| Copy number variations in neurodevelopmental disorders HM Grayton, C Fernandes, D Rujescu, DA Collier Progress in neurobiology 99 (1), 81-91, 2012 | 207 | 2012 |
| Altered social behaviours in neurexin 1α knockout mice resemble core symptoms in neurodevelopmental disorders HM Grayton, M Missler, DA Collier, C Fernandes PloS one 8 (6), e67114, 2013 | 197 | 2013 |
| Genetic targeting of NRXN2 in mice unveils role in excitatory cortical synapse function and social behaviors G Born, HM Grayton, H Langhorst, I Dudanova, A Rohlmann, ... Frontiers in synaptic neuroscience 7, 3, 2015 | 82 | 2015 |
| Ohnologs are overrepresented in pathogenic copy number mutations A McLysaght, T Makino, HM Grayton, M Tropeano, KJ Mitchell, E Vassos, ... Proceedings of the National Academy of Sciences 111 (1), 361-366, 2014 | 64 | 2014 |
| Prenatal exposure to maternal obesity leads to hyperactivity in offspring C Fernandes, H Grayton, L Poston, AM Samuelsson, PD Taylor, ... Molecular psychiatry 17 (12), 1159-1160, 2012 | 47 | 2012 |
| NRXN1 deletions identified by array comparative genome hybridisation in a clinical case series–further understanding of the relevance of NRXN1 to neurodevelopmental disorders S Curran, JW Ahn, H Grayton, DA Collier, CM Ogilvie Journal of molecular psychiatry 1, 1-7, 2013 | 46 | 2013 |
| The Role of Rare Copy Number Variation in Neurodevelopmental Disorders HM Grayton University of London, King's College London, Institute of Psychiatry, 2013 | | 2013 |
