| Sequenceserver: a modern graphical user interface for custom BLAST databases A Priyam, BJ Woodcroft, V Rai, I Moghul, A Munagala, F Ter, ... Molecular biology and evolution 36 (12), 2922-2924, 2019 | 277 | 2019 |
| Transcriptomic identification of starfish neuropeptide precursors yields new insights into neuropeptide evolution DC Semmens, O Mirabeau, I Moghul, MR Pancholi, Y Wurm, MR Elphick Open biology 6 (2), 150224, 2016 | 137 | 2016 |
| Discovery of novel representatives of bilaterian neuropeptide families and reconstruction of neuropeptide precursor evolution in ophiuroid echinoderms M Zandawala, I Moghul, LA Yañez Guerra, J Delroisse, N Abylkassimova, ... Open biology 7 (9), 170129, 2017 | 71 | 2017 |
| Phenopolis: an open platform for harmonization and analysis of genetic and phenotypic data N Pontikos, J Yu, I Moghul, L Withington, F Blanco-Kelly, T Vulliamy, ... Bioinformatics 33 (15), 2421-2423, 2017 | 47 | 2017 |
| GeneValidator: identify problems with protein-coding gene predictions MA Drăgan, I Moghul, A Priyam, C Bustos, Y Wurm Bioinformatics 32 (10), 1559-1561, 2016 | 42 | 2016 |
| SARS-CoV-2 3D database: understanding the coronavirus proteome and evaluating possible drug targets AF Alsulami, SE Thomas, AR Jamasb, CA Beaudoin, I Moghul, ... Briefings in bioinformatics, 2021 | 38 | 2021 |
| Echinoderms provide missing link in the evolution of PrRP/sNPF-type neuropeptide signalling LA Yañez-Guerra, X Zhong, I Moghul, T Butts, CG Zampronio, AM Jones, ... Elife 9, e57640, 2020 | 35* | 2020 |
| Personal Genome Project UK (PGP-UK): a research and citizen science hybrid project in support of personalized medicine BMC medical genomics 11, 1-12, 2018 | 31 | 2018 |
| Diagnostic approaches to neuroendocrine neoplasms of unknown primary site AM Berner, C Pipinikas, A Ryan, H Dibra, I Moghul, A Webster, TV Luong, ... Neuroendocrinology 110 (7-8), 563-573, 2020 | 30 | 2020 |
| The Personal Genome Project-UK, an open access resource of human multi-omics data O Chervova, L Conde, JA Guerra-Assunção, I Moghul, AP Webster, ... Scientific data 6 (1), 1-10, 2019 | 26 | 2019 |
| Machine learning algorithms to detect subclinical keratoconus: systematic review H Maile, JPO Li, D Gore, M Leucci, P Mulholland, S Hau, A Szabo, ... JMIR medical informatics 9 (12), e27363, 2021 | 21 | 2021 |
| ReLayer: a Free, Online Tool for Extracting Retinal Thickness From Cross-Platform OCT Images G Ometto, I Moghul, G Montesano, A Hunter, N Pontikos, PR Jones, ... Translational Vision Science & Technology 8 (3), 2019 | 19 | 2019 |
| SynthEye: investigating the impact of synthetic data on artificial intelligence-assisted gene diagnosis of inherited retinal disease YA Veturi, W Woof, T Lazebnik, I Moghul, P Woodward-Court, SK Wagner, ... Ophthalmology Science 3 (2), 100258, 2023 | 18 | 2023 |
| COSMIC Cancer Gene Census 3D database: understanding the impacts of mutations on cancer targets AF Alsulami, PHM Torres, I Moghul, SM Arif, AK Chaplin, SC Vedithi, ... Briefings in bioinformatics 22 (6), bbab220, 2021 | 15 | 2021 |
| Pheno4J: a gene to phenotype graph database S Mughal, I Moghul, J Yu, T Clark, DS Gregory, N Pontikos Bioinformatics 33 (20), 3317-3319, 2017 | 14 | 2017 |
| Comparison and imputation-aided integration of five commercial platforms for targeted DNA methylome analysis M Tanić, I Moghul, S Rodney, P Dhami, H Vaikkinen, J Ambrose, J Barrett, ... Nature Biotechnology 40 (10), 1478-1487, 2022 | 11 | 2022 |
| Personalized model to predict keratoconus progression from demographic, topographic, and genetic data HP Maile, JPO Li, MD Fortune, P Royston, MT Leucci, I Moghul, A Szabo, ... American journal of ophthalmology 240, 321-329, 2022 | 11 | 2022 |
| Factors in color fundus photographs that can be used by humans to determine sex of individuals S Dieck, M Ibarra, I Moghul, MW Yeung, JT Pantel, S Thiele, M Pfau, ... Translational vision science & technology 9 (7), 8-8, 2020 | 9 | 2020 |
| Can artificial intelligence accelerate the diagnosis of inherited retinal diseases? Protocol for a data-only retrospective cohort study (Eye2Gene) Q Nguyen, W Woof, N Kabiri, S Sen, MD Varela, TAC De Guimaraes, ... BMJ open 13 (3), e071043, 2023 | 8 | 2023 |
| Whole-genome sequencing reveals a recurrent missense mutation in the Connexin 46 (GJA3) gene causing autosomal-dominant lamellar cataract V Berry, ACW Ionides, N Pontikos, I Moghul, AT Moore, ME Cheetham, ... Eye 32 (10), 1661-1668, 2018 | 8 | 2018 |
Nikolas PontikosPrincipal Investigator at UCLVerified email at ucl.ac.uk
