Detalhe da pesquisa
1.
Comparing malignant monocytosis across the updated WHO and ICC classifications of 2022.
Blood
; 143(12): 1139-1156, 2024 Mar 21.
Artigo
em Inglês
| MEDLINE | ID: mdl-38064663
2.
Prevalence and Therapeutic Implications of Clonal Hematopoiesis of Indeterminate Potential in Young Patients With Stroke.
Stroke
; 54(4): 938-946, 2023 04.
Artigo
em Inglês
| MEDLINE | ID: mdl-36789775
3.
Clonal evolution in chronic lymphocytic leukemia is associated with an unmutated IGHV status and frequently leads to a combination of loss of TP53 and TP53 mutation.
Mol Biol Rep
; 49(12): 12247-12252, 2022 Dec.
Artigo
em Inglês
| MEDLINE | ID: mdl-36169893
4.
Dark-matter matters: Discriminating subtle blood cancers using the darkest DNA.
PLoS Comput Biol
; 15(8): e1007332, 2019 08.
Artigo
em Inglês
| MEDLINE | ID: mdl-31469830
5.
Identification of prognostic parameters in CLL with no abnormalities detected by chromosome banding and FISH analyses.
Br J Haematol
; 183(1): 47-59, 2018 10.
Artigo
em Inglês
| MEDLINE | ID: mdl-30022491
6.
Epigenetically induced ectopic expression of UNCX impairs the proliferation and differentiation of myeloid cells.
Haematologica
; 102(7): 1204-1214, 2017 07.
Artigo
em Inglês
| MEDLINE | ID: mdl-28411256
7.
Gain of chromosome 21 or amplification of chromosome arm 21q is one mechanism for increased ERG expression in acute myeloid leukemia.
Genes Chromosomes Cancer
; 55(2): 148-57, 2016 Feb.
Artigo
em Inglês
| MEDLINE | ID: mdl-26542308
8.
Application of an NGS-based 28-gene panel in myeloproliferative neoplasms reveals distinct mutation patterns in essential thrombocythaemia, primary myelofibrosis and polycythaemia vera.
Br J Haematol
; 175(3): 419-426, 2016 Nov.
Artigo
em Inglês
| MEDLINE | ID: mdl-27447873
9.
Ultra-deep sequencing leads to earlier and more sensitive detection of the tyrosine kinase inhibitor resistance mutation T315I in chronic myeloid leukemia.
Haematologica
; 101(7): 830-8, 2016 07.
Artigo
em Inglês
| MEDLINE | ID: mdl-27102501
10.
Molecular characterization of acute myeloid leukemia patients who relapse more than 3 years after diagnosis: an exome sequencing study of 31 patients.
Haematologica
; 105(4): e157-e159, 2020 04.
Artigo
em Inglês
| MEDLINE | ID: mdl-31371420
11.
BRCC3 mutations in myeloid neoplasms.
Haematologica
; 100(8): 1051-7, 2015 Aug.
Artigo
em Inglês
| MEDLINE | ID: mdl-26001790
12.
Multilineage dysplasia does not influence prognosis in CEBPA-mutated AML, supporting the WHO proposal to classify these patients as a unique entity.
Blood
; 119(20): 4719-22, 2012 May 17.
Artigo
em Inglês
| MEDLINE | ID: mdl-22442349
13.
Next-generation sequencing - feasibility and practicality in haematology.
Br J Haematol
; 160(6): 736-53, 2013 Mar.
Artigo
em Inglês
| MEDLINE | ID: mdl-23294427
14.
CEBPA double-mutated acute myeloid leukaemia harbours concomitant molecular mutations in 76·8% of cases with TET2 and GATA2 alterations impacting prognosis.
Br J Haematol
; 161(5): 649-658, 2013 Jun.
Artigo
em Inglês
| MEDLINE | ID: mdl-23521373
15.
Artificial intelligence in hematological diagnostics: Game changer or gadget?
Blood Rev
; 58: 101019, 2023 03.
Artigo
em Inglês
| MEDLINE | ID: mdl-36241586
16.
Interplay of TP53 allelic state, blast count, and complex karyotype on survival of patients with AML and MDS.
Blood Adv
; 7(18): 5540-5548, 2023 09 26.
Artigo
em Inglês
| MEDLINE | ID: mdl-37505914
17.
Molecular landscape of immune pressure and escape in aplastic anemia.
Leukemia
; 37(1): 202-211, 2023 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-36253429
18.
The clinical and genomic landscape of patients with DDX41 variants identified during diagnostic sequencing.
Blood Adv
; 7(23): 7346-7357, 2023 12 12.
Artigo
em Inglês
| MEDLINE | ID: mdl-37874914
19.
Aberrant somatic hypermutation of CCND1 generates non-coding drivers of mantle cell lymphomagenesis.
Cancer Gene Ther
; 29(5): 484-493, 2022 05.
Artigo
em Inglês
| MEDLINE | ID: mdl-35145272
20.
Indeterminate and oncogenic potential: CHIP vs CHOP mutations in AML with NPM1 alteration.
Leukemia
; 36(2): 394-402, 2022 02.
Artigo
em Inglês
| MEDLINE | ID: mdl-34376804