Detalhe da pesquisa
1.
Pitfalls in variant annotation for hereditary cancer diagnostics: The example of Illumina® VariantStudio®.
Genomics
; 113(1 Pt 2): 748-754, 2021 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-33053411
2.
CanVaS: Documenting the genetic variation spectrum of Greek cancer patients.
Hum Mutat
; 42(9): 1081-1093, 2021 09.
Artigo
em Inglês
| MEDLINE | ID: mdl-34174131
3.
BRCA1 and BRCA2 germline testing in Cretan isolates reveals novel and strong founder effects.
Int J Cancer
; 147(5): 1334-1342, 2020 09 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-32022259
4.
Functional characterization of CHEK2 variants in a Saccharomyces cerevisiae system.
Hum Mutat
; 40(5): 631-648, 2019 05.
Artigo
em Inglês
| MEDLINE | ID: mdl-30851065
5.
The spectrum of BRCA1 and BRCA2 pathogenic sequence variants in Middle Eastern, North African, and South European countries.
Hum Mutat
; 40(11): e1-e23, 2019 11.
Artigo
em Inglês
| MEDLINE | ID: mdl-31209999
6.
PALB2 c.2257C>T truncating variant is a Greek founder and is associated with high breast cancer risk.
J Hum Genet
; 64(8): 767-773, 2019 Aug.
Artigo
em Inglês
| MEDLINE | ID: mdl-31089269
7.
Germline deleterious mutations in genes other than BRCA2 are infrequent in male breast cancer.
Breast Cancer Res Treat
; 169(1): 105-113, 2018 May.
Artigo
em Inglês
| MEDLINE | ID: mdl-29335925
8.
Contribution of RAD51D germline mutations in breast and ovarian cancer in Greece.
J Hum Genet
; 63(11): 1149-1158, 2018 Nov.
Artigo
em Inglês
| MEDLINE | ID: mdl-30111881
9.
Characterization and prevalence of two novel CHEK2 large deletions in Greek breast cancer patients.
J Hum Genet
; 63(8): 877-886, 2018 Jul.
Artigo
em Inglês
| MEDLINE | ID: mdl-29785007
10.
DNA glycosylases involved in base excision repair may be associated with cancer risk in BRCA1 and BRCA2 mutation carriers.
PLoS Genet
; 10(4): e1004256, 2014 04.
Artigo
em Inglês
| MEDLINE | ID: mdl-24698998
11.
Genetic variation in mitotic regulatory pathway genes is associated with breast tumor grade.
Hum Mol Genet
; 23(22): 6034-46, 2014 Nov 15.
Artigo
em Inglês
| MEDLINE | ID: mdl-24927736
12.
An original phylogenetic approach identified mitochondrial haplogroup T1a1 as inversely associated with breast cancer risk in BRCA2 mutation carriers.
Breast Cancer Res
; 17: 61, 2015 Apr 25.
Artigo
em Inglês
| MEDLINE | ID: mdl-25925750
13.
Pathogenic Variants in Breast Cancer Susceptibility Genes in Older Women.
JAMA
; 324(4): 397, 2020 07 28.
Artigo
em Inglês
| MEDLINE | ID: mdl-32720998
14.
Epidemiological and clinicopathological characteristics of BRCA-positive and BRCA-negative breast cancer patients in Greece.
J BUON
; 20(4): 978-84, 2015.
Artigo
em Inglês
| MEDLINE | ID: mdl-26416046
15.
Genome-wide association study identifies 25 known breast cancer susceptibility loci as risk factors for triple-negative breast cancer.
Carcinogenesis
; 35(5): 1012-9, 2014 May.
Artigo
em Inglês
| MEDLINE | ID: mdl-24325915
16.
alphaB-crystallin is a marker of aggressive breast cancer behavior but does not independently predict for patient outcome: a combined analysis of two randomized studies.
BMC Clin Pathol
; 14: 28, 2014.
Artigo
em Inglês
| MEDLINE | ID: mdl-24987308
17.
Extending the clinical phenotype associated with biallelic NTHL1 germline mutations.
Clin Genet
; 94(6): 588-589, 2018 12.
Artigo
em Inglês
| MEDLINE | ID: mdl-30248171
18.
ENIGMA CHEK2gether Project: A Comprehensive Study Identifies Functionally Impaired CHEK2 Germline Missense Variants Associated with Increased Breast Cancer Risk.
Clin Cancer Res
; 29(16): 3037-3050, 2023 08 15.
Artigo
em Inglês
| MEDLINE | ID: mdl-37449874
19.
Prevalence of BRCA1 mutations among 403 women with triple-negative breast cancer: implications for genetic screening selection criteria: a Hellenic Cooperative Oncology Group Study.
Breast Cancer Res Treat
; 134(1): 353-62, 2012 Jul.
Artigo
em Inglês
| MEDLINE | ID: mdl-22434525
20.
Lung cancer as a predominant feature in a patient with Peutz-Jeghers syndrome: Case report.
Thorac Cancer
; 13(12): 1862-1865, 2022 06.
Artigo
em Inglês
| MEDLINE | ID: mdl-35543335