ERGONOMIC EZ SCOPE DIGITAL IMAGING SYSTEM von Ledwon, Anthony, Golub, Walter, Koch, Anne Lauren, Preiss, B Cooper, Rutter, Bryce, Gatti, John

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Ergonomic EZ scope digital imaging system von Ledwon, Anthony, Golub, Walter, Koch, Anne Lauren, Preiss, B Cooper, Rutter, Bryce, Gatti, John

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ERGONOMIC EZ SCOPE DIGITAL IMAGING SYSTEM von Ledwon, Anthony, Golub, Walter, Koch, Anne Lauren, Preiss, B Cooper, Rutter, Bryce, Gatti, John

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HMG-coenzyme A reductase inhibition, type 2 diabetes, and bodyweight: evidence from genetic analysis and randomised trials von Swerdlow, Daniel I, Dr, Preiss, David, Dr, Holmes, Michael V, PhD, Shah, Tina, PhD, Sofat, Reecha, MD, Johnson, Paul C D, PhD, Verweij, Niek, MD, Sharp, Stephen J, MSc, Giambartolomei, Claudia, MSc, Chung, Christina, MSc, Peasey, Anne, PhD, Amuzu, Antoinette, MSc, Li, KaWah, MSc, Cooper, Jackie A, MSc, Drenos, Fotios, PhD, Li, Yun R, BSc, Lowe, Gordon, Prof, Gallacher, John, PhD, Stewart, Marlene C W, PhD, Tzoulaki, Ioanna, PhD, van der A, Daphne L, PhD, Forouhi, Nita G, MRCP, Onland-Moret, N Charlotte, PhD, Schnabel, Renate B, MD, Hubacek, Jaroslav A, PhD, Kubinova, Ruzena, MD, Baceviciene, Migle, MD, Tamosiunas, Abdonas, Prof, Topor-Madry, Romanvan, MD, Stepaniak, Urszula, PhD, Malyutina, Sofia, Prof, Baldassarre, Damiano, PhD, Sennblad, Bengt, PhD, Tremoli, Elena, Prof, Veglia, Fabrizio, PhD, Ford, Ian, Prof, Westendorp, Rudi G J, Prof, Algra, Ale, Prof, der Zee, Anke H Maitland-van, PhD, Eaton, Charles B, Prof, Robinson, Jennifer G, Prof, Duggan, David, PhD, Downs, John R, MD, Gotto, Antonio M, MD, Keech, Anthony C, MD, Marchioli, Roberto, MD, Tognoni, Gianni, MD, Sever, Peter S, Prof, Waters, David D, MD, Pedersen, Terje R, MD, Nakamura, Haruo, MD, McMurray, John J V, Prof, Lewsey, James D, PhD, Chasman, Daniel I, PhD, Ridker, Paul M, MD, Maggioni, Aldo P, Prof, Tavazzi, Luigi, Prof, Manson, JoAnn E, Prof, Price, Jackie F, MD, Whincup, Peter H, Prof, Morris, Richard W, Prof, Lawlor, Debbie A, Prof, Ben-Shlomo, Yoav, Prof, Schreiner, Pamela J, Prof, Fornage, Myriam, Prof, Siscovick, David S, Prof, Cushman, Mary, MD, Kumari, Meena, PhD, Verschuren, W M Monique, PhD, Redline, Susan, Prof, Patel, Sanjay R, MD, Whittaker, John C, Prof, Hamsten, Anders, Prof, Delaney, Joseph A, PhD, Dale, Caroline, PhD, Gaunt, Tom R, PhD, Wong, Andrew, PhD, Hardy, Rebecca, Prof, Kathiresan, Sekar, MD, Castillo, Berta A, PhD, van der Harst, Pim, Prof, Brunner, Eric J, Prof, Tybjaerg-Hansen, Anne, Prof, Krauss, Ronald M, MD, Tsai, Michael, Prof, Coresh, Josef, Prof, Psaty, Bruce M, Prof, Hakonarson, Hakon, Prof, Dudbridge, Frank, PhD, Humphries, Steve E, Prof, Timpson, Nicholas J, PhD, Langenberg, Claudia, MD, Asselbergs, Folkert W, MD, Voevoda, Mikhail, Prof, Bobak, Martin, Prof, Pikhart, Hynek, PhD, Reiner, Alex P, Prof, Keating, Brendan J, PhD, Hingorani, Aroon D, Prof, Sattar, Naveed, Prof

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Manifesto for new directions in developmental science von Barbot, Baptiste, Hein, Sascha, Trentacosta, Christopher, Beckmann, Jens F, u.a

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Manifesto for new directions in developmental science von Barbot, Baptiste, Hein, Sascha, Trentacosta, Christopher, Beckmann, Jens F, Bick, Johanna, Crocetti, Elisabetta, Liu, Yangyang, Rao, Sylvia Fernandez, Liew, Jeffrey, Overbeek, Geertjan, Ponguta, Liliana A, Scheithauer, Herbert, Super, Charles, Arnett, Jeffrey, Bukowski, William, Cook, Thomas D, Cote, James, Eccles, Jacquelynne S, Eid, Michael, Hiraki, Kazuo, Johnson, Mark, Juang, Linda, Landi, Nicole, Leckman, James, McCardle, Peggy, Mulvey, Kelly Lynn, Piquero, Alex R, Preiss, David D, Siegler, Robert, Soenens, Bart, Yousafzai, Aisha Khizar, Bornstein, Marc H, Cooper, Catherine R, Goossens, Luc, Harkness, Sara, van IJzendoorn, Marinus H

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Phenome-wide association analysis of LDL-cholesterol lowering genetic variants in PCSK9 von Holmes, MV, Preiss, D, Swerdlow, DI, Fatemifar, G, Faraway, R, Fairhurst-Hunter, Z, Hartwig, FP, Hypponen, E, Power, C, Van Iperen, E, Hovingh, K, Demuth, I, Steinhagen-Thiessen, E, Bertram, L, Willeit, K, Mason, D, Wright, J, Morris, R, Whincup, P, Price, JF, Kivimaki, M, Sanchez-Galvez, A, Van der Schouw, YT, Fiorito, G, Guarrera, S, Sacerdote, C, Langenberg, C, Luan, J, Bobak, M, Pająk, A, Kubinova, R, Pikhart, H, Grarup, N, Jess, T, Humphries, SE, Brilliant, M, Hakonarson, H, Carrell, DS, McCarty, CA, Lester, KH, Roden, DM, Carty, C, Holliday, E, Scott, R, O'Donnell, M, Said, MA, Eppinga, RN, Verweij, N, Snieder, H, Lifelines Cohort authors, Christen, T, Mook-Kanamori, DO, ICBP Consortium, Lind, L, Pazoki, R, Hofman, A, Uitterlinden, A, Dehghan, A, Teumer, A, Baumeister, S, Lerch, MM, Völzke, H, Ward, J, Pell, JP, Christophersen, IE, Baranova, EV, Young, R, Ford, I, Campbell, A, Padmanabhan, S, Grobbee, DE, Froguel, P, Roussel, R, Cariou, B, Smart, M, Kumari, M, Seshadri, S, METASTROKE Consortium of the ISGC, Dale, C, Costa, RPE, Ridker, PM, Chasman, DI, Reiner, AP, Ritchie, MD, Labreche, K, Bondy, M, Law, P, Speedy, H, Allan, J, Went, M, Weinhold, N, Nilsson, B, Sud, A, Engert, A, Hansson, M, Hemingway, H, Asselbergs, FW, Houlston, R, Casas, JP, Hingorani, AD

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Phenome-wide association analysis of LDL-cholesterol lowering genetic variants in PCSK9 von Schmidt, Amand F, Swerdlow, Daniel I, Denaxas, Spiros, Faraway, Rupert, Finan, Chris, Fairhurst-Hunter, Zammy, Horta, Bernardo Lessa, Hypponen, Elina, Power, Christine, Van Iperen, Erik, Demuth, Ilja, Norman, Kristina, Steinhagen-Thiessen, Elisabeth, Demuth, Juri, Bertram, Lars, Lill, Christina M, Coassin, Stefan, Willeit, Johann, Kiechl, Stefan, Wanamethee, Goya, Whincup, Peter, Ben-Shlomo, Yoav, McLachlan, Stela, Welch, Catherine, Marques-Vidal, Pedro, Nicolaides, Andrew, Panayiotou, Andrie G, Onland-Moret, N. Charlotte, Van Der Schouw, Yvonne T, Matullo, Giuseppe, Fiorito, Giovanni, Guarrera, Simonetta, Sacerdote, Carlotta, Wareham, Nicholas J, Scott, Robert A, Bobak, Martin, Malyutina, Sofia, Grarup, Niels, Humphries, Steve E, Brilliant, Murray, Hakonarson, Hakon, Carrell, David S, McCarty, Catherine A, Lester, Kirchner H, Larson, Eric B, Crosslin, David R, De Andrade, Mariza, Denny, Joshua C, Carty, Cara, Hancock, Stephen, O'Donnell, Martin, Yusuf, Salim, Chong, Michael, Van Der Harst, Pim, Verweij, Niek, Snieder, Harold, Christen, Tim, Mook-Kanamori, D. O, Lind, Lars, Ingelsson, Erik, Pazoki, Raha, Franco, Oscar, Uitterlinden, Andre, Dehghan, Abbas, Teumer, Alexander, Baumeister, Sebastian, Dörr, Marcus, Völzke, Henry, Meade, Tom, Maitland-Van Der Zee, Anke H, Ford, Ian, Campbell, Archie, Froguel, Philippe, Thuillier, Dorothée, Bonnefond, Amélie, Kumari, Meena, Mahajan, Anubha, Hopewell, Jemma C, Seshadri, Sudha, Dale, Caroline, Costa, Rui Providencia E, Ridker, Paul M, Reiner, Alex P, Dobbins, Sara E, Labreche, Karim, Simon, Matthias, Bondy, Melissa, Law, Philip, Went, Molly, Weinhold, Niels, Morgan, Gareth, Sonneveld, Pieter, Nilsson, Björn, Goldschmidt, Hartmut, Engert, Andreas, Hansson, Markus, Hemingway, Harry, Asselbergs, Folkert W, Patel, Riyaz S, Casas, Juan P

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HMG-coenzyme A reductase inhibition, type 2 diabetes, and bodyweight: evidence from genetic analysis and randomised trials von Swerdlow, Daniel I, Preiss, David, Kuchenbaecker, Karoline B, Holmes, Michael V, Engmann, Jorgen E L, Shah, Tina, Sofat, Reecha, Stender, Stefan, Johnson, Paul C D, Scott, Robert A, Leusink, Maarten, Verweij, Niek, Sharp, Stephen J, Guo, Yiran, Giambartolomei, Claudia, Chung, Christina, Peasey, Anne, Amuzu, Antoinette, Li, KaWah, Palmen, Jutta, Howard, Philip, Cooper, Jackie A, Drenos, Fotios, Li, Yun R, Lowe, Gordon, Gallacher, John, Stewart, Marlene C W, Tzoulaki, Ioanna, Buxbaum, Sarah G, van der A, Daphne L, Forouhi, Nita G, Onland-Moret, N Charlotte, van der Schouw, Yvonne T, Schnabel, Renate B, Hubacek, Jaroslav A, Kubinova, Ruzena, Baceviciene, Migle, Tamosiunas, Abdonas, Pajak, Andrzej, Topor-Madry, Romanvan, Stepaniak, Urszula, Malyutina, Sofia, Baldassarre, Damiano, Sennblad, Bengt, Tremoli, Elena, de Faire, Ulf, der Zee, Anke H Maitland-van, Klungel, Olaf H, de Boer, Anthonius, Dale, Caroline, DIAGRAM Consortium, MAGIC Consortium, InterAct Consortium

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HMG-coenzyme A reductase inhibition, type 2 diabetes, and bodyweight: evidence from genetic analysis and randomised trials von Swerdlow, DI, Preiss, D, Holmes, MV, Engmann, JEL, Shah, T, Sofat, R, Stender, S, Scott, RA, Sharp, SJ, Guo, Y, Giambartolomei, C, Chung, C, Amuzu, A, Li, K, Palmen, J, Howard, P, Cooper, JA, Drenos, F, Li, YR, Lowe, G, Gallacher, J, Stewart, MCW, Tzoulaki, I, Forouhi, NG, Onland-Moret, NC, Van der Schouw, YT, Schnabel, RB, Kubinova, R, Baceviciene, M, Tamosiunas, A, Pajak, A, Topor-Madry, R, Stepaniak, U, Baldassarre, D, Tremoli, E, De Faire, U, Veglia, F, Ford, I, Jukema, JW, De Borst, GJ, Algra, A, De Boer, A, Eaton, CB, Robinson, JG, Duggan, D, Downs, JR, Gotto, AM, Keech, AC, Marchioli, R, Tognoni, G, Sever, PS, Waters, DD, Pedersen, TR, Amarenco, P, Nakamura, H, McMurray, JJV, Chasman, DI, Maggioni, AP, Ray, KK, Seshasai, SRK, Manson, JE, Whincup, PH, Morris, RW, Lawlor, DA, Smith, GD, Fornage, M, Siscovick, DS, Cushman, M, Kumari, M, Wareham, NJ, Verschuren, WMM, Redline, S, Patel, SR, Whittaker, JC, Hamsten, A, Delaney, JA, Gaunt, TR, Kuh, D, Hardy, R, Kathiresan, S, Brunner, EJ, Tybjaerg-Hansen, A, Marmot, MG, Krauss, RM, Tsai, M, Coresh, J, Psaty, BM, Hakonarson, H, Dudbridge, F, Humphries, SE, Talmud, PJ, Kivimaeki, M, Timpson, NJ, Voevoda, M, Bobak, M, Pikhart, H, Wilson, JG, Keating, BJ, Hingorani, AD, Sattar, N

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PCSK9 genetic variants and risk of type 2 diabetes: A mendelian randomisation study von Schmidt, Amand F, Holmes, Michael V, Fairhurst-Hunter, Zammy, Lyall, Donald M, Hartwig, Fernando Pires, Horta, Bernardo Lessa, Hyppönen, Elina, Power, Christine, Moldovan, Max, van Iperen, Erik, Steinhagen-Thiessen, Elisabeth, Demuth, Juri, Bertram, Lars, Liu, Tian, Coassin, Stefan, Willeit, Johann, Kiechl, Stefan, Willeit, Karin, Mason, Dan, Wright, John, Morris, Richard, Wanamethee, Goya, Whincup, Peter, Ben-Shlomo, Yoav, McLachlan, Stela, Price, Jackie F, Kivimaki, Mika, Sanchez-Galvez, Adelaida, Marques-Vidal, Pedro, Onland-Moret, N. Charlotte, van der Schouw, Yvonne T, Matullo, Giuseppe, Guarrera, Simonetta, Wareham, Nicholas J, Langenberg, Claudia, Scott, Robert, Malyutina, Sofia, Pajak, Andrzej, Kubinova, Ruzena, Tamosiunas, Abdonas, Pikhart, Hynek, Husemoen, Lise Lotte Nystrup, Grarup, Niels, Linneberg, Allan, Simonsen, Kenneth Starup, Humphries, Steve E, Hakonarson, Hakon, Carrell, David S, McCarty, Catherine A, Crosslin, David R, de Andrade, Mariza, Roden, Dan M, Denny, Joshua C, Carty, Cara, Hancock, Stephen, Attia, John, Holliday, Elizabeth, Donnell, Martin O, Yusuf, Salim, Chong, Michael, Said, M. Abdullah, Verweij, Niek, Snieder, Harold, Mook-Kanamori, Dennis O, Gustafsson, Stefan, Lind, Lars, Ingelsson, Erik, Franco, Oscar, Dehghan, Abbas, Teumer, Alexander, Baumeister, Sebastian, Dörr, Marcus, Lerch, Markus M, Völzke, Henry, Ward, Joey, Pell, Jill P, Smith, Daniel J, Maitland-van der Zee, Anke H, Baranova, Ekaterina V, Young, Robin, Ford, Ian, Campbell, Archie, Padmanabhan, Sandosh, Bots, Michiel L, Froguel, Philippe, Thuillier, Dorothée, Balkau, Beverley, Cariou, Bertrand, Smart, Melissa, Kumari, Meena, Mahajan, Anubha, Ridker, Paul M, Reiner, Alex P, Lange, Leslie A, Ritchie, Marylyn D, Asselbergs, Folkert W, Casas, Juan Pablo, Keating, Brendan J, Preiss, David, Sattar, Naveed

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PCSK9 genetic variants and risk of type 2 diabetes: a mendelian randomisation study von Swerdlow, DI, Holmes, MV, Fairhurst-Hunter, Z, Lyall, DM, Hartwig, FP, Horta, BL, Hypponen, E, Moldovan, M, Van Iperen, E, Hovingh, GK, Demuth, I, Norman, K, Steinhagen-Thiessen, E, Demuth, J, Coassin, S, Willeit, J, Kiechl, S, Willeit, K, Wright, J, Morris, R, Wanamethee, G, McLachlan, S, Price, JF, Kivimaki, M, Welch, C, Marques-Vidal, P, Nicolaides, A, Panayiotou, AG, Onland-Moret, NC, Van der Schouw, YT, Matullo, G, Fiorito, G, Sacerdote, C, Wareham, NJ, Langenberg, C, Luan, J, Malyutina, SA, Pajak, A, Tamosiunas, A, Hansen, T, Linneberg, A, Simonsen, KS, Cooper, J, Humphries, SE, Brilliant, M, Kitchner, T, Hakonarson, H, Carrell, DS, McCarty, CA, Kirchner, HL, Larson, EB, De Andrade, M, Roden, DM, Hancock, S, Attia, J, Holliday, E, Donnell, MO, Yusuf, S, Chong, M, Pare, G, Van der Harst, P, Said, MA, Eppinga, RN, Verweij, N, Snieder, H, Christen, T, Mook-Kanamori, DO, Gustafsson, S, Ingelsson, E, Pazoki, R, Franco, O, Hofman, A, Baumeister, S, Doerr, M, Lerch, MM, Voelker, U, Ward, J, Pell, JP, Meade, T, Maitland-van der Zee, AH, Baranova, EV, Ford, I, Padmanabhan, S, Bots, ML, Grobbee, DE, Thuillier, D, Balkau, B, Bonnefond, A, Cariou, B, Smart, M, Bao, Y, Mahajan, A, Reiner, AP, Lange, LA, Ritchie, MD, Asselbergs, FW, Casas, J-P, Preiss, D, Hingorani, AD, Sattar, N

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PCSK9 genetic variants and risk of type 2 diabetes: a mendelian randomisation study von Schmidt, Amand F, Holmes, Michael V, Fairhurst-Hunter, Zammy, Lyall, Donald M, Hartwig, Fernando Pires, Power, Christine, Moldovan, Max, van Iperen, Erik, Hovingh, G Kees, Steinhagen-Thiessen, Elisabeth, Demuth, Juri, Bertram, Lars, Liu, Tian, Coassin, Stefan, Willeit, Johann, Kiechl, Stefan, Willeit, Karin, Mason, Dan, Wright, John, Morris, Richard, Wanamethee, Goya, Whincup, Peter, Ben-Shlomo, Yoav, McLachlan, Stela, Price, Jackie F, Kivimaki, Mika, Sanchez-Galvez, Adelaida, Marques-Vidal, Pedro, van der Schouw, Yvonne T, Matullo, Giuseppe, Guarrera, Simonetta, Wareham, Nicholas J, Langenberg, Claudia, Scott, Robert, Malyutina, Sofia, Pająk, Andrzej, Kubinova, Ruzena, Tamosiunas, Abdonas, Pikhart, Hynek, Husemoen, Lise Lotte Nystrup, Grarup, Niels, Linneberg, Allan, Simonsen, Kenneth Starup, Humphries, Steve E, Carrell, David S, McCarty, Catherine A, Crosslin, David R, de Andrade, Mariza, Roden, Dan M, Denny, Joshua C, Carty, Cara, Hancock, Stephen, Attia, John, Holliday, Elizabeth, O'Donnell, Martin, Yusuf, Salim, Chong, Michael, Said, M Abdullah, Verweij, Niek, Snieder, Harold, LifeLines Cohort study group, Christen, Tim, Mook-Kanamori, Dennis O, Lind, Lars, Ingelsson, Erik, Pazoki, Raha, Franco, Oscar, Hofman, Albert, Uitterlinden, Andre, Dehghan, Abbas, Teumer, Alexander, Dörr, Marcus, Lerch, Markus M, Völker, Uwe, Ward, Joey, Pell, Jill P, Meade, Tom, Maitland-van der Zee, Anke H, Baranova, Ekaterina V, Young, Robin, Ford, Ian, Campbell, Archie, Padmanabhan, Sandosh, Bots, Michiel L, Grobbee, Diederick E, Froguel, Philippe, Thuillier, Dorothée, Balkau, Beverley, Bonnefond, Amélie, Cariou, Bertrand, Smart, Melissa, Bao, Yanchun, Kumari, Meena, Mahajan, Anubha, Chasman, Daniel I, Ritchie, Marylyn D, Casas, Juan-Pablo, Preiss, David, Hingorani, Aroon D, Sattar, Naveed

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Concurrent Oral 1 - Therapy of rheumatic disease: OP4. Effectiveness of Rituximab in Rheumatoid Arthritis: Results from the British Society for Rheumatology Biologics Register (BSR... von Soliman, M. M., Ashcroft, D. M., Watson, K. D., Lunt, M., Symmons, D., Hyrich, K. L., Lachmann, H. J., Quartier, P., Hachulla, E., Gattorno, M., Cartwright, R., Kone-Paut, I., Zulian, F., Weisbarth-Riedel, E., Lepore, L., Hoyer, J., Foeldvari, I., Ramos, E., Leslie, K., Krammer, G., Preiss, R., Incera, E., Kuemmerle-Deschner, J. B., Hawkins, P. N., So, A., De Meulemeester, M., Pikhlak, A., Yucel, A. E., Bodalia, B., Kerrane, J., Arulmani, U., Richard, D., Murphy, V., Sallstig, P., Schlesinger, N., Christidis, D., Hassan, N., Mapplebeck, S., Dasgupta, B., Genovese, M. C., Sebba, A., Rubbert-Roth, A., Scali, J., Zilberstein, M., ` Vernon, E., Vollenhoven, R., Choy, E., White-Alao, B., Ibrahim, F., Kowalczyk, A., Gordon, P., Hakim, A., Kitas, G., Isenberg, D., Griffiths, B., Lecky, B., Chakravarty, K., Winer, J., Danko, K., Cooper, R. G., Scott, D. L.

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Phenome-wide association analysis of LDL-cholesterol lowering genetic variants in PCSK9 von Holmes, MV, Preiss, D, Fatemifar, G, Faraway, R, Fairhurst-Hunter, Z, Hartwig, FP, Hypponen, E, Power, C, van Iperen, E, Hovingh, K, Demuth, I, Steinhagen-Thiessen, E, Bertram, L, Willeit, K, Mason, D, Wright, J, Morris, R, Whincup, P, Price, JF, Kivimaki, M, Sanchez-Galvez, A, van der Schouw, YT, Fiorito, G, Guarrera, S, Sacerdote, C, Langenberg, C, Luan, J, Bobak, M, Pająk, A, Kubinova, R, Pikhart, H, Grarup, N, Jess, T, Humphries, SE, Brilliant, M, Hakonarson, H, Carrell, DS, McCarty, CA, Lester, KH, de Andrade, M, Roden, DM, Carty, C, Holliday, E, Scott, R, O'Donnell, M, van der Harst, P, Said, MA, Eppinga, RN, Verweij, N, Snieder, H, Lifelines Cohort authors, Christen, T, Mook-Kanamori, DO, ICBP Consortium, Lind, L, Pazoki, R, Hofman, A, Uitterlinden, A, Dehghan, A, Teumer, A, Baumeister, S, Lerch, MM, Völzke, H, Ward, J, Pell, JP, Christophersen, IE, Baranova, EV, Young, R, Ford, I, Campbell, A, Padmanabhan, S, Grobbee, DE, Froguel, P, Roussel, R, Cariou, B, Smart, M, Kumari, M, Seshadri, S, METASTROKE Consortium of the ISGC, Dale, C, Costa, RPE, Ridker, PM, Chasman, DI, Reiner, AP, Ritchie, MD, Labreche, K, Bondy, M, Law, P, Speedy, H, Went, M, Weinhold, N, Nilsson, B, Sud, A, Engert, A, Hansson, M, Hemingway, H, Asselbergs, FW, Houlston, R, Casas, JP, Hingorani, AD

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Phenome-wide association analysis of LDL-cholesterol lowering genetic variants in PCSK9 von Schmidt, Amand F, Swerdlow, Daniel I, Denaxas, Spiros, Faraway, Rupert, Finan, Chris, Fairhurst-Hunter, Zammy, Horta, Bernardo Lessa, Hypponen, Elina, Power, Christine, van Iperen, Erik, Demuth, Ilja, Norman, Kristina, Steinhagen-Thiessen, Elisabeth, Demuth, Juri, Bertram, Lars, Lill, Christina M, Coassin, Stefan, Willeit, Johann, Kiechl, Stefan, Wanamethee, Goya, Whincup, Peter, Ben-Shlomo, Yoav, McLachlan, Stela, Welch, Catherine, Marques-Vidal, Pedro, Nicolaides, Andrew, Panayiotou, Andrie G, Onland-Moret, N. Charlotte, Matullo, Giuseppe, Fiorito, Giovanni, Guarrera, Simonetta, Sacerdote, Carlotta, Wareham, Nicholas J, Scott, Robert A, Luan, Jian’an, Bobak, Martin, Malyutina, Sofia, Pająk, Andrzej, Grarup, Niels, Humphries, Steve E, Brilliant, Murray, Hakonarson, Hakon, Carrell, David S, McCarty, Catherine A, Lester, Kirchner H, Larson, Eric B, Crosslin, David R, de Andrade, Mariza, Denny, Joshua C, Carty, Cara, Hancock, Stephen, Yusuf, Salim, Chong, Michael, van der Harst, Pim, Verweij, Niek, Snieder, Harold, Christen, Tim, Mook-Kanamori, D. O, Lind, Lars, Ingelsson, Erik, Pazoki, Raha, Franco, Oscar, Uitterlinden, Andre, Dehghan, Abbas, Teumer, Alexander, Baumeister, Sebastian, Dörr, Marcus, Völzke, Henry, Meade, Tom, Maitland-van der Zee, Anke H, Ford, Ian, Campbell, Archie, Froguel, Philippe, Thuillier, Dorothée, Bonnefond, Amélie, Kumari, Meena, Mahajan, Anubha, Hopewell, Jemma C, Seshadri, Sudha, Dale, Caroline, Costa, Rui Providencia E, Ridker, Paul M, Reiner, Alex P, Dobbins, Sara E, Labreche, Karim, Simon, Matthias, Bondy, Melissa, Law, Philip, Went, Molly, Weinhold, Niels, Morgan, Gareth, Sonneveld, Pieter, Nilsson, Björn, Goldschmidt, Hartmut, Engert, Andreas, Hansson, Markus, Hemingway, Harry, Asselbergs, Folkert W, Patel, Riyaz S, Casas, Juan P

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Phenome-wide association analysis of LDL-cholesterol lowering genetic variants in PCSK9 von Schmidt, Amand F, Swerdlow, Daniel I, Denaxas, Spiros, Faraway, Rupert, Finan, Chris, Fairhurst-Hunter, Zammy, Horta, Bernardo Lessa, Hypponen, Elina, Power, Christine, van Iperen, Erik, Demuth, Ilja, Norman, Kristina, Steinhagen-Thiessen, Elisabeth, Demuth, Juri, Bertram, Lars, Lill, Christina M, Coassin, Stefan, Willeit, Johann, Kiechl, Stefan, Wanamethee, Goya, Whincup, Peter, Ben-Shlomo, Yoav, McLachlan, Stela, Welch, Catherine, Marques-Vidal, Pedro, Nicolaides, Andrew, Panayiotou, Andrie G, Onland-Moret, N Charlotte, Fiorito, Giovanni, Guarrera, Simonetta, Sacerdote, Carlotta, Wareham, Nicholas J, Scott, Robert A, Luan, Jian'an, Bobak, Martin, Malyutina, Sofia, Pająk, Andrzej, Grarup, Niels, Humphries, Steve E, Brilliant, Murray, Carrell, David S, McCarty, Catherine A, Lester, Kirchner H, Larson, Eric B, Crosslin, David R, de Andrade, Mariza, Denny, Joshua C, Carty, Cara, Hancock, Stephen, O'Donnell, Martin, Yusuf, Salim, Chong, Michael, van der Harst, Pim, Verweij, Niek, Snieder, Harold, Lifelines Cohort authors, Mook-Kanamori, DO, ICBP Consortium, Ingelsson, Erik, Pazoki, Raha, Hofman, Albert, Teumer, Alexander, Baumeister, Sebastian, Dörr, Marcus, Lerch, Markus M, Völker, Uwe, Völzke, Henry, Pell, Jill P, Christophersen, Ingrid E, Baranova, Ekaterina V, Young, Robin, Bots, Michiel L, Grobbee, Diederick E, Froguel, Philippe, Roussel, Ronan, Bonnefond, Amélie, Cariou, Bertrand, Bao, Yanchun, METASTROKE Consortium of the ISGC, Dale, Caroline, Costa, Rui Providencia E, Chasman, Daniel I, Reiner, Alex P, Lange, Leslie A, Dobbins, Sara E, Labreche, Karim, Simon, Matthias, Bondy, Melissa, Speedy, Helen, Allan, James, Weinhold, Niels, Morgan, Gareth, Sonneveld, Pieter, Goldschmidt, Hartmut, Engert, Andreas, Hansson, Markus, Hemingway, Harry, Asselbergs, Folkert W, Patel, Riyaz S, Hingorani, Aroon D

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Phenome-wide association analysis of LDL-cholesterol lowering genetic variants in PCSK9 von Schmidt, Amand F, Swerdlow, Daniel I, Denaxas, Spiros, Faraway, Rupert, Finan, Chris, Fairhurst-Hunter, Zammy, Horta, Bernardo Lessa, Hypponen, Elina, Power, Christine, van Iperen, Erik, Demuth, Ilja, Norman, Kristina, Steinhagen-Thiessen, Elisabeth, Demuth, Juri, Bertram, Lars, Lill, Christina M, Coassin, Stefan, Willeit, Johann, Kiechl, Stefan, Wanamethee, Goya, Whincup, Peter, Ben-Shlomo, Yoav, McLachlan, Stela, Welch, Catherine, Marques-Vidal, Pedro, Nicolaides, Andrew, Panayiotou, Andrie G, Onland-Moret, N. Charlotte, Matullo, Giuseppe, Fiorito, Giovanni, Guarrera, Simonetta, Sacerdote, Carlotta, Wareham, Nicholas J, Scott, Robert A, Luan, Jian'an, Bobak, Martin, Malyutina, Sofia, Grarup, Niels, Humphries, Steve E, Brilliant, Murray, Hakonarson, Hakon, Carrell, David S, McCarty, Catherine A, Lester, Kirchner H, Larson, Eric B, Crosslin, David R, de Andrade, Mariza, Denny, Joshua C, Carty, Cara, Hancock, Stephen, O'Donnell, Martin, Yusuf, Salim, Chong, Michael, van der Harst, Pim, Verweij, Niek, Snieder, Harold, Christen, Tim, Mook-Kanamori, D. O, Lind, Lars, Ingelsson, Erik, Pazoki, Raha, Franco, Oscar, Uitterlinden, Andre, Dehghan, Abbas, Teumer, Alexander, Baumeister, Sebastian, Voelker, Uwe, Voelzke, Henry, Meade, Tom, Maitland-van der Zee, Anke H, Ford, Ian, Campbell, Archie, Froguel, Philippe, Thuillier, Dorothee, Bonnefond, Amelie, Kumari, Meena, Mahajan, Anubha, Hopewell, Jemma C, Seshadri, Sudha, Dale, Caroline, Costa, Rui Providencia E, Ridker, Paul M, Reiner, Alex P, Dobbins, Sara E, Labreche, Karim, Simon, Matthias, Bondy, Melissa, Law, Philip, Went, Molly, Weinhold, Niels, Morgan, Gareth, Sonneveld, Pieter, Nilsson, Bjorn, Goldschmidt, Hartmut, Engert, Andreas, Hansson, Markus, Hemingway, Harry, Asselbergs, Folkert W, Patel, Riyaz S, Casas, Juan P

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Phenome-wide association analysis of LDL-cholesterol lowering genetic variants in PCSK9 von Schmidt, Amand F, Swerdlow, Daniel I, Denaxas, Spiros, Faraway, Rupert, Finan, Chris, Fairhurst-Hunter, Zammy, Hartwig, Fernando P, Horta, Bernardo L, Hypponen, Elina, Power, Christine, van Iperen, Erik, Demuth, Ilja, Norman, Kristina, Steinhagen-Thiessen, Elisabeth, Demuth, Juri, Bertram, Lars, Lill, Christina M, Coassin, Stefan, Willeit, Johann, Kiechl, Stefan, Wanamethee, Goya, Whincup, Peter, Ben-Shlomo, Yoav, McLachlan, Stela, Welch, Catherine, Marques-Vidal, Pedro, Nicolaides, Andrew, Panayiotou, Andrie G, Onland-Moret, N. C, Matullo, Giuseppe, Fiorito, Giovanni, Guarrera, Simonetta, Sacerdote, Carlotta, Wareham, Nicholas J, Scott, Robert A, Luan, Jian’an, Bobak, Martin, Malyutina, Sofia, Pająk, Andrzej, Grarup, Niels, Humphries, Steve E, Brilliant, Murray, Carrell, David S, McCarty, Catherine A, Lester, Kirchner H, Larson, Eric B, Crosslin, David R, de Andrade, Mariza, Denny, Joshua C, Carty, Cara, Hancock, Stephen, Yusuf, Salim, Chong, Michael, van der Harst, Pim, Said, M. A, Verweij, Niek, Snieder, Harold, Christen, Tim, Mook-Kanamori, D. O, Lind, Lars, Ingelsson, Erik, Pazoki, Raha, Franco, Oscar, Uitterlinden, Andre, Dehghan, Abbas, Teumer, Alexander, Baumeister, Sebastian, Dörr, Marcus, Völzke, Henry, Meade, Tom, Maitland-van der Zee, Anke H, Ford, Ian, Campbell, Archie, Froguel, Philippe, Bonnefond, Amélie, Kumari, Meena, Mahajan, Anubha, Hopewell, Jemma C, Seshadri, Sudha, Dale, Caroline, Costa, Rui P E, Ridker, Paul M, Reiner, Alex P, Dobbins, Sara E, Labreche, Karim, Simon, Matthias, Bondy, Melissa, Law, Philip, Went, Molly, Weinhold, Niels, Morgan, Gareth, Sonneveld, Pieter, Nilsson, Björn, Goldschmidt, Hartmut, Engert, Andreas, Hansson, Markus, Hemingway, Harry, Asselbergs, Folkert W, Patel, Riyaz S, Casas, Juan P

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PCSK9 genetic variants and risk of type 2 diabetes: a mendelian randomisation study von Swerdlow, DI, Holmes, MV, Fairhurst-Hunter, Z, Lyall, DM, Hartwig, FP, Horta, BL, Hyppönen, E, Moldovan, M, Hovingh, GK, Demuth, I, Norman, K, Steinhagen-Thiessen, E, Demuth, J, Coassin, S, Willeit, J, Kiechl, S, Willeit, K, Wright, J, Morris, R, Wanamethee, G, McLachlan, S, Price, JF, Kivimaki, M, Welch, C, Marques-Vidal, P, Nicolaides, A, Panayiotou, AG, Onland-Moret, NC, van der Schouw, YT, Matullo, G, Fiorito, G, Sacerdote, C, Wareham, NJ, Langenberg, C, Luan, J, Malyutina, S, Pająk, A, Tamosiunas, A, Hansen, T, Linneberg, A, Simonsen, KS, Cooper, J, Humphries, SE, Brilliant, M, Kitchner, T, Hakonarson, H, Carrell, DS, McCarty, CA, Kirchner, HL, Larson, EB, Roden, DM, Hancock, S, Attia, J, Holliday, E, O'Donnell, M, Yusuf, S, Chong, M, Pare, G, van der Harst, P, Said, MA, Eppinga, RN, Verweij, N, Snieder, H, LifeLines Cohort study group, Lind, L, Ingelsson, E, Franco, O, Hofman, A, Uitterlinden, A, Dehghan, A, Teumer, A, Dörr, M, Lerch, MM, Pell, JP, Smith, DJ, Meade, T, Maitland-van der Zee, AH, Baranova, EV, Young, R, Ford, I, Campbell, A, Bots, ML, Grobbee, DE, Froguel, P, Thuillier, D, Balkau, B, Bao, Y, Kumari, M, Mahajan, A, Ridker, PM, Chasman, DI, Reiner, AP, Lange, LA, Ritchie, MD, Asselbergs, FW, Casas, J-P, Keating, BJ, Preiss, D, Hingorani, AD, Sattar, N

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