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Cited by in F6Publishing
For: Ellingford JM, Ahn JW, Bagnall RD, Baralle D, Barton S, Campbell C, Downes K, Ellard S, Duff-farrier C, Fitzpatrick DR, Ingles J, Krishnan N, Lord J, Martin HC, Newman WG, O’donnell-luria A, Ramsden SC, Rehm HL, Richardson E, Singer-berk M, Taylor JC, Williams M, Wood JC, Wright CF, Harrison SM, Whiffin N. Recommendations for clinical interpretation of variants found in non-coding regions of the genome.. [DOI: 10.1101/2021.12.28.21267792] [Cited by in Crossref: 1] [Cited by in F6Publishing: 1] [Article Influence: 0.5] [Reference Citation Analysis]
Number Citing Articles
1 Tabet D, Parikh V, Mali P, Roth FP, Claussnitzer M. Scalable Functional Assays for the Interpretation of Human Genetic Variation. Annu Rev Genet 2022;56:441-65. [PMID: 36055970 DOI: 10.1146/annurev-genet-072920-032107] [Reference Citation Analysis]
2 Dofash LN, Monahan G, Servián-morilla E, Rivas E, Faiz F, Sullivan P, Oates E, Clayton J, Taylor RL, Davis MR, Beilharz T, Laing NG, Cabrera-serrano M, Ravenscroft G. A KLHL40 3’ UTR splice-altering variant causes milder NEM8, an under-appreciated disease mechanism.. [DOI: 10.1101/2022.08.08.22278402] [Reference Citation Analysis]