Sugar-Sweetened Beverage Consumption May Modify Associations Between Genetic Variants in the CHREBP (Carbohydrate Responsive Element Binding Protein) Locus and HDL-C (High-Density Lipoprotein Cholesterol) and Triglyceride Concentrations

- Haslam, Danielle E., Peloso, Gina M., Guirette, Melanie, Imamura, Fumiaki, Bartz, Traci M., Pitsillides, Achilleas N., Wang, Carol A., Li-Gao, Ruifang, Westra, Jason M., Pitkanen, Niina, Young, Kristin L., Graff, Mariaelisa, Wood, Alexis C., Braun, Kim V. E., Luan, Jian'an, Kahonen, Mika, Kiefte-de Jong, Jessica C., Ghanbari, Mohsen, Tintle, Nathan, Lemaitre, Rozenn N., Mook-Kanamori, Dennis O., North, Kari, Helminen, Mika, Mossavar-Rahmani, Yasmin, Snetselaar, Linda, Martin, Lisa W., Viikari, Jorma S., Oddy, Wendy H., Pennell, Craig E., Rosendall, Frits R., Ikram, M. Arfan, Uitterlinden, Andre G., Psaty, Bruce M., Mozaffarian, Dariush, Rotter, Jerome, Taylor, Kent D., Lehtimaki, Terho, Raitakari, Olli T., Livingston, Kara A., Voortman, Trudy, Forouhi, Nita G., Wareham, Nick J., de Mutsert, Renee, Rich, Steven S., Manson, JoAnn E., Mora, Samia, Ridker, Paul M., Merino, Jordi, Meigs, James B., Dashti, Hassan S., Chasman, Daniel, Lichtenstein, Alice H., Smith, Caren E., Dupuis, Josee, Herman, Mark A., McKeown, Nicola M.

Genome-wide association study identifies nine novel loci for 2D:4D finger ratio, a putative retrospective biomarker of testosterone exposure in utero

- Warrington, Nicole M., Shevroja, Enisa, Hemani, Gibran, Hysi, Pirro G., Jiang, Yunxuan, Auton, Adam, Boer, Cindy G., Mangino, Massimo, Wang, Carol A., Kemp, John P., McMahon, George, Medina-Gomez, Carolina, Hickey, Martha, Trajanoska, Katerina, Wolke, Dieter, Ikram, M. Arfan, The 23and Me Research Team, Montgomery, Grant W., Felix, Janine F., Wright, Margaret J., Pennell, Craig E.

Genetic variation at 16q24.2 is associated with small vessel stroke

- Traylor, Matthew, Malik, Rainer, Yet, Idil, Spector, Tim D., Bell, Jordana T., Hannon, Ellis, Mill, Jonathan, Chauhan, Ganesh, Debette, Stephanie, Bis, Joshua C., Longstreth, W. T., Ikram, M. Arfan, Nalls, Mike A., Levi, Chris, Cotlarciuc, Iona, Radmanesh, Farid, Thorleifsson, Gudmar, Hanscombe, Ken B., Langefeld, Carl, Saleheen, Danish, Rost, Natalia S.

Genetic overlap between diagnostic subtypes of ischemic stroke

- Holliday, Elizabeth G., Traylor, Matthew, Boncoraglio, Giorgio B., Clarke, Robert, Cole, John W., Fornage, Myriam, Furie, Karen L., Ikram, M. Arfan, Jannes, Jim, Kittner, Steven J., Lincz, Lisa F., Maguire, Jane M., Malik, Rainer, Oldmeadow, Christopher, Scott, Rodney J., Levi, Christopher, Attia, John, Bevan, Steve, Falcone, Guido, Hopewell, Jemma C., Cheng, Yu-Ching, Cotlarciuc, Ioana, Bis, Joshua C., Boerwinkle, Eric

No additional prognostic value of genetic information in the prediction of vascular events after cerebral ischemia of arterial origin: The PROMISe study

- Achterberg, Sefanja, Kappelle, L. Jaap, Mali, W.P.T.M., Doevendans, P.A., Farrall, Martin, Holliday, Elizabeth G., Sudlow, Cathie, Hopewell, Jemma C., Cheng, Yu-Ching, Fornage, Myriam, Ikram, M. Arfan, Malik, Rainer, De Bakker, Paul I. W., Bevan, Steve, Thorsteinsdottir, Unnur, DeStefano, Anita L., Worrall, Bradford B., Reiner, Alex P., Mitchell, Braxtin D., Clarke, Robert, Levi, Christopher, Seshadri, Sudha, Boncoraglio, Giorgio B., Traylor, Matthew, Sharma, Pankaj, Bis, Joshua C., Gretarsdottir, Solveig, Psaty, Bruce M., Rothwell, Peter M., Rosand, Jonathan, Meschia, James F., Stefansson, Kari, Dichgans, Martin, Markus, Hugh S., Algra, Ale, Van Der Graaf, Y., Grobbee, D.E., Rutten, G.E.H.M., Visseren, F.L.J., Moll, F.L.

Shared genetic basis for migraine and ischemic stroke: a genome-wide analysis of common variants

- Malik, Rainer, Freilinger, Tobias, Bis, Joshua C., Hopewell, Jemma C., Ferrari, Michel D., Rannikmae, Kristiina, Wessman, Maija, Kallela, Mikko, Kubisch, Christian, Fornage, Myriam, Meschia, James F., Lehtimäki, Terho, Winsvold, Bendik S., Sudlow, Cathie, Clarke, Robert, Chasman, Daniel I., Mitchell, Braxton D., Maguire, Jane, Kaprio, Jakko, Farrall, Martin, Raitakari, Olli T., Kurth, Tobias, Ikram, M. Arfan, Anttila, Verneri, Reiner, Alex P., Longstreth, W. T., Rothwell, Peter M., Strachan, David P., Sharma, Pankaj, Seshadri, Sudha, Quaye, Lydia, Cherkas, Lynn, Schürks, Markus, Rosand, Jonathan, Vander Heiden, Jason, Ligthart, Lannie, Boncoraglio, Giorgio B., Davey Smith, George, van Duijn, Cornelia M., Stefansson, Kari, Worrall, Bradford B., Nyholt, Dale R., Markus, Hugh S., van den Maagdenberg, Arn M. J. M., Cotsapas, Chris, Traylor, Matthew, Zwart, John A., Palotie, Aarno, Dichgans, Martin, de Vries, Boukje, Holliday, Elizabeth G., Terwindt, Gisela M., Sturm, Jonathan

Effect of genetic variants associated with plasma homocysteine levels on stroke risk

- Cotlarciuc, Iona, Malik, Rainer, Markus, Hugh S., Rosand, Jonathan, Mitchell, Braxton D., Kittner, Steven J., Meschia, James F., van Meurs, Joyce B. J., Uitterlinden, Andre G., Worrall, Bradford B., Dichgans, Martin, Sharma, Pankaj, Holliday, Elizabeth G., Ahmadi, Kourosh R., Paré, Guillaume, Psaty, Bruce M., Fornage, Myriam, Hasan, Nazeeha, Rinne, Paul E., Ikram, M. Arfan

Meta-analysis in more than 17,900 cases of ischemic stroke reveals a novel association at 12q24.12

- Kilarski, Laura L., Achterberg, Sefanja, Walters, Matthew, Worrall, Bradford B., Sale, Michele M., Algra, Ale, Kappelle, L. Jaap, Wijmenga, Cisca, Norrving, Bo, Sandling, Johanna K., Röennblom, Lars, Goris, An, Devan, William J., Franke, Andre, Sudlow, Cathie, Rothwell, Peter M., Levi, Christopher, Holliday, Elizabeth G., Fornage, Myriam, Psaty, Bruce, Gretarsdottir, Solveig, Thorsteinsdottir, Unnar, Seshadri, Sudha, Traylor, Matthew, Mitchell, Braxton D., Kittner, Steven, Clarke, Robert, Hopewell, Jemma C., Bis, Joshua C., Boncoraglio, Giorgio B., Meschia, James, Ikram, M. Arfan, Hansen, Bjorn M., Montaner, Joan, Malik, Rainer, Thorleifsson, Gudmar, Stefanson, Kari, Rosand, Jonathan, de Bakker, Paul I. W., Farrall, Martin, Dichgans, Martin, Markus, Hugh S., Bevan, Steve, Lindgren, Arne, Pare, Guillame, Sharma, Pankaj, Slowik, Agniescka, Thijs, Vincent

Shared genetic susceptibility to ischemic stroke and coronary artery disease : a genome-wide analysis of common variants

- Dichgans, Martin, Malik, Rainer, Ódonnell, Christopher J., Fornage, Myriam, Thorsteinsdottir, Unnur, Psaty, Bruce M., Hengstenberg, Christian, Seshadri, Sudha, Erdmann, Jeanette, Bis, Joshua C., Peters, Annette, Boncoraglio, Giorgio B., König, Inke R., März, Winfred, Meschia, James F., Kathiresan, Sekar, Ikram, M. Arfan, McPherson, Ruth, Stefansson, Kari, Sudlow, Cathie, Reilly, Muredach, Thompson, John R., Sharma, Pankaj, Rosand, Jonathon, Hopewell, Jemma C., Chambers, John C., Watkins, Hugh, Rothwell, Peter M., Roberts, Robert, Markus, Hugh S., Samani, Nilesh J., Farrall, Martin, Schunkert, Heribert, Clarke, Robert, Gretarsdottir, Solveig, Thorleifsson, Gudmar, Mitchell, Branxton D., Assimes, Themistocles L., Levi, Christopher

Four novel loci (19q13, 6q24, 12q24, and 5q14) influence the microcirculation in vivo

- Ikram, M. Kamran, Xueling, Sim, Jensen, Richard A., Cotch, Mary Frances, Hewitt, Alex W., Attia, John, Holliday, Elizabeth G., Scott, Rodney J., Ikram, M. Arfan, Wang, Jie Jin, Klein, Ronald, Klein, Barbara E. K., Breteler, Monique M. B.