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Francesco Muntoni

ResearcherPublications, citations & collaboration network

Francesco Muntoni is a researcher indexed in ScholarIQ from OpenAlex & ORCID.

How many works does Francesco Muntoni have?

ScholarIQindexed works

Francesco Muntoni has 294 works in the ScholarIQ index. The count is the OpenAlex total, not the number of papers listed on this page.

How many citations does Francesco Muntoni have?

ScholarIQcitation count

Francesco Muntoni has 19,392 citations in the OpenAlex counts ScholarIQ stores.

What is the h-index of Francesco Muntoni?

ScholarIQh-index

Francesco Muntoni has an h-index of 76 in OpenAlex.

What is the i10-index of Francesco Muntoni?

ScholarIQi10-index

Francesco Muntoni has an i10-index of 180 in OpenAlex.

What is the OpenAlex record for Francesco Muntoni?

ScholarIQopenalex

The OpenAlex for Francesco Muntoni is on the source record.

What are the most-cited papers on Francesco Muntoni?

ScholarIQmost cited works
Diagnosis and management of spinal muscular atrophy: Part 2: Pulmonary and acute care; medications, supplements and immunizations; other organ systems; and ethics
Richard S. Finkel, Eugenio Mercuri, Oscar H. Meyer, Anita K. Simonds, Mary Schroth, Robert J. Graham, Janbernd Kirschner, Susan T. Iannaccone, Thomas O. Crawford, Simon Woods, Francesco Muntoni, Brunhilde Wirth, Jacqueline Montes, Marion Main, Elena Mazzone, Michael G. Vitale, Brian D. Snyder, Susana Quijano‐Roy, Enrico Bertini, Rebecca Hurst Davis, Ying Qian, Thomas Sejersen
Neuromuscular Disorders. 2017681 CitationsOPEN ACCESS
Ataluren in patients with nonsense mutation Duchenne muscular dystrophy (ACT DMD): a multicentre, randomised, double-blind, placebo-controlled, phase 3 trial
Craig M. McDonald, Craig Campbell, Ricardo Erazo Torricelli, Richard S. Finkel, Kevin M. Flanigan, Nathalie Goemans, Peter Heydemann, Anna Kamińska, Janbernd Kirschner, Francesco Muntoni, A. Nascimento Osorio, Ulrike Schara, Thomas Sejersen, Perry B. Shieh, H. Lee Sweeney, Haluk Topaloğlu, M. Tulinius, Juan J. Vílchez, Thomas Voït, Brenda Wong, Gary Elfring, Hans Kröger, Xiaohui Luo, Joseph McIntosh, Tuyen Ong, Peter Riebling, Marcio Ferreira de Souza, Robert J. Spiegel, Stuart W. Peltz, Eugenio Mercuri, Lindsay N. Alfano, Michelle Eagle, M. James, Linda Lowes, Anna Mayhew, Elena Mazzone, Leslie Nelson, Kristy Rose, Hoda Abdel‐Hamid, Susan Apkon, Richard J. Barohn, Enrico Bertini, Clemens Bloetzer, Lausanne Canton de Vaud, Russell J. Butterfield, B. Chabrol, Jong‐Hee Chae, Daehak-ro Jongno-gu, Giacomi Pietro Comi, Basil T. Darras, Jahannaz Dastgir, Isabelle Desguerre, Raúl G. Escobar, Erika Finanger, Michela Guglieri, Imelda Hughes, Susan T. Iannaccone, Kristi Jones, Peter Karachunski, Martin Kudr, Timothy Lotze, Jean K. Mah, Katherine D. Mathews, Yoram Nevo, Julie Parsons, Yann Péréon, Alexandra Prufer de Queiroz Campos Araújo, J. Ben Renfroe, Maria Bernadete Dutra de Resende, Monique M. Ryan, Kathryn Selby, Gihan Tennekoon, Giuseppe Vita
The Lancet. 2017459 CitationsOPEN ACCESS
Consensus Statement on Standard of Care for Congenital Muscular Dystrophies
Ching H. Wang, Carsten G. Bönnemann, A. Rutkowski, Thomas Sejersen, Jonathan Bellini, Vanessa Battista, Julaine Florence, Ulrike Schara, Pamela M. Schuler, Karim Wahbi, A. Aloysius, Robert O. Bash, Christophe Béroud, Enrico Bertini, Kate Bushby, Ronald D. Cohn, Anne M. Connolly, Nicolas Deconinck, Isabelle Desguerre, Michelle Eagle, Brigitte Estournet-Mathiaud, Ana Ferreiro, Albert Fujak, Nathalie Goemans, Susan T. Iannaccone, Patricia Jouinot, Marion Main, Paola Melacini, Wolfgang Mueller‐Felber, Francesco Muntoni, Leslie Nelson, Jes Rahbek, Susana Quijano-Roy, Caroline A. Sewry, Kari Storhaug, Anita K. Simonds, Brian S. Tseng, Jiri Vajsar, Andrea Vianello, Reinhard Zeller
Journal of Child Neurology. 2010217 CitationsOPEN ACCESS
Biallelic mutations in SORD cause a common and potentially treatable hereditary neuropathy with implications for diabetes
Andrea Cortese, Yi Zhu, Adriana Rebelo, Sara Negri, Steve Courel, Lisa Abreu, Chelsea J. Bacon, Yunhong Bai, Dana M. Bis‐Brewer, Enrico Bugiardini, Elena Buglo, Matt C. Danzi, Shawna Feely, Alkyoni Athanasiou‐Fragkouli, Nourelhoda A. Haridy, Aixa Rodríguez, Alexa Bacha, Ashley Kosikowski, Beth Wood, Brett A. McCray, Brianna Blume, Carly E. Siskind, Charlotte J. Sumner, Daniela Calabrese, David Walk, Dragan Vujović, Eun Hye Park, Francesco Muntoni, Gabrielle Donlevy, Gyula Acsádi, John Day, Joshua Burns, Jun Li, Karen Krajewski, Kate Eichinger, Kayla Cornett, Krista Mullen, Perez Quiros Laura, Laurie Gutmann, Maria Barrett, Mario Saporta, Mariola Skorupinska, Natalie Grant, Paula Bray, Reza Sadjadi, Riccardo Zuccarino, Richard S. Finkel, Richard A. Lewis, Rosemary Shy, Sabrina W. Yum, Sarah Hilbert, Simone Thomas, Steffen Behrens‐Spraggins, Tara Jones, Thomas E. Lloyd, Tiffany Grider, Tim Estilow, Vera Fridman, Rosario Isasi, Alaa Khan, Matilde Laurá, Stefania Magri, Menelaos Pipis, Chiara Pisciotta, Eric Powell, Alexander M. Rossor, Paola Saveri, Janet E. Sowden, Stefano Tozza, Jana Vandrovcová, Julia E. Dallman, Elena Grignani, Enrico Marchioni, Steven S. Scherer, Beisha Tang, Zhiqiang Lin, Abdullah Al‐Ajmi, Rebecca Schüle, Matthis Synofzik, Thierry Maisonobe, Tanya Stojkovic, Michaela Auer‐Grumbach, Mohamed A. Abdelhamed, Sherifa A. Hamed, Ruxu Zhang, Fiore Manganelli, Lucio Santoro, Franco Taroni, Davide Pareyson, Henry Houlden, David N. Herrmann, Mary M. Reilly, Michael E. Shy, R. Grace Zhai, Stephan Züchner
Nature Genetics. 2020177 CitationsOPEN ACCESS

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