ScholarIQanswers from OpenAlex
VIB-UAntwerp Center for Molecular Neurology
InstitutionResearch output, impact & collaborations
VIB-UAntwerp Center for Molecular Neurology is a institution indexed in ScholarIQ from OpenAlex.
What is known about VIB-UAntwerp Center for Molecular Neurology?
ScholarIQrecord summary
VIB-UAntwerp Center for Molecular Neurology is a research organisation in Antwerp, BE. OpenAlex records 1,580 works and 415,121 citations for it. 237 researchers list it as their most recent affiliation.
How many works does VIB-UAntwerp Center for Molecular Neurology have?
ScholarIQindexed works
VIB-UAntwerp Center for Molecular Neurology has 1,580 works in the ScholarIQ index. The count is the OpenAlex total, not the number of papers listed on this page.
How many citations does VIB-UAntwerp Center for Molecular Neurology have?
ScholarIQcitation count
VIB-UAntwerp Center for Molecular Neurology has 415,121 citations in the OpenAlex counts ScholarIQ stores.
How many researchers are at VIB-UAntwerp Center for Molecular Neurology?
ScholarIQresearcher count
VIB-UAntwerp Center for Molecular Neurology has 237 researchers in the ScholarIQ index.
What is the average h-index at VIB-UAntwerp Center for Molecular Neurology?
ScholarIQavg h-index
VIB-UAntwerp Center for Molecular Neurology has an average h-index of 139 in OpenAlex.
What is the ROR of VIB-UAntwerp Center for Molecular Neurology?
ScholarIQror
The ROR for VIB-UAntwerp Center for Molecular Neurology is on the source record.
What is the OpenAlex record for VIB-UAntwerp Center for Molecular Neurology?
ScholarIQopenalex
The OpenAlex for VIB-UAntwerp Center for Molecular Neurology is on the source record.
Who are the most-cited researchers behind VIB-UAntwerp Center for Molecular Neurology?
ScholarIQtop researchers by citations
What are the most-cited papers on VIB-UAntwerp Center for Molecular Neurology?
ScholarIQmost cited works
De Novo Mutations in the Sodium-Channel Gene SCN1A Cause Severe Myoclonic Epilepsy of Infancy
Lieve Claes, Jurgen Del‐Favero, Berten Ceulemans, Lieven Lagae, Christine Van Broeckhoven, Peter De Jonghe
VEGF is a modifier of amyotrophic lateral sclerosis in mice and humans and protects motoneurons against ischemic death
Diether Lambrechts, Erik Storkebaum, Masafumi Morimoto, Jurgen Del‐Favero, Frederik Desmet, Stefan L. Marklund, Sabine Wyns, Vincent Thijs, Jörgen Andersson, Ingrid van Marion, Ammar Al‐Chalabi, Stéphanie Bornes, Rhiannon Musson, Valerie K. Hansen, L. Beckman, Rolf Adolfsson, Hardev Pall, Hervé Prats, Séverine Vermeire, Paul Rutgeerts, Shigehiro Katayama, Takuya Awata, Nigel Leigh, Loı̈c Lang-Lazdunski, Mieke Dewerchin, Christopher E. Shaw, Lieve Moons, Robert Vlietinck, Karen Morrison, Wim Robberecht, Christine Van Broeckhoven, Désiré Collen, Peter M. Andersen, Peter Carmeliet
TREM2 mutations implicated in neurodegeneration impair cell surface transport and phagocytosis
Gernot Kleinberger, Yoshinori Yamanishi, Marc Suárez‐Calvet, Eva Czirr, Ebba Lohmann, Elise Cuyvers, Hanne Struyfs, Nadine Pettkus, Andrea Wenninger-Weinzierl, Fargol Mazaheri, Sabina Tahirović, Alberto Lleó, Daniel Alcolea, Juan Fortea, Michael Willem, Sven Lammich, José Luís Molinuevo, Raquel Sánchez‐Valle, Anna Antonell, Alfredo Ramı́rez, Michael T. Heneka, Kristel Sleegers, Julie van der Zee, Jean‐Jacques Martin, Sebastiaan Engelborghs, Aslı Demirtaş-Tatlıdede, Henrik Zetterberg, Christine Van Broeckhoven, Hakan Gürvıt, Tony Wyss‐Coray, John Hardy, Marco Colonna, Christian Haass
A C9orf72 promoter repeat expansion in a Flanders-Belgian cohort with disorders of the frontotemporal lobar degeneration-amyotrophic lateral sclerosis spectrum: a gene identification study
Ilse Gijselinck, Tim Van Langenhove, Julie van der Zee, Kristel Sleegers, Stéphanie Philtjens, Gernot Kleinberger, Jonathan Janssens, Karolien Bettens, Caroline Van Cauwenberghe, Sandra Pereson, Sebastiaan Engelborghs, Anne Sieben, Peter De Jonghe, Rik Vandenberghe, Patrick Santens, Jan De Bleecker, Githa Maes, Veerle Bäumer, Lubina Dillen, Geert Joris, Ivy Cuijt, Ellen Corsmit, Ellen Elinck, Jasper Van Dongen, Steven Vermeulen, Marleen Van den Broeck, C Vaerenberg, Maria Mattheijssens, Karin Peeters, Wim Robberecht, Patrick Cras, Jean‐Jacques Martin, Peter P. De Deyn, Marc Cruts, Christine Van Broeckhoven
Phenotype variability in progranulin mutation carriers: a clinical, neuropsychological, imaging and genetic study
Isabelle Le Ber, Agnès Camuzat, Didier Hannequin, Florence Pasquier, Éric Guedj, Anne Rovelet‐Lecrux, Valérie Hahn‐Barma, Julie van der Zee, Fabienne Clot, Serge Bakchine, Michèle Puel, Mustapha Ghanim, Lucette Lacomblez, Jacqueline Mikol, Vincent Deramecourt, Pascal Lejeune, Vincent de La Sayette, Serge Belliard, Martine Vercelletto, C Meyrignac, Christine Van Broeckhoven, Jean‐Charles Lambert, Patrice Verpillat, Dominique Campion, Marie‐Odile Habert, Bruno Dubois, Alexis Brice
How much of the research on VIB-UAntwerp Center for Molecular Neurology is open access?
ScholarIQopen access share
56%OPEN ACCESS