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Ismail Moghul
Ismail Moghul
在 ucl.ac.uk 的电子邮件经过验证 - 首页
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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
2662019
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
1332016
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
702017
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
462017
GeneValidator: identify problems with protein-coding gene predictions
MA Drăgan, I Moghul, A Priyam, C Bustos, Y Wurm
Bioinformatics 32 (10), 1559-1561, 2016
422016
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
352021
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
32*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
312018
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
282020
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
262019
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
212021
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
192019
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
142023
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
142021
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
142017
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
9*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
92022
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
92020
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
82018
Phenogenon: gene to phenotype associations for rare genetic diseases
N Pontikos, C Murphy, I Moghul, G Arno, K Fujinami, Y Fujinami, ...
PLoS One 15 (4), e0230587, 2020
72020
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