On this page:OverviewPublicationsKey papers
ScholarIQanswers from OpenAlex & ORCID

Stefan Kääb

ResearcherPublications, citations & collaboration network

Stefan Kääb is a researcher indexed in ScholarIQ from OpenAlex & ORCID.

How many works does Stefan Kääb have?

ScholarIQindexed works

Stefan Kääb has 451 works in the ScholarIQ index. The count is the OpenAlex total, not the number of papers listed on this page.

How many citations does Stefan Kääb have?

ScholarIQcitation count

Stefan Kääb has 31,594 citations in the OpenAlex counts ScholarIQ stores.

What is the h-index of Stefan Kääb?

ScholarIQh-index

Stefan Kääb has an h-index of 89 in OpenAlex.

What is the i10-index of Stefan Kääb?

ScholarIQi10-index

Stefan Kääb has an i10-index of 240 in OpenAlex.

What is the ORCID of Stefan Kääb?

ScholarIQorcid

The ORCID for Stefan Kääb is on the source record.

What is the OpenAlex record for Stefan Kääb?

ScholarIQopenalex

The OpenAlex for Stefan Kääb is on the source record.

What are the most-cited papers on Stefan Kääb?

ScholarIQmost cited works
2022 ESC Guidelines for the management of patients with ventricular arrhythmias and the prevention of sudden cardiac death
Katja Zeppenfeld, Jacob Tfelt‐Hansen, Marta Riva, Bo Gregers Winkel, Elijah R. Behr, Nico A. Blom, Philippe Charron, Domenico Corrado, Nikolaos Dagres, Christian de Chillou, Lars Eckardt, Tim Friede, Kristina H. Haugaa, Mélèze Hocini, Pier D. Lambiase, Éloi Marijon, José Luís Merino, Petr Peichl, Silvia G. Priori, Tobias Reichlin, Jeanette Schulz‐Menger, Christian Sticherling, Stylianos Tzeis, Axel Verstrael, Maurizio Volterrani, ESC Scientific Document Group, Maja Čikeš, Paulus Kirchhof, Magdy Abdelhamid, Victor Aboyans, Elena Arbelo, Fernando Arribas, Riccardo Asteggiano, Cristina Basso, Axel Bauer, Emanuele Bertaglia, Tor Biering‐Sørensen, C. Blomström‐Lundqvist, Michael A. Borger, Jelena Čelutkienė, Bernard Cosyns, Volkmar Falk, Laurent Fauchier, Bülent Görenek, Sigrun Halvorsen, Róbert Hatala, Hein Heidbüchel, Stefan Kääb, А. О. Конради, Konstantinos C. Koskinas, Dipak Kotecha, Ulf Landmesser, Basil S. Lewis, Aleš Linhart, Maja Lisa Løchen, Lars H. Lund, Andreas Metzner, Richard Mindham, Jens Cosedis Nielsen, Tone M Norekvål, Monica Patten, Eva Prescott, Amina Rakisheva, Carol Ann Remme, Ivo Roca‐Luque, Andrea Sarkozy, Daniel Scherr, Marta Sitges, Rhian M. Touyz, Nicolas M. Van Mieghem, Vedran Velagić, Sami Viskin, Paul G.A. Volders, B. Kichou, Mihran Martirosyan, Daniel Scherr, Farid Aliyev, Rik Willems, Nabil Naser, Tchavdar Shalganov, Davor Miličić, Theodoros Christophides, Josef Kautzner, J. P. Hart Hansen, Lamyaa Allam, Priit Kampus, Juhani Junttila, Christophe Leclercq, Kakhaber Etsadashvili, Daniel Steven, Konstantinos Gatzoulis, László Gellér, Davíð O. Arnar, Joseph Galvin, Moti Haim, Carlo Pappone, Shpend Elezi, Alina Kerimkulova, Oskars Kalējs, Ali Rabah
European Heart Journal. 20222,984 CitationsOPEN ACCESS
Simple Risk Model Predicts Incidence of Atrial Fibrillation in a Racially and Geographically Diverse Population: the CHARGE‐AF Consortium
Álvaro Alonso, Bouwe P. Krijthe, Thor Aspelund, Katherine A. Stepas, Michael Pencina, Carlee Moser, Moritz F. Sinner, Nona Sotoodehnia, João D. Fontes, A. Cecile J.W. Janssens, Richard A. Kronmal, Jared W. Magnani, Jacqueline C.M. Witteman, Alanna M. Chamberlain, Steven A. Lubitz, Renate B. Schnabel, Sunil Agarwal, David D. McManus, Patrick T. Ellinor, Martin G. Larson, Gregory L. Burke, Lenore J. Launer, Albert Hofman, Daniel Levy, John S. Gottdiener, Stefan Kääb, David Couper, Tamara B. Harris, Elsayed Z. Soliman, Bruno H. Stricker, Vilmundur Guðnason, Susan R. Heckbert, Emelia J. Benjamin
Journal of the American Heart Association. 2013892 CitationsOPEN ACCESS
Multi-ethnic genome-wide association study for atrial fibrillation
Carolina Roselli, Mark Chaffin, Lu‐Chen Weng, Stefanie Aeschbacher, Gustav Ahlberg, Christine M. Albert, Peter Almgren, Álvaro Alonso, Christopher D. Anderson, Krishna G. Aragam, Dan E. Arking, John Barnard, Traci M. Bartz, Emelia J. Benjamin, Nathan A. Bihlmeyer, Joshua C. Bis, Heather L. Bloom, Eric Boerwinkle, Erwin B. Bottinger, Jennifer A. Brody, Hugh Calkins, Archie Campbell, Thomas P. Cappola, John F. Carlquist, Daniel I. Chasman, Lin Y. Chen, Yii-Der Ida Chen, Eue‐Keun Choi, Seung Hoan Choi, Ingrid E. Christophersen, Mina K. Chung, John W. Cole, David Conen, James P. Cook, Harry J. Crijns, Michael J. Cutler, Scott M. Damrauer, Brian R. Daniels, Dawood Darbar, Graciela Delgado, Joshua C. Denny, Martin Dichgans, Marcus Dörr, Elton Dudink, Samuel C. Dudley, Nada Esa, Tõnu Esko, Markku Eskola, Diane Fatkin, Stephan B. Felix, Ian Ford, Oscar H. Franco, Bastiaan Geelhoed, Raji P. Grewal, Vilmundur Guðnason, Xiuqing Guo, Namrata Gupta, Stefan Gustafsson, Rebecca Gutmann, Anders Hamsten, Tamara B. Harris, Caroline Hayward, Susan R. Heckbert, Jussi Hernesniemi, Lynne J. Hocking, Albert Hofman, Andréa R. V. R. Horimoto, Jie Huang, Paul L. Huang, Jennifer E. Huffman, Erik Ingelsson, Esra Gücük İpek, Kaoru Ito, Jordi Jiménez‐Conde, Renée Johnson, J. Wouter Jukema, Stefan Kääb, Mika Kähönen, Yoichiro Kamatani, John P. Kane, Adnan Kastrati, Sekar Kathiresan, Petra Katschnig‐Winter, Maryam Kavousi, Thorsten Kessler, Bas Kietselaer, Paulus Kirchhof, Marcus E. Kleber, Stacey Knight, José Eduardo Krieger, Michiaki Kubo, Lenore J. Launer, Jari Laurikka, Terho Lehtimäki, Kirsten Leineweber, Rozenn N. Lemaître, Man Li, Hong Euy Lim, Henry J. Lin, Honghuang Lin
Nature Genetics. 2018824 CitationsOPEN ACCESS
Common variants at SCN5A-SCN10A and HEY2 are associated with Brugada syndrome, a rare disease with high risk of sudden cardiac death
Connie R. Bezzina, Julien Barc, Yuka Mizusawa, Carol Ann Remme, Jean‐Baptiste Gourraud, Floriane Simonet, Arie O. Verkerk, Peter J. Schwartz, Lia Crotti, Federica Dagradi, Pascale Guicheney, Véronique Fressart, Antoine Leenhardt, Charles Antzelevitch, S. Bartkowiak, Martin Borggrefe, Rainer Schimpf, Eric Schulze‐Bahr, Sven Zumhagen, Elijah R. Behr, Rachel Bastiaenen, Jacob Tfelt‐Hansen, Morten S. Olesen, Stefan Kääb, Britt Maria Beckmann, Peter Weeke, Hiroshi Watanabe, Naoto Endo, Tohru Minamino, Minoru Horie, Seiko Ohno, Kanae Hasegawa, Naomasa Makita, Akihiko Nogami, Wataru Shimizu, Takeshi Aiba, Philippe Froguel, Beverley Balkau, Olivier Lantieri, Margherita Torchio, Cornelia Wiese, David Weber, Rianne Wolswinkel, Ruben Coronel, Bastiaan J. Boukens, Stéphane Bezieau, Éric Charpentier, Stéphanie Chatel, Aurore Després, F Gros, Florence Kyndt, Simon Lecointe, Pierre Lindenbaum, Vincent Portero, Jade Violleau, Manfred Gessler, Hanno L. Tan, Dan M. Roden, Vincent M. Christoffels, Hervé Le Marec, Arthur A.M. Wilde, Vincent Probst, Jean‐Jacques Schott, Christian Dina, Richard Redon
Nature Genetics. 2013549 Citations
Variants in ZFHX3 are associated with atrial fibrillation in individuals of European ancestry
Emelia J. Benjamin, Kenneth Rice, Dan E. Arking, Arne Pfeufer, Charlotte van Noord, Albert V. Smith, Renate B. Schnabel, Joshua C Bis, Eric Boerwinkle, Moritz F. Sinner, Abbas Dehghan, Steven A. Lubitz, Ralph B. D’Agostino, Thomas Lumley, Georg Ehret, Jan Heeringa, Thor Aspelund, Christopher Newton‐Cheh, Martin G. Larson, Kristin D. Marciante, Elsayed Z. Soliman, Fernando Rivadeneira, Thomas J. Wang, Guðný Eiríksdóttir, Daniel Levy, Bruce M. Psaty, Man Li, Alanna M. Chamberlain, Albert Hofman, Ramachandran S. Vasan, Tamara B. Harris, Jerome I. Rotter, W.H. Linda Kao, Sunil Agarwal, Bruno H. Stricker, Ke Wang, Lenore J. Launer, Nicholas L. Smith, Aravinda Chakravarti, André G. Uitterlinden, Philip A. Wolf, Nona Sotoodehnia, Anna Köttgen, Cornelia M. van Duijn, Thomas Meitinger, Martina Mueller, Siegfried Perz, Gerhard Steinbeck, H‐Erich Wichmann, Kathryn L. Lunetta, Susan R. Heckbert, Vilmundur Guðnason, Álvaro Alonso, Stefan Kääb, Patrick T. Ellinor, Jacqueline C.M. Witteman
Nature Genetics. 2009390 CitationsOPEN ACCESS

Related on ScholarIQ

470M+ articles · free account