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Results: 1 to 20 of 43

1.

Role of BRCA1 and BRCA2 gene mutations in epithelial ovarian cancer in Indian population: a pilot study.

Sharma S, Rajaram S, Sharma T, Goel N, Agarwal S, Banerjee BD.

Int J Biochem Mol Biol. 2014 May 15;5(1):1-10. eCollection 2014.

PMID:
24955283
[PubMed]
Free PMC Article
2.

Probing structure-function relationships in missense variants in the carboxy-terminal region of BRCA1.

Carvalho RS, Abreu RB, Velkova A, Marsillac S, Rodarte RS, Suarez-Kurtz G, Iversen ES, Monteiro AN, Carvalho MA.

PLoS One. 2014 May 20;9(5):e97766. doi: 10.1371/journal.pone.0097766. eCollection 2014.

PMID:
24845084
[PubMed - in process]
Free PMC Article
3.

An analysis of polymorphisms within the Wnt signaling pathway in relation to ovarian cancer risk in a Polish population.

Mostowska A, Pawlik P, Sajdak S, Markowska J, Pawałowska M, Lianeri M, Jagodzinski PP.

Mol Diagn Ther. 2014 Feb;18(1):85-91.

PMID:
24078348
[PubMed - in process]
Free PMC Article
4.

Novel BRCA1 and BRCA2 pathogenic mutations in Slovene hereditary breast and ovarian cancer families.

Novaković S, Milatović M, Cerkovnik P, Stegel V, Krajc M, Hočevar M, Zgajnar J, Vakselj A.

Int J Oncol. 2012 Nov;41(5):1619-27. doi: 10.3892/ijo.2012.1595. Epub 2012 Aug 21.

PMID:
22923021
[PubMed - indexed for MEDLINE]
Free PMC Article
5.

Breast and ovarian cancer risk evaluation in families with a disease-causing mutation in BRCA1/2.

Beristain E, Ibáñez B, Vergara I, Martínez-Bouzas C, Guerra I, Tejada MI.

J Community Genet. 2010 Jun;1(2):91-9. doi: 10.1007/s12687-010-0014-0. Epub 2010 Aug 9.

PMID:
22460208
[PubMed]
Free PMC Article
6.

Ethnic, racial and cultural identity and perceived benefits and barriers related to genetic testing for breast cancer among at-risk women of African descent in New York City.

Sussner KM, Edwards TA, Thompson HS, Jandorf L, Kwate NO, Forman A, Brown K, Kapil-Pair N, Bovbjerg DH, Schwartz MD, Valdimarsdottir HB.

Public Health Genomics. 2011;14(6):356-70. doi: 10.1159/000325263. Epub 2011 May 3.

PMID:
21540561
[PubMed - indexed for MEDLINE]
Free PMC Article
7.

Do-it-yourself genetic testing.

Salzberg SL, Pertea M.

Genome Biol. 2010;11(10):404. doi: 10.1186/gb-2010-11-10-404. Epub 2010 Oct 7.

PMID:
20932271
[PubMed - indexed for MEDLINE]
Free PMC Article
8.

Detection of inherited mutations for breast and ovarian cancer using genomic capture and massively parallel sequencing.

Walsh T, Lee MK, Casadei S, Thornton AM, Stray SM, Pennil C, Nord AS, Mandell JB, Swisher EM, King MC.

Proc Natl Acad Sci U S A. 2010 Jul 13;107(28):12629-33. doi: 10.1073/pnas.1007983107. Epub 2010 Jun 28.

PMID:
20616022
[PubMed - indexed for MEDLINE]
Free PMC Article
9.

Pharmacogenetics and personal genomes.

Wagner MJ.

Per Med. 2009 Nov 1;6(6):643-652.

PMID:
20190862
[PubMed]
Free PMC Article
10.

Subjective versus objective risk in genetic counseling for hereditary breast and/or ovarian cancers.

Caruso A, Vigna C, Marozzo B, Sega FM, Sperduti I, Cognetti F, Savarese A.

J Exp Clin Cancer Res. 2009 Dec 21;28:157. doi: 10.1186/1756-9966-28-157.

PMID:
20025726
[PubMed - indexed for MEDLINE]
Free PMC Article
11.

Efficiency of BRCAPRO and Myriad II mutation probability thresholds versus cancer history criteria alone for BRCA1/2 mutation detection.

van Harssel JJ, van Roozendaal CE, Detisch Y, Brandão RD, Paulussen AD, Zeegers M, Blok MJ, Gómez García EB.

Fam Cancer. 2010 Jun;9(2):193-201. doi: 10.1007/s10689-009-9305-1.

PMID:
19949876
[PubMed - indexed for MEDLINE]
Free PMC Article
12.

Selecting for BRCA1 testing using a combination of homogeneous selection criteria and immunohistochemical characteristics of breast cancers.

Miolo G, Canzonieri V, De Giacomi C, Puppa LD, Dolcetti R, Lombardi D, Perin T, Scalone S, Veronesi A, Viel A.

BMC Cancer. 2009 Oct 10;9:360. doi: 10.1186/1471-2407-9-360.

PMID:
19818148
[PubMed - indexed for MEDLINE]
Free PMC Article
13.

Diffusion of breast cancer risk assessment in primary care.

Guerra CE, Sherman M, Armstrong K.

J Am Board Fam Med. 2009 May-Jun;22(3):272-9. doi: 10.3122/jabfm.2009.03.080153.

PMID:
19429733
[PubMed - indexed for MEDLINE]
Free PMC Article
14.

Age-dependent penetrance of different germline mutations in the BRCA1 gene.

Al-Mulla F, Bland JM, Serratt D, Miller J, Chu C, Taylor GT.

J Clin Pathol. 2009 Apr;62(4):350-6. doi: 10.1136/jcp.2008.062646.

PMID:
19329713
[PubMed - indexed for MEDLINE]
Free PMC Article
15.

Distress among women receiving uninformative BRCA1/2 results: 12-month outcomes.

O'Neill SC, Rini C, Goldsmith RE, Valdimarsdottir H, Cohen LH, Schwartz MD.

Psychooncology. 2009 Oct;18(10):1088-96. doi: 10.1002/pon.1467.

PMID:
19214961
[PubMed - indexed for MEDLINE]
Free PMC Article
16.

A method to assess the clinical significance of unclassified variants in the BRCA1 and BRCA2 genes based on cancer family history.

Gómez García EB, Oosterwijk JC, Timmermans M, van Asperen CJ, Hogervorst FB, Hoogerbrugge N, Oldenburg R, Verhoef S, Dommering CJ, Ausems MG, van Os TA, van der Hout AH, Ligtenberg M, van den Ouweland A, van der Luijt RB, Wijnen JT, Gille JJ, Lindsey PJ, Devilee P, Blok MJ, Vreeswijk MP.

Breast Cancer Res. 2009;11(1):R8. doi: 10.1186/bcr2223. Epub 2009 Feb 6.

PMID:
19200354
[PubMed - indexed for MEDLINE]
Free PMC Article
17.

The influence of acculturation and breast cancer-specific distress on perceived barriers to genetic testing for breast cancer among women of African descent.

Sussner KM, Thompson HS, Jandorf L, Edwards TA, Forman A, Brown K, Kapil-Pair N, Bovbjerg DH, Schwartz MD, Valdimarsdottir HB.

Psychooncology. 2009 Sep;18(9):945-55. doi: 10.1002/pon.1492.

PMID:
19090507
[PubMed - indexed for MEDLINE]
Free PMC Article
18.

Genetic counseling and testing for common hereditary breast cancer syndromes: a paper from the 2007 William Beaumont hospital symposium on molecular pathology.

Allain DC.

J Mol Diagn. 2008 Sep;10(5):383-95. doi: 10.2353/jmoldx.2008.070161. Epub 2008 Aug 7. Review.

PMID:
18687797
[PubMed - indexed for MEDLINE]
Free PMC Article
19.

Association between temporal orientation and attitudes about BRCA1/2 testing among women of African descent with family histories of breast cancer.

Edwards TA, Thompson HS, Kwate NO, Brown K, McGovern MM, Forman A, Kapil-Pair N, Jandorf L, Bovbjerg DH, Valdimarsdottir HB.

Patient Educ Couns. 2008 Aug;72(2):276-82. doi: 10.1016/j.pec.2008.03.021. Epub 2008 May 13.

PMID:
18479882
[PubMed - indexed for MEDLINE]
Free PMC Article
20.

Validity of models for predicting BRCA1 and BRCA2 mutations.

Parmigiani G, Chen S, Iversen ES Jr, Friebel TM, Finkelstein DM, Anton-Culver H, Ziogas A, Weber BL, Eisen A, Malone KE, Daling JR, Hsu L, Ostrander EA, Peterson LE, Schildkraut JM, Isaacs C, Corio C, Leondaridis L, Tomlinson G, Amos CI, Strong LC, Berry DA, Weitzel JN, Sand S, Dutson D, Kerber R, Peshkin BN, Euhus DM.

Ann Intern Med. 2007 Oct 2;147(7):441-50.

PMID:
17909205
[PubMed - indexed for MEDLINE]
Free PMC Article

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