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Fondazione IRCCS Istituto Neurologico Carlo Besta

InstitutionResearch output, impact & collaborations

Fondazione IRCCS Istituto Neurologico Carlo Besta is a research organisation in Milan, IT. OpenAlex records 13,285 works and 1,414,818 citations for it. 1,789 researchers list it as their most recent affiliation.

13,285
Works
1,414,818
Citations
1,789
Researchers
58.3
Avg h-index

How has Fondazione IRCCS Istituto Neurologico Carlo Besta's publication output changed over time?

ScholarIQpublication output · 2004–2017

Output grew100% over the shown period — from 1 works in 2004 to 2 in 2017.

1
1
1
1
1
2
1
1
1
2
2004200620082009201020122014201520162017

Who are the most-cited researchers behind Fondazione IRCCS Istituto Neurologico Carlo Besta?

ScholarIQtop researchers by citations
1
Alberto Raggi · Migraine and Headache Studies
326 works71,691 citations

What are the most-cited papers on Fondazione IRCCS Istituto Neurologico Carlo Besta?

ScholarIQmost cited works
The clinicopathologic spectrum of focal cortical dysplasias: A consensus classification proposed by an ad hoc Task Force of the ILAE Diagnostic Methods Commission1
Ingmar Blümcke, Maria Thom, Eleonora Aronica, Dawna D. Armstrong, Harry V. Vinters, André Palmini, Thomas S. Jacques, G. Avanzini, A. James Barkovich, Giorgio Battaglia, Albert J. Becker, Carlos Cepeda, Fernando Cendes, N. Colombo, Peter B. Crino, J. Helen Cross, Olivier Delalande, François Dubeau, John S. Duncan, Renzo Guerrini, Philippe Kahane, Gary W. Mathern, Imad Najm, Çiğdem Özkara, Charles Raybaud, Alfonso Represa, Steven N. Roper, Noriko Salamon, Andreas Schulze‐Bonhage, Laura Tassi, Annamaria Vezzani, Roberto Spreafico
Epilepsia. 20101,747 CitationsOPEN ACCESS
Terminology and classification of the cortical dysplasias
André Palmini, Imad Najm, G. Avanzini, Thomas L. Babb, Renzo Guerrini, Nancy Foldvary‐Schaefer, Graeme D. Jackson, Hans O. Lüders, Richard A. Prayson, Roberto Spreafico, Harry V. Vinters
Neurology. 2004952 Citations
Histopathological Findings in Brain Tissue Obtained during Epilepsy Surgery
Ingmar Blümcke, Roberto Spreafico, Gerrit Haaker, Roland Coras, Katja Kobow, Christian G. Bien, Margarete Pfäfflin, Christian E. Elger, Guido Widman, Johannes Schramm, Albert J. Becker, Kees P. J. Braun, Frans S. S. Leijten, Johannes C. Baayen, Eleonora Aronica, Francine Chassoux, Hajo M. Hamer, Hermann Stefan, Karl Rössler, Maria Thom, Matthew C. Walker, Sanjay M. Sisodiya, John S. Duncan, Andrew W. McEvoy, Tom Pieper, Hans Holthausen, Manfred Kudernatsch, H. J. Meencke, Philippe Kahane, Andreas Schulze‐Bonhage, Josef Zentner, Dieter Henrik Heiland, Horst Urbach, Bernhard J. Steinhoff, Thomas Bast, Laura Tassi, Giorgio Lo Russo, Çiğdem Özkara, Büğe Öz, Pavel Kršek, Silke Vogelgesang, Uwe Runge, Holger Lerche, Yvonne Weber, Mrinalini Honavar, José Pimentel, Alexis Arzimanoglou, Adriana Ulate-Campos, Soheyl Noachtar, Elisabeth Härtl, Olaf Schijns, Renzo Guerrini, Carmen Barba, Thomas S. Jacques, J. Helen Cross, Martha Feucht, Angelika Mühlebner, Thomas Grünwald, Eugen Trinka, Peter Winkler, António Gil‐Nagel, Rafael Toledano, Thomas Mayer, Martin Lutz, Basilios Zountsas, Kyriakos Garganis, Felix Rosenow, Anke Hermsen, Tim J. von Oertzen, Thomas L. Diepgen, G. Avanzini
New England Journal of Medicine. 2017929 CitationsOPEN ACCESS
Mutations in the profilin 1 gene cause familial amyotrophic lateral sclerosis
Chi-Hong Wu, Claudia Fallini, Nicola Ticozzi, Pamela Keagle, Peter C. Sapp, Katarzyna Piotrowska, Patrick Lowe, Max Koppers, Diane McKenna‐Yasek, Desiree M. Baron, Jason Kost, Paloma González-Pérez, Andrew Fox, Jenni Adams, Franco Taroni, Cinzia Tiloca, Ashley LeClerc, Shawn C. Chafe, Dev Mangroo, Melissa J. Moore, Jill A. Zitzewitz, Zuo-Shang Xu, Leonard H. van den Berg, Jonathan D. Glass, Gabriele Siciliano, Elizabeth T. Cirulli, David B. Goldstein, François Salachas, Vincent Meininger, Wilfried Rossoll, Antonia Ratti, Cinzia Gellera, Daryl A. Bosco, Gary J. Bassell, Vincenzo Silani, Vivian E. Drory, Robert H. Brown, John E. Landers
Nature. 2012601 Citations
Exome-wide Rare Variant Analysis Identifies TUBA4A Mutations Associated with Familial ALS
Bradley Smith, Nicola Ticozzi, Claudia Fallini, Soragia Athina Gkazi, Simon Topp, Kevin P. Kenna, Emma L. Scotter, Jason Kost, Pamela Keagle, Jack W. Miller, Daniela Calini, Caroline Vance, Eric Danielson, Claire Troakes, Cinzia Tiloca, Safa Al‐Sarraj, Elizabeth Lewis, Andrew King, Claudia Colombrita, Viviana Pensato, Barbara Castellotti, Jacqueline de Belleroche, Frank Baas, Anneloor L.M.A. ten Asbroek, Peter C. Sapp, Diane McKenna‐Yasek, Russell L. McLaughlin, Meraida Polak, Seneshaw Asress, Jesús Esteban‐Pérez, José Luís Muñoz-Blanco, Michael A. Simpson, Wouter van Rheenen, Frank P. Diekstra, Giuseppe Lauria, Stefano Duga, Stefania Corti, Cristina Cereda, Lucia Corrado, Gianni Sorarú, Karen Morrison, Kelly L. Williams, Garth A. Nicholson, Ian P. Blair, Patrick A. Dion, Claire S. Leblond, Guy A. Rouleau, Orla Hardiman, Jan H. Veldink, Leonard H. van den Berg, Ammar Al‐Chalabi, Hardev Pall, Pamela J. Shaw, Martin R. Turner, Kevin Talbot, Franco Taroni, Alberto García‐Redondo, Zheyang Wu, Jonathan D. Glass, Cinzia Gellera, Antonia Ratti, Robert H. Brown, Vincenzo Silani, Christopher E. Shaw, John E. Landers, Sandra D’Alfonso, Letizia Mazzini, Giacomo P. Comi, Roberto Del Bo, Mauro Ceroni, Stella Gagliardi, Giorgia Querin, Cinzia Bertolin
Neuron. 2014370 CitationsOPEN ACCESS

How much of the research on Fondazione IRCCS Istituto Neurologico Carlo Besta is open access?

ScholarIQopen access share
50%OPEN ACCESS
Gold
8%
Green
8%
Hybrid
0%
Bronze
33%
Closed
50%

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470M+ articles · free account