Resultats de la cerca - VanDenBerg, David J.

Reproducibility and reliability of SNP analysis using human cellular DNA at or near nanogram levels per Okitsu, Cindy Y, Van Den Berg, David J, Lieber, Michael R, Hsieh, Chih-Lin

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Snagger: A user-friendly program for incorporating additional information for tagSNP selection per Edlund, Christopher K, Lee, Won H, Li, Dalin, Van Den Berg, David J, Conti, David V

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Green tea intake, MTHFR/TYMS genotype and breast cancer risk: the Singapore Chinese Health Study per Inoue, Maki, Robien, Kim, Wang, Renwei, Van Den Berg, David J., Koh, Woon-Puay, Yu, Mimi C.

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Data-adaptive multi-locus association testing in subjects with arbitrary genealogical relationships per Gong, Gail, Wang, Wei, Hsieh, Chih-Lin, Van Den Berg, David J., Haiman, Christopher, Oakley-Girvan, Ingrid, Whittemore, Alice S.

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Genetic association between the COMT genotype and urinary levels of tea polyphenols and their metabolites among daily green tea drinkers per Inoue-Choi, Maki, Yuan, Jian-Min, Yang, Chung S, Van Den Berg, David J, Lee, Mao-Jung, Gao, Yu-Tang, Yu, Mimi C

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No association between the SRD5A2 gene A49T missense variant and prostate cancer risk: lessons learned per Pearce, C. Leigh, Van Den Berg, David J., Makridakis, Nick, Reichardt, Juergen K.V., Ross, Ronald K., Pike, Malcolm C., Kolonel, Laurence N., Henderson, Brian E.

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Polymorphisms in hormone metabolism and growth factor genes and mammographic density in Norwegian postmenopausal hormone therapy users and non-users per Ellingjord-Dale, Merete, Lee, Eunjung, Couto, Elisabeth, Ozhand, Ali, Qureshi, Samera Azeem, Hofvind, Solveig, Van Den Berg, David J, Akslen, Lars A, Grotmol, Tom, Ursin, Giske

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Genetic variations on chromosomes 5p15 and 15q25 and bladder cancer risk: findings from the Los Angeles–Shanghai bladder case–control study per Gago-Dominguez, Manuela, Jiang, Xuejuan, Conti, David V., Castelao, Jose Esteban, Stern, Mariana C., Cortessis, Victoria K., Pike, Malcolm C., Xiang, Yong-Bing, Gao, Yu-Tang, Yuan, Jian-Min, Van Den Berg, David J.

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Interleukin-2, interleukin-12, and interferon-γ levels and risk of young adult Hodgkin lymphoma per Cozen, Wendy, Gill, Parkash S., Salam, Muhammad T., Nieters, Alexandra, Masood, Rizwan, Cockburn, Myles G., Gauderman, W. James, Martínez-Maza, Otoniel, Nathwani, Bharat N., Pike, Malcolm C., Van Den Berg, David J., Hamilton, Ann S., Deapen, Dennis M., Mack, Thomas M.

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A Genome Screen of Families with Multiple Cases of Prostate Cancer: Evidence of Genetic Heterogeneity per Hsieh, Chih-lin, Oakley-Girvan, Ingrid, Balise, Raymond R., Halpern, Jerry, Gallagher, Richard P., Wu, Anna H., Kolonel, Laurence N., O'Brien, Laura E., Lin, Iping G., Van Den Berg, David J., Teh, Chong-Ze, West, Dee W., Whittemore, Alice S.

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A genome-wide meta-analysis of nodular sclerosing Hodgkin lymphoma identifies risk loci at 6p21.32 per Cozen, Wendy, Li, Dalin, Best, Timothy, Van Den Berg, David J., Gourraud, Pierre-Antoine, Cortessis, Victoria K., Skol, Andrew D., Mack, Thomas M., Glaser, Sally L., Weiss, Lawrence M., Nathwani, Bharat N., Bhatia, Smita, Schumacher, Fredrick R., Edlund, Christopher K., Hwang, Amie E., Slager, Susan L., Fredericksen, Zachary S., Strong, Louise C., Habermann, Thomas M., Link, Brian K., Cerhan, James R., Robison, Leslie L., Conti, David V., Onel, Kenan

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A Genome-Wide Scan for Breast Cancer Risk Haplotypes among African American Women per Song, Chi, Chen, Gary K., Millikan, Robert C., Ambrosone, Christine B., John, Esther M., Bernstein, Leslie, Zheng, Wei, Hu, Jennifer J., Ziegler, Regina G., Nyante, Sarah, Bandera, Elisa V., Ingles, Sue A., Press, Michael F., Deming, Sandra L., Rodriguez-Gil, Jorge L., Chanock, Stephen J., Wan, Peggy, Sheng, Xin, Pooler, Loreall C., Van Den Berg, David J., Le Marchand, Loic, Kolonel, Laurence N., Henderson, Brian E., Haiman, Chris A., Stram, Daniel O.

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Variability in Cytogenetic Testing for Multiple Myeloma: A Comprehensive Analysis From Across the United States per Yu, Yang, Brown Wade, Niquelle, Hwang, Amie E., Nooka, Ajay K., Fiala, Mark A., Mohrbacher, Ann, Peters, Edward S., Pawlish, Karen, Bock, Cathryn, Van Den Berg, David J., Rand, Kristin A., Stram, Daniel, Conti, David V., Auclair, Daniel, Colditz, Graham A., Mehta, Jayesh, Haiman, Christopher A., Terebelo, Howard, Janakiraman, Nalini, Singhal, Seema, Chiu, Brian, Vij, Ravi, Bernal-Mizrachi, Leon, Zonder, Jeffrey A., Huff, Carol A., Lonial, Sagar, Orlowski, Robert Z., Cozen, Wendy, Ailawadhi, Sikander

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Epigenome-wide association study of mitochondrial genome copy number per Wang, Penglong, Castellani, Christina A, Yao, Jie, Huan, Tianxiao, Bielak, Lawrence F, Zhao, Wei, Haessler, Jeffrey, Joehanes, Roby, Sun, Xianbang, Guo, Xiuqing, Longchamps, Ryan J, Manson, JoAnn E, Grove, Megan L, Bressler, Jan, Taylor, Kent D, Lappalainen, Tuuli, Kasela, Silva, Van Den Berg, David J, Hou, Lifang, Reiner, Alexander, Liu, Yongmei, Boerwinkle, Eric, Smith, Jennifer A, Peyser, Patricia A, Fornage, Myriam, Rich, Stephen S, Rotter, Jerome I, Kooperberg, Charles, Arking, Dan E, Levy, Daniel, Liu, Chunyu

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Progesterone Receptor Gene Polymorphisms and Risk of Endometriosis: Results from an International Collaborative Effort per Near, Aimee M., Wu, Anna H., Templeman, Claire, Van Den Berg, David J., Doherty, Jennifer A., Rossing, Mary Anne, Goode, Ellen L., Cunningham, Julie M., Vierkant, Robert A., Fridley, Brooke L., Chenevix-Trench, Georgia, Webb, Penelope M., Kjær, Susanne Krüger, Hogdall, Estrid, Gayther, Simon A., Ramus, Susan J., Menon, Usha, Gentry-Maharaj, Aleksandra, Schildkraut, Joellen M., Moorman, Patricia G., Palmieri, Rachel T., Ness, Roberta B., Moysich, Kirsten, Cramer, Daniel W., Terry, Kathryn L., Vitonis, Allison F., Pike, Malcolm C., Berchuck, Andrew, Pearce, Celeste Leigh

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Genetic variation in insulin-like growth factor 2 may play a role in ovarian cancer risk per 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, Wu, Anna H.

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Testicular germ cell tumor susceptibility associated with the UCK2 locus on chromosome 1q23 per Schumacher, Fredrick R., Wang, Zhaoming, Skotheim, Rolf I., Koster, Roelof, Chung, Charles C., Hildebrandt, Michelle A. T., Kratz, Christian P., Bakken, Anne C., Timothy Bishop, D., Cook, Michael B., Erickson, R. Loren, Fosså, Sophie D., Greene, Mark H., Jacobs, Kevin B., Kanetsky, Peter A., Kolonel, Laurence N., Loud, Jennifer T., Korde, Larissa A., Le Marchand, Loic, Pablo Lewinger, Juan, Lothe, Ragnhild A., Pike, Malcolm C., Rahman, Nazneen, Rubertone, Mark V., Schwartz, Stephen M., Siegmund, Kimberly D., Skinner, Eila C., Turnbull, Clare, Van Den Berg, David J., Wu, Xifeng, Yeager, Meredith, Nathanson, Katherine L., Chanock, Stephen J., Cortessis, Victoria K., McGlynn, Katherine A.

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Genome-wide interaction studies reveal sex-specific asthma risk alleles per Myers, Rachel A., Scott, Nicole M., Gauderman, W. James, Qiu, Weiliang, Mathias, Rasika A., Romieu, Isabelle, Levin, Albert M., Pino-Yanes, Maria, Graves, Penelope E., Villarreal, Albino Barraza, Beaty, Terri H., Carey, Vincent J., Croteau-Chonka, Damien C., del Rio Navarro, Blanca, Edlund, Christopher, Hernandez-Cadena, Leticia, Navarro-Olivos, Efrain, Padhukasahasram, Badri, Salam, Muhammad T., Torgerson, Dara G., Van den Berg, David J., Vora, Hita, Bleecker, Eugene R., Meyers, Deborah A., Williams, L. Keoki, Martinez, Fernando D., Burchard, Esteban G., Barnes, Kathleen C., Gilliland, Frank D., Weiss, Scott T., London, Stephanie J., Raby, Benjamin A., Ober, Carole, Nicolae, Dan L.

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Consortium analysis of 7 candidate SNPs for ovarian cancer per Ramus, Susan J., Vierkant, Robert A., Johnatty, Sharon E., Pike, Malcolm C., Van Den Berg, David J., Wu, Anna H., Pearce, Celeste Leigh, Menon, Usha, Gentry-Maharaj, Aleksandra, Gayther, Simon A., DiCioccio, Richard A., McGuire, Valerie, Whittemore, Alice S., Song, Honglin, Easton, Douglas F., Pharoah, Paul D.P., Garcia-Closas, Montserrat, Chanock, Stephen, Lissowska, Jolanta, Brinton, Louise, Terry, Kathryn L., Cramer, Daniel W., Tworoger, Shelley S., Hankinson, Susan E., Berchuck, Andrew, Moorman, Patricia G., Schildkraut, Joellen M., Cunningham, Julie M., Liebow, Mark, Kjaer, Susanne Krüger, Hogdall, Estrid, Hogdall, Claus, Blaakaer, Jan, Ness, Roberta B., Moysich, Kirsten B., Edwards, Robert P., Carney, Michael E., Lurie, Galina, Goodman, Marc T., Wang-Gohrke, Shan, Kropp, Silke, Chang-Claude, Jenny, Webb, Penelope M., Chen, Xiaoqing, Beesley, Jonathan, Chenevix-Trench, Georgia, Goode, Ellen L.

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Association between invasive ovarian cancer susceptibility and 11 best candidate SNPs from breast cancer genome-wide association study per Song, Honglin, Ramus, Susan J., Kjaer, Susanne Krüger, DiCioccio, Richard A., Chenevix-Trench, Georgia, Pearce, Celeste Leigh, Hogdall, Estrid, Whittemore, Alice S., McGuire, Valerie, Hogdall, Claus, Blaakaer, Jan, Wu, Anna H., Van Den Berg, David J., Stram, Daniel O., Menon, Usha, Gentry-Maharaj, Aleksandra, Jacobs, Ian J., Webb, Penny M., Beesley, Jonathan, Chen, Xiaoqing, Rossing, Mary Anne, Doherty, Jennifer A., Chang-Claude, Jenny, Wang-Gohrke, Shan, Goodman, Marc T., Lurie, Galina, Thompson, Pamela J., Carney, Michael E., Ness, Roberta B., Moysich, Kirsten, Goode, Ellen L., Vierkant, Robert A., Cunningham, Julie M., Anderson, Stephanie, Schildkraut, Joellen M., Berchuck, Andrew, Iversen, Edwin S., Moorman, Patricia G., Garcia-Closas, Montserrat, Chanock, Stephen, Lissowska, Jolanta, Brinton, Louise, Anton-Culver, Hoda, Ziogas, Argyrios, Brewster, Wendy R., Ponder, Bruce A.J., Easton, Douglas F., Gayther, Simon A., Pharoah, Paul D.P.

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