| Signaling through the primary cilium G Wheway, L Nazlamova, JT Hancock Frontiers in cell and developmental biology 6, 8, 2018 | 506 | 2018 |
| Loss-of-function mutations in MICU1 cause a brain and muscle disorder linked to primary alterations in mitochondrial calcium signaling CV Logan, G Szabadkai, JA Sharpe, DA Parry, S Torelli, AM Childs, ... Nature genetics 46 (2), 188-193, 2014 | 389 | 2014 |
| An siRNA-based functional genomics screen for the identification of regulators of ciliogenesis and ciliopathy genes G Wheway, M Schmidts, DA Mans, K Szymanska, TMT Nguyen, H Racher, ... Nature cell biology 17 (8), 1074-1087, 2015 | 256 | 2015 |
| Disrupted alternative splicing for genes implicated in splicing and ciliogenesis causes PRPF31 retinitis pigmentosa A Buskin, L Zhu, V Chichagova, B Basu, S Mozaffari-Jovin, D Dolan, ... Nature communications 9 (1), 4234, 2018 | 191 | 2018 |
| The SYSCILIA gold standard (SCGSv1) of known ciliary components and its applications within a systems biology consortium TJP Van Dam, G Wheway, GG Slaats, SYSCILIA Study Group, ... Cilia 2, 1-5, 2013 | 172* | 2013 |
| Meckel–Gruber syndrome: an update on diagnosis, clinical management, and research advances V Hartill, K Szymanska, SM Sharif, G Wheway, CA Johnson Frontiers in pediatrics 5, 244, 2017 | 160 | 2017 |
| Nesprin-2 interacts with meckelin and mediates ciliogenesis via remodelling of the actin cytoskeleton HR Dawe, M Adams, G Wheway, K Szymanska, CV Logan, AA Noegel, ... Journal of cell science 122 (15), 2716-2726, 2009 | 158 | 2009 |
| A novel ACE2 isoform is expressed in human respiratory epithelia and is upregulated in response to interferons and RNA respiratory virus infection C Blume, CL Jackson, CM Spalluto, J Legebeke, L Nazlamova, F Conforti, ... Nature genetics 53 (2), 205-214, 2021 | 152 | 2021 |
| The role of primary cilia in the development and disease of the retina G Wheway, DA Parry, CA Johnson Organogenesis 10 (1), 69-85, 2014 | 152 | 2014 |
| A meckelin–filamin A interaction mediates ciliogenesis M Adams, RJ Simms, Z Abdelhamed, HR Dawe, K Szymanska, CV Logan, ... Human molecular genetics 21 (6), 1272-1286, 2012 | 128 | 2012 |
| CiliaCarta: An integrated and validated compendium of ciliary genes TJP Van Dam, J Kennedy, R van Der Lee, E De Vrieze, KA Wunderlich, ... PloS one 14 (5), e0216705, 2019 | 121 | 2019 |
| Variable expressivity of ciliopathy neurological phenotypes that encompass Meckel–Gruber syndrome and Joubert syndrome is caused by complex de-regulated ciliogenesis, Shh and … ZA Abdelhamed, G Wheway, K Szymanska, S Natarajan, C Toomes, ... Human molecular genetics 22 (7), 1358-1372, 2013 | 121 | 2013 |
| Opportunities and challenges for molecular understanding of ciliopathies–the 100,000 genomes project G Wheway, Genomics England Research Consortium, HM Mitchison Frontiers in genetics 10, 127, 2019 | 93 | 2019 |
| Aberrant Wnt signalling and cellular over-proliferation in a novel mouse model of Meckel–Gruber syndrome G Wheway, Z Abdelhamed, S Natarajan, C Toomes, C Inglehearn, ... Developmental biology 377 (1), 55-66, 2013 | 61 | 2013 |
| The Meckel-Gruber syndrome protein TMEM67 controls basal body positioning and epithelial branching morphogenesis in mice via the non-canonical Wnt pathway ZA Abdelhamed, S Natarajan, G Wheway, CF Inglehearn, C Toomes, ... Disease models & mechanisms 8 (6), 527-541, 2015 | 52 | 2015 |
| Mutation spectrum of PRPF31, genotype-phenotype correlation in retinitis pigmentosa, and opportunities for therapy G Wheway, A Douglas, D Baralle, E Guillot Experimental eye research 192, 107950, 2020 | 51 | 2020 |
| ATMIN is a transcriptional regulator of both lung morphogenesis and ciliogenesis P Goggolidou, J L. Stevens, F Agueci, J Keynton, G Wheway, DT Grimes, ... Development 141 (20), 3966-3977, 2014 | 51 | 2014 |
| 661W photoreceptor cell line as a cell model for studying retinal ciliopathies G Wheway, L Nazlamova, D Turner, S Cross Frontiers in genetics 10, 308, 2019 | 45 | 2019 |
| DYNC2H1 hypomorphic or retina-predominant variants cause nonsyndromic retinal degeneration A Vig, JA Poulter, D Ottaviani, E Tavares, K Toropova, AM Tracewska, ... Genetics in Medicine 22 (12), 2041-2051, 2020 | 43 | 2020 |
| Genome sequencing reveals underdiagnosis of primary ciliary dyskinesia in bronchiectasis A Shoemark, H Griffin, G Wheway, C Hogg, JS Lucas, C Camps, J Taylor, ... European Respiratory Journal 60 (5), 2022 | 41 | 2022 |
