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For: Shen T, Lee A, Shen C, Lin CJ. The long tail and rare disease research: the impact of next-generation sequencing for rare Mendelian disorders. Genet Res (Camb) 2015;97:e15. [PMID: 26365496 DOI: 10.1017/S0016672315000166] [Cited by in Crossref: 13] [Cited by in F6Publishing: 9] [Article Influence: 1.9] [Reference Citation Analysis]
Number Citing Articles
1 Hong S, Wang L, Zhao D, Zhang Y, Chen Y, Tan J, Liang L, Zhu T. Clinical utility in infants with suspected monogenic conditions through next-generation sequencing. Mol Genet Genomic Med 2019;7:e684. [PMID: 30968598 DOI: 10.1002/mgg3.684] [Cited by in Crossref: 1] [Cited by in F6Publishing: 2] [Article Influence: 0.3] [Reference Citation Analysis]
2 Sayyab S, Viluma A, Bergvall K, Brunberg E, Jagannathan V, Leeb T, Andersson G, Bergström TF. Whole-Genome Sequencing of a Canine Family Trio Reveals a FAM83G Variant Associated with Hereditary Footpad Hyperkeratosis. G3 (Bethesda) 2016;6:521-7. [PMID: 26747202 DOI: 10.1534/g3.115.025643] [Cited by in Crossref: 14] [Cited by in F6Publishing: 13] [Article Influence: 2.3] [Reference Citation Analysis]
3 Yan T, Li J, Zhou X, Yang Z, Zhang Y, Zhang J, Xu N, Huang Y, Yang H. Genetic determinants of fracture non-union: A systematic review from the literature. Gene 2020;751:144766. [PMID: 32413481 DOI: 10.1016/j.gene.2020.144766] [Cited by in Crossref: 1] [Article Influence: 0.5] [Reference Citation Analysis]
4 Ekins S. Industrializing rare disease therapy discovery and development. Nat Biotechnol 2017;35:117-8. [PMID: 28178258 DOI: 10.1038/nbt.3787] [Cited by in Crossref: 17] [Cited by in F6Publishing: 15] [Article Influence: 4.3] [Reference Citation Analysis]
5 Cremers S, Aronson JK. Drugs for rare disorders. Br J Clin Pharmacol 2017;83:1607-13. [PMID: 28653488 DOI: 10.1111/bcp.13331] [Cited by in Crossref: 9] [Cited by in F6Publishing: 7] [Article Influence: 1.8] [Reference Citation Analysis]
6 Yates J, Gutiérrez-Sacristán A, Jouhet V, LeBlanc K, Esteves C, DeSain TN, Benik N, Stedman J, Palmer N, Mellon G, Kohane I, Avillach P; Undiagnosed Diseases Network. Finding commonalities in rare diseases through the undiagnosed diseases network. J Am Med Inform Assoc 2021;28:1694-702. [PMID: 34009343 DOI: 10.1093/jamia/ocab050] [Reference Citation Analysis]
7 Mossotto E, Ashton JJ, O'Gorman L, Pengelly RJ, Beattie RM, MacArthur BD, Ennis S. GenePy - a score for estimating gene pathogenicity in individuals using next-generation sequencing data. BMC Bioinformatics 2019;20:254. [PMID: 31096927 DOI: 10.1186/s12859-019-2877-3] [Cited by in Crossref: 5] [Cited by in F6Publishing: 5] [Article Influence: 1.7] [Reference Citation Analysis]
8 Schwarz JM, Hombach D, Köhler S, Cooper DN, Schuelke M, Seelow D. RegulationSpotter: annotation and interpretation of extratranscriptic DNA variants. Nucleic Acids Res 2019;47:W106-13. [PMID: 31106382 DOI: 10.1093/nar/gkz327] [Cited by in Crossref: 3] [Cited by in F6Publishing: 3] [Article Influence: 1.5] [Reference Citation Analysis]
9 Blazejewski SM, Bennison SA, Smith TH, Toyo-Oka K. Neurodevelopmental Genetic Diseases Associated With Microdeletions and Microduplications of Chromosome 17p13.3. Front Genet 2018;9:80. [PMID: 29628935 DOI: 10.3389/fgene.2018.00080] [Cited by in Crossref: 28] [Cited by in F6Publishing: 23] [Article Influence: 7.0] [Reference Citation Analysis]
10 Seoighe C, Bracken AP, Buckley P, Doran P, Green R, Healy S, Kavanagh D, Kenny E, Lawler M, Lowery M, Morris D, Morrissey D, O'Byrne JJ, Shields D, Smith O, Steward CA, Sweeney B, Kolch W. The future of genomics in Ireland - focus on genomics for health. HRB Open Res 2020;3:89. [PMID: 33855271 DOI: 10.12688/hrbopenres.13187.1] [Reference Citation Analysis]