ScholarIQanswers from OpenAlex & ORCID
Ivona Aksentijevich
ResearcherPublications, citations & collaboration network
Ivona Aksentijevich is a researcher indexed in ScholarIQ from OpenAlex & ORCID.
How many works does Ivona Aksentijevich have?
ScholarIQindexed works
Ivona Aksentijevich has 264 works in the ScholarIQ index. The count is the OpenAlex total, not the number of papers listed on this page.
How many citations does Ivona Aksentijevich have?
ScholarIQcitation count
Ivona Aksentijevich has 25,503 citations in the OpenAlex counts ScholarIQ stores.
What is the h-index of Ivona Aksentijevich?
ScholarIQh-index
Ivona Aksentijevich has an h-index of 74 in OpenAlex.
What is the i10-index of Ivona Aksentijevich?
ScholarIQi10-index
Ivona Aksentijevich has an i10-index of 164 in OpenAlex.
What is the ORCID of Ivona Aksentijevich?
ScholarIQorcid
The ORCID for Ivona Aksentijevich is on the source record.
What is the OpenAlex record for Ivona Aksentijevich?
ScholarIQopenalex
The OpenAlex for Ivona Aksentijevich is on the source record.
What are the most-cited papers on Ivona Aksentijevich?
ScholarIQmost cited works
Germline Mutations in the Extracellular Domains of the 55 kDa TNF Receptor, TNFR1, Define a Family of Dominantly Inherited Autoinflammatory Syndromes
Michael McDermott, Ivona Aksentijevich, Jérôme Galon, Elizabeth McDermott, B Ogunkolade, Michael Centola, Elizabeth Mansfield, Massimo Gadina, Leena Karenko, Tom Pettersson, John McCarthy, David M. Frucht, Martin Aringer, Yelizaveta Torosyan, Anna‐Maija Teppo, Meredith Wilson, H.Mehmet Karaarslan, Ying Wan, Ian Todd, Geryl Wood, Ryan Schlimgen, Thisum R. Kumarajeewa, Sheldon M. Cooper, John P. Vella, Christopher I. Amos, John C. Mulley, Kathleen A. Quane, Michael G. Molloy, Annamari Ranki, Richard J. Powell, G. A. Hitman, John J. O’Shea, Daniel L. Kastner
Early-Onset Stroke and Vasculopathy Associated with Mutations in ADA2
Qing Zhou, Dan Yang, Amanda K. Ombrello, Andrey V. Zavialov, Camilo Toro, Anton V. Zavialov, Deborah L. Stone, Jae Jin Chae, Sergio D. Rosenzweig, Kevin Bishop, Karyl S. Barron, Hye Sun Kuehn, Patrycja Hoffmann, Alejandra Negro, Wanxia Li Tsai, Edward W. Cowen, Wuhong Pei, Joshua D. Milner, Christopher Silvin, Theo Heller, David T. Chin, Nicholas J. Patronas, John S. Barber, Chyi‐Chia Richard Lee, Geryl Wood, Alexander Ling, Susan J. Kelly, David E. Kleiner, James C. Mullikin, Nancy J. Ganson, Heidi H. Kong, Sophie Hambleton, Fabio Candotti, Martha Quezado, Katherine R. Calvo, Hawwa Alao, Beverly Barham, Anne Jones, James F. Meschia, Bradford B. Worrall, Scott E. Kasner, Stephen S. Rich, Raphaela Goldbach‐Mansky, Mario Abinun, Elizabeth Chalom, Alisa Gotte, Marilynn Punaro, Virginia Pascual, James Verbsky, Troy R. Torgerson, Nora G. Singer, Timothy R. Gershon, Seza Özen, Ömer Karadağ, Thomas A. Fleisher, Elaine F. Remmers, Shawn M. Burgess, Susan Moir, Massimo Gadina, Raman Sood, Michael S. Hershfield, Manfred Boehm, Daniel L. Kastner, Ivona Aksentijevich
Loss-of-function mutations in TNFAIP3 leading to A20 haploinsufficiency cause an early-onset autoinflammatory disease
Qing Zhou, Hongying Wang, Daniella M. Schwartz, Monique Stoffels, Yong Hwan Park, Yuan Zhang, Dan Yang, Erkan Demirkaya, Masaki Takeuchi, Wanxia Li Tsai, Jonathan J. Lyons, Xiaomin Yu, Claudia Ouyang, Celeste Chen, David T. Chin, Kristien J.M. Zaal, Settara C. Chandrasekharappa, Eric P. Hanson, Zhen Yu, James C. Mullikin, Sarfaraz Hasni, Ingrid E. Wertz, Amanda K. Ombrello, Deborah L. Stone, Patrycja Hoffmann, Anne Jones, Beverly Barham, Helen L. Leavis, Annet van Royen-Kerkof, Cailin H. Sibley, Ezgi Deniz Batu, Ahmet Gül, Richard M. Siegel, Manfred Boehm, Joshua D. Milner, Seza Özen, Massimo Gadina, JaeJin Chae, Ronald M. Laxer, Daniel L. Kastner, Ivona Aksentijevich
Non-type I cystinuria caused by mutations in SLC7A9, encoding a subunit (bo,+AT) of rBAT
Lídia Feliubadaló, Mariona Font, Jesús Purroy, F. Rousaud, Xavier Estivill, Virginia Nunes, Eliahu Golomb, Michael Centola, Ivona Aksentijevich, Yitshak Kreiss, Boleslaw Goldman, Mordechai Pras, Daniel L. Kastner, Elon Pras, Paolo Gasparini, Luigi Bisceglia, Ercole Beccia, Michele Gallucci, Luisa De Sanctis, Alberto Ponzone, Gian Franco Rizzoni, Leopoldo Zelante, Maria Teresa Bassi, Alfred L. George, Marta Manzoni, Alessandro De Grandi, Mirko Riboni, John K. Endsley, Andrea Ballabio, Giuseppe Borsani, Núria Reig, Esperanza Fernández, Raúl Estévez, Marta Pineda, David Torrents, Marta Camps, Jorge Lloberas, António Zorzano, Manuel Palacı́n
ADA2 deficiency (DADA2) as an unrecognised cause of early onset polyarteritis nodosa and stroke: a multicentre national study
Roberta Caorsi, Federica Penco, Alice Grossi, Antonella Insalaco, Alessia Omenetti, Maria Alessio, Giovanni Conti, Federico Marchetti, Paolo Picco, Alberto Tommasini, Silvana Martino, Clara Malattia, Romina Gallizi, Rosa Anna Podda, Annalisa Salis, Fernanda Falcini, Francesca Schena, Francesca Garbarino, Alessia Morreale, Manuela Pardeo, Claudia Ventrici, Chiara Passarelli, Qing Zhou, Mariasavina Severino, Carlo Gandolfo, Gianluca Damonte, Alberto Martini, Angelo Ravelli, Ivona Aksentijevich, Isabella Ceccherini, Marco Gattorno