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/vufind/Search/Results?lookfor=%22Benelli%2C+Matteo%22&type=Person&page=8
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PubPharm (116)
71
Validation of a method for noninvasive prenatal testing for fetal aneuploidies risk and considerations for its introduction in the Public Health System
enthalten in:
The journal of maternal-fetal & neonatal medicine
| 2017
von
Gerundino, F.
|
Giachini, C.
|
Contini, E.
| +23
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72
N-Myc Induces an EZH2-Mediated Transcriptional Program Driving Neuroendocrine Prostate Cancer
enthalten in:
Cancer cell
| 2016
von
Dardenne, E.
|
Beltran, H.
|
Benelli, M.
| +18
CommentIn: Transl Cancer Res. 2017 Feb;6(Suppl 1):S104-S108. - PMID 30613478
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73
Thin and thick primary cutaneous melanomas reveal distinct patterns of somatic copy number alterations
enthalten in:
Oncotarget
| 2016
von
Montagnani, V.
|
Benelli, M.
|
Apollo, A.
| +7
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74
Divergent clonal evolution of castration-resistant neuroendocrine prostate cancer
enthalten in:
Nature medicine
| 2016
von
Beltran, H.
|
Prandi, D.
|
Mosquera, J.
| +16
CommentIn: Nat Rev Urol. 2016 Apr;13(4):179. - PMID 26902334
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75
Divergent clonal evolution of castration-resistant neuroendocrine prostate cancer
enthalten in:
Nature medicine
| 2016
von
Beltran, H.
|
Prandi, D.
|
Mosquera, J.
| +16
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76
A novel founder MYO15A frameshift duplication is the major cause of genetic hearing loss in Oman
enthalten in:
Journal of human genetics
| 2016
von
Palombo, F.
|
Al-Wardy, N.
|
Ruscone, G.
| +15
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77
N-Myc Induces an EZH2-Mediated Transcriptional Program Driving Neuroendocrine Prostate Cancer
enthalten in:
Cancer cell
| 2016
von
Dardenne, E.
|
Beltran, H.
|
Benelli, M.
| +18
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78
A novel founder MYO15A frameshift duplication is the major cause of genetic hearing loss in Oman
enthalten in:
Journal of human genetics
| 2016
von
Palombo, F.
|
Al-Wardy, N.
|
Ruscone, G.
| +15
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79
Multilineage dysplasia as assessed by immunophenotype has no impact on clinical-biological features and outcome of NPM1-mutated acute myeloid leukemia
enthalten in:
Experimental hematology
| 2015
von
Mannelli, F.
|
Ponziani, V.
|
Bonetti, M.
| +12
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80
Expanding the mutational spectrum of LZTR1 in schwannomatosis
enthalten in:
European journal of human genetics : EJHG
| 2015
von
Paganini, I.
|
Chang, V.
|
Capone, G.
| +9
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75
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42
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14
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9
Biomarkers, Tumor
8
EC 2.7.10.1
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palbociclib
7
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7
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7
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7
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7
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2020-
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2010-2019
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