1991 …2020

Research output per year

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Fingerprint Dive into the research topics where Massimo Carella is active. These topic labels come from the works of this person. Together they form a unique fingerprint.

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Research Output

  • 215 Article
  • 2 Conference contribution
  • 2 Comment/debate
  • 1 Review article

ACE2 gene variants may underlie interindividual variability and susceptibility to COVID-19 in the Italian population

GEN-COVID Multicenter Study, 2020, (Accepted/In press) In : European Journal of Human Genetics.

Research output: Contribution to journalArticle

Open Access
  • Clinical Significance of Circulating miR-1273g-3p and miR-122-5p in Pancreatic Cancer

    Mazza, T., Gioffreda, D., Fontana, A., Biagini, T., Carella, M., Palumbo, O., Maiello, E., Bazzocchi, F., Andriulli, A. & Tavano, F., Feb 4 2020, In : Frontiers in Oncology. 10, 44.

    Research output: Contribution to journalArticle

    Open Access
  • Compound phenotype due to recessive variants in larp7 and otog genes disclosed by an integrated approach of snp-array and whole exome sequencing

    Palumbo, P., Palumbo, O., Leone, M. P., Di Muro, E., Castellana, S., Bisceglia, L., Mazza, T., Carella, M. & Castori, M., Apr 2020, In : Genes. 11, 4, 379.

    Research output: Contribution to journalArticle

    Open Access
  • 1q23.1 homozygous deletion and downregulation of Fc receptor-like family genes confer poor prognosis in chronic lymphocytic leukemia

    Daniele, G., L’Abbate, A., Turchiano, A., Palumbo, O., Carella, M., Lo Cunsolo, C., Iuzzolino, P., Lonoce, A., Hernández-Sánchez, M., Minoia, C., Leone, P., Hernandez-Rivas, J. M. & Storlazzi, C. T., Jan 1 2019, In : Clinical and Experimental Medicine.

    Research output: Contribution to journalArticle

  • A novel dominant-negative FGFR1 variant causes Hartsfield syndrome by deregulating RAS/ERK1/2 pathway

    Palumbo, P., Petracca, A., Maggi, R., Biagini, T., Nardella, G., Sacco, M. C., Di Schiavi, E., Carella, M., Micale, L. & Castori, M., Jan 1 2019, In : European Journal of Human Genetics.

    Research output: Contribution to journalArticle