Detalhe da pesquisa
1.
The association between age at breast cancer diagnosis and prevalence of pathogenic variants.
Breast Cancer Res Treat
; 199(3): 617-626, 2023 Jun.
Artigo
em Inglês
| MEDLINE | ID: mdl-37084156
2.
Systematic mapping review of guidelines for BRCA1/2 genetic testing globally: investigating geographic and regional disparities in health equity for women and families at risk for hereditary ovarian cancer.
Int J Gynecol Cancer
; 33(2): 250-256, 2023 02 06.
Artigo
em Inglês
| MEDLINE | ID: mdl-36368709
3.
The emerging field of polygenic risk scores and perspective for use in clinical care.
Hum Mol Genet
; 29(R2): R165-R176, 2020 10 20.
Artigo
em Inglês
| MEDLINE | ID: mdl-32620971
4.
Multigene assessment of genetic risk for women for two or more breast cancers.
Breast Cancer Res Treat
; 188(3): 759-768, 2021 Aug.
Artigo
em Inglês
| MEDLINE | ID: mdl-33826040
5.
Risk assessment and genetic counseling for hereditary breast and ovarian cancer syndromes-Practice resource of the National Society of Genetic Counselors.
J Genet Couns
; 30(2): 342-360, 2021 04.
Artigo
em Inglês
| MEDLINE | ID: mdl-33410258
6.
Comprehensive sequencing of PALB2 in patients with breast cancer suggests PALB2 mutations explain a subset of hereditary breast cancer.
Cancer
; 120(7): 963-7, 2014 Apr 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-24415441
7.
NSGC practice guideline: risk assessment and genetic counseling for hereditary breast and ovarian cancer.
J Genet Couns
; 22(2): 155-63, 2013 Apr.
Artigo
em Inglês
| MEDLINE | ID: mdl-23188549
8.
Cancer Risk Associated With PTEN Pathogenic Variants Identified Using Multigene Hereditary Cancer Panel Testing.
JCO Precis Oncol
; 7: e2200415, 2023 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-36634299
9.
Association of Genomic Instability Score, Tumor Mutational Burden, and Tumor-Infiltrating Lymphocytes as Biomarkers in Uterine Serous Carcinoma.
Cancers (Basel)
; 15(2)2023 Jan 15.
Artigo
em Inglês
| MEDLINE | ID: mdl-36672477
10.
Pancreatic Ductal Carcinoma Risk Associated With Hereditary Cancer-Risk Genes.
J Natl Cancer Inst
; 114(7): 996-1002, 2022 07 11.
Artigo
em Inglês
| MEDLINE | ID: mdl-35445726
11.
Age of ovarian cancer diagnosis among BRIP1, RAD51C, and RAD51D mutation carriers identified through multi-gene panel testing.
J Ovarian Res
; 14(1): 61, 2021 Apr 29.
Artigo
em Inglês
| MEDLINE | ID: mdl-33926482
12.
Prospective Statewide Study of Universal Screening for Hereditary Colorectal Cancer: The Ohio Colorectal Cancer Prevention Initiative.
JCO Precis Oncol
; 52021.
Artigo
em Inglês
| MEDLINE | ID: mdl-34250417
13.
No Evidence of Increased Risk of Breast Cancer in Women With Lynch Syndrome Identified by Multigene Panel Testing.
JCO Precis Oncol
; 4: 51-60, 2020 Nov.
Artigo
em Inglês
| MEDLINE | ID: mdl-35050728
14.
Utilization of Complementary Alternative Medicine, Diet, and Exercise Among Women at High Risk for Developing Breast Cancer.
Integr Cancer Ther
; 19: 1534735420922610, 2020.
Artigo
em Inglês
| MEDLINE | ID: mdl-32448019
15.
Learning of your parent's BRCA mutation during adolescence or early adulthood: a study of offspring experiences.
Psychooncology
; 18(2): 200-8, 2009 Feb.
Artigo
em Inglês
| MEDLINE | ID: mdl-18702049
16.
Translational integrity and continuity: personalized biomedical data integration.
J Biomed Inform
; 42(1): 100-12, 2009 Feb.
Artigo
em Inglês
| MEDLINE | ID: mdl-18760382
17.
Should genetic testing for BRCA1/2 be permitted for minors? Opinions of BRCA mutation carriers and their adult offspring.
Am J Med Genet C Semin Med Genet
; 148C(1): 70-7, 2008 Feb 15.
Artigo
em Inglês
| MEDLINE | ID: mdl-18200524
18.
Infertility, treatment of infertility, and the risk of breast cancer among women with BRCA1 and BRCA2 mutations: a case-control study.
Cancer Causes Control
; 19(10): 1111-9, 2008 Dec.
Artigo
em Inglês
| MEDLINE | ID: mdl-18509731
19.
Uptake and timing of bilateral prophylactic salpingo-oophorectomy among BRCA1 and BRCA2 mutation carriers.
Genet Med
; 10(3): 161-166, 2008 Mar.
Artigo
em Inglês
| MEDLINE | ID: mdl-18344704
20.
Response to article: Langford et al. racial and ethnic differences in direct-to-consumer genetic tests awareness in HINTS 2007: sociodemographic and numeracy correlates. J Genet Counsel (2012) 21:440-447.
J Genet Couns
; 22(1): 152-3, 2013 Feb.
Artigo
em Inglês
| MEDLINE | ID: mdl-23097085