-
1
-
-
0029741063
-
The future of genetic studies of complex human diseases
-
Risch, N. and Merikangas, K. The future of genetic studies of complex human diseases, Science, 273: 1516-1517, 1996.
-
(1996)
Science
, vol.273
, pp. 1516-1517
-
-
Risch, N.1
Merikangas, K.2
-
2
-
-
0027092659
-
Characteristics relating to ovarian cancer risk. Collaborative analysis of twelve US case-control studies. II. Invasive epithelial ovarian cancers in white women
-
Whittemore, A.S., Harris, R. and Itnyre, J. Characteristics relating to ovarian cancer risk. Collaborative analysis of twelve US case-control studies. II. Invasive epithelial ovarian cancers in white women, Am J Epidemiol, 136: 1184-1203, 1992.
-
(1992)
Am J Epidemiol
, vol.136
, pp. 1184-1203
-
-
Whittemore, A.S.1
Harris, R.2
Itnyre, J.3
-
3
-
-
0032477328
-
Hormonal etiology of epithelial ovarian cancer, with a hypothesis concerning the role of androgens and progesterone
-
Risch, H.A. Hormonal etiology of epithelial ovarian cancer, with a hypothesis concerning the role of androgens and progesterone, J Natl Cancer Inst, 90: 1774-1786, 1998.
-
(1998)
J Natl Cancer Inst
, vol.90
, pp. 1774-1786
-
-
Risch, H.A.1
-
4
-
-
0031783028
-
Effect of progestin on the ovarian epithelium of macaques: Cancer prevention through apoptosis?
-
Rodriguez, G.C., Walmer, D.K., Cline, M., Krigman, H.R., Lessey, B.A., Whitaker, R.S., Dodge, R.K. and Hughes, C.L. Effect of progestin on the ovarian epithelium of macaques: Cancer prevention through apoptosis? J Soc Gynecol Invest, 5: 271-276, 1998.
-
(1998)
J Soc Gynecol Invest
, vol.5
, pp. 271-276
-
-
Rodriguez, G.C.1
Walmer, D.K.2
Cline, M.3
Krigman, H.R.4
Lessey, B.A.5
Whitaker, R.S.6
Dodge, R.K.7
Hughes, C.L.8
-
5
-
-
0037005938
-
Progestin-induced apoptosis in the macaque ovarian epithelium: Differential regulation of transforming growth factor-beta
-
Rodriguez, G.C., Nagarsheth, N.P., Lee, K.L., Bentley, R.C., Walmer, D.K., Cline, M., Whitaker, R.S., Isner, P., Berchuck, A., Dodge, R.K. and Hughes, C.L. Progestin-induced apoptosis in the macaque ovarian epithelium: Differential regulation of transforming growth factor-beta, J Natl Cancer Inst, 94: 50-60, 2002.
-
(2002)
J Natl Cancer Inst
, vol.94
, pp. 50-60
-
-
Rodriguez, G.C.1
Nagarsheth, N.P.2
Lee, K.L.3
Bentley, R.C.4
Walmer, D.K.5
Cline, M.6
Whitaker, R.S.7
Isner, P.8
Berchuck, A.9
Dodge, R.K.10
Hughes, C.L.11
-
6
-
-
0037005946
-
Impact of progestin and estrogen potency in oral contraceptives on ovarian cancer risk
-
Schildkraut, J.M., Calingaert, B., Marchbanks, P.A., Moorman, P.G. and Rodriguez, G.C. Impact of progestin and estrogen potency in oral contraceptives on ovarian cancer risk, J Natl Cancer Inst, 94: 32-38, 2002.
-
(2002)
J Natl Cancer Inst
, vol.94
, pp. 32-38
-
-
Schildkraut, J.M.1
Calingaert, B.2
Marchbanks, P.A.3
Moorman, P.G.4
Rodriguez, G.C.5
-
7
-
-
3242786474
-
Hormonal factors and the risk of invasive ovarian cancer: A population-based case-control study
-
Pike, M.C., Pearce, C.L., Peters, R., Cozen, W., Wan, P. and Wu, A.H. Hormonal factors and the risk of invasive ovarian cancer: A population-based case-control study, Fertil Steril, 82:186-95, 2004.
-
(2004)
Fertil Steril
, vol.82
, pp. 186-195
-
-
Pike, M.C.1
Pearce, C.L.2
Peters, R.3
Cozen, W.4
Wan, P.5
Wu, A.H.6
-
8
-
-
0038675036
-
Endometriosis and ovarian cancer: Thoughts on shared pathophysiology
-
Ness, R.B. Endometriosis and ovarian cancer: Thoughts on shared pathophysiology, Am J Obstet Gynecol, 189: 280-294, 2003.
-
(2003)
Am J Obstet Gynecol
, vol.189
, pp. 280-294
-
-
Ness, R.B.1
-
9
-
-
0028580071
-
Sunlight, vitamin D, and ovarian cancer mortality rates in US women
-
Lefkowitz, E.S. and Garland, C.F. Sunlight, vitamin D, and ovarian cancer mortality rates in US women, Int J Epidemiol, 23: 1133-1136, 1994.
-
(1994)
Int J Epidemiol
, vol.23
, pp. 1133-1136
-
-
Lefkowitz, E.S.1
Garland, C.F.2
-
10
-
-
0036331457
-
Aspirin, other NSAIDs, and ovarian cancer risk
-
Fairfield, K.M., Hunter, D.J., Fuchs, C.S., Colditz, G.A. and Hankinson, S.E. Aspirin, other NSAIDs, and ovarian cancer risk, Cancer Causes Control, 13: 535-542, 2002.
-
(2002)
Cancer Causes Control
, vol.13
, pp. 535-542
-
-
Fairfield, K.M.1
Hunter, D.J.2
Fuchs, C.S.3
Colditz, G.A.4
Hankinson, S.E.5
-
11
-
-
0034644185
-
Environmental and heritable factors in the causation of cancer - analyses of cohorts of twins from Sweden, Denmark, and Finland
-
Lichtenstein, P., Holm, N.V., Verkasalo, P.K., Iliadou, A., Kaprio, J., Koskenvuo, M., Pukkala, E., Skytthe, A. and Hemminki, K. Environmental and heritable factors in the causation of cancer - analyses of cohorts of twins from Sweden, Denmark, and Finland, N Engl J Med, 343: 78-85, 2000.
-
(2000)
N Engl J Med
, vol.343
, pp. 78-85
-
-
Lichtenstein, P.1
Holm, N.V.2
Verkasalo, P.K.3
Iliadou, A.4
Kaprio, J.5
Koskenvuo, M.6
Pukkala, E.7
Skytthe, A.8
Hemminki, K.9
-
12
-
-
0033408439
-
Managing hereditary ovarian cancer risk
-
Berchuck, A., Schildkraut, J.M., Marks, J.R. and Futreal, P.A. Managing hereditary ovarian cancer risk, Cancer, 86: 2517-2524, 1999.
-
(1999)
Cancer
, vol.86
, pp. 2517-2524
-
-
Berchuck, A.1
Schildkraut, J.M.2
Marks, J.R.3
Futreal, P.A.4
-
13
-
-
0031832541
-
Sequence analysis of BRCA1 and BRCA2: Correlation of mutations with family history and ovarian cancer risk
-
Frank, T.S., Manley, S.A., Olopade, O.I., Cummings, S., Garber, J.E., Bernhardt, B., Antman, K., Russo, D., Wood, M.E., Mullineau, L., Isaacs, C., Peshkin, B., Buys, S., Venne, V., Rowley, P.T., Loader, S., Offit, K., Robson, M., Hampel, H., Brener, D., Winer, E.P., Clark, S., Weber, B., Strong, L.C. and Thomas, A. Sequence analysis of BRCA1 and BRCA2: Correlation of mutations with family history and ovarian cancer risk, J Clin Oncol, 16: 2417-2425, 1998.
-
(1998)
J Clin Oncol
, vol.16
, pp. 2417-2425
-
-
Frank, T.S.1
Manley, S.A.2
Olopade, O.I.3
Cummings, S.4
Garber, J.E.5
Bernhardt, B.6
Antman, K.7
Russo, D.8
Wood, M.E.9
Mullineau, L.10
Isaacs, C.11
Peshkin, B.12
Buys, S.13
Venne, V.14
Rowley, P.T.15
Loader, S.16
Offit, K.17
Robson, M.18
Hampel, H.19
Brener, D.20
Winer, E.P.21
Clark, S.22
Weber, B.23
Strong, L.C.24
Thomas, A.25
more..
-
14
-
-
0029980129
-
Mutations and polymorphisms in the familial early-onset breast cancer (BRCA1) gene
-
Couch, F.J. and Weber, B.L. Mutations and polymorphisms in the familial early-onset breast cancer (BRCA1) gene, Hum Mutat, 8: 8-18, 1996.
-
(1996)
Hum Mutat
, vol.8
, pp. 8-18
-
-
Couch, F.J.1
Weber, B.L.2
-
15
-
-
85136349359
-
-
Shattuck-Eidens, D., Oliphant, A., McClure, M., McBride, C., Gupte, J., Rubano, T., Pruss, D., Tavtigian, S.V., Teng, D.H., Adey, N., Staebell, M., Gumpper, K., Lundstrom, R., Hulick, M., Kelly, M., Holmen, J., Lingenfelter, B., Manley, S., Fujimura, F., Luce, M., Ward, B., Cannon-Albright, L., Steele, L., Offit, K., Thomas, A., et al. BRCA1 sequence analysis in women at high risk for susceptibility mutations. Risk factor analysis and implications for genetic testing, JAMA, 278: 1242-1250, 1997.
-
Shattuck-Eidens, D., Oliphant, A., McClure, M., McBride, C., Gupte, J., Rubano, T., Pruss, D., Tavtigian, S.V., Teng, D.H., Adey, N., Staebell, M., Gumpper, K., Lundstrom, R., Hulick, M., Kelly, M., Holmen, J., Lingenfelter, B., Manley, S., Fujimura, F., Luce, M., Ward, B., Cannon-Albright, L., Steele, L., Offit, K., Thomas, A., et al. BRCA1 sequence analysis in women at high risk for susceptibility mutations. Risk factor analysis and implications for genetic testing, JAMA, 278: 1242-1250, 1997.
-
-
-
-
16
-
-
0031025322
-
Prevalence and contribution of BRCA1 mutations in breast cancer and ovarian cancer: Results from three U.S. population-based case-control studies of ovarian cancer
-
Whittemore, A.S., Gong, G. and Itnyre, J. Prevalence and contribution of BRCA1 mutations in breast cancer and ovarian cancer: Results from three U.S. population-based case-control studies of ovarian cancer, Am J Hum Genet, 60: 496-504, 1997.
-
(1997)
Am J Hum Genet
, vol.60
, pp. 496-504
-
-
Whittemore, A.S.1
Gong, G.2
Itnyre, J.3
-
17
-
-
0030910022
-
The risk of cancer associated with specific mutations of BRCA1 and BRCA2 among Ashkenazi Jews
-
Struewing, J.P., Hartge, P., Wacholder, S., Baker, S.M., Berlin, M., McAdams, M., Timmerman, M.M., Brody, L.C. and Tucker, M.A. The risk of cancer associated with specific mutations of BRCA1 and BRCA2 among Ashkenazi Jews, N Engl J Med, 336: 1401-1408, 1997.
-
(1997)
N Engl J Med
, vol.336
, pp. 1401-1408
-
-
Struewing, J.P.1
Hartge, P.2
Wacholder, S.3
Baker, S.M.4
Berlin, M.5
McAdams, M.6
Timmerman, M.M.7
Brody, L.C.8
Tucker, M.A.9
-
18
-
-
0035098503
-
Prevalence and penetrance of germline BRCA1 and BRCA2 mutations in a population series of 649 women with ovarian cancer
-
Risch, H.A., McLaughlin, J.R., Cole, D.E., Rosen, B., Bradley, L., Kwan, E., Jack, E., Vesprini, D.J., Kuperstein, G., Abrahamson, J.L., Fan, I., Wong, B. and Narod, S.A. Prevalence and penetrance of germline BRCA1 and BRCA2 mutations in a population series of 649 women with ovarian cancer, Am J Hum Genet, 68: 700-710, 2001.
-
(2001)
Am J Hum Genet
, vol.68
, pp. 700-710
-
-
Risch, H.A.1
McLaughlin, J.R.2
Cole, D.E.3
Rosen, B.4
Bradley, L.5
Kwan, E.6
Jack, E.7
Vesprini, D.J.8
Kuperstein, G.9
Abrahamson, J.L.10
Fan, I.11
Wong, B.12
Narod, S.A.13
-
19
-
-
0030902227
-
Invited editorial: Population genetics of BRCA1 and BRCA2
-
Szabo, C.I. and King, M.C. Invited editorial: Population genetics of BRCA1 and BRCA2, Am J Hum Genet, 60: 1013-1020, 1997.
-
(1997)
Am J Hum Genet
, vol.60
, pp. 1013-1020
-
-
Szabo, C.I.1
King, M.C.2
-
20
-
-
33750596601
-
-
Guillem, J., Wood, W., Berchuck, Karlan, B., Mutch, D., Gagel, R., Weitzel, J., Morrow, M., Weber, B., Giardiello, F., Rodriguez-Bigas, M., Church, J., Gruber, S. and Offit, K. ASCO/ SSO review of current role of risk-reducing surgery in common hereditary cancer syndromes, J Clin Oncol, 24: 4642-60, 2006.
-
Guillem, J., Wood, W., Berchuck, Karlan, B., Mutch, D., Gagel, R., Weitzel, J., Morrow, M., Weber, B., Giardiello, F., Rodriguez-Bigas, M., Church, J., Gruber, S. and Offit, K. ASCO/ SSO review of current role of risk-reducing surgery in common hereditary cancer syndromes, J Clin Oncol, 24: 4642-60, 2006.
-
-
-
-
21
-
-
0032991552
-
Characterization of single-nucleotide polymorphisms in coding regions of human genes
-
Cargill, M., Altshuler, D., Ireland, J., Sklar, P., Ardlie, K., Patil, N., Shaw, N., Lane, C.R., Lim, E.P., Kalyanaraman, N., Nemesh, J., Ziaugra, L., Friedland, L., Rolfe, A., Warrington, J., Lipshutz, R., Daley, G.Q. and Lander, E.S. Characterization of single-nucleotide polymorphisms in coding regions of human genes, Nat Genet, 22: 231-8, 1999.
-
(1999)
Nat Genet
, vol.22
, pp. 231-238
-
-
Cargill, M.1
Altshuler, D.2
Ireland, J.3
Sklar, P.4
Ardlie, K.5
Patil, N.6
Shaw, N.7
Lane, C.R.8
Lim, E.P.9
Kalyanaraman, N.10
Nemesh, J.11
Ziaugra, L.12
Friedland, L.13
Rolfe, A.14
Warrington, J.15
Lipshutz, R.16
Daley, G.Q.17
Lander, E.S.18
-
22
-
-
0032990407
-
Patterns of single-nucleotide polymorphisms in candidate genes for blood-pressure homeostasis
-
Halushka, M.K., Fan, J.B., Bentley, K., Hsie, L., Shen, N., Weder, A., Cooper, R., Lipshutz, R. and Chakravarti, A. Patterns of single-nucleotide polymorphisms in candidate genes for blood-pressure homeostasis, Nat Genet, 22: 239-47, 1999.
-
(1999)
Nat Genet
, vol.22
, pp. 239-247
-
-
Halushka, M.K.1
Fan, J.B.2
Bentley, K.3
Hsie, L.4
Shen, N.5
Weder, A.6
Cooper, R.7
Lipshutz, R.8
Chakravarti, A.9
-
23
-
-
0035865322
-
-
Sachidanandam, R., Weissman, D., Schmidt, S.C., Kakol, J.M., Stein, L.D., Marth, G., Sherry, S., Mullikin, J.C., Mortimore, B.J., Willey, D.L., Hunt, S.E., Cole, C.G., Coggill, P.C., Rice, C. M., Ning, Z., Rogers, J., Bentley, D.R., Kwok, P.Y., Mardis, E.R., Yeh, R.T., Schultz, B., Cook, L., Davenport, R., Dante, M., Fulton, L., Hillier, L., Waterston, R.H., McPherson, J.D., Gilman, B., Schaffner, S., Van Etten, W.J., Reich, D., Higgins, J., Daly, M.J., Blumenstiel, B., Baldwin, J., Stange-Thomann, N., Zody, M.C., Linton, L., Lander, E.S. and Altshuler, D. A map of human genome sequence variation containing 1.42 million single nucleotide polymorphisms, Nature, 409: 928-33, 2001.
-
Sachidanandam, R., Weissman, D., Schmidt, S.C., Kakol, J.M., Stein, L.D., Marth, G., Sherry, S., Mullikin, J.C., Mortimore, B.J., Willey, D.L., Hunt, S.E., Cole, C.G., Coggill, P.C., Rice, C. M., Ning, Z., Rogers, J., Bentley, D.R., Kwok, P.Y., Mardis, E.R., Yeh, R.T., Schultz, B., Cook, L., Davenport, R., Dante, M., Fulton, L., Hillier, L., Waterston, R.H., McPherson, J.D., Gilman, B., Schaffner, S., Van Etten, W.J., Reich, D., Higgins, J., Daly, M.J., Blumenstiel, B., Baldwin, J., Stange-Thomann, N., Zody, M.C., Linton, L., Lander, E.S. and Altshuler, D. A map of human genome sequence variation containing 1.42 million single nucleotide polymorphisms, Nature, 409: 928-33, 2001.
-
-
-
-
24
-
-
79959503826
-
-
The International HapMap Project
-
The International HapMap Project, Nature, 426: 789-96, 2003.
-
(2003)
Nature
, vol.426
, pp. 789-796
-
-
-
25
-
-
2642583283
-
Mapping complex disease loci in whole-genome association studies
-
Carlson, C.S., Eberle, M.A., Kruglyak, L. and Nickerson, D.A. Mapping complex disease loci in whole-genome association studies, Nature, 429: 446-452, 2004.
-
(2004)
Nature
, vol.429
, pp. 446-452
-
-
Carlson, C.S.1
Eberle, M.A.2
Kruglyak, L.3
Nickerson, D.A.4
-
26
-
-
0028923170
-
A germline TaqI restriction fragment length polymorphism in the progesterone receptor gene in ovarian carcinoma
-
McKenna, N.J., Kieback, D.G., Carney, D.N., Fanning, M., McLinden, J. and Headon, D.R. A germline TaqI restriction fragment length polymorphism in the progesterone receptor gene in ovarian carcinoma, Br J Cancer, 71: 451-455, 1995.
-
(1995)
Br J Cancer
, vol.71
, pp. 451-455
-
-
McKenna, N.J.1
Kieback, D.G.2
Carney, D.N.3
Fanning, M.4
McLinden, J.5
Headon, D.R.6
-
27
-
-
0029041961
-
Ovarian carcinoma-associated TaqI restriction fragment length polymorphism in intron G of the progesterone receptor gene is due to an Alu sequence insertion
-
Rowe, S.M., Coughlan, S.J., McKenna, N.J., Garrett, E., Kieback, D.G., Carney, D.N. and Headon, D.R. Ovarian carcinoma-associated TaqI restriction fragment length polymorphism in intron G of the progesterone receptor gene is due to an Alu sequence insertion, Cancer Res, 55: 2743-2745, 1995.
-
(1995)
Cancer Res
, vol.55
, pp. 2743-2745
-
-
Rowe, S.M.1
Coughlan, S.J.2
McKenna, N.J.3
Garrett, E.4
Kieback, D.G.5
Carney, D.N.6
Headon, D.R.7
-
28
-
-
0035026849
-
No significant association between progesterone receptor exon 4 Val660Leu G/T polymorphism and risk of ovarian cancer
-
Spurdle, A.B., Webb, P.M., Purdie, D.M., Chen, X., Green, A. and Chenevix-Trench, G. No significant association between progesterone receptor exon 4 Val660Leu G/T polymorphism and risk of ovarian cancer, Carcinogenesis, 22: 717-721, 2001.
-
(2001)
Carcinogenesis
, vol.22
, pp. 717-721
-
-
Spurdle, A.B.1
Webb, P.M.2
Purdie, D.M.3
Chen, X.4
Green, A.5
Chenevix-Trench, G.6
-
29
-
-
85045226092
-
Progesterone receptor gene and risk of breast and ovarian cancer
-
Lancaster, J.M., Berchuck, A., Carney, M., Wiseman, R.W. and Taylor, J.A. Progesterone receptor gene and risk of breast and ovarian cancer, Br J Cancer, 78: 277, 1997.
-
(1997)
Br J Cancer
, vol.78
, pp. 277
-
-
Lancaster, J.M.1
Berchuck, A.2
Carney, M.3
Wiseman, R.W.4
Taylor, J.A.5
-
30
-
-
0030938425
-
No association of a 306-bp insertion polymorphism in the progesterone receptor gene with ovarian and breast cancer
-
Manolitsas, T.P., Englefield, P., Eccles, D.M. and Campbell, I.G. No association of a 306-bp insertion polymorphism in the progesterone receptor gene with ovarian and breast cancer, Br J Cancer, 75: 1398-1399, 1900.
-
(1900)
Br J Cancer
, vol.75
, pp. 1398-1399
-
-
Manolitsas, T.P.1
Englefield, P.2
Eccles, D.M.3
Campbell, I.G.4
-
31
-
-
0037359229
-
No relationship between ovarian cancer risk and progesterone receptor gene polymorphism in a population-based, case-control study in North Carolina
-
Lancaster, J.M., Wenham, R.M., Halabi, S., Calingaert, B., Marks, J.R., Moorman, P.G., Bentley, R.C., Berchuck, A. and Schildkraut, J.M. No relationship between ovarian cancer risk and progesterone receptor gene polymorphism in a population-based, case-control study in North Carolina, Cancer Epidemiol Biomarkers Prev, 12: 226-227, 2003.
-
(2003)
Cancer Epidemiol Biomarkers Prev
, vol.12
, pp. 226-227
-
-
Lancaster, J.M.1
Wenham, R.M.2
Halabi, S.3
Calingaert, B.4
Marks, J.R.5
Moorman, P.G.6
Bentley, R.C.7
Berchuck, A.8
Schildkraut, J.M.9
-
32
-
-
19944433097
-
Clarifying the PROGINS allele association in ovarian and breast cancer risk: A haplotype-based analysis
-
Pearce, C.L., Hirschhorn, J.N., Wu, A.H., Burtt, N.P., Stram, D.O., Young, S., Kolonel, L.N., Henderson, B.E., Altshuler, D. and Pike, M.C. Clarifying the PROGINS allele association in ovarian and breast cancer risk: A haplotype-based analysis, J Natl Cancer Inst, 97: 51-59, 2005.
-
(2005)
J Natl Cancer Inst
, vol.97
, pp. 51-59
-
-
Pearce, C.L.1
Hirschhorn, J.N.2
Wu, A.H.3
Burtt, N.P.4
Stram, D.O.5
Young, S.6
Kolonel, L.N.7
Henderson, B.E.8
Altshuler, D.9
Pike, M.C.10
-
33
-
-
19944428552
-
Progesterone receptor promoter +331A polymorphism is associated with increased risk of endometrioid and clear cell ovarian cancers
-
Berchuck, A., Schildkraut, J.M., Wenham, R.M., Calingaert, B., Ali, S., Henriott, A., Halabi, S., Rodriguez, G.C., Gertig, D., Purdie, D.M., Kelemen, L., Spurdle, A.B., Marks, J. and Chenevix-Trench, G. Progesterone receptor promoter +331A polymorphism is associated with increased risk of endometrioid and clear cell ovarian cancers, Cancer Epidemiol Biomarkers Prev, 13: 2141-2147, 2004.
-
(2004)
Cancer Epidemiol Biomarkers Prev
, vol.13
, pp. 2141-2147
-
-
Berchuck, A.1
Schildkraut, J.M.2
Wenham, R.M.3
Calingaert, B.4
Ali, S.5
Henriott, A.6
Halabi, S.7
Rodriguez, G.C.8
Gertig, D.9
Purdie, D.M.10
Kelemen, L.11
Spurdle, A.B.12
Marks, J.13
Chenevix-Trench, G.14
-
34
-
-
0033865368
-
Androgen receptor exon 1 CAG repeat length and risk of ovarian cancer
-
Spurdle, A.B., Webb, P.M., Chen, X., Martin, N.G., Giles, G.G., Hopper, J.L. and Chenevix- Trench, G. Androgen receptor exon 1 CAG repeat length and risk of ovarian cancer, Int J Cancer, 87: 637-643, 2000.
-
(2000)
Int J Cancer
, vol.87
, pp. 637-643
-
-
Spurdle, A.B.1
Webb, P.M.2
Chen, X.3
Martin, N.G.4
Giles, G.G.5
Hopper, J.L.6
Chenevix- Trench, G.7
-
35
-
-
0035110955
-
The androgen receptor and genetic susceptibility to ovarian cancer: Results from a case series
-
Levine, D.A. and Boyd, J. The androgen receptor and genetic susceptibility to ovarian cancer: results from a case series, Cancer Res, 61: 908-911, 2001.
-
(2001)
Cancer Res
, vol.61
, pp. 908-911
-
-
Levine, D.A.1
Boyd, J.2
-
36
-
-
0036606681
-
Polymorphisms of the estrogen-metabolizing genes CYP17 and catechol-O-methyltransferase and risk of epithelial ovarian cancer
-
Garner, E.I., Stokes, E.E., Berkowitz, R.S., Mok, S.C. and Cramer, D.W. Polymorphisms of the estrogen-metabolizing genes CYP17 and catechol-O-methyltransferase and risk of epithelial ovarian cancer, Cancer Res, 62: 3058-3062, 2002.
-
(2002)
Cancer Res
, vol.62
, pp. 3058-3062
-
-
Garner, E.I.1
Stokes, E.E.2
Berkowitz, R.S.3
Mok, S.C.4
Cramer, D.W.5
-
37
-
-
0034183322
-
CYP17 promotor polymorphism and ovarian cancer risk
-
Spurdle, A.B., Chen, X., Abbazadegan, M., Martin, N., Khoo, S.K., Hurst, T., Ward, B., Webb, P.M. and Chenevix-Trench, G. CYP17 promotor polymorphism and ovarian cancer risk, Int J Cancer, 86: 436-439, 2000.
-
(2000)
Int J Cancer
, vol.86
, pp. 436-439
-
-
Spurdle, A.B.1
Chen, X.2
Abbazadegan, M.3
Martin, N.4
Khoo, S.K.5
Hurst, T.6
Ward, B.7
Webb, P.M.8
Chenevix-Trench, G.9
-
38
-
-
0028905769
-
-
Runnebaum, I.B., Tong, X.W., Konig, R., Zhao, H., Korner, K., Atkinson, E.N., Kreienberg, R., Kieback, D.G. and Hong, Z.c.t.Z.H. p53-based blood test for p53PIN3 and risk for sporadic ovarian cancer, Lancet, 345: 994, 1995.
-
Runnebaum, I.B., Tong, X.W., Konig, R., Zhao, H., Korner, K., Atkinson, E.N., Kreienberg, R., Kieback, D.G. and Hong, Z.c.t.Z.H. p53-based blood test for p53PIN3 and risk for sporadic ovarian cancer, Lancet, 345: 994, 1995.
-
-
-
-
39
-
-
0029035011
-
p53 polymorphism in ovarian and bladder cancer
-
Lancaster, J.M., Brownlee, H.A., Wiseman, R.W. and Taylor, J. p53 polymorphism in ovarian and bladder cancer, Lancet, 346: 182, 1995.
-
(1995)
Lancet
, vol.346
, pp. 182
-
-
Lancaster, J.M.1
Brownlee, H.A.2
Wiseman, R.W.3
Taylor, J.4
-
40
-
-
0038500734
-
The prohibitin 3 untranslated region polymorphism is not associated with risk of ovarian cancer
-
Spurdle, A.B., Purdie, D., Chen, X. and Chenevix-Trench, G. The prohibitin 3 untranslated region polymorphism is not associated with risk of ovarian cancer, Cancer Res, 90: 145-149, 2003.
-
(2003)
Cancer Res
, vol.90
, pp. 145-149
-
-
Spurdle, A.B.1
Purdie, D.2
Chen, X.3
Chenevix-Trench, G.4
-
41
-
-
0029961198
-
Microsomal epoxide hydrolase polymorphism as a risk factor for ovarian cancer
-
Lancaster, J.M., Taylor, J.A., Brownlee, H.A., Bell, D.A., Berchuck, A. and Wiseman, R.W. Microsomal epoxide hydrolase polymorphism as a risk factor for ovarian cancer, Mol Carcinog, 17: 160-162, 1996.
-
(1996)
Mol Carcinog
, vol.17
, pp. 160-162
-
-
Lancaster, J.M.1
Taylor, J.A.2
Brownlee, H.A.3
Bell, D.A.4
Berchuck, A.5
Wiseman, R.W.6
-
42
-
-
0035143142
-
The microsomal epoxide hydrolase Tyr113His polymorphism: Association with risk of ovarian cancer
-
Spurdle, A.B., Purdie, D.M., Webb, P.M., Chen, X., Green, A. and Chenevix-Trench, G. The microsomal epoxide hydrolase Tyr113His polymorphism: Association with risk of ovarian cancer, Mol Carcinog, 30: 71-78, 2001.
-
(2001)
Mol Carcinog
, vol.30
, pp. 71-78
-
-
Spurdle, A.B.1
Purdie, D.M.2
Webb, P.M.3
Chen, X.4
Green, A.5
Chenevix-Trench, G.6
-
43
-
-
0037454803
-
BRCA2 Arg372His polymorphism and epithelial ovarian cancer risk
-
Auranen, A., Spurdle, A.B., Chen, X., Lipscombe, J., Purdie, D.M., Hopper, J.L., Green, A., Healey, C.S., Redman, K., Dunning, A.M., Pharoah, P.D., Easton, D.F., Ponder, B.A., Chenevix-Trench, G. and Novik, K.L. BRCA2 Arg372His polymorphism and epithelial ovarian cancer risk, Int J Cancer, 103: 427-430, 2003.
-
(2003)
Int J Cancer
, vol.103
, pp. 427-430
-
-
Auranen, A.1
Spurdle, A.B.2
Chen, X.3
Lipscombe, J.4
Purdie, D.M.5
Hopper, J.L.6
Green, A.7
Healey, C.S.8
Redman, K.9
Dunning, A.M.10
Pharoah, P.D.11
Easton, D.F.12
Ponder, B.A.13
Chenevix-Trench, G.14
Novik, K.L.15
-
44
-
-
0141925969
-
Polymorphisms in BRCA1 and BRCA2 and risk of epithelial ovarian cancer
-
Wenham, R.M., Schildkraut, J.M., McLean, K., Calingaert, B., Bentley, R.C., Marks, J.R. and Berchuck, A. Polymorphisms in BRCA1 and BRCA2 and risk of epithelial ovarian cancer, Clin Cancer Res, 9: 4396-4403, 2003.
-
(2003)
Clin Cancer Res
, vol.9
, pp. 4396-4403
-
-
Wenham, R.M.1
Schildkraut, J.M.2
McLean, K.3
Calingaert, B.4
Bentley, R.C.5
Marks, J.R.6
Berchuck, A.7
-
45
-
-
0036277684
-
Point: Population stratification: A problem for case-control studies of candidate-gene associations?
-
Thomas, D.C. and Witte, J.S. Point: Population stratification: A problem for case-control studies of candidate-gene associations? Cancer Epidemiol Biomarkers Prev, 11: 505-512, 2002.
-
(2002)
Cancer Epidemiol Biomarkers Prev
, vol.11
, pp. 505-512
-
-
Thomas, D.C.1
Witte, J.S.2
-
46
-
-
0033768238
-
A common variant in BRCA2 is associated with both breast cancer risk and prenatal viability
-
Healey, C.S., Dunning, A.M., Teare, M.D., Chase, D., Parker, L., Burn, J., Chang-Claude, J., Mannermaa, A., Kataja, V., Huntsman, D.G., Pharoah, P.D., Luben, R.N., Easton, D.F. and Ponder, B.A. A common variant in BRCA2 is associated with both breast cancer risk and prenatal viability, Nat Genet, 26: 362-364, 2000.
-
(2000)
Nat Genet
, vol.26
, pp. 362-364
-
-
Healey, C.S.1
Dunning, A.M.2
Teare, M.D.3
Chase, D.4
Parker, L.5
Burn, J.6
Chang-Claude, J.7
Mannermaa, A.8
Kataja, V.9
Huntsman, D.G.10
Pharoah, P.D.11
Luben, R.N.12
Easton, D.F.13
Ponder, B.A.14
-
47
-
-
0029939505
-
Comparison of BRCA1 polymorphisms, rare sequence variants and/or missense mutations in unaffected and breast/ovarian cancer populations
-
Durocher, F., Shattuck-Eidens, D., McClure, M., Labrie, F., Skolnick, M.H., Goldgar, D.E. and Simard, J. Comparison of BRCA1 polymorphisms, rare sequence variants and/or missense mutations in unaffected and breast/ovarian cancer populations, Hum Mol Genet, 5: 835-842, 1996.
-
(1996)
Hum Mol Genet
, vol.5
, pp. 835-842
-
-
Durocher, F.1
Shattuck-Eidens, D.2
McClure, M.3
Labrie, F.4
Skolnick, M.H.5
Goldgar, D.E.6
Simard, J.7
-
48
-
-
8044228419
-
Common BRCA1 variants and susceptibility to breast and ovarian cancer in the general population
-
Dunning, A.M., Chiano, M., Smith, N.R., Dearden, J., Gore, M., Oakes, S., Wilson, C., Stratton, M., Peto, J., Easton, D., Clayton, D. and Ponder, B.A. Common BRCA1 variants and susceptibility to breast and ovarian cancer in the general population, Hum Mol Genet, 6:285-289, 1997.
-
(1997)
Hum Mol Genet
, vol.6
, pp. 285-289
-
-
Dunning, A.M.1
Chiano, M.2
Smith, N.R.3
Dearden, J.4
Gore, M.5
Oakes, S.6
Wilson, C.7
Stratton, M.8
Peto, J.9
Easton, D.10
Clayton, D.11
Ponder, B.A.12
-
49
-
-
0032945329
-
Germline BRCA1 alterations in a population- based series of ovarian cancer cases
-
Janezic, S.A., Ziogas, A., Krumroy, L.M., Krasner, M., Plummer, S.J., Cohen, P., Gildea, M., Barker, D., Haile, R., Casey, G. and Anton-Culver, H. Germline BRCA1 alterations in a population- based series of ovarian cancer cases, Hum Mol Genet, 8: 889-897, 1999.
-
(1999)
Hum Mol Genet
, vol.8
, pp. 889-897
-
-
Janezic, S.A.1
Ziogas, A.2
Krumroy, L.M.3
Krasner, M.4
Plummer, S.J.5
Cohen, P.6
Gildea, M.7
Barker, D.8
Haile, R.9
Casey, G.10
Anton-Culver, H.11
-
50
-
-
10344234708
-
A germline variation in the progesterone receptor gene increases transcriptional activity and may modify ovarian cancer risk
-
Agoulnik, I.U., Tong, X.W., Fischer, D.C., Korner, K., Atkinson, N.E., Edwards, D.P., Headon, D.R., Weigel, N.L. and Kieback, D.G. A germline variation in the progesterone receptor gene increases transcriptional activity and may modify ovarian cancer risk, J Clin Endocrinol Metab, 89: 6340-6347, 2004.
-
(2004)
J Clin Endocrinol Metab
, vol.89
, pp. 6340-6347
-
-
Agoulnik, I.U.1
Tong, X.W.2
Fischer, D.C.3
Korner, K.4
Atkinson, N.E.5
Edwards, D.P.6
Headon, D.R.7
Weigel, N.L.8
Kieback, D.G.9
-
51
-
-
0037126067
-
A functional polymorphism in the promoter of the progesterone receptor gene associated with endometrial cancer risk
-
DeVivo, I, Huggins, G.S., Hankinson, S.E., Lescault, P.J., Boezen, M., Colditz, G.A. and Hunter, D.J. A functional polymorphism in the promoter of the progesterone receptor gene associated with endometrial cancer risk, Proc Natl Acad Sci USA, 99: 12263-12268, 2002.
-
(2002)
Proc Natl Acad Sci USA
, vol.99
, pp. 12263-12268
-
-
DeVivo, I.1
Huggins, G.S.2
Hankinson, S.E.3
Lescault, P.J.4
Boezen, M.5
Colditz, G.A.6
Hunter, D.J.7
-
52
-
-
0034000089
-
The opposing transcriptional activities of the two isoforms of the human progesterone receptor are due to differential cofactor binding
-
Giangrande, P.H., Kimbrel, E.A., Edwards, D.P. and McDonnell, D.P. The opposing transcriptional activities of the two isoforms of the human progesterone receptor are due to differential cofactor binding, Mol Cell Biol, 20: 3102-3115, 2000.
-
(2000)
Mol Cell Biol
, vol.20
, pp. 3102-3115
-
-
Giangrande, P.H.1
Kimbrel, E.A.2
Edwards, D.P.3
McDonnell, D.P.4
-
53
-
-
0141705455
-
A functional polymorphism in the progesterone receptor gene is associated with an increase in breast cancer risk
-
DeVivo, I., Hankinson, S.E., Colditz, G.A. and Hunter, D.J. A functional polymorphism in the progesterone receptor gene is associated with an increase in breast cancer risk, Cancer Res, 63: 5236-5238, 2003.
-
(2003)
Cancer Res
, vol.63
, pp. 5236-5238
-
-
DeVivo, I.1
Hankinson, S.E.2
Colditz, G.A.3
Hunter, D.J.4
-
54
-
-
2942588593
-
No association between the progesterone receptor gene +331G/A polymorphism and breast cancer
-
Feigelson, H.S., Rodriguez, C., Jacobs, E.J., Diver, W.R., Thun, M.J. and Calle, E.E. No association between the progesterone receptor gene +331G/A polymorphism and breast cancer, Cancer Epidemiol Biomarkers Prev, 13: 1084-5, 2004.
-
(2004)
Cancer Epidemiol Biomarkers Prev
, vol.13
, pp. 1084-1085
-
-
Feigelson, H.S.1
Rodriguez, C.2
Jacobs, E.J.3
Diver, W.R.4
Thun, M.J.5
Calle, E.E.6
-
55
-
-
0037312921
-
Meta-analysis of genetic association studies supports a contribution of common variants to susceptibility to common disease
-
Lohmueller, K.E., Pearce, C.L., Pike, M., Lander, E.S. and Hirschhorn, J.N. Meta-analysis of genetic association studies supports a contribution of common variants to susceptibility to common disease, Nat Genet, 33: 177-82, 2003.
-
(2003)
Nat Genet
, vol.33
, pp. 177-182
-
-
Lohmueller, K.E.1
Pearce, C.L.2
Pike, M.3
Lander, E.S.4
Hirschhorn, J.N.5
-
56
-
-
0344395002
-
Bayesian modeling of complex metabolic pathways
-
Conti, D.V., Cortessis,V., Molitor, J. and Thomas, D.C. Bayesian modeling of complex metabolic pathways, Hum Hered, 56: 83-93, 2003.
-
(2003)
Hum Hered
, vol.56
, pp. 83-93
-
-
Conti, D.V.1
Cortessis, V.2
Molitor, J.3
Thomas, D.C.4
-
57
-
-
10044292874
-
SNPs, haplotypes, and model selection in a candidate gene region: The SIMPle analysis for multilocus data
-
Conti, D.V. and Gauderman, W.J. SNPs, haplotypes, and model selection in a candidate gene region: The SIMPle analysis for multilocus data, Genet Epidemiol, 27: 429-41, 2004.
-
(2004)
Genet Epidemiol
, vol.27
, pp. 429-441
-
-
Conti, D.V.1
Gauderman, W.J.2
-
58
-
-
0043175289
-
Choosing haplotype-tagging SNPS based on unphased genotype data using a preliminary sample of unrelated subjects with an example from the Multiethnic Cohort Study
-
Stram, D.O., Haiman, C.A., Hirschhorn, J.N., Altshuler, D., Kolonel, L.N., Henderson, B.E. and Pike, M.C. Choosing haplotype-tagging SNPS based on unphased genotype data using a preliminary sample of unrelated subjects with an example from the Multiethnic Cohort Study, Hum Hered, 55: 27-36, 2003.
-
(2003)
Hum Hered
, vol.55
, pp. 27-36
-
-
Stram, D.O.1
Haiman, C.A.2
Hirschhorn, J.N.3
Altshuler, D.4
Kolonel, L.N.5
Henderson, B.E.6
Pike, M.C.7
-
59
-
-
0034789532
-
Haplotype tagging for the identification of common disease genes
-
Johnson, G.C., Esposito, L., Barratt, B.J., Smith, A.N., Heward, J., Di Genova, G., Ueda, H., Cordell, H.J., Eaves, I.A., Dudbridge, F., Twells, R.C., Payne, F., Hughes, W., Nutland, S., Stevens, H., Carr, P., Tuomilehto-Wolf, E., Tuomilehto, J., Gough, S.C., Clayton, D.G. and Todd, J.A. Haplotype tagging for the identification of common disease genes, Nat Genet, 29:233-237, 2001.
-
(2001)
Nat Genet
, vol.29
, pp. 233-237
-
-
Johnson, G.C.1
Esposito, L.2
Barratt, B.J.3
Smith, A.N.4
Heward, J.5
Di Genova, G.6
Ueda, H.7
Cordell, H.J.8
Eaves, I.A.9
Dudbridge, F.10
Twells, R.C.11
Payne, F.12
Hughes, W.13
Nutland, S.14
Stevens, H.15
Carr, P.16
Tuomilehto-Wolf, E.17
Tuomilehto, J.18
Gough, S.C.19
Clayton, D.G.20
Todd, J.A.21
more..
-
60
-
-
16844369571
-
The need for a systematic approach to complex pathways in molecular epidemiology
-
Thomas, D.C. The need for a systematic approach to complex pathways in molecular epidemiology, Cancer Epidemiol Biomarkers Prev, 14: 557-559, 2005.
-
(2005)
Cancer Epidemiol Biomarkers Prev
, vol.14
, pp. 557-559
-
-
Thomas, D.C.1
|