-
1
-
-
0001422175
-
Some observations on the epidemiology of breast cancer among males
-
Schottenfeld, D., Lilienfeld, A. M., and Diamond, H. Some observations on the epidemiology of breast cancer among males. Am. J. Publ. Health, 53: 890-897, 1963.
-
(1963)
Am. J. Publ. Health
, vol.53
, pp. 890-897
-
-
Schottenfeld, D.1
Lilienfeld, A.M.2
Diamond, H.3
-
2
-
-
0028967165
-
Male breast cancer
-
Schön, M., Zaiac, M., and Schlag, P. M. Male breast cancer. Onkologie, 18: 16-21, 1995.
-
(1995)
Onkologie
, vol.18
, pp. 16-21
-
-
Schön, M.1
Zaiac, M.2
Schlag, P.M.3
-
3
-
-
0028936995
-
Carcinoma of the male breast: Update 1994
-
Wagner, J. L., Thomas, C. R., Koh, W-J., and Rudolph, R. H. Carcinoma of the male breast: update 1994. Med. Pediatr. Oncol., 24: 123-132, 1995.
-
(1995)
Med. Pediatr. Oncol.
, vol.24
, pp. 123-132
-
-
Wagner, J.L.1
Thomas, C.R.2
Koh, W.-J.3
Rudolph, R.H.4
-
4
-
-
0023780504
-
Endocrine epidemiology of male breast cancer
-
Rose, D. P. Endocrine epidemiology of male breast cancer. Anticancer Res., 8: 45-850, 1988.
-
(1988)
Anticancer Res.
, vol.8
, pp. 45-850
-
-
Rose, D.P.1
-
5
-
-
0026935782
-
A germline mutation in the androgen receptor gene in two brothers with breast cancer and Reifenstein syndrome
-
Wooster, R., Mangion, J., Eeles, R., Smith, S., Dowsett, M., Averill, D., Barrett-Lee, P., Easton, D. F., Ponder, B. A. J., and Stratton, M. R. A germline mutation in the androgen receptor gene in two brothers with breast cancer and Reifenstein syndrome. Nat. Genet., 2: 132-134, 1992.
-
(1992)
Nat. Genet.
, vol.2
, pp. 132-134
-
-
Wooster, R.1
Mangion, J.2
Eeles, R.3
Smith, S.4
Dowsett, M.5
Averill, D.6
Barrett-Lee, P.7
Easton, D.F.8
Ponder, B.A.J.9
Stratton, M.R.10
-
6
-
-
0027381049
-
Androgen receptor gene mutation in male breast cancer
-
Lobaccaro, J-M., Lumbroso, S., Belon, C., Galtier-Dereure, F., Bringer, J., Lesimple, T., Namer, M., Cutuli, F., Pujoi, H., and Sultan, C. Androgen receptor gene mutation in male breast cancer. Hum. Mol. Genet., 2: 1799-1802, 1993.
-
(1993)
Hum. Mol. Genet.
, vol.2
, pp. 1799-1802
-
-
Lobaccaro, J.-M.1
Lumbroso, S.2
Belon, C.3
Galtier-Dereure, F.4
Bringer, J.5
Lesimple, T.6
Namer, M.7
Cutuli, F.8
Pujoi, H.9
Sultan, C.10
-
7
-
-
0028006563
-
Localization of a breast cancer susceptibility gene, BRCA2, to chromosome 13q12-13
-
Washington DC
-
Wooster, R., Neuhausen, S. L., Mangion, J., Quirk, Y., Ford, D., Collins, N., Nguyen, K., Seal, S., Tran, T., Averill, D., Fields, P., Marshall, G., Narod, S., Lenoir, G. M., Lynch, H., Feunteun, J., Devilee, P., Cornelisse, C. J., Menko, F. H., Daly, P. A., Ormiston, W., McManus, R., Pye, C., Lewis, C. M., Cannon-Albright, L. A., Peto, J., Ponder, B. A. J., Skolnick, M. H., Easton, D. F., Goldgar, D. E., and Stratton, M. R. Localization of a breast cancer susceptibility gene, BRCA2, to chromosome 13q12-13. Science (Washington DC), 265: 2088-2090, 1994.
-
(1994)
Science
, vol.265
, pp. 2088-2090
-
-
Wooster, R.1
Neuhausen, S.L.2
Mangion, J.3
Quirk, Y.4
Ford, D.5
Collins, N.6
Nguyen, K.7
Seal, S.8
Tran, T.9
Averill, D.10
Fields, P.11
Marshall, G.12
Narod, S.13
Lenoir, G.M.14
Lynch, H.15
Feunteun, J.16
Devilee, P.17
Cornelisse, C.J.18
Menko, F.H.19
Daly, P.A.20
Ormiston, W.21
McManus, R.22
Pye, C.23
Lewis, C.M.24
Cannon-Albright, L.A.25
Peto, J.26
Ponder, B.A.J.27
Skolnick, M.H.28
Easton, D.F.29
Goldgar, D.E.30
Stratton, M.R.31
more..
-
8
-
-
0029160005
-
Linkage to BRCA2 region in hereditary male breast cancer
-
Thorlacius, S., Tryggvardottir, L., Olafsdottir, G. H., Jonasson, J. G., Ogmundsdottir, H. M., Tulinius, H., and Eyfjord, J. E. Linkage to BRCA2 region in hereditary male breast cancer. Lancet, 346: 544-545, 1995.
-
(1995)
Lancet
, vol.346
, pp. 544-545
-
-
Thorlacius, S.1
Tryggvardottir, L.2
Olafsdottir, G.H.3
Jonasson, J.G.4
Ogmundsdottir, H.M.5
Tulinius, H.6
Eyfjord, J.E.7
-
9
-
-
0006713602
-
Identification of the breast cancer susceptibility gene BRCA2
-
Wooster, R., Bignell, G., Lancaster, J., Swift, S., Seal, S., Mangion, J., Collins, N., Gregory, S., Gumbs, C., Micklem, G., Barfoot, R., Hamoudi, R., Patel, S., Rice, C., Biggs. P., Hashim, Y., Smith, A., Connor, F., Arason, A., Gudmundsson, J., Ficenec, D., Kelsell, D., Ford, D., Tonin, P., Bishop, D. T., Spurr, N. K., Ponder, B. A. J., Eeles, R., Peto, J., Devilee, P., Cornelisse, C., Lynch, H., Narod, S., Lenoir, G., Egilsson, V., Barkadottir, R. B., Easton, D. F., Bentley, D. R., Futreal, P. A., Ashworth, A., and Stratton, M. R. Identification of the breast cancer susceptibility gene BRCA2. Nature (Lond.), 378: 789-792, 1995.
-
(1995)
Nature (Lond.)
, vol.378
, pp. 789-792
-
-
Wooster, R.1
Bignell, G.2
Lancaster, J.3
Swift, S.4
Seal, S.5
Mangion, J.6
Collins, N.7
Gregory, S.8
Gumbs, C.9
Micklem, G.10
Barfoot, R.11
Hamoudi, R.12
Patel, S.13
Rice, C.14
Biggs, P.15
Hashim, Y.16
Smith, A.17
Connor, F.18
Arason, A.19
Gudmundsson, J.20
Ficenec, D.21
Kelsell, D.22
Ford, D.23
Tonin, P.24
Bishop, D.T.25
Spurr, N.K.26
Ponder, B.A.J.27
Eeles, R.28
Peto, J.29
Devilee, P.30
Cornelisse, C.31
Lynch, H.32
Narod, S.33
Lenoir, G.34
Egilsson, V.35
Barkadottir, R.B.36
Easton, D.F.37
Bentley, D.R.38
Futreal, P.A.39
Ashworth, A.40
Stratton, M.R.41
more..
-
10
-
-
0030139524
-
BRCA2 germline mutations in male breast cancer cases and breast cancer families
-
Couch, F. J., Farid, L. M., DeShano, M. L., Tavtigian, S. V., Calzone, K., Campeau, L., Peng, Y., Bogden, B., Chen, Q., Neuhausen, S., Shattuck-Eidens, D., Godwin, A. K., Daly, M., Radford, D. M., Sedlacek, S., Rommens, J., Simard, J., Garber, J., Merajver, S., and Weber, B. L. BRCA2 germline mutations in male breast cancer cases and breast cancer families. Nat. Genet., 13: 123-125, 1996.
-
(1996)
Nat. Genet.
, vol.13
, pp. 123-125
-
-
Couch, F.J.1
Farid, L.M.2
DeShano, M.L.3
Tavtigian, S.V.4
Calzone, K.5
Campeau, L.6
Peng, Y.7
Bogden, B.8
Chen, Q.9
Neuhausen, S.10
Shattuck-Eidens, D.11
Godwin, A.K.12
Daly, M.13
Radford, D.M.14
Sedlacek, S.15
Rommens, J.16
Simard, J.17
Garber, J.18
Merajver, S.19
Weber, B.L.20
more..
-
11
-
-
0030137718
-
Mutation analysis of the BRCA2 gene in 49 site-specific breast cancer families
-
Phelan, C. M., Lancaster, J. M., Tonin, P., Gumbs, C., Cochran, C., Carter, R., Ghadirian, P., Perret, C., Moslehi, R., Dion, F., Faucher, M-C., Dole, K., Karimi, S., Foulkes, W., Lounis, H., Warner, E., Goss, P., Anderson, D., Larsson, C., Narod, S. A., and Futreal, P. A. Mutation analysis of the BRCA2 gene in 49 site-specific breast cancer families. Nat. Genet., 13: 120-122, 1996.
-
(1996)
Nat. Genet.
, vol.13
, pp. 120-122
-
-
Phelan, C.M.1
Lancaster, J.M.2
Tonin, P.3
Gumbs, C.4
Cochran, C.5
Carter, R.6
Ghadirian, P.7
Perret, C.8
Moslehi, R.9
Dion, F.10
Faucher, M.-C.11
Dole, K.12
Karimi, S.13
Foulkes, W.14
Lounis, H.15
Warner, E.16
Goss, P.17
Anderson, D.18
Larsson, C.19
Narod, S.A.20
Futreal, P.A.21
more..
-
12
-
-
13344269668
-
The complete BRCA2 gene and mutations in chromosome 13q-linked kindreds
-
Tavtigian, S. V., Simard, J., Rommens, J., Couch, F., Shattuck-Eidens, D., Neuhausen, S., Merajver, S., Thorlacius, S., Offit, K., Stoppa-Lyonnet, D., Belanger, C., Bell, R., Berry, S., Bogden, R., Chen, Q., Davis, T., Dumont, M., Frye, C., Hattier, T., Jammulapati, S., Janecki, T., Jiang, P., Kehrer, R., Leblanc, J-F., Mitchell, J. T., McArthur-Morrison, J., Nguyen, K., Peng, Y., Samson, C., Schroeder, M., Snyder, S. C., Steele, L., Stringfellow, M., Stroup, C., Swedlund, B., Swensen, J., Teng, D., Thomas, A., Tran, T., Tranchant, M., Weaver-Feldhaus, J., Wong, A. K. C., Shizuya, H., Eyfjord, J. E., Cannon-Albright, L., Labrie, F., Skolnick, M. H., Weber, B., Kamb, A., and Goldgar, D. E. The complete BRCA2 gene and mutations in chromosome 13q-linked kindreds. Nat. Genet., 12: 333-337, 1996.
-
(1996)
Nat. Genet.
, vol.12
, pp. 333-337
-
-
Tavtigian, S.V.1
Simard, J.2
Rommens, J.3
Couch, F.4
Shattuck-Eidens, D.5
Neuhausen, S.6
Merajver, S.7
Thorlacius, S.8
Offit, K.9
Stoppa-Lyonnet, D.10
Belanger, C.11
Bell, R.12
Berry, S.13
Bogden, R.14
Chen, Q.15
Davis, T.16
Dumont, M.17
Frye, C.18
Hattier, T.19
Jammulapati, S.20
Janecki, T.21
Jiang, P.22
Kehrer, R.23
Leblanc, J.-F.24
Mitchell, J.T.25
McArthur-Morrison, J.26
Nguyen, K.27
Peng, Y.28
Samson, C.29
Schroeder, M.30
Snyder, S.C.31
Steele, L.32
Stringfellow, M.33
Stroup, C.34
Swedlund, B.35
Swensen, J.36
Teng, D.37
Thomas, A.38
Tran, T.39
Tranchant, M.40
Weaver-Feldhaus, J.41
Wong, A.K.C.42
Shizuya, H.43
Eyfjord, J.E.44
Cannon-Albright, L.45
Labrie, F.46
Skolnick, M.H.47
Weber, B.48
Kamb, A.49
Goldgar, D.E.50
more..
-
13
-
-
0030140026
-
A single BRCA2 mutation in male and female breast cancer families from Iceland with varied cancer phenotypes
-
Thorlacius, S., Olafsdottir, G., Tryggvardottir, L., Neuhausen, S., Jonasson, J. G., Tavtigian, S. V., Tulinius, H., Ogmundsdottir, H. M., and Eyfjord, J. E. A single BRCA2 mutation in male and female breast cancer families from Iceland with varied cancer phenotypes. Nat. Genet., 13: 117-119, 1996.
-
(1996)
Nat. Genet.
, vol.13
, pp. 117-119
-
-
Thorlacius, S.1
Olafsdottir, G.2
Tryggvardottir, L.3
Neuhausen, S.4
Jonasson, J.G.5
Tavtigian, S.V.6
Tulinius, H.7
Ogmundsdottir, H.M.8
Eyfjord, J.E.9
-
14
-
-
0031018551
-
Mutation analysis of BRCA1 and BRCA2 in a male breast cancer population
-
Friedman, L. S., Gayther, S. A., Kurosaki, T., Gordon, D., Noble, B., Casey, G., Ponder, B. A., and Anton-Culver, H. Mutation analysis of BRCA1 and BRCA2 in a male breast cancer population. Am. J. Hum. Genet., 60: 313-319, 1997.
-
(1997)
Am. J. Hum. Genet.
, vol.60
, pp. 313-319
-
-
Friedman, L.S.1
Gayther, S.A.2
Kurosaki, T.3
Gordon, D.4
Noble, B.5
Casey, G.6
Ponder, B.A.7
Anton-Culver, H.8
-
15
-
-
0031012305
-
Variation of risks of breast and ovarian cancer associated with different germline mutations of the BRCA2 gene
-
Gayther, S. A., Mangion, J., Russel, P., Seal, S., Barfoot, R., Ponder, B. A., Stratton, M. R., and Easton, D. Variation of risks of breast and ovarian cancer associated with different germline mutations of the BRCA2 gene. Nat. Genet., 15: 103-105, 1997.
-
(1997)
Nat. Genet.
, vol.15
, pp. 103-105
-
-
Gayther, S.A.1
Mangion, J.2
Russel, P.3
Seal, S.4
Barfoot, R.5
Ponder, B.A.6
Stratton, M.R.7
Easton, D.8
-
16
-
-
16944367027
-
Moderate frequency of BRCA1 and BRCA2 germline mutations in Scandinavian familial breast cancer
-
Hakansson, S., Johansson, O., Johansson, U., Sellberg, G., Loman, N., Gerdes, A-M., Holmberg, E., Dahl, N., Pandis, N., Kristoffersson, U., Olsson, H., and Borg, A. Moderate frequency of BRCA1 and BRCA2 germline mutations in Scandinavian familial breast cancer. Am. J. Hum. Genet., 60: 1068-1078, 1997.
-
(1997)
Am. J. Hum. Genet.
, vol.60
, pp. 1068-1078
-
-
Hakansson, S.1
Johansson, O.2
Johansson, U.3
Sellberg, G.4
Loman, N.5
Gerdes, A.-M.6
Holmberg, E.7
Dahl, N.8
Pandis, N.9
Kristoffersson, U.10
Olsson, H.11
Borg, A.12
-
17
-
-
0030902559
-
BRCA2 in American families with four or more cases of breast or ovarian cancer: Recurrent and novel mutations, variable expression, penetrance and the possibility of families whose breast cancer is not attributable to BRCA1 or BRCA2
-
Schubert, E. L., Lee, M. K., Mefford, H. C., Argonza, R. H., Morrow, J. E., Hull, J., Dann, J. L., and King, M-C. BRCA2 in American families with four or more cases of breast or ovarian cancer: recurrent and novel mutations, variable expression, penetrance and the possibility of families whose breast cancer is not attributable to BRCA1 or BRCA2. Am. J. Hum. Genet., 60: 1031-1040, 1997.
-
(1997)
Am. J. Hum. Genet.
, vol.60
, pp. 1031-1040
-
-
Schubert, E.L.1
Lee, M.K.2
Mefford, H.C.3
Argonza, R.H.4
Morrow, J.E.5
Hull, J.6
Dann, J.L.7
King, M.-C.8
-
18
-
-
16944361810
-
Mutations in BRCA1 and BRCA2 in breast cancer families: Are there more breast cancer susceptibility genes
-
Serova, O. M., Mazoyer, S., Puget, N., Dubois, V., Tonin, P., Shugart, Y. Y., Goldgar, D., Narod, S. A., Lynch, H. T., and Lenoir, G. M. Mutations in BRCA1 and BRCA2 in breast cancer families: are there more breast cancer susceptibility genes. Am. J. Hum. Genet., 60: 486-595, 1997.
-
(1997)
Am. J. Hum. Genet.
, vol.60
, pp. 486-595
-
-
Serova, O.M.1
Mazoyer, S.2
Puget, N.3
Dubois, V.4
Tonin, P.5
Shugart, Y.Y.6
Goldgar, D.7
Narod, S.A.8
Lynch, H.T.9
Lenoir, G.M.10
-
19
-
-
0030956589
-
Study of a single BRCA2 mutation with high carrier frequency in a small population
-
Thorlacius, S., Sigurdsson, S., Bjarnadottir, H., Olafsdottir, G., Jonasson, J. G., Tryggvardottir, L., Tulinius, H., and Eyfjord, J. Study of a single BRCA2 mutation with high carrier frequency in a small population. Am. J. Hum. Genet., 60: 1079-1084, 1997.
-
(1997)
Am. J. Hum. Genet.
, vol.60
, pp. 1079-1084
-
-
Thorlacius, S.1
Sigurdsson, S.2
Bjarnadottir, H.3
Olafsdottir, G.4
Jonasson, J.G.5
Tryggvardottir, L.6
Tulinius, H.7
Eyfjord, J.8
-
20
-
-
0028023048
-
Translocation involving 1p and 17q is a recurrent genetic alteration of human neuroblastoma cells
-
Savelyeva, L., Corvi, R., and Schwab, M. Translocation involving 1p and 17q is a recurrent genetic alteration of human neuroblastoma cells. Am. J. Hum. Genet., 55: 334-340, 1994.
-
(1994)
Am. J. Hum. Genet.
, vol.55
, pp. 334-340
-
-
Savelyeva, L.1
Corvi, R.2
Schwab, M.3
-
21
-
-
0028305310
-
MYCN is retained in single copy at chromosome band 2p23-24 during amplification in human neuroblastoma cells
-
Corvi, R., Amler, L. C., Savelyeva, L., Gehring, M., and Schwab, M. MYCN is retained in single copy at chromosome band 2p23-24 during amplification in human neuroblastoma cells. Proc. Natl. Acad. Sci. USA, 91: 5523-5527, 1994.
-
(1994)
Proc. Natl. Acad. Sci. USA
, vol.91
, pp. 5523-5527
-
-
Corvi, R.1
Amler, L.C.2
Savelyeva, L.3
Gehring, M.4
Schwab, M.5
-
22
-
-
0016316563
-
Pericentric inversion of human chromosomes 9 and 10
-
de la Chapelle, A., Schröder, J., Stensand, K., Fellman, J., Herva, R., Saarni, M., Auttolainen, I., Tallila, L., Tervilae, L., Husa, L., Tallquist, G., Robson, E. B., Cook, P. J. L., and Sanger, R. Pericentric inversion of human chromosomes 9 and 10. Am. J. Hum. Genet., 26: 746-765, 1974.
-
(1974)
Am. J. Hum. Genet.
, vol.26
, pp. 746-765
-
-
De La Chapelle, A.1
Schröder, J.2
Stensand, K.3
Fellman, J.4
Herva, R.5
Saarni, M.6
Auttolainen, I.7
Tallila, L.8
Tervilae, L.9
Husa, L.10
Tallquist, G.11
Robson, E.B.12
Cook, P.J.L.13
Sanger, R.14
-
23
-
-
0022257061
-
C-band heteromorphism in breast cancer patients
-
Berger, R., Bernheim, A., Kristoffersson, U., Mitelman, F., and Olsson, H. C-band heteromorphism in breast cancer patients. Cancer Genet. Cytogenet., 18: 37-42, 1985.
-
(1985)
Cancer Genet. Cytogenet.
, vol.18
, pp. 37-42
-
-
Berger, R.1
Bernheim, A.2
Kristoffersson, U.3
Mitelman, F.4
Olsson, H.5
-
24
-
-
0022596452
-
Constitutive heterochromatin studies in patients with solid tumors
-
Suciu, S. Constitutive heterochromatin studies in patients with solid tumors. J. Cancer Res. Clin. Oncol., 111: 291-294, 1986.
-
(1986)
J. Cancer Res. Clin. Oncol.
, vol.111
, pp. 291-294
-
-
Suciu, S.1
-
25
-
-
0028060062
-
Molecular cytogenetic characterization of two types of chromosome 9 variants
-
Wang, J-C. C., and Miller, W. A. Molecular cytogenetic characterization of two types of chromosome 9 variants. Cytogenet. Cell Genet., 67: 190-192, 1994.
-
(1994)
Cytogenet. Cell Genet.
, vol.67
, pp. 190-192
-
-
Wang, J.-C.C.1
Miller, W.A.2
-
26
-
-
0028121279
-
A cell cycle regulator potentially involved in genesis of many tumor types
-
Washington DC
-
Kamb, A., Gruis, N. A., Weaver-Feldhaus, J., Liu, Q., Harshman, K., Tavtigian, S. V., Stockert, E., Day, R. S., Johnson, B. E., and Skolnick, M. H. A cell cycle regulator potentially involved in genesis of many tumor types. Science (Washington DC), 264: 436-440, 1994.
-
(1994)
Science
, vol.264
, pp. 436-440
-
-
Kamb, A.1
Gruis, N.A.2
Weaver-Feldhaus, J.3
Liu, Q.4
Harshman, K.5
Tavtigian, S.V.6
Stockert, E.7
Day, R.S.8
Johnson, B.E.9
Skolnick, M.H.10
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