Detalhe da pesquisa
1.
Exome sequencing identified rare recurrent copy number variants and hereditary breast cancer susceptibility.
PLoS Genet
; 19(8): e1010889, 2023 08.
Artigo
em Inglês
| MEDLINE | ID: mdl-37578974
2.
PALB2-mutated human mammary cells display a broad spectrum of morphological and functional abnormalities induced by increased TGFß signaling.
Cell Mol Life Sci
; 81(1): 173, 2024 Apr 10.
Artigo
em Inglês
| MEDLINE | ID: mdl-38597967
3.
ATM c.7570G>C is a high-risk allele for breast cancer.
Int J Cancer
; 152(3): 429-435, 2023 02 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-36161273
4.
Tumor suppressor MCPH1 regulates gene expression profiles related to malignant conversion and chromosomal assembly.
Int J Cancer
; 145(8): 2070-2081, 2019 10 15.
Artigo
em Inglês
| MEDLINE | ID: mdl-30809794
5.
Targeted Next-Generation Sequencing Identifies a Recurrent Mutation in MCPH1 Associating with Hereditary Breast Cancer Susceptibility.
PLoS Genet
; 12(1): e1005816, 2016 Jan.
Artigo
em Inglês
| MEDLINE | ID: mdl-26820313
6.
Rare missense mutations in RECQL and POLG associate with inherited predisposition to breast cancer.
Int J Cancer
; 142(11): 2286-2292, 2018 06 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-29341116
7.
FANCM mutation c.5791C>T is a risk factor for triple-negative breast cancer in the Finnish population.
Breast Cancer Res Treat
; 166(1): 217-226, 2017 Nov.
Artigo
em Inglês
| MEDLINE | ID: mdl-28702895
8.
FANCM c.5101C>T mutation associates with breast cancer survival and treatment outcome.
Int J Cancer
; 139(12): 2760-2770, 2016 Dec 15.
Artigo
em Inglês
| MEDLINE | ID: mdl-27542569
9.
Recurrent CYP2C19 deletion allele is associated with triple-negative breast cancer.
BMC Cancer
; 14: 902, 2014 Dec 02.
Artigo
em Inglês
| MEDLINE | ID: mdl-25466287
10.
Truncating TINF2 p.Tyr312Ter variant and inherited breast cancer susceptibility.
Fam Cancer
; 22(1): 13-17, 2023 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-35590014
11.
Exome sequencing identifies a recurrent variant in SERPINA3 associating with hereditary susceptibility to breast cancer.
Eur J Cancer
; 143: 46-51, 2021 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-33279852
12.
Genetic contributions to the expression of acquired causes of cardiac hypertrophy in non-ischemic sudden cardiac death victims.
Sci Rep
; 11(1): 11171, 2021 05 27.
Artigo
em Inglês
| MEDLINE | ID: mdl-34045587
13.
Evaluating the role of NTHL1 p.Q90* allele in inherited breast cancer predisposition.
Mol Genet Genomic Med
; 8(11): e1493, 2020 11.
Artigo
em Inglês
| MEDLINE | ID: mdl-32949222
14.
Case-control analysis of truncating mutations in DNA damage response genes connects TEX15 and FANCD2 with hereditary breast cancer susceptibility.
Sci Rep
; 7(1): 681, 2017 04 06.
Artigo
em Inglês
| MEDLINE | ID: mdl-28386063