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David J. Tester

1994–2025 年に発表

121
論文数
20,136
被引用数
86
h 指数
119
i10 指数

被引用数

David J. Tester の年別被引用数1995 年: 被引用 9 件1996 年: 被引用 5 件1997 年: 被引用 10 件1998 年: 被引用 25 件1999 年: 被引用 69 件2000 年: 被引用 76 件2001 年: 被引用 72 件2002 年: 被引用 69 件2003 年: 被引用 51 件2004 年: 被引用 79 件2005 年: 被引用 118 件2006 年: 被引用 115 件2007 年: 被引用 147 件2008 年: 被引用 208 件2009 年: 被引用 223 件2010 年: 被引用 198 件2011 年: 被引用 255 件2012 年: 被引用 219 件2013 年: 被引用 240 件2014 年: 被引用 137 件2015 年: 被引用 187 件2016 年: 被引用 165 件2017 年: 被引用 127 件2018 年: 被引用 150 件2019 年: 被引用 453 件2020 年: 被引用 512 件2021 年: 被引用 466 件2022 年: 被引用 484 件2023 年: 被引用 265 件2024 年: 被引用 373 件2025 年: 被引用 152 件2026 年: 被引用 7 件

引用元

国・地域

この著者を引用した国・地域の世界地図アメリカ合衆国: 引用元論文 1,669 件、この内訳の 26.9%イギリス: 引用元論文 460 件、この内訳の 7.4%イタリア: 引用元論文 412 件、この内訳の 6.6%オランダ: 引用元論文 351 件、この内訳の 5.7%カナダ: 引用元論文 296 件、この内訳の 4.8%ドイツ: 引用元論文 294 件、この内訳の 4.7%中国: 引用元論文 282 件、この内訳の 4.6%フランス: 引用元論文 236 件、この内訳の 3.8%日本: 引用元論文 229 件、この内訳の 3.7%オーストラリア: 引用元論文 228 件、この内訳の 3.7%スペイン: 引用元論文 184 件、この内訳の 3%デンマーク: 引用元論文 125 件、この内訳の 2%
0%26.9%その他 23.1%

機関

分野

  • Medicine72.3%
  • Biochemistry, Genetics and Molecular Biology23.3%
  • Neuroscience2.8%
  • Computer Science0.3%
  • Pharmacology, Toxicology and Pharmaceutics0.3%
  • Agricultural and Biological Sciences0.2%
  • その他0.8%

トピック

  • Cardiac electrophysiology and arrhythmias15.2%
  • Ion channel regulation and function9.2%
  • Cardiovascular Effects of Exercise4.7%
  • Cardiomyopathy and Myosin Studies4.7%
  • Genetic factors in colorectal cancer4.7%
  • Cardiac Arrhythmias and Treatments3.4%
  • その他58.1%

共著者

全論文

検索で開く
  1. Transethnic Genome-Wide Association Study Provides Insights in the Genetic Architecture and Heritability of Long QT Syndrome

    著者: Najim Lahrouchi, Rafik Tadros, Lia Crotti, Yuka Mizusawa, Pieter G. Postema, Leander Beekman, Roddy Walsh, Kanae Hasegawa, Julien Barc, Marko Ernsting, Kari L. Turkowski, Andrea Mazzanti, Britt M. Beckmann, Keiko Shimamoto, Ulla‐Britt Diamant, Yanushi D. Wijeyeratne, Yu Kucho, Tomas Robyns, Taisuke Ishikawa, Elena Arbelo, Michael Christiansen, Annika Winbo, Reza Jabbari, Steven A. Lubitz, Johannes Steinfurt, Boris Rudic, Bart Loeys, Moore B. Shoemaker, Peter Weeke, Ryan Pfeiffer, Brianna Davies, Antoine Andorin, Nynke Hofman, Federica Dagradi, Matteo Pedrazzini, David J. Tester, J. Martijn Bos, Georgia Sarquella‐Brugada, Óscar Campuzano, Pyotr G. Platonov, Birgit Stallmeyer, Sven Zumhagen, Eline A. Nannenberg, Jan H. Veldink, Leonard H. van den Berg, Ammar Al‐Chalabi, Christopher E. Shaw, Pamela J. Shaw, Karen Morrison, Peter M. Andersen, Martina Müller‐Nurasyid, Daniele Cusi, Cristina Barlassina, Pilar Galán, Mark Lathrop, Markus Munter, Thomas Werge, Marta Ribasés, Tin Aung, Chiea Chuen Khor, Mineo Ozaki, Peter Lichtner, Thomas Meitinger, J. Peter van Tintelen, Yvonne M. Hoedemaekers, Isabelle Denjoy, Antoine Leenhardt, Carlo Napolitano, Wataru Shimizu, Jean‐Jacques Schott, Jean‐Baptiste Gourraud, Takeru Makiyama, Seiko Ohno, Hideki Itoh, Andrew D. Krahn, Charles Antzelevitch, Dan M. Roden, Johan Saenen, Martin Borggrefe, Katja E. Odening, Patrick T. Ellinor, Jacob Tfelt‐Hansen, Jonathan R. Skinner, Maarten P. van den Berg, Morten S. Olesen, Josép Brugada, Ramón Brugada, Naomasa Makita, Jeroen Breckpot, Masao Yoshinaga, Elijah R. Behr, Annika Rydberg, Takeshi Aiba, Stefan Kääb, Silvia G. Priori, Pascale Guicheney, Hanno L. Tan, Christopher Newton‐Cheh, Michael Ackerman, Peter J. Schwartz ほか 6 名 - Circulation 2020 被引用: 141

  2. An international compendium of mutations in the SCN5A-encoded cardiac sodium channel in patients referred for Brugada syndrome genetic testing

    著者: Jamie D. Kapplinger, David J. Tester, Mariëlle Alders, Begoña Benito, Myriam Berthet, Josép Brugada, Pedro Brugada, Véronique Fressart, Alejandra Guerchicoff, Carole Harris‐Kerr, Shiro Kamakura, Florence Kyndt, Tamara T. Koopmann, Yoshihiro Miyamoto, Ryan Pfeiffer, Guido D. Pollevick, Vincent Probst, Sven Zumhagen, Matteo Vatta, Jeffrey A. Towbin, Wataru Shimizu, Eric Schulze‐Bahr, Charles Antzelevitch, Benjamin A. Salisbury, Pascale Guicheney, Arthur A.M. Wilde, Ramón Brugada, Jean‐Jacques Schott, Michael J. Ackerman - Heart Rhythm 2009 被引用: 764

  3. Plakophilin-2 is required for transcription of genes that control calcium cycling and cardiac rhythm

    著者: Marina Cerrone, Jérôme Montnach, Xianming Lin, Yan-Ting Zhao, Mingliang Zhang, Esperanza Agulló-Pascual, Alejandra Leo‐Macías, Francisco Alvarado, Igor Dolgalev, Thomas V. Karathanos, Kabir Malkani, Chantal J.M. van Opbergen, Joanne J.A. van Bavel, Hua-Qian Yang, Carolina Vásquez, David J. Tester, Steven J. Fowler, Feng‐Xia Liang, Eli Rothenberg, Adriana Heguy, Gregory E. Morley, William A. Coetzee, Natalia A. Trayanova, Michael J. Ackerman, Toon A.B. van Veen, Héctor H. Valdivia, Mario Delmar - Nature Communications 2017 被引用: 202

  4. Suppression-Replacement KCNQ1 Gene Therapy for Type 1 Long QT Syndrome

    著者: Steven M. Dotzler, C.S. John Kim, William A.C. Gendron, Wei Zhou, Dan Ye, J. Martijn Bos, David J. Tester, Michael A. Barry, Michael J. Ackerman - Circulation 2021 被引用: 86

  5. Systematic Review of the Genetics of Sudden Unexpected Death in Epilepsy: Potential Overlap With Sudden Cardiac Death and Arrhythmia‐Related Genes

    著者: C. Anwar A. Chahal, Mohammad N. Salloum, Fares Alahdab, Joseph A. Gottwald, David J. Tester, Lucman A. Anwer, Elson L. So, M. Hassan Murad, Erik K. St. Louis, Michael J. Ackerman, Virend K. Somers - Journal of the American Heart Association 2019 被引用: 126

  6. Enhancing rare variant interpretation in inherited arrhythmias through quantitative analysis of consortium disease cohorts and population controls

    著者: Roddy Walsh, Najim Lahrouchi, Rafik Tadros, Florence Kyndt, Charlotte Glinge, Pieter G. Postema, Ahmad S. Amin, Eline A. Nannenberg, James S. Ware, Nicola Whiffin, Francesco Mazzarotto, Doris Škorić‐Milosavljević, Christian Krijger, Elena Arbelo, Dominique Babuty, Héctor Barajas-Martínez, Britt Maria Beckmann, Stéphane Bezieau, J. Martijn Bos, Jeroen Breckpot, Óscar Campuzano, Silvia Castelletti, Candan Celen, Sebastian Clauß, Anniek Corveleyn, Lia Crotti, Federica Dagradi, Carlo de Asmundis, Isabelle Denjoy, Sven Dittmann, Patrick T. Ellinor, Cristina Gil, Carla Giustetto, Jean‐Baptiste Gourraud, Daisuke Hazeki, Minoru Horie, Taisuke Ishikawa, Hideki Itoh, Yoshiaki Kaneko, Jørgen K. Kanters, Hiroki Kimoto, Maria‐Christina Kotta, Ingrid P.C. Krapels, Masahiko Kurabayashi, Julieta Lazarte, Antoine Leenhardt, Bart Loeys, Catarina Lundin, Takeru Makiyama, Jacques Mansourati, Raphaël P. Martins, Andrea Mazzanti, Stellan Mörner, Carlo Napolitano, Kimie Ohkubo, Michael Papadakis, Boris Rudic, María Sabater‐Molina, Frédéric Sacher, Hatice Şahin, Georgia Sarquella‐Brugada, Regina Sebastiano, Sanjay Sharma, Mary N. Sheppard, Keiko Shimamoto, M. Benjamin Shoemaker, Birgit Stallmeyer, Johannes Steinfurt, Yuji Tanaka, David J. Tester, Keisuke Usuda, Paul A. van der Zwaag, Sonia Van Dooren, Lut Van Laer, Annika Winbo, Bo Gregers Winkel, Kenichiro Yamagata, Sven Zumhagen, Paul G.A. Volders, Steven A. Lubitz, Charles Antzelevitch, Pyotr G. Platonov, Katja E. Odening, Dan M. Roden, Jason D. Roberts, Jonathan R. Skinner, Jacob Tfelt-Hansen, Maarten P. van den Berg, Morten S. Olesen, Pier D. Lambiase, Martin Borggrefe, Kenshi Hayashi, Annika Rydberg, Tadashi Nakajima, Masao Yoshinaga, Johan Saenen, Stefan Kääb, Pedro Brugada, Tomas Robyns, Daniela Giachino ほか 30 名 - Genetics in Medicine 2020 被引用: 105

  7. Hypermethylation of the hMLH1 promoter in colon cancer with microsatellite instability.

    著者: Julie M. Cunningham, Eric R. Christensen, David J. Tester, Cheong Yong Kim, Patrick C. Roche, Lawrence J. Burgart, Stephen N. Thibodeau - 1998 被引用: 875

  8. Spectrum and prevalence of mutations from the first 2,500 consecutive unrelated patients referred for the FAMILION® long QT syndrome genetic test

    著者: Jamie D. Kapplinger, David J. Tester, Benjamin A. Salisbury, Janet L. Carr, Carole Harris‐Kerr, Guido D. Pollevick, Arthur A.M. Wilde, Michael J. Ackerman - Heart Rhythm 2009 被引用: 469

  9. Calmodulin mutations and life-threatening cardiac arrhythmias: insights from the International Calmodulinopathy Registry

    著者: Lia Crotti, Carla Spazzolini, David J. Tester, Alice Ghidoni, Alban‐Elouen Baruteau, Britt Maria Beckmann, Elijah R. Behr, Jeffrey S. Bennett, Connie R. Bezzina, Zahurul A. Bhuiyan, Alpay Çeliker, Marina Cerrone, Federica Dagradi, Gaetano Maria De Ferrari, Susan P. Etheridge, Meena Fatah, Pablo García‐Pavía, Saleh Alghamdi, Robert M. Hamilton, Zuhair N. Al‐Hassnan, Minoru Horie, Juan Jiménez‐Jáimez, Ronald J. Kanter, Juan Pablo Kaski, Maria‐Christina Kotta, Najim Lahrouchi, Naomasa Makita, Gabrielle Norrish, Hans Henrik Odland, Seiko Ohno, John Papagiannis, Gianfranco Parati, Nicole Sekarski, Kristian Tveten, Matteo Vatta, Gregory Webster, Arthur A.M. Wilde, Julianne Wojciak, Alfred L. George, Michael J. Ackerman, Peter J. Schwartz - European Heart Journal 2019 被引用: 184

  10. Long QT Syndrome–Associated Mutations in Intrauterine Fetal Death

    著者: Lia Crotti, David J. Tester, Wendy White, Daniel C. Bartos, Roberto Insolia, Alessandra Besana, Jennifer D. Kunic, Melissa L. Will, Ellyn J. Velasco, Jennifer J. Bair, Alice Ghidoni, Irene Cetin, Daniel L. Van Dyke, Myra Wick, Brian Brost, Brian P. Delisle, Fabio Facchinetti, Alfred L. George, Peter J. Schwartz, Michael J. Ackerman - JAMA 2013 被引用: 173

  11. Cardiac Genetic Predisposition in Sudden Infant Death Syndrome

    著者: David J. Tester, Leonie C.H. Wong, Pritha Chanana, Amie Jaye, Jared M. Evans, David Fitzpatrick, Margaret J. Evans, Peter Fleming, Iona Jeffrey, Marta C. Cohen, Jacob Tfelt‐Hansen, Michael A. Simpson, Elijah R. Behr, Michael J. Ackerman - Journal of the American College of Cardiology 2018 被引用: 103

  12. SCN5A Mutation Type and a Genetic Risk Score Associate Variably With Brugada Syndrome Phenotype in SCN5A Families

    著者: Yanushi D. Wijeyeratne, Michael W.T. Tanck, Yuka Mizusawa, Velislav N. Batchvarov, Julien Barc, Lia Crotti, J. Martijn Bos, David J. Tester, Alison Muir, Christian Veltmann, Seiko Ohno, Stephen P Page, Joseph Galvin, Rafik Tadros, Martina Muggenthaler, Hariharan Raju, Isabelle Denjoy, Jean‐Jacques Schott, Jean‐Baptiste Gourraud, Doris Škorić‐Milosavljević, Eline A. Nannenberg, Richard Redon, Michael Papadakis, Florence Kyndt, Federica Dagradi, Silvia Castelletti, Margherita Torchio, Thomas Meitinger, Peter Lichtner, Taisuke Ishikawa, Arthur A.M. Wilde, Kazuhiro Takahashi, Sanjay Sharma, Dan M. Roden, Martin Borggrefe, Pascal McKeown, Wataru Shimizu, Minoru Horie, Naomasa Makita, Takeshi Aiba, Michael J. Ackerman, Peter J. Schwartz, Vincent Probst, Connie R. Bezzina, Elijah R. Behr - Circulation Genomic and Precision Medicine 2020 被引用: 64

  13. A Precision Medicine Approach to the Rescue of Function on Malignant Calmodulinopathic Long-QT Syndrome

    著者: Worawan B. Limpitikul, Ivy E. Dick, David J. Tester, Nicole J. Boczek, Pattraranee Limphong, Wanjun Yang, Myoung Hyun Choi, Jennifer Babich, Deborah DiSilvestre, Ronald J. Kanter, Gordon F. Tomaselli, Michael J. Ackerman, David T. Yue - Circulation Research 2016 被引用: 165

  14. Distinguishing Arrhythmogenic Right Ventricular Cardiomyopathy/Dysplasia–Associated Mutations From Background Genetic Noise

    著者: Jamie D. Kapplinger, Andrew P. Landstrom, Benjamin A. Salisbury, Thomas E. Callis, Guido D. Pollevick, David J. Tester, Moniek G.P.J. Cox, Zahir A. Bhuiyan, Hennie Bikker, Ans C.P. Wiesfeld, Richard N.W. Hauer, J. Peter van Tintelen, Jan D.H. Jongbloed, Hugh Calkins, Daniel P. Judge, Arthur A.M. Wilde, Michael J. Ackerman - Journal of the American College of Cardiology 2011 被引用: 301

  15. Genetic association study of QT interval highlights role for calcium signaling pathways in myocardial repolarization

    著者: Dan E. Arking, DCCT/EDIC, Sara L. Pulit, Lia Crotti, Pim van der Harst, Patricia B. Munroe, Tamara T. Koopmann, Nona Sotoodehnia, Elizabeth J. Rossin, Michael P. Morley, Xinchen Wang, Andrew D. Johnson, Alicia Lundby, Daníel F. Guðbjartsson, Peter A. Noseworthy, Mark Eijgelsheim, Yuki Bradford, Kirill V. Tarasov, Marcus Dörr, Martina Müller‐Nurasyid, Annukka M. Lahtinen, Ilja M. Nolte, Albert V. Smith, Joshua C Bis, Aaron Isaacs, Stephen Newhouse, Daniel S. Evans, Wendy S. Post, Daryl Waggott, Leo‐Pekka Lyytikäinen, Andrew A. Hicks, Lewin Eisele, David Ellinghaus, Caroline Hayward, Pau Navarro, Sheila Ulivi, Toshiko Tanaka, David J. Tester, Stéphanie Chatel, Stefan Gustafsson, Meena Kumari, Richard Morris, Åsa Torinsson Naluai, Sandosh Padmanabhan, Alexander Kluttig, Bernhard Strohmer, Andrie G. Panayiotou, María Torres, Michael Knoflach, Jaroslav A. Hubáček, Kamil Slowikowski, Soumya Raychaudhuri, Runjun D. Kumar, Tamara B. Harris, Lenore J. Launer, Alan R. Shuldiner, Álvaro Alonso, Joel S. Bader, Georg Ehret, Hailiang Huang, W.H. Linda Kao, James B. Strait, Peter W. Macfarlane, Morris Brown, Mark J. Caulfield, Nilesh J. Samani, Florian Kronenberg, Johann Willeit, J. Gustav Smith, Karin Halina Greiser, Henriette E. Meyer zu Schwabedissen, Karl Werdan, Massimo Carella, Leopoldo Zelante, Susan R. Heckbert, Bruce M. Psaty, Jerome I. Rotter, Ivana Kolčić, Ozren Polašek, Alan F. Wright, Maura Griffin, Mark J. Daly, Davíð O. Arnar, Hilma Hólm, Unnur Þorsteinsdóttir, Joshua C. Denny, Dan M. Roden, Rebecca L. Zuvich, Valur Emilsson, Andrew Plump, Martin G. Larson, Christopher J. O’Donnell, Xiaoyan Yin, Marco Bobbo, Pio D’Adamo, Annamaria Iorio, Gianfranco Sinagra, Ángel Carracedo, Steven R. Cummings, Michael A. Nalls ほか 131 名 - Nature Genetics 2014 被引用: 335

  16. Cardiac Channel Molecular Autopsy: Insights From 173 Consecutive Cases of Autopsy-Negative Sudden Unexplained Death Referred for Postmortem Genetic Testing

    著者: David J. Tester, Argelia Medeiros‐Domingo, Melissa L. Will, Carla M. Haglund, Michael J. Ackerman - Mayo Clinic Proceedings 2012 被引用: 277

  17. Clinical Aspects of Type 3 Long-QT Syndrome

    著者: Arthur A.M. Wilde, Arthur J. Moss, Elizabeth S. Kaufman, Wataru Shimizu, Derick R. Peterson, Jesaia Benhorin, Coeli M. Lopes, Jeffrey A. Towbin, Carla Spazzolini, Lia Crotti, Wojciech Zaręba, Ilan Goldenberg, Jørgen K. Kanters, Jennifer L. Robinson, Ming Qi, Nynke Hofman, David J. Tester, Connie R. Bezzina, Mariëlle Alders, Takeshi Aiba, Shiro Kamakura, Yoshihiro Miyamoto, Mark Andrews, Scott McNitt, Bronislava Polonsky, Peter J. Schwartz, Michael J. Ackerman - Circulation 2016 被引用: 192

  18. Prevalence of early-onset atrial fibrillation in congenital long QT syndrome

    著者: Jonathan N. Johnson, David J. Tester, James C. Perry, Benjamin A. Salisbury, Carol R. Reed, Michael J. Ackerman - Heart Rhythm 2008 被引用: 178

  19. Molecular Diagnosis of the Inherited Long-QT Syndrome in a Woman Who Died after Near-Drowning

    著者: Michael J. Ackerman, David J. Tester, Co-burn J. Porter, William D. Edwards - New England Journal of Medicine 1999 被引用: 143

  20. Compendium of cardiac channel mutations in 541 consecutive unrelated patients referred for long QT syndrome genetic testing

    著者: David J. Tester, Melissa L. Will, Carla M. Haglund, Michael J. Ackerman - Heart Rhythm 2005 被引用: 564

  21. SCN4B -Encoded Sodium Channel β4 Subunit in Congenital Long-QT Syndrome

    著者: Argelia Medeiros‐Domingo, Toshihiko Kaku, David J. Tester, Pedro Iturralde-Torres, Ajit Itty, Bin Ye, Carmen R. Valdivia, Kazuo Ueda, Samuel Canizales‐Quinteros, Marı́a Teresa Tusié-Luna, Jonathan C. Makielski, Michael J. Ackerman - Circulation 2007 被引用: 359

  22. Spectrum and Prevalence of CALM1 -, CALM2 -, and CALM3 -Encoded Calmodulin Variants in Long QT Syndrome and Functional Characterization of a Novel Long QT Syndrome–Associated Calmodulin Missense Variant, E141G

    著者: Nicole J. Boczek, Nieves Gómez‐Hurtado, Dan Ye, Melissa L. Calvert, David J. Tester, Dmytro O. Kryshtal, Hyun Seok Hwang, Christopher N. Johnson, Walter Chazin, Christina G. Loporcaro, Maully J. Shah, Andrew L. Papez, Yung R. Lau, Ronald J. Kanter, Björn C. Knollmann, Michael J. Ackerman - Circulation Cardiovascular Genetics 2016 被引用: 134

  23. Elucidation of MRAS-mediated Noonan syndrome with cardiac hypertrophy

    著者: Erin M. Higgins, J. Martijn Bos, Heather Mason‐Suares, David J. Tester, Jaeger P. Ackerman, Calum A. MacRae, Katia Sol‐Church, Karen W. Gripp, Raúl Urrutia, Michael J. Ackerman - JCI Insight 2017 被引用: 93

  24. Enhancing rare variant interpretation in inherited arrhythmias through quantitative analysis of consortium disease cohorts and population controls.

    著者: Roddy Walsh, Najim Lahrouchi, Rafik Tadros, Florence Kyndt, Charlotte Glinge, Pieter G. Postema, Ahmad S. Amin, Eline A. Nannenberg, James S. Ware, Nicola Whiffin, Francesco Mazzarotto, Doris Škorić‐Milosavljević, Christian Krijger, Elena Arbelo, Dominique Babuty, Héctor Barajas-Martínez, Britt Maria Beckmann, Stéphane Bezieau, J Martijn Bos, Jeroen Breckpot, Óscar Campuzano, Silvia Castelletti, Candan Celen, Sebastian Clauß, Anniek Corveleyn, Lia Crotti, Federica Dagradi, Carlo de Asmundis, Isabelle Denjoy, Sven Dittmann, Patrick T. Ellinor, Cristina Gil, Carla Giustetto, Jean‐Baptiste Gourraud, Daisuke Hazeki, Minoru Horie, Taisuke Ishikawa, Hideki Itoh, Yoshiaki Kaneko, Jørgen K. Kanters, Hiroki Kimoto, Maria‐Christina Kotta, Ingrid P.C. Krapels, Masahiko Kurabayashi, Julieta Lazarte, Antoine Leenhardt, Bart Loeys, Catarina Lundin, Takeru Makiyama, Jacques Mansourati, Raphaël P. Martins, Andrea Mazzanti, Stellan Mörner, Carlo Napolitano, Kimie Ohkubo, Michael Papadakis, Boris Rudic, María Sabater‐Molina, Frédéric Sacher, Hatice Şahin, Georgia Sarquella‐Brugada, Regina Sebastiano, Sanjay Sharma, Mary N. Sheppard, Keiko Shimamoto, M. Benjamin Shoemaker, Birgit Stallmeyer, Johannes Steinfurt, Yuji Tanaka, David J. Tester, Keisuke Usuda, Paul A. van der Zwaag, Sonia Van Dooren, Lut Van Laer, Annika Winbo, Bo Gregers Winkel, Kenichiro Yamagata, Sven Zumhagen, Paul G.A. Volders, Steven A. Lubitz, Charles Antzelevitch, Pyotr G. Platonov, Katja E. Odening, Dan M. Roden, Jason D. Roberts, Jonathan R. Skinner, Jacob Tfelt‐Hansen, Maarten P. van den Berg, Morten S. Olesen, Pier D. Lambiase, Martin Borggrefe, Kenshi Hayashi, Annika Rydberg, Tadashi Nakajima, Masao Yoshinaga, Johan Saenen, Stefan Kääb, Pedro Brugada, Tomas Robyns, Daniela Giachino ほか 19 名 - 2020 被引用: 58