ScholarIQanswers from OpenAlex & ORCID
Arthur A.M. Wilde
ResearcherPublications, citations & collaboration network
Arthur A.M. Wilde is a researcher indexed in ScholarIQ from OpenAlex & ORCID.
How many works does Arthur A.M. Wilde have?
ScholarIQindexed works
Arthur A.M. Wilde has 1,194 works in the ScholarIQ index. The count is the OpenAlex total, not the number of papers listed on this page.
How many citations does Arthur A.M. Wilde have?
ScholarIQcitation count
Arthur A.M. Wilde has 77,554 citations in the OpenAlex counts ScholarIQ stores.
What is the h-index of Arthur A.M. Wilde?
ScholarIQh-index
Arthur A.M. Wilde has an h-index of 149 in OpenAlex.
What is the i10-index of Arthur A.M. Wilde?
ScholarIQi10-index
Arthur A.M. Wilde has an i10-index of 607 in OpenAlex.
What is the ORCID of Arthur A.M. Wilde?
ScholarIQorcid
The ORCID for Arthur A.M. Wilde is on the source record.
What is the OpenAlex record for Arthur A.M. Wilde?
ScholarIQopenalex
The OpenAlex for Arthur A.M. Wilde is on the source record.
What are the most-cited papers on Arthur A.M. Wilde?
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
Genotype-Phenotype Correlation in the Long-QT Syndrome
Peter J. Schwartz, Silvia G. Priori, Carla Spazzolini, Arthur J. Moss, G. Michael Vincent, Carlo Napolitano, Isabelle Denjoy, Pascale Guicheney, Günter Breithardt, Mark T. Keating, Jeffrey A. Towbin, Alan H. Beggs, Paul A. Brink, Arthur A.M. Wilde, Lauri Toivonen, Wojciech Zaręba, Jennifer L. Robinson, Katherine W. Timothy, Valerie A. Corfield, Duangrurdee Wattanasirichaigoon, Clive Corbett, Wilhelm Haverkamp, Eric Schulze‐Bahr, Michael H. Lehmann, Ketty Schwartz, P Coumel, Raffaella Bloise
2019 HRS expert consensus statement on evaluation, risk stratification, and management of arrhythmogenic cardiomyopathy
Jeffrey A. Towbin, William J. McKenna, Dominic J. Abrams, Michael J. Ackerman, Hugh Calkins, Francisco Darrieux, James P. Daubert, Christian de Chillou, E.C. DePasquale, Milind Y. Desai, N.A. Mark Estes, Wei Hua, Julia H. Indik, Jodie Ingles, Cynthia A. James, Roy M. John, Daniel P. Judge, Roberto Keegan, Andrew D. Krahn, Mark S. Link, Gregory M. Marcus, Christopher J. McLeod, Luisa Mestroni, Silvia G. Priori, Jeffrey E. Saffitz, Shubhayan Sanatani, Wataru Shimizu, J. Peter van Tintelen, Arthur A.M. Wilde, Wojciech Zaręba
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
Clinical Aspects of Type-1 Long-QT Syndrome by Location, Coding Type, and Biophysical Function of Mutations Involving the KCNQ1 Gene
Arthur J. Moss, Wataru Shimizu, Arthur A.M. Wilde, Jeffrey A. Towbin, Wojciech Zaręba, Jennifer L. Robinson, Ming Qi, G. Michael Vincent, Michael J. Ackerman, Elizabeth S. Kaufman, Nynke Hofman, Rahul Seth, Shiro Kamakura, Yoshihiro Miyamoto, Ilan Goldenberg, Mark Andrews, Scott McNitt