Detalhe da pesquisa
1.
GATA2 gene analysis in several forms of hematological malignancies including familial aggregations.
Ann Hematol
; 96(10): 1635-1639, 2017 Oct.
Artigo
em Inglês
| MEDLINE | ID: mdl-28752392
2.
GENESIS: a French national resource to study the missing heritability of breast cancer.
BMC Cancer
; 16: 13, 2016 Jan 12.
Artigo
em Inglês
| MEDLINE | ID: mdl-26758370
3.
Mutational analysis of JAK2, CBL, RUNX1, and NPM1 genes in familial aggregation of hematological malignancies.
Ann Hematol
; 95(7): 1043-50, 2016 Jun.
Artigo
em Inglês
| MEDLINE | ID: mdl-27106701
4.
Familial hematological malignancies: new IDH2 mutation.
Ann Hematol
; 95(12): 1943-1947, 2016 Dec.
Artigo
em Inglês
| MEDLINE | ID: mdl-27591990
5.
High cumulative risks of cancer in patients with PTEN hamartoma tumour syndrome.
J Med Genet
; 50(4): 255-63, 2013 Apr.
Artigo
em Inglês
| MEDLINE | ID: mdl-23335809
6.
Variation in breast cancer risk associated with factors related to pregnancies according to truncating mutation location, in the French National BRCA1 and BRCA2 mutations carrier cohort (GENEPSO).
Breast Cancer Res
; 14(4): R99, 2012 Jul 03.
Artigo
em Inglês
| MEDLINE | ID: mdl-22762150
7.
Novel FH mutations in families with hereditary leiomyomatosis and renal cell cancer (HLRCC) and patients with isolated type 2 papillary renal cell carcinoma.
J Med Genet
; 48(4): 226-34, 2011 Apr.
Artigo
em Inglês
| MEDLINE | ID: mdl-21398687
8.
Mutational analysis of apoptotic genes in familial aggregation of hematological malignancies.
Bull Cancer
; 108(9): 798-805, 2021 Sep.
Artigo
em Inglês
| MEDLINE | ID: mdl-34140154
9.
Molecular apocrine differentiation is a common feature of breast cancer in patients with germline PTEN mutations.
Breast Cancer Res
; 12(4): R63, 2010.
Artigo
em Inglês
| MEDLINE | ID: mdl-20712882
10.
BRCA1 allele-specific expression in genetic predisposed breast/ovarian cancer.
Fam Cancer
; 16(2): 167-171, 2017 04.
Artigo
em Inglês
| MEDLINE | ID: mdl-27783335
11.
ARLTS1, potential candidate gene in familial aggregation of hematological malignancies.
Bull Cancer
; 104(2): 123-127, 2017 Feb.
Artigo
em Inglês
| MEDLINE | ID: mdl-27866680
12.
Mutation screening of MIR146A/B and BRCA1/2 3'-UTRs in the GENESIS study.
Eur J Hum Genet
; 24(9): 1324-9, 2016 08.
Artigo
em Inglês
| MEDLINE | ID: mdl-26785832
13.
Clinical relevance of 8q23, 15q13 and 18q21 SNP genotyping to evaluate colorectal cancer risk.
Eur J Hum Genet
; 24(1): 99-105, 2016 Jan.
Artigo
em Inglês
| MEDLINE | ID: mdl-25873010
14.
EFGR-mutant lung adenocarcinoma and Li-Fraumeni syndrome: report of two cases and review of the literature.
Lung Cancer
; 87(1): 80-4, 2015 Jan.
Artigo
em Inglês
| MEDLINE | ID: mdl-25433984
15.
Idiopathic gastric acid hypersecretion in a patient with MUTYH-associated polyposis.
Am J Gastroenterol
; 104(10): 2648-9, 2009 Oct.
Artigo
em Inglês
| MEDLINE | ID: mdl-19806110
16.
Next-generation sequencing for the diagnosis of hereditary breast and ovarian cancer using genomic capture targeting multiple candidate genes.
Eur J Hum Genet
; 22(11): 1305-13, 2014 Nov.
Artigo
em Inglês
| MEDLINE | ID: mdl-24549055
17.
Uptake of a randomized breast cancer prevention trial comparing letrozole to placebo in BRCA1/2 mutations carriers: the LIBER trial.
Fam Cancer
; 11(1): 77-84, 2012 Mar.
Artigo
em Inglês
| MEDLINE | ID: mdl-22076253
18.
Molecular study of the perforin gene in familial hematological malignancies.
Hered Cancer Clin Pract
; 9(1): 9, 2011 Sep 21.
Artigo
em Inglês
| MEDLINE | ID: mdl-21936944
19.
Breast cancer in a male with ankylosing spondylitis treated with TNFalpha antagonists.
Joint Bone Spine
; 76(4): 421-3, 2009 Jul.
Artigo
em Inglês
| MEDLINE | ID: mdl-19457692
20.
Colorectal adenomatous polyposis Associated with MYH mutations: genotype and phenotype characteristics.
Dis Colon Rectum
; 50(10): 1612-7, 2007 Oct.
Artigo
em Inglês
| MEDLINE | ID: mdl-17674103