Knowledge as a Service at the Point of Care von Shellum, Jane L, Freimuth, Robert R, Peters, Steve G, Nishimura, Rick A, Chaudhry, Rajeev, Demuth, Steve J, Knopp, Amy L, Miksch, Timothy A, Milliner, Dawn S

Volltext

Detection of Hypertrophic Cardiomyopathy Using a Convolutional Neural Network-Enabled Electrocardiogram von Ko, Wei-Yin, Siontis, Konstantinos C., Attia, Zachi I., Carter, Rickey E., Kapa, Suraj, Ommen, Steve R., Demuth, Steven J., Ackerman, Michael J., Gersh, Bernard J., Arruda-Olson, Adelaide M., Geske, Jeffrey B., Asirvatham, Samuel J., Lopez-Jimenez, Francisco, Nishimura, Rick A., Friedman, Paul A., Noseworthy, Peter A.

Volltext

Phenome-wide association analysis of LDL-cholesterol lowering genetic variants in PCSK9 von Schmidt, Amand F, Holmes, Michael V, Preiss, David, Swerdlow, Daniel I, 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 M, 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, Welch, Catherine, Sanchez-Galvez, Adelaida, 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, Langenberg, Claudia, Scott, Robert A, 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 E, Brilliant, Murray, Kitchner, Terrie, Hakonarson, Hakon, Carrell, David S, McCarty, Catherine A, Lester, Kirchner H, Larson, Eric B, Crosslin, David R, de Andrade, Mariza, Roden, Dan M, Denny, Joshua C, 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 N, Verweij, Niek, Snieder, Harold, Christen, Tim, Mook-Kanamori, D O, Gustafsson, Stefan, Lind, Lars, Ingelsson, Erik, Pazoki, Raha, Franco, Oscar, Hofman, Albert, Uitterlinden, Andre, Dehghan, Abbas

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, 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

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