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Cited by in F6Publishing
For: Pal LR, Kundu K, Yin Y, Moult J. Matching whole genomes to rare genetic disorders: Identification of potential causative variants using phenotype-weighted knowledge in the CAGI SickKids5 clinical genomes challenge. Hum Mutat 2020;41:347-62. [PMID: 31680375 DOI: 10.1002/humu.23933] [Cited by in F6Publishing: 2] [Reference Citation Analysis]
Number Citing Articles
1 Katsonis P, Wilhelm K, Williams A, Lichtarge O. Genome interpretation using in silico predictors of variant impact. Hum Genet 2022. [PMID: 35488922 DOI: 10.1007/s00439-022-02457-6] [Reference Citation Analysis]
2 Andreoletti G, Pal LR, Moult J, Brenner SE. Reports from the fifth edition of CAGI: The Critical Assessment of Genome Interpretation. Hum Mutat 2019;40:1197-201. [PMID: 31334884 DOI: 10.1002/humu.23876] [Cited by in Crossref: 24] [Cited by in F6Publishing: 24] [Article Influence: 8.0] [Reference Citation Analysis]