-
1
-
-
0029125296
-
Inherited breast and ovarian cancer
-
Szabo CI, King MC: Inherited breast and ovarian cancer. Hum Mol Genet 1995;4:1811-1817.
-
(1995)
Hum Mol Genet
, vol.4
, pp. 1811-1817
-
-
Szabo, C.I.1
King, M.C.2
-
2
-
-
0029083814
-
The carrier frequency of the BRCA1 185de1AG mutation is approximately 1 percent in Ashkenazi Jewish individiuals
-
Streuwing JP, Abeliovitch D, Peretz T, Avishai N, Kaback MM, Collins FS, Brody LC: The carrier frequency of the BRCA1 185de1AG mutation is approximately 1 percent in Ashkenazi Jewish individiuals. Nat Genet 1995;11:198-200.
-
(1995)
Nat 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
-
3
-
-
0029794992
-
Ashkenazi Jewish population frequencies for common mutations in BRCA1 and BRCA2
-
Roa BB, Boyd AA, Volick K, Richards CS: Ashkenazi Jewish population frequencies for common mutations in BRCA1 and BRCA2. Nat Genet 1996;14:185-187.
-
(1996)
Nat 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 JP, Clayton CM, Neuhausen S, Brody LC, Kaback M, Haas B, Norton L, Borgen P, Jhanwar S, Goldgar D, Ostrer H, Offit K: The carrier frequency of the BRCA2 6174delT mutation among Ashkenazi Jewish individuals is approximately 1%. Nat Genet 1996;14:188-190.
-
(1996)
Nat 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
-
6
-
-
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, Peretz T: 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 1997;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
-
8
-
-
0018177059
-
Ethnic communities in Israel: The genetic blood markers of Babylonian Jews
-
Bonne-Tamir B, Asbel S, Bar-Shani S: Ethnic communities in Israel: The genetic blood markers of Babylonian Jews. Am J Phys Anthropol 1978;49:457-464.
-
(1978)
Am J Phys Anthropol
, vol.49
, pp. 457-464
-
-
Bonne-Tamir, B.1
Asbel, S.2
Bar-Shani, S.3
-
9
-
-
0001937175
-
Genetic diversity among Jews reexamined: Preliminary analysis at the DNA level
-
Bonne-Tamir B, Adam A (eds): Oxford, Oxford University Press
-
Bonne-Tamir B, Zoosman-Disakin A, Ticher A: Genetic diversity among Jews reexamined: Preliminary analysis at the DNA level; in Bonne-Tamir B, Adam A (eds): Genetic Diversity among Jews. Diseases and Markers at the DNA Level. Oxford, Oxford University Press, 1992, pp 80-94.
-
(1992)
Genetic Diversity among Jews. Diseases and Markers at the DNA Level
, pp. 80-94
-
-
Zoosman-Disakin A, B.B.1
Ticher, A.2
-
10
-
-
0028034348
-
Confirmation of BRCA1 by analysis of germline mutations linked to breast and ovarian cancer in ten families
-
Friedman LS, Ostermeyer EA, Szabo CI, Dowd P, Lynch ED, Powell SE, King MC: Confirmation of BRCA1 by analysis of germline mutations linked to breast and ovarian cancer in ten families. Nat Genet 1994;8:399-404.
-
(1994)
Nat 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
-
11
-
-
0029737763
-
Heteroduplex and protein truncation analysis of the BRCA1 185delAG mutation
-
Ozelik H, Antebi YJ, Cole DEC, Andrulis IL: Heteroduplex and protein truncation analysis of the BRCA1 185delAG mutation. Hum Genet 1996;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
-
12
-
-
10544234199
-
High frequency of the 185delAG mutation in ovarian cancer in Israel
-
Modan B, Gak E, Hirsch G, Bar-Sade Bruchim R, Theodor L, Lubin F, Ben-Baruch G, Beller U, Fishman A, Dgani R, Menczer J, Papa MZ, Friedman E: High frequency of the 185delAG mutation in ovarian cancer in Israel. JAMA 1996;276:1823-1825.
-
(1996)
JAMA
, vol.276
, pp. 1823-1825
-
-
Modan, B.1
Gak, E.2
Hirsch, G.3
Bar-Sade Bruchim, R.4
Theodor, L.5
Lubin, F.6
Ben-Baruch, G.7
Beller, U.8
Fishman, A.9
Dgani, R.10
Menczer, J.11
Papa, M.Z.12
Friedman, E.13
-
13
-
-
0024437865
-
Direct sequencing of affinity captured amplified human DNA: Application to the detection of apolipoprotein E polymorphism
-
Syvänen AC, Aalto-Setälä K, Kontula K, Soderlund H: Direct sequencing of affinity captured amplified human DNA: Application to the detection of apolipoprotein E polymorphism. FEBS Lett 1989;258:71-74.
-
(1989)
FEBS Lett
, vol.258
, pp. 71-74
-
-
Syvänen, A.C.1
Aalto-Setälä, K.2
Kontula, K.3
Soderlund, H.4
-
14
-
-
0028113345
-
A strong candidate for the breast and ovarian cancer susceptibility gene BRCA1
-
Miki Y, Swensen J, Shattuck-Eidens D, Futreal PA, Harsman K, Tavtigian S, Liu Q, Cochran C, Bennet LM, Ding W, Bell R, Rosenthal J, Hussey C, Tran T, McClure M, Frye C, Hattier T, Pelps R, Haugen-Strano A, Katcher H, Yakumo K, Gholami Z, Shaffer D, Stone S, Bayer S, Wray C, Bogden R, Dayananth P, Ward J, Tonin P, Narod S, Bristow PK, Norris FH, Helvering L, Morrison P, Rosteck P, Lai M, Barrett JC, Lewis C, Neuhausen S, Cannon-Albright L, Goldgar D, Wessman R, Kamb A, Skolnick MH: A strong candidate for the breast and ovarian cancer susceptibility gene BRCA1. Science 1994;266:66-71.
-
(1994)
Science
, vol.266
, pp. 66-71
-
-
Miki, Y.1
Swensen, J.2
Shattuck-Eidens, D.3
Futreal, P.A.4
Harsman, K.5
Tavtigian, S.6
Liu, Q.7
Cochran, C.8
Bennet, L.M.9
Ding, W.10
Bell, R.11
Rosenthal, J.12
Hussey, C.13
Tran, T.14
McClure, M.15
Frye, C.16
Hattier, T.17
Pelps, R.18
Haugen-Strano, A.19
Katcher, H.20
Yakumo, K.21
Gholami, Z.22
Shaffer, D.23
Stone, S.24
Bayer, S.25
Wray, C.26
Bogden, R.27
Dayananth, P.28
Ward, J.29
Tonin, P.30
Narod, S.31
Bristow, P.K.32
Norris, F.H.33
Helvering, L.34
Morrison, P.35
Rosteck, P.36
Lai, M.37
Barrett, J.C.38
Lewis, C.39
Neuhausen, S.40
Cannon-Albright, L.41
Goldgar, D.42
Wessman, R.43
Kamb, A.44
Skolnick, M.H.45
more..
-
15
-
-
19144362921
-
Haplotype and phenotype analysis of six recurrent BRCA1 mutations in 61 families: Results of an international study
-
Neuhausen SL, 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, Streuwing J, Tonin P, Durcher F, Narod S, Skolnick MH, Lenoir G, Serova O, Ponder B, Stoppa-Lynnrd D, Easton D, King MC, Goldgar D: Haplotype and phenotype analysis of six recurrent BRCA1 mutations in 61 families: Results of an international study. Am J Hum Genet 1996;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
Streuwing, 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..
-
17
-
-
0028899613
-
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: 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. Blood 1995;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
-
18
-
-
0029949217
-
Two distinct origins of a common mutation in breastovarian cancer families: A genetic study of 15 185delAG-mutation kindreds
-
Berman DB, Wagner-Costalas J, Schultz DC, Lynch DC, Daly M, Goodwin AK: Two distinct origins of a common mutation in breastovarian cancer families: A genetic study of 15 185delAG-mutation kindreds. Am J Hum Genet 1996;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
-
19
-
-
0028229223
-
The origin of the major cystic fibrosis mutation (delta F508) in European populations
-
Morral N, Bertranpetit J; Estivill X, Nunes V, Casals T, Gimenez J, Reis A, Varon Mateeva R, Macek M Jr, Kalaydjieva L: The origin of the major cystic fibrosis mutation (delta F508) in European populations. Nat Genet 1994;7: 169-175.
-
(1994)
Nat Genet
, vol.7
, pp. 169-175
-
-
Morral, N.1
Bertranpetit, J.2
Estivill, X.3
Nunes, V.4
Casals, T.5
Gimenez, J.6
Reis, A.7
Varon Mateeva, R.8
Macek Jr., M.9
Kalaydjieva, L.10
-
20
-
-
0029684888
-
Microsatellites are subject to directional evolution
-
William A, Rubinstein DC: Microsatellites are subject to directional evolution. Nat Genet 1996;12:13-14.
-
(1996)
Nat Genet
, vol.12
, pp. 13-14
-
-
William, A.1
Rubinstein, D.C.2
-
21
-
-
0030035824
-
Directional evolution in germline microsatellite mutations
-
Ellgern H, Saino N, Moller AP: Directional evolution in germline microsatellite mutations. Nat Genet 1996;13:391-393.
-
(1996)
Nat Genet
, vol.13
, pp. 391-393
-
-
Ellgern, H.1
Saino, N.2
Moller, A.P.3
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