-
3
-
-
8544278104
-
-
Central Bureau of Statistics, Jerusalem. Government Press
-
Statistic Abstracts of Israel, Central Bureau of Statistics, Jerusalem. Government Press 2000; 84-85.
-
(2000)
Statistic Abstracts of Israel
, pp. 84-85
-
-
-
4
-
-
0003018599
-
Genetic markers: Benign and normal traits of Ashkenazi Jews
-
Goodman RM, Motulsky AG (eds): New York: Raven Press
-
Bonné-Tamir B, Ashbel S, Kennet R. Genetic markers: benign and normal traits of Ashkenazi Jews. In Goodman RM, Motulsky AG (eds): Genetic Diseases Among Ashkenazi Jews. New York: Raven Press 1979; 54-76.
-
(1979)
Genetic Diseases among Ashkenazi Jews
, pp. 54-76
-
-
Bonné-Tamir, B.1
Ashbel, S.2
Kennet, R.3
-
5
-
-
0027429393
-
The differences among Jewish communities-maternal and paternal contributions
-
Ritte U, Neufeld E, Broit M et al. The differences among Jewish communities-maternal and paternal contributions. J Mol Evol 1993; 37: 435-40.
-
(1993)
J Mol Evol
, vol.37
, pp. 435-440
-
-
Ritte, U.1
Neufeld, E.2
Broit, M.3
-
6
-
-
12944286501
-
Jewish and Middle Eastern non-Jewish populations share a common pool of Y-chromosome biallelic haplotypes
-
Hammer MF, Redd AJ, Wood ET et al. Jewish and Middle Eastern non-Jewish populations share a common pool of Y-chromosome biallelic haplotypes. Proc Natl Acad Sci 2000; 97: 6769-74.
-
(2000)
Proc Natl Acad Sci
, vol.97
, pp. 6769-6774
-
-
Hammer, M.F.1
Redd, A.J.2
Wood, E.T.3
-
7
-
-
0034764750
-
The Y chromosome pool of Jews as part of the genetic landscape of the Middle East
-
Nebel A, Filon D, Brinkmann B et al. The Y chromosome pool of Jews as part of the genetic landscape of the Middle East. Am J Hum Genet 2001; 69: 1095-112.
-
(2001)
Am J Hum Genet
, vol.69
, pp. 1095-1112
-
-
Nebel, A.1
Filon, D.2
Brinkmann, B.3
-
8
-
-
18344362614
-
Founding mothers of Jewish communities: Geographically separated Jewish groups were independently founded by few female ancestors
-
Thomas MG, Weale ME, Jones AL et al. Founding mothers of Jewish communities: geographically separated Jewish groups were independently founded by few female ancestors. Am J Hum Genet 2002; 70: 1411-20.
-
(2002)
Am J Hum Genet
, vol.70
, pp. 1411-1420
-
-
Thomas, M.G.1
Weale, M.E.2
Jones, A.L.3
-
9
-
-
84862459217
-
-
March on 1 June 2004
-
MIM Statistics (March 2003). Retrieved from http:// www.ncbi.nlm.nih.gov/ Omim/Stats/mimstars.html on 1 June 2004.
-
(2003)
MIM Statistics
-
-
-
11
-
-
84911329245
-
Tay Sachs Disease mutations among Moroccan Jews
-
Bonné-Tamir B and Adam A (eds): New York: Oxford University Press
-
Navon R, Proia RL. Tay Sachs Disease mutations among Moroccan Jews. In Bonné-Tamir B and Adam A (eds): Genetic Diversity Among Jews. New York: Oxford University Press 1992.
-
(1992)
Genetic Diversity among Jews
-
-
Navon, R.1
Proia, R.L.2
-
12
-
-
0021045849
-
The Tay-Sachs disease gene in North American Jewish populations: Geographic variations and origin
-
Peterson GM, Rotter JI, Cantor RM et al. The Tay-Sachs disease gene in North American Jewish populations: geographic variations and origin. Am J Hum Genet 1983; 35: 1258-69.
-
(1983)
Am J Hum Genet
, vol.35
, pp. 1258-1269
-
-
Peterson, G.M.1
Rotter, J.I.2
Cantor, R.M.3
-
13
-
-
0037385394
-
Geographic distribution of disease mutations in the Ashkenazi Jewish population supports genetic drift over selection
-
Risch N, Tang H, Katzenstein H, Ekstein J. Geographic distribution of disease mutations in the Ashkenazi Jewish population supports genetic drift over selection. Am J Genet 2003; 72: 812-22.
-
(2003)
Am J Genet
, vol.72
, pp. 812-822
-
-
Risch, N.1
Tang, H.2
Katzenstein, H.3
Ekstein, J.4
-
14
-
-
0042164985
-
The possibility of a selection process in the Ashkenazi Jewish population
-
Zlotogora J, Bach G. The possibility of a selection process in the Ashkenazi Jewish population. Am J Genet 2003; 73: 438-40.
-
(2003)
Am J Genet
, vol.73
, pp. 438-440
-
-
Zlotogora, J.1
Bach, G.2
-
15
-
-
0036188591
-
Bloom syndrome and Fanconi's Anemia: Rate and ethnic origin of mutation carriers in Israel
-
Peleg L, Pesso R, Goldman B et al. Bloom syndrome and Fanconi's Anemia: rate and ethnic origin of mutation carriers in Israel. Isr Med Assoc J 2002; 4: 95-7.
-
(2002)
Isr Med Assoc J
, vol.4
, pp. 95-97
-
-
Peleg, L.1
Pesso, R.2
Goldman, B.3
-
16
-
-
0034903797
-
Numerous colonie adenomas in an individual with Bloom's syndrome
-
Lowy A, Kordich JJ, Gismondi V et al. Numerous colonie adenomas in an individual with Bloom's syndrome. Gastroenterology 2001; 121: 435-9.
-
(2001)
Gastroenterology
, vol.121
, pp. 435-439
-
-
Lowy, A.1
Kordich, J.J.2
Gismondi, V.3
-
17
-
-
0026604026
-
Fanconi Anemia and leukemia: Tracking the genes
-
Auerbach AD. Fanconi Anemia and leukemia: tracking the genes. Leukemia 1992; 6 (Suppl 1): 1-4.
-
(1992)
Leukemia
, vol.6
, Issue.1 SUPPL.
, pp. 1-4
-
-
Auerbach, A.D.1
-
18
-
-
0037306904
-
Cancer incidence in persons with Fanconi anemia
-
Rosenberg PS, Greene MH, Alter BP. Cancer incidence in persons with Fanconi anemia. Blood 2003; 101: 822-6.
-
(2003)
Blood
, vol.101
, pp. 822-826
-
-
Rosenberg, P.S.1
Greene, M.H.2
Alter, B.P.3
-
19
-
-
0033764862
-
Fanconi anaemia group a (FANCA) mutations in Israeli non-Ashkenazi Jewish patients
-
Tamary H, Bar-Yam R, Shalmon L et al. Fanconi anaemia group A (FANCA) mutations in Israeli non-Ashkenazi Jewish patients. Br J Haematol 2000; 111: 338-43.
-
(2000)
Br J Haematol
, vol.111
, pp. 338-343
-
-
Tamary, H.1
Bar-Yam, R.2
Shalmon, L.3
-
20
-
-
18444362122
-
Biallelic inactivation of BRCA2 in Fanconi Anemia
-
Howlett NG, Taniguchi T, Olson S et al. Biallelic inactivation of BRCA2 in Fanconi Anemia. Science 2002; 297: 606-9.
-
(2002)
Science
, vol.297
, pp. 606-609
-
-
Howlett, N.G.1
Taniguchi, T.2
Olson, S.3
-
21
-
-
0142054687
-
Shared genetic susceptibility to breast cancer, brain tumors, and Fanconi anemia
-
Offit K, Levran O, Mullaney B et al. Shared genetic susceptibility to breast cancer, brain tumors, and Fanconi anemia. J Natl Cancer Inst 2003; 95: 1548-51.
-
(2003)
J Natl Cancer Inst
, vol.95
, pp. 1548-1551
-
-
Offit, K.1
Levran, O.2
Mullaney, B.3
-
22
-
-
13344260688
-
Germ-line BRCA1 mutations in Jewish and non-Jewish women with early-onset breast cancer
-
Fitzgerald MG, MacDonald DJ, Krainer M et al. Germ-line BRCA1 mutations in Jewish and non-Jewish women with early-onset breast cancer. N Engl J Med 1996; 334: 143-9.
-
(1996)
N Engl J Med
, vol.334
, pp. 143-149
-
-
Fitzgerald, M.G.1
MacDonald, D.J.2
Krainer, M.3
-
23
-
-
13144305098
-
Could the 185delAG BRCA1 mutation be an ancient Jewish mutation?
-
Bruchim Bar-Sade R, Theodor L, Gak E et al. Could the 185delAG BRCA1 mutation be an ancient Jewish mutation? Eur J Hum Gene 1997; 51: 413-16.
-
(1997)
Eur J Hum Gene
, vol.51
, pp. 413-416
-
-
Bruchim Bar-Sade, R.1
Theodor, L.2
Gak, E.3
-
24
-
-
7144251883
-
The 185delAG BRCA1 mutation originated before the dispersion of Jews in the Diaspora and is not limited to Ashkenazim
-
Bruchim Bar-Sade R, Kruglikova A, Modan B et al. The 185delAG BRCA1 mutation originated before the dispersion of Jews in the Diaspora and is not limited to Ashkenazim. Hum Mol Genet 1998; 7: 801-5.
-
(1998)
Hum Mol Genet
, vol.7
, pp. 801-805
-
-
Bruchim Bar-Sade, R.1
Kruglikova, A.2
Modan, B.3
-
25
-
-
0034894831
-
The Tyr978X BRCA1 mutation in non-Ashkenazi Jews: Occurrence in high-risk families, general population and unselected ovarian cancer patients
-
Shiri-Sverdlov R. Gershoni-Baruch R, Ichezkel-Hirsch G et al. The Tyr978X BRCA1 mutation in non-Ashkenazi Jews: occurrence in high-risk families, general population and unselected ovarian cancer patients. Community Genet 2001; 4: 50-5.
-
(2001)
Community Genet
, vol.4
, pp. 50-55
-
-
Shiri-Sverdlov, R.1
Gershoni-Baruch, R.2
Ichezkel-Hirsch, G.3
-
26
-
-
16044366988
-
The carrier frequency of the BRCA2 6174delT mutation among Ashkenazi Jewish individuals is approximately 1%
-
Oddoux C, Struewing JP, Clayton CM et al. The carrier frequency of the BRCA2 6174delT mutation among Ashkenazi Jewish individuals is approximately 1%. Nat Genet 1996; 14: 188-90.
-
(1996)
Nat Genet
, vol.14
, pp. 188-190
-
-
Oddoux, C.1
Struewing, J.P.2
Clayton, C.M.3
-
27
-
-
0030138354
-
Recurrent BRCA2 6174delT mutations in Ashkenazi Jewish women affected by breast cancer
-
Neuhausen S, Gilewski LN, Tran T et al. Recurrent BRCA2 6174delT mutations in Ashkenazi Jewish women affected by breast cancer. Nat Genet 1996; 13: 126-8.
-
(1996)
Nat Genet
, vol.13
, pp. 126-128
-
-
Neuhausen, S.1
Gilewski, L.N.2
Tran, T.3
-
28
-
-
16944363862
-
Founder BRCA1 and BRCA2 mutations in Ashkenazi Jews in Israel: Frequency and differential penetrance in ovarian cancer and in breast-ovarian cancer families
-
Levy-Lahad E, Catane R, Eisenberg S et al. Founder BRCA1 and BRCA2 mutations in Ashkenazi Jews in Israel: frequency and differential penetrance in ovarian cancer and in breast-ovarian cancer families. Am J Hum Genet 1997; 60: 1059-67.
-
(1997)
Am J Hum Genet
, vol.60
, pp. 1059-1067
-
-
Levy-Lahad, E.1
Catane, R.2
Eisenberg, S.3
-
29
-
-
85048630959
-
The 8765delAG mutation in BRCA2 is common among Jews of Yemenite extraction
-
Lerer I, Wang T, Peretz T et al. The 8765delAG mutation in BRCA2 is common among Jews of Yemenite extraction. Am J Hum Genet 1998; 63: 272-4.
-
(1998)
Am J Hum Genet
, vol.63
, pp. 272-274
-
-
Lerer, I.1
Wang, T.2
Peretz, T.3
-
30
-
-
0031035359
-
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 et al. 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. Am J Hum Genet 1997; 60: 505-14.
-
(1997)
Am J Hum Genet
, vol.60
, pp. 505-514
-
-
Abeliovich, D.1
Kaduri, L.2
Lerer, I.3
-
31
-
-
16944365288
-
Familial colorectal cancer in Ashkenazim due to a hypermutable tract in APC
-
Laken SJ, Petersen GM, Gruber SB et al. Familial colorectal cancer in Ashkenazim due to a hypermutable tract in APC. Nat Genet 1997; 17: 79-83.
-
(1997)
Nat Genet
, vol.17
, pp. 79-83
-
-
Laken, S.J.1
Petersen, G.M.2
Gruber, S.B.3
-
32
-
-
0037093967
-
Clinical and screening implications of the I1307K adenomatous polyposis coli gene variant in Israeli Ashkenazi Jews with familial colorectal neoplasia. Evidence for a founder effect
-
Rozen P, Naiman T, Strul H et al. Clinical and screening implications of the I1307K adenomatous polyposis coli gene variant in Israeli Ashkenazi Jews with familial colorectal neoplasia. Evidence for a founder effect. Cancer 2002; 94; 2561-8.
-
(2002)
Cancer
, vol.94
, pp. 2561-2568
-
-
Rozen, P.1
Naiman, T.2
Strul, H.3
-
33
-
-
0037389343
-
Genetic analysis of familial colorectal cancer in Israeli Arabs
-
Chen-Shtoyerman R, Theodor L, Harmati E et al. Genetic analysis of familial colorectal cancer in Israeli Arabs. Hum Mut 2003; 21: 446-7.
-
(2003)
Hum Mut
, vol.21
, pp. 446-447
-
-
Chen-Shtoyerman, R.1
Theodor, L.2
Harmati, E.3
-
34
-
-
0036917758
-
The founder mutation MSH2*1906G>C is an important cause of hereditary non-polyposis colorectal cancer in the Ashkenazi Jewish population
-
Foulkes WD, Thiffault I, Gruber SB et al. The founder mutation MSH2*1906G>C is an important cause of hereditary non-polyposis colorectal cancer in the Ashkenazi Jewish population. Am J Hum Genet 2002; 71: 1395-412.
-
(2002)
Am J Hum Genet
, vol.71
, pp. 1395-1412
-
-
Foulkes, W.D.1
Thiffault, I.2
Gruber, S.B.3
-
35
-
-
0037324532
-
A636P is associated with early-onset colon cancer in Ashkenazi Jews
-
Guillem JG, Rapaport BS, Kirchhoff T et al. A636P is associated with early-onset colon cancer in Ashkenazi Jews. J Am Coll Surg 2003; 196: 222-5.
-
(2003)
J Am Coll Surg
, vol.196
, pp. 222-225
-
-
Guillem, J.G.1
Rapaport, B.S.2
Kirchhoff, T.3
-
36
-
-
0142214793
-
A prospective study of the clinical, genetic, screening and pathological features of a family with hereditary mixed polyposis syndrome
-
Rozen P, Samuel Z, Brazowski E. A prospective study of the clinical, genetic, screening and pathological features of a family with hereditary mixed polyposis syndrome. Am J Gastroenterol 2003; 98: 2317-20.
-
(2003)
Am J Gastroenterol
, vol.98
, pp. 2317-2320
-
-
Rozen, P.1
Samuel, Z.2
Brazowski, E.3
-
37
-
-
0037730140
-
An ancestral Ashkenazi haplotype at the HMPS/CRAC1 locus on 15q13-q14 is associated with hereditary mixed polyposis syndrome
-
Jaeger EEM, Woodford-Richens KL, Lockett M et al. An ancestral Ashkenazi haplotype at the HMPS/CRAC1 locus on 15q13-q14 is associated with hereditary mixed polyposis syndrome. Am J Hum Genet 2003; 72: 1261-7.
-
(2003)
Am J Hum Genet
, vol.72
, pp. 1261-1267
-
-
Jaeger, E.E.M.1
Woodford-Richens, K.L.2
Lockett, M.3
|