Similar articles for PMID: 25971130

Year	Number of Results
1947	1
1979	1
1996	1
1997	6
1998	5
1999	7
2000	6
2001	3
2002	8
2003	4
2004	2
2005	9
2006	10
2007	4
2008	5
2009	9
2010	13
2011	7
2012	5
2013	10
2014	7
2015	7
2016	8
2017	4
2018	4
2019	9
2020	12
2021	8
2022	6
2023	5
2024	0

1

[Ethnic aspects of hereditary breast cancer in the region of Siberia].

Cherdyntseva NV, Pisareva LF, Ivanova AA, Panferova YV, Malinovskaya EA, Odintsova IN, Doroshenko AV, Gervas PA, Slonimskaya EM, Shivit-ool AA, Dvornichenko VV, Choinzonov YL. Cherdyntseva NV, et al. Vestn Ross Akad Med Nauk. 2014;(11-12):72-9. doi: 10.15690/vramn.v69i11-12.1186. Vestn Ross Akad Med Nauk. 2014. PMID: 25971130 Russian.

2

Founder mutations in BRCA1/2 are not frequent in Canadian Ashkenazi Jewish men with prostate cancer.

Hamel N, Kotar K, Foulkes WD. Hamel N, et al. BMC Med Genet. 2003 Aug 11;4:7. doi: 10.1186/1471-2350-4-7. BMC Med Genet. 2003. PMID: 12911837 Free PMC article.

3

Frequency and spectrum of founder and non-founder BRCA1 and BRCA2 mutations in a large series of Russian breast cancer and ovarian cancer patients.

Sokolenko AP, Sokolova TN, Ni VI, Preobrazhenskaya EV, Iyevleva AG, Aleksakhina SN, Romanko AA, Bessonov AA, Gorodnova TV, Anisimova EI, Savonevich EL, Bizin IV, Stepanov IA, Krivorotko PV, Berlev IV, Belyaev AM, Togo AV, Imyanitov EN. Sokolenko AP, et al. Breast Cancer Res Treat. 2020 Nov;184(1):229-235. doi: 10.1007/s10549-020-05827-8. Epub 2020 Aug 9. Breast Cancer Res Treat. 2020. PMID: 32776218

4

The founder mutations 185delAG and 5382insC in BRCA1 and 6174delT in BRCA2 appear in 60% of ovarian cancer and 30% of early-onset breast cancer patients among Ashkenazi women.

Abeliovich D, Kaduri L, Lerer I, Weinberg N, Amir G, Sagi M, Zlotogora J, Heching N, Peretz T. Abeliovich D, et al. Am J Hum Genet. 1997 Mar;60(3):505-14. Am J Hum Genet. 1997. PMID: 9042909 Free PMC article.

5

High frequency of BRCA1 founder mutations in Polish women with nonfamilial breast cancer.

Gaj P, Kluska A, Nowakowska D, Bałabas A, Piątkowska M, Dabrowska M, Niwińska A, Ostrowski J. Gaj P, et al. Fam Cancer. 2012 Dec;11(4):623-8. doi: 10.1007/s10689-012-9560-4. Fam Cancer. 2012. PMID: 22864640

6

High incidence of BRCA1-2 germline mutations, previous breast cancer and familial cancer history in Jewish patients with uterine serous papillary carcinoma.

Biron-Shental T, Drucker L, Altaras M, Bernheim J, Fishman A. Biron-Shental T, et al. Eur J Surg Oncol. 2006 Dec;32(10):1097-100. doi: 10.1016/j.ejso.2006.03.032. Epub 2006 May 2. Eur J Surg Oncol. 2006. PMID: 16650962

7

Differences in the characteristics of families with BRCA1 and BRCA2 mutations in Israel.

Rennert G, Dishon S, Rennert HS, Fares F. Rennert G, et al. Eur J Cancer Prev. 2005 Aug;14(4):357-61. doi: 10.1097/00008469-200508000-00008. Eur J Cancer Prev. 2005. PMID: 16030426

8

Ashkenazi founder BRCA1/BRCA2 mutations in Slovak hereditary breast and/or ovarian cancer families.

Cierniková S, Tomka M, Kovác M, Stevurková V, Zajac V. Cierniková S, et al. Neoplasma. 2006;53(2):97-102. Neoplasma. 2006. PMID: 16575464

9

Prevalence of founder BRCA1 and BRCA2 mutations among breast and ovarian cancer patients in Hungary.

Van Der Looij M, Szabo C, Besznyak I, Liszka G, Csokay B, Pulay T, Toth J, Devilee P, King MC, Olah E. Van Der Looij M, et al. Int J Cancer. 2000 Jun 1;86(5):737-40. doi: 10.1002/(sici)1097-0215(20000601)86:5<737::aid-ijc21>3.0.co;2-1. Int J Cancer. 2000. PMID: 10797299 Free article.

10

Double heterozygosity in the BRCA1 and BRCA2 genes in the Jewish population.

Lavie O, Narod S, Lejbkowicz F, Dishon S, Goldberg Y, Gemer O, Rennert G. Lavie O, et al. Ann Oncol. 2011 Apr;22(4):964-966. doi: 10.1093/annonc/mdq460. Epub 2010 Oct 5. Ann Oncol. 2011. PMID: 20924075 Free PMC article.

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