• 7205 Citations
  • 41 h-Index
1976 …2018
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Fingerprint Dive into the research topics where Giuseppe Opocher is active. These topic labels come from the works of this person. Together they form a unique fingerprint.

  • 15 Similar Profiles
Pheochromocytoma Medicine & Life Sciences
Paraganglioma Medicine & Life Sciences
Aldosterone Medicine & Life Sciences
Mutation Medicine & Life Sciences
von Hippel-Lindau Disease Medicine & Life Sciences
Hyperaldosteronism Medicine & Life Sciences
Genes Medicine & Life Sciences
Neoplasms Medicine & Life Sciences

Network Recent external collaboration on country level. Dive into details by clicking on the dots.

Research Output 1976 2018

  • 7205 Citations
  • 41 h-Index
  • 193 Article
  • 3 Conference contribution
  • 2 Chapter
  • 1 Review article

65 YEARS OF THE DOUBLE HELIX: Genetics informs precision practice in the diagnosis and management of pheochromocytoma

Neumann, H. P., Young, W. F., Krauss, T., Bayley, J-P., Schiavi, F., Opocher, G., Boedeker, C. C., Tirosh, A., Castinetti, F., Ruf, J., Beltsevich, D., Walz, M., Groeben, H-T., von Dobschuetz, E., Gimm, O., Wohllk, N., Pfeifer, M., Lourenço, D. M., Peczkowska, M., Patocs, A. & 10 others, Ngeow, J., Makay, Ö., Shah, N. S., Tischler, A., Leijon, H., Pennelli, G., Villar Gómez de Las Heras, K., Links, T. P., Bausch, B. & Eng, C., Aug 2018, In : Endocrine-Related Cancer. 25, 8, p. T201-T219

Research output: Contribution to journalReview article

Pheochromocytoma
Paraganglioma
Genes
Neoplasms
Germ-Line Mutation

Correction to: Multiple endocrine neoplasia type 1: analysis of germline MEN1 mutations in the Italian multicenter MEN1 patient database (Endocrine, (2018), 10.1007/s12020-018-1566-8)

Marini, F., Giusti, F., Fossi, C., Cioppi, F., Cianferotti, L., Masi, L., Boaretto, F., Zovato, S., Cetani, F., Colao, A., Davì, M. V., Faggiano, A., Fanciulli, G., Ferolla, P., Ferone, D., Loli, P., Mantero, F., Marcocci, C., Opocher, G., Beck-Peccoz, P. & 7 others, Persani, L., Scillitani, A., Guizzardi, F., Spada, A., Tomassetti, P., Tonelli, F. & Brandi, M. L., Jan 1 2018, (Accepted/In press) In : Endocrine.

Research output: Contribution to journalArticle

Multiple Endocrine Neoplasia Type 1
Germ-Line Mutation
Publications
Databases

Gain-of-function mutations in DNMT3A in patients with paraganglioma

Remacha, L., Currás-Freixes, M., Torres-Ruiz, R., Schiavi, F., Torres-Pérez, R., Calsina, B., Letón, R., Comino-Méndez, I., Roldán-Romero, J. M., Montero-Conde, C., Santos, M., Pérez, L. I., Pita, G., Alonso, M. R., Honrado, E., Pedrinaci, S., Crespo-Facorro, B., Percesepe, A., Falcioni, M., Rodríguez-Perales, S. & 6 others, Korpershoek, E., Ramón-Maiques, S., Opocher, G., Rodríguez-Antona, C., Robledo, M. & Cascón, A., May 8 2018, In : Genetics in Medicine.

Research output: Contribution to journalArticle

Paraganglioma
Germ-Line Mutation
Clustered Regularly Interspaced Short Palindromic Repeats
Mutation
Pheochromocytoma

Multiple endocrine neoplasia type 1

Marini, F., Giusti, F., Fossi, C., Cioppi, F., Cianferotti, L., Masi, L., Boaretto, F., Zovato, S., Cetani, F., Colao, A., Davì, M. V., Faggiano, A., Fanciulli, G., Ferolla, P., Ferone, D., Loli, P., Mantero, F., Marcocci, C., Opocher, G., Beck-Peccoz, P. & 7 others, Persani, L., Scillitani, A., Guizzardi, F., Spada, A., Tomassetti, P., Tonelli, F. & Brandi, M. L., Oct 1 2018, In : Endocrine. 62, 1, p. 215-233 19 p.

Research output: Contribution to journalArticle

3 Citations (Scopus)

Multiple endocrine neoplasia type 1: analysis of germline MEN1 mutations in the Italian multicenter MEN1 patient database

Marini, F., Giusti, F., Fossi, C., Cioppi, F., Cianferotti, L., Masi, L., Boaretto, F., Zovato, S., Cetani, F., Colao, A., Davì, M. V., Faggiano, A., Fanciulli, G., Ferolla, P., Ferone, D., Loli, P., Mantero, F., Marcocci, C., Opocher, G., Beck-Peccoz, P. & 7 others, Persani, L., Scillitani, A., Guizzardi, F., Spada, A., Tomassetti, P., Tonelli, F. & Brandi, M. L., Oct 1 2018, In : Endocrine. 62, 1, p. 215-233 19 p.

Research output: Contribution to journalArticle

Multiple Endocrine Neoplasia Type 1
Databases
Mutation
Exons
Multiple Endocrine Neoplasia