Výsledky vyhledávání - Muralidharan Sargurupremraj

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  1. 1
    Burden of Dilated Perivascular Spaces, an Emerging Marker of Cerebral Small Vessel Disease, Is Highly Heritable

    Burden of Dilated Perivascular Spaces, an Emerging Marker of Cerebral Small Vessel Disease, Is Highly Heritable Autor Marie‐Gabrielle Duperron, Christophe Tzourio, Muralidharan Sargurupremraj, Bernard Mazoyer, Aïcha Soumaré, Sabrina Schilling, Philippe Amouyel, Ganesh Chauhan, Yi‐Cheng Zhu, Stéphanie Debette

    Vydáno 2018
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  2. 2
    Genome‐wide meta‐analysis identifies 3 novel loci associated with stroke

    Genome‐wide meta‐analysis identifies 3 novel loci associated with stroke Autor Rainer Malik, Kristiina Rannikmäe, Matthew Traylor, Marios K. Georgakis, Muralidharan Sargurupremraj, Hugh S. Markus, Jemma C. Hopewell, Stéphanie Debette, Cathie Sudlow, Martin Dichgans

    Vydáno 2018
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  3. 3
    Mendelian Randomization Applied to Neurology

    Mendelian Randomization Applied to Neurology Autor Éloi Gagnon, Iyas Daghlas, Loukas Zagkos, Muralidharan Sargurupremraj, Marios K. Georgakis, Christopher D. Anderson, Héléne T. Cronjé, Stephen Burgess, Benoît J. Arsenault, Dipender Gill

    Vydáno 2024
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  4. 4
    Migraine, Stroke, and Cervical Arterial Dissection

    Migraine, Stroke, and Cervical Arterial Dissection Autor Iyas Daghlas, Muralidharan Sargurupremraj, Rebecca Danning, Padhraig Gormley, Rainer Malik, Philippe Amouyel, Tiina M. Metso, Alessandro Pezzini, Tobias Kurth, Stéphanie Debette, Daniel I. Chasman

    Vydáno 2022
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  5. 5
    Migraine, Stroke, and Cervical Arterial Dissection: Shared Genetics for a Triad of Brain Disorders With Vascular Involvement.

    Migraine, Stroke, and Cervical Arterial Dissection: Shared Genetics for a Triad of Brain Disorders With Vascular Involvement. Autor Iyas Daghals, Muralidharan Sargurupremraj, Rebecca Danning, Padhraig Gormley, Rainer Malik, Philippe Amouyel, Tiina M. Metso, Alessandro Pezzini, Tobias Kurth, Stéphanie Debette, Daniel I. Chasman

    Vydáno 2022
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  6. 6
    Genetic Insights on the Relation of Vascular Risk Factors and Cervical Artery Dissection

    Genetic Insights on the Relation of Vascular Risk Factors and Cervical Artery Dissection Autor Quentin Le Grand, Leslie Ecker Ferreira, Tiina M. Metso, Sabrina Schilling, Turgut Tatlisumak, Caspar Grond‐Ginsbach, Stefan T. Engelter, Philippe Lyrer, Jennifer J. Majersik, Bradford B. Worrall, Andrew M. Southerland, Hugh S. Markus, Mark Lathrop, Vincent Thijs, Didier Leys, Philippe Amouyel, Jean Dallongeville, Martin Dichgans, Alessandro Pezzini, Anna Bersano, Muralidharan Sargurupremraj, Stéphanie Debette

    Vydáno 2023
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  7. 7
    Genome-wide associations of aortic distensibility suggest causality for aortic aneurysms and brain white matter hyperintensities

    Genome-wide associations of aortic distensibility suggest causality for aortic aneurysms and brain white matter hyperintensities Autor Catherine Francis, Matthias E. Futschik, Jian Huang, Wenjia Bai, Muralidharan Sargurupremraj, Alexander Teumer, Monique M.B. Breteler, Enrico Petretto, Amanda S. R. Ho, Philippe Amouyel, Stefan T. Engelter, Robin Bülow, Uwe Völker, Henry Völzke, Marcus Dörr, Mohammed Aslam Imtiaz, N. Ahmad Aziz, Valerie Lohner, James S. Ware, Stéphanie Debette, Paul Elliott, Abbas Dehghan, Paul M. Matthews

    Vydáno 2022
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  8. 8
    Polygenic score integrating neurodegenerative and vascular risk informs dementia risk stratification

    Polygenic score integrating neurodegenerative and vascular risk informs dementia risk stratification Autor Tim D'Aoust, Santiago Clocchiatti‐Tuozzo, Cyprien Rivier, Aniket Mishra, Tsuyoshi Hachiya, Benjamin Grenier‐Boley, Aïcha Soumaré, Marie‐Gabrielle Duperron, Quentin Le Grand, Vincent Bouteloup, Cécile Proust‐Lima, Cécilia Samieri, Jeanne Neuffer, Muralidharan Sargurupremraj, Geneviève Chêne, Catherine Helmer, M. C. Thibault, Philippe Amouyel, Jean‐Charles Lambert, Yoichiro Kamatani, Hélène Jacqmin‐Gadda, David‐Alexandre Trégouët, Michael Inouye, Carole Dufouil, Guido J. Falcone, Stéphanie Debette

    Vydáno 2025
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  9. 9
    Genome-wide association study of cerebral small vessel disease reveals established and novel loci

    Genome-wide association study of cerebral small vessel disease reveals established and novel loci Autor Jaeyoon Chung, Sandro Marini, Joanna Pera, Bo Norrving, Jordi Jiménez-Conde, Jaume Roquer, Israel Fernández‐Cadenas, David Tirschwell, Magdy Selim, Devin L. Brown, Scott Silliman, Bradford B. Worrall, James F. Meschia, Stacie L Demel, Steven M. Greenberg, Agnieszka Słowik, Cecilia M. Lindgren, Reinhold Schmidt, Matthew Traylor, Muralidharan Sargurupremraj, Steffen Tiedt, Rainer Malik, Stéphanie Debette, Martin Dichgans, Carl D. Langefeld, Daniel Woo, Jonathan Rosand, Christopher D. Anderson

    Vydáno 2019
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  10. 10
    Genetic Complexities of Cerebral Small Vessel Disease, Blood Pressure, and Dementia

    Genetic Complexities of Cerebral Small Vessel Disease, Blood Pressure, and Dementia Autor Muralidharan Sargurupremraj, Aïcha Soumaré, Joshua C. Bis, Ida Surakka, Tuuli Jürgenson, Pierre Joly, Maria J. Knol, Ruiqi Wang, Qiong Yang, Claudia L. Satizábal, Alexander Guðjónsson, Aniket Mishra, Vincent Bouteloup, Chia‐Ling Phuah, Cornelia M. van Duijn, Carlos Cruchaga, Carole Dufouil, Geneviève Chêne, Oscar L. López, Bruce M. Psaty, Christophe Tzourio, Philippe Amouyel, Hieab H.H. Adams, Hélène Jacqmin‐Gadda, M. Arfan Ikram, Vilmundur Guðnason, Lili Milani, Bendik S. Winsvold, Kristian Hveem, Paul M. Matthews, W.T. Longstreth, Sudha Seshadri, Lenore J. Launer, Stéphanie Debette

    Vydáno 2024
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  11. 11
    Circulating Metabolome and White Matter Hyperintensities in Women and Men

    Circulating Metabolome and White Matter Hyperintensities in Women and Men Autor Eeva Sliz, Jean Shin, Shahzad Ahmad, Dylan M. Williams, Stefan Frenzel, Friederike Gauß, Sarah E. Harris, Ann‐Kristin Henning, María Valdés Hernández, Yi‐Han Hu, Beatriz Jiménez, Muralidharan Sargurupremraj, Carole H. Sudre, Ruiqi Wang, Katharina Wittfeld, Qiong Yang, Joanna M. Wardlaw, Henry Völzke, Meike W. Vernooij, Jonathan M. Schott, Marcus Richards, Petroula Proitsi, Matthias Nauck, Matthew R. Lewis, Lenore J. Launer, Norbert Hosten, Hans J. Grabe, Mohsen Ghanbari, Ian J. Deary, Simon R. Cox, Nish Chaturvedi, Josephine Barnes, Jerome I. Rotter, Stéphanie Debette, M. Arfan Ikram, Myriam Fornage, Tomáš Paus, Sudha Seshadri, Zdenka Pausová

    Vydáno 2022
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  12. 12
    A genome-wide association study identifies new loci for factor VII and implicates factor VII in ischemic stroke etiology

    A genome-wide association study identifies new loci for factor VII and implicates factor VII in ischemic stroke etiology Autor Paul S. de Vries, Maria Sabater‐Lleal, Jennifer E. Huffman, Jonathan Marten, Ci Song, Nathan Pankratz, Traci M. Bartz, Hugoline G. de Haan, Graciela E. Delgado, John D. Eicher, Ángel Martínez-Pérez, Cavin Ward‐Caviness, Jennifer A. Brody, Ming‐Huei Chen, Moniek P.M. de Maat, Mattias Frånberg, Dipender Gill, Marcus E. Kleber, Fernando Rivadeneira, José Manuel Soria, Weihong Tang, Geoffrey H. Tofler, André G. Uitterlinden, Astrid van Hylckama Vlieg, Sudha Seshadri, Eric Boerwinkle, Neil M Davies, Anne‐Katrin Giese, M. Kamran Ikram, Steven J. Kittner, Barbara McKnight, Bruce M. Psaty, Alex P. Reiner, Muralidharan Sargurupremraj, Kent D. Taylor, Myriam Fornage, Anders Hamsten, Winfried März, Frits R. Rosendaal, Juan Carlos Souto, Abbas Dehghan, Andrew D. Johnson, Alanna C. Morrison, Christopher J. O’Donnell, Nicholas L. Smith

    Vydáno 2019
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  13. 13
    Genome-wide association study of intracranial aneurysms identifies 17 risk loci and genetic overlap with clinical risk factors

    Genome-wide association study of intracranial aneurysms identifies 17 risk loci and genetic overlap with clinical risk factors Autor Mark K. Bakker, Rick A. A. van der Spek, Wouter van Rheenen, Sandrine Morel, Romain Bourcier, Isabel C. Hostettler, Varinder S. Alg, Kristel R. van Eijk, Masaru Koido, Masato Akiyama, Chikashi Terao, Koichi Matsuda, Robin Walters, Kuang Lin, Liming Li, Iona Y. Millwood, Zhengming Chen, Guy A. Rouleau, Sirui Zhou, Kristiina Rannikmäe, Cathie Sudlow, Henry Houlden, Leonard H. van den Berg, Christian Dina, Olivier Naggara, Jean‐Christophe Gentric, Eimad Shotar, François Eugène, Hubert Desal, Bendik S. Winsvold, Sigrid Børte, Marianne Bakke Johnsen, Ben Brumpton, Marie Søfteland Sandvei, Cristen J. Willer, Kristian Hveem, John‐Anker Zwart, W. M. Monique Verschuren, Christoph M. Friedrich, Sven Hirsch, Sabine Schilling, Jérôme Dauvillier, O. Martin, Gregory T. Jones, Matthew J. Bown, Nerissa Ko, Helen Kim, Jonathan R. I. Coleman, Gerome Breen, Jonathan G. Zaroff, Catharina J.M. Klijn, Rainer Malik, Martin Dichgans, Muralidharan Sargurupremraj, Turgut Tatlisumak, Philippe Amouyel, Stéphanie Debette, Gabriël J.E. Rinkel, Bradford B. Worrall, Joanna Pera, Agnieszka Słowik, Emília Gaál‐Paavola, Mika Niemelä, Juha E. Jääskeläinen, Mikael von und zu Fraunberg, Antti Lindgren, Joseph Broderick, David J. Werring, Daniel Woo, Richard Redon, Philippe Bijlenga, Yoichiro Kamatani, Jan H. Veldink, Ynte M. Ruigrok

    Vydáno 2020
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  14. 14
    Common Genetic Variation Indicates Separate Causes for Periventricular and Deep White Matter Hyperintensities

    Common Genetic Variation Indicates Separate Causes for Periventricular and Deep White Matter Hyperintensities Autor Nicola J. Armstrong, Karen A. Mather, Muralidharan Sargurupremraj, Maria J. Knol, Rainer Malik, Claudia L. Satizábal, Lisa R. Yanek, Wei Wen, Vilmundur Guðnason, Nicole Dueker, Lloyd T. Elliott, Edith Hofer, Joshua C. Bis, Neda Jahanshad, Shuo Li, Mark Logue, Michelle Luciano, Markus Scholz, Albert V. Smith, Stella Trompet, Dina Vojinović, Rui Xia, Fidel Alfaro‐Almagro, David Ames, Najaf Amin, Philippe Amouyel, Alexa S. Beiser, Henry Brodaty, Ian J. Deary, Christine Fennema‐Notestine, Piyush Gampawar, Rebecca Gottesman, Ludovica Griffanti, Clifford R. Jack, Mark Jenkinson, Jiyang Jiang, Brian G. Kral, John B. Kwok, Leonie Lampe, David C. Liewald, Pauline Maillard, Jonathan Marchini, Mark E. Bastin, Bernard Mazoyer, Lukas Pirpamer, José R. Romero, Gennady V. Roshchupkin, Peter R. Schofield, Matthias L. Schroeter, David J. Stott, Anbupalam Thalamuthu, Julian N. Trollor, Christophe Tzourio, Jeroen van der Grond, Meike W. Vernooij, A. Veronica Witte, Margaret J. Wright, Qiong Yang, Zoë Morris, Siggi Siggurdsson, Bruce M. Psaty, Arno Villringer, Helena Schmidt, Asta K. Håberg, Cornelia M. van Duijn, J. Wouter Jukema, Martin Dichgans, Ralph L. Sacco, Clinton B. Wright, William S. Kremen, Lewis C. Becker, Paul M. Thompson, Thomas H. Mosley, Joanna M. Wardlaw, M. Arfan Ikram, Hieab H.H. Adams, Sudha Seshadri, Perminder S. Sachdev, Stephen M. Smith, L. J. Launer, W.T. Longstreth, Charles DeCarli, Reinhold Schmidt, Myriam Fornage, Stéphanie Debette, Paul Nyquist

    Vydáno 2020
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  15. 15
    Genomics of perivascular space burden unravels early mechanisms of cerebral small vessel disease

    Genomics of perivascular space burden unravels early mechanisms of cerebral small vessel disease Autor Marie‐Gabrielle Duperron, Maria J. Knol, Quentin Le Grand, Tavia E. Evans, Aniket Mishra, Ami Tsuchida, Gennady V. Roshchupkin, Takahiro Konuma, David‐Alexandre Trégouët, José R. Romero, Stefan Frenzel, Michelle Luciano, Edith Hofer, Mathieu Bourgey, Nicole Dueker, Pilar Delgado, Saima Hilal, Rick M. Tankard, Florian Dubost, Jean Shin, Yasaman Saba, Nicola J. Armstrong, Constance Bordes, Mark E. Bastin, Alexa Beiser, Henry Brodaty, Robin Bülow, Caty Carrera, Christopher Chen, Ching‐Yu Cheng, Ian J. Deary, Piyush Gampawar, Jayandra J. Himali, Jiyang Jiang, Takahisa Kawaguchi, Shuo Li, Mélissa Macalli, Pascale Marquis, Zoë Morris, Susana Muñoz Maniega, Susumu Miyamoto, Masakazu Okawa, Matthew Paradise, Pedram Parva, Tatjana Rundek, Muralidharan Sargurupremraj, Sabrina Schilling, Kazuya Setoh, Omar Soukarieh, Yasuharu Tabara, Alexander Teumer, Anbupalam Thalamuthu, Julian N. Trollor, Maria C. Valdés Hernández, Meike W. Vernooij, Uwe Völker, Katharina Wittfeld, Tien Yin Wong, Margaret J. Wright, Junyi Zhang, Wanting Zhao, Yi‐Cheng Zhu, Helena Schmidt, Perminder S. Sachdev, Wei Wen, Kazumichi Yoshida, Anne Joutel, Claudia L. Satizábal, Ralph L. Sacco, Guillaume Bourque, Quentin Le Grand, Mark Lathrop, Tomáš Paus, Israel Fernández‐Cadenas, Qiong Yang, Bernard Mazoyer, Philippe Boutinaud, Yukinori Okada, Hans J. Grabe, Karen A. Mather, Reinhold Schmidt, Marc Joliot, M. Arfan Ikram, Fumihiko Matsuda, Christophe Tzourio, Joanna M. Wardlaw, Sudha Seshadri, Hieab H.H. Adams, Stéphanie Debette

    Vydáno 2023
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  16. 16
    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 Autor 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

    Vydáno 2018
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  17. 17
    GWAS and colocalization analyses implicate carotid intima-media thickness and carotid plaque loci in cardiovascular outcomes

    GWAS and colocalization analyses implicate carotid intima-media thickness and carotid plaque loci in cardiovascular outcomes Autor Nora Franceschini, Claudia Giambartolomei, Paul S. de Vries, Chris Finan, Joshua C. Bis, Rachael P. Huntley, Ruth C. Lovering, Salman M. Tajuddin, Thomas W. Winkler, Misa Graff, Maryam Kavousi, Caroline Dale, Albert V. Smith, Edith Hofer, Jin‐Moo Lee, Ilja M. Nolte, Lingyi Lu, Markus Scholz, Muralidharan Sargurupremraj, Niina Pitkänen, Oscar Franzén, Peter K. Joshi, Raymond Noordam, Riccardo E. Marioni, Shih‐Jen Hwang, Solomon K. Musani, Ulf Schminke, Walter Palmas, Aaron Isaacs, Adolfo Correa, Alan B. Zonderman, Albert Hofman, Alexander Teumer, Amanda J. Cox, André G. Uitterlinden, Andrew Wong, Andries J. Smit, Anne B. Newman, Annie Britton, Arno Ruusalepp, Bengt Sennblad, Bo Hedblad, Bogdan Paşaniuc, Brenda W.J.H. Penninx, Carl D. Langefeld, Christina L. Wassel, Christophe Tzourio, Cristiano Fava, Damiano Baldassarre, Daniel H. O’Leary, Daniel Teupser, Diana Kuh, Elena Tremoli, Elmo Mannarino, Enzo Grossi, E BOERWINKLE, Eric E. Schadt, Erik Ingelsson, Fabrizio Veglia, Fernando Rivadeneira, Frank Beutner, Ganesh Chauhan, G. Heiss, Bram P. Prins, Harry Campbell, Henry Völzke, Hugh S. Markus, Ian J. Deary, J. Wouter Jukema, Jacqueline de Graaf, Jackie F. Price, Janne Pott, Jemma C. Hopewell, Jingjing Liang, Joachim Thiery, Jorgen Engmann, Karl Gertow, Kenneth Rice, Kent D. Taylor, Klodian Dhana, Lambertus A. Kiemeney, Lars Lind, Laura M. Raffield, Lenore J. Launer, Lesca M. Holdt, Marcus Dörr, Martin Dichgans, Matthew Traylor, Matthias Sitzer, Meena Kumari, Mika Kivimäki, Mike A. Nalls, Olle Melander, Olli T. Raitakari, Oscar H. Franco, Oscar L. Rueda‐Ochoa, Panos Roussos, Peter H. Whincup, Philippe Amouyel, Philippe Giral

    Vydáno 2018
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  18. 18
    Genetic architecture of subcortical brain structures in 38,851 individuals

    Genetic architecture of subcortical brain structures in 38,851 individuals Autor Claudia L. Satizábal, Hieab H.H. Adams, Derrek P. Hibar, Charles C. White, Maria J. Knol, Jason L. Stein, Markus Scholz, Muralidharan Sargurupremraj, Neda Jahanshad, Gennady V. Roshchupkin, Albert V. Smith, Joshua C. Bis, Xueqiu Jian, Michelle Luciano, Edith Hofer, Alexander Teumer, Sven J. van der Lee, Jingyun Yang, Lisa R. Yanek, Tom V. Lee, Shuo Li, Yanhui Hu, Jia Yu Koh, John D. Eicher, Sylvane Desrivières, Alejandro Arias Vásquez, Ganesh Chauhan, Lavinia Athanasiu, Miguel E. Rentería, Sung Eun Kim, David Hoehn, Nicola J. Armstrong, Qiang Chen, Avram J. Holmes, Anouk den Braber, Iwona Kłoszewska, Micael Andersson, Thomas Espeseth, O. Grimm, Lucija Abramovic, Saud Alhusaini, Yuri Milaneschi, Martina Papmeyer, Tomas Axelsson, Stefan Ehrlich, Roberto Roiz‐Santiáñez, Bernd Kraemer, Asta K. Håberg, Hannah Jones, G. Bruce Pike, Dan J. Stein, Allison Stevens, Janita Bralten, Meike W. Vernooij, Tamara B. Harris, Irina Filippi, A. Veronica Witte, Tulio Guadalupe, Katharina Wittfeld, Thomas H. Mosley, James T. Becker, Nhat Trung Doan, Saskia P. Hagenaars, Yasaman Saba, Gabriel Cuéllar-Partida, Najaf Amin, Saima Hilal, Kwangsik Nho, Nazanin Mirza‐Schreiber, Konstantinos Arfanakis, Diane M. Becker, David Ames, Aaron L. Goldman, Phil Hyu Lee, Dorret I. Boomsma, Simon Lovestone, Sudheer Giddaluru, Stéphanie Le Hellard, Manuel Mattheisen, Marc M. Bohlken, Dalia Kasperavičiūtė, Lianne Schmaal, Stephen M. Lawrie, Ingrid Agartz, Esther Walton, Diana Tordesillas‐Gutiérrez, Gareth E. Davies, Jean Shin, Jonathan Ipser, Louis Vinke, Martine Hoogman, Tianye Jia, Ralph Burkhardt, Marieke Klein, Fabrice Crivello, Deborah Janowitz, Owen Carmichael, Unn K. Haukvik, Benjamin S. Aribisala, Helena Schmidt

    Vydáno 2019
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  19. 19
    Stroke genetics informs drug discovery and risk prediction across ancestries

    Stroke genetics informs drug discovery and risk prediction across ancestries Autor Stéphanie Debette, Aniket Mishra, Rainer Malik, Tsuyoshi Hachiya, Tuuli Jürgenson, Shinichi Namba, Masaru Koido, Quentin Le Grand, Frederick Kamanu, Mingyang Shi, Yunye He, Marios K. Georgakis, Ilana Caro, Kristi Krebs, Felix Vaura, Naomi Habib, Bendik S. Winsvold, Yon Ho Jee, Jesper Qvist Thomassen, Vida Abedi, Jara Cárcel‐Márquez, Kuang Lin, Marianne Nygaard, Ganesh Chauhan, Hampton L. Leonard, Chaojie Yang, Ekaterina Yonova-Doing, Maria J. Knol, Tetsuro Ago, Philippe Amouyel, Christopher D. Anderson, Nicole D. Armstrong, Mark K. Bakker, Traci M. Bartz, Joshua C. Bis, Constance Bordes, Sigrid Børte, Anael Cain, Paul M. Ridker, Zhengming Chen, Michael Chong, John W. Cole, Rafael de Cid, Matthias Endres, Leslie Ecker Ferreira, Natalie C. Gasca, Vilmundur Guðnason, Jun Hata, Aki S. Havulinna, Jemma C. Hopewell, Hyacinth Hyacinth, Michael Inouye, Mina A. Jacob, Christina Jeon, Christina Jern, Masahiro Kamouchi, Keith L. Keene, Takanari Kitazono, Steven J. Kittner, Takahiro Konuma, Amit Kumar, Paul Lacaze, Lenore J. Launer, Kaido Lepik, Jiang Li, Liming Li, Ani Manichaikul, Hugh S. Markus, Nicholas Marston, Thomas Meitinger, Braxton D. Mitchell, Felipe A. Montellano, Takayuki Morisaki, Thomas H. Mosley, Mike A. Nalls, Børge G. Nordestgaard, Martin O’Donnell, Yukinori Okada, Guillaume Paré, Annette Peters, Bruce M. Psaty, Stephen S. Rich, Jonathan Rosand, Marc S. Sabatine, Ralph L. Sacco, Danish Saleheen, Else Charlotte Sandset, Muralidharan Sargurupremraj, Makoto Sasaki, Claudia L. Satizábal, Carsten Oliver Schmidt, Atsushi Shimizu, Nicholas L. Smith, Daniel Strbian, Yoichi Sutoh, Kozo Tanno, Steffen Tiedt, Nuria P. Torres‐Aguila, David‐Alexandre Trégouët, Stella Trompet

    Vydáno 2022
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  20. 20
    Cardiovascular Risk Factors and MRI Markers of Cerebral Small Vessel Disease

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    Vydáno 2021
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