Хайлтын үр дүнгүүд - Anuj Goel

Үр дүнг сайжруулах
  1. 1
    A Common <i>LPA</i> Null Allele Associates With Lower Lipoprotein(a) Levels and Coronary Artery Disease Risk

    A Common <i>LPA</i> Null Allele Associates With Lower Lipoprotein(a) Levels and Coronary Artery Disease Risk -н Theodosios Kyriakou, Udo Seedorf, Anuj Goel, Jemma C. Hopewell, Robert Clarke, Hugh Watkins, Martin Farrall

    Хэвлэсэн 2014
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    Artigo
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  2. 2
    Relationship between CAD Risk Genotype in the Chromosome 9p21 Locus and Gene Expression. Identification of Eight New ANRIL Splice Variants

    Relationship between CAD Risk Genotype in the Chromosome 9p21 Locus and Gene Expression. Identification of Eight New ANRIL Splice Variants -н Lasse Folkersen, Theodosios Kyriakou, Anuj Goel, John F. Peden, Anders Mälarstig, Gabrielle Paulsson‐Berne, Anders Hamsten, Anders Franco‐Cereceda, Anders Gabrielsen, Per Eriksson

    Хэвлэсэн 2009
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    Artigo
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  3. 3
    Susceptibility to coronary artery disease and diabetes is encoded by distinct, tightly linked SNPs in the ANRIL locus on chromosome 9p

    Susceptibility to coronary artery disease and diabetes is encoded by distinct, tightly linked SNPs in the ANRIL locus on chromosome 9p -н Helen M. Broadbent, John F. Peden, Stefan Lorkowski, Anuj Goel, Halit Ongen, Fiona Green, Robert Clarke, Rory Collins, Maria Grazia Franzosi, Gianni Tognoni, Udo Seedorf, Stephan Rust, Per Eriksson, Anders Hamsten, Martin Farrall, Hugh Watkins

    Хэвлэсэн 2007
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    Artigo
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  4. 4
    Meta-analysis of gene-level tests for rare variant association

    Meta-analysis of gene-level tests for rare variant association -н Dajiang J. Liu, Gina M. Peloso, Xiaowei Zhan, Oddgeir L. Holmen, Matthew Zawistowski, Shuang Feng, Majid Nikpay, Paul L. Auer, Anuj Goel, He Zhang, Ulrike Peters, Martin Farrall, Marju Orho‐Melander, Charles Kooperberg, Ruth McPherson, Hugh Watkins, Cristen J. Willer, Kristian Hveem, Olle Melander, Sekar Kathiresan, Gonçalo R. Abecasis

    Хэвлэсэн 2013
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  5. 5
    Genetic Variants Associated with Lp(a) Lipoprotein Level and Coronary Disease

    Genetic Variants Associated with Lp(a) Lipoprotein Level and Coronary Disease -н Robert Clarke, John F. Peden, Jemma C. Hopewell, Theodosios Kyriakou, Anuj Goel, Simon Heath, Sarah Parish, Simona Barlera, Maria Grazia Franzosi, Stephan Rust, Derrick Bennett, Angela Silveira, Anders Mälarstig, Fiona R. Green, Mark Lathrop, Bruna Gigante, Karin Leander, Ulf dé Fairé, Udo Seedorf, Anders Hamsten, Rory Collins, Hugh Watkins, Martin Farrall

    Хэвлэсэн 2009
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    Artigo
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  6. 6
    Genetic variation in CADM2 as a link between psychological traits and obesity

    Genetic variation in CADM2 as a link between psychological traits and obesity -н Julia Morris, Mark E.S. Bailey, Damiano Baldassarre, Breda Cullen, Ulf dé Fairé, Amy Ferguson, Bruna Gigante, Philippe Giral, Anuj Goel, Nicholas Graham, Anders Hamsten, Steve E. Humphries, Keira J.A. Johnston, Donald M. Lyall, Laura M. Lyall, Bengt Sennblad, Angela Silveira, Andries J. Smit, Elena Tremoli, Fabrizio Veglia, Joey Ward, Hugh Watkins, Daniel J. Smıth, Rona J. Strawbridge

    Хэвлэсэн 2019
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  7. 7
    Network analysis of coronary artery disease risk genes elucidates disease mechanisms and druggable targets

    Network analysis of coronary artery disease risk genes elucidates disease mechanisms and druggable targets -н Harri Lempiäinen, Ingrid Brænne, Tom Michoel, Vinicius Tragante, Baiba Vilne, Tom R. Webb, Theodosios Kyriakou, Johannes Eichner, Lingyao Zeng, Christina Willenborg, Oscar Franzén, Arno Ruusalepp, Anuj Goel, Sander W. van der Laan, Claudia Biegert, Stephen E. Hamby, Husain A. Talukdar, Hassan Foroughi Asl, Martin Dichgans, Tobias Dreker, Mira Graettinger, Philip Gribbon, Thorsten Kessler, Rainer Malik, Matthias Prestel, Barbara Stiller, Christine Schofield, Gerard Pasterkamp, Hugh Watkins, Nilesh J. Samani, Timo Wittenberger, Jeanette Erdmann, Heribert Schunkert, Folkert W. Asselbergs, Johan Björkegren

    Хэвлэсэн 2018
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    Artigo
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  8. 8
    Exome Sequencing and Directed Clinical Phenotyping Diagnose Cholesterol Ester Storage Disease Presenting as Autosomal Recessive Hypercholesterolemia

    Exome Sequencing and Directed Clinical Phenotyping Diagnose Cholesterol Ester Storage Disease Presenting as Autosomal Recessive Hypercholesterolemia -н Nathan O. Stitziel, Sigrid W. Fouchier, Barbara Sjouke, Gina M. Peloso, Alessa M. Moscoso, Paul L. Auer, Anuj Goel, Bruna Gigante, Timothy Barnes, Olle Melander, Marju Orho‐Melander, Stefano Duga, Suthesh Sivapalaratnam, Majid Nikpay, Nicola Martinelli, Domenico Girelli, Rebecca D. Jackson, Charles Kooperberg, Leslie A. Lange, Diego Ardissino, Ruth McPherson, Martin Farrall, Hugh Watkins, Muredach P. Reilly, Daniel J. Rader, Ulf dé Fairé, Heribert Schunkert, Jeanette Erdmann, Mark M. Iles, Lawrence Charnas, David Altshuler, Stacey Gabriel, John J.P. Kastelein, Joep C. Defesche, Aart J. Nederveen, Sekar Kathiresan, G. Kees Hovingh

    Хэвлэсэн 2013
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  9. 9
    Evaluation of polygenic scores for hypertrophic cardiomyopathy in the general population and across clinical settings

    Evaluation of polygenic scores for hypertrophic cardiomyopathy in the general population and across clinical settings -н Sean L. Zheng, Sean J. Jurgens, Kathryn A. McGurk, Xiao Yun Xu, Chris Grace, Pantazis Theotokis, Rachel Buchan, Catherine Francis, Antonio de Marvao, Lara Curran, Wenjia Bai, Chee Jian Pua, Hak Chiaw Tang, Paloma Jordà, Marjon A. van Slegtenhorst, Judith M.A. Verhagen, Andrew R. Harper, Elizabeth Ormondroyd, Calvin Chin, Antonio de Marvao, Marjon A. van Slegtenhorst, James S. Ware, Antonios Pantazis, John Baksi, Brian P. Halliday, Paul M. Matthews, Yigal M. Pinto, Roddy Walsh, Ahmad S. Amin, Arthur A.M. Wilde, Stuart A. Cook, Sanjay Prasad, Paul J.R. Barton, Declan P. O’Regan, R. Thomas Lumbers, Anuj Goel, Rafik Tadros, Michelle Michels, Hugh Watkins, Connie R. Bezzina, James S. Ware

    Хэвлэсэн 2025
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    Artigo
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  10. 10
    Association Between the Chromosome 9p21 Locus and Angiographic Coronary Artery Disease Burden

    Association Between the Chromosome 9p21 Locus and Angiographic Coronary Artery Disease Burden -н Kenneth Chan, Riyaz S. Patel, Paul J. Newcombe, Christopher P. Nelson, Atif Qasim, Stephen E. Epstein, Susan Burnett, Viola Vaccarino, A. Maziar Zafari, Svati H. Shah, Jeffrey L. Anderson, John F. Carlquist, Jaana Hartiala, Hooman Allayee, Kunihiko Hinohara, Bok-Soo Lee, Anna Erl, Katrina L. Ellis, Anuj Goel, Arne S. Schäefer, Nour Eddine El Mokhtari, Benjamin A. Goldstein, Mark A. Hlatky, Alan S. Go, Gong-Qing Shen, Yan Gong, Carl J. Pepine, Ross C. Laxton, John C. Whittaker, W.H. Wilson Tang, Julie A. Johnson, Qing K. Wang, Themistocles L. Assimes, Ute Nöthlings, Martin Farrall, Hugh Watkins, Mark Richards, Vicky A. Cameron, Axel Muendlein, Heinz Drexel, Werner Koch, Jeong Euy Park, Akinori Kimura, Weifeng Shen, Iain Simpson, Stanley L. Hazen, Benjamin D. Horne, Elizabeth R. Hauser, Arshed A. Quyyumi, Muredach P. Reilly, Nilesh J. Samani, Shu Ye

    Хэвлэсэн 2013
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  11. 11
    Coding Variation in<i>ANGPTL4,</i><i>LPL,</i>and<i>SVEP1</i>and the Risk of Coronary Disease

    Coding Variation in<i>ANGPTL4,</i><i>LPL,</i>and<i>SVEP1</i>and the Risk of Coronary Disease -н Nathan O. Stitziel, Kathleen Stirrups, Nicholas G. D. Masca, Jeanette Erdmann, Paola G. Ferrario, Inke R. König, Peter Weeke, Tom R. Webb, Paul L. Auer, Ursula M. Schick, Yingchang Lu, He Zhang, Marie‐Pierre Dubé, Anuj Goel, Martin Farrall, Gina M. Peloso, Hong‐Hee Won, Ron Do, Erik P.A. van Iperen, Stavroula Kanoni, Jochen Kruppa, Anubha Mahajan, Robert A. Scott, Christina Willenberg, Peter S. Braund, Julian C. van Capelleveen, Alex S. F. Doney, Louise A. Donnelly, Rosanna Asselta, Piera Angelica Merlini, Stefano Duga, Nicola Marziliano, Joshua C. Denny, Christian M. Shaffer, Nour Eddine El Mokhtari, Andre Franke, Omri Gottesman, Stefanie Heilmann‐Heimbach, Christian Hengstenberg, Per Hoffman, Oddgeir L. Holmen, Kristian Hveem, Jan‐Håkan Jansson, Karl‐Heinz Jöckel, Thorsten Kessler, Jennifer Kriebel, Karl‐Ludwig Laugwitz, Eirini Marouli, Nicola Martinelli, Børge G. Nordestgaard, Tibor V. Varga

    Хэвлэсэн 2016
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    Artigo
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  12. 12
    Distribution and Medical Impact of Loss-of-Function Variants in the Finnish Founder Population

    Distribution and Medical Impact of Loss-of-Function Variants in the Finnish Founder Population -н Elaine T. Lim, Peter Würtz, Aki S. Havulinna, Priit Palta, Taru Tukiainen, Karola Rehnström, Tõnu Esko, Reedik Mägi, Michael Inouye, Tuuli Lappalainen, Yingleong Chan, Rany M. Salem, Monkol Lek, Jason Flannick, Xueling Sim, Alisa K. Manning, Claes Ladenvall, Suzannah Bumpstead, Eija Hämäläinen, Kristiina Aalto, Mikael Maksimow, Marko Salmi, Stefan Blankenberg, Diego Ardissino, Svati H. Shah, Benjamin D. Horne, Ruth McPherson, Gerald K. Hovingh, Muredach P. Reilly, Hugh Watkins, Anuj Goel, Martin Farrall, Domenico Girelli, Alex P. Reiner, Nathan O. Stitziel, Sekar Kathiresan, Stacey Gabriel, Jeffrey C. Barrett, Terho Lehtimäki, Markku Laakso, Leif Groop, Jaakko Kaprio, Markus Perola, Mark I. McCarthy, Michael Boehnke, David Altshuler, Cecilia M. Lindgren, Joel N. Hirschhorn, Andres Metspalu, Nelson B. Freimer, Tanja Zeller, Sirpa Jalkanen, Seppo Koskinen, Olli T. Raitakari, Richard Durbin, Daniel G. MacArthur, Veikko Salomaa, Samuli Ripatti, Mark J. Daly, Aarno Palotie

    Хэвлэсэн 2014
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    Artigo
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  13. 13
    Causal Assessment of Serum Urate Levels in Cardiometabolic Diseases Through a Mendelian Randomization Study

    Causal Assessment of Serum Urate Levels in Cardiometabolic Diseases Through a Mendelian Randomization Study -н Tanya E. Keenan, Wei Zhao, Asif Rasheed, Weang-Kee Ho, Rainer Malik, Janine F. Felix, Robin Young, Nabi Shah, Maria Samuel, Nasir Sheikh, Megan Mucksavage, Omar J. Shah, Jin Li, Michael P. Morley, Annika Laser, Nadeem Hayat Mallick, Khan Shah Zaman, Mohammad Ishaq, Syed Zahed Rasheed, Fazal-ur-Rehman Memon, Faisal Ahmed, Bashir Hanif, Muhammad Shakir Lakhani, Muhammad Fahim, Madiha Ishaq, Naresh Kumar Shardha, Naveeduddin Ahmed, Khalid Mahmood, Waseem Iqbal, Saba Akhtar, Rabia Raheel, Christopher J. O’Donnell, Christian Hengstenberg, W. März, Sekar Kathiresan, Nilesh J. Samani, Anuj Goel, Jemma C. Hopewell, John C. Chambers, Yu-Ching Cheng, Pankaj Sharma, Qiong Yang, Jonathan Rosand, Giorgio B. Boncoraglio, Shahana Urooj Kazmi, Hákon Hákonarson, Anna Köttgen, Andreas P. Kalogeropoulos, Philippe Frossard, Ayeesha Kamran Kamal, Martin Dichgans, Thomas P. Cappola, Muredach P. Reilly, John Danesh, Daniel J. Rader, Benjamin F. Voight, Danish Saleheen

    Хэвлэсэн 2016
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    Artigo
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  14. 14
    Common genetic loci influencing plasma homocysteine concentrations and their effect on risk of coronary artery disease

    Common genetic loci influencing plasma homocysteine concentrations and their effect on risk of coronary artery disease -н Joyce B. J. van Meurs, Guillaume Paré, Stephen M. Schwartz, Aditi Hazra, Toshiko Tanaka, Sita H. Vermeulen, Ioana Cotlarciuc, Xin Yuan, Anders Mälarstig, Stefania Bandinelli, Joshua C. Bis, Henk J. Blom, Matthew A. Brown, Constance Chen, Yii-Der Chen, Robert Clarke, Abbas Dehghan, Jeanette Erdmann, Luigi Ferrucci, Anders Hamsten, Albert Hofman, David J. Hunter, Anuj Goel, Andrew D. Johnson, Sekar Kathiresan, Ellen Kampman, Douglas P. Kiel, Lambertus A. Kiemeney, John C. Chambers, Peter Kraft, Jan Lindemans, Barbara McKnight, Christopher P. Nelson, Christopher J. O’Donnell, Bruce M. Psaty, Paul M. Ridker, Fernando Rivadeneira, Lynda M. Rose, Udo Seedorf, David S. Siscovick, Heribert Schunkert, Jacob Selhub, Per Magne Ueland, Péter Vollenweider, Gérard Waeber, Dawn Waterworth, Hugh Watkins, Jacqueline C.M. Witteman, Martin den Heijer, Paul F. Jacques, André G. Uitterlinden, Jaspal S. Kooner, Dan Rader, Muredach P. Reilly, Vincent Mooser, Daniel I. Chasman, Nilesh J. Samani, Kourosh R. Ahmadi

    Хэвлэсэн 2013
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  15. 15
    Association analyses based on false discovery rate implicate new loci for coronary artery disease

    Association analyses based on false discovery rate implicate new loci for coronary artery disease -н Christopher P. Nelson, Anuj Goel, Adam S. Butterworth, Stavroula Kanoni, Tom R. Webb, Eirini Marouli, Lingyao Zeng, Ιωάννα Ντάλλα, Florence Lai, Jemma C. Hopewell, Olga Giannakopoulou, Tao Jiang, Stephen E. Hamby, Emanuele Di Angelantonio, Themistocles L. Assimes, Erwin P. Böttinger, John C. Chambers, Robert Clarke, Colin N. A. Palmer, Richard M. Cubbon, Patrick T. Ellinor, Raili Ermel, Εvangelos Εvangelou, Paul W. Franks, Christopher Grace, Dongfeng Gu, Aroon D. Hingorani, Joanna M. M. Howson, Erik Ingelsson, Adnan Kastrati, Thorsten Kessler, Theodosios Kyriakou, Terho Lehtimäki, Xiangfeng Lu, Yingchang Lu, Winfried März, Ruth McPherson, Andres Metspalu, Mar Pujades‐Rodríguez, Arno Ruusalepp, Eric E. Schadt, Amand F. Schmidt, Michael Sweeting, Pierre Zalloua, Kamal AlGhalayini, Bernard Keavney, Jaspal S. Kooner, Ruth J. F. Loos, Riyaz Patel, Martin K. Rutter, Maciej Tomaszewski, Ioanna Tzoulaki, Eleftheria Zeggini, Jeanette Erdmann, George Dedoussis, Johan Björkegren, Heribert Schunkert, Martin Farrall, John Danesh, Nilesh J. Samani, Hugh Watkins, Panos Deloukas

    Хэвлэсэн 2017
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    Artigo
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  16. 16
    Reevaluation of the South Asian <i>MYBPC3</i> <sup>Δ25bp</sup> Intronic Deletion in Hypertrophic Cardiomyopathy

    Reevaluation of the South Asian <i>MYBPC3</i> <sup>Δ25bp</sup> Intronic Deletion in Hypertrophic Cardiomyopathy -н Andrew R. Harper, Michael Bowman, Jesse B.G. Hayesmoore, Helen Sage, Silvia Salatino, Edward Blair, Carolyn Campbell, Bethany Currie, Anuj Goel, Karen McGuire, Elizabeth Ormondroyd, Kate Sergeant, Adam Waring, Jessica Woodley, Christopher M. Kramer, Stefan Neubauer, Martin Farrall, Hugh Watkins, Kate Thomson, Theodore P. Abraham, Lisa Anderson, Evan Appelbaum, Camillo Autore, Colin Berry, Elena Biagini, William Bradlow, Chiara Bucciarelli‐Ducci, Amedeo Chiribiri, Lubna Choudhury, Andrew M. Crean, Dana Dawson, Milind Y. Desai, Eleanor Elstein, Andrew Flett, Matthias G. Friedrich, Stephen B. Heitner, Adam S. Helms, Carolyn Y. Ho, Daniel Jacoby, Han Kim, Bette Kim, Éric Larose, Masliza Mahmod, Heiko Mahrholdt, Martin S. Maron, Gerry P McCann, Michelle Michaels, Saidi Mohiddin, Sherif F. Nagueh, David E. Newby, Iacopo Olivotto, Anjali Owens, François Pierre-Mongeon, Sanjay Prasad, Ornella Rimoldi, Michael Salerno, Jeanette Schulz‐Menger, Mark V. Sherrid, Peter Swoboda, Albert C. van Rossum, Jonathan W. Weinsaft, James A. White, Eric E. Williamson

    Хэвлэсэн 2020
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  17. 17
    Common genetic variants and modifiable risk factors underpin hypertrophic cardiomyopathy susceptibility and expressivity

    Common genetic variants and modifiable risk factors underpin hypertrophic cardiomyopathy susceptibility and expressivity -н Andrew R. Harper, Anuj Goel, Christopher Grace, Kate Thomson, Steffen E. Petersen, Xiao Hua Xu, Adam Waring, Elizabeth Ormondroyd, Christopher M. Kramer, Carolyn Y. Ho, Stefan Neubauer, Paul Kolm, Raymond Y. Kwong, Sarahfaye Dolman, Patrice Desvigne‐Nickens, John Dimarco, Nancy L. Geller, Dong‐Yun Kim, Cheng Zhang, William S. Weintraub, Theodore P. Abraham, Lisa Anderson, Evan Appelbaum, Camillo Autore, Colin Berry, Elena Biagini, William Bradlow, Chiara Bucciarelli‐Ducci, Amedeo Chiribiri, Lubna Choudhury, Andrew M. Crean, Dana Dawson, Milind Y. Desai, Eleanor Elstein, Andrew Flett, Matthias G. Friedrich, Stephen B. Heitner, Adam S. Helms, Daniel Jacoby, Han Kim, Bette Kim, Éric Larose, Masliza Mahmod, Heiko Mahrholdt, Martin S. Maron, Gerry P McCann, Michelle Michels, Saidi Mohiddin, Sherif F. Nagueh, David E. Newby, Iacopo Olivotto, Anjali Owens, François Pierre-Mongeon, Sanjay Prasad, Ornella Rimoldi, Michael Salerno, Jeanette Schulz‐Menger, Mark V. Sherrid, Peter Swoboda, Albert C. van Rossum, Jonathan W. Weinsaft, James A. White, Eric E. Williamson, Rafik Tadros, James S. Ware, Connie R. Bezzina, Martin Farrall, Hugh Watkins

    Хэвлэсэн 2021
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    Artigo
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  18. 18
    Large-scale genome-wide association analyses identify novel genetic loci and mechanisms in hypertrophic cardiomyopathy

    Large-scale genome-wide association analyses identify novel genetic loci and mechanisms in hypertrophic cardiomyopathy -н Rafik Tadros, Sean L. Zheng, Christopher Grace, Paloma Jordà, Catherine Francis, Dominique M West, Sean J. Jurgens, Kate Thomson, Andrew R. Harper, Elizabeth Ormondroyd, Xiao Yun Xu, Pantazis Theotokis, Rachel Buchan, Kathryn A. McGurk, Francesco Mazzarotto, Beatrice Boschi, Elisabetta Pelo, Michael Lee, Michela Noseda, Amanda Varnava, Alexa M.C. Vermeer, Roddy Walsh, Ahmad S. Amin, Marjon A. van Slegtenhorst, Nicole M. Roslin, Lisa J. Strug, Erika Salvi, Chiara Lanzani, Antonio de Marvao, Jason D. Roberts, Maxime Tremblay‐Gravel, Geneviève Giraldeau, Julia Cadrin‐Tourigny, Philippe L. L’Allier, Patrick Garceau, Mario Talajic, Sarah A. Gagliano Taliun, Yigal M. Pinto, Harry Rakowski, Antonis Pantazis, Wenjia Bai, John Baksi, Brian P. Halliday, Sanjay Prasad, Paul J.R. Barton, Declan P. O’Regan, Stuart A. Cook, Rudolf A. de Boer, Imke Christiaans, Michelle Michels, Christopher M. Kramer, Carolyn Y. Ho, Stefan Neubauer, Paul M. Matthews, Arthur A.M. Wilde, Jean‐Claude Tardif, Iacopo Olivotto, Arnon Adler, Anuj Goel, James S. Ware, Connie R. Bezzina, Hugh Watkins

    Хэвлэсэн 2025
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  19. 19
    Rare and low-frequency variants and their association with plasma levels of fibrinogen, FVII, FVIII, and vWF

    Rare and low-frequency variants and their association with plasma levels of fibrinogen, FVII, FVIII, and vWF -н Jennifer E. Huffman, Paul S. de Vries, Alanna C. Morrison, Maria Sabater‐Lleal, Tim Kacprowski, Paul L. Auer, Jennifer A. Brody, Daniel I. Chasman, Ming‐Huei Chen, Xiuqing Guo, Li‐An Lin, Riccardo E. Marioni, Martina Müller‐Nurasyid, Lisa R. Yanek, Nathan Pankratz, Megan L. Grove, Moniek P.M. de Maat, Mary Cushman, Kerri L. Wiggins, Lihong Qi, Bengt Sennblad, Sarah E. Harris, Ozren Polašek, Helene Riess, Fernando Rivadeneira, Lynda M. Rose, Anuj Goel, Kent D. Taylor, Alexander Teumer, André G. Uitterlinden, Dhananjay Vaidya, Jie Yao, Weihong Tang, Daniel Levy, Mélanie Waldenberger, Diane M. Becker, Aaron R. Folsom, Franco Giulianini, Andreas Greinacher, Albert Hofman, Chiang‐Ching Huang, Charles Kooperberg, Angela Silveira, John M. Starr, Konstantin Strauch, Rona J. Strawbridge, Alan F. Wright, Barbara McKnight, Oscar H. Franco, Neil A. Zakai, Rasika A. Mathias, Bruce M. Psaty, Paul M. Ridker, Geoffrey H. Tofler, Uwe Völker, Hugh Watkins, Myriam Fornage, Anders Hamsten, Ian J. Deary, Eric Boerwinkle, Wolfgang Köenig, Jerome I. Rotter, Caroline Hayward, Abbas Dehghan, Alex P. Reiner, Christopher J. O’Donnell, Nicholas L. Smith

    Хэвлэсэн 2015
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  20. 20
    Loss of Cardioprotective Effects at the <i>ADAMTS7</i> Locus as a Result of Gene-Smoking Interactions

    Loss of Cardioprotective Effects at the <i>ADAMTS7</i> Locus as a Result of Gene-Smoking Interactions -н Danish Saleheen, Wei Zhao, Robin Young, Christopher P. Nelson, Weang-Kee Ho, Jane F. Ferguson, Asif Rasheed, Kristy Ou, Sylvia Nürnberg, Robert C. Bauer, Anuj Goel, Ron Do, Alexandre F.R. Stewart, Jaana Hartiala, Weihua Zhang, Guðmar Þorleifsson, Rona J. Strawbridge, Juha Sinisalo, Stavroula Kanoni, Sanaz Sedaghat, Eirini Marouli, Kati Kristiansson, Wei Zhao, Robert A. Scott, Dominique Gauguier, Svati H. Shah, Albert V. Smith, Natalie Van Zuydam, Amanda J. Cox, Christina Willenborg, Thorsten Kessler, Lingyao Zeng, Michael A. Province, Andrea Ganna, Lars Lind, Nancy L. Pedersen, Charles C. White, Anni Joensuu, Marcus E. Kleber, Alistair S. Hall, Winfried März, Veikko Salomaa, Christopher J. O’Donnell, Erik Ingelsson, Mary F. Feitosa, Jeanette Erdmann, Donald W. Bowden, Colin N. A. Palmer, Vilmundur Guðnason, Ulf dé Fairé, Pierre Zalloua, Nicholas J. Wareham, John R. Thompson, Kari Kuulasmaa, George Dedoussis, Markus Perola, Abbas Dehghan, John C. Chambers, Jaspal S. Kooner, Hooman Allayee, Panos Deloukas, Ruth McPherson, Kāri Stefánsson, Heribert Schunkert, Sekar Kathiresan, Martin Farrall, Philippe M. Frossard, Daniel J. Rader, Nilesh J. Samani, Muredach P. Reilly

    Хэвлэсэн 2017
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    Artigo
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