Detalhe da pesquisa
1.
AXIN2 germline testing in a French cohort validates pathogenic variants as a rare cause of predisposition to colorectal polyposis and cancer.
Genes Chromosomes Cancer
; 62(4): 210-222, 2023 04.
Artigo
em Inglês
| MEDLINE | ID: mdl-36502525
2.
Identification and Characterization of an Exonic Duplication in PALB2 in a Man with Synchronous Breast and Prostate Cancer.
Int J Mol Sci
; 23(2)2022 Jan 08.
Artigo
em Inglês
| MEDLINE | ID: mdl-35054852
3.
Diagnostic chest X-rays and breast cancer risk among women with a hereditary predisposition to breast cancer unexplained by a BRCA1 or BRCA2 mutation.
Breast Cancer Res
; 23(1): 79, 2021 08 03.
Artigo
em Inglês
| MEDLINE | ID: mdl-34344426
4.
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
5.
Familial breast cancer and DNA repair genes: Insights into known and novel susceptibility genes from the GENESIS study, and implications for multigene panel testing.
Int J Cancer
; 144(8): 1962-1974, 2019 04 15.
Artigo
em Inglês
| MEDLINE | ID: mdl-30303537
6.
Endoscopic Phenotype of Monoallelic Carriers of MUTYH Gene Mutations in the Family of Polyposis Patients: A Prospective Study.
Dis Colon Rectum
; 62(4): 470-475, 2019 04.
Artigo
em Inglês
| MEDLINE | ID: mdl-30640315
7.
"Double-hit" chronic lymphocytic leukemia: An aggressive subgroup with 17p deletion and 8q24 gain.
Am J Hematol
; 93(3): 375-382, 2018 03.
Artigo
em Inglês
| MEDLINE | ID: mdl-29194741
8.
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
9.
Overview of the Genetic Causes of Hereditary Breast and Ovarian Cancer Syndrome in a Large French Patient Cohort.
Cancers (Basel)
; 15(13)2023 Jun 29.
Artigo
em Inglês
| MEDLINE | ID: mdl-37444530
10.
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
11.
Chronic lymphocytic leukemia and prolymphocytic leukemia with MYC translocations: a subgroup with an aggressive disease course.
Ann Hematol
; 91(6): 863-73, 2012 Jun.
Artigo
em Inglês
| MEDLINE | ID: mdl-22205151
12.
Three new cases of non-Hodgkin lymphoma with t(9;14)(p13;q32).
Cancer Genet Cytogenet
; 145(1): 65-9, 2003 Aug.
Artigo
em Inglês
| MEDLINE | ID: mdl-12885465
13.
GEMO, a National Resource to Study Genetic Modifiers of Breast and Ovarian Cancer Risk in BRCA1 and BRCA2 Pathogenic Variant Carriers.
Front Oncol
; 8: 490, 2018.
Artigo
em Inglês
| MEDLINE | ID: mdl-30430080
14.
Specific chromosomal IG translocations have different prognoses in chronic lymphocytic leukemia.
Am J Blood Res
; 1(1): 13-21, 2011.
Artigo
em Inglês
| MEDLINE | ID: mdl-22432063
15.
Gain of the short arm of chromosome 2 (2p) is a frequent recurring chromosome aberration in untreated chronic lymphocytic leukemia (CLL) at advanced stages.
Leuk Res
; 34(1): 63-8, 2010 Jan.
Artigo
em Inglês
| MEDLINE | ID: mdl-19406473
16.
Overexpression of CEBPA resulting from the translocation t(14;19)(q32;q13) of human precursor B acute lymphoblastic leukemia.
Blood
; 108(10): 3560-3, 2006 Nov 15.
Artigo
em Inglês
| MEDLINE | ID: mdl-16873674
17.
Interstitial deletion of the short arm of chromosome 1: attempt to establish a clinical phenotype (46,XX,del (1)(p22p32)).
Am J Med Genet A
; 118A(2): 176-9, 2003 Apr 15.
Artigo
em Inglês
| MEDLINE | ID: mdl-12655498