Detalhe da pesquisa
1.
VTRNA2-1: Genetic Variation, Heritable Methylation and Disease Association.
Int J Mol Sci;
22(5)2021 Mar 03.
Artigo
em Inglês
| MEDLINE
| ID: mdl-33802562
2.
Rare germline genetic variants and risk of aggressive prostate cancer.
Int J Cancer;
147(8): 2142-2149, 2020 10 15.
Artigo
em Inglês
| MEDLINE
| ID: mdl-32338768
3.
Genetic testing in Poland and Ukraine: should comprehensive germline testing of BRCA1 and BRCA2 be recommended for women with breast and ovarian cancer?
Genet Res (Camb);
102: e6, 2020 08 10.
Artigo
em Inglês
| MEDLINE
| ID: mdl-32772980
4.
FANCM and RECQL genetic variants and breast cancer susceptibility: relevance to South Poland and West Ukraine.
BMC Med Genet;
19(1): 12, 2018 01 19.
Artigo
em Inglês
| MEDLINE
| ID: mdl-29351780
5.
Is RNASEL:p.Glu265* a modifier of early-onset breast cancer risk for carriers of high-risk mutations?
BMC Cancer;
18(1): 165, 2018 02 08.
Artigo
em Inglês
| MEDLINE
| ID: mdl-29422015
6.
Mutation screening of PALB2 in clinically ascertained families from the Breast Cancer Family Registry.
Breast Cancer Res Treat;
149(2): 547-54, 2015 Jan.
Artigo
em Inglês
| MEDLINE
| ID: mdl-25575445
7.
FAVR (Filtering and Annotation of Variants that are Rare): methods to facilitate the analysis of rare germline genetic variants from massively parallel sequencing datasets.
BMC Bioinformatics;
14: 65, 2013 Feb 25.
Artigo
em Inglês
| MEDLINE
| ID: mdl-23441864
8.
Low penetrance breast cancer susceptibility loci are associated with specific breast tumor subtypes: findings from the Breast Cancer Association Consortium.
Hum Mol Genet;
20(16): 3289-303, 2011 Aug 15.
Artigo
em Inglês
| MEDLINE
| ID: mdl-21596841
9.
Associations of common variants at 1p11.2 and 14q24.1 (RAD51L1) with breast cancer risk and heterogeneity by tumor subtype: findings from the Breast Cancer Association Consortium.
Hum Mol Genet;
20(23): 4693-706, 2011 Dec 01.
Artigo
em Inglês
| MEDLINE
| ID: mdl-21852249
10.
Using SNP genotypes to improve the discrimination of a simple breast cancer risk prediction model.
Breast Cancer Res Treat;
139(3): 887-96, 2013 Jun.
Artigo
em Inglês
| MEDLINE
| ID: mdl-23774992
11.
Cross-platform compatibility of Hi-Plex, a streamlined approach for targeted massively parallel sequencing.
Anal Biochem;
442(2): 127-9, 2013 Nov 15.
Artigo
em Inglês
| MEDLINE
| ID: mdl-23933242
12.
Maternal SARS-CoV-2 exposure alters infant DNA methylation.
Brain Behav Immun Health;
27: 100572, 2023 Feb.
Artigo
em Inglês
| MEDLINE
| ID: mdl-36570792
13.
FAN1 variants identified in multiple-case early-onset breast cancer families via exome sequencing: no evidence for association with risk for breast cancer.
Breast Cancer Res Treat;
130(3): 1043-9, 2011 Dec.
Artigo
em Inglês
| MEDLINE
| ID: mdl-21858661
14.
Repeatability of methylation measures using a QIAseq targeted methyl panel and comparison with the Illumina HumanMethylation450 assay.
BMC Res Notes;
14(1): 394, 2021 Oct 24.
Artigo
em Inglês
| MEDLINE
| ID: mdl-34689793
15.
Population-Based Estimates of the Age-Specific Cumulative Risk of Breast Cancer for Pathogenic Variants in CHEK2: Findings from the Australian Breast Cancer Family Registry.
Cancers (Basel);
13(6)2021 Mar 18.
Artigo
em Inglês
| MEDLINE
| ID: mdl-33803639
16.
Rare Germline Pathogenic Variants Identified by Multigene Panel Testing and the Risk of Aggressive Prostate Cancer.
Cancers (Basel);
13(7)2021 Mar 24.
Artigo
em Inglês
| MEDLINE
| ID: mdl-33804961
17.
Population-based estimates of breast cancer risk for carriers of pathogenic variants identified by gene-panel testing.
NPJ Breast Cancer;
7(1): 153, 2021 Dec 09.
Artigo
em Inglês
| MEDLINE
| ID: mdl-34887416
18.
Mismatch repair gene pathogenic germline variants in a population-based cohort of breast cancer.
Fam Cancer;
19(3): 197-202, 2020 07.
Artigo
em Inglês
| MEDLINE
| ID: mdl-32060697
19.
Hi-Plex2: a simple and robust approach to targeted sequencing-based genetic screening.
Biotechniques;
67(3): 118-122, 2019 09.
Artigo
em Inglês
| MEDLINE
| ID: mdl-31267764
20.
Hi-Plex for Simple, Accurate, and Cost-Effective Amplicon-based Targeted DNA Sequencing.
Methods Mol Biol;
1712: 53-70, 2018.
Artigo
em Inglês
| MEDLINE
| ID: mdl-29224068