Peretz T - Search Results

1

The carrier frequency of the BRCA1 185delAG mutation is approximately 1 percent in Ashkenazi Jewish individuals.

Struewing JP, Abeliovich D, Peretz T, Avishai N, Kaback MM, Collins FS, Brody LC. Struewing JP, et al. Among authors: peretz t. Nat Genet. 1995 Oct;11(2):198-200. doi: 10.1038/ng1095-198. Nat Genet. 1995. PMID: 7550349

2

Low-penetrance susceptibility to breast cancer due to CHEK2(*)1100delC in noncarriers of BRCA1 or BRCA2 mutations.

Meijers-Heijboer H, van den Ouweland A, Klijn J, Wasielewski M, de Snoo A, Oldenburg R, Hollestelle A, Houben M, Crepin E, van Veghel-Plandsoen M, Elstrodt F, van Duijn C, Bartels C, Meijers C, Schutte M, McGuffog L, Thompson D, Easton D, Sodha N, Seal S, Barfoot R, Mangion J, Chang-Claude J, Eccles D, Eeles R, Evans DG, Houlston R, Murday V, Narod S, Peretz T, Peto J, Phelan C, Zhang HX, Szabo C, Devilee P, Goldgar D, Futreal PA, Nathanson KL, Weber B, Rahman N, Stratton MR; CHEK2-Breast Cancer Consortium. Meijers-Heijboer H, et al. Among authors: peretz t. Nat Genet. 2002 May;31(1):55-9. doi: 10.1038/ng879. Epub 2002 Apr 22. Nat Genet. 2002. PMID: 11967536

3

Haplotype analysis of BRCA2 8765delAG mutation carriers in French Canadian and Yemenite Jewish hereditary breast cancer families.

Manning AP, Abelovich D, Ghadirian P, Lambert JA, Frappier D, Provencher D, Robidoux A, Peretz T, Narod SA, Mes-Masson AM, Foulkes WD, Wang T, Morgan K, Fujiwara TM, Tonin PN. Manning AP, et al. Among authors: peretz t. Hum Hered. 2001;52(2):116-20. doi: 10.1159/000053364. Hum Hered. 2001. PMID: 11512557

4

The Jewish Ashkenazi founder mutations in the BRCA1/BRCA2 genes are not found at an increased frequency in Ashkenazi patients with prostate cancer.

Hubert A, Peretz T, Manor O, Kaduri L, Wienberg N, Lerer I, Sagi M, Abeliovich D. Hubert A, et al. Among authors: peretz t. Am J Hum Genet. 1999 Sep;65(3):921-4. doi: 10.1086/302525. Am J Hum Genet. 1999. PMID: 10441598 Free PMC article. No abstract available.

5

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. Among authors: peretz t. Am J Hum Genet. 1997 Mar;60(3):505-14. Am J Hum Genet. 1997. PMID: 9042909 Free PMC article.

6

Double heterozygotes for the Ashkenazi founder mutations in BRCA1 and BRCA2 genes.

Friedman E, Bar-Sade Bruchim R, Kruglikova A, Risel S, Levy-Lahad E, Halle D, Bar-On E, Gershoni-Baruch R, Dagan E, Kepten I, Peretz T, Lerer I, Wienberg N, Shushan A, Abeliovich AD. Friedman E, et al. Among authors: peretz t. Am J Hum Genet. 1998 Oct;63(4):1224-7. doi: 10.1086/302040. Am J Hum Genet. 1998. PMID: 9758598 Free PMC article. No abstract available.

7

The 8765delAG mutation in BRCA2 is common among Jews of Yemenite extraction.

Lerer I, Wang T, Peretz T, Sagi M, Kaduri L, Orr-Urtreger A, Stadler J, Gutman H, Abeliovich D. Lerer I, et al. Among authors: peretz t. Am J Hum Genet. 1998 Jul;63(1):272-4. doi: 10.1086/301924. Am J Hum Genet. 1998. PMID: 9634522 Free PMC article. No abstract available.

8

Genetic counseling for women with breast cancer: the importance of evaluating the spouse.

Allweis TM, Sagi M, Peretz T. Allweis TM, et al. Among authors: peretz t. Clin Genet. 2004 Dec;66(6):573-4. doi: 10.1111/j.1399-0004.2004.00336.x. Clin Genet. 2004. PMID: 15521992 No abstract available.

9

BRCA1 mutations in women with ovarian cancer.

Shushan A, Abeliovich D, Peretz T, Weinberg N, Paltiel O. Shushan A, et al. Among authors: peretz t. JAMA. 1997 Mar 26;277(12):963. JAMA. 1997. PMID: 9091664 No abstract available.

10

[Inherited breast cancer].

Kaduri L, Heshing N, Abeliovich D, Peretz T. Kaduri L, et al. Among authors: peretz t. Harefuah. 1996 Nov 15;131(10):418-21. Harefuah. 1996. PMID: 8981821 Review. Hebrew. No abstract available.

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