ScholarIQanswers from OpenAlex & ORCID
Vincent Meininger
ResearcherPublications, citations & collaboration network
Vincent Meininger is a researcher indexed in ScholarIQ from OpenAlex & ORCID.
How many works does Vincent Meininger have?
ScholarIQindexed works
Vincent Meininger has 311 works in the ScholarIQ index. The count is the OpenAlex total, not the number of papers listed on this page.
How many citations does Vincent Meininger have?
ScholarIQcitation count
Vincent Meininger has 22,919 citations in the OpenAlex counts ScholarIQ stores.
What is the h-index of Vincent Meininger?
ScholarIQh-index
Vincent Meininger has an h-index of 80 in OpenAlex.
What is the i10-index of Vincent Meininger?
ScholarIQi10-index
Vincent Meininger has an i10-index of 208 in OpenAlex.
What is the ORCID of Vincent Meininger?
ScholarIQorcid
The ORCID for Vincent Meininger is on the source record.
What is the OpenAlex record for Vincent Meininger?
ScholarIQopenalex
The OpenAlex for Vincent Meininger is on the source record.
What are the most-cited papers on Vincent Meininger?
ScholarIQmost cited works
TARDBP mutations in individuals with sporadic and familial amyotrophic lateral sclerosis
Edor Kabashi, Paul N. Valdmanis, Patrick A. Dion, Dan Spiegelman, Brendan J. McConkey, Christine Vande Velde, Jean‐Pierre Bouchard, Lucette Lacomblez, Ksenia Pochigaeva, François Salachas, Pierre‐François Pradat, William Camu, Vincent Meininger, Nicolas Dupré, Guy A. Rouleau
Genome-wide association analyses identify new risk variants and the genetic architecture of amyotrophic lateral sclerosis
PARALS Registry, Wouter van Rheenen, SLALOM Group, SLAP Registry, NNIPPS Study Group, Aleksey Shatunov, Annelot M. Dekker, Russell L. McLaughlin, Frank P. Diekstra, Sara L. Pulit, Rick A. A. van der Spek, Urmo Võsa, Simone de Jong, Matthew R. Robinson, Jian Yang, Isabella Fogh, Perry Tc van Doormaal, Gijs Tazelaar, Max Koppers, Anna M. Blokhuis, William Sproviero, Ashley R Jones, Kevin P. Kenna, Kristel R. van Eijk, Oliver Harschnitz, Raymond D. Schellevis, William J. Brands, Jelena Medic, Androniki Menelaou, Alice Vajda, Nicola Ticozzi, Kuang Lin, Boris Rogelj, Katarina Vrabec, Metka Ravnik‐Glavač, Blaž Koritnik, Janez Zidar, Lea Leonardis, Leja Dolenc Grošelj, Stéphanie Millecamps, François Salachas, Vincent Meininger, Mamede de Carvalho, Susana Pinto, Jesús S. Mora, Ricardo Rojas-García, Meraida Polak, Siddharthan Chandran, Shuna Colville, Robert Swingler, Karen Morrison, Pamela J. Shaw, John Hardy, Richard W. Orrell, Alan Pittman, Katie Sidle, Pietro Fratta, Andrea Malaspina, Simon Topp, Susanne Petri, Susanne Abdulla, Carsten Drepper, Michael Sendtner, Thomas Meyer, Roel A. Ophoff, Kim A. Staats, Martina Wiedau‐Pazos, Catherine Lomen‐Hoerth, Vivianna M. Van Deerlin, John Q. Trojanowski, Lauren Elman, Leo McCluskey, A. Nazlı Başak, Ceren Tunca, Hamid Hamzeiy, Yeşim Parman, Thomas Meitinger, Peter Lichtner, Milena Radivojkov‐Blagojevic, Christian Andrés, Cindy Maurel, Gilbert Bensimon, G. Bernhard Landwehrmeyer, Alexis Brice, Christine Payan, Safaa Saker-Delye, Alexandra Dürr, Nicholas Wood, Lukas Tittmann, Wolfgang Lieb, André Franke, Marcella Rietschel, Sven Cichon, Markus M. Nöthen, Philippe Amouyel, Christophe Tzourio, Jean‐François Dartigues, André G. Uitterlinden, Fernando Rivadeneira, Karol Estrada
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
<i>TARDBP</i> mutations in motoneuron disease with frontotemporal lobar degeneration
Lina Benajiba, Isabelle Le Ber, Agnès Camuzat, Mathieu Lacoste, Catherine Thomas-Antérion, Philippe Couratier, Solenn Legallic, François Salachas, Didier Hannequin, M. Décousus, Lucette Lacomblez, Eric Guedj, Véronique Golfier, William Camu, Bruno Dubois, Dominique Campion, Vincent Meininger, Alexis Brice
<i>SOD1</i>, <i>ANG</i>, <i>VAPB</i>, <i>TARDBP</i>, and <i>FUS</i> mutations in familial amyotrophic lateral sclerosis: genotype–phenotype correlations
Stéphanie Millecamps, François Salachas, C. Cazeneuve, Paul Gordon, Bernard Bricka, A. Camuzat, Léna Guillot‐Noël, Odile Russaouen, Gaëlle Bruneteau, Pierre‐François Pradat, Nadine Le Forestier, N. Vandenberghe, Véronique Danel-Brunaud, Nathalie Guy, Christel Thauvin-Robinet, Lucette Lacomblez, P. Couratier, Didier Hannequin, Danielle Seilhean, Isabelle Le Ber, Philippe Corcia, William Camu, Alexis Brice, Guy A. Rouleau, Eric Leguern, Vincent Meininger