ScholarIQanswers from OpenAlex & ORCID
Bart Loeys
ResearcherPublications, citations & collaboration network
Bart Loeys is a researcher indexed in ScholarIQ from OpenAlex & ORCID.
How many works does Bart Loeys have?
ScholarIQindexed works
Bart Loeys has 474 works in the ScholarIQ index. The count is the OpenAlex total, not the number of papers listed on this page.
How many citations does Bart Loeys have?
ScholarIQcitation count
Bart Loeys has 35,818 citations in the OpenAlex counts ScholarIQ stores.
What is the h-index of Bart Loeys?
ScholarIQh-index
Bart Loeys has an h-index of 83 in OpenAlex.
What is the i10-index of Bart Loeys?
ScholarIQi10-index
Bart Loeys has an i10-index of 234 in OpenAlex.
What is the ORCID of Bart Loeys?
ScholarIQorcid
The ORCID for Bart Loeys is on the source record.
What is the OpenAlex record for Bart Loeys?
ScholarIQopenalex
The OpenAlex for Bart Loeys is on the source record.
What are the most-cited papers on Bart Loeys?
ScholarIQmost cited works
2023 ESC Guidelines for the management of cardiomyopathies
Elena Arbelo, Alexandros Protonotarios, Juan R. Gimeno, Eloisa Arbustini, Roberto Barriales‐Villa, Cristina Basso, Connie R. Bezzina, Elena Biagini, Nico A. Blom, Rudolf A. de Boer, Tim De Winter, Perry Elliott, Marcus Flather, Pablo García‐Pavía, Kristina H. Haugaa, Jodie Ingles, Ruxandra Jurcuţ, Sabine Klaassen, Giuseppe Limongelli, Bart Loeys, Jens Mogensen, Iacopo Olivotto, Antonios Pantazis, Sanjay Sharma, J. Peter van Tintelen, James S. Ware, Juan Pablo Kaski, ESC Scientific Document Group, Philippe Charron, Massimo Imazio, Magdy Abdelhamid, Victor Aboyans, Michael Arad, Folkert W. Asselbergs, Riccardo Asteggiano, Zofia T. Bilińska, Damien Bonnet, Henning Bundgaard, Nuno Cardim, Jelena Čelutkienė, Maja Čikeš, Gaetano Maria De Ferrari, Veronica Dusi, Volkmar Falk, Laurent Fauchier, Estelle Gandjbakhch, Tiina Heliö, Konstantinos C. Koskinas, Dipak Kotecha, Ulf Landmesser, George Lazaros, Basil S. Lewis, Aleš Linhart, Maja‐Lisa Løchen, Benjamin Meder, Richard Mindham, James Moon, Jens Cosedis Nielsen, Steffen E. Petersen, Eva Prescott, Mary N. Sheppard, Gianfranco Sinagra, Marta Sitges, Jacob Tfelt‐Hansen, Rhian M. Touyz, Rogier J. A. Veltrop, Josef Veselka, Karim Wahbi, Arthur A.M. Wilde, Katja Zeppenfeld, B. Kichou, Hamayak Sisakian, Daniel Scherr, Bernhard Gerber, Alen Džubur, Мариана Господинова, Ivo Planinc, Hera Heracleous Moustra, David Zemánek, Morten K. Jensen, Ahmad Samir, Kairit Palm, Tiina Heliö, Karim Wahbi, Eric Schulze‐Bahr, Vlachopoulos Haralambos, Róbert Sepp, Berglind Aðalsteinsdóttir, Deirdre Ward, Miry Blich, Gianfranco Sinagra, Afrim Poniku, Olga Lunegova, Ainārs Rudzītis, Roland Kassab, Jūratė Barysienė, Steve Huijnen, Tiziana Felice, Eleonora Vataman, Nikola Pavlović
Loeys–Dietz syndrome: a primer for diagnosis and management
Gretchen MacCarrick, James H. Black, Sarah Bowdin, Ismaı̈l El-Hamamsy, Pamela A. Frischmeyer‐Guerrerio, Anthony L. Guerrerio, Paul D. Sponseller, Bart Loeys, Harry C. Dietz
Nephrocystin-5, a ciliary IQ domain protein, is mutated in Senior-Loken syndrome and interacts with RPGR and calmodulin
Edgar A. Otto, Bart Loeys, Hemant Khanna, Jan Hellemans, Ralf Sudbrak, Shuling Fan, Ulla Muerb, John F. O’Toole, Juliana Helou, Massimo Attanasio, Boris Utsch, John A. Sayer, Concepción Lillo, David Jimeno, Paul Coucke, Anne De Paepe, Richard Reinhardt, Sven Klages, Motoyuki Tsuda, I. Kawakami, Takehiro Kusakabe, Heymut Omran, Anita Imm, Melissa Tippens, Pamela A. Raymond, JO Hill, Phil Beales, Shirley He, Andreas Kispert, Benjamin Margolis, David S. Williams, Anand Swaroop, Friedhelm Hildebrandt
Phenotypic spectrum of the SMAD3-related aneurysms–osteoarthritis syndrome
Ingrid M.B.H. van de Laar, Denise van der Linde, E.H. Oei, P.K. Bos, J. H. J. M. Bessems, Sita Bierma‐Zeinstra, Belle L. van Meer, Gerard Pals, Rogier A. Oldenburg, Jos A. Bekkers, Adriaan Moelker, Bianca M. de Graaf, Gábor Mátyás, Ingrid M.E. Frohn-Mulder, Janneke Timmermans, Yvonne Hilhorst‐Hofstee, Jan M. Cobben, Hennie T. Brüggenwirth, Lut Van Laer, Bart Loeys, Julie De Backer, Paul Coucke, Harry C. Dietz, Patrick J. Willems, Ben A. Oostra, Anne De Paepe, Jolien W. Roos‐Hesselink, Aida M. Bertoli‐Avella, Marja W. Wessels
Transethnic Genome-Wide Association Study Provides Insights in the Genetic Architecture and Heritability of Long QT Syndrome
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