A DNA methylation biomarker of alcohol consumption von Liu, C, Marioni, R E, Hedman, Å K, Pfeiffer, L, Tsai, P-C, Reynolds, L M, Just, A C, Duan, Q, Boer, C G, Tanaka, T, Elks, C E, Aslibekyan, S, Brody, J A, Kühnel, B, Herder, C, Almli, L M, Zhi, D, Wang, Y, Huan, T, Yao, C, Mendelson, M M, Joehanes, R, Liang, L, Love, S-A, Guan, W, Shah, S, McRae, A F, Kretschmer, A, Prokisch, H, Strauch, K, Peters, A, Visscher, P M, Wray, N R, Guo, X, Wiggins, K L, Smith, A K, Binder, E B, Ressler, K J, Irvin, M R, Absher, D M, Hernandez, D, Ferrucci, L, Bandinelli, S, Lohman, K, Ding, J, Trevisi, L, Gustafsson, S, Sandling, J H, Stolk, L, Uitterlinden, A G, Yet, I, Castillo-Fernandez, J E, Spector, T D, Schwartz, J D, Vokonas, P, Lind, L, Li, Y, Fornage, M, Arnett, D K, Wareham, N J, Sotoodehnia, N, Ong, K K, van Meurs, J B J, Conneely, K N, Baccarelli, A A, Deary, I J, Bell, J T, North, K E, Liu, Y, Waldenberger, M, London, S J, Ingelsson, E, Levy, D

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Genome-wide association studies suggest sex-specific loci associated with abdominal and visceral fat von Sung, Y J, Pérusse, L, Sarzynski, M A, Fornage, M, Sidney, S, Sternfeld, B, Rice, T, Terry, J G, Jacobs, D R, Katzmarzyk, P, Curran, J E, Jeffrey Carr, J, Blangero, J, Ghosh, S, Després, J-P, Rankinen, T, Rao, D C, Bouchard, C

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Genetic variants of the NOTCH3 gene in the elderly and magnetic resonance imaging correlates of age-related cerebral small vessel disease von Schmidt, Helena, Zeginigg, Marion, Wiltgen, Marco, Freudenberger, Paul, Petrovic, Katja, Cavalieri, Margherita, Gider, Pierre, Enzinger, Christian, Fornage, Myriam, Debette, Stephanie, Rotter, Jerome I., Ikram, Mohammad A., Launer, Lenore J., Schmidt, Reinhold

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A genotype risk score predicts type 2 diabetes from young adulthood: the CARDIA study von Vassy, J. L., Durant, N. H., Kabagambe, E. K., Carnethon, M. R., Rasmussen-Torvik, L. J., Fornage, M., Lewis, C. E., Siscovick, D. S., Meigs, J. B.

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The Alzheimer's Disease Sequencing Project: Study design and sample selection von Beecham, Gary W, Bis, J C, Martin, E R, Choi, S-H, DeStefano, A L, van Duijn, C M, Fornage, M, Gabriel, S B, Koboldt, D C, Larson, D E, Naj, A C, Psaty, B M, Salerno, W, Bush, W S, Foroud, T M, Wijsman, E, Farrer, L A, Goate, A, Haines, J L, Pericak-Vance, Margaret A, Boerwinkle, E, Mayeux, R, Seshadri, S, Schellenberg, G

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Replication of genetic loci for ages at menarche and menopause in the multi-ethnic Population Architecture using Genomics and Epidemiology (PAGE) study von Carty, C.L., Spencer, K.L., Setiawan, V.W., Fernandez-Rhodes, L., Malinowski, J., Buyske, S., Young, A., Jorgensen, N.W., Cheng, I., Carlson, C.S., Brown-Gentry, K., Goodloe, R., Park, A., Parikh, N.I., Henderson, B., Le Marchand, L., Wactawski-Wende, J., Fornage, M., Matise, T.C., Hindorff, L.A., Arnold, A.M., Haiman, C.A., Franceschini, N., Peters, U., Crawford, D.C.

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Common genetic variants may identify women with large uterine fibroids on ultrasound: the cardia women’s study (CWS) von Wellons, M, Edwards, T.L, Hartmann, K.E, Fornage, M, Velez Edwards, D.R

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Association of 25-Hydroxyvitamin D status and genetic variation in the vitamin D metabolic pathway with FEV1 in the Framingham Heart Study von Hansen, J G, Gao, W, Dupuis, J, O'Connor, G T, Tang, W, Kowgier, M, Sood, A, Gharib, S A, Palmer, L J, Fornage, M, Heckbert, S R, Psaty, B M, Booth, S L, Cassano, Patricia A

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Association of coagulation‐related and inflammation‐related genes and factor VIIc levels with stroke: the Cardiovascular Health Study von ZAKAI, N. A., LANGE, L., LONGSTRETH, W. T., O’MEARA, E. S., KELLEY, J. L., FORNAGE, M., NIKERSON, D., CUSHMAN, M., REINER, A. P.

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Proceedings of the 21st International Stroke Genetics Consortium Workshop von Fornage, M.

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SNP-by-fitness and SNP-by-BMI interactions from seven candidate genes and incident hypertension after 20 years of follow-up: the CARDIA Fitness Study von Sarzynski, M A, Rankinen, T, Sternfeld, B, Fornage, M, Sidney, S, Bouchard, C

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Circulating Metabolome and White Matter Hyperintensities in Women and Men von Sliz, Eeva, Shin, Jean, Ahmad, Shahzad, Williams, Dylan M., Frenzel, Stefan, Gauß, Friederike, Harris, Sarah E., Henning, Ann-Kristin, Hernandez, Maria Valdes, Hu, Yi-Han, Jiménez, Beatriz, Sargurupremraj, Muralidharan, Sudre, Carole, Wang, Ruiqi, Wittfeld, Katharina, Yang, Qiong, Wardlaw, Joanna M., Völzke, Henry, Vernooij, Meike W., Schott, Jonathan M., Richards, Marcus, Proitsi, Petroula, Nauck, Matthias, Lewis, Matthew R., Launer, Lenore, Hosten, Norbert, Grabe, Hans J., Ghanbari, Mohsen, Deary, Ian J., Cox, Simon R., Chaturvedi, Nishi, Barnes, Josephine, Rotter, Jerome I., Debette, Stephanie, Ikram, M. Arfan, Fornage, Myriam, Paus, Tomas, Seshadri, Sudha, Pausova, Zdenka

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Association between patterns of nucleotide variation across the three fibrinogen genes and plasma fibrinogen levels: the Coronary Artery Risk Development in Young Adults (CARDIA) s... von REINER, A. P., CARTY, C. L., CARLSON, C. S., WAN, J. Y., RIEDER, M. J., SMITH, J. D., RICE, K., FORNAGE, M., JAQUISH, C. E., WILLIAMS, O. D., TRACY, R. P., LEWIS, C. E., SISCOVICK, D. S., BOERWINKLE, E., NICKERSON, D. A.

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A genome-wide association study identifies new loci for factor VII and implicates factor VII in ischemic stroke etiology von de Vries, Paul S., Sabater-Lleal, Maria, Huffman, Jennifer E., Marten, Jonathan, Song, Ci, Pankratz, Nathan, Bartz, Traci M., de Haan, Hugoline G., Delgado, Graciela E., Eicher, John D., Martinez-Perez, Angel, Ward-Caviness, Cavin K., Brody, Jennifer A., Chen, Ming-Huei, de Maat, Moniek P.M., Frånberg, Mattias, Gill, Dipender, Kleber, Marcus E., Rivadeneira, Fernando, Soria, José Manuel, Tang, Weihong, Tofler, Geoffrey H., Uitterlinden, André G., van Hylckama Vlieg, Astrid, Seshadri, Sudha, Boerwinkle, Eric, Davies, Neil M., Giese, Anne-Katrin, Ikram, M. Kamran, Kittner, Steven J., McKnight, Barbara, Psaty, Bruce M., Reiner, Alex P., Sargurupremraj, Muralidharan, Taylor, Kent D., Fornage, Myriam, Hamsten, Anders, März, Winfried, Rosendaal, Frits R., Souto, Juan Carlos, Dehghan, Abbas, Johnson, Andrew D., Morrison, Alanna C., O’Donnell, Christopher J., Smith, Nicholas L.

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Genome-wide analysis of mitochondrial DNA copy number reveals loci implicated in nucleotide metabolism, platelet activation, and megakaryocyte proliferation von Longchamps, R. J., Yang, S. Y., Castellani, C. A., Shi, W., Lane, J., Grove, M. L., Bartz, T. M., Sarnowski, C., Liu, C., Burrows, K., Guyatt, A. L., Gaunt, T. R., Kacprowski, T., Yang, J., De Jager, P. L., Yu, L., Bergman, A., Xia, R., Fornage, M., Feitosa, M. F., Wojczynski, M. K., Kraja, A. T., Province, M. A., Amin, N., Rivadeneira, F., Tiemeier, H., Uitterlinden, A. G., Broer, L., Van Meurs, J. B. J., Van Duijn, C. M., Raffield, L. M., Lange, L., Rich, S. S., Lemaitre, R. N., Goodarzi, M. O., Sitlani, C. M., Mak, A. C. Y., Bennett, D. A., Rodriguez, S., Murabito, J. M., Lunetta, K. L., Sotoodehnia, N., Atzmon, G., Ye, K., Barzilai, N., Brody, J. A., Psaty, B. M., Taylor, K. D., Rotter, J. I., Boerwinkle, E., Pankratz, N., Arking, D. E.

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DNA methylation analysis is used to identify novel genetic loci associated with circulating fibrinogen levels in blood von Hahn, Julie, Bressler, Jan, Domingo-Relloso, Arce, Chen, Ming-Huei, McCartney, Daniel L., Teumer, Alexander, van Dongen, Jenny, Kleber, Marcus E., Aïssi, Dylan, Swenson, Brenton R., Yao, Jie, Zhao, Wei, Huang, Jian, Xia, Yujing, Brown, Michael R., Costeira, Ricardo, de Geus, Eco J.C., Delgado, Graciela E., Dobson, Dre'Von A., Elliott, Paul, Grabe, Hans J., Guo, Xiuqing, Harris, Sarah E., Huffman, Jennifer E., Kardia, Sharon L.R., Liu, Yongmei, Lorkowski, Stefan, Marioni, Riccardo E., Nauck, Matthias, Ratliff, Scott M., Sabater-Lleal, Maria, Spector, Tim D., Suchon, Pierre, Taylor, Kent D., Thibord, Florian, Trégouët, David-Alexandre, Wiggins, Kerri L., Willemsen, Gonneke, Bell, Jordana T., Boomsma, Dorret I., Cole, Shelley A., Cox, Simon R., Dehghan, Abbas, Greinacher, Andreas, Haack, Karin, März, Winfried, Morange, Pierre-Emmanuel, Rotter, Jerome I., Sotoodehnia, Nona, Tellez-Plaza, Maria, Navas-Acien, Ana, Smith, Jennifer A., Johnson, Andrew D., Fornage, Myriam, Smith, Nicholas L., Wolberg, Alisa S., Morrison, Alanna C., de Vries, Paul S.

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Comparison of smoking-related DNA methylation between newborns from prenatal exposure and adults from personal smoking von Sikdar, Sinjini, Joehanes, Roby, Joubert, Bonnie R, Xu, Cheng-Jian, Vives-Usano, Marta, Rezwan, Faisal I, Felix, Janine F, Ward, James M, Guan, Weihua, Richmond, Rebecca C, Brody, Jennifer A, Küpers, Leanne K, Baïz, Nour, Håberg, Siri E, Smith, Jennifer A, Reese, Sarah E, Aslibekyan, Stella, Hoyo, Cathrine, Dhingra, Radhika, Markunas, Christina A, Xu, Tao, Reynolds, Lindsay M, Just, Allan C, Mandaviya, Pooja R, Ghantous, Akram, Bennett, Brian D, Wang, Tianyuan, Consortium, The Bios, Bakulski, Kelly M, Melen, Erik, Zhao, Shanshan, Jin, Jianping, Herceg, Zdenko, Meurs, Joyce van, Taylor, Jack A, Baccarelli, Andrea A, Murphy, Susan K, Liu, Yongmei, Munthe-Kaas, Monica Cheng, Deary, Ian J, Nystad, Wenche, Waldenberger, Melanie, Annesi-Maesano, Isabella, Conneely, Karen, Jaddoe, Vincent Wv, Arnett, Donna, Snieder, Harold, Kardia, Sharon Lr, Relton, Caroline L, Ong, Ken K, Ewart, Susan, Moreno-Macias, Hortensia, Romieu, Isabelle, Sotoodehnia, Nona, Fornage, Myriam, Motsinger-Reif, Alison, Koppelman, Gerard H, Bustamante, Mariona, Levy, Daniel, London, Stephanie J

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Genome-Wide Association Studies of Cerebral White Matter Lesion Burden: The CHARGE Consortium von FORNAGE, Myriam, DEBETTE, Stephanie, VROOMAN, Henri A, SHIBATA, Dean K, MAILLARD, Pauline, ZIJDENBOS, Alex, SMITH, Albert V, GUDNASON, Haukur, DE BOER, Renske, CUSHMAN, Mary, MAZOYER, Bernard, HEISS, Gerardo, BIS, Joshua C, VERNOOIJ, Meike W, ENZINGER, Christian, GLAZER, Nicole L, BEISER, Alexa, KNOPMAN, David S, CAVALIERI, Margherita, NIESSEN, WiroJ, HARRIS, TamaraB, PETROVIC, Katja, LOPEZ, Oscar L, SCHMIDT, Helena, AU, Rhoda, LAMBERT, Jean-Charles, HOFMAN, Albert, GOTTESMAN, Rebecca F, GARCIA, Melissa, HECKBERT, SusanR, ATWOOD, LarryD, CATELLIER, DianeJ, UITTERLINDEN, Andre G, QIONG YANG, ARFAN IKRAM, M, SMITH, Nicholas L, ASPELUND, Thor, ROMERO, Jose R, RICE, Kenneth, TAYLOR, Kent D, NALLS, Michael A, ROTTER, Jerome I, SHARRETT, Richey, VAN DUIJN, Cornelia M, AMOUYEL, Philippe, DUFOUIL, Carole, WOLF, Philip A, GUDNASON, Vilmundur, VAN DER LUGT, Aad, BOERWINKLE, Eric, PSATY, Bruce M, SESHADRI, Sudha, TZOURIO, Christophe, BRETELER, Monique M. B, MOSLEY, Thomas H, SCHMIDT, Reinhold, SIGURDSSON, Sigurdur, LUMLEY, Thomas, DESTEFANO, Anita L, FAZEKAS, Franz

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Rare and low-frequency variants and their association with plasma levels of fibrinogen, FVII, FVIII, and vWF von Huffman, Jennifer E., de Vries, Paul S., Morrison, Alanna C., Sabater-Lleal, Maria, Kacprowski, Tim, Auer, Paul L., Brody, Jennifer A., Chasman, Daniel I., Chen, Ming-Huei, Guo, Xiuqing, Lin, Li-An, Marioni, Riccardo E., Müller-Nurasyid, Martina, Yanek, Lisa R., Pankratz, Nathan, Grove, Megan L., de Maat, Moniek P.M., Cushman, Mary, Wiggins, Kerri L., Qi, Lihong, Sennblad, Bengt, Harris, Sarah E., Polasek, Ozren, Riess, Helene, Rivadeneira, Fernando, Rose, Lynda M., Goel, Anuj, Taylor, Kent D., Teumer, Alexander, Uitterlinden, André G., Vaidya, Dhananjay, Yao, Jie, Tang, Weihong, Levy, Daniel, Waldenberger, Melanie, Becker, Diane M., Folsom, Aaron R., Giulianini, Franco, Greinacher, Andreas, Hofman, Albert, Huang, Chiang-Ching, Kooperberg, Charles, Silveira, Angela, Starr, John M., Strauch, Konstantin, Strawbridge, Rona J., Wright, Alan F., McKnight, Barbara, Franco, Oscar H., Zakai, Neil, Mathias, Rasika A., Psaty, Bruce M., Ridker, Paul M., Tofler, Geoffrey H., Völker, Uwe, Watkins, Hugh, Fornage, Myriam, Hamsten, Anders, Deary, Ian J., Boerwinkle, Eric, Koenig, Wolfgang, Rotter, Jerome I., Hayward, Caroline, Dehghan, Abbas, Reiner, Alex P., O'Donnell, Christopher J., Smith, Nicholas L.

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Multilocus Genetic Risk Score Associates With Ischemic Stroke in Case-Control and Prospective Cohort Studies von MALIK, Rainer, BEVAN, Steve, DE STEFANO, Anita L, FORNAGE, Myriam, PSATY, Bruce M, IKRAM, M. Arfan, LAUNER, Lenore J, VAN DUIJN, Cornelia M, SHARMA, Pankaj, MITCHELL, Braxton D, ROSAND, Jonathan, MESCHIA, James F, NALLS, Michael A, LEVI, Christopher, ROTHWELL, Peter M, SUDLOW, Cathie, MARKUS, Hugh S, SESHADRI, Sudha, DICHGANS, Martin, HOLLIDAY, Elizabeth G, DEVAN, William J, CHENG, Yu-Ching, IBRAHIM-VERBAAS, Carla A, VERHAAREN, Benjamin F. J, BIS, Joshua C, JOON, Aron Y

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