Detalhe da pesquisa
1.
Predictors of long-term cancer-related distress among female BRCA1 and BRCA2 mutation carriers without a cancer diagnosis: an international analysis.
Br J Cancer
; 123(2): 268-274, 2020 07.
Artigo
em Inglês
| MEDLINE | ID: mdl-32393849
2.
Preferences for breast cancer prevention among women with a BRCA1 or BRCA2 mutation.
Hered Cancer Clin Pract
; 18: 20, 2020.
Artigo
em Inglês
| MEDLINE | ID: mdl-33014209
3.
Oestrogen receptor status and survival in women with BRCA2-associated breast cancer.
Br J Cancer
; 120(4): 398-403, 2019 02.
Artigo
em Inglês
| MEDLINE | ID: mdl-30723304
4.
Physical activity during adolescence and young adulthood and the risk of breast cancer in BRCA1 and BRCA2 mutation carriers.
Breast Cancer Res Treat
; 169(3): 561-571, 2018 Jun.
Artigo
em Inglês
| MEDLINE | ID: mdl-29404807
5.
Preferences for breast cancer risk reduction among BRCA1/BRCA2 mutation carriers: a discrete-choice experiment.
Breast Cancer Res Treat
; 165(2): 433-444, 2017 Sep.
Artigo
em Inglês
| MEDLINE | ID: mdl-28624978
6.
Screening for familial and hereditary prostate cancer.
Int J Cancer
; 138(11): 2579-91, 2016 Jun 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-26638190
7.
Two PALB2 germline mutations found in both BRCA1+ and BRCAx familial breast cancer.
Breast Cancer Res Treat
; 151(1): 219-24, 2015 May.
Artigo
em Inglês
| MEDLINE | ID: mdl-25833210
8.
Endometrial cancers in mutation carriers from hereditary breast ovarian cancer syndrome kindreds: report from the Creighton University Hereditary Cancer Registry with review of the implications.
Int J Gynecol Cancer
; 25(4): 650-6, 2015 May.
Artigo
em Inglês
| MEDLINE | ID: mdl-25756400
9.
Genome instability in blood cells of a BRCA1+ breast cancer family.
BMC Cancer
; 14: 342, 2014 May 19.
Artigo
em Inglês
| MEDLINE | ID: mdl-24884718
10.
Family-specific, novel, deleterious germline variants provide a rich resource to identify genetic predispositions for BRCAx familial breast cancer.
BMC Cancer
; 14: 470, 2014 Jun 26.
Artigo
em Inglês
| MEDLINE | ID: mdl-24969172
11.
Aspirin use is associated with lower prostate cancer risk in male carriers of BRCA mutations.
J Genet Couns
; 23(2): 187-91, 2014 Apr.
Artigo
em Inglês
| MEDLINE | ID: mdl-23881471
12.
Can unknown predisposition in familial breast cancer be family-specific?
Breast J
; 19(5): 520-8, 2013.
Artigo
em Inglês
| MEDLINE | ID: mdl-23800003
13.
Hereditary breast cancer: practical pursuit for clinical translation.
Ann Surg Oncol
; 19(6): 1723-31, 2012 Jun.
Artigo
em Inglês
| MEDLINE | ID: mdl-22434244
14.
Lynch syndrome-associated extracolonic tumors are rare in two extended families with the same EPCAM deletion.
Am J Gastroenterol
; 106(10): 1829-36, 2011 Oct.
Artigo
em Inglês
| MEDLINE | ID: mdl-21769135
15.
Genetic counseling and the advanced practice oncology nursing role in a hereditary cancer prevention clinic: hereditary breast cancer focus (part I).
Breast J
; 15 Suppl 1: S2-10, 2009.
Artigo
em Inglês
| MEDLINE | ID: mdl-19775325
16.
Genetic counseling and the advanced practice oncology nursing role in a hereditary cancer prevention clinic: hereditary breast cancer focus (part II).
Breast J
; 15 Suppl 1: S11-9, 2009.
Artigo
em Inglês
| MEDLINE | ID: mdl-19775324
17.
Family information service participation increases the rates of mutation testing among members of families with BRCA1/2 mutations.
Breast J
; 15 Suppl 1: S20-4, 2009.
Artigo
em Inglês
| MEDLINE | ID: mdl-19775326
18.
Hereditary Colorectal Cancer Syndromes.
Semin Oncol Nurs
; 35(1): 58-78, 2019 02.
Artigo
em Inglês
| MEDLINE | ID: mdl-30665732
19.
The benefits of a model of interval comprehensive assessments (MICA) in hereditary cancer Syndromes: Hereditary diffuse gastric cancer (HDGC) as an example.
Cancer Genet
; 233-234: 43-47, 2019 04.
Artigo
em Inglês
| MEDLINE | ID: mdl-31109593
20.
Common genetic variants contribute to incomplete penetrance: evidence from cancer-free BRCA1 mutation carriers.
Eur J Cancer
; 107: 68-78, 2019 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-30551077