Similar articles for PMID: 10827109

Year	Number of Results
1996	2
1997	8
1998	3
1999	11
2000	10
2001	11
2002	5
2003	6
2004	4
2005	3
2006	8
2007	4
2008	4
2009	6
2010	10
2011	3
2013	1
2014	2
2016	1
2017	1
2018	1
2019	1
2024	0

1

The exon 13 duplication in the BRCA1 gene is a founder mutation present in geographically diverse populations. The BRCA1 Exon 13 Duplication Screening Group.

The BRCA1 Exon 13 Duplication Screening Group. The BRCA1 Exon 13 Duplication Screening Group. Am J Hum Genet. 2000 Jul;67(1):207-12. Epub 2000 May 25. Am J Hum Genet. 2000. PMID: 10827109 Free PMC article.

2

Comprehensive analysis of 989 patients with breast or ovarian cancer provides BRCA1 and BRCA2 mutation profiles and frequencies for the German population.

Meindl A; German Consortium for Hereditary Breast and Ovarian Cancer. Meindl A, et al. Int J Cancer. 2002 Feb 1;97(4):472-80. doi: 10.1002/ijc.1626. Int J Cancer. 2002. PMID: 11802209 Free article.

3

Association between BRCA1 and BRCA2 mutations and cancer phenotype in Spanish breast/ovarian cancer families: implications for genetic testing.

de la Hoya M, Osorio A, Godino J, Sulleiro S, Tosar A, Perez-Segura P, Fernandez C, Rodríguez R, Díaz-Rubio E, Benítez J, Devilee P, Caldés T. de la Hoya M, et al. Int J Cancer. 2002 Feb 1;97(4):466-71. doi: 10.1002/ijc.1627. Int J Cancer. 2002. PMID: 11802208 Free article.

4

Screening for genomic rearrangements in families with breast and ovarian cancer identifies BRCA1 mutations previously missed by conformation-sensitive gel electrophoresis or sequencing.

Unger MA, Nathanson KL, Calzone K, Antin-Ozerkis D, Shih HA, Martin AM, Lenoir GM, Mazoyer S, Weber BL. Unger MA, et al. Am J Hum Genet. 2000 Oct;67(4):841-50. doi: 10.1086/303076. Epub 2000 Sep 7. Am J Hum Genet. 2000. PMID: 10978226 Free PMC article.

5

BRCA1 sequence analysis in women at high risk for susceptibility mutations. Risk factor analysis and implications for genetic testing.

Shattuck-Eidens D, Oliphant A, McClure M, McBride C, Gupte J, Rubano T, Pruss D, Tavtigian SV, Teng DH, Adey N, Staebell M, Gumpper K, Lundstrom R, Hulick M, Kelly M, Holmen J, Lingenfelter B, Manley S, Fujimura F, Luce M, Ward B, Cannon-Albright L, Steele L, Offit K, Thomas A, et al. Shattuck-Eidens D, et al. JAMA. 1997 Oct 15;278(15):1242-50. JAMA. 1997. PMID: 9333265

6

BRCA1 1675delA and 1135insA account for one third of Norwegian familial breast-ovarian cancer and are associated with later disease onset than less frequent mutations.

Borg A, Dørum A, Heimdal K, Maehle L, Hovig E, Møller P. Borg A, et al. Dis Markers. 1999 Oct;15(1-3):79-84. doi: 10.1155/1999/278269. Dis Markers. 1999. PMID: 10595257 Free PMC article.

7

BRCA1 and BRCA2 mutation analysis of 208 Ashkenazi Jewish women with ovarian cancer.

Moslehi R, Chu W, Karlan B, Fishman D, Risch H, Fields A, Smotkin D, Ben-David Y, Rosenblatt J, Russo D, Schwartz P, Tung N, Warner E, Rosen B, Friedman J, Brunet JS, Narod SA. Moslehi R, et al. Am J Hum Genet. 2000 Apr;66(4):1259-72. doi: 10.1086/302853. Epub 2000 Mar 16. Am J Hum Genet. 2000. PMID: 10739756 Free PMC article.

8

Frequency of BRCA1 and BRCA2 germline mutations in Japanese breast cancer families.

Ikeda N, Miyoshi Y, Yoneda K, Shiba E, Sekihara Y, Kinoshita M, Noguchi S. Ikeda N, et al. Int J Cancer. 2001 Jan 1;91(1):83-8. doi: 10.1002/1097-0215(20010101)91:1<83::aid-ijc1013>3.0.co;2-5. Int J Cancer. 2001. PMID: 11149425 Free article.

9

First BRCA1 and BRCA2 gene testing implemented in the health care system of Stockholm.

Arver B, Borg A, Lindblom A. Arver B, et al. Genet Test. 2001 Spring;5(1):1-8. doi: 10.1089/109065701750168581. Genet Test. 2001. PMID: 11336395

10

Identification of a founder BRCA2 mutation in Sardinian breast cancer families.

Monne M, Piras G, Fancello P, Santona MC, Uras A, Landriscina G, Mastio G, Gabbas A. Monne M, et al. Fam Cancer. 2007;6(1):73-9. doi: 10.1007/s10689-006-9107-7. Fam Cancer. 2007. PMID: 17216544

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