| 06-P023–Withdrawn S Castro, KY Leung, D Savery, P Gustavsson, AJ Copp, NDE Greene MECHANISMS OF DEVELOPMENT 126, S120-S136, 2009 | | 2009 |
| 06-P024 Identification of Lmnb1 as a possible modifier gene for neural tube defects in the mouse S Castro, KY Leung, D Savery, P Gustavsson, AJ Copp, NDE Greene Mechanisms of Development, S127, 2009 | | 2009 |
| 06-P032 Human Developmental Biology Resource (HDBR): A unique resource for studying human embryo and fetal development D Gerrelli, S Lisgo, A Copp, S Lindsay Mechanisms of Development, S129, 2009 | | 2009 |
| 06-P051 Mechanisms of spina bifida in the Zic2-Kumba mouse S Raza, V Massa, N Greene, A Copp Mechanisms of Development, S134-S135, 2009 | | 2009 |
| 17th Mammalian Genetics and Development Workshop of the Genetics Society-November 9-10, 2006-London, England, UK-Abstracts AJ Copp, NDE Greene, EMC Fisher CAMBRIDGE UNIV PRESS 89 (3), 181-181, 2007 | | 2007 |
| 561 Maternal Lifestyle Interventions: Targeting Preconception Health F Facchinetti, MSB Espinola, D Dewailly, AC Ozay, N Prapas, ... Metabolism 31 (8), 2020 | | 2020 |
| A cell-type-specific abnormality of cell proliferation in mutant (curly tail) mouse embryos developing spinal neural tube defects AJ Copp, FA Brook, HJ Roberts Development 104 (2), 285-295, 1988 | 166 | 1988 |
| A curly-tail modifier locus, mct1, on mouse chromosome 17 VA Letts, NJ Schork, AJ Copp, M Bernfield, WN Frankel Genomics 29 (3), 719-724, 1995 | 59 | 1995 |
| A gene for autosomal dominant sacral agenesis maps to the holoprosencephaly region at 7q36 SA Lynch, PM Bond, AJ Copp, WO Kirwan, S Nour, R Balling, E Mariman, ... Nature genetics 11 (1), 93-95, 1995 | 173 | 1995 |
| A genetic risk factor for mouse neural tube defects: defining the embryonic basis A Fleming, AJ Copp Human molecular genetics 9 (4), 575-581, 2000 | 85 | 2000 |
| A non-coding insertional mutation of Grhl2 causes gene over-expression and multiple structural anomalies including cleft palate, spina bifida and encephalocele Z Crane-Smith, SCP De Castro, E Nikolopoulou, P Wolujewicz, ... Human Molecular Genetics 32 (17), 2681-2692, 2023 | 3 | 2023 |
| A possible interaction between retarded splotch and curly tail JP Estibeiro, AJ Copp Mouse Genome 86, 245-, 1990 | | 1990 |
| A roadmap for the human developmental cell atlas M Haniffa, D Taylor, S Linnarsson, BJ Aronow, GD Bader, RA Barker, ... Nature 597 (7875), 196-205, 2021 | 138 | 2021 |
| A single center study of epidemiology of neural tube defects M Al-Mendalawi Journal of Neurosciences in Rural Practice 8 (1), 2017 | | 2017 |
| A summary of the registration process and the conditions of use S Lindsay, AJ Copp Trends in Genetics 11 (21), 586-590, 2005 | | 2005 |
| A targeted sequencing panel identifies rare damaging variants in multiple genes in the cranial neural tube defect, anencephaly M Ishida, T Cullup, C Boustred, C James, J Docker, C English, GOSgene, ... Clinical genetics 93 (4), 870-879, 2018 | 27 | 2018 |
| A topographical analysis of encephalocele locations: generation of a standardised atlas and cluster analysis VN Vakharia, S Toescu, AJ Copp, DNP Thompson Child's Nervous System 39 (7), 1911-1920, 2023 | 2 | 2023 |
| AAV-mediated expression of mouse or human GLDC normalises metabolic biomarkers in a GLDC-deficient mouse model of Non-Ketotic Hyperglycinemia KY Leung, C Santos, SCP De Castro, DG Diaz, AJ Copp, S Waddington, ... Molecular Genetics and Metabolism 142 (3), 108496, 2024 | | 2024 |
| AAV-mediated gene therapy in a GLDC-deficient mouse model of Non-Ketotic Hyperglycinemia KY Leung, C Santos, SCP De Castro, D Gold-Diaz, A Copp, ... bioRxiv, 2023.12. 15.571844, 2023 | | 2023 |
| Abnormal accumulation of chondroitin sulphate in the splotch G Yip, P Ferretti, A Copp GLYCOBIOLOGY 11, 10-56, 2001 | | 2001 |
