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Cited by in F6Publishing
For: [DOI: 10.1101/459123] [Cited by in Crossref: 7] [Cited by in F6Publishing: 6] [Reference Citation Analysis]
Number Citing Articles
1 Povysil G, Petrovski S, Hostyk J, Aggarwal V, Allen AS, Goldstein DB. Rare-variant collapsing analyses for complex traits: guidelines and applications. Nat Rev Genet 2019;20:747-59. [PMID: 31605095 DOI: 10.1038/s41576-019-0177-4] [Cited by in Crossref: 90] [Cited by in F6Publishing: 97] [Article Influence: 22.5] [Reference Citation Analysis]
2 Yao DW, O’connor LJ, Price AL, Gusev A. Quantifying genetic effects on disease mediated by assayed gene expression levels.. [DOI: 10.1101/730549] [Cited by in Crossref: 12] [Cited by in F6Publishing: 11] [Article Influence: 3.0] [Reference Citation Analysis]
3 Verweij N, Benjamins J, Morley MP, van de Vegte Y, Teumer A, Trenkwalder T, Reinhard W, Cappola TP, van der Harst P. The genetic makeup of the electrocardiogram.. [DOI: 10.1101/648527] [Cited by in Crossref: 1] [Article Influence: 0.3] [Reference Citation Analysis]
4 Mohammadi P, Castel SE, Cummings BB, Einson J, Sousa C, Hoffman P, Donkervoort S, Mohassel P, Foley R, Wheeler HE, Im HK, Bonnemann CG, Macarthur DG, Lappalainen T. Quantifying genetic regulatory variation in human populations improves transcriptome analysis in rare disease patients.. [DOI: 10.1101/632794] [Cited by in Crossref: 2] [Cited by in F6Publishing: 2] [Article Influence: 0.5] [Reference Citation Analysis]
5 [DOI: 10.1101/655670] [Cited by in Crossref: 11] [Cited by in F6Publishing: 10] [Reference Citation Analysis]
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