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Thomas Wieland

Active 1979–2026

120
Papers
18,187
Citations
74
h-index
96
i10-index

Citations

Citations per year for Thomas Wieland1980: 5 citations1981: 3 citations1983: 7 citations1984: 10 citations1985: 5 citations1986: 11 citations1987: 11 citations1988: 11 citations1989: 14 citations1990: 6 citations1991: 1 citations1992: 8 citations1993: 6 citations1994: 9 citations1995: 16 citations1996: 14 citations1997: 26 citations1998: 29 citations1999: 34 citations2000: 20 citations2001: 17 citations2002: 11 citations2003: 28 citations2004: 21 citations2005: 23 citations2006: 22 citations2007: 29 citations2008: 34 citations2009: 50 citations2010: 50 citations2011: 51 citations2012: 62 citations2013: 173 citations2014: 298 citations2015: 321 citations2016: 341 citations2017: 301 citations2018: 285 citations2019: 774 citations2020: 823 citations2021: 752 citations2022: 532 citations2023: 387 citations2024: 506 citations2025: 225 citations2026: 13 citations1982: no citations, so this year is not shown

Citation sources

Countries

World map of the countries and regions citing this authorUnited States: 2,773 citing papers, 23.1% of this breakdownGermany: 1,132 citing papers, 9.4% of this breakdownUnited Kingdom: 973 citing papers, 8.1% of this breakdownChina: 785 citing papers, 6.5% of this breakdownItaly: 552 citing papers, 4.6% of this breakdownFrance: 489 citing papers, 4.1% of this breakdownNetherlands: 464 citing papers, 3.9% of this breakdownCanada: 453 citing papers, 3.8% of this breakdownAustralia: 407 citing papers, 3.4% of this breakdownJapan: 366 citing papers, 3.1% of this breakdownSwitzerland: 309 citing papers, 2.6% of this breakdownSpain: 303 citing papers, 2.5% of this breakdown
0%23.1%Other 24.9%

Institutions

Fields

  • Biochemistry, Genetics and Molecular Biology50.1%
  • Medicine36.4%
  • Neuroscience6%
  • Immunology and Microbiology2.1%
  • Chemistry1.5%
  • Computer Science1.1%
  • Other2.8%

Topics

  • Cardiac electrophysiology and arrhythmias2.6%
  • Mitochondrial Function and Pathology2.5%
  • Genomics and Rare Diseases2.5%
  • RNA modifications and cancer2.2%
  • Genetics and Neurodevelopmental Disorders1.9%
  • Amyotrophic Lateral Sclerosis Research1.8%
  • Other86.5%

Coauthors

All papers

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  1. A deep proteome and transcriptome abundance atlas of 29 healthy human tissues

    Authors: Dongxue Wang, Basak Eraslan, Thomas Wieland, Björn M. Hallström, Thomas A. Hopf, Daniel P. Zolg, Jana Zecha, Anna Asplund, Lihua Li, Chen Meng, Martin Frejno, Tobias Schmidt, Karsten Schnatbaum, Mathias Wilhelm, Fredrik Pontén, Mathias Uhlén, Julien Gagneur, Hannes Hahne, Bernhard Küster - Molecular Systems Biology 2019 cited by 796

  2. Transcriptome and genome sequencing uncovers functional variation in humans

    Authors: Tuuli Lappalainen, Michael Sammeth, Marc R. Friedländer, Peter A.C. ’t Hoen, Jean Monlong, Manuel A. Rivas, Mar Gonzàlez-Porta, Natalja Kurbatova, Thasso Griebel, Pedro G. Ferreira, Matthias Barann, Thomas Wieland, Liliana Greger, Maarten van Iterson, Jonas Carlsson Almlöf, Paolo Ribeca, Irina Pulyakhina, Daniela Esser, Thomas Giger, Andrew Tikhonov, Marc Sultan, Gabrielle Bertier, Daniel G. MacArthur, Monkol Lek, Esther Lizano, Henk P.J. Buermans, Ismaël Padioleau, Thomas Schwarzmayr, Olof Karlberg, Halit Ongen, Helena Kilpinen, Sergi Beltrán, Marta Gut, Katja Kahlem, Vyacheslav Amstislavskiy, Oliver Stegle, Matti Pirinen, Stephen B. Montgomery, Peter Donnelly, Mark I. McCarthy, Paul Flicek, Tim M. Strom, Hans Lehrach, Stefan Schreiber, Ralf Sudbrak, Ángel Carracedo, Stylianos E. Antonarakis, Robert Häsler, Ann‐Christine Syvänen, Gert‐Jan B. van Ommen, Alvis Brāzma, Thomas Meitinger, Philip Rosenstiel, Roderic Guigó, Marta Gut, Xavier Estivill, Emmanouil T. Dermitzakis - Nature 2013 cited by 2,195

  3. Haploinsufficiency of TBK1 causes familial ALS and fronto-temporal dementia

    Authors: Axel Freischmidt, Thomas Wieland, Benjamin Richter, Wolfgang Ruf, Véronique Schaeffer, Kathrin Müller, Nicolai Marroquin, Frida Nordin, Annemarie Hübers, Patrick Weydt, Susana Pinto, Rayomond Press, Stéphanie Millecamps, Nicolas Molko, E Bernard, Claude Desnuelle, Marie‐Hélène Soriani, Johannes Dorst, Elisabeth Graf, Ulrika Nordström, Marisa S. Feiler, Stefan Putz, Tobias M. Boeckers, Thomas Meyer, Andrea Sylvia Winkler, Juliane Winkelman, Mamede de Carvalho, Dietmar Rudolf Thal, Markus Otto, Thomas Brännström, Alexander E. Volk, Petri Kursula, Karin M. Danzer, Peter Lichtner, Ivan Đikić, Thomas Meitinger, Albert C. Ludolph, Tim M. Strom, Peter M. Andersen, Jochen H. Weishaupt - Nature Neuroscience 2015 cited by 783

  4. Enhanced Sarcoplasmic Reticulum Ca 2+ Leak and Increased Na + -Ca 2+ Exchanger Function Underlie Delayed Afterdepolarizations in Patients With Chronic Atrial Fibrillation

    Authors: Niels Voigt, Na Li, Qiongling Wang, Wei Wang, Andrew W. Trafford, Issam Abu-Taha, Qiang Sun, Thomas Wieland, Ursula Ravens, Stanley Nattel, Xander H.T. Wehrens, Dobromir Dobrev - Circulation 2012 cited by 622

  5. Mutations in the deubiquitinase gene USP8 cause Cushing's disease

    Authors: Martín Reincke, Silviu Sbiera, Akira Hayakawa, Marily Theodoropoulou, Andrea Oßwald, Felix Beuschlein, Thomas Meitinger, Emi Mizuno-Yamasaki, Kohei Kawaguchi, Yasushi Saeki, Keiji Tanaka, Thomas Wieland, Elisabeth Graf, Wolfgang Saeger, Cristina L. Ronchi, Bruno Allolio, Michael Buchfelder, Tim M. Strom, Martin Faßnacht, Masayuki Komada - Nature Genetics 2014 cited by 591

  6. Angiopoietin-2 differentially regulates angiogenesis through TIE2 and integrin signaling

    Authors: Moritz Felcht, Robert Luck, Alexander Schering, Philipp Seidel, Kshitij Srivastava, Junhao Hu, Arne Bartol, Yvonne Kienast, Christiane Vettel, Elias K. Loos, Simone Kutschera, Susanne Bartels, Sila Appak‐Baskoy, Eva Besemfelder, Dorothee Terhardt, Emmanouil Chavakis, Thomas Wieland, Christian Klein, Markus Thomas, Akiyoshi Uemura, Sergij Goerdt, Hellmut G. Augustin - Journal of Clinical Investigation 2012 cited by 476

  7. Constitutive Activation of PKA Catalytic Subunit in Adrenal Cushing's Syndrome

    Authors: Felix Beuschlein, Martin Faßnacht, Guillaume Assié, Davide Calebiro, Constantine A. Stratakis, Andrea Oßwald, Cristina L. Ronchi, Thomas Wieland, Silviu Sbiera, Fábio R. Faucz, Katrin Schaak, Anett Schmittfull, Thomas Schwarzmayr, Olivia Barreau, Delphine Vezzosi, Marthe Rizk‐Rabin, Ulrike Zabel, Eva Szarek, Paraskevi Salpea, Antonella Forlino, Annalisa Vetro, Orsetta Zuffardi, Caroline Kisker, Susanne Diener, Thomas Meitinger, Martin J. Lohse, Martín Reincke, Jérôme Bertherat, Tim M. Strom, Bruno Allolio - New England Journal of Medicine 2014 cited by 431

  8. Lipopolysaccharides induced inflammatory responses and electrophysiological dysfunctions in human-induced pluripotent stem cell derived cardiomyocytes

    Authors: Gökhan Yücel, Zhihan Zhao, Ibrahim El‐Battrawy, Huan Lan, Siegfried Lang, Xin Li, Fanis Buljubasic, Wolfram‐Hubertus Zimmermann, Lukas Cyganek, Jochen Utikal, Ursula Ravens, Thomas Wieland, Martin Borggrefe, Xiaobo Zhou, İbrahim Akın - Scientific Reports 2017 cited by 159

  9. Lamin A/C-dependent chromatin architecture safeguards naïve pluripotency to prevent aberrant cardiovascular cell fate and function

    Authors: Yinuo Wang, Adel Elsherbiny, Linda Kessler, Julio Cordero, Haojie Shi, Heike Serke, Olga Lityagina, Felix A. Trogisch, Mona Malek Mohammadi, Ibrahim El‐Battrawy, Johannes Backs, Thomas Wieland, Joerg Heineke, Gergana Dobreva - Nature Communications 2022 cited by 66

  10. Range of genetic mutations associated with severe non-syndromic sporadic intellectual disability: an exome sequencing study

    Authors: Anita Rauch, Dagmar Wieczorek, Elisabeth Graf, Thomas Wieland, Sabine Endele, Thomas Schwarzmayr, Beate Albrecht, Deborah Bartholdi, Jasmin Beygo, Nataliya Di Donato, Andreas Dufke, Kirsten Cremer, Maja Hempel, Denise Horn, Juliane Hoyer, Pascal Joset, Albrecht Röpke, Ute Moog, Angelika Rieß, Christian T. Thiel, Andreas Tzschach, Antje Wiesener, Eva Wohlleber, Christiane Zweier, Arif B. Ekici, Alexander M. Zink, Andreas Rump, Christa Meisinger, Harald Grallert, Heinrich Sticht, Annette Schenck, Hartmut Engels, Gudrun Rappold, Evelin Schröck, Peter Wieacker, Olaf Rieß, Thomas Meitinger, André Reis, Tim M. Strom - The Lancet 2012 cited by 1,065

  11. Exome Sequencing Reveals De Novo WDR45 Mutations Causing a Phenotypically Distinct, X-Linked Dominant Form of NBIA

    Authors: Tobias B. Haack, Penelope Hogarth, Michael C. Kruer, Allison Gregory, Thomas Wieland, Thomas Schwarzmayr, Elisabeth Graf, Lynn Sanford, Esther Meyer, Eleanna Kara, Stephan M. Cuno, Sami I. Harik, Vasuki Dandu, Nardo Nardocci, Giovanna Zorzi, Todd Dunaway, Mark A. Tarnopolsky, Steven A. Skinner, Steven J. Frucht, Era Hanspal, Connie Schrander‐Stumpel, Delphine Héron, Cyril Mignot, Barbara Garavaglia, Kailash P. Bhatia, John Hardy, Tim M. Strom, Nathalie Boddaert, Henry Houlden, Manju A. Kurian, Thomas Meitinger, Holger Prokisch, Susan J. Hayflick - The American Journal of Human Genetics 2012 cited by 359

  12. Somatic mutations in ATP1A1 and ATP2B3 lead to aldosterone-producing adenomas and secondary hypertension

    Authors: Felix Beuschlein, Sheerazed Boulkroun, Andrea Oßwald, Thomas Wieland, Hang N. Nielsen, Urs Lichtenauer, David Pentón, Vivien R. Schack, Laurence Amar, Evelyn Fischer, Anett Walther, Philipp Tauber, Thomas Schwarzmayr, Susanne Diener, Elisabeth Graf, Bruno Allolio, Benoît Samson-Couterie, Arndt Benecke, Marcus Quinkler, Francesco Fallo, Pierre‐François Plouin, Franco Mantero, Thomas Meitinger, Paolo Mulatero, Xavier Jeunemaı̂tre, Richard Warth, Bente Vilsen, Maria‐Christina Zennaro, Tim M. Strom, Martín Reincke - Nature Genetics 2013 cited by 568

  13. Calmodulin Mutations Associated With Recurrent Cardiac Arrest in Infants

    Authors: Lia Crotti, Christopher N. Johnson, Elisabeth Graf, Gaetano Maria De Ferrari, Bettina F. Cuneo, Marc Ovadia, John Papagiannis, Michael D. Feldkamp, Subodh Rathi, Jennifer D. Kunic, Matteo Pedrazzini, Thomas Wieland, Peter Lichtner, Britt Maria Beckmann, Travis Clark, Christian M. Shaffer, D. Woodrow Benson, Stefan Kääb, Thomas Meitinger, Tim M. Strom, Walter Chazin, Peter J. Schwartz, Alfred L. George - Circulation 2013 cited by 389

  14. NEK1mutations in familial amyotrophic lateral sclerosis

    Authors: David A. Brenner, Kathrin Müller, Thomas Wieland, Patrick Weydt, Sarah Böhm, Dorothée Lulé, Annemarie Hübers, Christoph Neuwirth, Markus Weber, Guntram Borck, Magnus Wahlqvist, Karin M. Danzer, Alexander E. Volk, Thomas Meitinger, Tim M. Strom, Markus Otto, Jan Kassubek, Albert C. Ludolph, Peter M. Andersen, Jochen H. Weishaupt - Brain 2016 cited by 139

  15. Exome Sequence Reveals Mutations in CoA Synthase as a Cause of Neurodegeneration with Brain Iron Accumulation

    Authors: Sabrina Dusi, Lorella Valletta, Tobias B. Haack, Yugo Tsuchiya, Paola Venco, Sebastiano Pasqualato, P Goffrini, Marco Tigano, Nikita Demchenko, Thomas Wieland, Thomas Schwarzmayr, Tim M. Strom, Federica Invernizzi, Barbara Garavaglia, Allison Gregory, Lynn Sanford, Jeffrey Hamada, Conceição Bettencourt, Henry Houlden, Luisa Chiapparini, Giovanna Zorzi, Manju A. Kurian, Nardo Nardocci, Holger Prokisch, Susan J. Hayflick, Ivan Gout, Valeria Tiranti - The American Journal of Human Genetics 2013 cited by 204

  16. Mutations in FBXL4, Encoding a Mitochondrial Protein, Cause Early-Onset Mitochondrial Encephalomyopathy

    Authors: Xiaowu Gai, Daniele Ghezzi, Mark Johnson, Caroline Biagosch, Hanan E. Shamseldin, Tobias B. Haack, Aurelio Reyes, Mai Tsukikawa, Claire A. Sheldon, Satish Srinivasan, Matteo Gorza, Laura S. Kremer, Thomas Wieland, Tim M. Strom, Erzsébet Polyák, Emily Place, Mark Consugar, Julian Ostrovsky, Sara Vidoni, Alan J. Robinson, Lee-Jun Wong, Neal Sondheimer, Mustafa A. Salih, Emtethal Al-Jishi, Christopher Raab, Charles Bean, Francesca Furlan, Rossella Parini, Costanza Lamperti, Johannes A. Mayr, Vassiliki Konstantopoulou, Martina Huemer, Eric A. Pierce, Thomas Meitinger, Peter Freisinger, Wolfgang Sperl, Holger Prokisch, Fowzan S. Alkuraya, Marni J. Falk, Massimo Zeviani - The American Journal of Human Genetics 2013 cited by 179

  17. Lack of the Mitochondrial Protein Acylglycerol Kinase Causes Sengers Syndrome

    Authors: Johannes A. Mayr, Tobias B. Haack, Elisabeth Graf, Franz Zimmermann, Thomas Wieland, Birgit Haberberger, Andrea Superti‐Furga, Janbernd Kirschner, Beat Steinmann, Matthias R. Baumgartner, Isabella Moroni, Eleonora Lamantea, Massimo Zeviani, Richard J. Rodenburg, Jan Smeıtınk, Tim M. Strom, Thomas Meitinger, Wolfgang Sperl, Holger Prokisch - The American Journal of Human Genetics 2012 cited by 218

  18. Chronic isoprenaline/phenylephrine vs. exclusive isoprenaline stimulation in mice: critical contribution of alpha1-adrenoceptors to early cardiac stress responses

    Authors: Matthias Dewenter, Jianyuan Pan, Laura Knödler, Niklas Tzschöckel, Julian Henrich, Julio Cordero, Gergana Dobreva, Susanne Lutz, Johannes Backs, Thomas Wieland, Christiane Vettel - Basic Research in Cardiology 2022 cited by 36

  19. Molecular diagnosis in mitochondrial complex I deficiency using exome sequencing

    Authors: Tobias B. Haack, Birgit Haberberger, Eva-Maria Frisch, Thomas Wieland, Arcangela Iuso, Matteo Gorza, Valentina Strecker, Elisabeth Graf, Johannes A. Mayr, Ulrike Herberg, Julia B. Hennermann, Thomas Klopstock, Klaus A. Kuhn, Uwe Ahting, Wolfgang Sperl, Ekkehard Wilichowski, Georg F. Hoffmann, Markéta Tesařová, Hana Hansíková, J Zeman, Barbara Plecko, Massimo Zeviani, Ilka Wittig, Tim M. Strom, Markus Schuelke, Peter Freisinger, Thomas Meitinger, Holger Prokisch - Journal of Medical Genetics 2012 cited by 185

  20. Biallelic Mutations of Methionyl-tRNA Synthetase Cause a Specific Type of Pulmonary Alveolar Proteinosis Prevalent on Réunion Island

    Authors: Alice Hadchouel, Thomas Wieland, Matthias Griese, Enrico Baruffini, Bettina Lorenz‐Depiereux, Laurent Enaud, Elisabeth Graf, J.‐C. Dubus, S. Halioui-Louhaichi, Aurore Coulomb, Christophe Delacourt, Gertrud Eckstein, Ralf Zarbock, Thomas Schwarzmayr, François Cartault, Thomas Meitinger, Tiziana Lodi, Jacques de Blic, Tim M. Strom - The American Journal of Human Genetics 2015 cited by 127

  21. Modeling Short QT Syndrome Using Human‐Induced Pluripotent Stem Cell–Derived Cardiomyocytes

    Authors: Ibrahim El‐Battrawy, Huan Lan, Lukas Cyganek, Zhihan Zhao, Xin Li, Fanis Buljubasic, Siegfried Lang, Gökhan Yücel, Katherine Sattler, Wolfram‐Hubertus Zimmermann, Jochen Utikal, Thomas Wieland, Ursula Ravens, Martin Borggrefe, Xiaobo Zhou, İbrahim Akın - Journal of the American Heart Association 2018 cited by 119

  22. Quantification and discovery of sequence determinants of protein‐per‐mRNA amount in 29 human tissues

    Authors: Basak Eraslan, Dongxue Wang, Mirjana Gušić, Holger Prokisch, Björn M. Hallström, Mathias Uhlén, Anna Asplund, Fredrik Pontén, Thomas Wieland, Thomas A. Hopf, Hannes Hahne, Bernhard Küster, Julien Gagneur - Molecular Systems Biology 2019 cited by 100

  23. Alterations in cardiac DNA methylation in human dilated cardiomyopathy

    Authors: Jan Haas, Karen Frese, Yoon Jung Park, Andreas Keller, Britta Vogel, Anders M. Lindroth, Dieter Weichenhan, Jennifer Franke, Simon Fischer, Andrea S. Bauer, Sabine Marquart, Farbod Sedaghat‐Hamedani, Elham Kayvanpour, Doreen Köhler, Nadine M. Wolf, Sarah Hassel, Rouven Nietsch, Thomas Wieland, Philipp Ehlermann, Jobst‐Hendrik Schultz, Andreas Dösch, Derliz Mereles, Stefan Hardt, Johannes Backs, Jörg D. Hoheisel, Christoph Plass, Hugo A. Katus, Benjamin Meder - EMBO Molecular Medicine 2013 cited by 246

  24. ELAC2 Mutations Cause a Mitochondrial RNA Processing Defect Associated with Hypertrophic Cardiomyopathy

    Authors: Tobias B. Haack, Robert Kopajtich, Peter Freisinger, Thomas Wieland, Joanna Rorbach, Thomas J. Nicholls, Enrico Baruffini, Anett Walther, Katharina Danhauser, Franz Zimmermann, Ralf A. Husain, Jessica Schum, Helen Mundy, Ileana Ferrero, Tim M. Strom, Thomas Meitinger, Robert W. Taylor, Michal Minczuk, Johannes A. Mayr, Holger Prokisch - The American Journal of Human Genetics 2013 cited by 147