Detalhe da pesquisa
1.
Impact of cytogenetic abnormalities on the risk of disease progression in solitary bone plasmacytomas.
Blood
; 142(22): 1871-1878, 2023 11 30.
Artigo
em Inglês
| MEDLINE | ID: mdl-37494698
2.
Section E6.1-6.6 of the American College of Medical Genetics and Genomics (ACMG) Technical Laboratory Standards: Cytogenomic studies of acquired chromosomal abnormalities in neoplastic blood, bone marrow, and lymph nodes.
Genet Med
; 26(4): 101054, 2024 Apr.
Artigo
em Inglês
| MEDLINE | ID: mdl-38349293
3.
Guiding the global evolution of cytogenetic testing for hematologic malignancies.
Blood
; 139(15): 2273-2284, 2022 04 14.
Artigo
em Inglês
| MEDLINE | ID: mdl-35167654
4.
Role of Dot1L and H3K79 methylation in regulating somatic hypermutation of immunoglobulin genes.
Proc Natl Acad Sci U S A
; 118(29)2021 07 20.
Artigo
em Inglês
| MEDLINE | ID: mdl-34253616
5.
Typical, atypical and cryptic t(15;17)(q24;q21) (PML::RARA) observed in acute promyelocytic leukemia: A retrospective review of 831 patients with concurrent chromosome and PML::RARA dual-color dual-fusion FISH studies.
Genes Chromosomes Cancer
; 61(10): 629-634, 2022 10.
Artigo
em Inglês
| MEDLINE | ID: mdl-35639830
6.
Characterization of unusual iAMP21 B-lymphoblastic leukemia (iAMP21-ALL) from the Mayo Clinic and Children's Oncology Group.
Genes Chromosomes Cancer
; 61(12): 710-719, 2022 12.
Artigo
em Inglês
| MEDLINE | ID: mdl-35771717
7.
Comparative study of therapy-related and de novo adult b-cell acute lymphoblastic leukaemia.
Br J Haematol
; 196(4): 963-968, 2022 02.
Artigo
em Inglês
| MEDLINE | ID: mdl-34697797
8.
Prognostic significance of acquired 1q22 gain in multiple myeloma.
Am J Hematol
; 97(1): 52-59, 2022 01 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-34710241
9.
Identification of EWSR1 rearrangements in patients with immature hematopoietic neoplasms: A case series and review of literature.
Ann Diagn Pathol
; 58: 151942, 2022 Jun.
Artigo
em Inglês
| MEDLINE | ID: mdl-35344861
10.
Increased complexity of t(11;14) rearrangements in plasma cell neoplasms compared with mantle cell lymphoma.
Genes Chromosomes Cancer
; 60(10): 678-686, 2021 10.
Artigo
em Inglês
| MEDLINE | ID: mdl-34124820
11.
Identification of a novel KMT2A/GIMAP8 gene fusion in a pediatric patient with acute undifferentiated leukemia.
Genes Chromosomes Cancer
; 60(2): 108-111, 2021 02.
Artigo
em Inglês
| MEDLINE | ID: mdl-33078871
12.
Clinical utility of next generation sequencing to detect IGH/IL3 rearrangements [t(5;14)(q31.1;q32.1)] in B-lymphoblastic leukemia/lymphoma.
Ann Diagn Pathol
; 53: 151761, 2021 Aug.
Artigo
em Inglês
| MEDLINE | ID: mdl-33991782
13.
Cryptic and atypical KMT2A-USP2 and KMT2A-USP8 rearrangements identified by mate pair sequencing in infant and childhood leukemia.
Genes Chromosomes Cancer
; 59(7): 422-427, 2020 07.
Artigo
em Inglês
| MEDLINE | ID: mdl-32196814
14.
Limited diagnostic impact of duplications <1 Mb of uncertain clinical significance: a 10-year retrospective analysis of reporting practices at the Mayo Clinic.
Genet Med
; 22(12): 2120-2124, 2020 12.
Artigo
em Inglês
| MEDLINE | ID: mdl-32820244
15.
Fluorescence in-situ hybridisation for TP63 rearrangements in T cell lymphomas: single-site experience of 470 patients and implications for clinical testing.
Histopathology
; 76(3): 481-485, 2020 Feb.
Artigo
em Inglês
| MEDLINE | ID: mdl-31557339
16.
Functional convergence of histone methyltransferases EHMT1 and KMT2C involved in intellectual disability and autism spectrum disorder.
PLoS Genet
; 13(10): e1006864, 2017 Oct.
Artigo
em Inglês
| MEDLINE | ID: mdl-29069077
17.
Siblings with ETV6/RUNX1-positive B-lymphoblastic leukemia: A single site experience and review of the literature.
Ann Diagn Pathol
; 48: 151588, 2020 Oct.
Artigo
em Inglês
| MEDLINE | ID: mdl-32836179
18.
Detection of cryptic CCND1 rearrangements in mantle cell lymphoma by next generation sequencing.
Ann Diagn Pathol
; 46: 151533, 2020 Jun.
Artigo
em Inglês
| MEDLINE | ID: mdl-32408254
19.
A near-haploid clone harboring a BCR/ABL1 gene fusion in an adult patient with newly diagnosed B-lymphoblastic leukemia.
Genes Chromosomes Cancer
; 58(9): 665-668, 2019 09.
Artigo
em Inglês
| MEDLINE | ID: mdl-30790375
20.
Acute leukemias harboring KMT2A/MLLT10 fusion: a 10-year experience from a single genomics laboratory.
Genes Chromosomes Cancer
; 58(8): 567-577, 2019 08.
Artigo
em Inglês
| MEDLINE | ID: mdl-30707474