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Table representation of search results timeline featuring number of search results per year.

Year Number of Results
1972 1
1995 3
1997 1
1998 1
1999 1
2001 1
2003 2
2004 1
2005 3
2006 1
2007 4
2008 3
2009 2
2010 5
2011 3
2012 4
2013 3
2014 2
2015 2
2016 2
2017 2
2018 3
2019 1
2020 5
2021 5
2022 5
2023 3
2024 0

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64 results

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Page 1
A guilt-by-association mutation network in LGL leukemia.
Andersson EI, Coppe A, Bortoluzzi S. Andersson EI, et al. Among authors: coppe a. Oncotarget. 2017 Oct 9;8(55):93299-93300. doi: 10.18632/oncotarget.21699. eCollection 2017 Nov 7. Oncotarget. 2017. PMID: 29212142 Free PMC article. No abstract available.
Optical coherence tomography.
Ripandelli G, Coppé AM, Capaldo A, Stirpe M. Ripandelli G, et al. Among authors: coppe am. Semin Ophthalmol. 1998 Dec;13(4):199-202. doi: 10.3109/08820539809056053. Semin Ophthalmol. 1998. PMID: 9878670 Review.
A Novel Autosomal Recessive Variant of the NRL Gene Causing Enhanced S-Cone Syndrome: A Morpho-Functional Analysis of Two Unrelated Pediatric Patients.
Iarossi G, Sinibaldi L, Passarelli C, Coppe' AM, Cappelli A, Petrocelli G, Catena G, Perrone C, Falsini B, Novelli A, Bartuli A, Buzzonetti L. Iarossi G, et al. Among authors: coppe am. Diagnostics (Basel). 2022 Sep 9;12(9):2183. doi: 10.3390/diagnostics12092183. Diagnostics (Basel). 2022. PMID: 36140584 Free PMC article.
A high definition picture of key genes and pathways mutated in pediatric follicular lymphoma.
Lovisa F, Binatti A, Coppe A, Primerano S, Carraro E, Pillon M, Pizzi M, Guzzardo V, Buffardi S, Porta F, Farruggia P, De Santis R, Bulian P, Basso G, Lazzari E, d'Amore ESG, Bortoluzzi S, Mussolin L. Lovisa F, et al. Among authors: coppe a. Haematologica. 2019 Sep;104(9):e406-e409. doi: 10.3324/haematol.2018.211631. Epub 2019 Feb 28. Haematologica. 2019. PMID: 30819919 Free PMC article. No abstract available.
Multiomic analysis of HER2-enriched and AR-positive breast carcinoma with apocrine differentiation and an oligometastatic course: a case report.
Poggiali B, Ponzetti A, Malerba M, Landuzzi F, Furia F, Charrance D, Trova S, Perseghin V, Falcone PA, Alliod V, Malossi A, Carassai P, Familiari U, Vecchi M, Gustincich S, Schena M, Cavalli A, Coppe A. Poggiali B, et al. Among authors: coppe a. Front Oncol. 2023 Jul 31;13:1240865. doi: 10.3389/fonc.2023.1240865. eCollection 2023. Front Oncol. 2023. PMID: 37583932 Free PMC article.
MAGIA, a web-based tool for miRNA and Genes Integrated Analysis.
Sales G, Coppe A, Bisognin A, Biasiolo M, Bortoluzzi S, Romualdi C. Sales G, et al. Among authors: coppe a. Nucleic Acids Res. 2010 Jul;38(Web Server issue):W352-9. doi: 10.1093/nar/gkq423. Epub 2010 May 19. Nucleic Acids Res. 2010. PMID: 20484379 Free PMC article.
A data-driven network model of primary myelofibrosis: transcriptional and post-transcriptional alterations in CD34+ cells.
Calura E, Pizzini S, Bisognin A, Coppe A, Sales G, Gaffo E, Fanelli T, Mannarelli C, Zini R, Norfo R, Pennucci V, Manfredini R, Romualdi C, Guglielmelli P, Vannucchi AM, Bortoluzzi S. Calura E, et al. Among authors: coppe a. Blood Cancer J. 2016 Jun 24;6(6):e439. doi: 10.1038/bcj.2016.47. Blood Cancer J. 2016. PMID: 27341078 Free PMC article.
64 results