ScholarIQanswers from OpenAlex & ORCID
Mamede de Carvalho
ResearcherPublications, citations & collaboration network
Mamede de Carvalho is a researcher indexed in ScholarIQ from OpenAlex & ORCID.
How many works does Mamede de Carvalho have?
ScholarIQindexed works
Mamede de Carvalho has 644 works in the ScholarIQ index. The count is the OpenAlex total, not the number of papers listed on this page.
How many citations does Mamede de Carvalho have?
ScholarIQcitation count
Mamede de Carvalho has 20,889 citations in the OpenAlex counts ScholarIQ stores.
What is the h-index of Mamede de Carvalho?
ScholarIQh-index
Mamede de Carvalho has an h-index of 66 in OpenAlex.
What is the i10-index of Mamede de Carvalho?
ScholarIQi10-index
Mamede de Carvalho has an i10-index of 281 in OpenAlex.
What is the ORCID of Mamede de Carvalho?
ScholarIQorcid
The ORCID for Mamede de Carvalho is on the source record.
What is the OpenAlex record for Mamede de Carvalho?
ScholarIQopenalex
The OpenAlex for Mamede de Carvalho is on the source record.
What are the most-cited papers on Mamede de Carvalho?
ScholarIQmost cited works
Evidence-based guidelines on the therapeutic use of repetitive transcranial magnetic stimulation (rTMS)
Jean‐Pascal Lefaucheur, Nathalie André‐Obadia, Andrea Antal, Samar S. Ayache, Chris Baeken, David Benninger, Roberto Cantello, M. Cincotta, Mamede de Carvalho, Dirk De Ridder, H. Devanne, Vincenzo Di Lazzaro, Saša R. Filipović, Friedhelm C. Hummel, Satu K. Jääskeläinen, Vasilios Κ. Kimiskidis, Giacomo Koch, Berthold Langguth, Thomas Nyffeler, Antonio Oliviero, Frank Padberg, Emmanuel Poulet, Símone Rossi, Paolo Maria Rossini, John C. Rothwell, Carlos Schönfeldt‐Lecuona, Hartwig R. Siebner, Christina W. Slotema, Charlotte J. Stagg, Josep Valls‐Solé, Ulf Ziemann, Walter Paulus, Luis Garcı́a-Larrea
EFNS guidelines on the Clinical Management of Amyotrophic Lateral Sclerosis (MALS) – revised report of an EFNS task force
The EFNS Task Force on Diagnosis and Management of Amyotrophic Lateral Sclerosis:, Peter M. Andersen, Sharon Abrahams, Gian Domenico Borasio, Mamede de Carvalho, Adriano Chiò, Philip Van Damme, Orla Hardiman, Katja Kollewe, Karen Morrison, Susanne Petri, Pierre‐François Pradat, Vincenzo Silani, Barbara Tomik, Maria Wasner, Markus Weber
Haploinsufficiency of TBK1 causes familial ALS and fronto-temporal dementia
Axel Freischmidt, Thomas Wieland, Benjamin Richter, Wolfgang Ruf, Véronique Schaeffer, Kathrin Müller, Nicolai Marroquin, Frida Nordin, Annemarie Hübers, Patrick Weydt, Susana Pinto, Rayomond Press, Stéphanie Millecamps, Nicolas Molko, E Bernard, Claude Desnuelle, Marie‐Hélène Soriani, Johannes Dorst, Elisabeth Graf, Ulrika Nordström, Marisa S. Feiler, Stefan Putz, Tobias M. Boeckers, Thomas Meyer, Andrea Sylvia Winkler, Juliane Winkelman, Mamede de Carvalho, Dietmar Rudolf Thal, Markus Otto, Thomas Brännström, Alexander E. Volk, Petri Kursula, Karin M. Danzer, Peter Lichtner, Ivan Đikić, Thomas Meitinger, Albert C. Ludolph, Tim M. Strom, Peter M. Andersen, Jochen H. Weishaupt
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
A proposal for new diagnostic criteria for ALS
Jeremy M. Shefner, Ammar Al‐Chalabi, Mark R. Baker, Liying Cui, Mamede de Carvalho, Andrew Eisen, Julian Großkreutz, Orla Hardiman, Robert D. Henderson, José Manuel Matamala, Hiroshi Mitsumoto, Walter J. Paulus, Neil G. Simon, Michael Swash, Kevin Talbot, Martin R. Turner, Yoshikazu Ugawa, Leonard H. van den Berg, Renato J. Verdugo, S. Vucic, Ryuji Kaji, David Burke, Matthew C. Kiernan