Systems and methods for providing image portions for progressive images von Sacerdote, David Andrew, Larumbe, Federico Daniel, Berenger, Georges Edouard Maurice

Volltext bestellen

Systems and methods for providing progressive images based on data range requests von Sacerdote, David Andrew, Larumbe, Federico Daniel, Berenger, Georges Edouard Maurice

Volltext bestellen

SYSTEMS AND METHODS FOR PROVIDING PROGRESSIVE IMAGES BASED ON DATA RANGE REQUESTS von Berenger Georges Edouard Maurice, Larumbe Federico Daniel, Sacerdote David Andrew

Volltext bestellen

SYSTEMS AND METHODS FOR PROVIDING IMAGE PORTIONS FOR PROGRESSIVE IMAGES von Berenger Georges Edouard Maurice, Larumbe Federico Daniel, Sacerdote David Andrew

Volltext bestellen

Integrative genomic analysis implicates limited peripheral adipose storage capacity in the pathogenesis of human insulin resistance von Lotta, Luca A, Gulati, Pawan, Day, Felix R, Payne, Felicity, Ongen, Halit, van de Bunt, Martijn, Gaulton, Kyle J, Eicher, John D, Sharp, Stephen J, Luan, Jian'an, De Lucia Rolfe, Emanuella, Stewart, Isobel D, Wheeler, Eleanor, Willems, Sara M, Adams, Claire, Yaghootkar, Hanieh, Forouhi, Nita G, Khaw, Kay-Tee, Johnson, Andrew D, Semple, Robert K, Frayling, Timothy, Perry, John R B, Dermitzakis, Emmanouil, McCarthy, Mark I, Barroso, Inês, Wareham, Nicholas J, Savage, David B, Langenberg, Claudia, O'Rahilly, Stephen, Scott, Robert A

Volltext

Parent-of-origin-specific allelic associations among 106 genomic loci for age at menarche von Perry, John R. B., Ferreira, Teresa, Chasman, Daniel I., Esko, Tõnu, Thorleifsson, Gudmar, Albrecht, Eva, Ang, Wei Q., Corre, Tanguy, Cousminer, Diana L., Franceschini, Nora, Ganna, Andrea, Johnson, Andrew D., Kjellqvist, Sanela, Lunetta, Kathryn L., Porcu, Eleonora, Teumer, Alexander, Tikkanen, Emmi, Hottenga, Jouke-Jan, Pers, Tune H., Yerges-Armstrong, Laura M., Hua Zhao, Jing, Andrulis, Irene L., Anton-Culver, Hoda, Benitez, Javier, Blomqvist, Carl, Bolla, Manjeet K., Brenner, Hermann, Chang-Claude, Jenny, Chanock, Stephen, Chen, Jinhui, Chenevix-Trench, Georgia, Collée, J. Margriet, Davey Smith, George, Demerath, Ellen W., Dieffenbach, Aida K., Eriksson, Johan G., Flyger, Henrik, Franke, Lude, Gudbjartsson, Daniel F., Gudnason, Vilmundur, Guénel, Pascal, Guo, Suiqun, Hall, Per, Hartman, Catharina A., Heath, Andrew C., Hofman, Albert, Hooning, Maartje J., Hu, Frank B., Karasik, David, Kiel, Douglas P., Knight, Julia A., Kutalik, Zoltan, Lambrechts, Diether, Lindblom, Annika, Mägi, Reedik, Mannermaa, Arto, Martin, Nicholas G., Masson, Gisli, McArdle, Patrick F., Mihailov, Evelin, Nohr, Ellen A., Oostra, Ben A., Peacock, Munro, Peterlongo, Paolo, Peto, Julian, Postma, Dirkje S., Radice, Paolo, Rivadeneira, Fernando, Rose, Lynda M., Rudolph, Anja, Schlessinger, David, Sovio, Ulla, Tyrer, Jonathan, Vollenweider, Peter, Winqvist, Robert, Wolffenbuttel, Bruce H. R., Wright, Margaret J., Econs, Michael J., Loos, Ruth J. F., McCarthy, Mark I., Montgomery, Grant W., Rice, John P., Thorsteinsdottir, Unnur, van Duijn, Cornelia M., Alizadeh, Behrooz Z., Bergmann, Sven, Boerwinkle, Eric, Crisponi, Laura, Gasparini, Paolo, Gieger, Christian, Järvelin, Marjo-Riitta, Kraft, Peter, Ridker, Paul M., Snieder, Harold, Sørensen, Thorkild I. A., Spector, Tim D., Uitterlinden, André G., Zygmunt, Marek, Murray, Anna, Ong, Ken K.

Volltext

Alcohol and lung cancer risk among never smokers: A pooled analysis from the international lung cancer consortium and the SYNERGY study von Fehringer, Gordon, Brenner, Darren R., Zhang, Zuo‐Feng, Lee, Yuan‐Chin Amy, Matsuo, Keitaro, Ito, Hidemi, Lan, Qing, Vineis, Paolo, Johansson, Mattias, Overvad, Kim, Riboli, Elio, Trichopoulou, Antonia, Sacerdote, Carlotta, Stucker, Isabelle, Boffetta, Paolo, Brennan, Paul, Christiani, David. C., Hong, Yun‐Chul, Landi, Maria Teresa, Morgenstern, Hal, Schwartz, Ann G., Wenzlaff, Angela S., Rennert, Gad, McLaughlin, John R., Harris, Curtis C., Olivo‐Marston, Susan, Orlow, Irene, Park, Bernard J., Zauderer, Marjorie, Barros Dios, Juan M., Ruano Raviña, Alberto, Siemiatycki, Jack, Koushik, Anita, Lazarus, Philip, Fernández‐Somoano, Ana, Tardon, Adonina, Le Marchand, Loic, Brenner, Hermann, Saum, Kai‐Uwe, Duell, Eric J., Andrew, Angeline S., Szeszenia‐Dabrowska, Neonila, Lissowska, Jolanta, Zaridze, David, Rudnai, Peter, Fabianova, Eleonora, Mates, Dana, Foretova, Lenka, Janout, Vladimir, Bencko, Vladimir, Holcatova, Ivana, Pesatori, Angela Cecilia, Consonni, Dario, Olsson, Ann, Straif, Kurt, Hung, Rayjean J.

Volltext

Four novel Loci (19q13, 6q24, 12q24, and 5q14) influence the microcirculation in vivo von Ikram, M Kamran, Sim, Xueling, Xueling, Sim, Jensen, Richard A, Cotch, Mary Frances, Hewitt, Alex W, Ikram, M Arfan, Wang, Jie Jin, Klein, Ronald, Klein, Barbara E K, Breteler, Monique M B, Cheung, Ning, Liew, Gerald, Mitchell, Paul, Uitterlinden, Andre G, Rivadeneira, Fernando, Hofman, Albert, de Jong, Paulus T V M, van Duijn, Cornelia M, Kao, Linda, Cheng, Ching-Yu, Smith, Albert Vernon, Glazer, Nicole L, Lumley, Thomas, McKnight, Barbara, Psaty, Bruce M, Jonasson, Fridbert, Eiriksdottir, Gudny, Aspelund, Thor, Harris, Tamara B, Launer, Lenore J, Taylor, Kent D, Li, Xiaohui, Iyengar, Sudha K, Xi, Quansheng, Sivakumaran, Theru A, Mackey, David A, Macgregor, Stuart, Martin, Nicholas G, Young, Terri L, Bis, Josh C, Wiggins, Kerri L, Heckbert, Susan R, Hammond, Christopher J, Andrew, Toby, Fahy, Samantha, Attia, John, Holliday, Elizabeth G, Scott, Rodney J, Islam, F M Amirul, Rotter, Jerome I, McAuley, Annie K, Boerwinkle, Eric, Tai, E Shyong, Gudnason, Vilmundur, Siscovick, David S, Vingerling, Johannes R, Wong, Tien Y

Volltext

Rare coding variants and X-linked loci associated with age at menarche von Lunetta, Kathryn L., Day, Felix R., Sulem, Patrick, Ruth, Katherine S., Tung, Joyce Y., Hinds, David A., Esko, Tõnu, Elks, Cathy E., Altmaier, Elisabeth, He, Chunyan, Huffman, Jennifer E., Mihailov, Evelin, Porcu, Eleonora, Robino, Antonietta, Rose, Lynda M., Schick, Ursula M., Stolk, Lisette, Teumer, Alexander, Thompson, Deborah J., Traglia, Michela, Wang, Carol A., Yerges-Armstrong, Laura M., Antoniou, Antonis C., Barbieri, Caterina, Coviello, Andrea D., Cucca, Francesco, Demerath, Ellen W., Dunning, Alison M., Gandin, Ilaria, Grove, Megan L., Gudbjartsson, Daniel F., Hocking, Lynne J., Hofman, Albert, Huang, Jinyan, Jackson, Rebecca D., Karasik, David, Kriebel, Jennifer, Lange, Ethan M., Lange, Leslie A., Langenberg, Claudia, Li, Xin, Luan, Jian'an, Mägi, Reedik, Morrison, Alanna C., Padmanabhan, Sandosh, Pirie, Ailith, Polasek, Ozren, Porteous, David, Reiner, Alex P., Rivadeneira, Fernando, Rudan, Igor, Sala, Cinzia F., Schlessinger, David, Scott, Robert A., Stöckl, Doris, Visser, Jenny A., Völker, Uwe, Vozzi, Diego, Wilson, James G., Zygmunt, Marek, Boerwinkle, Eric, Buring, Julie E., Crisponi, Laura, Easton, Douglas F., Hayward, Caroline, Hu, Frank B., Liu, Simin, Metspalu, Andres, Pennell, Craig E., Ridker, Paul M., Strauch, Konstantin, Streeten, Elizabeth A., Toniolo, Daniela, Uitterlinden, André G., Ulivi, Sheila, Völzke, Henry, Wareham, Nicholas J., Wellons, Melissa, Franceschini, Nora, Chasman, Daniel I., Thorsteinsdottir, Unnur, Murray, Anna, Stefansson, Kari, Murabito, Joanne M., Ong, Ken K., Perry, John R. B.

Volltext

Phenome-wide association analysis of LDL-cholesterol lowering genetic variants in PCSK9 von Schmidt, Amand, Holmes, Michael, Preiss, David, Swerdlow, Daniel, Denaxas, Spiros, Fatemifar, Ghazaleh, Faraway, Rupert, Finan, Chris, Valentine, Dennis, Fairhurst-Hunter, Zammy, Hartwig, Fernando Pires, Horta, Bernardo Lessa, Hypponen, Elina, Power, Christine, Moldovan, Max, van Iperen, Erik, Hovingh, Kees, Demuth, Ilja, Norman, Kristina, Steinhagen-Thiessen, Elisabeth, Demuth, Juri, Bertram, Lars, Lill, Christina, 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, Kivimaki, Mika, Welch, Catherine, Sanchez-Galvez, Adelaida, Marques-Vidal, Pedro, Nicolaides, Andrew, Panayiotou, Andrie, Onland-Moret, N. Charlotte, van der Schouw, Yvonne, Matullo, Giuseppe, Fiorito, Giovanni, Guarrera, Simonetta, Sacerdote, Carlotta, Wareham, Nicholas, Langenberg, Claudia, Scott, Robert, Luan, Jian’an, Bobak, Martin, Malyutina, Sofia, Pająk, Andrzej, Kubinova, Ruzena, Tamosiunas, Abdonas, Pikhart, Hynek, Grarup, Niels, Pedersen, Oluf, Hansen, Torben, Linneberg, Allan, Jess, Tine, Cooper, Jackie, Humphries, Steve, Brilliant, Murray, Kitchner, Terrie, Hakonarson, Hakon, Carrell, David, Mccarty, Catherine, Lester, Kirchner, Larson, Eric, Crosslin, David, de Andrade, Mariza, Roden, Dan, Denny, Joshua, Carty, Cara, Hancock, Stephen, Attia, John, Holliday, Elizabeth, Scott, Rodney, Schofield, Peter, O’donnell, Martin, Yusuf, Salim, Chong, Michael, Pare, Guillaume, van der Harst, Pim, Said, M. Abdullah, Eppinga, Ruben, Verweij, Niek, Snieder, Harold, Christen, Tim, Mook-Kanamori, D., Gustafsson, Stefan, Lind, Lars, Ingelsson, Erik, Pazoki, Raha, Franco, Oscar, Hofman, Albert, Uitterlinden, Andre, Dehghan, Abbas

Volltext

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

Volltext

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

Volltext

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

Volltext

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

Volltext bestellen

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

Volltext bestellen

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

Volltext bestellen

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

Volltext bestellen

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, 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, 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, O'Donnell, Martin, 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

Volltext bestellen

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, Hypponen, 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, Sofi A, 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, Doerr, Marcus, Lerch, Markus M, Voelzke, 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, Balkau, Beverley, Cariou, Bertrand, Smart, Melissa, Kumari, Meena, Mahajan, Anubha, Ridker, Paul M, Chasman, Daniel I, Reiner, Alex P, Lange, Leslie A, Ritchie, Marylyn D, Asselbergs, Folkert W, Casas, Juan-Pablo, Keating, Brendan J, Preiss, David, Sattar, Naveed

Volltext bestellen

Additional file 1: of Phenome-wide association analysis of LDL-cholesterol lowering genetic variants in PCSK9 von Schmidt, Amand, Preiss, David, Faraway, Rupert, Valentine, Dennis, Fairhurst-Hunter, Zammy, Hartwig, Fernando, Power, Christine, Moldovan, Max, Hovingh, Kees, Demuth, Ilja, Norman, Kristina, Steinhagen-Thiessen, Elisabeth, Demuth, Juri, Lill, Christina, Coassin, Stefan, Willeit, Johann, Kiechl, Stefan, Willeit, Karin, Wright, John, Morris, Richard, Wanamethee, Goya, Kivimaki, Mika, Welch, Catherine, Sanchez-Galvez, Adelaida, Marques-Vidal, Pedro, Nicolaides, Andrew, Panayiotou, Andrie, Onland-Moret, N., Matullo, Giuseppe, Fiorito, Giovanni, Sacerdote, Carlotta, Wareham, Nicholas, Luan, Jian’an, Malyutina, Sofia, Kubinova, Ruzena, Tamosiunas, Abdonas, Pikhart, Hynek, Grarup, Niels, Pedersen, Oluf, Hansen, Torben, Linneberg, Allan, Cooper, Jackie, Carrell, David, Larson, Eric, Roden, Dan, Holliday, Elizabeth, Scott, Rodney, Chong, Michael, Pare, Guillaume, Said, M., Eppinga, Ruben, Verweij, Niek, Christen, Tim, Mook-Kanamori, D., Gustafsson, Stefan, Franco, Oscar, Hofman, Albert, Uitterlinden, Andre, Dehghan, Abbas, Teumer, Alexander, Baumeister, Sebastian, Dörr, Marcus, Völker, Uwe, Völzke, Henry, Ward, Joey, Pell, Jill, Maitland-van der Zee, Anke, Baranova, Ekaterina, Campbell, Archie, Padmanabhan, Sandosh, Bots, Michiel, Froguel, Philippe, Thuillier, Dorothée, Roussel, Ronan, Bonnefond, Amélie, Cariou, Bertrand, Smart, Melissa, Kumari, Meena, Ridker, Paul, Chasman, Daniel, Reiner, Alex, Lange, Leslie, Cornish, Alex, Dobbins, Sara, Kinnersley, Ben, Sanson, Marc, Simon, Matthias, Bondy, Melissa, Law, Philip, Allan, James, Li, Ni, Went, Molly, Morgan, Gareth, Goldschmidt, Hartmut, Sud, Amit, Engert, Andreas, Hansson, Markus, Houlston, Richard, Casas, Juan, Hingorani, Aroon

Volltext bestellen