Milan Radovich

  • 1764 Citations
  • 22 h-Index
20062019

Research output per year

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Publications

  • 1764 Citations
  • 22 h-Index
  • 50 Article
  • 4 Review article
  • 1 Comment/debate
  • 1 Letter

Precision prevention: The current state and future of genomically guided cancer prevention

Kassem, N., Stout, L. A., Hunter, C., Schneider, B. & Radovich, M., Jan 1 2019, In : JCO Precision Oncology. 3, p. 96-108 13 p.

Research output: Contribution to journalReview article

  • Profiling molecular regulators of recurrence in chemorefractory triple-negative breast cancers

    Hancock, B. A., Chen, Y. H., Solzak, J. P., Ahmad, M. N., Wedge, D. C., Brinza, D., Scafe, C., Veitch, J., Gottimukkala, R., Short, W., Atale, R. V., Ivan, M., Badve, S. S., Schneider, B. P., Lu, X., Miller, K. D. & Radovich, M., Aug 5 2019, In : Breast Cancer Research. 21, 1, 87.

    Research output: Contribution to journalArticle

    Open Access
  • 2 Scopus citations

    The nuclear hypoxia-regulated NLUCAT1 long non-coding RNA contributes to an aggressive phenotype in lung adenocarcinoma through regulation of oxidative stress

    Moreno Leon, L., Gautier, M., Allan, R., Ilié, M., Nottet, N., Pons, N., Paquet, A., Lebrigand, K., Truchi, M., Fassy, J., Magnone, V., Kinnebrew, G., Radovich, M., Cheok, M. H. C., Barbry, P., Vassaux, G., Marquette, C. H., Ponzio, G., Ivan, M., Pottier, N. & 3 others, Hofman, P., Mari, B. & Rezzonico, R., Nov 14 2019, In : Oncogene. 38, 46, p. 7146-7165 20 p.

    Research output: Contribution to journalArticle

  • 3 Scopus citations

    Allelic decomposition and exact genotyping of highly polymorphic and structurally variant genes

    Numanagić, I., Malikić, S., Ford, M., Qin, X., Toji, L., Radovich, M., Skaar, T. C., Pratt, V. M., Berger, B., Scherer, S. & Sahinalp, S. C., Dec 1 2018, In : Nature communications. 9, 1, 828.

    Research output: Contribution to journalArticle

  • 7 Scopus citations

    Cancer-associated rs6983267 SNP and its accompanying long noncoding RNA CCAT2 induce myeloid malignancies via unique SNP-specific RNA mutations

    Shah, M. Y., Ferracin, M., Pileczki, V., Chen, B., Redis, R., Fabris, L., Zhang, X., Ivan, C., Shimizu, M., Rodriguez-Aguayo, C., Dragomir, M., Van Roosbroeck, K., Almeida, M. I., Ciccone, M., Nedelcu, D., Cortez, M. A., Manshouri, T., Calin, S., Muftuoglu, M., Banerjee, P. P. & 24 others, Badiwi, M. H., Parker-Thornburg, J., Multani, A., Welsh, J. W., Estecio, M. R., Ling, H., Tomuleasa, C., Dima, D., Yang, H., Alvarez, H., You, M. J., Radovich, M., Shpall, E., Fabbri, M., Rezvani, K., Girnita, L., Berindan-Neagoe, I., Maitra, A., Verstovsek, S., Fodde, R., Bueso-Ramos, C., Gagea, M., Manero, G. G. & Calin, G. A., Apr 2018, In : Genome research. 28, 4, p. 432-447 16 p.

    Research output: Contribution to journalArticle

  • 20 Scopus citations