Seligsohn U - Search Results

1

Age estimates of two common mutations causing factor XI deficiency: recent genetic drift is not necessary for elevated disease incidence among Ashkenazi Jews.

Goldstein DB, Reich DE, Bradman N, Usher S, Seligsohn U, Peretz H. Goldstein DB, et al. Among authors: seligsohn u. Am J Hum Genet. 1999 Apr;64(4):1071-5. doi: 10.1086/302313. Am J Hum Genet. 1999. PMID: 10090892 Free PMC article.

2

One of the two common mutations causing factor XI deficiency in Ashkenazi Jews (type II) is also prevalent in Iraqi Jews, who represent the ancient gene pool of Jews.

Shpilberg O, Peretz H, Zivelin A, Yatuv R, Chetrit A, Kulka T, Stern C, Weiss E, Seligsohn U. Shpilberg O, et al. Among authors: seligsohn u. Blood. 1995 Jan 15;85(2):429-32. Blood. 1995. PMID: 7811996 Free article.

3

Molecular genetics aspects of factor XI deficiency and Glanzmann thrombasthenia.

Seligsohn U, Peretz H. Seligsohn U, et al. Haemostasis. 1994 Mar-Apr;24(2):81-5. doi: 10.1159/000217088. Haemostasis. 1994. PMID: 7959366 Review.

4

A 14-bp deletion (codon 554 del AAGgtaacagagtg) at exon 14/intron N junction of the coagulation factor XI gene disrupts splicing and causes severe factor XI deficiency.

Peretz H, Zivelin A, Usher S, Seligsohn U. Peretz H, et al. Among authors: seligsohn u. Hum Mutat. 1996;8(1):77-8. doi: 10.1002/(SICI)1098-1004(1996)8:1<77::AID-HUMU12>3.0.CO;2-O. Hum Mutat. 1996. PMID: 8807341 No abstract available.

5

The two common mutations causing factor XI deficiency in Jews stem from distinct founders: one of ancient Middle Eastern origin and another of more recent European origin.

Peretz H, Mulai A, Usher S, Zivelin A, Segal A, Weisman Z, Mittelman M, Lupo H, Lanir N, Brenner B, Shpilberg O, Seligsohn U. Peretz H, et al. Among authors: seligsohn u. Blood. 1997 Oct 1;90(7):2654-9. Blood. 1997. PMID: 9326232 Free article.

6

Type I mutation in the F11 gene is a third ancestral mutation which causes factor XI deficiency in Ashkenazi Jews.

Peretz H, Salomon O, Mor-Cohen R, Usher S, Zucker M, Zivelin A, Seligsohn U. Peretz H, et al. Among authors: seligsohn u. J Thromb Haemost. 2013 Apr;11(4):724-30. doi: 10.1111/jth.12137. J Thromb Haemost. 2013. PMID: 23332144 Free article.

7

A common ancestral mutation (C128X) occurring in 11 non-Jewish families from the UK with factor XI deficiency.

Bolton-Maggs PH, Peretz H, Butler R, Mountford R, Keeney S, Zacharski L, Zivelin A, Seligsohn U. Bolton-Maggs PH, et al. Among authors: seligsohn u. J Thromb Haemost. 2004 Jun;2(6):918-24. doi: 10.1111/j.1538-7836.2004.00723.x. J Thromb Haemost. 2004. PMID: 15140127 Free article.

8

Mendelian diseases among Roman Jews: implications for the origins of disease alleles.

Oddoux C, Guillen-Navarro E, Ditivoli C, Dicave E, Cilio MR, Clayton CM, Nelson H, Sarafoglou K, McCain N, Peretz H, Seligsohn U, Luzzatto L, Nafa K, Nardi M, Karpatkin M, Aksentijevich I, Kastner D, Axelrod F, Ostrer H. Oddoux C, et al. Among authors: seligsohn u. J Clin Endocrinol Metab. 1999 Dec;84(12):4405-9. doi: 10.1210/jcem.84.12.6268. J Clin Endocrinol Metab. 1999. PMID: 10599695 Review.

9

Point mutations regarded as missense mutations cause splicing defects in the factor XI gene.

Zucker M, Rosenberg N, Peretz H, Green D, Bauduer F, Zivelin A, Seligsohn U. Zucker M, et al. Among authors: seligsohn u. J Thromb Haemost. 2011 Oct;9(10):1977-84. doi: 10.1111/j.1538-7836.2011.04426.x. J Thromb Haemost. 2011. PMID: 21718436 Free article.

10

Discerning the ancestry of European Americans in genetic association studies.

Price AL, Butler J, Patterson N, Capelli C, Pascali VL, Scarnicci F, Ruiz-Linares A, Groop L, Saetta AA, Korkolopoulou P, Seligsohn U, Waliszewska A, Schirmer C, Ardlie K, Ramos A, Nemesh J, Arbeitman L, Goldstein DB, Reich D, Hirschhorn JN. Price AL, et al. Among authors: seligsohn u. PLoS Genet. 2008 Jan;4(1):e236. doi: 10.1371/journal.pgen.0030236. Epub 2007 Nov 19. PLoS Genet. 2008. PMID: 18208327 Free PMC article.

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