| Impaired B and T cell antigen receptor signaling in p110δ PI 3-kinase mutant mice K Okkenhaug, A Bilancio, G Farjot, H Priddle, S Sancho, E Peskett, ... Science 297 (5583), 1031-1034, 2002 | 1167 | 2002 |
| Impaired B and T cell antigen receptor signaling in p110δ PI 3-kinase mutant mice K Okkenhaug, A Bilancio, G Farjot, H Priddle, S Sancho, E Peskett, ... Science 297 (5583), 1031-1034, 2002 | 1167 | 2002 |
| Critical role for the p110α phosphoinositide-3-OH kinase in growth and metabolic regulation LC Foukas, M Claret, W Pearce, K Okkenhaug, S Meek, E Peskett, ... Nature 441 (7091), 366-370, 2006 | 565 | 2006 |
| Essential role for the p110δ phosphoinositide 3-kinase in the allergic response K Ali, A Bilancio, M Thomas, W Pearce, AM Gilfillan, C Tkaczyk, N Kuehn, ... Nature 431 (7011), 1007-1011, 2004 | 506 | 2004 |
| Mice with endogenous TDP‐43 mutations exhibit gain of splicing function and characteristics of amyotrophic lateral sclerosis P Fratta, P Sivakumar, J Humphrey, K Lo, T Ricketts, H Oliveira, ... The EMBO journal 37 (11), e98684, 2018 | 151 | 2018 |
| SNX14 mutations affect endoplasmic reticulum-associated neutral lipid metabolism in autosomal recessive spinocerebellar ataxia 20 D Bryant, Y Liu, S Datta, H Hariri, M Seda, G Anderson, E Peskett, ... Human molecular genetics 27 (11), 1927-1940, 2018 | 66 | 2018 |
| Mechanistic insights into arrhythmogenic right ventricular cardiomyopathy caused by desmocollin-2 mutations K Gehmlich, P Syrris, E Peskett, A Evans, E Ehler, A Asimaki, ... Cardiovascular research 90 (1), 77-87, 2011 | 61 | 2011 |
| Genetic analyses in small-for-gestational-age newborns SE Stalman, N Solanky, M Ishida, C Alemán-Charlet, S Abu-Amero, ... The Journal of Clinical Endocrinology & Metabolism 103 (3), 917-925, 2018 | 51 | 2018 |
| Mechanical properties of calvarial bones in a mouse model for craniosynostosis M Moazen, E Peskett, C Babbs, E Pauws, MJ Fagan PloS one 10 (5), e0125757, 2015 | 41 | 2015 |
| Impaired neutrophil migration and phagocytosis in IRAK-4 deficiency G Bouma, R Doffinger, SY Patel, E Peskett, JC Sinclair, ... British journal of haematology 147 (1), 153-156, 2009 | 35 | 2009 |
| Impact of rare variants in ARHGAP29 to the etiology of oral clefts: role of loss‐of‐function vs missense variants CP Savastano, LA Brito, ÁC Faria, N Setó‐Salvia, E Peskett, CM Musso, ... Clinical genetics 91 (5), 683-689, 2017 | 31 | 2017 |
| Investigation of the Annexin A5 M2 haplotype in 500 white European couples who have experienced recurrent spontaneous abortion C Demetriou, S Abu-Amero, S White, E Peskett, A Markoff, P Stanier, ... Reproductive biomedicine online 31 (5), 681-688, 2015 | 28 | 2015 |
| Analysis of the Fgfr2C342Y mouse model shows condensation defects due to misregulation of Sox9 expression in prechondrocytic mesenchyme E Peskett, S Kumar, W Baird, J Jaiswal, M Li, P Patel, JA Britto, E Pauws Biology Open 6 (2), 223-231, 2017 | 25 | 2017 |
| X‐linked CHARGE‐like Abruzzo–Erickson syndrome and classic cleft palate with ankyloglossia result from TBX22 splicing mutations E Pauws, E Peskett, C Boissin, A Hoshino, K Mengrelis, E Carta, ... Clinical genetics 83 (4), 352-358, 2013 | 19 | 2013 |
| Diverse species-specific phenotypic consequences of loss of function sorting nexin 14 mutations D Bryant, M Seda, E Peskett, C Maurer, G Pomeranz, M Ghosh, ... Scientific reports 10 (1), 13763, 2020 | 18 | 2020 |
| Overexpression of Fgfr2c causes craniofacial bone hypoplasia and ameliorates craniosynostosis in the Crouzon mouse KKL Lee, E Peskett, CM Quinn, R Aiello, L Adeeva, DA Moulding, ... Disease Models & Mechanisms 11 (11), dmm035311, 2018 | 14 | 2018 |
| Analysis of transgenic zebrafish expressing the Lenz-Majewski syndrome gene PTDSS1 in skeletal cell lineages M Seda, E Peskett, C Demetriou, D Bryant, GE Moore, P Stanier, ... F1000Research 8, 2019 | 12 | 2019 |
| Disruption of FOXF2 as a Likely Cause of Absent Uvula in an Egyptian Family R Seselgyte, D Bryant, C Demetriou, M Ishida, E Peskett, N Moreno, ... Journal of Dental Research 98 (6), 659-665, 2019 | 4 | 2019 |
| De-Suppression of Mesenchymal Cell Identities and Variable Phenotypic Outcomes Associated with Knockout of Bbs1 GM Freke, T Martins, RJ Davies, T Beyer, M Seda, E Peskett, N Haq, ... Cells 12 (22), 2662, 2023 | | 2023 |
| Affinity Purification of Intraflagellar Transport (IFT) Proteins in Mice Using Endogenous Streptavidin/FLAG Tags T Beyer, T Martins, JJ Srikaran, M Seda, E Peskett, F Klose, K Junger, ... Cilia: Methods and Protocols, 199-212, 2023 | | 2023 |
