Výsledky vyhledávání - Sonali Pechlivanis

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  1. 1
    A statistical model for the analysis of beta values in DNA methylation studies

    A statistical model for the analysis of beta values in DNA methylation studies Autor Leonie Weinhold, Simone Wahl, Sonali Pechlivanis, Per Hoffmann, Matthias Schmid

    Vydáno 2016
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  2. 2
    Tumor Suppressive MicroRNAs miR-34a/c Control Cancer Cell Expression of ULBP2, a Stress-Induced Ligand of the Natural Killer Cell Receptor NKG2D

    Tumor Suppressive MicroRNAs miR-34a/c Control Cancer Cell Expression of ULBP2, a Stress-Induced Ligand of the Natural Killer Cell Receptor NKG2D Autor Anja Heinemann, Fang Zhao, Sonali Pechlivanis, Jürgen Eberle, Alexander Steinle, Sven Diederichs, Dirk Schadendorf, Annette Paschen

    Vydáno 2011
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  3. 3
    Anthropometric markers and their association with incident type 2 diabetes mellitus: which marker is best for prediction? Pooled analysis of four German population-based cohort studies and comparison with a nationwide cohort study

    Anthropometric markers and their association with incident type 2 diabetes mellitus: which marker is best for prediction? Pooled analysis of four German population-based cohort stu... Autor Saskia Hartwig, Alexander Kluttig, Daniel Tiller, Julia Fricke, Grit Müller, Sabine Schipf, Henry Völzke, Michaela Schunk, Christa Meisinger, Anja Schienkiewitz, Christin Heidemann, Susanne Moebus, Sonali Pechlivanis, Karl Werdan, Oliver Kuß, Teresa Tamayo, Johannes Haerting, Karin Halina Greiser

    Vydáno 2016
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  4. 4
    Identification and characterisation of pathogenic and non-pathogenic FGF14 repeat expansions

    Identification and characterisation of pathogenic and non-pathogenic FGF14 repeat expansions Autor Lars Mohren, Friedrich Erdlenbruch, Elsa Leitão, Fabian Kilpert, Georg Sebastian Hönes, Sabine Kaya, Christopher Schröder, Andreas Thieme, Marc Sturm, Joohyun Park, Agatha Schlüter, Montserrat Ruíz, Moisés Morales de la Prida, Carlos Casasnovas, Kerstin Becker, Ulla Roggenbuck, Sonali Pechlivanis, Frank J. Kaiser, Matthis Synofzik, Thomas Wirth, Mathieu Anheim, Tobias B. Haack, Paul J. Lockhart, Karl‐Heinz Jöckel, Aurora Pujol, Stephan Klebe, Dagmar Timmann, Christel Depienne

    Vydáno 2024
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  5. 5
    Genome-wide analysis of rare copy number variations reveals PARK2 as a candidate gene for attention-deficit/hyperactivity disorder

    Genome-wide analysis of rare copy number variations reveals PARK2 as a candidate gene for attention-deficit/hyperactivity disorder Autor Ivonne Jarick, A-L Volckmar, Carolin Pütter, Sonali Pechlivanis, Thuy Trang Nguyen, Maria R. Dauvermann, Sebastian Beck, Özgür Albayrak, Susann Scherag, Susanne Gilsbach, Sven Cichon, Per Hoffmann, Franziska Degenhardt, Markus M. Nöthen, S. Schreiber, H-E Wichmann, KH Jöckel, Joachim Heinrich, Carla M. T. Tiesler, Stephen V. Faraone, Susanne Walitza, Judith Sinzig, Christine M. Freitag, Jobst Meyer, B Herpertz‐Dahlmann, Gerd Lehmkuhl, Tobias Renner, Andreas Warnke, Marcel Romanos, Klaus‐Peter Lesch, Andreas Reif, Benno G. Schimmelmann, Johannes Hebebrand, André Scherag, Anke Hinney

    Vydáno 2012
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  6. 6
    Meta-analysis identifies novel risk loci and yields systematic insights into the biology of male-pattern baldness

    Meta-analysis identifies novel risk loci and yields systematic insights into the biology of male-pattern baldness Autor Stefanie Heilmann‐Heimbach, Christine Herold, Lara M. Hochfeld, Axel M. Hillmer, Dale R. Nyholt, Julian Hecker, Asif Javed, Elaine Guo Yan Chew, Sonali Pechlivanis, Dmitriy Drichel, Xiu Ting Heng, Ricardo C.H. del Rosario, Heide Fier, Ralf Paus, Rico Rueedi, Tessel E. Galesloot, Susanne Moebus, Thomas Anhalt, Shyam Prabhakar, Rui Li, Stavroula Kanoni, George Papanikolaou, Zoltán Kutalik, Panos Deloukas, Michael P. Philpott, Gérard Waeber, Tim D. Spector, Péter Vollenweider, Lambertus A. Kiemeney, George Dedoussis, J. Brent Richards, Michael Nothnagel, Nicholas G. Martin, Tim Becker, David A. Hinds, Markus M. Nöthen

    Vydáno 2017
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  7. 7
    Genetic Associations with Valvular Calcification and Aortic Stenosis

    Genetic Associations with Valvular Calcification and Aortic Stenosis Autor George Thanassoulis, Catherine Y. Campbell, David S. Owens, J. G. Smith, Albert V. Smith, Gina M. Peloso, Kathleen F. Kerr, Sonali Pechlivanis, Matthew J. Budoff, Tamara B. Harris, Rajeev Malhotra, Kevin D. O’Brien, Pia R. Kamstrup, Børge G. Nordestgaard, Anne Tybjærg‐Hansen, Matthew Allison, Thor Aspelund, Michael H. Criqui, Susan R. Heckbert, Shih Jen Hwang, Yongmei Liu, Marketa Sjögren, Jesper van der Pals, Hagen Kälsch, Hae‐Won Uh, Markus M. Nöthen, L. Adrienne Cupples, Muriel Caslake, Emanuele Di Angelantonio, John Danesh, Jerome I. Rotter, Sigurður Sigurðsson, Quenna Wong, Raimund Erbel, Sekar Kathiresan, Olle Melander, Vilmundur Guðnason, Christopher J. O’Donnell, Wendy S. Post

    Vydáno 2013
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  8. 8
    HDAC9 is implicated in atherosclerotic aortic calcification and affects vascular smooth muscle cell phenotype

    HDAC9 is implicated in atherosclerotic aortic calcification and affects vascular smooth muscle cell phenotype Autor Rajeev Malhotra, Andreas C. Mauer, Christian L. Lino Cardenas, Xiuqing Guo, Jie Yao, Xiaoling Zhang, Florian Wunderer, Albert V. Smith, Quenna Wong, Sonali Pechlivanis, Shih‐Jen Hwang, Judy Wang, Lingyi Lu, Christopher J. Nicholson, Georgia Shelton, Mary D. Buswell, Hanna J. Barnes, Haakon H. Sigurslid, Charles Slocum, Caitlin O’ Rourke, David K. Rhee, Aranya Bagchi, Sagar U. Nigwekar, Emmanuel S. Buys, Catherine Y. Campbell, Tamara Harris, Matthew J. Budoff, Michael H Criqui, Jerome I. Rotter, Andrew D. Johnson, Ci Song, Nora Franceschini, Stéphanie Debette, Udo Hoffmann, Hagen Kälsch, Markus M. Nöthen, Sigurður Sigurðsson, Barry I. Freedman, Donald W. Bowden, Karl-Heinz Jöckel, Susanne Moebus, Raimund Erbel, Mary F. Feitosa, Vilmundur Guðnason, George Thanassoulis, Warren M. Zapol, Mark E. Lindsay, Donald B. Bloch, Wendy S. Post, Christopher J. O’Donnell

    Vydáno 2019
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  9. 9
    Large-scale association analysis provides insights into the genetic architecture and pathophysiology of type 2 diabetes

    Large-scale association analysis provides insights into the genetic architecture and pathophysiology of type 2 diabetes Autor Andrew P. Morris, Benjamin F. Voight, Tanya M. Teslovich, Teresa Ferreira, Ayellet V. Segrè, Valgerður Steinthórsdóttir, Rona J. Strawbridge, Hassan Khan, Harald Grallert, Anubha Mahajan, Inga Prokopenko, Hyun Min Kang, Christian Dina, Tõnu Esko, Ross M. Fraser, Stavroula Kanoni, Ashish Kumar, Vasiliki Lagou, Claudia Langenberg, Jian’an Luan, Cecilia M. Lindgren, Martina Müller‐Nurasyid, Sonali Pechlivanis, Nigel W. Rayner, Laura J. Scott, Steven Wiltshire, Loïc Yengo, Leena Kinnunen, Elizabeth J. Rossin, Soumya Raychaudhuri, Andrew D. Johnson, Antigone S. Dimas, Ruth J. F. Loos, Sailaja Vedantam, Han Chen, José C. Florez, Caroline S. Fox, Yongmei Liu, Denis Rybin, David Couper, Wen Hong Linda Kao, Man Li, Marilyn C. Cornelis, Peter Kraft, Qi Sun, Rob M. van Dam, Heather M. Stringham, Peter S. Chines, Krista Fischer, Pierre Fontanillas, Oddgeir L. Holmen, Sarah Hunt, Anne Jackson, Augustine Kong, Robert Lawrence, Julia Meyer, John R. B. Perry, Carl Platou, Simon Potter, Emil Rehnberg, Neil Robertson, Suthesh Sivapalaratnam, Alena Stančáková, Kathleen Stirrups, Guðmar Þorleifsson, Emmi Tikkanen, Andrew R. Wood, Peter Almgren, Mustafa Atalay, Rafn Benediktsson, Lori L. Bonnycastle, Noël P. Burtt, Jason Carey, G. Charpentier, Andrew Crenshaw, Alex S. F. Doney, Mozhgan Dorkhan, Sarah Edkins, Valur Emilsson, Elodie Eury, Tom Forsén, Karl Gertow, Bruna Gigante, George Grant, Christopher J. Groves, Candace Guiducci, Christian Herder, Ástráður B. Hreiðarsson, Jennie Hui, Anthony James, Anna Jonsson, Wolfgang Rathmann, Norman Klopp, Jasmina Kravić, Kaarel Krjutškov, Cordelia Langford, Karin Leander, Eero Lindholm, Stéphane Lobbens, Satu Männistö

    Vydáno 2012
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  10. 10
    Genome-wide meta-analysis identifies 11 new loci for anthropometric traits and provides insights into genetic architecture

    Genome-wide meta-analysis identifies 11 new loci for anthropometric traits and provides insights into genetic architecture Autor Sonja I. Berndt, Stefan Gustafsson, Reedik Mägi, Andrea Ganna, Eleanor Wheeler, Mary F. Feitosa, Anne E. Justice, Keri L. Monda, Damien C. Croteau‐Chonka, Felix R. Day, Tõnu Esko, Tove Fall, Teresa Ferreira, Davide Gentilini, Anne Jackson, Jian’an Luan, Joshua C. Randall, Sailaja Vedantam, Cristen J. Willer, Thomas W. Winkler, Andrew R. Wood, Tsegaselassie Workalemahu, Yi‐Juan Hu, Sang Lee, Liming Liang, Dan-Yu Lin, Josine L. Min, Benjamin M. Neale, Guðmar Þorleifsson, Jian Yang, Eva Albrecht, Najaf Amin, Jennifer L. Bragg‐Gresham, Gemma Cadby, Martin den Heijer, Niina Eklund, Krista Fischer, Anuj Goel, Jouke‐Jan Hottenga, Jennifer E. Huffman, Ivonne Jarick, Åsa Johansson, Toby Johnson, Stavroula Kanoni, Marcus E. Kleber, Inke R. König, Kati Kristiansson, Zoltán Kutalik, Claudia Lamina, Cécile Lecœur, Li Guo, Massimo Mangino, Wendy L. McArdle, Carolina Medina‐Gómez, Martina Müller‐Nurasyid, Julius S. Ngwa, Ilja M. Nolte, Lavinia Paternoster, Sonali Pechlivanis, Markus Perola, Marjolein J. Peters, Michael Preuß, Lynda M. Rose, Jianxin Shi, Dmitry Shungin, Albert V. Smith, Rona J. Strawbridge, Ida Surakka, Alexander Teumer, Mieke D. Trip, Jonathan P. Tyrer, Jana V. van Vliet‐Ostaptchouk, Liesbeth Vandenput, Lindsay L. Waite, Wei Zhao, Devin Absher, Folkert W. Asselbergs, Mustafa Atalay, Antony Attwood, Anthony J. Balmforth, Hanneke Basart, John Beilby, Lori L. Bonnycastle, Paolo Brambilla, Marcel Bruinenberg, Harry Campbell, Daniel I. Chasman, Peter S. Chines, Francis S. Collins, John Connell, William Cookson, Ulf dé Fairé, Femmie de Vegt, Mariano Dei, Maria Dimitriou, Sarah Edkins, Karol Estrada, David M. Evans, Martin Farrall, Maurizio Ferrario

    Vydáno 2013
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  11. 11
    New genetic loci link adipose and insulin biology to body fat distribution

    New genetic loci link adipose and insulin biology to body fat distribution Autor Dmitry Shungin, Thomas W. Winkler, Damien C. Croteau‐Chonka, Teresa Ferreira, Adam E. Locke, Reedik Mägi, Rona J. Strawbridge, Tune H. Pers, Krista Fischer, Anne E. Justice, Tsegaselassie Workalemahu, Joseph Wu, Martin L. Buchkovich, Nancy L. Heard‐Costa, Tamara S. Roman, Alexander Drong, Ci Song, Stefan Gustafsson, Felix R. Day, Tõnu Esko, Tove Fall, Zoltán Kutalik, Jian’an Luan, Joshua C. Randall, André Scherag, Sailaja Vedantam, Andrew R. Wood, Ming‐Huei Chen, Rudolf S.N. Fehrmann, Juha Karjalainen, Bratati Kahali, Yongmei Liu, Ellen M. Schmidt, Devin Absher, Najaf Amin, Denise Anderson, Marian Beekman, Jennifer L. Bragg‐Gresham, Steven Buyske, Ayşe Demirkan, Georg Ehret, Mary F. Feitosa, Anuj Goel, Anne Jackson, Toby Johnson, Marcus E. Kleber, Kati Kristiansson, Massimo Mangino, Irene Mateo Leach, Carolina Medina‐Gómez, Colin N. A. Palmer, Dorota Pasko, Sonali Pechlivanis, Marjolein J. Peters, Inga Prokopenko, Alena Stančáková, Yan V. Sun, Toshiko Tanaka, Alexander Teumer, Jana V. van Vliet‐Ostaptchouk, Loïc Yengo, Weihua Zhang, Eva Albrecht, Johan Ärnlöv, Gillian M. Arscott, Stefania Bandinelli, Amy Barrett, Claire Bellis, Amanda J. Bennett, Christian Berne, Matthias Blüher, Stefan Böhringer, Fabrice Bonnet, Yvonne Böttcher, Marcel Bruinenberg, Delia B. Carba, Ida Henriette Caspersen, Robert Clarke, E. Warwick Daw, Joris Deelen, Ewa Deelman, Graciela Delgado, Alex S. F. Doney, Niina Eklund, Michael R. Erdos, Karol Estrada, Elodie Eury, Nele Friedrich, Melissa E. Garcia, Vilmantas Giedraitis, Bruna Gigante, Alan S. Go, Alain Golay, Harald Grallert, Tanja B. Grammer, Jürgen Gräßler, Jagvir Grewal, Christopher J. Groves, Toomas Haller, Göran Hallmans

    Vydáno 2015
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  12. 12
    Defining the role of common variation in the genomic and biological architecture of adult human height

    Defining the role of common variation in the genomic and biological architecture of adult human height Autor Andrew R. Wood, Tõnu Esko, Jian Yang, Sailaja Vedantam, Tune H. Pers, Stefan Gustafsson, Audrey Y. Chu, Karol Estrada, Jian’an Luan, Zoltán Kutalik, Najaf Amin, Martin L. Buchkovich, Damien C. Croteau‐Chonka, Felix R. Day, Yanan Duan, Tove Fall, Rudolf S.N. Fehrmann, Teresa Ferreira, Anne Jackson, Juha Karjalainen, Ken Sin Lo, Adam E. Locke, Reedik Mägi, Evelin Mihailov, Eleonora Porcu, Joshua C. Randall, André Scherag, Anna A. E. Vinkhuyzen, Harm-Jan Westra, Thomas W. Winkler, Tsegaselassie Workalemahu, Wei Zhao, Devin Absher, Eva Albrecht, Denise Anderson, Jeffrey Baron, Marian Beekman, Ayşe Demirkan, Georg Ehret, Bjarke Feenstra, Mary F. Feitosa, Krista Fischer, Ross M. Fraser, Anuj Goel, Jian Gong, Anne E. Justice, Stavroula Kanoni, Marcus E. Kleber, Kati Kristiansson, Unhee Lim, Vaneet Lotay, Julian C. Lui, Massimo Mangino, Irene Mateo Leach, Carolina Medina‐Gómez, Michael A. Nalls, Dale R. Nyholt, Cameron D. Palmer, Dorota Pasko, Sonali Pechlivanis, Inga Prokopenko, Janina S. Ried, Stephan Ripke, Dmitry Shungin, Alena Stančáková, Rona J. Strawbridge, Yan V. Sun, Toshiko Tanaka, Alexander Teumer, Stella Trompet, Sander W. van der Laan, Jessica van Setten, Jana V. van Vliet‐Ostaptchouk, Thomas J. Wang, Loïc Yengo, Weihua Zhang, Uzma Afzal, Johan Ärnlöv, Gillian M. Arscott, Stefania Bandinelli, Amy Barrett, Claire Bellis, Amanda J. Bennett, Christian Berne, Matthias Blüher, Jennifer L. Bolton, Yvonne Böttcher, Heather A. Boyd, Marcel Bruinenberg, Brendan M. Buckley, Steven Buyske, Ida Henriette Caspersen, Peter S. Chines, Robert Clarke, Xueling Sim, Matthew N. Cooper, E. Warwick Daw, Pim A. de Jong, Joris Deelen, Graciela Delgado

    Vydáno 2014
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  13. 13
    An Expanded Genome-Wide Association Study of Type 2 Diabetes in Europeans

    An Expanded Genome-Wide Association Study of Type 2 Diabetes in Europeans Autor Robert A. Scott, Laura J. Scott, Reedik Mägi, Letizia Marullo, Kyle J. Gaulton, Marika Kaakinen, Natalia Pervjakova, Tune H. Pers, Andrew D. Johnson, John D. Eicher, Anne Jackson, Teresa Ferreira, Yeji Lee, Clement Ma, Valgerður Steinthórsdóttir, Guðmar Þorleifsson, Lu Qi, Natalie R. van Zuydam, Anubha Mahajan, Han Chen, Peter Almgren, Benjamin F. Voight, Harald Grallert, Martina Müller‐Nurasyid, Janina S. Ried, Nigel W. Rayner, Neil Robertson, Lennart C. Karssen, Jin‐Moo Lee, Sara M. Willems, Christian Fuchsberger, Phoenix Kwan, Tanya M. Teslovich, Pritam Chanda, Man Li, Yingchang Lu, Christian Dina, Dorothée Thuillier, Loïc Yengo, Longda Jiang, Thomas Sparsø, Hans A. Kestler, Himanshu Chheda, Lewin Eisele, Stefan Gustafsson, Mattias Frånberg, Rona J. Strawbridge, Rafn Benediktsson, Ástráður B. Hreiðarsson, Augustine Kong, Gunnar Sigurðsson, Nicola D. Kerrison, Jian’an Luan, Liming Liang, Thomas Meitinger, Michael Roden, Barbara Thorand, Tõnu Esko, Evelin Mihailov, Caroline S. Fox, Yongmei Liu, Denis Rybin, Bo Isomaa, Valeriya Lyssenko, Jaakko Tuomilehto, David Couper, James S. Pankow, Niels Grarup, Henri Theil, Marit E. Jørgensen, Torben Jørgensen, Allan Linneberg, Marilyn C. Cornelis, Rob M. van Dam, Sarah Hunt, Peter Kraft, Qi Sun, Sarah Edkins, Katharine R. Owen, John R. B. Perry, Andrew R. Wood, Eleftheria Zeggini, Juan Tajes-Fernandes, Gonçalo R. Abecasis, Lori L. Bonnycastle, Peter S. Chines, Heather M. Stringham, Heikki A. Koistinen, Leena Kinnunen, Bengt Sennblad, Hae‐Won Uh, Markus M. Nöthen, Sonali Pechlivanis, Damiano Baldassarre, Karl Gertow, Steve E. Humphries, Elena Tremoli, Norman Klopp, Julia Meyer, Gerald Steinbach

    Vydáno 2017
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  14. 14
    Genetic studies of body mass index yield new insights for obesity biology

    Genetic studies of body mass index yield new insights for obesity biology Autor Adam E. Locke, Bratati Kahali, Sonja I. Berndt, Anne E. Justice, Tune H. Pers, Felix R. Day, C. E. Powell, Sailaja Vedantam, Martin L. Buchkovich, Jian Yang, Damien C. Croteau‐Chonka, Tõnu Esko, Tove Fall, Teresa Ferreira, Stefan Gustafsson, Zoltán Kutalik, Jian’an Luan, Reedik Mägi, Joshua C. Randall, Thomas W. Winkler, Andrew R. Wood, Tsegaselassie Workalemahu, Jessica D. Faul, Jennifer A. Smith, Wei Zhao, Wei Zhao, Ming‐Huei Chen, Rudolf S.N. Fehrmann, Åsa K. Hedman, Juha Karjalainen, Ellen M. Schmidt, Devin Absher, Najaf Amin, Denise Anderson, Marian Beekman, Jennifer L. Bolton, Jennifer L. Bragg‐Gresham, Steven Buyske, Ayşe Demirkan, Guohong Deng, Georg Ehret, Bjarke Feenstra, Mary F. Feitosa, Krista Fischer, Anuj Goel, Jian Gong, Anne Jackson, Stavroula Kanoni, Marcus E. Kleber, Kati Kristiansson, Unhee Lim, Vaneet Lotay, Massimo Mangino, Irene Mateo Leach, Carolina Medina‐Gómez, Sarah E. Medland, Michael A. Nalls, Lyle J. Palmer, Dorota Pasko, Sonali Pechlivanis, Marjolein J. Peters, Inga Prokopenko, Dmitry Shungin, Alena Stančáková, Rona J. Strawbridge, Yan V. Sun, Toshiko Tanaka, Alexander Teumer, Stella Trompet, Sander W. van der Laan, Jessica van Setten, Jana V. van Vliet‐Ostaptchouk, Thomas J. Wang, Loïc Yengo, Weihua Zhang, Aaron Isaacs, Eva Albrecht, Johan Ärnlöv, Gillian M. Arscott, Antony Attwood, Stefania Bandinelli, Amy Barrett, Isabelita Bas, Claire Bellis, Amanda J. Bennett, Christian Berne, Roza Blagieva, Matthias Blüher, Stefan Böhringer, Lori L. Bonnycastle, Yvonne Böttcher, Heather A. Boyd, Marcel Bruinenberg, Ida Henriette Caspersen, Yii‐Der Ida Chen, Robert Clarke, E. Warwick Daw, Anton J. M. de Craen, Graciela Delgado, Maria Dimitriou

    Vydáno 2015
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  15. 15
    Meta-analysis of Gene-Level Associations for Rare Variants Based on Single-Variant Statistics

    Meta-analysis of Gene-Level Associations for Rare Variants Based on Single-Variant Statistics Autor Yi‐Juan Hu, Sonja I. Berndt, Stefan Gustafsson, Andrea Ganna, Joel N. Hirschhorn, Kari E. North, Erik Ingelsson, D. Y. Lin, Sonja I. Berndt, Stefan Gustafsson, Reedik Mägi, Andrea Ganna, Eleanor Wheeler, Mary F. Feitosa, Anne E. Justice, Keri L. Monda, Damien C. Croteau‐Chonka, Felix R. Day, Tõnu Esko, Tove Fall, Teresa Ferreira, Davide Gentilini, Anne Jackson, Jian’an Luan, Joshua C. Randall, Sailaja Vedantam, Cristen J. Willer, Thomas W. Winkler, Andrew R. Wood, Tsegaselassie Workalemahu, Yi‐Juan Hu, Sang Lee, Liming Liang, D. Y. Lin, Josine L. Min, Benjamin M. Neale, Guðmar Þorleifsson, Jian Yang, Eva Albrecht, Najaf Amin, Jennifer L. Bragg‐Gresham, Gemma Cadby, Martin den Heijer, Niina Eklund, Krista Fischer, Anuj Goel, Jouke‐Jan Hottenga, Jennifer E. Huffman, Ivonne Jarick, Åsa Johansson, Toby Johnson, Stavroula Kanoni, Marcus E. Kleber, Inke R. König, Kati Kristiansson, Zoltán Kutalik, Claudia Lamina, Cécile Lecœur, Li Guo, Massimo Mangino, Wendy L. McArdle, Carolina Medina‐Gómez, Martina Müller‐Nurasyid, Julius S. Ngwa, Ilja M. Nolte, Lavinia Paternoster, Sonali Pechlivanis, Markus Perola, Marjolein J. Peters, Michael Preuß, Lynda M. Rose, Jianxin Shi, Dmitry Shungin, Albert V. Smith, Rona J. Strawbridge, Ida Surakka, Alexander Teumer, Mieke D. Trip, Jonathan P. Tyrer, Jana V. van Vliet‐Ostaptchouk, Liesbeth Vandenput, Lindsay L. Waite, Jing Hua Zhao, Devin Absher, Folkert W. Asselbergs, Mustafa Atalay, Antony Attwood, Anthony J. Balmforth, Hanneke Basart, John Beilby, Lori L. Bonnycastle, Paolo Brambilla, Marcel Bruinenberg, Harry Campbell, Daniel I. Chasman, Peter S. Chines, Francis S. Collins, John Connell, William Cookson, Ulf dé Fairé

    Vydáno 2013
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  16. 16
    Genetic insights into resting heart rate and its role in cardiovascular disease

    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 2023
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