Detalhe da pesquisa
1.
CTNND1 is involved in germline predisposition to early-onset gastric cancer by affecting cell-to-cell interactions.
Gastric Cancer
; 2024 May 25.
Artigo
em Inglês
| MEDLINE | ID: mdl-38796558
2.
Quality of Colonoscopy Is Associated With Adenoma Detection and Postcolonoscopy Colorectal Cancer Prevention in Lynch Syndrome.
Clin Gastroenterol Hepatol
; 20(3): 611-621.e9, 2022 03.
Artigo
em Inglês
| MEDLINE | ID: mdl-33157315
3.
Clinical and Pathological Characterization of Lynch-Like Syndrome.
Clin Gastroenterol Hepatol
; 18(2): 368-374.e1, 2020 02.
Artigo
em Inglês
| MEDLINE | ID: mdl-31220642
4.
Role of POLE and POLD1 in familial cancer.
Genet Med
; 22(12): 2089-2100, 2020 12.
Artigo
em Inglês
| MEDLINE | ID: mdl-32792570
5.
Analysis of Lynch Syndrome Mismatch Repair Genes in Women with Endometrial Cancer.
Oncology
; 91(3): 171-6, 2016.
Artigo
em Inglês
| MEDLINE | ID: mdl-27398995
6.
Mammographic density and breast cancer in women from high risk families.
Breast Cancer Res
; 17: 93, 2015 Jul 11.
Artigo
em Inglês
| MEDLINE | ID: mdl-26163143
7.
Capillary electrophoresis analysis of conventional splicing assays: IARC analytical and clinical classification of 31 BRCA2 genetic variants.
Hum Mutat
; 35(1): 53-7, 2014 Jan.
Artigo
em Inglês
| MEDLINE | ID: mdl-24123850
8.
Prevalence of Homologous Recombination Deficiency Among Patients With Germline RAD51C/D Breast or Ovarian Cancer.
JAMA Netw Open
; 7(4): e247811, 2024 Apr 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-38648056
9.
Impact of concurrent tumour events on the prostate cancer outcomes of germline BRCA2 mutation carriers.
Eur J Cancer
; 185: 105-118, 2023 05.
Artigo
em Inglês
| MEDLINE | ID: mdl-36972661
10.
Genome-wide linkage scan reveals three putative breast-cancer-susceptibility loci.
Am J Hum Genet
; 84(2): 115-22, 2009 Feb.
Artigo
em Inglês
| MEDLINE | ID: mdl-19147119
11.
Transcriptional characteristics of familial non-BRCA1/BRCA2 breast tumors.
Int J Cancer
; 128(11): 2635-44, 2011 Jun 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-20715112
12.
Paired Somatic-Germline Testing of 15 Polyposis and Colorectal Cancer-Predisposing Genes Highlights the Role of APC Mosaicism in de Novo Familial Adenomatous Polyposis.
J Mol Diagn
; 23(11): 1452-1459, 2021 11.
Artigo
em Inglês
| MEDLINE | ID: mdl-34454113
13.
Identification of a new complex deleterious mutation in exon 18 of the BRCA2 gene in a hereditary male/female breast cancer family.
Breast Cancer Res Treat
; 123(2): 587-90, 2010 Sep.
Artigo
em Inglês
| MEDLINE | ID: mdl-20232139
14.
Association of premenopausal risk-reducing salpingo-oophorectomy with breast cancer risk in BRCA1/2 mutation carriers: Maximising bias-reduction.
Eur J Cancer
; 132: 53-60, 2020 06.
Artigo
em Inglês
| MEDLINE | ID: mdl-32325420
15.
Complete Loss of EPCAM Immunoexpression Identifies EPCAM Deletion Carriers in MSH2-Negative Colorectal Neoplasia.
Cancers (Basel)
; 12(10)2020 Sep 29.
Artigo
em Inglês
| MEDLINE | ID: mdl-33003511
16.
Hereditary Leiomyomatosis and Renal Cell Cancer Syndrome in Spain: Clinical and Genetic Characterization.
Cancers (Basel)
; 12(11)2020 Nov 05.
Artigo
em Inglês
| MEDLINE | ID: mdl-33167498
17.
Risk of Cancer in Family Members of Patients with Lynch-Like Syndrome.
Cancers (Basel)
; 12(8)2020 Aug 09.
Artigo
em Inglês
| MEDLINE | ID: mdl-32784934
18.
Analysis of FANCB and FANCN/PALB2 fanconi anemia genes in BRCA1/2-negative Spanish breast cancer families.
Breast Cancer Res Treat
; 113(3): 545-51, 2009 Feb.
Artigo
em Inglês
| MEDLINE | ID: mdl-18302019
19.
The average cumulative risks of breast and ovarian cancer for carriers of mutations in BRCA1 and BRCA2 attending genetic counseling units in Spain.
Clin Cancer Res
; 14(9): 2861-9, 2008 May 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-18451254
20.
[Hereditary breast and ovarian cancer: primary and secondary prevention for BRCA1 and BRCA2 mutation carriers]. / Cáncer de mama y ovario hereditario: prevención primaria y secundaria en mujeres portadoras de mutación en los genes BRCA1 y BRCA2.
Med Clin (Barc)
; 128(12): 468-76, 2007 Mar 31.
Artigo
em Espanhol
| MEDLINE | ID: mdl-17408542