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Year Number of Results
2014 1
2015 3
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2017 3
2019 2
2020 2
2021 6
2022 1
2023 2
2024 2

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Page 1
Clinical significance of somatic mutation in unexplained blood cytopenia.
Malcovati L, Gallì A, Travaglino E, Ambaglio I, Rizzo E, Molteni E, Elena C, Ferretti VV, Catricalà S, Bono E, Todisco G, Bianchessi A, Rumi E, Zibellini S, Pietra D, Boveri E, Camaschella C, Toniolo D, Papaemmanuil E, Ogawa S, Cazzola M. Malcovati L, et al. Among authors: rizzo e. Blood. 2017 Jun 22;129(25):3371-3378. doi: 10.1182/blood-2017-01-763425. Epub 2017 Apr 19. Blood. 2017. PMID: 28424163 Free PMC article.
Critical assessment of variant prioritization methods for rare disease diagnosis within the Rare Genomes Project.
Stenton SL, O'Leary M, Lemire G, VanNoy GE, DiTroia S, Ganesh VS, Groopman E, O'Heir E, Mangilog B, Osei-Owusu I, Pais LS, Serrano J, Singer-Berk M, Weisburd B, Wilson M, Austin-Tse C, Abdelhakim M, Althagafi A, Babbi G, Bellazzi R, Bovo S, Carta MG, Casadio R, Coenen PJ, De Paoli F, Floris M, Gajapathy M, Hoehndorf R, Jacobsen JOB, Joseph T, Kamandula A, Katsonis P, Kint C, Lichtarge O, Limongelli I, Lu Y, Magni P, Mamidi TKK, Martelli PL, Mulargia M, Nicora G, Nykamp K, Pejaver V, Peng Y, Pham THC, Podda MS, Rao A, Rizzo E, Saipradeep VG, Savojardo C, Schols P, Shen Y, Sivadasan N, Smedley D, Soru D, Srinivasan R, Sun Y, Sunderam U, Tan W, Tiwari N, Wang X, Wang Y, Williams A, Worthey EA, Yin R, You Y, Zeiberg D, Zucca S, Bakolitsa C, Brenner SE, Fullerton SM, Radivojac P, Rehm HL, O'Donnell-Luria A. Stenton SL, et al. Among authors: rizzo e. medRxiv [Preprint]. 2023 Aug 4:2023.08.02.23293212. doi: 10.1101/2023.08.02.23293212. medRxiv. 2023. PMID: 37577678 Free PMC article. Preprint.
Mutational and immunogenetic landscape of HCV-associated B-cell lymphoproliferative disorders.
Defrancesco I, Visentini M, Zibellini S, Minafò YA, Rattotti S, Ferretti VV, Rizzo E, Varettoni M, Frigeni M, Pulsoni A, Casato M, Colantuono S, Rossi M, Candido C, Zerbi C, Bergamini F, Cristinelli C, Fabbri N, Merli M, Zuccaro V, Bruno R, Paulli M, Arcaini L. Defrancesco I, et al. Among authors: rizzo e. Am J Hematol. 2021 Jun 1;96(6):E210-E214. doi: 10.1002/ajh.26167. Epub 2021 Apr 9. Am J Hematol. 2021. PMID: 33755245 Free PMC article. No abstract available.
Comprehensive kinome NGS targeted expression profiling by KING-REX.
Carapezza G, Cusi C, Rizzo E, Raddrizzani L, Di Bella S, Somaschini A, Leone A, Lupi R, Mutarelli M, Nigro V, di Bernardo D, Magni P, Isacchi A, Bosotti R. Carapezza G, et al. Among authors: rizzo e. BMC Genomics. 2019 Apr 23;20(1):307. doi: 10.1186/s12864-019-5676-3. BMC Genomics. 2019. PMID: 31014245 Free PMC article.
Relationship between clone metrics and clinical outcome in clonal cytopenia.
Gallì A, Todisco G, Catamo E, Sala C, Elena C, Pozzi S, Bono E, Ferretti VV, Rizzo E, Molteni E, Zibellini S, Sarchi M, Boveri E, Ferrari J, Fiorelli N, Camaschella C, Gasparini P, Toniolo D, Cazzola M, Malcovati L. Gallì A, et al. Among authors: rizzo e. Blood. 2021 Sep 16;138(11):965-976. doi: 10.1182/blood.2021011323. Blood. 2021. PMID: 34255818 Free article.
Sequential next generation sequencing analysis in homogeneously treated low risk NPM1-mutated acute myeloid leukemia with an adverse clinical outcome.
Rossi M, Nizzoli ME, Gallì A, Roncoroni E, Zibellini S, Merati G, Rizzo E, Rocca B, Pietra D, Picone C, Brociner M, Tobar Cabrera CP, Gelli E, Santacroce E, Arcaini L, Zappasodi P. Rossi M, et al. Among authors: rizzo e. Am J Hematol. 2022 Apr;97(4):E135-E138. doi: 10.1002/ajh.26469. Epub 2022 Jan 24. Am J Hematol. 2022. PMID: 35041232 Free article. No abstract available.
Incidence and prognosis of clonal hematopoiesis in patients with chronic idiopathic neutropenia.
Tsaknakis G, Gallì A, Papadakis S, Kanellou P, Elena C, Todisco G, Bono E, Rizzo E, Molteni E, Fragiadaki I, Mavroudi I, Pontikoglou C, Batas A, Maxouri S, Linardaki E, Tavernarakis N, Malcovati L, Papadaki HA. Tsaknakis G, et al. Among authors: rizzo e. Blood. 2021 Oct 7;138(14):1249-1257. doi: 10.1182/blood.2021010815. Blood. 2021. PMID: 34166485 Free article.
Enrichment of Double RUNX1 Mutations in Acute Leukemias of Ambiguous Lineage.
Merati G, Rossi M, Gallì A, Roncoroni E, Zibellini S, Rizzo E, Pietra D, Picone C, Rocca B, Cabrera CPT, Gelli E, Santacroce E, Arcaini L, Zappasodi P. Merati G, et al. Among authors: rizzo e. Front Oncol. 2021 Aug 31;11:726637. doi: 10.3389/fonc.2021.726637. eCollection 2021. Front Oncol. 2021. PMID: 34540694 Free PMC article.
Scalable and cost-effective NGS genotyping in the cloud.
Souilmi Y, Lancaster AK, Jung JY, Rizzo E, Hawkins JB, Powles R, Amzazi S, Ghazal H, Tonellato PJ, Wall DP. Souilmi Y, et al. Among authors: rizzo e. BMC Med Genomics. 2015 Oct 15;8:64. doi: 10.1186/s12920-015-0134-9. BMC Med Genomics. 2015. PMID: 26470712 Free PMC article.
23 results