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Cited by in F6Publishing
For: Duran-lozano L, Montalban G, Bonache S, Moles-fernández A, Tenés A, Castroviejo-bermejo M, Carrasco E, López-fernández A, Torres-esquius S, Gadea N, Stjepanovic N, Balmaña J, Gutiérrez-enríquez S, Diez O. Alternative transcript imbalance underlying breast cancer susceptibility in a family carrying PALB2 c.3201+5G>T. Breast Cancer Res Treat 2019;174:543-50. [DOI: 10.1007/s10549-018-05094-8] [Cited by in Crossref: 5] [Cited by in F6Publishing: 3] [Article Influence: 1.3] [Reference Citation Analysis]
Number Citing Articles
1 Grasel RS, Felicio PS, de Paula AE, Campacci N, Garcia FAO, de Andrade ES, Evangelista AF, Fernandes GC, Sabato CDS, De Marchi P, Souza CP, de Paula CAA, Torrezan GT, Galvão HCR, Carraro DM, Palmero EI. Using Co-segregation and Loss of Heterozygosity Analysis to Define the Pathogenicity of Unclassified Variants in Hereditary Breast Cancer Patients. Front Oncol 2020;10:571330. [PMID: 33134171 DOI: 10.3389/fonc.2020.571330] [Cited by in Crossref: 1] [Cited by in F6Publishing: 1] [Article Influence: 0.5] [Reference Citation Analysis]
2 Robles-Espinoza CD, Mohammadi P, Bonilla X, Gutierrez-Arcelus M. Allele-specific expression: applications in cancer and technical considerations. Curr Opin Genet Dev 2021;66:10-9. [PMID: 33383480 DOI: 10.1016/j.gde.2020.10.007] [Reference Citation Analysis]
3 Lian DS, Chen XY, Zeng HS, Wang YY. Capillary electrophoresis based on nucleic acid analysis for diagnosing inherited diseases. Clin Chem Lab Med 2020;59:249-66. [PMID: 32374277 DOI: 10.1515/cclm-2020-0186] [Reference Citation Analysis]