pp. 2379-2388. ISSN 1863-2653.

    Campbell, L.E. and Daly, E. and Toal, F. and Stevens, A. and Azuma, R. and Karmiloff-Smith, Annette and Murphy, D.G.M. and Murphy, K.C. (2009) Brain structural differences associated with the behavioural phenotype in children with Williams syndrome. Brain Research 1258 , pp. 96-107. ISSN 0006-8993.

    Campbell, L.E. and Stevens, A. and Daly, E. and Toal, F. and Azuma, R. and Karmiloff-Smith, Annette and Murphy, D.G.M. and Murphy, K.C. (2009) A comparative study of cognition and brain anatomy between two neurodevelopmental disorders: 22q11.2 deletion syndrome and Williams syndrome. Neuropsychologia 47 (4), pp. 1034-1044. ISSN 0028-3932.

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