Prospective evaluation of a breast-cancer risk model integrating classical risk factors and polygenic risk in 15 cohorts from six countries by Hurson, Amber N, Pal Choudhury, Parichoy, Gao, Chi, Hüsing, Anika, Eriksson, Mikael, Shi, Min, Jones, Michael E, Evans, D Gareth R, Milne, Roger L, Gaudet, Mia M, Vachon, Celine M, Chasman, Daniel I, Easton, Douglas F, Schmidt, Marjanka K, Kraft, Peter, Garcia-Closas, Montserrat, Chatterjee, Nilanjan

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Genome-wide analysis of dental caries and periodontitis combining clinical and self-reported data by Shungin, Dmitry, Haworth, Simon, Divaris, Kimon, Agler, Cary S., Kamatani, Yoichiro, Keun Lee, Myoung, Grinde, Kelsey, Hindy, George, Alaraudanjoki, Viivi, Pesonen, Paula, Teumer, Alexander, Holtfreter, Birte, Sakaue, Saori, Hirata, Jun, Yu, Yau-Hua, Ridker, Paul M., Giulianini, Franco, Chasman, Daniel I., Magnusson, Patrik K. E., Sudo, Takeaki, Okada, Yukinori, Völker, Uwe, Kocher, Thomas, Anttonen, Vuokko, Laitala, Marja-Liisa, Orho-Melander, Marju, Sofer, Tamar, Shaffer, John R., Vieira, Alexandre, Marazita, Mary L., Kubo, Michiaki, Furuichi, Yasushi, North, Kari E., Offenbacher, Steve, Ingelsson, Erik, Franks, Paul W., Timpson, Nicholas J., Johansson, Ingegerd

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Meta-analysis of 65,734 Individuals Identifies TSPAN15 and SLC44A2 as Two Susceptibility Loci for Venous Thromboembolism by Germain, Marine, Chasman, Daniel I., de Haan, Hugoline, Tang, Weihong, Lindström, Sara, Weng, Lu-Chen, de Andrade, Mariza, de Visser, Marieke C.H., Wiggins, Kerri L., Suchon, Pierre, Saut, Noémie, Smadja, David M., Le Gal, Grégoire, van Hylckama Vlieg, Astrid, Di Narzo, Antonio, Hao, Ke, Nelson, Christopher P., Rocanin-Arjo, Ares, Folkersen, Lasse, Monajemi, Ramin, Rose, Lynda M., Brody, Jennifer A., Slagboom, Eline, Aïssi, Dylan, Gagnon, France, Deleuze, Jean-Francois, Deloukas, Panos, Tzourio, Christophe, Dartigues, Jean-Francois, Berr, Claudine, Taylor, Kent D., Civelek, Mete, Eriksson, Per, Psaty, Bruce M., Houwing-Duitermaat, Jeanine, Goodall, Alison H., Cambien, François, Kraft, Peter, Amouyel, Philippe, Samani, Nilesh J., Basu, Saonli, Ridker, Paul M., Rosendaal, Frits R., Kabrhel, Christopher, Folsom, Aaron R., Heit, John, Reitsma, Pieter H., Trégouët, David-Alexandre, Smith, Nicholas L., Morange, Pierre-Emmanuel

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Forty-three loci associated with plasma lipoprotein size, concentration, and cholesterol content in genome-wide analysis by Chasman, Daniel I, Paré, Guillaume, Mora, Samia, Hopewell, Jemma C, Peloso, Gina, Clarke, Robert, Cupples, L Adrienne, Hamsten, Anders, Kathiresan, Sekar, Mälarstig, Anders, Ordovas, José M, Ripatti, Samuli, Parker, Alex N, Miletich, Joseph P, Ridker, Paul M

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Pharmacogenetic Study of Statin Therapy and Cholesterol Reduction by Chasman, Daniel I, Posada, David, Subrahmanyan, Lakshman, Cook, Nancy R, Stanton, Jr, Vincent P, Ridker, Paul M

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Meta-analysis identifies five novel loci associated with endometriosis highlighting key genes involved in hormone metabolism by Sapkota, Yadav, Steinthorsdottir, Valgerdur, Morris, Andrew P., Fassbender, Amelie, Rahmioglu, Nilufer, De Vivo, Immaculata, Buring, Julie E., Zhang, Futao, Edwards, Todd L., Jones, Sarah, O, Dorien, Peterse, Daniëlle, Rexrode, Kathryn M., Ridker, Paul M., Schork, Andrew J., MacGregor, Stuart, Martin, Nicholas G., Becker, Christian M., Adachi, Sosuke, Yoshihara, Kosuke, Enomoto, Takayuki, Takahashi, Atsushi, Kamatani, Yoichiro, Matsuda, Koichi, Kubo, Michiaki, Thorleifsson, Gudmar, Geirsson, Reynir T., Thorsteinsdottir, Unnur, Wallace, Leanne M., Yang, Jian, Velez Edwards, Digna R., Nyegaard, Mette, Low, Siew-Kee, Zondervan, Krina T., Missmer, Stacey A., D'Hooghe, Thomas, Montgomery, Grant W., Chasman, Daniel I., Stefansson, Kari, Tung, Joyce Y., Nyholt, Dale R.

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Loci Related to Metabolic-Syndrome Pathways Including LEPR,HNF1A, IL6R, and GCKR Associate with Plasma C-Reactive Protein: The Women's Genome Health Study by Ridker, Paul M., Pare, Guillaume, Parker, Alex, Zee, Robert Y.L., Danik, Jacqueline S., Buring, Julie E., Kwiatkowski, David, Cook, Nancy R., Miletich, Joseph P., Chasman, Daniel I.

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Association between ABO haplotypes and the risk of venous thrombosis: impact on disease risk estimation by Goumidi, Louisa, Thibord, Florian, Wiggins, Kerri L., Li-Gao, Ruifang, Brown, Mickael R., van Hylckama Vlieg, Astrid, Souto, Joan-Carles, Soria, José-Manuel, Ibrahim-Kosta, Manal, Saut, Noémie, Daian, Delphine, Olaso, Robert, Amouyel, Philippe, Debette, Stéphanie, Boland, Anne, Bailly, Pascal, Morrison, Alanna C., Mook-Kanamori, Denis O., Deleuze, Jean-François, Johnson, Andrew, de Vries, Paul S., Sabater-Lleal, Maria, Chiaroni, Jacques, Smith, Nicholas L., Rosendaal, Frits R., Chasman, Daniel I., Trégouët, David-Alexandre, Morange, Pierre-Emmanuel

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Family History of MI, Smoking, and Risk of Periodontal Disease by Yu, Y.H., Doucette-Stamm, L., Rogus, J., Moss, K., Zee, R.Y.L., Steffensen, B., Ridker, P.M., Buring, J.E., Offenbacher, S., Kornman, K., Chasman, D.I.

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Common genetic loci influencing plasma homocysteine concentrations and their effect on risk of coronary artery disease by van Meurs, Joyce BJ, Pare, Guillaume, Schwartz, Stephen M, Hazra, Aditi, Tanaka, Toshiko, Vermeulen, Sita H, Cotlarciuc, Ioana, Yuan, Xin, Mälarstig, Anders, Bandinelli, Stefania, Bis, Joshua C, Blom, Henk, Brown, Morris J, Chen, Constance, Chen, Yii-Der, Clarke, Robert J, Dehghan, Abbas, Erdmann, Jeanette, Ferrucci, Luigi, Hamsten, Anders, Hofman, Albert, Hunter, David J, Goel, Anuj, Johnson, Andrew D, Kathiresan, Sekar, Kampman, Ellen, Kiel, Douglas P, Kiemeney, Lambertus ALM, Chambers, John C, Kraft, Peter, Lindemans, Jan, McKnight, Barbara, Nelson, Christopher P, O'Donnell, Christopher J, Psaty, Bruce M, Ridker, Paul M, Rivadeneira, Fernando, Rose, Lynda M, Seedorf, Udo, Siscovick, David S, Schunkert, Heribert, Selhub, Jacob, Ueland, Per M, Vollenweider, Peter, Waeber, Gérard, Waterworth, Dawn M, Watkins, Hugh, Witteman, Jacqueline CM, den Heijer, Martin, Jacques, Paul, Uitterlinden, Andre G, Kooner, Jaspal S, Rader, Dan J, Reilly, Muredach P, Mooser, Vincent, Chasman, Daniel I, Samani, Nilesh J, Ahmadi, Kourosh R

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Polymorphisms of the HNF1A Gene Encoding Hepatocyte Nuclear Factor-1α are Associated with C-Reactive Protein by Reiner, Alexander P., Barber, Mathew J., Guan, Yongtao, Ridker, Paul M., Lange, Leslie A., Chasman, Daniel I., Walston, Jeremy D., Cooper, Gregory M., Jenny, Nancy S., Rieder, Mark J., Durda, J. Peter, Smith, Joshua D., Novembre, John, Tracy, Russell P., Rotter, Jerome I., Stephens, Matthew, Nickerson, Deborah A., Krauss, Ronald M.

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Cross-Ancestry Investigation of Venous Thromboembolism Genomic Predictors by Thibord, Florian, Klarin, Derek, Brody, Jennifer A., Chen, Ming-Huei, Levin, Michael G., Chasman, Daniel I., Goode, Ellen L., Hveem, Kristian, Teder-Laving, Maris, Martinez-Perez, Angel, Aïssi, Dylan, Daian-Bacq, Delphine, Ito, Kaoru, Natarajan, Pradeep, Lutsey, Pamela L., Nadkarni, Girish N., de Vries, Paul S., Cuellar-Partida, Gabriel, Wolford, Brooke N., Pattee, Jack W., Kooperberg, Charles, Braekkan, Sigrid K., Li-Gao, Ruifang, Saut, Noemie, Sept, Corriene, Germain, Marine, Judy, Renae L., Wiggins, Kerri L., Ko, Darae, O’Donnell, Christopher J., Taylor, Kent D., Giulianini, Franco, De Andrade, Mariza, Nøst, Therese H., Boland, Anne, Empana, Jean-Philippe, Koyama, Satoshi, Gilliland, Thomas, Do, Ron, Huffman, Jennifer E., Wang, Xin, Zhou, Wei, Manuel Soria, Jose, Carlos Souto, Juan, Pankratz, Nathan, Haessler, Jeffery, Hindberg, Kristian, Rosendaal, Frits R., Turman, Constance, Olaso, Robert, Kember, Rachel L., Bartz, Traci M., Lynch, Julie A., Heckbert, Susan R., Armasu, Sebastian M., Brumpton, Ben, Smadja, David M., Jouven, Xavier, Komuro, Issei, Clapham, Katharine R., Loos, Ruth J.F., Willer, Cristen J., Sabater-Lleal, Maria, Pankow, James S., Reiner, Alexander P., Morelli, Vania M., Ridker, Paul M, Vlieg, Astrid van Hylckama, Deleuze, Jean-François, Kraft, Peter, Rader, Daniel J., Min Lee, Kyung, Psaty, Bruce M., Heidi Skogholt, Anne, Emmerich, Joseph, Suchon, Pierre, Rich, Stephen S., Vy, Ha My T., Tang, Weihong, Jackson, Rebecca D., Hansen, John-Bjarne, Morange, Pierre-Emmanuel, Kabrhel, Christopher, Trégouët, David-Alexandre, Damrauer, Scott M., Johnson, Andrew D., Smith, Nicholas L.

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Polymorphism in the apolipoprotein(a) gene, plasma lipoprotein(a), cardiovascular disease, and low-dose aspirin therapy by Chasman, Daniel I, Shiffman, Dov, Zee, Robert Y.L, Louie, Judy Z, Luke, May M, Rowland, Charles M, Catanese, Joseph J, Buring, Julie E, Devlin, James J, Ridker, Paul M

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Gene × physical activity interactions in obesity: combined analysis of 111,421 individuals of European ancestry by Ahmad, Shafqat, Rukh, Gull, Varga, Tibor V, Ali, Ashfaq, Kurbasic, Azra, Shungin, Dmitry, Ericson, Ulrika, Koivula, Robert W, Chu, Audrey Y, Rose, Lynda M, Ganna, Andrea, Qi, Qibin, Stančáková, Alena, Sandholt, Camilla H, Elks, Cathy E, Curhan, Gary, Jensen, Majken K, Tamimi, Rulla M, Allin, Kristine H, Jørgensen, Torben, Brage, Soren, Langenberg, Claudia, Aadahl, Mette, Grarup, Niels, Linneberg, Allan, Paré, Guillaume, Magnusson, Patrik K E, Pedersen, Nancy L, Boehnke, Michael, Hamsten, Anders, Mohlke, Karen L, Pasquale, Louis T, Pedersen, Oluf, Scott, Robert A, Ridker, Paul M, Ingelsson, Erik, Laakso, Markku, Hansen, Torben, Qi, Lu, Wareham, Nicholas J, Chasman, Daniel I, Hallmans, Göran, Hu, Frank B, Renström, Frida, Orho-Melander, Marju, Franks, Paul W

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Novel Associations of CPS1, MUT, NOX4, and DPEP1 With Plasma Homocysteine in a Healthy Population: A Genome-Wide Evaluation of 13 974 Participants in the Women's Genome Health Stud... by Pare, Guillaume, Chasman, Daniel I, Parker, Alexander N, Zee, Robert R.Y, Malarstig, Anders, Seedorf, Udo, Collins, Rory, Watkins, Hugh, Hamsten, Anders, Miletich, Joseph P, Ridker, Paul M

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Association of Common CRP Gene Variants with CRP Levels and Cardiovascular Events by Miller, D. T., Zee, R. Y. L., Suk Danik, J., Kozlowski, P., Chasman, D. I., Lazarus, R., Cook, N. R., Ridker, P. M., Kwiatkowski, D. J.

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DNA mismatch repair gene MSH6 implicated in determining age at natural menopause by Perry, John R B, Hsu, Yi-Hsiang, Chasman, Daniel I, Johnson, Andrew D, Elks, Cathy, Albrecht, Eva, Andrulis, Irene L, Beesley, Jonathan, Berenson, Gerald S, Bergmann, Sven, Bojesen, Stig E, Bolla, Manjeet K, Brown, Judith, Buring, Julie E, Campbell, Harry, Chang-Claude, Jenny, Chenevix-Trench, Georgia, Corre, Tanguy, Couch, Fergus J, Cox, Angela, Czene, Kamila, D'adamo, Adamo Pio, Davies, Gail, Deary, Ian J, Dennis, Joe, Easton, Douglas F, Engelhardt, Ellen G, Eriksson, Johan G, Esko, Tõnu, Fasching, Peter A, Figueroa, Jonine D, Flyger, Henrik, Fraser, Abigail, Garcia-Closas, Montse, Gasparini, Paolo, Gieger, Christian, Giles, Graham, Guenel, Pascal, Hägg, Sara, Hall, Per, Hayward, Caroline, Hopper, John, Ingelsson, Erik, Kardia, Sharon L R, Kasiman, Katherine, Knight, Julia A, Lahti, Jari, Lawlor, Debbie A, Magnusson, Patrik K E, Margolin, Sara, Marsh, Julie A, Metspalu, Andres, Olson, Janet E, Pennell, Craig E, Polasek, Ozren, Rahman, Iffat, Ridker, Paul M, Robino, Antonietta, Rudan, Igor, Rudolph, Anja, Salumets, Andres, Schmidt, Marjanka K, Schoemaker, Minouk J, Smith, Erin N, Smith, Jennifer A, Southey, Melissa, Stöckl, Doris, Swerdlow, Anthony J, Thompson, Deborah J, Truong, Therese, Ulivi, Sheila, Waldenberger, Melanie, Wang, Qin, Wild, Sarah, Wilson, James F, Wright, Alan F, Zgaga, Lina, Ong, Ken K, Murabito, Joanne M, Karasik, David, Murray, Anna

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Vitamin D-associated genetic variation and risk of breast cancer in the breast and prostate cancer cohort consortium (BPC3) by Mondul, Alison M, Shui, Irene M, Yu, Kai, Weinstein, Stephanie J, Tsilidis, Konstantinos K, Joshi, Amit D, Agudo, Antonio, Berg, Christine D, Black, Amanda, Buring, Julie E, Chasman, Daniel I, Gaudet, Mia M, Haiman, Christopher, Hankinson, Susan E, Henderson, Brian E, Hoover, Robert N, Hunter, David J, Khaw, Kay-Tee, Kühn, Tilman, Kvaskoff, Marina, Le Marchand, Loic, Lindström, Sara, McCullough, Marjorie L, Overvad, Kim, Peeters, Petra H, Riboli, Elio, Ridker, Paul M, Stram, Daniel O, Sund, Malin, Trichopoulos, Dimitrios, Tumino, Rosario, Weiderpass, Elisabete, Willett, Walter, Kraft, Peter, Ziegler, Regina G, Albanes, Demetrius

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Detection of Protein Folding Defects Caused by BRCA1-BRCT Truncation and Missense Mutations by Williams, R. Scott, Chasman, Daniel I., Hau, D. Duong, Hui, Benjamin, Lau, Albert Y., Glover, J. N. Mark

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Influence of Genetic Variation in the C‐Reactive Protein Gene on the Inflammatory Response During and After Acute Coronary Ischemia by Suk Danik, J., Chasman, D. I., Cannon, C. P., Miller, D. T., Zee, R. Y. L., Kozlowski, P., Kwiatkowski, D. J., Ridker, P. M.

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