ScholarIQanswers from OpenAlex & ORCID
G. Meco
ResearcherPublications, citations & collaboration network
G. Meco is a researcher indexed in ScholarIQ from OpenAlex & ORCID.
How many works does G. Meco have?
ScholarIQindexed works
G. Meco has 218 works in the ScholarIQ index. The count is the OpenAlex total, not the number of papers listed on this page.
How many citations does G. Meco have?
ScholarIQcitation count
G. Meco has 16,448 citations in the OpenAlex counts ScholarIQ stores.
What is the h-index of G. Meco?
ScholarIQh-index
G. Meco has an h-index of 60 in OpenAlex.
What is the i10-index of G. Meco?
ScholarIQi10-index
G. Meco has an i10-index of 125 in OpenAlex.
What is the OpenAlex record for G. Meco?
ScholarIQopenalex
The OpenAlex for G. Meco is on the source record.
What are the most-cited papers on G. Meco?
ScholarIQmost cited works
Mutations in the <i>DJ-1</i> Gene Associated with Autosomal Recessive Early-Onset Parkinsonism
Vincenzo Bonifati, Patrizia Rizzu, Marijke J. van Baren, Onno Schaap, Guido J. Breedveld, Elmar Krieger, Marieke Dekker, Ferdinando Squitieri, Pablo Ibáñez, Marijke Joosse, Jeroen W. van Dongen, Nicola Vanacore, John C. van Swieten, Alexis Brice, G. Meco, Cornelia M. van Duijn, Ben A. Oostra, Peter Heutink
The PRIAMO study: A multicenter assessment of nonmotor symptoms and their impact on quality of life in Parkinson's disease
Paolo Barone, Angelo Antonini, Carlo Colosimo, Roberto Marconi, Letterio Morgante, Tania P. Avarello, Eugenio Bottacchi, Antonino Cannas, Maria Gabriella Ceravolo, Roberto Ceravolo, Giulio Cicarelli, Roberto M. Gaglio, Rosa M. Giglia, Francesco Iemolo, M. Manfredi, G. Meco, Alessandra Nicoletti, Massimo Pederzoli, Alfredo Petrone, Antonio Pisani, Francesco E. Pontieri, R. Quatrale, Silvia Ramat, Rosanna Scala, Giuseppe Volpe, Salvatore Zappulla, Anna Rita Bentivoglio, Fabrizio Stocchi, Giorgio Trianni, Paolo Del Dotto
The natural history of multiple system atrophy: a prospective European cohort study
Gregor K. Wenning, Felix Geser, Florian Krismer, Klaus Seppi, Susanne Duerr, Sylvia Boesch, Martin Köllensperger, Georg Goebel, Karl Pfeiffer, Paolo Barone, Maria Teresa Pellecchia, Niall Quinn, Vasiliki Koukouni, Clare J. Fowler, Anette Schrag, Christopher J. Mathias, Nir Giladi, Tanya Gurevich, E. Dupont, Karen Østergaard, Christer Nilsson, Håkan Widner, Wolfgang H. Oertel, Karla Eggert, Alberto Albanese, Francesca Del Sorbo, Eduardo Tolosa, Adriana Cardozo, Günther Deuschl, Helge Hellriegel, Thomas Klockgether, Richard Dodel, Cristina Sampaio, Miguel Coelho, Ruth Djaldetti, Eldad Melamed, Thomas Gasser, Christoph Kamm, G. Meco, Carlo Colosimo, Olivier Rascol, Wassilios G. Meissner, François Tison, Werner Poewe
<i>ATP13A2</i> missense mutations in juvenile parkinsonism and young onset Parkinson disease
Alessio Di Fonzo, Hsin Fen Chien, Mariana P. Socal, Sabrina Giraudo, C. Tassorelli, Gianni Iliceto, Giovanni Fabbrini, R. Marconi, E. Fincati, Giovanni Abbruzzese, P. Marini, Ferdinando Squitieri, M.W.I.M. Horstink, P. Montagna, A. Dalla Libera, Fabrizio Stocchi, Stefano Goldwurm, Joaquim J. Ferreira, G. Meco, E. Martignoni, Leonardo Lopiano, Laura Bannach Jardim, Ben A. Oostra, Egberto Reis Barbosa, The Italian Parkinson Genetics Network, V. Bonifati
Early-onset parkinsonism associated with <i>PINK1</i> mutations
Vincenzo Bonifati, Christan F. Rohé, Guido J. Breedveld, E. Fabrizio, Michele De Mari, C. Tassorelli, A. Tavella, R. Marconi, David Nicholl, Hsin Fen Chien, E. Fincati, Giovanni Abbruzzese, P. Marini, Antonio De Gaetano, M.W.I.M. Horstink, J A Maat-Kievit, Cristina Sampaio, Angelo Antonini, Fabrizio Stocchi, P. Montagna, V. Toni, Marco Guidi, A. Dalla Libera, Michèle Tinazzi, Francesca De Pandis, Giovanni Fabbrini, Stefano Goldwurm, Annelies de Klein, Egberto Reis Barbosa, Leonardo Lopiano, E. Martignoni, P. Lamberti, N. Vanacore, G. Meco, Ben A. Oostra, The Italian Parkinson Genetics Network