Detalhe da pesquisa
1.
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
2.
Gene- and pathway-level analyses of iCOGS variants highlight novel signaling pathways underlying familial breast cancer susceptibility.
Int J Cancer;
148(8): 1895-1909, 2021 04 15.
Artigo
em Inglês
| MEDLINE
| ID: mdl-33368296
3.
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
4.
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
5.
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
6.
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
7.
Familial hematological malignancies: new IDH2 mutation.
Ann Hematol;
95(12): 1943-1947, 2016 Dec.
Artigo
em Inglês
| MEDLINE
| ID: mdl-27591990
8.
Squamous Cell Carcinoma of the Lung With Microsatellite Instability in a Patient With Lynch Syndrome: A Case Report.
JTO Clin Res Rep;
5(1): 100595, 2024 Jan.
Artigo
em Inglês
| MEDLINE
| ID: mdl-38229768
9.
Prediction of BRCA1 germ-line mutation status in patients with breast cancer using histoprognosis grade, MS110, Lys27H3, vimentin, and KI67.
Pathobiology;
80(5): 219-27, 2013.
Artigo
em Inglês
| MEDLINE
| ID: mdl-23614934
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.
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
12.
TUMOSPEC: A Nation-Wide Study of Hereditary Breast and Ovarian Cancer Families with a Predicted Pathogenic Variant Identified through Multigene Panel Testing.
Cancers (Basel);
13(15)2021 Jul 21.
Artigo
em Inglês
| MEDLINE
| ID: mdl-34359559
13.
Time to prophylactic surgery in BRCA1/2 carriers depends on psychological and other characteristics.
Genet Med;
12(12): 801-7, 2010 Dec.
Artigo
em Inglês
| MEDLINE
| ID: mdl-20921896
14.
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
15.
The genomic architecture of NLRP7 is Alu rich and predisposes to disease-associated large deletions.
Eur J Hum Genet;
24(10): 1445-52, 2016 10.
Artigo
em Inglês
| MEDLINE
| ID: mdl-26956250
16.
Breast radiotherapy in the lateral decubitus position: A technique to prevent lung and heart irradiation.
Int J Radiat Oncol Biol Phys;
61(5): 1348-54, 2005 Apr 01.
Artigo
em Inglês
| MEDLINE
| ID: mdl-15817336
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.
The genomic architecture of NLRP7 is Alu rich and predisposes to disease-associated large deletions.
Eur J Hum Genet;
24(10): 1516, 2016 10.
Artigo
em Inglês
| MEDLINE
| ID: mdl-27628567
20.
Common genetic variation at BARD1 is not associated with breast cancer risk in BRCA1 or BRCA2 mutation carriers.
Cancer Epidemiol Biomarkers Prev;
20(5): 1032-8, 2011 May.
Artigo
em Inglês
| MEDLINE
| ID: mdl-21393566