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A. Børresen (1992)
Oncogenesis in ovarian cancerActa Obstetricia et Gynecologica Scandinavica, 71
Harris R Whittemore AS (1992)
Characteristics relating to ovarian cancer risk: collaborative analysis of 12 US case-control studies, IV: the pathogenesis of epithelial ovarian cancer.Am J Epidemiol, 136
Dembo A Berek JS (1993)
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Nutrient intake and ovarian cancer.American journal of epidemiology, 130 3
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Pike MC Preston-Martin S (1991)
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Utah Cancer Registry (1992)
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Reproductive, genetic, and dietary risk factors for ovarian cancer.American journal of epidemiology, 128 4
C. Amos, J. Struewing (2010)
Genetic epidemiology of epithelial ovarian cancerCancer, 71
D. Malkin, F. Li, L. Strong, J. Fraumeni, C. Nelson, D. Kim, J. Kassel, M. Gryka, F. Bischoff, M. Tainsky (1990)
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Genetic instability of microsatellites in endometrial carcinoma.Cancer research, 53 21
D. Cramer (1989)
Lactase persistence and milk consumption as determinants of ovarian cancer risk.American journal of epidemiology, 130 5
Li FP Malkin D (1990)
Germ line p53 mutations in a familial syndrome of breast cancer, sarcomas, and other neoplasms [see comments].Science, 250
A. Polychronopoulou, A. Tzonou, C. Hsieh, D. Trichopoulos, G. Kaprinis, A. Rebelakos, N. Toupadaki (1993)
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D. Easton, D. Bishop, D. Ford, G. Crockford (1993)
Genetic linkage analysis in familial breast and ovarian cancer: results from 214 families. The Breast Cancer Linkage Consortium.American journal of human genetics, 52 4
D. Cramer, W. Welch (1983)
Determinants of ovarian cancer risk. II. Inferences regarding pathogenesis.Journal of the National Cancer Institute, 71 4
Thompson WD Schildkraut JM (1988)
Familial ovarian cancer: a population-based case-control study [see comments].Am J Epidemiol, 128
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Alcohol and epithelial ovarian cancer.Journal of clinical epidemiology, 45 9
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Dietary factors and the risk of epithelial ovarian cancer.Journal of the National Cancer Institute, 79 4
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A case-control study of epithelial ovarian cancer.American journal of obstetrics and gynecology, 161 1
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Chromosome 17q linkage studies of 18 Utah breast cancer kindreds.American journal of human genetics, 52 4
A. Whittemore, M. Wu, R. Paffenbarger, D. Sarles, J. Kampert, S. Grosser, D. Jung, S. Ballon, M. Hendrickson, J. Mohle-Boetani (1989)
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A. Engle, J. Muscat, R. Harris (1991)
Nutritional risk factors and ovarian cancer.Nutrition and cancer, 15 3-4
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Characteristics relating to ovarian cancer risk: collaborative analysis of 12 US case-control studies, II: invasive epithelial ovarian cancers in white women [see comments].J Epidemiol, 136
G. Malécot (1948)
Les mathématiques de l'hérédité
S. Narod, P. Tonin, H. Lynch, P. Watson, J. Feunteun, G. Lenoir (1994)
Histology of BRCA1-associated ovarian tumoursThe Lancet, 343
Clive Osmond, N. Breslow, N. Day (1987)
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Lubin JH Preston DL (1992)
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Jolly Kw, D. Malkin, Douglass Ec, Brown Tf, Sinclair Ae, Look At (1994)
Splice-site mutation of the p53 gene in a family with hereditary breast-ovarian cancer.Oncogene, 9 1
S. Preston‐Martin, M. Pike, R. Ross, B. Henderson (1993)
Epidemiologic evidence for the increased cell proliferation model of carcinogenesis.Environmental Health Perspectives, 101
M. Koch, H. Gaedke, H. Jenkins (1989)
Family history of ovarian cancer patients: a case-control study.International journal of epidemiology, 18 4
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Family history of reproductive cancers and ovarian cancer risk: an Italian case-control study.American journal of epidemiology, 135 1
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Galactose consumption and metabolism in relation to the risk of ovarian cancer [see comments].Lancet, 2
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Determinants of ovarian cancer risk. I. Reproductive experiences and family history.Journal of the National Cancer Institute, 71 4
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Hereditary ovarian cancer: heterogeneity in age at onset.Cancer, 71
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Risk factors in ovarian cancer.European journal of gynaecological oncology, 9 3
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Bishop DT Easton DF (1993)
Genetic linkage analysis in familial breast and ovarian cancer: results from 214 families.Am J Hum Genet, 52
J. Schildkraut, W. Thompson (1988)
Familial ovarian cancer: a population-based case-control study.American journal of epidemiology, 128 3
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M. Piver, T. Baker, M. Jishi, A. Sandecki, Y. Tsukada, N. Natarajan, C. Mettlin, C. Blake (2010)
Familial ovarian cancer: A report of 658 families from the gilda radner familial ovarian cancer registry 1981–1991Cancer, 71
Malecot G (1948)
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Jean Feunteun, A. Steven, Narod, T. Henry, Lynch, Patrice, Watson, Theresa Conway, Jane, Jillian Parboosingh, Peter O'Connell, Ray White, M. Gilbert, LenoirlI (1993)
A breast-ovarian cancer susceptibility gene maps to chromosome 17q21.American journal of human genetics, 52 4
B. Ames, M. Shigenaga, T. Hagen (1993)
Oxidants, antioxidants, and the degenerative diseases of aging.Proceedings of the National Academy of Sciences of the United States of America, 90 17
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Abstract Objective: To estimate the relative risks and population attributable risks of ovarian cancer associated with family histories of cancer at several sites. Methods: A matched case-control analytic study (662 cases, 2647 controls), employing the Utah Population Database, a genealogy of approximately 1 million individuals linked to cancer incidence data from the Utah Cancer Registry. Family history was assessed using kinship order and a kinship-weighted familial standardized incidence ratio statistic. Results: Family histories of ovarian, uterine, breast, and pancreatic cancer were significantly associated with increased risk of ovarian cancer. The relative risk of ovarian cancer was 4.31 (95% confidence interval [CI], 2.35 to 7.90) for women with a first-degree relative with ovarian cancer, 2.12 (95% CI, 1.19 to 3.78) for women with an affected second-degree relative, and 1.48 (95% CI, 0.98 to 2.24) for women with an affected third-degree relative. The odds ratio (OR) was 2.06 (95% CI, 1.44 to 2.93) for those with the highest familial standardized incidence ratio. No age differences were observed between cases with and without a family history of ovarian cancer. There was substantial heterogeneity of family history effects by cell type. Increased parity was not protective among women with a strong family history of cancer at the sites studied (OR, 1.11; 95% CI, 0.38 to 3.26), although it was protective among women without a family history of these cancers (OR, 0.29; 95% CI, 0.11 to 0.62). Conclusions: The risk of ovarian cancer was substantially increased among women with family histories of ovarian, uterine, pancreatic, and, to a lesser degree, breast cancer. Among women with family histories of any of these cancers, the risk of ovarian cancer is not diminished by high parity.(Arch Intern Med. 1995;155:905-912) References 1. Berek JS, Dembo A, Ozols RF. Ovarian cancer. 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Archives of Internal Medicine – American Medical Association
Published: May 8, 1995
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