| The genetic basis of mammalian neurulation AJ Copp, NDE Greene, JN Murdoch Nature Reviews Genetics 4 (10), 784-793, 2003 | 904 | 2003 |
| Mutation of Celsr1 disrupts planar polarity of inner ear hair cells and causes severe neural tube defects in the mouse JA Curtin, E Quint, V Tsipouri, RM Arkell, B Cattanach, AJ Copp, ... Current Biology 13 (13), 1129-1133, 2003 | 711 | 2003 |
| FOXP2 and the neuroanatomy of speech and language F Vargha-Khadem, DG Gadian, A Copp, M Mishkin Nature Reviews Neuroscience 6 (2), 131-138, 2005 | 698 | 2005 |
| Disruption of Bardet-Biedl syndrome ciliary proteins perturbs planar cell polarity in vertebrates AJ Ross, H May-Simera, ER Eichers, M Kai, J Hill, DJ Jagger, CC Leitch, ... Nature genetics 37 (10), 1135-1140, 2005 | 673 | 2005 |
| Neural tube defects: recent advances, unsolved questions, and controversies AJ Copp, P Stanier, NDE Greene The Lancet Neurology 12 (8), 799-810, 2013 | 672 | 2013 |
| Neural tube defects NDE Greene, AJ Copp Annual review of neuroscience 37, 221-242, 2014 | 657 | 2014 |
| Spina bifida AJ Copp, NS Adzick, LS Chitty, JM Fletcher, GN Holmbeck, GM Shaw Nature reviews Disease primers 1 (1), 1-18, 2015 | 645 | 2015 |
| Genetics and development of neural tube defects AJ Copp, NDE Greene The Journal of Pathology: A Journal of the Pathological Society of Great …, 2010 | 567 | 2010 |
| FOXP2 expression during brain development coincides with adult sites of pathology in a severe speech and language disorder CSL Lai, D Gerrelli, AP Monaco, SE Fisher, AJ Copp Brain 126 (11), 2455-2462, 2003 | 529 | 2003 |
| Death before birth: clues from gene knockouts and mutations AJ Copp Trends in Genetics 11 (3), 87-93, 1995 | 488 | 1995 |
| Neural tube closure: cellular, molecular and biomechanical mechanisms E Nikolopoulou, GL Galea, A Rolo, NDE Greene, AJ Copp Development 144 (4), 552-566, 2017 | 481 | 2017 |
| Genetics of human neural tube defects NDE Greene, P Stanier, AJ Copp Human molecular genetics 18 (R2), R113-R129, 2009 | 423 | 2009 |
| The embryonic development of mammalian neural tube defects AJ Copp, FA Brook, JP Estibeiro, ASW Shum, DL Cockroft Progress in neurobiology 35 (5), 363-403, 1990 | 419 | 1990 |
| Severe neural tube defects in the loop-tail mouse result from mutation of Lpp1, a novel gene involved in floor plate specification JN Murdoch, K Doudney, C Paternotte, AJ Copp, P Stanier Human molecular genetics 10 (22), 2593-2601, 2001 | 369 | 2001 |
| Convergent extension, planar-cell-polarity signalling and initiation of mouse neural tube closure P Ybot-Gonzalez, D Savery, D Gerrelli, M Signore, CE Mitchell, CH Faux, ... Oxford University Press for The Company of Biologists Limited 134 (4), 789-799, 2007 | 366 | 2007 |
| Pax3 is required for cardiac neural crest migration in the mouse: evidence from the splotch (Sp2H) mutant SJ Conway, DJ Henderson, AJ Copp Development 124 (2), 505-514, 1997 | 359 | 1997 |
| The chromosome 6p22 haplotype associated with dyslexia reduces the expression of KIAA0319 , a novel gene involved in neuronal migration S Paracchini, A Thomas, S Castro, C Lai, M Paramasivam, Y Wang, ... Human molecular genetics 15 (10), 1659-1666, 2006 | 356 | 2006 |
| Disruption of scribble (Scrb1) causes severe neural tube defects in the circletail mouse JN Murdoch, DJ Henderson, K Doudney, C Gaston-Massuet, HM Phillips, ... Human molecular genetics 12 (2), 87-98, 2003 | 348 | 2003 |
| The Meckel–Gruber syndrome proteins MKS1 and meckelin interact and are required for primary cilium formation HR Dawe, UM Smith, AR Cullinane, D Gerrelli, P Cox, JL Badano, ... Human molecular genetics 16 (2), 173-186, 2007 | 321 | 2007 |
| Embryonic folate metabolism and mouse neural tube defects A Fleming, AJ Copp Science 280 (5372), 2107-2109, 1998 | 317 | 1998 |
