-
3
-
-
0029794992
-
Ashkenazi Jewish population frequencies for common mutations in BRCA1 and BRCA2
-
Roa, B.B., Boyd, A.A., Volick, K. and Richards, C.S. (1996) Ashkenazi Jewish population frequencies for common mutations in BRCA1 and BRCA2. Nature Genet., 14, 185-187.
-
(1996)
Nature Genet.
, vol.14
, pp. 185-187
-
-
Roa, B.B.1
Boyd, A.A.2
Volick, K.3
Richards, C.S.4
-
4
-
-
16044366988
-
The carrier frequency of the BRCA2 6174delT mutation among Ashkenazi Jewish individuals is approximately 1%
-
Odduoux, C., Streuwing, J.P., Clayton, C.M., Neuhausen, S., Brody, L.C., Kaback, M., Haas, B., Norton, L., Borgen, P., Jhanwar, S., Goldgar, D., Ostrer, H. and Offit, K. (1996) The carrier frequency of the BRCA2 6174delT mutation among Ashkenazi Jewish individuals is approximately 1%. Nature Genet., 14, 188-190.
-
(1996)
Nature Genet.
, vol.14
, pp. 188-190
-
-
Odduoux, C.1
Streuwing, J.P.2
Clayton, C.M.3
Neuhausen, S.4
Brody, L.C.5
Kaback, M.6
Haas, B.7
Norton, L.8
Borgen, P.9
Jhanwar, S.10
Goldgar, D.11
Ostrer, H.12
Offit, K.13
-
5
-
-
0029083814
-
The carrier frequency of the BRCA1 185delAG mutation is approximately 1 percent in Ashkenazi Jewish individuals
-
Streuwing, J.P., Abeliovitch, D., Peretz, T., Avishai, N., Kaback, M.M., Collins, F.S. and Brody, L.C. (1995) The carrier frequency of the BRCA1 185delAG mutation is approximately 1 percent in Ashkenazi Jewish individuals. Nature Genet., 11, 198-200.
-
(1995)
Nature Genet.
, vol.11
, pp. 198-200
-
-
Streuwing, J.P.1
Abeliovitch, D.2
Peretz, T.3
Avishai, N.4
Kaback, M.M.5
Collins, F.S.6
Brody, L.C.7
-
6
-
-
0030049823
-
BRCA1 mutations in a population-based sample of young women with breast cancer
-
Langston, A.A., Malone, K.E., Thompson, J.D. and Ostrander, E.A. (1996) BRCA1 mutations in a population-based sample of young women with breast cancer. N. Engl. J. Med., 334, 137-142.
-
(1996)
N. Engl. J. Med.
, vol.334
, pp. 137-142
-
-
Langston, A.A.1
Malone, K.E.2
Thompson, J.D.3
Ostrander, E.A.4
-
7
-
-
13344260688
-
Germ-line BRCA1 mutations in Jewish and non-Jewish women with early onset breast cancer
-
FitzGerald, M.G., MacDonald, D.J., Krainer, M., Hoover, I., O'Neil, E., Unsal, H., Silva-Arielo, H., Finkelstein, D.M., Beer-Romero, P., Englert, C., Sgori, D.C., Smith, B.L., Younger, I.W., Garber, J.E., Duda, A.B., Mayzel, K.A., Isselbacher, K.J., Friend, S.H. and Haber, D.H. (1996) Germ-line BRCA1 mutations in Jewish and non-Jewish women with early onset breast cancer. N. Engl. J. Med., 334, 143-149.
-
(1996)
N. Engl. J. Med.
, vol.334
, pp. 143-149
-
-
FitzGerald, M.G.1
MacDonald, D.J.2
Krainer, M.3
Hoover, I.4
O'Neil, E.5
Unsal, H.6
Silva-Arielo, H.7
Finkelstein, D.M.8
Beer-Romero, P.9
Englert, C.10
Sgori, D.C.11
Smith, B.L.12
Younger, I.W.13
Garber, J.E.14
Duda, A.B.15
Mayzel, K.A.16
Isselbacher, K.J.17
Friend, S.H.18
Haber, D.H.19
-
8
-
-
0029949217
-
Two distinct origins of a common mutation in breast-ovarian cancer families: A genetic study of 15 185delAG-mutation kindreds
-
Berman, D.B., Wagner-Costalas, J., Schultz, D.C., Lynch, D.C., Daly, M. and Goodwin, A.K. (1996) Two distinct origins of a common mutation in breast-ovarian cancer families: a genetic study of 15 185delAG-mutation kindreds. Am. J. Hum. Genet., 58, 1166-1176.
-
(1996)
Am. J. Hum. Genet.
, vol.58
, pp. 1166-1176
-
-
Berman, D.B.1
Wagner-Costalas, J.2
Schultz, D.C.3
Lynch, D.C.4
Daly, M.5
Goodwin, A.K.6
-
9
-
-
19144362921
-
Haplotype and phenotype analysis of six recurrent BRCA1 mutations in 61 families: Results of an international study
-
Neuhausen, S.L., Mazoyer, S., Friedman, L., Stratton, M., Offit, K., Caligo, A.,Tomlinson, G., Cannon-Albright, L., Bishop, T., Kelsell, D., Solomon, E., Weber, B., Couch, F., Streuwitig, J., Tonin, P., Durcher, F., Narod, S., Skolnick, M.H., Lenoir, G., Serova, O., Ponder, B., Stoppa-Lynnrd, D., Easton, D., King, M.C. and Goldgar, D. (1996) Haplotype and phenotype analysis of six recurrent BRCA1 mutations in 61 families: results of an international study. Am. J. Hum. Genet., 58, 271-280.
-
(1996)
Am. J. Hum. Genet.
, vol.58
, pp. 271-280
-
-
Neuhausen, S.L.1
Mazoyer, S.2
Friedman, L.3
Stratton, M.4
Offit, K.5
Caligo, A.6
Tomlinson, G.7
Cannon-Albright, L.8
Bishop, T.9
Kelsell, D.10
Solomon, E.11
Weber, B.12
Couch, F.13
Streuwitig, J.14
Tonin, P.15
Durcher, F.16
Narod, S.17
Skolnick, M.H.18
Lenoir, G.19
Serova, O.20
Ponder, B.21
Stoppa-Lynnrd, D.22
Easton, D.23
King, M.C.24
Goldgar, D.25
more..
-
10
-
-
0012614805
-
Breast cancer and BRCA1
-
Sher, C., Sharabani-Gargir, L. and Shohat, M. (1996) Breast cancer and BRCA1. N. Engl. J. Med., 334, 1199.
-
(1996)
N. Engl. J. Med.
, vol.334
, pp. 1199
-
-
Sher, C.1
Sharabani-Gargir, L.2
Shohat, M.3
-
11
-
-
0031035359
-
The founder mutation 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. and Peretz, T. (1997) The founder mutation 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., 60, 505-514.
-
(1997)
Am. J. Hum. Genet.
, vol.60
, pp. 505-514
-
-
Abeliovich, D.1
Kaduri, L.2
Lerer, I.3
Weinberg, N.4
Amir, G.5
Sagi, M.6
Zlotogora, J.7
Heching, N.8
Peretz, T.9
-
12
-
-
13144305098
-
Could the 185delAG BRCA1 mutation be an ancient Jewish mutation?
-
Bruchim Bar-Sade, R., Theodor, L., Gak, E., Kruglikova, A., Hirsh-Yechezkel, G., Modan, B., Kuperstein, G., Seligsohn, U., Rechavi, G. and Friedman, E. (1997) Could the 185delAG BRCA1 mutation be an ancient Jewish mutation? Eur. J. Hum. Genet., 51, 413-416.
-
(1997)
Eur. J. Hum. Genet.
, vol.51
, pp. 413-416
-
-
Bruchim Bar-Sade, R.1
Theodor, L.2
Gak, E.3
Kruglikova, A.4
Hirsh-Yechezkel, G.5
Modan, B.6
Kuperstein, G.7
Seligsohn, U.8
Rechavi, G.9
Friedman, E.10
-
13
-
-
0028899613
-
One of the two common mutations causing factor X1 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. and Seligsohn, U. (1995) One of the two common mutations causing factor X1 deficiency in Ashkenazi Jews (type II) is also prevalent in Iraqi Jews, who represent the ancient gene pool of Jews. Blood, 85, 429-432.
-
(1995)
Blood
, vol.85
, pp. 429-432
-
-
Shpilberg, O.1
Peretz, H.2
Zivelin, A.3
Yatuv, R.4
Chetrit, A.5
Kulka, T.6
Stern, C.7
Weiss, E.8
Seligsohn, U.9
-
14
-
-
0029684888
-
Microsatellites are subject to directional evolution
-
William, A. and Rubinstein, D.C. (1996) Microsatellites are subject to directional evolution. Nature Genet., 12, 13-14.
-
(1996)
Nature Genet.
, vol.12
, pp. 13-14
-
-
William, A.1
Rubinstein, D.C.2
-
15
-
-
0030017038
-
Microsatellites show mutational bias and heterozygote instability
-
William, A. and Rubinstein, D.S. (1996) Microsatellites show mutational bias and heterozygote instability. Nature Genet., 13, 390-391.
-
(1996)
Nature Genet.
, vol.13
, pp. 390-391
-
-
William, A.1
Rubinstein, D.S.2
-
16
-
-
0003010558
-
A perspective of genetic diseases among the Jewish people
-
Goodman, R.M and Moutulsky, A.G. (eds), Raven Press, New York
-
Goodman, R.M. (1979) A perspective of genetic diseases among the Jewish people. In Goodman, R.M and Moutulsky, A.G. (eds), Genetic Diseases among Ashkena:i Jews. Raven Press, New York.
-
(1979)
Genetic Diseases among Ashkena:i Jews
-
-
Goodman, R.M.1
-
17
-
-
0001937175
-
Genetic diversity among Jews re-examined: Preliminary analysis at the DNA level
-
Bonne-Tamir, B. and Adam, A. (eds), Oxford University Press, Oxford
-
Bonne-Tamir, B., Zoosman-Disakin, A. and Ticher, A. (1992) Genetic diversity among Jews re-examined: preliminary analysis at the DNA level. In Bonne-Tamir, B. and Adam, A. (eds), Genetic Diversity among Jews. Diseases and Markers at the DNA Level. Oxford University Press, Oxford, pp. 80-94.
-
(1992)
Genetic Diversity among Jews. Diseases and Markers at the DNA Level
, pp. 80-94
-
-
Bonne-Tamir, B.1
Zoosman-Disakin, A.2
Ticher, A.3
-
18
-
-
0030902227
-
Population genetics of BRCA1 and BRCA2
-
Szabo, C.I. and King, M.C. (1997) Population genetics of BRCA1 and BRCA2. Am. J. Hum. Genet., 60, 1013-1020.
-
(1997)
Am. J. Hum. Genet.
, vol.60
, pp. 1013-1020
-
-
Szabo, C.I.1
King, M.C.2
-
19
-
-
0028034348
-
Confirmation of BRCA1 by analysis of germline mutations linked to breast and ovarian cancer in ten families
-
Friedman, L.S., Ostermeyer, E.A., Szabo, C.I., Dowd, P., Lynch, E.D., Powell, S.E. and King, M.C. (1994) Confirmation of BRCA1 by analysis of germline mutations linked to breast and ovarian cancer in ten families. Nature Genet., 8, 399-404.
-
(1994)
Nature Genet.
, vol.8
, pp. 399-404
-
-
Friedman, L.S.1
Ostermeyer, E.A.2
Szabo, C.I.3
Dowd, P.4
Lynch, E.D.5
Powell, S.E.6
King, M.C.7
-
20
-
-
0029737763
-
Heteroduplex and protein truncation analysis of the BRCA1 185delAG mutation
-
Ozelik, H., Antebi, Y.J., Cole, D.E.C. and Andrulis, I.L. (1996) Heteroduplex and protein truncation analysis of the BRCA1 185delAG mutation. Hum Genet., 98, 310-312.
-
(1996)
Hum Genet.
, vol.98
, pp. 310-312
-
-
Ozelik, H.1
Antebi, Y.J.2
Cole, D.E.C.3
Andrulis, I.L.4
-
21
-
-
0024437865
-
Direct sequencing of affinity captured amplified human DNA: Application to the detection of apolipoprotein e polymorphism
-
Syvänen, A.C., Aalto-Setälä, K., Kontula, K. and Söderlund, H. (1989) Direct sequencing of affinity captured amplified human DNA: application to the detection of apolipoprotein E polymorphism. FEBS Lett., 258, 71-74.
-
(1989)
FEBS Lett.
, vol.258
, pp. 71-74
-
-
Syvänen, A.C.1
Aalto-Setälä, K.2
Kontula, K.3
Söderlund, H.4
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