Detalhe da pesquisa
1.
Analysis of 11 candidate genes in 849 adult patients with suspected hereditary cancer predisposition.
Genes Chromosomes Cancer
; 60(2): 73-78, 2021 02.
Artigo
em Inglês
| MEDLINE | ID: mdl-33099839
2.
Feedback of extended panel sequencing in 1530 patients referred for suspicion of hereditary predisposition to adult cancers.
Clin Genet
; 99(1): 166-175, 2021 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-33047316
3.
Further delineation of the NTHL1 associated syndrome: A report from the French Oncogenetic Consortium.
Clin Genet
; 99(5): 662-672, 2021 05.
Artigo
em Inglês
| MEDLINE | ID: mdl-33454955
4.
Is BRCA2 involved in early onset colorectal cancer risk?
Clin Genet
; 97(4): 668-669, 2020 04.
Artigo
em Inglês
| MEDLINE | ID: mdl-31875949
5.
Interactions between microsatellite instability and human gut colonization by Escherichia coli in colorectal cancer.
Clin Sci (Lond)
; 131(6): 471-485, 2017 Mar 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-28093453
6.
Diet-induced hypoxia responsive element demethylation increases CEACAM6 expression, favouring Crohn's disease-associated Escherichia coli colonisation.
Gut
; 64(3): 428-37, 2015 Mar.
Artigo
em Inglês
| MEDLINE | ID: mdl-24898815
7.
BRCA1 and BRCA2 mutations in ethnic Lebanese Arab women with high hereditary risk breast cancer.
Oncologist
; 20(4): 357-64, 2015 Apr.
Artigo
em Inglês
| MEDLINE | ID: mdl-25777348
8.
The UMD-APC database, a model of nation-wide knowledge base: update with data from 3,581 variations.
Hum Mutat
; 35(5): 532-6, 2014 May.
Artigo
em Inglês
| MEDLINE | ID: mdl-24599579
9.
Positive link between variant Toll-like receptor 4 (Asp299Gly and Thr399Ile) and colorectal cancer patients with advanced stage and lymph node metastasis.
Tumour Biol
; 35(1): 545-51, 2014 Jan.
Artigo
em Inglês
| MEDLINE | ID: mdl-23949880
10.
Significant association between interleukin-17A polymorphism and colorectal cancer.
Tumour Biol
; 35(7): 6627-32, 2014 Jul.
Artigo
em Inglês
| MEDLINE | ID: mdl-24699997
11.
Mutation screening of the BRCA1 gene in early onset and familial breast/ovarian cancer in Moroccan population.
Int J Med Sci
; 10(1): 60-7, 2013.
Artigo
em Inglês
| MEDLINE | ID: mdl-23289006
12.
Case Series of 11 CDH1 Families (47 Carriers) Including Incidental Findings, Signet Ring Cell Colon Cancer and Review of the Literature.
Genes (Basel)
; 14(9)2023 Aug 25.
Artigo
em Inglês
| MEDLINE | ID: mdl-37761816
13.
Detection Rate and Spectrum of Pathogenic Variations in a Cohort of 83 Patients with Suspected Hereditary Risk of Kidney Cancer.
Genes (Basel)
; 14(11)2023 Oct 25.
Artigo
em Inglês
| MEDLINE | ID: mdl-38002934
14.
Rare duplication of the CDC73 gene and atypical hyperparathyroidism-jaw tumor syndrome: A case report and review of the literature.
Mol Genet Genomic Med
; 11(5): e2133, 2023 05.
Artigo
em Inglês
| MEDLINE | ID: mdl-36639964
15.
Diagnosis of PTEN mosaicism: the relevance of additional tumor DNA sequencing. A case report and review of the literature.
BMC Med Genomics
; 16(1): 166, 2023 07 13.
Artigo
em Inglês
| MEDLINE | ID: mdl-37442961
16.
Hereditary breast cancer in Middle Eastern and North African (MENA) populations: identification of novel, recurrent and founder BRCA1 mutations in the Tunisian population.
Mol Biol Rep
; 39(2): 1037-46, 2012 Feb.
Artigo
em Inglês
| MEDLINE | ID: mdl-21603858
17.
CHEK2 contribution to hereditary breast cancer in non-BRCA families.
Breast Cancer Res
; 13(6): R119, 2011.
Artigo
em Inglês
| MEDLINE | ID: mdl-22114986
18.
Germline mutations of the E-cadherin gene in families with inherited invasive lobular breast carcinoma but no diffuse gastric cancer.
Cancer
; 117(14): 3112-7, 2011 Jul 15.
Artigo
em Inglês
| MEDLINE | ID: mdl-21271559
19.
International distribution and age estimation of the Portuguese BRCA2 c.156_157insAlu founder mutation.
Breast Cancer Res Treat
; 127(3): 671-9, 2011 Jun.
Artigo
em Inglês
| MEDLINE | ID: mdl-20652400
20.
Genomic variations integrated database for MUTYH-associated adenomatous polyposis.
J Med Genet
; 52(1): 25-7, 2015 Jan.
Artigo
em Inglês
| MEDLINE | ID: mdl-25368107