Objects
Temprano-Sagrera, Gerard, Sitlani, Colleen M., Dehghan, Abbas, Heath, Adam S., Reiner, Alex P., Johnson, Andrew, Richmond, Anne, Peters, Annette, van Hylckama Vlieg, Astrid, McKnight, Barbara, Psaty, Bruce M., Hayward, Caroline, Bone, William P., Holliday, Elizabeth G., Attia, John, Levi, Christopher R., Chasman, D, Strachan, DP, Tregouet, DA, Mook-Kanamori, D, Gill, D, Thibord, F, Asselbergs, FW, Martin-Bornez, Miguel, Leebeek, FWG, Rosendaal, FR, Davies, G, Homuth, G, Temprano, G, Campbell, H, Taylor, HA, Bressler, J, Huffman, JE, Rotter, JI, Voight, Benjamin F., Yao, J, Wilson, JF, Bis, JC, Hahn, JM, Desch, KC, Wiggins, KL, Raffield, LM, Bielak, LF, Yanek, LR, Kleber, ME, Morrison, Alanna C., Sabater-Lleal, M, Mueller, M, Kavousi, M, Mangino, M, Liu, M, Brown, MR, Conomos, MP, Jhun, MA, Chen, MH, de Maat, MPM, Damrauer, Scott M., Pankratz, N, Peyser, PA, Elliot, P, Wei, P, Wild, PS, Morange, PE, van der Harst, P, Yang, Q, Le, NQ, Marioni, R, de Vries, Paul S., Li, R, Damrauer, SM, Cox, SR, Trompet, S, Felix, SB, Völker, U, Tang, W, Koenig, W, Jukema, JW, Guo, X, Smith, Nicholas L., Lindstrom, S, Wang, L, Smith, EN, Gordon, W, van Hylckama Vlieg, A, de Andrade, M, Brody, JA, Pattee, JW, Haessler, J, Brumpton, BM, Sabater-Lleal, Maria, Chasman, DI, Suchon, P, Chen, MH, Turman, C, Germain, M, Wiggins, KL, MacDonald, J, Braekkan, SK, Armasu, SM. Wiley-Blackwell; 2022. Multi-phenotype analyses of hemostatic traits with cardiovascular events reveal novel genetic associations.
Malik, Rainer, Bevan, Steve, de Stefano, Anita L., Fornage, Myriam, Psaty, Bruce M., Ikram, M. Afran, 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, MD Wellcome Trust Case Control Consortium 2,, Holliday, Elizabeth G., Devan, William J., Cheng, Yu-Ching, Ibrahim-Verbaas, Carla A., Verhaaren, Benjamin F. J., Bis, Joshua C., Joon, Aron Y.. Lippincott Williams & Wilkins; 2014. Multilocus genetic risk score associates with ischemic stroke in case-control and prospective cohort studies.
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. Lippincott Williams & Wilkins; 2014. Shared genetic susceptibility to ischemic stroke and coronary artery disease : a genome-wide analysis of common variants.
Loth, Daan W., Artigas, María Soler, Lee, Mi Kyeong, Scott, Rodney J., Karrasch, Stefan, Grallert, Harald, Gaddis, Nathan C., Starr, John M., Wijmenga, Cisca, Minster, Ryan L., Lederer, David J., Pekkanen, Juha, Gyllensten, Ulf, Strachan, David P., Campbell, Harry, Morris, Andrew P., Gläeser, Sven, Hammond, Christopher J., Burkart, Kristin M., Beilby, John, Kritchevsky, Stephen B., Gucinason, Vilmundur, Hancock, Dana B., Williams, O. Dale, James, Alan L., Polasek, Ozren, Zemunik, Tatijana, Kolcic, Ivana, Petrini, Marcy F., Wjst, Matthias, Kim, Woo Jin, Porteous, David J., Scotland, Generation, Smith, Blair H., Viljanen, Anne, Huffman, Jennifer E., Heliovaara, Markku, Attia, John R., Sayers, Ian, Hampel, Regina, Gieger, Christian, Deary, Ian J., Boezen, H. Marike, Newman, Anne, Jarvelin, Marjo-Riitta, Wilson, James F., Vitart, Veronique, Lind, Lars, Stricker, Bruno H., Teumer, Alexander, Spector, Timothy D., Melén, Erik, Peters, Marjolein J., Lange, Leslie A., Barr, R. Graham, Bracke, Ken R., Verhamme, Fien M., Ramasamy, Adaikalavan, Sung, Joohon, Hiemstra, Pieter S., Cassano, Patricia A., Sood, Akshay, Hayward, Caroline, Dupuis, Josée, Hall, Ian P., Brusselle, Guy G., Tobin, Martin D., London, Stephanie J., Wareham, Nicholas J., Kaprio, Jaakko, Wang, Xin-Qun, Trochet, Holly, Gharib, Sina A., Kähönen, Mika, Flexeder, Claudia, Albrecht, Eva, Lopez, Lorna M., de Jong, Kim, Thyagarajan, Bharat, Alves, Alexessander Couto, Enroth, Stefan, Omenaas, Ernst, Joshi, Peter K., Wain, Louise V., Fall, Tove, Viñuela, Ana, Launer, Lenore J., Loehr, Laura R., Fornage, Myriam, Li, Guo, Wik, Jemma B., Tang, Wenbo, Manichaikul, Ani, Lahousse, Lies, Franceschini, Nora, Harris, Tamara B., North, Kari E., Rudnicka, Alicja R., Hui, Jennie, Gu, Xiangjun, Lumley, Thomas, Wright, Alan F., Hastie, Nicholas D., Campbell, Susan, Kumar, Rajesh, Koch, Beate, Pin, Isabelle, Scott, Robert A., Pietilainen, Kirsi H., Surakka, Ida, Liu, Yongmei, Holliday, Elizabeth G., Schulz, Holger, Heinrich, Joachim, Davies, Gail, Vonk, Judith M., Pottinger, Tess D., Wojczynski, Mary, Pouta, Anneli, Johansson, Åsa, Wild, Sarah H., Ingelsson, Erik, Rivadeneira, Fernando, Vöezke, Henry, Hysi, Pirro G., Eiriksdottir, Gudny, Morrison, Alanna C., Smith, Albert Vernon, Rotter, Jerome I., Gao, Wei, Postma, Dirkje S., White, Wendy B., Rich, Stephen S., Hofman, Albert, Aspelund, Thor, Couper, David, Smith, Lewis J., Psaty, Bruce M., Duan, Qing, Lohman, Kurt, Burchard, Esteban G., Uitterlinden, André G., Garcia, Melissa, Joubert, Bonnie R., McArdle, Wendy L., Musk, A. Bill, Hansel, Nadia, Heckbert, Susan R., Zgaga, Lina, Oldmeadow, Chris, van Meurs, Joyce B. J., Navarro, Pau, Rudan, Igor, Oh, Yeon-Mok, Redline, Susan, Jarvis, Deborah L., Zhao, Jing Hua, Rantanen, Taina, O'Connor, George T., Ripatti, Samuli. Nature Publishing Group; 2014. Genome-wide association analysis identifies six new loci associated with forced vital capacity.
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.. Lippincott Williams & Wilkins; 2021. 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.
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. Lippincott Williams & Wilkins; 2014. Effect of genetic variants associated with plasma homocysteine levels on stroke risk.
Traylor, Matthew, Farrall, Martin, Thorsteinsdottir, Unnur, Nalls, Mike A., Longstreth, W. T., Wiggins, Kerri L., Yadav, Sunaina, Parati, Eugenio A., Destefano, Anita L., Worrall, Bradford B., Kittner, Steven J., Khan, Muhammad Saleem, Holliday, Elizabeth G., Reiner, Alex P., Helgadottir, Anna, Achterberg, Sefanja, Fernandez-Cadenas, Israel, Abboud, Sherine, Schmidt, Reinhold, Walters, Matthew, Chen, Wei-Min, Ringelstein, E. Bernd, O'Donnell, Martin, Sudlow, Cathie, Ho, Weang Kee, Pera, Joanna, Lemmens, Robin, Norrving, Bo, Higgins, Peter, Benn, Marianne, Sale, Michele, Kuhlenbaumer, Gregor, Doney, Alexander S. F., Vicente, Astrid M., Hopewell, Jemma C., Delavaran, Hossein, Algra, Ale, Davies, Gail, Oliveira, Sophia A., Palmer, Colin N. A., Deary, Ian, Schmidt, Helena, Pandolfo, Massimo, Montaner, Joan, Carty, Cara, Cheng, Yu-Ching, De Bakker, Paul I. W., Kostulas, Konstantinos, Ferro, Jose M., Van Zuydam, Natalie R., Valdimarsson, Einar, Nordestgaard, Berge G., Lindgren, Anne, Thijs, Vincent, Slowik, Agnieszka, Saleheen, Danish, Fornage, Myriam, Paré, Guillaume, Berger, Klaus, Thorleifsson, Gudmar, Astc, W., Hofman, Albert, Mosley, Thomas H., Mitchell, Branxton D., Furie, Karen, Clarke, Robert, Levi, Christopher, Arfan Ikram, M,, Seshadri, Sudha, Gschwendtner, Andreas, Boncoraglio, Giorgio B., Sharma, Pankaj, Bis, Joshua C., Gretarsdottir, Solveig, Psaty, Bruce M., Rothwell, Peter M., Rosand, Jonathan, Meschia, James F., Malik, Rainer, Stefansson, Kari, Dichgans, Martin, Markus, Hugh S., Bevan, Steve. The Lancet Publishing Group; 2012. Genetic risk factors for ischaemic stroke and its subtypes (the METASTROKE Collaboration): a meta-analysis of genome-wide association studies.
Valdes-Marquez, Elsa, Parish, Sarah, Clarke, Robert, Stari, Traiani, Worrall, Bradford B., Slowik, Agnieszka, Hofman, Albert, Algra, Ale, Reiner, Alex P., Doney, Alexander S. F., Gschwendtner, Andreas, Ilinca, Andreea, Giese, Anne-Katrin, Lindgren, Arne, Vicente, Astrid M., Norrving, Bo, Nordestgaard, Borge G., Mitchell, Braxton D., Psaty, Bruce M., Carty, Cara L., Cheng, Y-C, Holliday, Elizabeth G.. Lippincott Williams & Wilkins; 2019. Relative effects of LDL-C on ischemic stroke and coronary disease: a Mendelian randomization 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.. Public Library of Science; 2015. No additional prognostic value of genetic information in the prediction of vascular events after cerebral ischemia of arterial origin: The PROMISe study.
Sim, Xueling, Jensen, Richard A., Klein, Ronald, Klein, Barbara E. K., Glazer, Nicole L., Lumley, Thomas, McKnight, Barbara, Psaty, Bruce M., de Jong, Paulus T. V. M., Hofman, Albert, Rivadeneira, Fernando, Uitterlinden, Andre G., Ikram, M. Kamran, van Duijn, Cornelia M., Aspelund, Thor, Eiriksdottir, Gudny, Harris, Tamara B., Jonasson, Fridbert, Launer, Lenore J., The Wellcome Trust Case Control Consortium, Attia, John, Baird, Paul N., Harrap, Stephen, Cotch, Mary Frances, Holliday, Elizabeth G., Inouye, Michael, Rochtchina, Elena, Scott, Rodney J., Viswanathan, Ananth, Global BPGen Consortium, Li, Guo, Smith, Nicholas L., Wiggins, Kerri L., Kuo, Jane Z., Li, Xiaohui, Taylor, Kent D., Hewitt, Alex W., Martin, Nicholas G., Montgomery, Grant W., Sun, Cong, Young, Terri L., Mackey, David A., van Zuydam, Natalie R., Doney, Alex S. F., Palmer, Colin N. A., MacGregor, Stuart, Morris, Andrew D., Rotter, Jerome I., Tai, E. Shyong, Gudnason, Vilmundur, Vingerling, Johannes R., Siscovick, David S., Wang, Jie Jin, Wong, Tien Y., Xie, Jing, Smith, Albert Vernon, Boerwinkle, Eric, Mitchell, Paul. Public Library of Science; 2013. Genetic loci for retinal arteriolar microcirculation.
Jensen, Richard A., Sim, Xueling, Launer, Lenore J., Smith, Albert Vernon, Boerwinkle, Eric, Cheung, Ning, Hewitt, Alex W., Liew, Gerald, Mitchell, Paul, Wang, Jie Jin, Attia, John, Scott, Rodney, Li, Xiaohui, Glazer, Nicole L., Lumley, Thomas, McKnight, Barbara, Psaty, Bruce M., Taylor, Kent, Hofman, Albert, de Jong, Paulus T. V. M., Rivadeneira, Fernando, Uitterlinden, Andre G., Tay, Wan-Ting, Cotch, Mary Frances, Teo, Yik Ying, Seielstad, Mark, Liu, Jianjun, Cheng, Ching-Yu, Saw, Seang-Mei, Aung, Tin, Ganesh, Santhi K., O'Donnell, Christopher J., Nalls, Mike A., Wiggins, Kerri L., Ikram, M. Kamran, Kuo, Jane Z., The Blue Mountains Eye Study GWAS Team, CKDGen Consortium, Klein, Cornelia M., van Duijn, Cornelia M., Gudnason, Vilmundur, Klein, Ronald, Siscovick, David S., Rotter, Jerome I., Tai, E. Shong, Holliday, Elizabeth G., Vingerling, Johannes, Wong, Tien Y., Eiriksdottir, Gudny, Harris, Tamara B., Jonasson, Fridbert, Klein, Barbara E. K.. Public Library of Science; 2013. Genome-wide association study of retinopathy in individuals without diabetes.
Holliday, Elizabeth G., Smith, Albert V., Cheng, Ching Yu, Van Duijn, Cornelia M., Eiriksdottir, Gudny, Gudnason, Vilmundur, Harris, Tamara, Hewitt, Alex W., Inouye, Michael, Jonasson, Fridbert, Klein, Barbara E. K., Launer, Lenore, Cornes, Belinda K., Li, Xiaohui, Liew, Gerald, Lumley, Thomas, McElduff, Patrick, McKnight, Barbara, Mitchell, Paul, Psaty, Bruce M., Rochtchina, Elena, Rotter, Jerome I., Scott, Rodney J., Buitendijk, Gabrielle H. S., Tay, Wanting, Taylor, Kent, Teo, Yik Ying, Uitterlinden, Andre G., Viswanathan, Ananth, Xie, Sophia, Wellcome Trust Case Control Consortium, Vingerling, Johannes R., Klaver, Caroline C. W., Tai, E. Shyong, Jensen, Richard A., Siscovick, David, Klein, Ronald, Cotch, Mary Frances, Wong, Tien Y., Attia, John, Wang, Jie Jin, Sim, Xueling, Aspelund, Thor, Aung, Tin, Baird, Paul N., Boerwinkle, Eric. Public Library of Science; 2013. Insights into the genetic architecture of early stage age-related macular degeneration: a genome-wide association study meta-analysis.
de Vries, Paul S., Sabater-Lleal, Maria, Marioni, Riccardo E., Steri, Maristella, Weng, Lu-Chen, Pool, Rene, Grossmann, Vera, Brody, Jennifer A., Venturini, Cristina, Tanaka, Toshiko, Rose, Lynda M., Oldmeadow, Christopher, Chasman, Daniel I., Mazur, Johanna, Basu, Saonli, Frånberg, Mattias, Yang, Qiong, Ligthart, Symen, Hottenga, Jouke J., Rumley, Ann, Mulas, Antonella, de Craen, Anton J. M., Grotevendt, Anne, Trompet, Stella, Taylor, Kent D., Delgado, Graciela E., Kifley, Annette, Lopez, Lorna M., Berentzen, Tina L., Mangino, Massimo, Bandinelli, Stefania, Morrison, Alanna C., Hamsten, Anders, Tofler, Geoffrey, Ahluwalia, Tarunveer S., de Maat, Moniek P. M., Draisma, Harmen H. M., Lowe, Gordon D., Zoledziewska, Magdalena, Sattar, Naveed, Lackner, Karl J., Völker, Uwe, McKnight, Barbara, Huang, Jie, Holliday, Elizabeth G., Teumer, Alexander, McEvoy, Mark A., Starr, John M., Hysi, Pirro G., Hernandez, Dena G., Guan, Weihua, Rivadeneira, Fernando, McArdle, Wendy L., Slagboom, P. Eline, Zeller, Tanja, Psaty, Bruce M., Kleber, Marcus E., Uitterlinden, André G., de Geus, Eco J. C., Stott, David J., Binder, Harald, Hofman, Albert, Franco, Oscar H., Rotter, Jerome I., Ferrucci, Luigi, Spector, Tim D., Deary, Ian J., Chen, Ming-Huei, März, Winfried, Greinacher, Andreas, Wild, Philipp S., Cucca, Francesco, Boomsma, Dorret I., Watkins, Hugh, Tang, Weihong, Ridker, Paul M., Jukema, Jan W., Scott, Rodney J., Wang, Jie Jin, Mitchell, Paul, Hansen, Torben, O'Donnell, Christopher J., Smith, Nicholas L., Strachan, David P., Dehghan, Abbas, Attia, John R.. Public Library of Science (PLoS); 2017. Comparison of HapMap and 1000 genomes reference panels in a large-scale genome-wide association study.
Adib-Samii, Poneh, Rost, Natalia, Gschwendtner, Andreas, Malik, Rainer, Richie, Alexa, Gamble, Dale, Segal, Helen, Parati, Eugenio A., Ciusani, Emilio, Holliday, Elizabeth G., Maguire, Jane, Wardlaw, Joanna, Traylor, Matthew, Worrall, Bradford, Bis, Joshua, Wiggins, Kerri L., Longstreth, Will, Kittner, Steve J., Cheng, Yu-Ching, Mosley, Thomas, Falcone, Guido J., Furie, Karen L., Leiva-Salinas, Carlos, Devan, William, Lau, Benison C., Saleem Khan, Muhammed, Australian Stroke Genetics Collaborative, Wellcome Trust Case-Control Consortium-2, METASTROKE, Sharma, Pankaj, Fornage, Miriam, Mitchell, Braxton D., Psaty, Bruce M., Sudlow, Cathie, Biffi, Alessandro, Levi, Christopher, Boncoraglio, Giorgio B., Rothwell, Peter M., Meschia, James, Dichgans, Martin, Rosand, Jonathan, Markus, Hugh S., Lanfranconi, Silvia, Fitzpatrick, Kaitlin, Bevan, Steve, Kanakis, Allison, Valant, Valerie. Lippincott Williams & Wilkins; 2013. 17q25 Locus is associated with white matter hyperintensity volume in ischemic stroke, but not with lacunar stroke status.