Хайлтын үр дүнгүүд - Raha Pazoki

Үр дүнг сайжруулах
  1. 1
    Effects of a community-based healthy heart program on increasing healthy women's physical activity: a randomized controlled trial guided by Community-based Participatory Research (CBPR)

    Effects of a community-based healthy heart program on increasing healthy women's physical activity: a randomized controlled trial guided by Community-based Participatory Research (... -н Raha Pazoki, Iraj Nabipour, Nasrin Seyednezami, Seyed Reza Imami

    Хэвлэсэн 2007
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    Artigo
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  2. 2
    The association of metabolic syndrome and Chlamydia pneumoniae, Helicobacter pylori, cytomegalovirus, and herpes simplex virus type 1: the Persian Gulf Healthy Heart Study.

    The association of metabolic syndrome and Chlamydia pneumoniae, Helicobacter pylori, cytomegalovirus, and herpes simplex virus type 1: the Persian Gulf Healthy Heart Study. -н Iraj Nabipour, Katayoun Vahdat, Seyed Mojtaba Jafari, Raha Pazoki, Zahra Sanjdideh

    Хэвлэсэн 2006
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    Artigo
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  3. 3
    Genetic Predisposition to High Blood Pressure and Lifestyle Factors

    Genetic Predisposition to High Blood Pressure and Lifestyle Factors -н Raha Pazoki, Abbas Dehghan, Εvangelos Εvangelou, Helen R. Warren, He Gao, Mark J. Caulfield, Paul Elliott, Ioanna Tzoulaki

    Хэвлэсэн 2017
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    Artigo
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  4. 4
    Estimated 24-Hour Urinary Sodium Excretion and Incident Cardiovascular Disease and Mortality Among 398 628 Individuals in UK Biobank

    Estimated 24-Hour Urinary Sodium Excretion and Incident Cardiovascular Disease and Mortality Among 398 628 Individuals in UK Biobank -н Paul Elliott, David C. Muller, Deborah Schneider-Luftman, Raha Pazoki, Εvangelos Εvangelou, Abbas Dehghan, Bruce Neal, Ioanna Tzoulaki

    Хэвлэсэн 2020
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    Artigo
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  5. 5
    Determinants of accelerated metabolomic and epigenetic aging in a UK cohort

    Determinants of accelerated metabolomic and epigenetic aging in a UK cohort -н Oliver Robinson, Marc Chadeau‐Hyam, İbrahim Karaman, Rui Pinto, Mika Ala‐Korpela, Evangelos Handakas, Giovanni Fiorito, He Gao, Andy Heard, Marjo‐Riitta Järvelin, Matthew R. Lewis, Raha Pazoki, Silvia Polidoro, Ioanna Tzoulaki, Matthias Wielscher, Paul Elliott, Paolo Vineis

    Хэвлэсэн 2020
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    Artigo
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  6. 6
    Genetic analysis of over half a million people characterises C-reactive protein loci

    Genetic analysis of over half a million people characterises C-reactive protein loci -н Saredo Said, Raha Pazoki, Ville Karhunen, Urmo Võsa, Symen Ligthart, Barbara Bodinier, Fotios Koskeridis, Paul Welsh, Behrooz Z. Alizadeh, Daniel I. Chasman, Naveed Sattar, Marc Chadeau‐Hyam, Εvangelos Εvangelou, Marjo‐Riitta Järvelin, Paul Elliott, Ioanna Tzoulaki, Abbas Dehghan

    Хэвлэсэн 2022
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    Artigo
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  7. 7
    Genome-wide association study identifies a susceptibility locus at 21q21 for ventricular fibrillation in acute myocardial infarction

    Genome-wide association study identifies a susceptibility locus at 21q21 for ventricular fibrillation in acute myocardial infarction -н Connie R. Bezzina, Raha Pazoki, Abdennasser Bardai, Roos F. Marsman, Jonas S.S.G. de Jong, Marieke T. Blom, Brendon P. Scicluna, J. Wouter Jukema, Navin R. Bindraban, Peter Lichtner, Arne Pfeufer, Nanette H. Bishopric, Dan M. Roden, Thomas Meitinger, Sumeet S. Chugh, Robert J. Myerburg, Xavier Jouven, Stefan Kääb, Henk L. Dekker, Hanno L. Tan, Michael W.T. Tanck, Arthur A.M. Wilde

    Хэвлэсэн 2010
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  8. 8
    Whole-Exome Sequencing Identifies Loci Associated with Blood Cell Traits and Reveals a Role for Alternative GFI1B Splice Variants in Human Hematopoiesis

    Whole-Exome Sequencing Identifies Loci Associated with Blood Cell Traits and Reveals a Role for Alternative GFI1B Splice Variants in Human Hematopoiesis -н Linda M. Polfus, Rajiv K. Khajuria, Ursula M. Schick, Nathan Pankratz, Raha Pazoki, Jennifer A. Brody, Ming‐Huei Chen, Paul L. Auer, James S. Floyd, Jie Huang, Leslie A. Lange, Frank J.A. van Rooij, Richard A. Gibbs, Ginger Metcalf, Donna M. Muzny, Narayanan Veeraraghavan, Klaudia Walter, Lu Chen, Lisa R. Yanek, Lewis C. Becker, Gina M. Peloso, Aoi Wakabayashi, Mart Kals, Andres Metspalu, Tõnu Esko, Keolu Fox, Robert B. Wallace, Nora Franceschini, Nena Matijevic, Kenneth Rice, Traci M. Bartz, Leo‐Pekka Lyytikäinen, Mika Kähönen, Terho Lehtimäki, Olli Raitakari, Ruifang Li‐Gao, Dennis O. Mook‐Kanamori, Guillaume Lettre, Cornelia M. van Duijn, Oscar H. Franco, Stephen S. Rich, Fernando Rivadeneira, Albert Hofman, André G. Uitterlinden, James Wilson, Bruce M. Psaty, Nicole Soranzo, Abbas Dehghan, Eric Boerwinkle, Xiaoling Zhang, Andrew D. Johnson, Christopher J. O’Donnell, Jill M. Johnsen, Alexander P. Reiner, Santhi K. Ganesh, Vijay G. Sankaran

    Хэвлэсэн 2016
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  9. 9
    Identification of a Sudden Cardiac Death Susceptibility Locus at 2q24.2 through Genome-Wide Association in European Ancestry Individuals

    Identification of a Sudden Cardiac Death Susceptibility Locus at 2q24.2 through Genome-Wide Association in European Ancestry Individuals -н Dan E. Arking, Juhani Junttila, Philippe Goyette, Adriana Huertas‐Vázquez, Mark Eijgelsheim, Marieke T. Blom, Christopher Newton‐Cheh, Kyndaron Reinier, Carmen Teodorescu, Audrey Uy‐Evanado, Naima Carter‐Monroe, Kari Kaikkonen, Marja‐Leena Kortelainen, Gabrielle Boucher, Caroline Lagacé, Anna Moes, Xiaoqing Zhao, Frank D. Kolodgie, Fernando Rivadeneira, Albert Hofman, Jacqueline C.M. Witteman, André G. Uitterlinden, Roos F. Marsman, Raha Pazoki, Abdennasser Bardai, Rudolph W. Koster, Abbas Dehghan, Shih‐Jen Hwang, Pallav Bhatnagar, Wendy S. Post, Gina M. Hilton, Ronald J. Prineas, Man Li, Anna Köttgen, Georg Ehret, Eric Boerwinkle, Josef Coresh, W.H. Linda Kao, Bruce M. Psaty, Gordon F. Tomaselli, Nona Sotoodehnia, David S. Siscovick, Greg Burke, Eduardo Marbán, Peter M. Spooner, L. Adrienne Cupples, Jonathan Jui, Karen Gunson, Y. Antero Kesäniemi, Arthur A.M. Wilde, Jean‐Claude Tardif, Christopher J. O’Donnell, Connie R. Bezzina, Renu Virmani, Bruno H. Stricker, Hanno L. Tan, Christine M. Albert, Aravinda Chakravarti, John D. Rioux, Heikki V. Huikuri, Sumeet S. Chugh

    Хэвлэсэн 2011
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    Artigo
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  10. 10
    Discovery and refinement of genetic loci associated with cardiometabolic risk using dense imputation maps

    Discovery and refinement of genetic loci associated with cardiometabolic risk using dense imputation maps -н Valentina Iotchkova, Jie Huang, John Morris, Deepti Jain, Caterina Barbieri, Klaudia Walter, Josine L. Min, Lu Chen, William J. Astle, Massimiliano Cocca, Patrick Deelen, Heather Elding, Aliki‐Eleni Farmaki, Christopher S. Franklin, Mattias Frånberg, Tom R. Gaunt, Albert Hofman, Tao Jiang, Marcus E. Kleber, Geneviève Lachance, Jian’an Luan, Giovanni Malerba, Angela Matchan, Daniel G. Mead, Yasin Memari, Ιωάννα Ντάλλα, Kalliope Panoutsopoulou, Raha Pazoki, John R. B. Perry, Fernando Rivadeneira, Maria Sabater‐Lleal, Bengt Sennblad, So–Youn Shin, Lorraine Southam, Michela Traglia, Freerk van Dijk, Jin‐Moo Lee, Gianluigi Zaza, Weihua Zhang, Najaf Amin, Adam S. Butterworth, John C. Chambers, George Dedoussis, Abbas Dehghan, Oscar H. Franco, Lude Franke, Mattia Frontini, Giovanni Gambaro, Paolo Gasparini, Anders Hamsten, Aaron Issacs, Jaspal S. Kooner, Charles Kooperberg, Claudia Langenberg, Winfried März, Robert A. Scott, Morris A. Swertz, Daniela Toniolo, André G. Uitterlinden, Cornelia M. van Duijn, Hugh Watkins, Eleftheria Zeggini, Mathew T Maurano, Nicholas J. Timpson, Alexander P. Reiner, Paul L. Auer, Nicole Soranzo

    Хэвлэсэн 2016
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    Artigo
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  11. 11
    A comprehensive evaluation of the genetic architecture of sudden cardiac arrest

    A comprehensive evaluation of the genetic architecture of sudden cardiac arrest -н Foram N. Ashar, Rebecca Mitchell, Christine M. Albert, Christopher Newton‐Cheh, Jennifer A. Brody, Martina Müller‐Nurasyid, Anna Moes, Thomas Meitinger, Angel C. Y. Mak, Heikki V. Huikuri, Juhani Junttila, Philippe Goyette, Sara L. Pulit, Raha Pazoki, Michael W.T. Tanck, Marieke T. Blom, Xiaoqing Zhao, Aki S. Havulinna, Reza Jabbari, Charlotte Glinge, Vinicius Tragante, Stefan Andersson Escher, Aravinda Chakravarti, Georg Ehret, Josef Coresh, Man Li, Ronald J. Prineas, Oscar H. Franco, Pui‐Yan Kwok, Thomas Lumley, Florence Dumas, Barbara McKnight, Jerome I. Rotter, Rozenn N. Lemaître, Susan R. Heckbert, Christopher J. O’Donnell, Shih‐Jen Hwang, Jean‐Claude Tardif, Martin VanDenburgh, André G. Uitterlinden, Albert Hofman, Bruno H. Stricker, Paul I. W. de Bakker, Paul W. Franks, Jan‐Håkan Jansson, Folkert W. Asselbergs, Marc K. Halushka, Joseph J. Maleszewski, Jacob Tfelt‐Hansen, Thomas Engstrøm, Veikko Salomaa, Renu Virmani, Frank D. Kolodgie, Arthur A.M. Wilde, Hanno L. Tan, Connie R. Bezzina, Mark Eijgelsheim, John D. Rioux, Xavier Jouven, Stefan Kääb, Bruce M. Psaty, David S. Siscovick, Dan E. Arking, Nona Sotoodehnia

    Хэвлэсэн 2018
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  12. 12
    Phenome-wide association analysis of LDL-cholesterol lowering genetic variants in <i>PCSK9</i>

    Phenome-wide association analysis of LDL-cholesterol lowering genetic variants in <i>PCSK9</i> -н 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

    Хэвлэсэн 2018
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    Pré-impressão
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  13. 13
    Genetic analysis of over 1 million people identifies 535 new loci associated with blood pressure traits

    Genetic analysis of over 1 million people identifies 535 new loci associated with blood pressure traits -н Εvangelos Εvangelou, Helen R. Warren, David Mosén-Ansorena, Borbála Mifsud, Raha Pazoki, He Gao, Georgios Ntritsos, Niki Dimou, Claudia P. Cabrera, İbrahim Karaman, Fu Liang Ng, Marina Evangelou, Katarzyna Witkowska, Evan Tzanis, Jacklyn N. Hellwege, Ayush Giri, Digna R. Velez Edwards, Yan V. Sun, Kelly Cho, J. Michael Gaziano, Peter W.F. Wilson, Philip S. Tsao, Csaba P. Kövesdy, Tõnu Esko, Reedik Mägi, Lili Milani, Peter Almgren, Thibaud Boutin, Stéphanie Debette, Jun Ding, Franco Giulianini, Elizabeth Holliday, Anne Jackson, Ruifang Li‐Gao, Wei‐Yu Lin, Jian’an Luan, Massimo Mangino, Christopher Oldmeadow, Bram P. Prins, Yong Qian, Muralidharan Sargurupremraj, Nabi Shah, Praveen Surendran, Sébastien Thériault, Niek Verweij, Sara M. Willems, Jing-Hua Zhao, Philippe Amouyel, John Connell, Renée de Mutsert, Alex S. F. Doney, Martin Farrall, Cristina Menni, Andrew D. Morris, Raymond Noordam, Guillaume Paré, Neil R Poulter, Denis C. Shields, Alice Stanton, Simon Thom, Gonçalo Abecasis, Najaf Amin, Dan E. Arking, Kristin L. Ayers, Caterina Barbieri, Chiara Batini, Joshua C. Bis, Tineka Blake, Murielle Bochud, Michael Boehnke, Eric Boerwinkle, Dorret I. Boomsma, Erwin P. Böttinger, Peter S. Braund, Marco Brumat, Archie Campbell, Harry Campbell, Aravinda Chakravarti, John C. Chambers, Ganesh Chauhan, Marina Ciullo, Massimiliano Cocca, Francis S. Collins, Heather J. Cordell, Gail Davies, Martin H. de Borst, Eco J. C. de Geus, Ian J. Deary, Joris Deelen, Fabiola Del Greco M, Cumhur Yusuf Demirkale, Marcus Dörr, Georg Ehret, Roberto Elosúa, Stefan Enroth, A. Mesut Erzurumluoglu, Teresa Ferreira, Mattias Frånberg, Oscar H. Franco, Ilaria Gandin

    Хэвлэсэн 2018
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  14. 14
    Phenome-wide association analysis of LDL-cholesterol lowering genetic variants in PCSK9

    Phenome-wide association analysis of LDL-cholesterol lowering genetic variants in PCSK9 -н 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

    Хэвлэсэн 2019
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  15. 15
    Exome Genotyping Identifies Pleiotropic Variants Associated with Red Blood Cell Traits

    Exome Genotyping Identifies Pleiotropic Variants Associated with Red Blood Cell Traits -н Nathalie Chami, Ming‐Huei Chen, Andrew J. Slater, John D. Eicher, Εvangelos Εvangelou, Salman M. Tajuddin, Latisha Love‐Gregory, Tim Kacprowski, Ursula M. Schick, Akihiro Nomura, Ayush Giri, Samuel Lessard, Jennifer A. Brody, Claudia Schurmann, Nathan Pankratz, Lisa R. Yanek, Ani Manichaikul, Raha Pazoki, Evelin Mihailov, W. David Hill, Laura M. Raffield, Amber Burt, Traci M. Bartz, Diane M. Becker, Lewis C. Becker, Eric Boerwinkle, Jette Bork‐Jensen, Erwin P. Böttinger, Michelle L. O’Donoghue, David R. Crosslin, Simon de Denus, Marie‐Pierre Dubé, Paul Elliott, Gunnar Engström, Michele K. Evans, James S. Floyd, Myriam Fornage, He Gao, Andreas Greinacher, Vilmundur Guðnason, Torben Hansen, Tamara B. Harris, Caroline Hayward, Jussi Hernesniemi, Heather M. Highland, Joel N. Hirschhorn, Albert Hofman, Marguerite R. Irvin, Mika Kähönen, Ethan M. Lange, Lenore J. Launer, Terho Lehtimäki, Jin Li, David C. Liewald, Allan Linneberg, Yongmei Liu, Yingchang Lu, Leo‐Pekka Lyytikäinen, Reedik Mägi, Rasika A. Mathias, Olle Melander, Andres Metspalu, Nina Mononen, Mike A. Nalls, Deborah A. Nickerson, Kjell Nikus, Chris O’Donnell, Marju Orho‐Melander, Oluf Pedersen, Astrid Petersmann, Linda M. Polfus, Bruce M. Psaty, Olli T. Raitakari, Emma Raitoharju, Melissa A. Richard, Kenneth Rice, Fernando Rivadeneira, Jerome I. Rotter, Frank Schmidt, Albert V. Smith, John M. Starr, Kent D. Taylor, Alexander Teumer, Betina H. Thuesen, Eric S. Torstenson, Russell P. Tracy, Ioanna Tzoulaki, Neil A. Zakai, Caterina Vacchi‐Suzzi, Cornelia M. van Duijn, Frank J.A. van Rooij, Mary Cushman, Ian J. Deary, Digna R. Velez Edwards, Anne‐Claire Vergnaud, Lars Wallentin, Dawn Waterworth, Harvey D. White, James G. Wilson, Alan B. Zonderman

    Хэвлэсэн 2016
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  16. 16
    Large-Scale Exome-wide Association Analysis Identifies Loci for White Blood Cell Traits and Pleiotropy with Immune-Mediated Diseases

    Large-Scale Exome-wide Association Analysis Identifies Loci for White Blood Cell Traits and Pleiotropy with Immune-Mediated Diseases -н Salman M. Tajuddin, Ursula M. Schick, John D. Eicher, Nathalie Chami, Ayush Giri, Jennifer A. Brody, W. David Hill, Tim Kacprowski, Jin Li, Leo‐Pekka Lyytikäinen, Ani Manichaikul, Evelin Mihailov, Michelle L. O’Donoghue, Nathan Pankratz, Raha Pazoki, Linda M. Polfus, Albert V. Smith, Claudia Schurmann, Caterina Vacchi‐Suzzi, Dawn Waterworth, Εvangelos Εvangelou, Lisa R. Yanek, Amber Burt, Ming‐Huei Chen, Frank J.A. van Rooij, James S. Floyd, Andreas Greinacher, Tamara B. Harris, Heather M. Highland, Leslie A. Lange, Yongmei Liu, Reedik Mägi, Mike A. Nalls, Rasika A. Mathias, Deborah A. Nickerson, Kjell Nikus, John M. Starr, Jean‐Claude Tardif, Ioanna Tzoulaki, Digna R. Velez Edwards, Lars Wallentin, Traci M. Bartz, Lewis C. Becker, Joshua C. Denny, Laura M. Raffield, John D. Rioux, Nele Friedrich, Myriam Fornage, He Gao, Joel N. Hirschhorn, David C. Liewald, Stephen S. Rich, André G. Uitterlinden, Lisa Bastarache, Diane M. Becker, Eric Boerwinkle, Simon de Denus, Erwin P. Böttinger, Caroline Hayward, Albert Hofman, Georg Homuth, Ethan M. Lange, Lenore J. Launer, Terho Lehtimäki, Yingchang Lu, Andres Metspalu, Chris O’Donnell, Rakale C. Quarells, Melissa A. Richard, Eric S. Torstenson, Kent D. Taylor, Anne‐Claire Vergnaud, Alan B. Zonderman, David R. Crosslin, Ian J. Deary, Marcus Dörr, Paul Elliott, Michele K. Evans, Vilmundur Guðnason, Mika Kähönen, Bruce M. Psaty, Jerome I. Rotter, Andrew J. Slater, Abbas Dehghan, Harvey D. White, Santhi K. Ganesh, Ruth J. F. Loos, Tõnu Esko, Nauder Faraday, James G. Wilson, Mary Cushman, Andrew D. Johnson, Todd L. Edwards, Neil A. Zakai, Guillaume Lettre, Alex P. Reiner, Paul L. Auer

    Хэвлэсэн 2016
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  17. 17
    Platelet-Related Variants Identified by Exomechip Meta-analysis in 157,293 Individuals

    Platelet-Related Variants Identified by Exomechip Meta-analysis in 157,293 Individuals -н John D. Eicher, Nathalie Chami, Tim Kacprowski, Akihiro Nomura, Ming‐Huei Chen, Lisa R. Yanek, Salman M. Tajuddin, Ursula M. Schick, Andrew J. Slater, Nathan Pankratz, Linda M. Polfus, Claudia Schurmann, Ayush Giri, Jennifer A. Brody, Leslie A. Lange, Ani Manichaikul, W. David Hill, Raha Pazoki, Paul Elliot, Εvangelos Εvangelou, Ioanna Tzoulaki, He Gao, Anne‐Claire Vergnaud, Rasika A. Mathias, Diane M. Becker, Lewis C. Becker, Amber Burt, David R. Crosslin, Leo‐Pekka Lyytikäinen, Kjell Nikus, Jussi Hernesniemi, Mika Kähönen, Emma Raitoharju, Nina Mononen, Olli T. Raitakari, Terho Lehtimäki, Mary Cushman, Neil A. Zakai, Deborah A. Nickerson, Laura M. Raffield, Rakale C. Quarells, Cristen J. Willer, Gina M. Peloso, Gonçalo R. Abecasis, Dajiang J. Liu, Panos Deloukas, Nilesh J. Samani, Heribert Schunkert, Jeanette Erdmann, Myriam Fornage, Melissa A. Richard, Jean‐Claude Tardif, John D. Rioux, Marie‐Pierre Dubé, Simon de Denus, Yingchang Lu, Erwin P. Böttinger, Ruth J. F. Loos, Albert V. Smith, Tamara B. Harris, Lenore J. Launer, Vilmundur Guðnason, Digna R. Velez Edwards, Eric S. Torstenson, Yongmei Liu, Russell P. Tracy, Jerome I. Rotter, Stephen S. Rich, Heather M. Highland, Eric Boerwinkle, Jin Li, Ethan M. Lange, James G. Wilson, Evelin Mihailov, Reedik Mägi, Joel N. Hirschhorn, Andres Metspalu, Tõnu Esko, Caterina Vacchi‐Suzzi, Mike A. Nalls, Alan B. Zonderman, Michele K. Evans, Gunnar Engström, Marju Orho‐Melander, Olle Melander, Michelle L. O’Donoghue, Dawn Waterworth, Lars Wallentin, Harvey D. White, James S. Floyd, Traci M. Bartz, Kenneth Rice, Bruce M. Psaty, John M. Starr, David C. Liewald, Caroline Hayward, Ian J. Deary, Andreas Greinacher, Uwe Völker, Thomas Thiele

    Хэвлэсэн 2016
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  18. 18
    PCSK9 genetic variants and risk of type 2 diabetes: a mendelian randomisation study

    PCSK9 genetic variants and risk of type 2 diabetes: a mendelian randomisation study -н 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

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    Study of 300,486 individuals identifies 148 independent genetic loci influencing general cognitive function

    Study of 300,486 individuals identifies 148 independent genetic loci influencing general cognitive function -н Gail Davies, Max Lam, Sarah E. Harris, Joey W. Trampush, Michelle Luciano, W. David Hill, Saskia P. Hagenaars, Stuart J. Ritchie, Riccardo E. Marioni, Chloe Fawns‐Ritchie, David C. Liewald, Judith A. Okely, Ari Ahola‐Olli, Catriona L. K. Barnes, Lars Bertram, Joshua C. Bis, Katherine E. Burdick, Andrea Christoforou, Pamela DeRosse, Srdjan Djurovic, Thomas Espeseth, Stella G. Giakoumaki, Sudheer Giddaluru, Daniel E. Gustavson, Caroline Hayward, Edith Hofer, M. Arfan Ikram, Robert Karlsson, Emma Knowles, Jari Lahti, Markus Leber, Shuo Li, Karen A. Mather, Ingrid Melle, Derek W. Morris, Christopher Oldmeadow, Teemu Palviainen, Antony Payton, Raha Pazoki, Katja Petrovic, Chandra A. Reynolds, Muralidharan Sargurupremraj, Markus Scholz, Jennifer A. Smith, Albert V. Smith, Natalie Terzikhan, Anbupalam Thalamuthu, Stella Trompet, Sven J. van der Lee, Erin B. Ware, B. Gwen Windham, Margaret J. Wright, Jingyun Yang, Jin Yu, David Ames, Najaf Amin, Philippe Amouyel, Ole A. Andreassen, Nicola J. Armstrong, Amelia A. Assareh, John Attia, Deborah K. Attix, Dimitrios Avramopoulos, David A. Bennett, Anne C. Böhmer, Patricia A. Boyle, Henry Brodaty, Harry Campbell, Tyrone D. Cannon, Elizabeth T. Cirulli, Eliza Congdon, Emily Drabant Conley, Janie Corley, Simon R. Cox, Anders M. Dale, Abbas Dehghan, Danielle M. Dick, Dwight Dickinson, Johan G. Eriksson, Εvangelos Εvangelou, Jessica D. Faul, Ian Ford, Nelson B. Freimer, He Gao, Ina Giegling, Nathan A. Gillespie, Scott D. Gordon, Rebecca F. Gottesman, Michael Griswold, Vilmundur Guðnason, Tamara B. Harris, Annette M. Hartmann, Alex Hatzimanolis, Gerardo Heiss, Elizabeth G. Holliday, Peter K. Joshi, Mika Kähönen, Sharon L. R. Kardia, Ida Karlsson, Luca Kleineidam

    Хэвлэсэн 2018
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    New alcohol-related genes suggest shared genetic mechanisms with neuropsychiatric disorders

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    Хэвлэсэн 2019
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