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For: Harbers L, Agostini F, Nicos M, Poddighe D, Bienko M, Crosetto N. Somatic Copy Number Alterations in Human Cancers: An Analysis of Publicly Available Data From The Cancer Genome Atlas. Front Oncol 2021;11:700568. [PMID: 34395272 DOI: 10.3389/fonc.2021.700568] [Cited by in Crossref: 10] [Cited by in F6Publishing: 11] [Article Influence: 5.0] [Reference Citation Analysis]
Number Citing Articles
1 Doig KD, Fellowes AP, Fox SB. Homologous Recombination Repair Deficiency: An Overview for Pathologists. Mod Pathol 2023;36:100049. [PMID: 36788098 DOI: 10.1016/j.modpat.2022.100049] [Reference Citation Analysis]
2 Wang L, Sun L, Sun H, Xing Y, Zhou S, An G, Li J, Ren K, Sun J. GPR65 as a potential immune checkpoint regulates the immune microenvironment according to pan-cancer analysis. Heliyon 2023;9:e13617. [PMID: 36852075 DOI: 10.1016/j.heliyon.2023.e13617] [Reference Citation Analysis]
3 Moorthi S, Paguirigan A, Ko M, Pettinger M, Hoge ACH, Nag A, Patel NA, Wu F, Sather C, Fitzgibbon MP, Thorner AR, Anderson GL, Ha G, Berger AH. Somatic mutation but not aneuploidy differentiates lung cancer in never-smokers and smokers. bioRxiv 2023:2023. [PMID: 36712079 DOI: 10.1101/2023.01.05.522947] [Reference Citation Analysis]
4 Cleynen A, Avet-loiseau H, Corre J. Unsupervized identification of prognostic copy-number alterations using segmentation and lasso regularization.. [DOI: 10.1101/2022.12.14.520497] [Reference Citation Analysis]
5 Traweek RS, Cope BM, Roland CL, Keung EZ, Nassif EF, Erstad DJ. Targeting the MDM2-p53 pathway in dedifferentiated liposarcoma. Front Oncol 2022;12. [DOI: 10.3389/fonc.2022.1006959] [Reference Citation Analysis]
6 Abujudeh S, Zeki SS, van Lanschot MCJ, Pusung M, Weaver JMJ, Li X, Noorani A, Metz AJ, Bornschein J, Bower L, Miremadi A, Fitzgerald RC, Morrissey ER, Lynch AG. Low-cost and clinically applicable copy number profiling using repeat DNA. BMC Genomics 2022;23:599. [PMID: 35978291 DOI: 10.1186/s12864-022-08681-8] [Reference Citation Analysis]
7 Jin S, Huang D, Jin W, Wang Y, Shao H, Gong L, Luo Z, Yang Z, Luan J, Xie D, Ding C. Detection of DNA copy number alterations by matrix-assisted laser desorption/ionization time-of-flight mass spectrometric analysis of single nucleotide polymorphisms. Clin Chem Lab Med 2022. [PMID: 35938948 DOI: 10.1515/cclm-2022-0511] [Cited by in F6Publishing: 1] [Reference Citation Analysis]
8 Striker SS, Wilferd SF, Lewis EM, O’connor SA, Plaisier CL. Systematic integration of protein affecting mutations, gene fusions, and copy number alterations into a comprehensive somatic mutational profile.. [DOI: 10.1101/2022.07.22.501139] [Reference Citation Analysis]
9 Peng A, Peng W, Wang R, Zhao H, Yu X, Sun Y. Regulation of 3D Organization and Its Role in Cancer Biology. Front Cell Dev Biol 2022;10:879465. [PMID: 35757006 DOI: 10.3389/fcell.2022.879465] [Reference Citation Analysis]
10 Ghose N, Kaliki S. Liquid biopsy in Retinoblastoma: A review. Semin Ophthalmol 2022;:1-7. [PMID: 35604935 DOI: 10.1080/08820538.2022.2078165] [Reference Citation Analysis]
11 Minkina A, Cao J, Shendure J. Tethering distinct molecular profiles of single cells by their lineage histories to investigate sources of cell state heterogeneity.. [DOI: 10.1101/2022.05.12.491602] [Cited by in Crossref: 1] [Cited by in F6Publishing: 1] [Article Influence: 1.0] [Reference Citation Analysis]
12 Ciccarone F, Bruno M, De Paolis E, Piermattei A, De Bonis M, Lorusso D, Zannoni GF, Normanno N, Minucci A, Scambia G, Ferrandina G. Role of Homologous Recombination Repair (HRR) Genes in Uterine Leiomyosarcomas: A Retrospective Analysis. Cancers (Basel) 2022;14:1934. [PMID: 35454841 DOI: 10.3390/cancers14081934] [Cited by in Crossref: 1] [Cited by in F6Publishing: 1] [Article Influence: 1.0] [Reference Citation Analysis]
13 Mcevoy AM, Schlessinger DI, Council ML. Cells to Surgery Quiz: January 2022. Journal of Investigative Dermatology 2022;142:e9-e14. [DOI: 10.1016/j.jid.2021.11.006] [Reference Citation Analysis]
14 Rozhoňová H, Danciu D, Stark S, Rätsch G, Kahles A, Lehmann K. SECEDO: SNV-based subclone detection using ultra-low coverage single-cell DNA sequencing.. [DOI: 10.1101/2021.11.08.467510] [Cited by in Crossref: 1] [Cited by in F6Publishing: 1] [Article Influence: 0.5] [Reference Citation Analysis]