Clinical Utility of Implementing a Frontline NGS-Based DNA and RNA Fusion Panel Test for Patients with Suspected Myeloid Malignancies
暂无分享,去创建一个
B. Sadikovic | L. Schenkel | Hanxin Lin | A. Xenocostas | I. Chin-Yee | P. Bhai | M. Levy | J. Kerkhof | A. Stuart | B. Hedley | C. Hsia | Ping Yang | Stephanie Santos | R. Broadbent | Shirley Nan
[1] C. Howlett,et al. Reducing cytogenetic testing in the era of next generation sequencing: Are we choosing wisely? , 2021, International journal of laboratory hematology.
[2] P. Guglielmelli,et al. Impact of Mutational Profile on the Management of Myeloproliferative Neoplasms: A Short Review of the Emerging Data , 2020, OncoTargets and therapy.
[3] A. Gerasimova,et al. Analytical validation and performance characteristics of a 48-gene next-generation sequencing panel for detecting potentially actionable genomic alterations in myeloid neoplasms , 2020, bioRxiv.
[4] W. Blum,et al. Treating acute myeloid leukemia in the modern era: A primer , 2020, Cancer.
[5] A. Trumpp,et al. Survival differences and associated molecular signatures of DNMT3A-mutant acute myeloid leukemia patients , 2020, Scientific Reports.
[6] Ping Yang,et al. Clinical value of next‐generation sequencing compared to cytogenetics in patients with suspected myelodysplastic syndrome , 2020, British journal of haematology.
[7] P. Johansson,et al. ASXL1 mutations, previous vascular complications and age at diagnosis predict survival in 85 WHO‐defined polycythaemia vera patients , 2020, British journal of haematology.
[8] S. Saad,et al. Co-occurrence of DNMT3A, NPM1, FLT3 mutations identifies a subset of acute myeloid leukemia with adverse prognosis. , 2020, Blood.
[9] J. Cigudosa,et al. Spanish Guidelines for the use of targeted deep sequencing in myelodysplastic syndromes and chronic myelomonocytic leukaemia , 2019, British journal of haematology.
[10] P. Szankasi,et al. Chronic myelomonocytic leukemia with ETV6-ABL1 rearrangement and SMC1A mutation. , 2019, Cancer genetics.
[11] H. Feilotter,et al. Implementation of an NGS‐based sequencing and gene fusion panel for clinical screening of patients with suspected hematologic malignancies , 2019, European journal of haematology.
[12] E. Fermo,et al. The Role of New Technologies in Myeloproliferative Neoplasms , 2019, Front. Oncol..
[13] S. Ogawa. Genetics of MDS. , 2019, Blood.
[14] Annette S. Kim,et al. Clinical Significance of DNA Variants in Chronic Myeloid Neoplasms: A Report of the Association for Molecular Pathology. , 2018, The Journal of molecular diagnostics : JMD.
[15] U. Amstutz,et al. Challenges in the introduction of next-generation sequencing (NGS) for diagnostics of myeloid malignancies into clinical routine use , 2018, Blood Cancer Journal.
[16] Chieh-Yu Liu,et al. Incorporation of mutations in five genes in the revised International Prognostic Scoring System can improve risk stratification in the patients with myelodysplastic syndrome , 2018, Blood Cancer Journal.
[17] O. Abdel-Wahab,et al. Diagnosis and classification of hematologic malignancies on the basis of genetics. , 2017, Blood.
[18] K. Patel,et al. Diagnostic, Prognostic, and Predictive Utility of Recurrent Somatic Mutations in Myeloid Neoplasms , 2017, Clinical lymphoma, myeloma & leukemia.
[19] B. Ebert,et al. Clinical Implications of Genetic Mutations in Myelodysplastic Syndrome. , 2017, Journal of clinical oncology : official journal of the American Society of Clinical Oncology.
[20] Bob Löwenberg,et al. Diagnosis and management of AML in adults: 2017 ELN recommendations from an international expert panel. , 2017, Blood.
[21] B. Ebert,et al. The genetics of myelodysplastic syndrome: from clonal haematopoiesis to secondary leukaemia , 2016, Nature Reviews Cancer.
[22] J. Maciejewski,et al. Incorporation of molecular data into the Revised International Prognostic Scoring System in treated patients with myelodysplastic syndromes , 2016, Leukemia.
[23] Nicola D. Roberts,et al. Genomic Classification and Prognosis in Acute Myeloid Leukemia. , 2016, The New England journal of medicine.
[24] Mario Cazzola,et al. The 2016 revision to the World Health Organization classification of myeloid neoplasms and acute leukemia. , 2016, Blood.
[25] G. Marcucci,et al. Molecular prognostic factors in cytogenetically normal acute myeloid leukemia , 2012, Expert review of hematology.
[26] N. Socci,et al. Prognostic relevance of integrated genetic profiling in acute myeloid leukemia. , 2012, The New England journal of medicine.
[27] B. Smith,et al. Prognostically important molecular markers in cytogenetically normal acute myeloid leukemia. , 2011, The American journal of the medical sciences.
[28] D. Steensma. Novel therapies for myelodysplastic syndromes. , 2010, Hematology/oncology clinics of North America.
[29] Marilyn M. Li,et al. Standards and Guidelines for the Interpretation and Reporting of Sequence Variants in Cancer: A Joint Consensus Recommendation of the Association for Molecular Pathology, American Society of Clinical Oncology, and College of American Pathologists. , 2017, The Journal of molecular diagnostics : JMD.
[30] H. Deeg,et al. Myelodysplastic Syndromes, Version 2.2017, NCCN Clinical Practice Guidelines in Oncology. , 2017, Journal of the National Comprehensive Cancer Network : JNCCN.