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Items: 1 to 20 of 87

1.

Analysis of allelic association between D6S461 marker and multiple sclerosis in Ashkenazi and Iraqi Jewish patients.

Shinar Y, Pras E, Siev-Ner I, Gamus D, Brautbar C, Israel S, Achiron A.

J Mol Neurosci. 1998 Dec;11(3):265-9.

PMID:
10344796
2.

Genetic contribution to multiple sclerosis risk among Ashkenazi Jews.

Khankhanian P, Matsushita T, Madireddy L, Lizée A, Din L, Moré JM, Gourraud PA, Hauser SL, Baranzini SE, Oksenberg JR.

BMC Med Genet. 2015 Jul 28;16:55. doi: 10.1186/s12881-015-0201-2.

3.

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.

Blood. 1995 Jan 15;85(2):429-32.

PMID:
7811996
4.

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.

Blood. 1997 Oct 1;90(7):2654-9.

PMID:
9326232
5.

Genetic association between polymorphisms in the ADAMTS14 gene and multiple sclerosis.

Goertsches R, Comabella M, Navarro A, Perkal H, Montalban X.

J Neuroimmunol. 2005 Jul;164(1-2):140-7.

PMID:
15913795
6.

The I1307K APC polymorphism: prevalence in non-Ashkenazi Jews and evidence for a founder effect.

Shtoyerman-Chen R, Friedman E, Figer A, Carmel M, Patael Y, Rath P, Fidder HH, Bar-Meir S, Theodor L.

Genet Test. 2001 Summer;5(2):141-6.

PMID:
11551102
7.

Familial Mediterranean fever in Ashkenazi Jews: the mild end of the clinical spectrum.

Lidar M, Kedem R, Berkun Y, Langevitz P, Livneh A.

J Rheumatol. 2010 Feb;37(2):422-5. doi: 10.3899/jrheum.090401. Epub 2009 Dec 15.

PMID:
20008924
8.

The IBD1 locus for susceptibility to Crohn's disease has a greater impact in Ashkenazi Jews with early onset disease.

Akolkar PN, Gulwani-Akolkar B, Lin XY, Zhou Z, Daly M, Katz S, Levine J, Present D, Gelb B, Desnick R, Mayer L, Silver J.

Am J Gastroenterol. 2001 Apr;96(4):1127-32.

PMID:
11316159
9.
10.

Polymorphisms in the tumor necrosis factor/lipopolysaccharides pathway in Crohn disease in the Jewish Ashkenazi population.

Silbermintz A, Levine J, Weinstein T, Silver J.

J Pediatr Gastroenterol Nutr. 2008 May;46(5):546-50. doi: 10.1097/MPG.0b013e3181653ab5.

PMID:
18493210
11.

Linkage disequilibrium between the FES, D15S127, and BLM loci in Ashkenazi Jews with Bloom syndrome.

Ellis NA, Roe AM, Kozloski J, Proytcheva M, Falk C, German J.

Am J Hum Genet. 1994 Sep;55(3):453-60.

12.

The HLA locus and multiple sclerosis in Sicily.

Brassat D, Salemi G, Barcellos LF, McNeill G, Proia P, Hauser SL, Oksenberg JR, Savettieri G.

Neurology. 2005 Jan 25;64(2):361-3.

PMID:
15668443
13.
14.

Specific mutations in the HEXA gene among Iraqi Jewish Tay-Sachs disease carriers: dating of founder ancestor.

Karpati M, Gazit E, Goldman B, Frisch A, Colombo R, Peleg L.

Neurogenetics. 2004 Feb;5(1):35-40. Epub 2003 Nov 27.

PMID:
14648242
15.

Genetic anthropology of the colorectal cancer-susceptibility allele APC I1307K: evidence of genetic drift within the Ashkenazim.

Niell BL, Long JC, Rennert G, Gruber SB.

Am J Hum Genet. 2003 Dec;73(6):1250-60. Epub 2003 Nov 17.

16.

NOD2/CARD15 genotype and phenotype differences between Ashkenazi and Sephardic Jews with Crohn's disease.

Karban A, Waterman M, Panhuysen CI, Pollak RD, Nesher S, Datta L, Weiss B, Suissa A, Shamir R, Brant SR, Eliakim R.

Am J Gastroenterol. 2004 Jun;99(6):1134-40.

PMID:
15180737
17.

Familial Mediterranean fever: high gene frequency among the non-Ashkenazic and Ashkenazic Jewish populations in Israel.

Daniels M, Shohat T, Brenner-Ullman A, Shohat M.

Am J Med Genet. 1995 Jan 30;55(3):311-4.

PMID:
7726228
18.

Chromosome 19 locus apolipoprotein C-II association with multiple sclerosis.

Zouali H, Faure-Delanef L, Lucotte G.

Mult Scler. 1999 Apr;5(2):134-6.

PMID:
10335523
19.

Strong allelic association between the torsion dystonia gene (DYT1) andloci on chromosome 9q34 in Ashkenazi Jews.

Ozelius LJ, Kramer PL, de Leon D, Risch N, Bressman SB, Schuback DE, Brin MF, Kwiatkowski DJ, Burke RE, Gusella JF, et al.

Am J Hum Genet. 1992 Mar;50(3):619-28.

20.

A novel NOD2/CARD15 haplotype conferring risk for Crohn disease in Ashkenazi Jews.

Sugimura K, Taylor KD, Lin YC, Hang T, Wang D, Tang YM, Fischel-Ghodsian N, Targan SR, Rotter JI, Yang H.

Am J Hum Genet. 2003 Mar;72(3):509-18. Epub 2003 Feb 7.

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