Detalhe da pesquisa
1.
Low risk of embryonic and other cancers in PIK3CA-related overgrowth spectrum: Impact on screening recommendations.
Clin Genet
; 104(5): 554-563, 2023 11.
Artigo
em Inglês
| MEDLINE | ID: mdl-37580112
2.
Clinical and biological features of B-cell neoplasms with CDK6 translocations: an association with a subgroup of splenic marginal zone lymphomas displaying frequent CD5 expression, prolymphocytic cells, and TP53 abnormalities.
Br J Haematol
; 193(1): 72-82, 2021 04.
Artigo
em Inglês
| MEDLINE | ID: mdl-33314017
3.
Genetic characterization of B-cell prolymphocytic leukemia: a prognostic model involving MYC and TP53.
Blood
; 134(21): 1821-1831, 2019 11 21.
Artigo
em Inglês
| MEDLINE | ID: mdl-31527074
4.
Plasmacytoid dendritic cells proliferation associated with acute myeloid leukemia: phenotype profile and mutation landscape
Haematologica
; 106(12): 3056-3066, 2021 12 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-33054115
5.
Post-Essential Thrombocythemia Myelofibrosis and Multiple Isodicentric Y Chromosomes: A Unique Case among a Rare Association.
Cytogenet Genome Res
; 160(1): 18-21, 2020.
Artigo
em Inglês
| MEDLINE | ID: mdl-32008001
6.
Polygenic risk scores and breast and epithelial ovarian cancer risks for carriers of BRCA1 and BRCA2 pathogenic variants.
Genet Med
; 22(10): 1653-1666, 2020 10.
Artigo
em Inglês
| MEDLINE | ID: mdl-32665703
7.
Mendelian randomisation study of height and body mass index as modifiers of ovarian cancer risk in 22,588 BRCA1 and BRCA2 mutation carriers.
Br J Cancer
; 121(2): 180-192, 2019 07.
Artigo
em Inglês
| MEDLINE | ID: mdl-31213659
8.
The t(X;20)(q13;q13) translocation is a good prognostic factor in myeloid neoplasms: A report of 25 cases from the Groupe Francophone de Cytogénétique Hématologique.
Am J Hematol
; 2024 Apr 13.
Artigo
em Inglês
| MEDLINE | ID: mdl-38613825
9.
Efficacy of pembrolizumab in a patient with xeroderma pigmentosum variant and advanced cutaneous squamous-cell carcinoma.
Acta Oncol
; 61(9): 1140-1142, 2022 09.
Artigo
em Inglês
| MEDLINE | ID: mdl-35950634
10.
Pregnancy outcomes in prenatally diagnosed 47, XXX and 47, XYY syndromes: a 30-year French, retrospective, multicentre study.
Prenat Diagn
; 36(6): 523-9, 2016 Jun.
Artigo
em Inglês
| MEDLINE | ID: mdl-27018091
11.
14q deletions are associated with trisomy 12, NOTCH1 mutations and unmutated IGHV genes in chronic lymphocytic leukemia and small lymphocytic lymphoma.
Genes Chromosomes Cancer
; 53(8): 657-66, 2014 Aug.
Artigo
em Inglês
| MEDLINE | ID: mdl-24729385
12.
Patterns of genomic aberrations suggest that Burkitt lymphomas with complex karyotype are distinct from other aggressive B-cell lymphomas with MYC rearrangement.
Genes Chromosomes Cancer
; 52(1): 81-92, 2013 Jan.
Artigo
em Inglês
| MEDLINE | ID: mdl-23012230
13.
Cytogenetics in the management of bone marrow failure syndromes: Guidelines from the Groupe Francophone de Cytogénétique Hématologique (GFCH).
Curr Res Transl Med
; 71(4): 103423, 2023.
Artigo
em Inglês
| MEDLINE | ID: mdl-38016422
14.
Cytogenetics in the management of hematologic neoplasms with germline predisposition: guidelines from the Groupe Francophone de Cytogénétique Hématologique (GFCH).
Curr Res Transl Med
; 71(4): 103416, 2023.
Artigo
em Inglês
| MEDLINE | ID: mdl-37865978
15.
The "extreme phenotype approach" applied to male breast cancer allows the identification of rare variants of ATR as potential breast cancer susceptibility alleles.
Oncotarget
; 14: 111-125, 2023 02 07.
Artigo
em Inglês
| MEDLINE | ID: mdl-36749285
16.
Association and performance of polygenic risk scores for breast cancer among French women presenting or not a familial predisposition to the disease.
Eur J Cancer
; 179: 76-86, 2023 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-36509001
17.
Systematic donor blood qualification by flow cytometry would have been able to avoid CLL-type MBL transmission after unrelated hematopoietic stem cell transplantation.
Eur J Haematol
; 88(3): 269-72, 2012 Mar.
Artigo
em Inglês
| MEDLINE | ID: mdl-22168404
18.
Copy number variants as modifiers of breast cancer risk for BRCA1/BRCA2 pathogenic variant carriers.
Commun Biol
; 5(1): 1061, 2022 10 06.
Artigo
em Inglês
| MEDLINE | ID: mdl-36203093
19.
The CADM1 tumor suppressor gene is a major candidate gene in MDS with deletion of the long arm of chromosome 11.
Blood Adv
; 6(2): 386-398, 2022 01 25.
Artigo
em Inglês
| MEDLINE | ID: mdl-34638130
20.
Chromosomal abnormalities in transformed Ph-negative myeloproliferative neoplasms are associated to the transformation subtype and independent of JAK2 and the TET2 mutations.
Genes Chromosomes Cancer
; 49(10): 919-27, 2010 Oct.
Artigo
em Inglês
| MEDLINE | ID: mdl-20629097