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For: Muskens IS, Zhang C, de Smith AJ, Biegel JA, Walsh KM, Wiemels JL. Germline genetic landscape of pediatric central nervous system tumors. Neuro Oncol 2019;21:1376-88. [PMID: 31247102 DOI: 10.1093/neuonc/noz108] [Cited by in Crossref: 7] [Cited by in F6Publishing: 4] [Article Influence: 3.5] [Reference Citation Analysis]
Number Citing Articles
1 Hakar MH, Wood MD. Updates in Pediatric Glioma Pathology. Surg Pathol Clin 2020;13:801-16. [PMID: 33183734 DOI: 10.1016/j.path.2020.08.006] [Reference Citation Analysis]
2 Huang W, Sundquist K, Sundquist J, Ji J. Psychiatric disorders in offspring of childhood or adolescent central nervous system tumor survivors: a national cohort study. Cancer Med 2021;10:675-83. [PMID: 33135321 DOI: 10.1002/cam4.3591] [Reference Citation Analysis]
3 Foss-Skiftesvik J, Stoltze UK. Genetic predisposition to central nervous system tumors in children - what the neurosurgeon should know. Acta Neurochir (Wien) 2022. [PMID: 35660974 DOI: 10.1007/s00701-022-05258-y] [Reference Citation Analysis]
4 Giannikou K, Zhu Z, Kim J, Winden KD, Tyburczy ME, Marron D, Parker JS, Hebert Z, Bongaarts A, Taing L, Long HW, Pisano WV, Alexandrescu S, Godlewski B, Nellist M, Kotulska K, Jozwiak S, Roszkowski M, Mandera M, Thiele EA, Lidov H, Getz G, Devinsky O, Lawrence MS, Ligon KL, Ellison DW, Sahin M, Aronica E, Meredith DM, Kwiatkowski DJ. Subependymal giant cell astrocytomas are characterized by mTORC1 hyperactivation, a very low somatic mutation rate, and a unique gene expression profile. Mod Pathol 2021;34:264-79. [PMID: 33051600 DOI: 10.1038/s41379-020-00659-9] [Reference Citation Analysis]
5 Chen W, Wang S, Tithi SS, Ellison DW, Schaid DJ, Wu G. A rare variant analysis framework using public genotype summary counts to prioritize disease-predisposition genes. Nat Commun 2022;13:2592. [PMID: 35545612 DOI: 10.1038/s41467-022-30248-0] [Reference Citation Analysis]
6 Hahn G, Mentzel HJ. [Tumors of the central nervous system in children and adolescents]. Radiologe 2021;61:601-10. [PMID: 34191042 DOI: 10.1007/s00117-021-00860-0] [Reference Citation Analysis]