Výsledky vyhledávání - Ruben N. Eppinga
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Phenome-wide association analysis of LDL-cholesterol lowering genetic variants in <i>PCSK9</i> Autor Amand F. Schmidt, Michael V. Holmes, David Preiss, Daniel I. Swerdlow, Spiros Denaxas, Ghazaleh Fatemifar, Rupert Faraway, Chris Finan, Tom Lumbers, Albert Henry, Dennis Valentine, Zammy Fairhurst-Hunter, Fernando Pires Hartwig, Bernardo Lessa Horta, Elina Hyppönen, Christine Power, Max Moldovan, Erik Van Iperen, Kees Hovingh, Ilja Demuth, Kristina Norman, Elisabeth Steinhagen‐Thiessen, Juri Demuth, Lars Bertram, Christina M. Lill, Stefan Coassin, Johann Willeit, Stefan Kiechl, Karin Willeit, Dan Mason, John Wright, Richard Morris, Goya Wanamethee, Peter H. Whincup, Yoav Ben‐Shlomo, Stela McLachlan, Jackie F. Price, Mika Kivimäki, Catherine Welch, Adelaida Sánchez-Gálvez, Pedro Marques‐Vidal, Andrew Nicolaides, Andrie G. Panayiotou, N. Charlotte Onland‐Moret, Yvonne T. van der Schouw, Giuseppe Matullo, Giovanni Fiorito, Simonetta Guarrera, Carlotta Sacerdote, Nicholas J. Wareham, Claudia Langenberg, Robert A. Scott, Jian’an Luan, Martin Bobák, Sofia Malyutina, Andrzej Pająk, Růžena Kubínová, Abdonas Tamošiūnas, Hynek Pikhart, Niels Grarup, Oluf Pedersen, Torben Hansen, Allan Linneberg, Tine Jess, Jackie A. Cooper, Steve E. Humphries, Murray H. Brilliant, Terrie Kitchner, Hákon Hákonarson, David Carrell, Catherine A. McCarty, Kirchner H. Lester, Eric B. Larson, David R. Crosslin, Mariza de Andrade, Dan M. Roden, Joshua C. Denny, Cara L. Carty, Stephen Hancock, John Attia, Elizabeth Holliday, Rodney J. Scott, Peter W. Schofield, Martin O’Donnell, Salim Yusuf, Michael Chong, Guillaume Paré, Pim van der Harst, M. Abdullah Said, Ruben N. Eppinga, Niek Verweij, Harold Snieder, Tim Christen, Dennis O. Mook‐Kanamori, Stefan Gustafsson, Lars Lind, Erik Ingelsson, Raha Pazoki, Oscar H. Franco, Albert Hofman
Vydáno 2018Pré-impressão -
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Phenome-wide association analysis of LDL-cholesterol lowering genetic variants in PCSK9 Autor Amand F. Schmidt, Michael V. Holmes, David Preiss, Daniel I. Swerdlow, Spiros Denaxas, Ghazaleh Fatemifar, Rupert Faraway, Chris Finan, Dennis Valentine, Zammy Fairhurst-Hunter, Fernando Pires Hartwig, Bernardo Lessa Horta, Elina Hyppönen, Christine Power, Max Moldovan, Erik Van Iperen, Kees Hovingh, Ilja Demuth, Kristina Norman, Elisabeth Steinhagen‐Thiessen, Juri Demuth, Lars Bertram, Christina M. Lill, Stefan Coassin, Johann Willeit, Stefan Kiechl, Karin Willeit, Dan Mason, John Wright, Richard Morris, Goya Wanamethee, Peter H. Whincup, Yoav Ben‐Shlomo, Stela McLachlan, Jackie F. Price, Mika Kivimäki, Catherine Welch, Adelaida Sánchez-Gálvez, Pedro Marques‐Vidal, Andrew Nicolaides, Andrie G. Panayiotou, N. Charlotte Onland‐Moret, Yvonne T. van der Schouw, Giuseppe Matullo, Giovanni Fiorito, Simonetta Guarrera, Carlotta Sacerdote, Nicholas J. Wareham, Claudia Langenberg, Robert A. Scott, Jian’an Luan, Martin Bobák, Sofia Malyutina, Andrzej Pająk, Růžena Kubínová, Abdonas Tamošiūnas, Hynek Pikhart, Niels Grarup, Oluf Pedersen, Torben Hansen, Allan Linneberg, Tine Jess, Jackie A. Cooper, Steve E. Humphries, Murray H. Brilliant, Terrie Kitchner, Hákon Hákonarson, David Carrell, Catherine A. McCarty, Kirchner H. Lester, Eric B. Larson, David R. Crosslin, Mariza de Andrade, Dan M. Roden, Joshua C. Denny, Cara L. Carty, Stephen Hancock, John Attia, Elizabeth G. Holliday, Rodney J. Scott, Peter W. Schofield, Martin O’Donnell, Salim Yusuf, Michael Chong, Guillaume Paré, Pim van der Harst, M. Abdullah Said, Ruben N. Eppinga, Niek Verweij, Harold Snieder, Tim Christen, Dennis O. Mook‐Kanamori, Stefan Gustafsson, Lars Lind, Erik Ingelsson, Raha Pazoki, Oscar H. Franco, Albert Hofman, André G. Uitterlinden, Abbas Dehghan
Vydáno 2019Artigo -
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PCSK9 genetic variants and risk of type 2 diabetes: a mendelian randomisation study Autor Amand F. Schmidt, Daniel I. Swerdlow, Michael V. Holmes, Riyaz Patel, Zammy Fairhurst-Hunter, Donald M. Lyall, Fernando Pires Hartwig, Bernardo Lessa Horta, Elina Hyppönen, Christine Power, Max Moldovan, Erik Van Iperen, G. Kees Hovingh, Ilja Demuth, Kristina Norman, Elisabeth Steinhagen‐Thiessen, Juri Demuth, Lars Bertram, Tian Liu, Stefan Coassin, Johann Willeit, Stefan Kiechl, Karin Willeit, Dan Mason, John Wright, Richard Morris, Goya Wanamethee, Peter H. Whincup, Yoav Ben‐Shlomo, Stela McLachlan, Jackie F. Price, Mika Kivimäki, Catherine Welch, Adelaida Sánchez-Gálvez, Pedro Marques‐Vidal, Andrew Nicolaides, Andrie G. Panayiotou, N. Charlotte Onland‐Moret, Yvonne T. van der Schouw, Giuseppe Matullo, Giovanni Fiorito, Simonetta Guarrera, Carlotta Sacerdote, Nicholas J. Wareham, Claudia Langenberg, Robert A. Scott, Jian’an Luan, Martin Bobák, Sofia Malyutina, Andrzej Pająk, Růžena Kubínová, Abdonas Tamošiūnas, Hynek Pikhart, Lise Lotte N. Husemoen, Niels Grarup, Oluf Pedersen, Torben Hansen, Allan Linneberg, Kenneth Starup Simonsen, Jackie A. Cooper, Steve E. Humphries, Murray H. Brilliant, Terrie Kitchner, Hákon Hákonarson, David Carrell, Catherine A. McCarty, H. Lester Kirchner, Eric B. Larson, David R. Crosslin, Mariza de Andrade, Dan M. Roden, Joshua C. Denny, Cara L. Carty, Stephen Hancock, John Attia, Elizabeth G. Holliday, Martin O’Donnell, Salim Yusuf, Michael Chong, Guillaume Paré, Pim van der Harst, M. Abdullah Said, Ruben N. Eppinga, Niek Verweij, Harold Snieder, Tim Christen, Dennis O. Mook‐Kanamori, Stefan Gustafsson, Lars Lind, Erik Ingelsson, Raha Pazoki, Oscar H. Franco, Albert Hofman, André G. Uitterlinden, Abbas Dehghan, Alexander Teumer, Sebastian E. Baumeister, Marcus Dörr, Markus M. Lerch, Uwe Völker
Vydáno 2016Artigo -
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Multiancestry Genome-Wide Association Study of Lipid Levels Incorporating Gene-Alcohol Interactions Autor Paul S. de Vries, Michael R. Brown, Amy R. Bentley, Yan V. Sun, Thomas W Winkler, Ιωάννα Ντάλλα, Karen Schwander, Aldi T. Kraja, Xiuqing Guo, Nora Franceschini, Ching‐Yu Cheng, Xueling Sim, Dina Vojinović, Jennifer E. Huffman, Solomon K. Musani, Changwei Li, Mary F. Feitosa, Melissa A. Richard, Raymond Noordam, Hugues Aschard, Traci M. Bartz, Lawrence F. Bielak, Xuan Deng, Rajkumar Dorajoo, Kurt K. Lohman, Man Li, Tuomo Rankinen, Albert V. Smith, Salman M. Tajuddin, Εvangelos Εvangelou, Mariaelisa Graff, Maris Alver, Mathilde Boissel, Jin Fang Chai, Xu Chen, Jasmin Divers, Ilaria Gandin, Chuan Gao, Anuj Goel, Yanick Hagemeijer, Sarah E. Harris, Fernando Pires Hartwig, Meian He, Andréa R. V. R. Horimoto, Fang‐Chi Hsu, Anne Jackson, Anuradhani Kasturiratne, Pirjo Komulainen, Brigitte Kühnel, Federica Laguzzi, Joseph H. Lee, Jian’an Luan, Leo‐Pekka Lyytikäinen, Nana Matoba, Ilja M. Nolte, Maik Pietzner, Muhammad Riaz, M. Abdullah Said, Robert A. Scott, Tamar Sofer, Alena Stančáková, Fumihiko Takeuchi, Bamidele O. Tayo, Peter J. van der Most, Tibor V. Varga, Yajuan Wang, Erin B. Ware, Wanqing Wen, Lisa R. Yanek, Weihua Zhang, Jing Hua Zhao, Saima Afaq, Najaf Amin, Marzyeh Amini, Dan E. Arking, Tin Aung, Christie M. Ballantyne, Eric Boerwinkle, Ulrich Broeckel, Archie Campbell, Mickaël Canouil, Charumathi Sabanayagam, Yii‐Der Ida Chen, John Connell, Ulf dé Fairé, Lisa de las Fuentes, Renée de Mutsert, H Janaka de Silva, Jingzhong Ding, Anna F. Dominiczak, Qing Duan, Charles B. Eaton, Ruben N. Eppinga, Jessica D. Faul, Virginia Fisher, Terrence Forrester, Oscar H. Franco, Yechiel Friedlander, Mohsen Ghanbari, Franco Giulianini
Vydáno 2019Revisão -
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Genetic insights into resting heart rate and its role in cardiovascular disease Autor Yordi J. van de Vegte, Ruben N. Eppinga, M. Yldau van der Ende, Yanick Hagemeijer, Yuvaraj Mahendran, Elias Salfati, Albert V. Smith, Vanessa Y. Tan, Dan E. Arking, Ιωάννα Ντάλλα, Emil V. R. Appel, Claudia Schurmann, Jennifer A. Brody, Rico Rueedi, Ozren Polašek, Garðar Sveinbjörnsson, Cécile Lecœur, Claes Ladenvall, Jing Hua Zhao, Aaron Isaacs, Lihua Wang, Jian’an Luan, Shih‐Jen Hwang, Nina Mononen, Kirsi Auro, Anne Jackson, Lawrence F. Bielak, Linyao Zeng, Nabi Shah, Maria Nethander, Archie Campbell, Tuomo Rankinen, Sonali Pechlivanis, Lu Qi, Wei Zhao, Federica Rizzi, Toshiko Tanaka, Antonietta Robino, Massimiliano Cocca, Leslie A. Lange, Martina Müller‐Nurasyid, Carolina Roselli, Weihua Zhang, Marcus E. Kleber, Xiuqing Guo, Henry J. Lin, Francesca Pavani, Tessel E. Galesloot, Raymond Noordam, Yuri Milaneschi, Katharina E. Schraut, Marcel den Hoed, Frauke Degenhardt, Stella Trompet, Marten E. van den Berg, Giorgio Pistis, Yih‐Chung Tham, Stefan Weiß, Xueling Sim, Hengtong L. Li, Peter J. van der Most, Ilja M. Nolte, Leo‐Pekka Lyytikäinen, M. Abdullah Said, Daniel R. Witte, Carlos Iribarren, Lenore J. Launer, Susan M. Ring, Paul S. de Vries, Peter Sever, Allan Linneberg, Erwin P. Böttinger, Sandosh Padmanabhan, Bruce M. Psaty, Nona Sotoodehnia, Ivana Kolčić, Delnaz Roshandel, Andrew D. Paterson, Davíð O. Arnar, Daníel F. Guðbjartsson, Hilma Hólm, Beverley Balkau, Claudia Silva, Christopher Newton‐Cheh, Kjell Nikus, Perttu Salo, Karen L. Mohlke, Patricia A. Peyser, Heribert Schunkert, Mattias Lorentzon, Jari Lahti, D. C. Rao, Marilyn C. Cornelis, Jessica D. Faul, Jennifer A. Smith, Katarzyna Stolarz‐Skrzypek, Stefania Bandinelli, Maria Pina Concas, Gianfranco Sinagra, Thomas Meitinger
Vydáno 2023Revisão
Vyhledávací nástroje:
Související témata
Medicine
Biology
Gene
Genetics
Genotype
Internal medicine
Single-nucleotide polymorphism
Genetic variants
Mendelian randomization
Bioinformatics
Cardiology
Cholesterol
Diabetes mellitus
Endocrinology
Genome-wide association study
Heart failure
LDL receptor
Lipoprotein
PCSK9
Type 2 diabetes
Alternative medicine
Biochemistry
Blood pressure
Coronary artery disease
Disease
Myocardial infarction
Odds ratio
Pathology
Placebo
Alcohol