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For: Sarkadi B, Liko I, Nyiro G, Igaz P, Butz H, Patocs A. Analytical Performance of NGS-Based Molecular Genetic Tests Used in the Diagnostic Workflow of Pheochromocytoma/Paraganglioma. Cancers (Basel) 2021;13:4219. [PMID: 34439371 DOI: 10.3390/cancers13164219] [Cited by in Crossref: 1] [Cited by in F6Publishing: 1] [Article Influence: 0.5] [Reference Citation Analysis]
Number Citing Articles
1 Li C, Li J, Han C, Wang T, Zhang L, Wang Z, Wang T, Xu L, Qi G, Qin G, Li X, Zheng L. Novel and recurrent genetic variants of VHL, SDHB, and RET genes in Chinese pheochromocytoma and paraganglioma patients. Front Genet 2023;14:959989. [PMID: 36936415 DOI: 10.3389/fgene.2023.959989] [Reference Citation Analysis]
2 Grolmusz VK, Nagy P, Likó I, Butz H, Pócza T, Bozsik A, Papp J, Oláh E, Patócs A. A common genetic variation in GZMB may associate with cancer risk in patients with Lynch syndrome. Front Oncol 2023;13:1005066. [PMID: 36890824 DOI: 10.3389/fonc.2023.1005066] [Reference Citation Analysis]
3 Igaz P. New Insights in the Genetics and Genomics of Adrenocortical Tumors and Pheochromocytomas. Cancers (Basel) 2022;14:1094. [PMID: 35205841 DOI: 10.3390/cancers14041094] [Reference Citation Analysis]