ScholarIQanswers from OpenAlex
AGCO (Netherlands)
InstitutionResearch output, impact & collaborations
AGCO (Netherlands) is a institution indexed in ScholarIQ from OpenAlex.
What is known about AGCO (Netherlands)?
ScholarIQrecord summary
AGCO (Netherlands) is a research organisation in Helmond, Netherlands. OpenAlex records 839 works and 17,238 citations for it. 1 researchers list it as their most recent affiliation.
How many works does AGCO (Netherlands) have?
ScholarIQindexed works
AGCO (Netherlands) has 839 works in the ScholarIQ index. The count is the OpenAlex total, not the number of papers listed on this page.
How many citations does AGCO (Netherlands) have?
ScholarIQcitation count
AGCO (Netherlands) has 17,238 citations in the OpenAlex counts ScholarIQ stores.
How many researchers are at AGCO (Netherlands)?
ScholarIQresearcher count
AGCO (Netherlands) has 1 researchers in the ScholarIQ index.
What is the average h-index at AGCO (Netherlands)?
ScholarIQavg h-index
AGCO (Netherlands) has an average h-index of 35 in OpenAlex.
What is the ROR of AGCO (Netherlands)?
ScholarIQror
The ROR for AGCO (Netherlands) is on the source record.
What is the OpenAlex record for AGCO (Netherlands)?
ScholarIQopenalex
The OpenAlex for AGCO (Netherlands) is on the source record.
Who are the most-cited researchers behind AGCO (Netherlands)?
ScholarIQtop researchers by citations
What are the most-cited papers on AGCO (Netherlands)?
ScholarIQmost cited works
Mutations in Cu/Zn superoxide dismutase gene are associated with familial amyotrophic lateral sclerosis
D.R. Rosen, Teepu Siddique, David T. Patterson, Denise A. Figlewicz, Peter C. Sapp, Afif Hentati, Deirdre Donaldson, Jun Goto, J. O'Regan, Han‐Xiang Deng, Zohra Rahmani, Aldis Krizus, Diane McKenna‐Yasek, Annarueber Cayabyab, Sandra M. Gaston, Ralph Berger, Rudolph E. Tanzi, John Halperin, Brian Herzfeldt, R. van den Bergh, W.‐Y. Hung, Thomas D. Bird, Gang Deng, Donald W. Mulder, Celestine Smyth, Nigel G. Laing, Edwin Soriano, Margaret A. Pericak‐Vance, Jonathan Haines, Guy A. Rouleau, James S. Gusella, H. Robert Horvitz, Robert Brown
Mutations in the <i>FUS/TLS</i> Gene on Chromosome 16 Cause Familial Amyotrophic Lateral Sclerosis
Thomas J. Kwiatkowski, Daryl A. Bosco, Aurélie Leclerc, Eric Tamrazian, Charles Vanderburg, C Russ, Adam Davis, James M. Gilchrist, Edward J. Kasarskis, T. L. Munsat, Paul N. Valdmanis, Guy A. Rouleau, Betsy A. Hosler, Pietro Cortelli, Pieter J. de Jong, Yuko Yoshinaga, J. L. Haines, Margaret A. Pericak‐Vance, J Yan, Nicola Ticozzi, Teepu Siddique, D. McKenna‐Yasek, Peter C. Sapp, H. Robert Horvitz, John E. Landers, Robert H. Brown
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
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
Mutations in the vesicular trafficking protein annexin A11 are associated with amyotrophic lateral sclerosis
Bradley Smith, Simon Topp, Claudia Fallini, Hideki Shibata, Han-Jou Chen, Claire Troakes, Andrew King, Nicola Ticozzi, Kevin P. Kenna, Athina Soragia-Gkazi, Jack W. Miller, Akane Sato, Diana Marques Dias, Maryangel Jeon, Caroline Vance, Chun Hao Wong, Martina de Majo, Wejdan Kattuah, Jacqueline C. Mitchell, Emma L. Scotter, Nicholas Parkin, Peter C. Sapp, Matthew Nolan, Peter J. Nestor, Michael A. Simpson, Michael E. Weale, Monkel Lek, Frank Baas, J. M. Vianney de Jong, Anneloor L.M.A. ten Asbroek, Alberto García‐Redondo, Jesús Esteban‐Pérez, Cinzia Tiloca, Federico Verde, Stefano Duga, Nigel Leigh, Hardev Pall, Karen Morrison, Ammar Al‐Chalabi, Pamela J. Shaw, Janine Kirby, Martin R. Turner, Kevin Talbot, Orla Hardiman, Jonathan D. Glass, Jacqueline de Belleroche, Masatoshi Maki, Stephen E. Moss, Christopher C.J. Miller, Cinzia Gellera, Antonia Ratti, Safa Al‐Sarraj, Robert H. Brown, Vincenzo Silani, John E. Landers, Christopher E. Shaw
How much of the research on AGCO (Netherlands) is open access?
ScholarIQopen access share
57%OPEN ACCESS