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Table representation of search results timeline featuring number of search results per year.

Year Number of Results
2016 2
2017 3
2018 1
2019 7
2020 6
2021 2
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Page 1
Phenogenon: Gene to phenotype associations for rare genetic diseases.
Pontikos N, Murphy C, Moghul I, Arno G, Fujinami K, Fujinami Y, Sumodhee D, Downes S, Webster A, Yu J; UK Inherited Retinal Dystrophy Consortium, Phenopolis Consortium. Pontikos N, et al. Among authors: moghul i. PLoS One. 2020 Apr 9;15(4):e0230587. doi: 10.1371/journal.pone.0230587. eCollection 2020. PLoS One. 2020. PMID: 32271766 Free PMC article.
Diagnostic Approaches to Neuroendocrine Neoplasms of Unknown Primary Site.
Berner AM, Pipinikas C, Ryan A, Dibra H, Moghul I, Webster A, Luong TV, Thirlwell C. Berner AM, et al. Among authors: moghul i. Neuroendocrinology. 2020;110(7-8):563-573. doi: 10.1159/000504370. Epub 2019 Oct 28. Neuroendocrinology. 2020. PMID: 31658461 Free article. Review.
GenomeChronicler: The Personal Genome Project UK Genomic Report Generator Pipeline.
Guerra-Assunção JA, Conde L, Moghul I, Webster AP, Ecker S, Chervova O, Chatzipantsiou C, Prieto PP, Beck S, Herrero J. Guerra-Assunção JA, et al. Among authors: moghul i. Front Genet. 2020 Sep 24;11:518644. doi: 10.3389/fgene.2020.518644. eCollection 2020. Front Genet. 2020. PMID: 33193602 Free PMC article.
Sequenceserver: A Modern Graphical User Interface for Custom BLAST Databases.
Priyam A, Woodcroft BJ, Rai V, Moghul I, Munagala A, Ter F, Chowdhary H, Pieniak I, Maynard LJ, Gibbins MA, Moon H, Davis-Richardson A, Uludag M, Watson-Haigh NS, Challis R, Nakamura H, Favreau E, Gómez EA, Pluskal T, Leonard G, Rumpf W, Wurm Y. Priyam A, et al. Among authors: moghul i. Mol Biol Evol. 2019 Dec 1;36(12):2922-2924. doi: 10.1093/molbev/msz185. Mol Biol Evol. 2019. PMID: 31411700 Free PMC article.
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