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Davíð O. Arnar

ResearcherPublications, citations & collaboration network

Davíð O. Arnar is a researcher indexed in ScholarIQ from OpenAlex & ORCID.

How many works does Davíð O. Arnar have?

ScholarIQindexed works

Davíð O. Arnar has 168 works in the ScholarIQ index. The count is the OpenAlex total, not the number of papers listed on this page.

How many citations does Davíð O. Arnar have?

ScholarIQcitation count

Davíð O. Arnar has 17,970 citations in the OpenAlex counts ScholarIQ stores.

What is the h-index of Davíð O. Arnar?

ScholarIQh-index

Davíð O. Arnar has an h-index of 48 in OpenAlex.

What is the i10-index of Davíð O. Arnar?

ScholarIQi10-index

Davíð O. Arnar has an i10-index of 76 in OpenAlex.

What is the ORCID of Davíð O. Arnar?

ScholarIQorcid

The ORCID for Davíð O. Arnar is on the source record.

What is the OpenAlex record for Davíð O. Arnar?

ScholarIQopenalex

The OpenAlex for Davíð O. Arnar is on the source record.

What are the most-cited papers on Davíð O. Arnar?

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
Variants conferring risk of atrial fibrillation on chromosome 4q25
Daníel F. Guðbjartsson, Davíð O. Arnar, Anna Helgadóttir, Sólveig Grétarsdóttir, Hilma Hólm, Ásgeir Sigurðsson, Aðalbjörg Jónasdóttir, Adam Baker, Guðmar Þorleifsson, Kristleifur Kristjánsson, Arnar Pálsson, Thórarinn Blöndal, Patrick Sulem, Valgerdur M. Backman, Gudmundur A. Hardarson, Ebba Pálsdóttir, Agnar Helgason, Rúna Sigurjónsdóttir, Jon T. Sverrisson, Konstantinos Kostulas, Maggie C. Y. Ng, Larry Baum, Wing Yee So, Ka Sing Wong, Juliana C.N. Chan, Karen L. Furie, Steven M. Greenberg, Michelle Sale, Peter J. Kelly, Calum A. MacRae, Eric E. Smith, Jonathan Rosand, Jan Hillert, Ronald C.W., Patrick T. Ellinor, Guðmundur Þorgeirsson, Jeffrey R. Gulcher, Augustine Kong, Unnur Þorsteinsdóttir, Kāri Stefánsson
Nature. 2007958 Citations
Sequence variants affecting eosinophil numbers associate with asthma and myocardial infarction
Daníel F. Guðbjartsson, Unnur Steina Björnsdóttir, Eva Halapi, Anna Helgadóttir, Patrick Sulem, G.M. Jonsdottir, Guðmar Þorleifsson, Hafdís T. Helgadóttir, Valgerður Steinthórsdóttir, Hreinn Stefánsson, Carolyn Williams, Jennie Hui, John Beilby, Nicole M. Warrington, Alan James, Lyle J. Palmer, Gerard H. Koppelman, Andrea Heinzmann, Marcus Krueger, H. Marike Boezen, Amanda Wheatley, Janine Altmüller, Hyoung Doo Shin, Soo‐Taek Uh, Hyun Sub Cheong, Brynja Jónsdóttir, Davíð Gíslason, Choon‐Sik Park, Linda Makowska Rasmussen, Celeste Porsbjerg, Jakob Werner Hansen, Vibeke Backer, Thomas Werge, Christer Janson, Ulla‐Britt Jönsson, Maggie Ng, Juliana C.N. Chan, Wing Yee So, Ronald C.W., Svati H. Shah, Christopher B. Granger, Arshed A. Quyyumi, Allan I. Levey, Viola Vaccarino, Muredach P. Reilly, Daniel J. Rader, Michael Williams, André M. van Rij, Gregory T. Jones, Elisabetta Trabetti, Giovanni Malerba, Pier Franco Pignatti, Attilio Boner, Lydia Pescollderungg, Domenico Girelli, Oliviero Olivieri, Nicola Martinelli, Björn R. Lúdvíksson, Dóra Lúðvíksdóttir, Guðmundur I. Eyjólfsson, Davíð O. Arnar, Guðmundur Þorgeirsson, Klaus A. Deichmann, Philip J. Thompson, Matthias Wjst, Ian P. Hall, Dirkje S. Postma, Þórarinn Gíslason, Jeffrey R. Gulcher, Augustine Kong, Ingileif Jónsdóttir, Unnur Þorsteinsdóttir, Kāri Stefánsson
Nature Genetics. 2009770 Citations
Discovery and systematic characterization of risk variants and genes for coronary artery disease in over a million participants
Krishna G. Aragam, Tao Jiang, Anuj Goel, Stavroula Kanoni, Brooke N. Wolford, Deepak Atri, E. Weeks, Minxian Wang, George Hindy, Wei Zhou, Christopher Grace, Carolina Roselli, Nicholas Marston, Frederick Kamanu, Ida Surakka, Loreto Muñoz Venegas, Paul Sherliker, Satoshi Koyama, Kazuyoshi Ishigaki, Bjørn Olav Åsvold, Michael R. Brown, Ben Brumpton, Paul S. de Vries, Olga Giannakopoulou, Tota Giardoglou, Daníel F. Guðbjartsson, Ulrich Güldener, Syed M. Ijlal Haider, Anna Helgadóttir, M Ibrahim, Adnan Kastrati, Thorsten Kessler, Theodosios Kyriakou, Tomasz Konopka, Ling Li, Lijiang Ma, Thomas Meitinger, Sören Mucha, Matthias Munz, Federico Murgia, Jonas B. Nielsen, Markus M. Nöthen, Shichao Pang, Tobias Reinberger, Gavin R. Schnitzler, Damian Smedley, Guðmar Þorleifsson, Moritz von Scheidt, Jacob C. Ulirsch, Biobank Japan, EPIC-CVD, John Danesh, Davíð O. Arnar, Noël P. Burtt, Maria C. Costanzo, Jason Flannick, Kaoru Ito, Dongkeun Jang, Yoichiro Kamatani, Amit V. Khera, Issei Komuro, Iftikhar J. Kullo, Luca A. Lotta, Christopher P. Nelson, Robert Roberts, Guðmundur Þorgeirsson, Unnur Þorsteinsdóttir, Tom R. Webb, Aris Baras, Johan Björkegren, Eric Boerwinkle, George Dedoussis, Hilma Hólm, Kristian Hveem, Olle Melander, Alanna C. Morrison, Marju Orho‐Melander, Lοukianos S. Rallidis, Arno Ruusalepp, Marc S. Sabatine, Kāri Stefánsson, Pierre Zalloua, Patrick T. Ellinor, Martin Farrall, John Danesh, Christian T. Ruff, Hilary K. Finucane, Jemma C. Hopewell, Robert Clarke, Rajat M. Gupta, Jeanette Erdmann, Nilesh J. Samani, Heribert Schunkert, Hugh Watkins, Cristen J. Willer, Panos Deloukas, Sekar Kathiresan, Adam S. Butterworth, Paul S. de Vries, Moritz von Scheidt
Nature Genetics. 2022728 CitationsOPEN ACCESS
A sequence variant in ZFHX3 on 16q22 associates with atrial fibrillation and ischemic stroke
Daníel F. Guðbjartsson, Hilma Hólm, Sólveig Grétarsdóttir, Guðmar Þorleifsson, G. Bragi Walters, Guðmundur Þorgeirsson, Jeffrey R. Gulcher, Ellisiv B. Mathiesen, Inger Njølstad, Audhild Nyrnes, Tom Wilsgaard, Erin Mathiesen Hald, Kristian Hveem, Camilla Stoltenberg, Gayle Kucera, Tanya Stubblefield, Shannon Carter, Dan M. Roden, Maggie Ng, Larry Baum, Wing Yee So, Ka Sing Wong, Juliana C.N. Chan, Christian Gieger, H‐Erich Wichmann, Andreas Gschwendtner, Martin Dichgans, Gregor Kuhlenbäumer, Klaus Berger, E. Bernd Ringelstein, Steve Bevan, Hugh S. Markus, Konstantinos Kostulas, Jan Hillert, Sigurlaug Sveinbjörnsdóttir, Einar Már Valdimarsson, Maja‐Lisa Løchen, Ronald C.W., Dawood Darbar, Augustine Kong, Davíð O. Arnar, Unnur Þorsteinsdóttir, Kāri Stefánsson
Nature Genetics. 2009493 CitationsOPEN ACCESS

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