Risk Prediction for Epithelial Ovarian Cancer in 11 United States-Based Case-Control Studies: Incorporation of Epidemiologic Risk Factors and 17 Confirmed Genetic Loci

Autor: Clyde, Merlise A, Palmieri Weber, Rachel, Iversen, Edwin S, Poole, Elizabeth M, Doherty, Jennifer A, Goodman, Marc T, Ness, Roberta B, Risch, Harvey A, Rossing, Mary Anne, Terry, Kathryn L, Wentzensen, Nicolas, Whittemore, Alice S, Anton-Culver, Hoda, Bandera, Elisa V, Berchuck, Andrew, Carney, Michael E, Cramer, Daniel W, Cunningham, Julie M, Cushing-Haugen, Kara L, Edwards, Robert P, Fridley, Brooke L, Goode, Ellen L, Lurie, Galina, McGuire, Valerie, Modugno, Francesmary, Moysich, Kirsten B, Olson, Sara H, Pearce, Celeste Leigh, Pike, Malcolm C, Rothstein, Joseph H, Sellers, Thomas A, Sieh, Weiva, Stram, Daniel, Thompson, Pamela J, Vierkant, Robert A, Wicklund, Kristine G, Wu, Anna H, Ziogas, Argyrios, Tworoger, Shelley S, Schildkraut, Joellen M, on behalf of the Ovarian Cancer Association Consortium

Publikováno v: Clyde, Merlise A; Palmieri Weber, Rachel; Iversen, Edwin S; Poole, Elizabeth M; Doherty, Jennifer A; Goodman, Marc T; et al.(2016). Risk Prediction for Epithelial Ovarian Cancer in 11 United States-Based Case-Control Studies: Incorporation of Epidemiologic Risk Factors and 17 Confirmed Genetic Loci.. American journal of epidemiology, 184(8), 579-589. doi: 10.1093/aje/kww091. UC Irvine: Retrieved from: http://www.escholarship.org/uc/item/4qd5v32h

Previously developed models for predicting absolute risk of invasive epithelial ovarian cancer have included a limited number of risk factors and have had low discriminatory power (area under the receiver operating characteristic curve (AUC) < 0.60).

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=od_______325::d7fb3f85984dcc8e206bf08e253c97bb
http://www.escholarship.org/uc/item/4qd5v32h

POST TRAUMATIC STRESS DISORDER IN CHILDREN RELATED TO CHILD ABUSE NEW GENETIC AND EPIGENETIC EVIDENCES

Autor: E. Parano, X. G. Pappalardo, P. Pavone, M. Ruggieri, S. Cavallaro

Publikováno v: 1st International Congress on Advances Pediatrics-New frontiers in neurological surgery, neonatology, nutrition, broncopneumoallergology, gastroenterology and skin diseases, Conrnell university-Uris auditorium Weill Medical College (New York), USA, 3-6 Dicembre 2016
info:cnr-pdr/source/autori:E. Parano; X. G. Pappalardo; P. Pavone; M. Ruggieri; S. Cavallaro/congresso_nome:1st International Congress on Advances Pediatrics-New frontiers in neurological surgery, neonatology, nutrition, broncopneumoallergology, gastroenterology and skin diseases/congresso_luogo:Conrnell university-Uris auditorium Weill Medical College (New York), USA/congresso_data:3-6 Dicembre 2016/anno:2015/pagina_da:/pagina_a:/intervallo_pagine

In children or adolescents who experiences severe traumatic events, including situations where someone's life (themselves and/or parents' lives) is threatened, or when major injuries occur (e.g., victims or witnesses of physical/sexual abuse), or vic

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=cnr_________::fe7f8279f1acb9c2445225d7b95acd8c
http://www.cnr.it/prodotto/i/356283

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Common genetic variation in the Estrogen Receptor Beta (ESR2) gene and osteoarthritis: results of a meta-analysis

Autor: Nancy E Lane, Fernando Rivadeneira, Michael C. Nevitt, Albert Hofman, Huibert A. P. Pols, Ingrid Meulenbelt, André G. Uitterlinden, Margreet Kloppenburg, John Loughlin, Antonio Gonzalez, Tim D. Spector, Hanneke J. M. Kerkhof, Andrew Carr, Eline Slagboom, Aspasia Tsezou, Deborah J. Hart, Ana M. Valdes, Joyce B. J. van Meurs, Lisette Stolk

Publikováno v: BMC Medical Genetics, 11. BioMed Central Ltd.
BMC Medical Genetics, Vol 11, Iss 1, p 164 (2010)
BMC Medical Genetics
Kerkhof, Hanneke JM; Meulenbelt, Ingrid; Carr, Andrew; Gonzalez, Antonio; Hart, Deborah; Hofman, Albert; et al.(2010). Common genetic variation in the Estrogen Receptor Beta (ESR2) gene and osteoarthritis: results of a meta-analysis. BMC Medical Genetics, 11(1), 164. doi: http://dx.doi.org/10.1186/1471-2350-11-164. Retrieved from: http://www.escholarship.org/uc/item/706319bd
BMC Medical Genetics, 11

Background The objective of this study was to examine the relationship between common genetic variation of the ESR2 gene and osteoarthritis. Methods In the discovery study, the Rotterdam Study-I, 7 single nucleotide polymorphisms (SNPs) were genotype

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6a4d1123beb0a4a4f4a6a06c1c2e721d
https://hdl.handle.net/1887/110843

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