The Polygenic and Monogenic Basis of Blood Traits and Diseases by Vuckovic, Dragana, Bao, Erik L., Akbari, Parsa, Mousas, Abdou, Jiang, Tao, Chen, Ming-Huei, Raffield, Laura M., Huffman, Jennifer E., Ritchie, Scott C., Megy, Karyn, Ponstingl, Hannes, Penkett, Christopher J., Albers, Patrick K., Wigdor, Emilie M., Sakaue, Saori, Moscati, Arden, Manansala, Regina, Lo, Ken Sin, Qian, Huijun, Akiyama, Masato, Bartz, Traci M., Beswick, Andrew, Bork-Jensen, Jette, Bottinger, Erwin P., van Rooij, Frank J.A., Chitrala, Kumaraswamy N., Wilson, Peter W.F., Choquet, Hélène, Danesh, John, Di Angelantonio, Emanuele, Dimou, Niki, Ding, Jingzhong, Elliott, Paul, Esko, Tõnu, Evans, Michele K., Felix, Stephan B., Floyd, James S., Grarup, Niels, Guo, Michael H., Guo, Qi, Greinacher, Andreas, Haessler, Jeff, Howson, Joanna M.M., Huang, Wei, Kacprowski, Tim, Kähönen, Mika, Kamatani, Yoichiro, Kanai, Masahiro, Karthikeyan, Savita, Koskeridis, Fotios, Lange, Leslie A., Lehtimäki, Terho, Linneberg, Allan, Liu, Yongmei, Lyytikäinen, Leo-Pekka, Manichaikul, Ani, Matsuda, Koichi, Mohlke, Karen L., Mononen, Nina, Murakami, Yoshinori, Nikus, Kjell, Pankratz, Nathan, Pedersen, Oluf, Preuss, Michael, Psaty, Bruce M., Rich, Stephen S., Rodriguez, Benjamin A.T., Rosen, Jonathan D., Rotter, Jerome I., Spracklen, Cassandra N., Surendran, Praveen, Tang, Hua, Tardif, Jean-Claude, Ghanbari, Mohsen, Völzke, Henry, Watkins, Nicholas A., Cai, Na, Kundu, Kousik, Watt, Stephen B., Walter, Klaudia, Zonderman, Alan B., Cho, Kelly, Li, Yun, Loos, Ruth J.F., Knight, Julian C., Georges, Michel, Stegle, Oliver, Evangelou, Evangelos, Okada, Yukinori, Roberts, David J., Inouye, Michael, Johnson, Andrew D., Auer, Paul L., Astle, William J., Reiner, Alexander P., Butterworth, Adam S., Ouwehand, Willem H., Lettre, Guillaume, Sankaran, Vijay G., Soranzo, Nicole

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Trans-ethnic and Ancestry-Specific Blood-Cell Genetics in 746,667 Individuals from 5 Global Populations by Chen, Ming-Huei, Raffield, Laura M., Mousas, Abdou, Sakaue, Saori, Huffman, Jennifer E., Moscati, Arden, Trivedi, Bhavi, Jiang, Tao, Akbari, Parsa, Vuckovic, Dragana, Bao, Erik L., Zhong, Xue, Manansala, Regina, Laplante, Véronique, Chen, Minhui, Lo, Ken Sin, Qian, Huijun, Lareau, Caleb A., Beaudoin, Mélissa, Akiyama, Masato, Ben-Shlomo, Yoav, Beswick, Andrew, Bottinger, Erwin P., Brody, Jennifer A., van Rooij, Frank J.A., Cho, Kelly, Choquet, Hélène, Correa, Adolfo, Di Angelantonio, Emanuele, Dimou, Niki, Ding, Jingzhong, Elliott, Paul, Esko, Tõnu, Evans, Michele K., Floyd, James S., Broer, Linda, Grarup, Niels, Guo, Michael H., Greinacher, Andreas, Haessler, Jeff, Hansen, Torben, Howson, Joanna M.M., Huang, Qin Qin, Huang, Wei, Jorgenson, Eric, Kacprowski, Tim, Kanai, Masahiro, Karthikeyan, Savita, Koskeridis, Fotis, Lange, Leslie A., Lerch, Markus M., Linneberg, Allan, Liu, Yongmei, Lyytikäinen, Leo-Pekka, Manichaikul, Ani, Martin, Hilary C., Matsuda, Koichi, Mohlke, Karen L., Mononen, Nina, Murakami, Yoshinori, Nadkarni, Girish N., Nauck, Matthias, Nikus, Kjell, Ouwehand, Willem H., Pankratz, Nathan, Pedersen, Oluf, Preuss, Michael, Psaty, Bruce M., Raitakari, Olli T., Roberts, David J., Rich, Stephen S., Rodriguez, Benjamin A.T., Rosen, Jonathan D., Rotter, Jerome I., Schubert, Petra, Spracklen, Cassandra N., Surendran, Praveen, Tang, Hua, Tardif, Jean-Claude, Trembath, Richard C., Ghanbari, Mohsen, Völker, Uwe, Völzke, Henry, Watkins, Nicholas A., Zonderman, Alan B., Wilson, Peter W.F., Li, Yun, Butterworth, Adam S., Gauchat, Jean-François, Chiang, Charleston W.K., Li, Bingshan, Loos, Ruth J.F., Astle, William J., Evangelou, Evangelos, van Heel, David A., Sankaran, Vijay G., Okada, Yukinori, Johnson, Andrew D., Reiner, Alexander P., Auer, Paul L.

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New evidence from plasma ceramides links apoE polymorphism to greater risk of coronary artery disease in Finnish adults[S] by Karjalainen, Juho-Pekka, Mononen, Nina, Hutri-Kähönen, Nina, Lehtimäki, Miikael, Hilvo, Mika, Kauhanen, Dimple, Juonala, Markus, Viikari, Jorma, Kähönen, Mika, Raitakari, Olli, Laaksonen, Reijo, Lehtimäki, Terho

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Genetic analyses of the electrocardiographic QT interval and its components identify additional loci and pathways by Isaacs, Aaron, Duong, ThuyVy, Foco, Luisa, Ahmed, Farah, Brody, Jennifer A., Salman, Reem, Noordam, Raymond, Benjamins, Jan-Walter, Repetto, Linda, Concas, Maria Pina, van den Berg, Marten E., Weiss, Stefan, Baldassari, Antoine R., Bartz, Traci M., Cook, James P., Evans, Daniel S., Freudling, Rebecca, Mei, Hao, Moscati, Arden, Müller-Nurasyid, Martina, Nursyifa, Casia, Ryan, Kathleen A., Tarazona-Santos, Eduardo, van Duijvenboden, Stefan, Yao, Jie, Andreasen, Laura, Bis, Joshua C., Cutler, Michael J., Ellervik, Christina, Ellinor, Patrick T., Felix, Stephan B., Graff, Mariaelisa, Guo, Xiuqing, Heckbert, Susan R., Huang, Paul L., Hutri-Kähönen, Nina, Ikram, M. Arfan, Jackson, Rebecca D., Junttila, Juhani, Kavousi, Maryam, Kors, Jan A., Leal, Thiago P., Lemaitre, Rozenn N., Lind, Lars, Liu, Simin, MacFarlane, Peter W., Mangino, Massimo, Meitinger, Thomas, Mezzavilla, Massimo, Mishra, Pashupati P., Montasser, May E., Navarro, Pau, Nikus, Kjell, Pare, Guillaume, Patton, Kristen K., Pelliccione, Giulia, Porteous, David J., Pramstaller, Peter P., Preuss, Michael H., Risch, Lorenz, Schurmann, Claudia, Sinner, Moritz F., Stoll, Monika, Tarasov, Kirill, Taylor, Kent D., Trompet, Stella, Uitterlinden, André, Völker, Uwe, Waldenberger, Melanie, Weng, Lu-Chen, Whitsel, Eric A., Wilson, James G., Avery, Christy L., Conen, David, Dörr, Marcus, Gharib, Sina A., Girotto, Giorgia, Grarup, Niels, Hayward, Caroline, Jamshidi, Yalda, Kähönen, Mika, Kanters, Jørgen K., Lima-Costa, Maria Fernanda, Liu, Yongmei, Loos, Ruth J. F., Mook-Kanamori, Dennis O., Morris, Andrew P., O’Connell, Jeffrey R., Olesen, Morten Salling, Orini, Michele, Pattaro, Cristian, Psaty, Bruce M., Rotter, Jerome I., Stricker, Bruno, van der Harst, Pim, van Duijn, Cornelia M., Arking, Dan E., Ramirez, Julia, Sotoodehnia, Nona, Munroe, Patricia B.

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Early resilience and epigenetic ageing: Results from the prospective Young Finns Study with a 31-year follow-up by Aino, Saarinen, Saara, Marttila, Mishra Pashupati, P, Leo-Pekka, Lyytikäinen, Binisha, Hamal Mishra, Emma, Raitoharju, Nina, Mononen, Mika, Kähönen, Olli, Raitakari, Terho, Lehtimäki, Liisa, Keltikangas-Järvinen

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The effect of apolipoprotein E polymorphism on serum metabolome – a population-based 10-year follow-up study by Karjalainen, Juho-Pekka, Mononen, Nina, Hutri-Kähönen, Nina, Lehtimäki, Miikael, Juonala, Markus, Ala-Korpela, Mika, Kähönen, Mika, Raitakari, Olli, Lehtimäki, Terho

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Trans-ancestral genome-wide association study of longitudinal pubertal height growth and shared heritability with adult health outcomes by Bradfield, Jonathan P, Kember, Rachel L, Ulrich, Anna, Balkhiyarova, Zhanna, Alyass, Akram, Aris, Izzuddin M, Bell, Joshua A, Broadaway, K Alaine, Chen, Zhanghua, Chai, Jin-Fang, Davies, Neil M, Fernandez-Orth, Dietmar, Bustamante, Mariona, Fore, Ruby, Ganguli, Amitavo, Heiskala, Anni, Hottenga, Jouke-Jan, Íñiguez, Carmen, Kobes, Sayuko, Leinonen, Jaakko, Lowry, Estelle, Lyytikainen, Leo-Pekka, Mahajan, Anubha, Pitkänen, Niina, Schnurr, Theresia M, Have, Christian Theil, Strachan, David P, Thiering, Elisabeth, Vogelezang, Suzanne, Wade, Kaitlin H, Wang, Carol A, Wong, Andrew, Holm, Louise Aas, Chesi, Alessandra, Choong, Catherine, Cruz, Miguel, Elliott, Paul, Franks, Steve, Frithioff-Bøjsøe, Christine, Gauderman, W James, Glessner, Joseph T, Gilsanz, Vicente, Griesman, Kendra, Hanson, Robert L, Kaakinen, Marika, Kalkwarf, Heidi, Kelly, Andrea, Kindler, Joseph, Kähönen, Mika, Lanca, Carla, Lappe, Joan, Lee, Nanette R, McCormack, Shana, Mentch, Frank D, Mitchell, Jonathan A, Mononen, Nina, Niinikoski, Harri, Oken, Emily, Pahkala, Katja, Sim, Xueling, Teo, Yik-Ying, Baier, Leslie J, van Beijsterveldt, Toos, Adair, Linda S, Boomsma, Dorret I, de Geus, Eco, Guxens, Mònica, Eriksson, Johan G, Felix, Janine F, Gilliland, Frank D, Biobank, Penn Medicine, Hansen, Torben, Hardy, Rebecca, Hivert, Marie-France, Holm, Jens-Christian, Jaddoe, Vincent W V, Järvelin, Marjo-Riitta, Lehtimäki, Terho, Mackey, David A, Meyre, David, Mohlke, Karen L, Mykkänen, Juha, Oberfield, Sharon, Pennell, Craig E, Perry, John R B, Raitakari, Olli, Rivadeneira, Fernando, Saw, Seang-Mei, Sebert, Sylvain, Shepherd, John A, Standl, Marie, Sørensen, Thorkild I A, Timpson, Nicholas J, Torrent, Maties, Willemsen, Gonneke, Hypponen, Elina, Power, Chris, McCarthy, Mark I, Freathy, Rachel M, Widén, Elisabeth

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Identification and functional characterisation of DNA methylation differences between East- and West-originating Finns by Ciantar, Joanna, Marttila, Saara, Rajić, Sonja, Kostiniuk, Daria, Mishra, Pashupati P, Lyytikäinen, Leo-Pekka, Mononen, Nina, Kleber, Marcus E, März, Winfried, Kähönen, Mika, Raitakari, Olli, Lehtimäki, Terho, Raitoharju, Emma

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X-chromosome and kidney function: evidence from a multi-trait genetic analysis of 908,697 individuals reveals sex-specific and sex-differential findings in genes regulated by andro... by Scholz, Markus, Horn, Katrin, Pott, Janne, Wuttke, Matthias, Nasr, M. Kamal, Kirsten, Holger, Li, Yong, Hoppmann, Anselm, Gorski, Mathias, Chai, Jin-Fang, Wang, Judy, Nutile, Teresa, Åsvold, Bjørn Olav, Bansal, Nisha, Biggs, Mary L., Boutin, Thibaud, Brenner, Hermann, Burkhardt, Ralph, Cai, Jianwen, Chasman, Daniel I., Chee, Miao Ling, Chee, Miao Li, Cheng, Ching-Yu, Delgado, Graciela, Dittrich, Katalin, Giri, Ayush, Gordon, Scott D., Hallan, Stein, Hamet, Pavel, Holleczek, Bernd, Holm, Hilma, Hutri-Kähönen, Nina, Isermann, Berend, Jonas, Jost B., Kastarinen, Mika, Kiess, Wieland, Kleber, Marcus E., Kovacs, Peter, Krajcoviechova, Alena, Krämer, Bernhard K., Kähönen, Mika, Lange, Leslie A., Lash, James P., Lehtimäki, Terho, Li, Hengtong, Lin, Bridget M., Liu, Jianjun, Loeffler, Markus, Martin, Nicholas G., Milaneschi, Yuri, Mishra, Pashupati P., Mononen, Nina, Montgomery, Grant W., Mook-Kanamori, Dennis O., Mychaleckyj, Josyf C., Nikus, Kjell, Nolte, Ilja M., Okada, Yukinori, Oldehinkel, Albertine J., Penninx, Brenda W. J. H., Perola, Markus, Pirastu, Nicola, Polasek, Ozren, Porteous, David J., Psaty, Bruce M., Raitakari, Olli T., Rasheed, Humaira, Reilly, Dermot F., Rice, Kenneth M., Ridker, Paul M., Rotter, Jerome I., Schöttker, Ben, Sims, Mario, Snieder, Harold, Stark, Klaus J., Stumvoll, Michael, Sulem, Patrick, Sveinbjornsson, Gardar, Tayo, Bamidele O., Teren, Andrej, Tham, Yih-Chung, Thiery, Joachim, Thio, Chris H. L., Thomas, Laurent F., Tremblay, Johanne, Tönjes, Anke, Vitart, Veronique, Wang, Ya Xing, Wang, Chaolong, Wei, Wen Bin, Whitfield, John B., Wild, Sarah H., Wong, Tien-Yin, Woodward, Mark, Sim, Xueling, Feitosa, Mary F., Hung, Adriana M., Teumer, Alexander, Köttgen, Anna, Schlosser, Pascal

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Author Correction: Trans-ancestral genome-wide association study of longitudinal pubertal height growth and shared heritability with adult health outcomes by Bradfeld, Jonathan P, Kember, Rachel L, Ulrich, Anna, Balkhiyarova, Zhanna, Alyass, Akram, Aris, Izzuddin M, Bell, Joshua A, Broadaway, K Alaine, Chen, Zhanghua, Chai, Jin-Fang, Davies, Neil M, Fernandez-Orth, Dietmar, Bustamante, Mariona, Fore, Ruby, Ganguli, Amitavo, Heiskala, Anni, Hottenga, Jouke-Jan, Íñiguez, Carmen, Kobes, Sayuko, Leinonen, Jaakko, Lowry, Estelle, Lyytikainen, Leo-Pekka, Mahajan, Anubha, Pitkänen, Niina, Schnurr, Theresia M, Have, Christian Theil, Strachan, David P, Thiering, Elisabeth, Vogelezang, Suzanne, Wade, Kaitlin H, Wang, Carol A, Wong, Andrew, Holm, Louise Aas, Chesi, Alessandra, Choong, Catherine, Cruz, Miguel, Elliott, Paul, Franks, Steve, Frithiof-Bøjsøe, Christine, Gauderman, W James, Glessner, Joseph T, Gilsanz, Vicente, Griesman, Kendra, Hanson, Robert L, Kaakinen, Marika, Kalkwarf, Heidi, Kelly, Andrea, Kindler, Joseph, Kähönen, Mika, Lanca, Carla, Lappe, Joan, Lee, Nanette R, McCormack, Shana, Mentch, Frank D, Mitchell, Jonathan A, Mononen, Nina, Niinikoski, Harri, Oken, Emily, Pahkala, Katja, Sim, Xueling, Teo, Yik-Ying, Baier, Leslie J, van Beijsterveldt, Toos, Adair, Linda S, Boomsma, Dorret I, de Geus, Eco, Guxens, Mònica, Eriksson, Johan G, Felix, Janine F, Gilliland, Frank D, Hansen, Torben, Hardy, Rebecca, Hivert, Marie-France, Holm, Jens-Christian, Jaddoe, Vincent W V, Järvelin, Marjo-Riitta, Lehtimäki, Terho, Mackey, David A, Meyre, David, Mohlke, Karen L, Mykkänen, Juha, Oberfeld, Sharon, Pennell, Craig E, Perry, John R B, Raitakari, Olli, Rivadeneira, Fernando, Saw, Seang-Mei, Sebert, Sylvain, Shepherd, John A, Standl, Marie, Sørensen, Thorkild I A, Timpson, Nicholas J, Torrent, Maties, Willemsen, Gonneke, Hypponen, Elina, Power, Chris, McCarthy, Mark I, Freathy, Rachel M, Widén, Elisabeth, Hakonarson, Hakon

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Modular genome-wide gene expression architecture shared by early traits of osteoporosis and atherosclerosis in the Young Finns Study by Mishra, Binisha H., Mishra, Pashupati P., Raitoharju, Emma, Marttila, Saara, Mononen, Nina, Sievänen, Harri, Viikari, Jorma, Juonala, Markus, Laaksonen, Marika, Hutri-Kähönen, Nina, Kähönen, Mika, Raitakari, Olli T., Lehtimäki, Terho

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Platelet-Related Variants Identified by Exomechip Meta-analysis in 157,293 Individuals by Eicher, John D., Kacprowski, Tim, Nomura, Akihiro, Chen, Ming-Huei, Yanek, Lisa R., Tajuddin, Salman M., Slater, Andrew J., Polfus, Linda, Schurmann, Claudia, Brody, Jennifer A., Manichaikul, Ani, Hill, W. David, Pazoki, Raha, Elliot, Paul, Evangelou, Evangelos, Tzoulaki, Ioanna, Gao, He, Vergnaud, Anne-Claire, Mathias, Rasika A., Becker, Diane M., Becker, Lewis C., Burt, Amber, Crosslin, David R., Lyytikäinen, Leo-Pekka, Nikus, Kjell, Hernesniemi, Jussi, Kähönen, Mika, Raitoharju, Emma, Mononen, Nina, Raitakari, Olli T., Lehtimäki, Terho, Cushman, Mary, Zakai, Neil A., Nickerson, Deborah A., Raffield, Laura M., Quarells, Rakale, Willer, Cristen J., Peloso, Gina M., Abecasis, Goncalo R., Liu, Dajiang J., Deloukas, Panos, Samani, Nilesh J., Schunkert, Heribert, Erdmann, Jeanette, Fornage, Myriam, Richard, Melissa, Tardif, Jean-Claude, Rioux, John D., Dube, Marie-Pierre, de Denus, Simon, Bottinger, Erwin P., Loos, Ruth J.F., Smith, Albert Vernon, Harris, Tamara B., Launer, Lenore J., Gudnason, Vilmundur, Velez Edwards, Digna R., Torstenson, Eric S., Liu, Yongmei, Tracy, Russell P., Rotter, Jerome I., Rich, Stephen S., Highland, Heather M., Li, Jin, Lange, Ethan, Wilson, James G., Mihailov, Evelin, Hirschhorn, Joel, Metspalu, Andres, Esko, Tõnu, Vacchi-Suzzi, Caterina, Zonderman, Alan B., Evans, Michele K., Engström, Gunnar, Orho-Melander, Marju, Melander, Olle, O’Donoghue, Michelle L., Waterworth, Dawn M., Floyd, James S., Rice, Kenneth M., Psaty, Bruce M., Starr, J.M., Liewald, David C.M., Hayward, Caroline, Deary, Ian J., Greinacher, Andreas, Völker, Uwe, Thiele, Thomas, Völzke, Henry, van Rooij, Frank J.A., Uitterlinden, André G., Franco, Oscar H., Dehghan, Abbas, Edwards, Todd L., Ganesh, Santhi K., Kathiresan, Sekar, Faraday, Nauder, Reiner, Alex P., Lettre, Guillaume, Johnson, Andrew D.

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Examining the effect of mitochondrial DNA variants on blood pressure in two Finnish cohorts by Laaksonen, Jaakko, Mishra, Pashupati P., Seppälä, Ilkka, Lyytikäinen, Leo-Pekka, Raitoharju, Emma, Mononen, Nina, Lepistö, Maija, Almusa, Henrikki, Ellonen, Pekka, Hutri-Kähönen, Nina, Juonala, Markus, Raitakari, Olli, Kähönen, Mika, Salonen, Jukka T., Lehtimäki, Terho

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Identification of gene networks jointly associated with depressive symptoms and cardiovascular health metrics using whole blood transcriptome in the Young Finns Study by Mishra, Binisha H, Raitoharju, Emma, Mononen, Nina, Saarinen, Aino, Viikari, Jorma, Juonala, Markus, Hutri-Kähönen, Nina, Kähönen, Mika, Raitakari, Olli T, Lehtimäki, Terho, Mishra, Pashupati P

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Genetic and environmental perturbations lead to regulatory decoherence by Lea, Amanda, Subramaniam, Meena, Ko, Arthur, Lehtimäki, Terho, Raitoharju, Emma, Kähönen, Mika, Seppälä, Ilkka, Mononen, Nina, Raitakari, Olli T, Ala-Korpela, Mika, Pajukanta, Päivi, Zaitlen, Noah, Ayroles, Julien F

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Sex-specific associations of TCF7L2 variants with fasting glucose, type 2 diabetes and coronary heart disease among Turkish adults by Yüzbaşıoğulları, Ayşe Berna, Kömürcü-Bayrak, Evrim, Onat, Altan, Can, Gunay, Mononen, Nina, Laaksonen, Reijo, Kähönen, Mika, Lehtimäki, Terho, Erginel-Ünaltuna, Nihan

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Polymorphism in the IL10 promoter region and early markers of atherosclerosis: The Cardiovascular Risk in Young Finns Study by Heiskanen, Miikael, Kähönen, Mika, Hurme, Mikko, Lehtimäki, Terho, Mononen, Nina, Juonala, Markus, Hutri-Kähönen, Nina, Viikari, Jorma, Raitakari, Olli, Hulkkonen, Janne

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Genetic variants and their interactions in the prediction of increased pre-clinical carotid atherosclerosis: the cardiovascular risk in young Finns study by Okser, Sebastian, Lehtimäki, Terho, Elo, Laura L, Mononen, Nina, Peltonen, Nina, Kähönen, Mika, Juonala, Markus, Fan, Yue-Mei, Hernesniemi, Jussi A, Laitinen, Tomi, Lyytikäinen, Leo-Pekka, Rontu, Riikka, Eklund, Carita, Hutri-Kähönen, Nina, Taittonen, Leena, Hurme, Mikko, Viikari, Jorma S A, Raitakari, Olli T, Aittokallio, Tero

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Erratum: Genetic loci associated with heart rate variability and their effects on cardiac disease risk by Munoz, M. Loretto, Amare, Azmeraw T., Jansen, Rick, Vaez, Ahmad, Avery, Christy L., van Dongen, Jenny, Goyette, Philippe, Hernesniemi, Jussi, Huikari, Ville, Hwang, Shih-Jen, Kluttig, Alexander, Krijthe, Bouwe P., Kumar, Jitender, Lyytikäinen, Leo-Pekka, Maihofer, Adam X., van der Most, Peter J., Müller-Nurasyid, Martina, Nivard, Michel, Salvi, Erika, Thayer, Julian F., Zabaneh, Delilah, Abdellaoui, Abdel, Albarwani, Sulayma, Albert, Christine, Ashar, Foram, Auvinen, Juha, Axelsson, Tomas, Baker, Dewleen G., Bayoumi, Riad, Britton, Annie R., Christophersen, Ingrid, Dietrich, Andrea, Ehret, George B., Ellinor, Patrick T., Felix, Janine F., Floras, John S., Franco, Oscar H., Gademan, Maaike G. J., Giedraitis, Vilmantas, Hartman, Catharina A., Hemerich, Daiane, Hofman, Albert, Hottenga, Jouke-Jan, Juonala, Markus, Kiviniemi, Antti M., Kumari, Meena, Lefrandt, Joop D., Limacher, Marian C., Lin, Henry J., Lindgren, Cecilia M., Lubitz, Steven A., Mahajan, Anubha, McKnight, Barbara, zu Schwabedissen, Henriette Meyer, Milaneschi, Yuri, Mononen, Nina, Morris, Andrew P., Nalls, Mike A., Navis, Gerjan, Neijts, Melanie, North, Kari E., Perz, Siegfried, Peters, Annette, Raitakari, Olli T., Risbrough, Victoria B., Sinner, Moritz F., Smit, Johannes H., Smith, Nicholas L., Sotoodehnia, Nona, Staessen, Jan A., Stolarz-Skrzypek, Katarzyna, Swenne, Cees A., Syvänen, Ann-Christine, Taylor, Kent D., Teumer, Alexander, Tinker, Lesley E., Uitterlinden, André G., Voss, Andreas, Willemsen, Gonneke, Zhang, Zhu-Ming, Zonderman, Alan B, Cusi, Daniele, van der Harst, Pim, Hassan, Mohammad, Ingelsson, Erik, Järvelin, Marjo-Riitta, Kääb, Stefan, Kähönen, Mika, Kuh, Diana, Lind, Lars, Nievergelt, Caroline M., Oldehinkel, Albertine J., Penninx, Brenda, Rioux, John D., Rotter, Jerome I., Vrijkotte, Tanja G. M., Asselbergs, Folkert W., Heckbert, Susan R., Whitsel, Eric A., Snieder, Harold

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Genetic profiling using genome-wide significant coronary artery disease risk variants does not improve the prediction of subclinical atherosclerosis: the Cardiovascular Risk in You... by Hernesniemi, Jussi A, Seppälä, Ilkka, Lyytikäinen, Leo-Pekka, Mononen, Nina, Oksala, Niku, Hutri-Kähönen, Nina, Juonala, Markus, Taittonen, Leena, Smith, Erin N, Schork, Nicholas J, Chen, Wei, Srinivasan, Sathanur R, Berenson, Gerald S, Murray, Sarah S, Laitinen, Tomi, Jula, Antti, Kettunen, Johannes, Ripatti, Samuli, Laaksonen, Reijo, Viikari, Jorma, Kähönen, Mika, Raitakari, Olli T, Lehtimäki, Terho

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