{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2026,5,9]],"date-time":"2026-05-09T06:31:59Z","timestamp":1778308319213,"version":"3.51.4"},"reference-count":26,"publisher":"Wiley","issue":"5-7","license":[{"start":{"date-parts":[[2006,10,15]],"date-time":"2006-10-15T00:00:00Z","timestamp":1160870400000},"content-version":"vor","delay-in-days":4597,"URL":"http:\/\/onlinelibrary.wiley.com\/termsAndConditions#vor"}],"content-domain":{"domain":[],"crossmark-restriction":false},"short-container-title":["Statistics in Medicine"],"published-print":{"date-parts":[[1994,3,15]]},"abstract":"<jats:title>Abstract<\/jats:title><jats:p>In population\u2010based case\u2010control studies, an attempt is made to identify all incident cases diagnosed in a specified population during a fixed time interval. Assuming that this goal is met allows one to obtain measures of risk other than relative risks. In this paper, we describe three approaches to estimate exposure\u2010specific incidence rates. Approach 1 relies on estimating crude incidence rates of the disease in strata defined, for instance, by age and geographic area, and combining them with relative risk estimates from the case\u2010control data. In approaches 2 and 3, baseline incidence rates and relative risks are estimated jointly. Approach 2 is based on a pseudo\u2010likelihood, while, in approach 3, the problem is regarded as a missing data problem and a full likelihood is maximized. We applied these three approaches to a study of bladder cancer. Our three sets of estimates of exposure\u2010specific incidence rates were in close agreement, while there appeared to be greater precision with approaches 2 and 3.<\/jats:p>","DOI":"10.1002\/sim.4780130526","type":"journal-article","created":{"date-parts":[[2007,4,28]],"date-time":"2007-04-28T21:18:12Z","timestamp":1177795092000},"page":"651-661","source":"Crossref","is-referenced-by-count":23,"title":["A comparison of three approaches to estimate exposure\u2010specific incidence rates from population\u2010based case\u2010control data"],"prefix":"10.1002","volume":"13","author":[{"given":"Jacques","family":"Benichou","sequence":"first","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Sholom","family":"Wacholder","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]}],"member":"311","published-online":{"date-parts":[[2006,10,15]]},"reference":[{"key":"e_1_2_1_2_2","first-page":"1269","article-title":"A method for estimating comparative rates from clinical data: Applications to cancer of the lung, breast and cervix","volume":"11","author":"Cornfield J.","year":"1951","journal-title":"Journal of the National Cancer Institute"},{"key":"e_1_2_1_3_2","first-page":"133","volume-title":"Proceedings of the Third Berkeley Symposium","author":"Cornfield J.","year":"1956"},{"key":"e_1_2_1_4_2","first-page":"1173","article-title":"Prenatal X\u2010ray exposure and childhood cancer","volume":"28","author":"MacMahon B.","year":"1962","journal-title":"Journal of the National Cancer Institute"},{"key":"e_1_2_1_5_2","doi-asserted-by":"publisher","DOI":"10.1093\/oxfordjournals.aje.a121617"},{"key":"e_1_2_1_6_2","doi-asserted-by":"publisher","DOI":"10.1093\/oxfordjournals.aje.a112614"},{"key":"e_1_2_1_7_2","doi-asserted-by":"publisher","DOI":"10.1016\/0021-9681(81)90004-7"},{"key":"e_1_2_1_8_2","doi-asserted-by":"publisher","DOI":"10.1093\/jnci\/81.24.1879"},{"key":"e_1_2_1_9_2","doi-asserted-by":"publisher","DOI":"10.2105\/AJPH.74.1.52"},{"key":"e_1_2_1_10_2","doi-asserted-by":"publisher","DOI":"10.1093\/jnci\/81.19.1472"},{"key":"e_1_2_1_11_2","unstructured":"Miller B. 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