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1,361 results on '"Whittemore, Alice S"'

171. Consortium analysis of gene and gene–folate interactions in purine and pyrimidine metabolism pathways with ovarian carcinoma risk

Author

Kelemen, Linda E., Terry, Kathryn L., Goodman, Marc T., Webb, Penelope M., Bandera, Elisa V., McGuire, Valerie, Rossing, Mary Anne, Wang, Qinggang, Dicks, Ed, Tyrer, Jonathan P., Song, Honglin, Kupryjanczyk, Jolanta, Dansonka-Mieszkowska, Agnieszka, Plisiecka-Halasa, Joanna, Timorek, Agnieszka, Menon, Usha, Gentry-Maharaj, Aleksandra, Gayther, Simon A., Ramus, Susan J., Narod, Steven A., Risch, Harvey A., McLaughlin, John R., Siddiqui, Nadeem, Glasspool, Rosalind, Paul, James, Carty, Karen, Gronwald, Jacek, Lubiński, Jan, Jakubowska, Anna, Cybulski, Cezary, Kiemeney, Lambertus A., Massuger, Leon F. A. G., van Altena, Anne M., Aben, Katja K. H., Olson, Sara H., Orlow, Irene, Cramer, Daniel W., Levine, Douglas A., Bisogna, Maria, Giles, Graham G., Southey, Melissa C., Bruinsma, Fiona, Kjær, Susanne K., Hgdall, Estrid, Jensen, Allan, Hgdall, Claus K., Lundvall, Lene, Engelholm, Svend-Aage, Heitz, Florian, du Bois, Andreas, Harter, Philipp, Schwaab, Ira, Butzow, Ralf, Nevanlinna, Heli, Pelttari, Liisa M., Leminen, Arto, Thompson, Pamela J., Lurie, Galina, Wilkens, Lynne R., Lambrechts, Diether, Van Nieuwenhuysen, Els, Lambrechts, Sandrina, Vergote, Ignace, Beesley, Jonathan, Fasching, Peter A., Beckmann, Matthias W., Hein, Alexander, Ekici, Arif B., Doherty, Jennifer A., Wu, Anna H., Pearce, Celeste L., Pike, Malcolm C., Stram, Daniel, Chang-Claude, Jenny, Rudolph, Anja, Dörk, Thilo, Dürst, Matthias, Hillemanns, Peter, Runnebaum, Ingo B., Bogdanova, Natalia, Antonenkova, Natalia, Odunsi, Kunle, Edwards, Robert P., Kelley, Joseph L., Modugno, Francesmary, Ness, Roberta B., Karlan, Beth Y., Walsh, Christine, Lester, Jenny, Orsulic, Sandra, Fridley, Brooke L., Vierkant, Robert A., Cunningham, Julie M., Wu, Xifeng, Lu, Karen, Liang, Dong, Hildebrandt, Michelle A.T., Weber, Rachel Palmieri, Iversen, Edwin S., Tworoger, Shelley S., Poole, Elizabeth M., Salvesen, Helga B., Krakstad, Camilla, Bjorge, Line, Tangen, Ingvild L., Pejovic, Tanja, Bean, Yukie, Kellar, Melissa, Wentzensen, Nicolas, Brinton, Louise A., Lissowska, Jolanta, Garcia-Closas, Montserrat, Campbell, Ian G., Eccles, Diana, Whittemore, Alice S., Sieh, Weiva, Rothstein, Joseph H., Anton-Culver, Hoda, Ziogas, Argyrios, Phelan, Catherine M., Moysich, Kirsten B., Goode, Ellen L., Schildkraut, Joellen M., Berchuck, Andrew, Pharoah, Paul D.P., Sellers, Thomas A., Brooks-Wilson, Angela, Cook, Linda S., and Le, Nhu D.

Published
2014
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172. Cigarette smoking and risk of ovarian cancer: a pooled analysis of 21 case–control studies

Author

Faber, Mette T., Kjær, Susanne K., Dehlendorff, Christian, Chang-Claude, Jenny, Andersen, Klaus K., Høgdall, Estrid, Webb, Penelope M., Jordan, Susan J., Rossing, Mary Anne, Doherty, Jennifer A., Lurie, Galina, Thompson, Pamela J., Carney, Michael E., Goodman, Marc T., Ness, Roberta B., Modugno, Francesmary, Edwards, Robert P., Bunker, Clareann H., Goode, Ellen L., Fridley, Brooke L., Vierkant, Robert A., Larson, Melissa C., Schildkraut, Joellen, Cramer, Daniel W., Terry, Kathryn L., Vitonis, Allison F., Bandera, Elisa V., Olson, Sara H., King, Melony, Chandran, Urmila, Kiemeney, Lambertus A., Massuger, Leon F. A. G., van Altena, Anne M., Vermeulen, Sita H., Brinton, Louise, Wentzensen, Nicolas, Lissowska, Jolanta, Yang, Hannah P., Moysich, Kirsten B., Odunsi, Kunle, Kasza, Karin, Odunsi-Akanji, Oluwatosin, Song, Honglin, Pharaoh, Paul, Shah, Mitul, Whittemore, Alice S., McGuire, Valerie, Sieh, Weiva, Sutphen, Rebecca, Menon, Usha, Gayther, Simon A., Ramus, Susan J., Gentry-Maharaj, Aleksandra, Pearce, Celeste Leigh, Wu, Anna H., Pike, Malcolm C., Risch, Harvey A., Jensen, Allan, The Australian Cancer Study (Ovarian Cancer), Australian Ovarian Cancer Study Group, and On behalf of the Ovarian Cancer Association Consortium

Published
2013
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173. HOXB13 is a susceptibility gene for prostate cancer: results from the International Consortium for Prostate Cancer Genetics (ICPCG)

Author

Xu, Jianfeng, Lange, Ethan M., Lu, Lingyi, Zheng, Siqun L., Wang, Zhong, Thibodeau, Stephen N., Cannon-Albright, Lisa A., Teerlink, Craig C., Camp, Nicola J., Johnson, Anna M., Zuhlke, Kimberly A., Stanford, Janet L., Ostrander, Elaine A., Wiley, Kathleen E., Isaacs, Sarah D., Walsh, Patrick C., Maier, Christiane, Luedeke, Manuel, Vogel, Walther, Schleutker, Johanna, Wahlfors, Tiina, Tammela, Teuvo, Schaid, Daniel, McDonnell, Shannon K., DeRycke, Melissa S., Cancel-Tassin, Geraldine, Cussenot, Olivier, Wiklund, Fredrik, Grönberg, Henrik, Eeles, Ros, Easton, Doug, Kote-Jarai, Zsofia, Whittemore, Alice S., Hsieh, Chih-Lin, Giles, Graham G., Hopper, John L., Severi, Gianluca, Catalona, William J., Mandal, Diptasri, Ledet, Elisa, Foulkes, William D., Hamel, Nancy, Mahle, Lovise, Moller, Pal, Powell, Isaac, Bailey-Wilson, Joan E., Carpten, John D., Seminara, Daniela, Cooney, Kathleen A., Isaacs, William B., and International Consortium for Prostate Cancer Genetics

Published
2013
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174. Validation of prostate cancer risk-related loci identified from genome-wide association studies using family-based association analysis: evidence from the International Consortium for Prostate Cancer Genetics (ICPCG)

Author

Jin, Guangfu, Lu, Lingyi, Cooney, Kathleen A., Ray, Anna M., Zuhlke, Kimberly A., Lange, Ethan M., Cannon-Albright, Lisa A., Camp, Nicola J., Teerlink, Craig C., FitzGerald, Liesel M., Stanford, Janet L., Wiley, Kathleen E., Isaacs, Sarah D., Walsh, Patrick C., Foulkes, William D., Giles, Graham G., Hopper, John L., Severi, Gianluca, Eeles, Ros, Easton, Doug, Kote-Jarai, Zsofia, Guy, Michelle, Rinckleb, Antje, Maier, Christiane, Vogel, Walther, Cancel-Tassin, Geraldine, Egrot, Christophe, Cussenot, Olivier, Thibodeau, Stephen N., McDonnell, Shannon K., Schaid, Daniel J., Wiklund, Fredrik, Grönberg, Henrik, Emanuelsson, Monica, Whittemore, Alice S., Oakley-Girvan, Ingrid, Hsieh, Chih-Lin, Wahlfors, Tiina, Tammela, Teuvo, Schleutker, Johanna, Catalona, William J., Zheng, S. Lilly, Ostrander, Elaine A., Isaacs, William B., Xu, Jianfeng, and International Consortium for Prostate Cancer Genetics

Published
2012
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177. Family history of breast cancer and all-cause mortality after breast cancer diagnosis in the Breast Cancer Family Registry

Author

Chang, Ellen T., Milne, Roger L., Phillips, Kelly-Anne, Figueiredo, Jane C., Sangaramoorthy, Meera, Keegan, Theresa H. M., Andrulis, Irene L., Hopper, John L., Goodwin, Pamela J., O’Malley, Frances P., Weerasooriya, Nayana, Apicella, Carmel, Southey, Melissa C., Friedlander, Michael L., Giles, Graham G., Whittemore, Alice S., West, Dee W., and John, Esther M.

Published
2009
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178. Finding the missing heritability of complex diseases

Author

Manolio, Teri A., Collins, Francis S., Cox, Nancy J., Goldstein, David B., Hindorffs, Lucia A., Hunter, David J., McCarthy, Mark I., Ramos, Erin M., Cardon, Lon R., Chakravarti, Aravinda, Cho, Judy H., Guttmacher, Alan E., Kong, Augustine, Kruglyak, Leonid, Mardis, Elaine, Rotimi, Charles N., Slatkin, Montgomery, Valle, David, Whittemore, Alice S., Boehnke, Michael, Clark, Andrew G., Eichler, Evan E., Gibson, Greg, Haines, Jonathan L., Mackay, Trudy F.C., McCarroll, Steven A., and Visscher, Peter M.

Subjects
Diseases -- United States -- Genetic aspects -- Research, Genomes -- Health aspects -- Research -- Genetic aspects, Heritability -- Research -- Genetic aspects -- Health aspects, Environmental issues, Science and technology, Zoology and wildlife conservation
Abstract

Genome-wide association studies have identified hundreds of genetic variants associated with complex human diseases and traits, and have provided valuable insights into their genetic architecture. Most variants identified so far confer relatively small increments in risk, and explain only a small proportion of familial clustering, leading many to question how the remaining, 'missing' heritability can be explained. Here we examine potential sources of missing heritability and search strategies, including and extending beyond current genome-wide association approaches, to illuminate the genetics of complex diseases and enhance its potential to enable effective disease prevention or treatment., Many common human diseases and traits are known to cluster in families and are believed to be influenced by several genetic and environmental factors, but until recently the identification of [...]

Published
2009

179. Common variants on chromosome 6p22.1 are associated with schizophrenia

Author

Shi, Jianxin, Levinson, Douglas F., Duan, Jubao, Sanders, Alan R., Zheng, Yonglan, Pe'er, Itsik, Dudbridge, Frank, Holmans, Peter A., Whittemore, Alice S., Mowry, Bryan J., Olincy, Ann, Amin, Farooq, Cloninger, C. Robert, Silverman, Jeremy M., Buccola, Nancy G., Byerley, William F., Black, Donald W., Crowe, Raymond R., Oksenberg, Jorge R., Mirel, Daniel B., Kendler, Kenneth S., Freedman, Robert, and Gejman, Pablo V.

Subjects
Schizophrenia -- Genetic aspects -- Diagnosis -- Research, Single nucleotide polymorphisms -- Research -- Health aspects -- Genetic aspects, Disease susceptibility -- Health aspects -- Genetic aspects -- Research -- Diagnosis, Environmental issues, Science and technology, Zoology and wildlife conservation, Diagnosis, Genetic aspects, Research, Health aspects
Abstract

Schizophrenia, a devastating psychiatric disorder, has a prevalence of 0.5-1%, with high heritability (80-85%)and complex transmission (1). Recent studies implicate rare, large, high-penetrante copy number variants in some cases (2), but the genes or biological mechanisms that underlie susceptibility are not known. Here we show that schizophrenia is significantly associated with single nucleotide polymorphisms (SNPs) in the extended major histocompatibility complex region on chromosome 6. We carried out a genome-wide association study of common SNPs in the Molecular Genetics of Schizophrenia (MGS) case-control sample, and then a meta-analysis of data from the MGS, International Schizophrenia Consortium and SGENE data sets. No MGS finding achieved genome-wide statistical significance. In the meta-analysis of European-ancestry subjects (8,008 cases, 19,077 controls), significant association with schizophrenia was observed in a region of linkage disequilibrium on chromosome 6p22.1 (P = 9.54 x [10.sup.-9]). This region includes a histone gene cluster and several immunity-related genes--possibly implicating aetiological mechanisms involving chromatin modification, transcriptional regulation, autoimmunity and/or infection. These results demonstrate that common schizophrenia susceptibility alleles can be detected. The characterization of these signals will suggest important directions for research on susceptibility mechanisms., The symptoms and course of schizophrenia are variable, without forming distinct familial subtypes (1). There are positive (delusions and hallucinations), negative (reduced emotions, speech and interest), and disorganized (disrupted syntax [...]

Published
2009

181. Two-stage Study of Familial Prostate Cancer by Whole-exome Sequencing and Custom Capture Identifies 10 Novel Genes Associated with the Risk of Prostate Cancer

Author

Schaid, Daniel J., primary, McDonnell, Shannon K., additional, FitzGerald, Liesel M., additional, DeRycke, Lissa, additional, Fogarty, Zachary, additional, Giles, Graham G., additional, MacInnis, Robert J., additional, Southey, Melissa C., additional, Nguyen-Dumont, Tu, additional, Cancel-Tassin, Geraldine, additional, Cussenot, Oliver, additional, Whittemore, Alice S., additional, Sieh, Weiva, additional, Ioannidis, Nilah Monnier, additional, Hsieh, Chih-Lin, additional, Stanford, Janet L., additional, Schleutker, Johanna, additional, Cropp, Cheryl D., additional, Carpten, John, additional, Hoegel, Josef, additional, Eeles, Rosalind, additional, Kote-Jarai, Zsofia, additional, Ackerman, Michael J., additional, Klein, Christopher J., additional, Mandal, Diptasri, additional, Cooney, Kathleen A., additional, Bailey-Wilson, Joan E., additional, Helfand, Brian, additional, Catalona, William J., additional, Wiklund, Fredrick, additional, Riska, Shaun, additional, Bahetti, Saurabh, additional, Larson, Melissa C., additional, Cannon Albright, Lisa, additional, Teerlink, Craig, additional, Xu, Jianfeng, additional, Isaacs, William, additional, Ostrander, Elaine A., additional, and Thibodeau, Stephen N., additional

Published
2021
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182. Prevalence of pathogenic BRCA1 mutation carriers in 5 US racial/ethnic groups

Author

John, Esther M., Miron, Alexander, Gong, Gail, Phipps, Amanda I., Felberg, Anna, Li, Frederick P., West, Dee W., and Whittemore, Alice S.

Subjects
African Americans -- Health aspects, African Americans -- Genetic aspects, Asian Americans -- Health aspects, Asian Americans -- Genetic aspects, Hispanic Americans -- Health aspects, Hispanic Americans -- Genetic aspects, Tumor suppressor genes -- Research
Abstract

A study to compare the extent Hispanics, African Americans and Asian Americans as carriers of the tumor suppressor gene BRCA1 compared to white non-Hispanics with and without Ashkenazi Jewish ancestry is conducted. Results reveal that the mutated gene was highest in Hispanics and Asian Americans displayed the lowest.

Published
2007

184. Accuracy of Risk Estimates from the iPrevent Breast Cancer Risk Assessment and Management Tool

Author

Phillips, Kelly-Anne, Liao, Yuyan, Milne, Roger L, MacInnis, Robert J, Collins, Ian M, Buchsbaum, Richard, Weideman, Prue C, Bickerstaffe, Adrian, Nesci, Stephanie, Chung, Wendy K, Southey, Melissa C, Knight, Julia A, Whittemore, Alice S, Dite, Gillian S, Goldgar, David, Giles, Graham G, Glendon, Gord, Cuzick, Jack, Antoniou, Antonis C, Andrulis, Irene L, John, Esther M, Daly, Mary B, Buys, Saundra S, Hopper, John L, Terry, Mary Beth, kConFab Investigators, Phillips, Kelly-Anne [0000-0002-0475-1771], Milne, Roger L [0000-0001-5764-7268], Collins, Ian M [0000-0001-6936-0942], Weideman, Prue C [0000-0002-3672-5201], Dite, Gillian S [0000-0002-2448-2548], Giles, Graham G [0000-0003-4946-9099], and Apollo - University of Cambridge Repository

Subjects
kConFab Investigators
Abstract

BACKGROUND: iPrevent is an online breast cancer (BC) risk management decision support tool. It uses an internal switching algorithm, based on a woman's risk factor data, to estimate her absolute BC risk using either the International Breast Cancer Intervention Study (IBIS) version 7.02, or Breast and Ovarian Analysis of Disease Incidence and Carrier Estimation Algorithm version 3 models, and then provides tailored risk management information. This study assessed the accuracy of the 10-year risk estimates using prospective data. METHODS: iPrevent-assigned 10-year invasive BC risk was calculated for 15 732 women aged 20-70 years and without BC at recruitment to the Prospective Family Study Cohort. Calibration, the ratio of the expected (E) number of BCs to the observed (O) number and discriminatory accuracy were assessed. RESULTS: During the 10 years of follow-up, 619 women (3.9%) developed BC compared with 702 expected (E/O = 1.13; 95% confidence interval [CI] =1.05 to 1.23). For women younger than 50 years, 50 years and older, and BRCA1/2-mutation carriers and noncarriers, E/O was 1.04 (95% CI = 0.93 to 1.16), 1.24 (95% CI = 1.11 to 1.39), 1.13 (95% CI = 0.96 to 1.34), and 1.13 (95% CI = 1.04 to 1.24), respectively. The C-statistic was 0.70 (95% CI = 0.68 to 0.73) overall and 0.74 (95% CI = 0.71 to 0.77), 0.63 (95% CI = 0.59 to 0.66), 0.59 (95% CI = 0.53 to 0.64), and 0.65 (95% CI = 0.63 to 0.68), respectively, for the subgroups above. Applying the newer IBIS version 8.0b in the iPrevent switching algorithm improved calibration overall (E/O = 1.06, 95% CI = 0.98 to 1.15) and in all subgroups, without changing discriminatory accuracy. CONCLUSIONS: For 10-year BC risk, iPrevent had good discriminatory accuracy overall and was well calibrated for women aged younger than 50 years. Calibration may be improved in the future by incorporating IBIS version 8.0b.

Published
2019

186. A combined genomewide linkage scan of 1,233 families for prostate cancer-susceptibility genes conducted by the International Consortium for Prostate Cancer Genetics

Author

Xu, Jianfeng, Dimitrov, Latchezar, Chang, Bao-Li, Adams, Tamara S., Turner, Aubrey R., Meyers, Deborah A., Eeles, Rosalind A., Easton, Douglas F., Foulkes, William D., Simard, Jacques, Giles, Graham G., Hopper, John L., Mahle, Lovise, Moller, Pal, Bishop, Tim, Evans, Chris, Edwards, Steve, Meitz, Julia, Bullock, Sarah, Hope, Questa, Hsieh, Chih-lin, Halpern, Jerry, Balise, Raymond N., Oakley-Girvan, Ingrid, Whittemore, Alice S., Ewing, Charles M., Gielzak, Marta, Isaacs, Sarah D., Walsh, Patrick C., Wiley, Kathleen E., Isaacs, William B., Thibodeau, Stephen N., McDonnell, Shannon K., Cunningham, Julie M., Zarfas, Katherine E., Hebbring, Scott, Schaid, Daniel J., Friedrichsen, Danielle M., Deutsch, Kerry, Kolb, Suzanne, Badzioch, Michael, Jarvik, Gail P., Janer, Marta, Hood, Leroy, Ostrander, Elaine A., Stanford, Janet L., Lange, Ethan M., Beebe-Dimmer, Jennifer L., Mohai, Caroline E., Cooney, Kathleen A., Ikonen, Tarja, Baffoe-Bonnie, Agnes, Fredriksson, Henna, Matikainen, Mika P., Tammela, Teuvo LJ, Bailey-Wilson, Joan, Schleutker, Johanna, Maier, Christiane, Herkommer, Kathleen, Hoegel, Josef J., Vogel, Walther, Paiss, Thomas, Wiklund, Fredrik, Emanuelsson, Monica, Stenman, Elisabeth, Jonsson, Bjorn-Anders, Gronberg, Henrik, Camp, Nicola J., Farnham, James, Cannon-Albright, Lisa A., and Seminara, Daniela

Subjects
Prostate cancer -- Genetic aspects, Human genetics -- Research, Biological sciences
Published
2005

187. Identification of 31 loci for mammographic density phenotypes and their associations with breast cancer risk

Author

Sieh, Weiva, primary, Rothstein, Joseph H., additional, Klein, Robert J., additional, Alexeeff, Stacey E., additional, Sakoda, Lori C., additional, Jorgenson, Eric, additional, McBride, Russell B., additional, Graff, Rebecca E., additional, McGuire, Valerie, additional, Achacoso, Ninah, additional, Acton, Luana, additional, Liang, Rhea Y., additional, Lipson, Jafi A., additional, Rubin, Daniel L., additional, Yaffe, Martin J., additional, Easton, Douglas F., additional, Schaefer, Catherine, additional, Risch, Neil, additional, Whittemore, Alice S., additional, and Habel, Laurel A., additional

Published
2020
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188. Breast cancer risks for BRCA 1/2 carriers

Author

Easton, Douglas F., Hopper, John L., Thomas, Duncan C., Antoniou, Antonis, Pharoah, Paul D.P., Whittemore, Alice S., Haile, Robert W., Wacholder, Sholom, Greene, Mark H., Tucker, Margaret A., and King, Mary-Claire

Abstract

THE REPORT BY M.-C. KING ET AL. ESTIMATES breast cancer risks in carriers of the Ashkenazi Jewish founder mutations in BRCA1 and BRCA2 ('Breast and ovarian cancer risks due to [...]

Published
2004

189. Tubal ligation and risk of ovarian cancer subtypes: a pooled analysis of case-control studies

Author

Sieh, Weiva, Salvador, Shannon, McGuire, Valerie, Weber, Rachel Palmieri, Terry, Kathryn L, Rossing, Mary Anne, Risch, Harvey, Wu, Anna H, Webb, Penelope M, Moysich, Kirsten, Doherty, Jennifer A, Felberg, Anna, Miller, Dianne, Jordan, Susan J, Goodman, Marc T, Lurie, Galina, Chang-Claude, Jenny, Rudolph, Anja, Kjær, Susanne Krüger, Jensen, Allan, Høgdall, Estrid, Bandera, Elisa V, Olson, Sara H, King, Melony G, Rodriguez-Rodriguez, Lorna, Kiemeney, Lambertus A, Marees, Tamara, Massuger, Leon F, van Altena, Anne M, Ness, Roberta B, Cramer, Daniel W, Pike, Malcolm C, Pearce, Celeste Leigh, Berchuck, Andrew, Schildkraut, Joellen M, and Whittemore, Alice S

Published
2013
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191. Stage at diagnosis survival in a multiethnic cohort of prostate cancer patients

Author

Oakley-Girvan, Ingrid, Kolonel, Laurence N., Gallagher, Richard P., Wu, Anna H., Felberg, Anna, and Whittemore, Alice S.

Subjects
Cancer patients -- Health aspects, Social status -- Health aspects, Prostate cancer, Government, Health care industry
Abstract

Objectives. We evaluated the effects of socioeconomic status and comorbidity on stage of disease and survival among 1,509 population-based prostate cancer patients. Methods. We applied logistic regression and Cox proportional hazards regression to data from Whites, African Americans, and Asian Americans who were diagnosed from 1987 to 1991. Results. Patients with existing comorbid conditions were less likely than those without these conditions to be diagnosed with advanced cancer. Compared with Whites, African Americans (odds ratio [OR] = 1.5; 95% confidence interval [CI]= 1.1, 2.2) and foreign-born Asian Americans (OR=1.6; 95% CI=1.0, 2.4) were more likely to be diagnosed with advanced cancer. Among men with localized disease, prostate cancer death rates were higher for African Americans than for Whites (death rate ratio=2.3; 95% CI=1.2, 4.7). Conclusions. These findings support the need for further investigation of factors that affect access to and use of health care among African Americans and Asian Americans.

Published
2003

193. Chromosomes 4 and 8 implicated in a genome wide SNP linkage scan of 762 prostate cancer families collected by the ICPCG

Author

Lu, Lingyi, Cancel-Tassin, Geraldine, Valeri, Antoine, Cussenot, Olivier, Lange, Ethan M., Cooney, Kathleen A., Farnham, James M., Camp, Nicola J., Cannon-Albright, Lisa A., Tammela, Teuvo L.J., Schleutker, Johanna, Hoegel, Josef, Herkommer, Kathleen, Maier, Christiane, Vogel, Walther, Wiklund, Fredrik, Emanuelsson, Monica, Grönberg, Henrik, Wiley, Kathleen E., Isaacs, Sarah D., Walsh, Patrick C., Helfand, Brian T., Kan, Donghui, Catalona, William J., Stanford, Janet L., FitzGerald, Liesel M., Johanneson, Bo, Deutsch, Kerry, McIntosh, Laura, Ostrander, Elaine A., Thibodeau, Stephen N., McDonnell, Shannon K., Hebbring, Scott, Schaid, Daniel J., Whittemore, Alice S., Oakley-Girvan, Ingrid, Hsieh, Chih-Lin, Powell, Isaac, Bailey-Wilson, Joan E., Cropp, Cheryl D., Simpson, Claire, Carpten, John D., Seminara, Daniela, Zheng, Lilly S., Xu, Jianfen, Giles, Graham G., Severi, Gianluca, Hopper, John L., English, Dallas R., Foulkes, William D., Maehle, Lovise, Moller, Pal, Badzioch, Michael D., Edwards, Steve, Guy, Michelle, Eeles, Ros, Easton, Douglas, and Isaacs, William B.

Published
2012
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194. Association Between BRCA1 and BRCA2 Mutations and Survival in Women With Invasive Epithelial Ovarian Cancer

Author

Bolton, Kelly L., Chenevix- Trench, Georgia, Goh, Cindy, Sadetzki, Siegal, Ramus, Susan J., Karlan, Beth Y., Lambrechts, Diether, Despierre, Evelyn, Barrowdale, Daniel, McGuffog, Lesley, Healey, Sue, Easton, Douglas F., Sinilnikova, Olga, Benítez, Javier, García, María J., Neuhausen, Susan, Gail, Mitchell H., Hartge, Patricia, Peock, Susan, Frost, Debra, Evans, D. Gareth, Eeles, Rosalind, Godwin, Andrew K., Daly, Mary B., Kwong, Ava, Ma, Edmond S., Lázaro, Conxi, Blanco, Ignacio, Montagna, Marco, DʼAndrea, Emma, Nicoletto, Maria Ornella, Johnatty, Sharon E., Kjær, Susanne Krüger, Jensen, Allan, Høgdall, Estrid, Goode, Ellen L., Fridley, Brooke L., Loud, Jennifer T., Greene, Mark H., Mai, Phuong L., Chetrit, Angela, Lubin, Flora, Hirsh-Yechezkel, Galit, Glendon, Gord, Andrulis, Irene L., Toland, Amanda E., Senter, Leigha, Gore, Martin E., Gourley, Charlie, Michie, Caroline O., Song, Honglin, Tyrer, Jonathan, Whittemore, Alice S., McGuire, Valerie, Sieh, Weiva, Kristoffersson, Ulf, Olsson, Håkan, Borg, Åke, Levine, Douglas A., Steele, Linda, Beattie, Mary S., Chan, Salina, Nussbaum, Robert L., Moysich, Kirsten B., Gross, Jenny, Cass, Ilana, Walsh, Christine, Li, Andrew J., Leuchter, Ronald, Gordon, Ora, Garcia-Closas, Montserrat, Gayther, Simon A., Chanock, Stephen J., Antoniou, Antonis C., and Pharoah, Paul D.

Published
2012
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197. Genetic variation in insulin-like growth factor 2 may play a role in ovarian cancer risk

Author

Pearce, Celeste Leigh, Doherty, Jennifer A., Van Den Berg, David J., Moysich, Kirsten, Hsu, Chris, Cushing-Haugen, Kara L., Conti, David V., Ramus, Susan J., Gentry-Maharaj, Aleksandra, Menon, Usha, Gayther, Simon A., Pharoah, Paul D.P., Song, Honglin, Kjaer, Susanne K., Hogdall, Estrid, Hogdall, Claus, Whittemore, Alice S., McGuire, Valerie, Sieh, Weiva, Gronwald, Jacek, Medrek, Krzysztof, Jakubowska, Anna, Lubinski, Jan, Chenevix-Trench, Georgia, Beesley, Jonathan, Webb, Penelope M., Berchuck, Andrew, Schildkraut, Joellen M., Iversen, Edwin S., Moorman, Patricia G., Edlund, Christopher K., Stram, Daniel O., Pike, Malcolm C., Ness, Roberta B., Rossing, Mary Anne, and Wu, Anna H.

Published
2011
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198. Common alleles in candidate susceptibility genes associated with risk and development of epithelial ovarian cancer

Author

Notaridou, Maria, Quaye, Lydia, Dafou, Dimitra, Jones, Chris, Song, Honglin, Hgdall, Estrid, Kjaer, Susanne K., Christensen, Lise, Hgdall, Claus, Blaakaer, Jan, McGuire, Valerie, Wu, Anna H., Van Den Berg, David J., Pike, Malcolm C., Gentry-Maharaj, Aleksandra, Wozniak, Eva, Sher, Tanya, Jacobs, Ian J., Tyrer, Jonathan, Schildkraut, Joellen M., Moorman, Patricia G., Iversen, Edwin S., Jakubowska, Anna, Mędrek, Krzysztof, Lubiński, Jan, Ness, Roberta B., Moysich, Kirsten B., Lurie, Galina, Wilkens, Lynne R., Carney, Michael E., Wang-Gohrke, Shan, Doherty, Jennifer A., Rossing, Mary Anne, Beckmann, Matthias W., Thiel, Falk C., Ekici, Arif B., Chen, Xiaoqing, Beesley, Jonathan, Gronwald, Jacek, Fasching, Peter A., Chang-Claude, Jenny, Goodman, Marc T., Chenevix-Trench, Georgia, Berchuck, Andrew, Pearce, Leigh C., Whittemore, Alice S., Menon, Usha, Pharoah, Paul D.P., Gayther, Simon A., and Ramus, Susan J.

Published
2011
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199. Vitamin D receptor rs2228570 polymorphism and invasive ovarian carcinoma risk: Pooled analysis in five studies within the Ovarian Cancer Association Consortium

Author

Lurie, Galina, Wilkens, Lynne R., Thompson, Pamela J., Carney, Michael E., Palmieri, Rachel T., Pharoah, Paul D. P., Song, Honglin, Hogdall, Estrid, Kjaer, Susanne Kruger, DiCioccio, Richard A., McGuire, Valerie, Whittemore, Alice S., Gayther, Simon A., Gentry-Maharaj, Aleksandra, Menon, Usha, Ramus, Susan J., and Goodman, Marc T.

Published
2011
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