Ana Ferreiro

6.8k citations

87 papers · 3.3k · h-index 31

Impact in

Cardiology and Cardiovascular Medicine top 1%
- Cardiomyopathy and Myosin Studies
Genetics top 2%
- Neurogenetic and Muscular Disorders Research

Papers in

Molecular Biology 69
- Muscle Physiology and Disorders 46
- Nuclear Structure and Function 18
- Mitochondrial Function and Pathology 13
- Ion channel regulation and function 13
Cardiology and Cardiovascular Medicine 28
- Cardiomyopathy and Myosin Studies 27

Co-authors: Pascale Guicheney (24 shared papers)Sandrine Arbogast (10 shared papers)Michel Fardeau (14 shared papers)Pascale Richard (14 shared papers)Claire Chauveau (4 shared papers)John Rowell (1 shared paper)Carsten G. Bönnemann (11 shared papers)Heinz Jungbluth (13 shared papers)
Journals: Neuromuscular Disorders (29 papers)Annals of Neurology (7 papers)Human Mutation (4 papers)Neurology (3 papers)Neuropediatrics (2 papers)
Partner nations: France United States United Kingdom

In The Last Decade

Ana Ferreiro

83 papers receiving 3.3k citations

Peers

Countries citing papers authored by Ana Ferreiro

Since Specialization

Citations

This map shows the geographic impact of Ana Ferreiro's research. It shows the number of citations coming from papers published by authors working in each country. You can also color the map by specialization and compare the number of citations received by Ana Ferreiro with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Ana Ferreiro more than expected).

Fields of papers citing papers by Ana Ferreiro

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Ana Ferreiro. Nodes represent research fields, and links connect fields that are likely to share authors. Colored nodes show fields that tend to cite the papers produced by Ana Ferreiro. The network helps show where Ana Ferreiro may publish in the future.

Co-authors

The 25 scholars most cited alongside Ana Ferreiro, linked wherever they have co-authored with each other. Click a name or a connecting line to browse the papers they share.

Border = papers with Ana Ferreiro Line = papers co-authored together Ana Ferreiro links everyone, so they are left out of the graph.

All Works

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20 of 20 papers shown

Showing the 20 most-cited of 87 papers — load more, or switch the sort, to bring in the rest.

#	Work
1	Mutations of the Selenoprotein N Gene, Which Is Implicated in Rigid Spine Muscular Dystrophy, Cause the Classical Phenotype of Multiminicore Disease: Reassessing the Nosology of Early-Onset Myopathies The American Journal of Human Genetics ·Ana Ferreiro, Susana Quijano-Roy, Claire Pichereau, Behzad Moghadaszadeh, Nathalie Goemans, Carsten G. Bönnemann, Heinz Jungbluth, Volker Straub, Marcello Villanova, Jean‐Paul Leroy, Norma B. Romero, Jean‐Jacques Martin, Francesco Muntoni, Thomas Voit, B. Estournet, Pascale Richard, Michel Fardeau, Pascale Guicheney	2002	234
2	Diagnostic approach to the congenital muscular dystrophies Neuromuscular Disorders ·Carsten G. Bönnemann, Ching H. Wang, Susana Quijano‐Roy, Nicolas Deconinck, Enrico Bertini, Ana Ferreiro, Francesco Muntoni, Caroline Sewry, Christophe Béroud, Katherine D. Mathews, Steven A. Moore, Jonathan Bellini, Anne Rutkowski, Kathryn N. North	2014	207
3	A Rising Titan:TTNReview and Mutation Update Human Mutation ·Claire Chauveau, John Rowell, Ana Ferreiro	2014	170
4	C‐terminal titin deletions cause a novel early‐onset myopathy with fatal cardiomyopathy Annals of Neurology ·Virginie Carmignac, Mustafa A. Salih, Susana Quijano‐Roy, Sylvie Marchand, Molham M. Al Rayess, Maowia M. Mukhtar, Jon Andoni Urtizberea, Siegfried Labeit, Pascale Guicheney, France Leturcq, Mathias Gautel, Michel Fardeau, Kevin P. Campbell, Isabelle Richard, B. Estournet, Ana Ferreiro	2007	156
5	Interactions with titin and myomesin target obscurin and obscurin-like 1 to the M-band – implications for hereditary myopathies Journal of Cell Science ·Atsushi Fukuzawa, Stephan Lange, Mark Holt, Anna Vihola, Virginie Carmignac, Ana Ferreiro, Bjarne Udd, Mathias Gautel	2008	152
6	A recessive form of central core disease, transiently presenting as multi‐minicore disease, is associated with a homozygous mutation in the ryanodine receptor type 1 gene Annals of Neurology ·Ana Ferreiro, Nicole Monnier, Norma B. Romero, Jean‐Paul Leroy, Carsten G. Bönnemann, Charles‐Antoine Haenggeli, Volker Straub, W Voss, Y. Nivoche, Heinz Jungbluth, Arnaud Lemainque, Thomas Voit, Joël Lunardi, Michel Fardeau, Pascale Guicheney	2002	137
7	Desmin‐related myopathy with mallory body–like inclusions is caused by mutations of the selenoprotein N gene Annals of Neurology ·Ana Ferreiro, Chantal Ceuterick‐de Groote, Jared J. Marks, Nathalie Goemans, Gudrun Schreiber, F. Hanefeld, Michel Fardeau, Jean‐Jacques Martin, Hans H. Goebel, Pascale Richard, Pascale Guicheney, Carsten G. Bönnemann	2004	134
8	Selenoproteins and Protection against Oxidative Stress: Selenoprotein N as a Novel Player at the Crossroads of Redox Signaling and Calcium Homeostasis Antioxidants and Redox Signaling ·Sandrine Arbogast, Ana Ferreiro	2009	125
9	Mutations in COL6A3 Cause Severe and Mild Phenotypes of Ullrich Congenital Muscular Dystrophy The American Journal of Human Genetics ·Ercan Demir, Patrizia Sabatelli, Valérie Allamand, Ana Ferreiro, Behzad Moghadaszadeh, Mohamed Makrelouf, Haluk Topaloğlu, Bernard Échenne, Luciano Merlini, Pascale Guicheney	2002	119
10	SEPN1: Associated with congenital fiber‐type disproportion and insulin resistance Annals of Neurology ·Nigel F. Clarke, Warren Kidson, Susana Quijano‐Roy, B. Estournet, Ana Ferreiro, Pascale Guicheney, James Manson, Andrew J. Kornberg, Lloyd K. Shield, Kathryn N. North	2006	114
11	Autosomal recessive inheritance of RYR1 mutations in a congenital myopathy with cores Neurology ·Heinz Jungbluth, C. R. Müller, B. Halliger–Keller, Martin Brockington, S. Brown, L. Feng, Arijit Chattopadhyay, Eugenio Mercuri, A. Manzur, Ana Ferreiro, Nigel G. Laing, Mark R. Davis, Helen P. Roper, Victor Dubowitz, Graeme M. Bydder, Caroline A. Sewry, Francesco Muntoni	2002	114
12	Oxidative stress in SEPN1‐related myopathy: From pathophysiology to treatment Annals of Neurology ·Sandrine Arbogast, Maud Beuvin, B. Fraysse, Haïyan Zhou, Francesco Muntoni, Ana Ferreiro	2009	111
13	Minicore myopathy with ophthalmoplegia caused by mutations in the ryanodine receptor type 1 gene Neurology ·Heinz Jungbluth, Haiyan Zhou, Louise Hartley, B. Halliger–Keller, Sonia Messina, Cheryl Longman, Martin Brockington, S. Robb, Volker Straub, Thomas Voit, Michael Swash, Ana Ferreiro, Graeme M. Bydder, Caroline A. Sewry, C. R. Müller, Francesco Muntoni	2005	100
14	Oxidative stress and successful antioxidant treatment in models of RYR1-related myopathy Brain ·James J. Dowling, Sandrine Arbogast, Junguk Hur, Darcee D. Nelson, Anna McEvoy, Trent A. Waugh, Isabelle Marty, Joël Lunardi, Susan V. Brooks, John Y. Kuwada, Ana Ferreiro	2012	95
15	Recessive RYR1 mutations cause unusual congenital myopathy with prominent nuclear internalization and large areas of myofibrillar disorganization Neuropathology and Applied Neurobiology ·Jorge A. Bevilacqua, Nicole Monnier, Marc Bitoun, B. Eymard, Ana Ferreiro, Soledad Monges, F. Lubieniecki, Analía Taratuto, A. Laquérrière, Kristl G. Claeys, Isabelle Marty, Michel Fardeau, Pascale Guicheney, Joël Lunardi, Norma B. Romero	2010	75
16	Null mutations causing depletion of the type 1 ryanodine receptor (RYR1) are commonly associated with recessive structural congenital myopathies with cores Human Mutation ·Nicole Monnier, Isabelle Marty, Julien Fauré, Claudia Castiglioni, Claude Desnuelle, Sabrina Sacconi, B. Estournet, Ana Ferreiro, Norma B. Romero, Annie Laquerrière, Leïla Lazaro, Jean‐Jacques Martin, Éva Morava, Annick Rossi, Anneke J. van der Kooi, Marianne de Visser, Corien Verschuuren, Joël Lunardi	2008	75
17	Multi-minicore disease-searching for boundaries: Phenotype analysis of 38 cases Annals of Neurology ·Ana Ferreiro, B. Estournet, Danielle Château, Norma B. Romero, C Laroche, Sylvie Odent, Annick Toutain, Ana Cabello, D Fontan, Helo�sa G. Dos Santos, Charles-Antoine Haenggeli, Enrico Bertini, Jon-Andoni Urtizberea, Pascale Guicheney, Michel Fardeau	2000	75
18	A single homozygous point mutation in a 3′untranslated region motif of selenoprotein N mRNA causes SEPN1‐related myopathy EMBO Reports ·Valérie Allamand, Pascale Richard, Alain Lescure, C. Ledeuil, Delphine Desjardin, Nathalie Petit, Corine Gartioux, Ana Ferreiro, Alain Krol, N. Pellegrini, Jon Andoni Urtizberea, Pascale Guicheney	2006	68
19	Increased Muscle Stress-Sensitivity Induced by Selenoprotein N Inactivation in Mouse: A Mammalian Model for SEPN1-Related Myopathy PLoS ONE ·Mathieu Rederstorff, Perrine Castets, Sandrine Arbogast, Jeanne Lainé, Stéphane Vassilopoulos, Maud Beuvin, O. Dubourg, Alban Vignaud, Arnaud Ferry, Alain Krol, Valérie Allamand, Pascale Guicheney, Ana Ferreiro, Alain Lescure	2011	53
20	A mutation in theSEPN1selenocysteine redefinition element (SRE) reduces selenocysteine incorporation and leads toSEPN1-related myopathy Human Mutation ·Baijayanta Maiti, Sandrine Arbogast, Val��rie Allamand, Mark W. Moyle, Christine B. Anderson, Pascale Richard, Pascale Guicheney, Ana Ferreiro, Kevin M. Flanigan, Michael Howard	2008	50

About Ana Ferreiro

Ana Ferreiro is a scholar working on Molecular Biology, Cardiology and Cardiovascular Medicine, Cell Biology, Nutrition and Dietetics and Genetics, having authored 87 papers that have together received 3.3k indexed citations. Recurring topics across this work include Muscle Physiology and Disorders (46 papers), Cardiomyopathy and Myosin Studies (27 papers), Nuclear Structure and Function (18 papers), Mitochondrial Function and Pathology (13 papers), Ion channel regulation and function (13 papers), Selenium in Biological Systems (11 papers), Genetic Neurodegenerative Diseases (10 papers) and Neurogenetic and Muscular Disorders Research (10 papers). The work is most often cited by research in Cardiology and Cardiovascular Medicine (1.3k citations), Genetics (578 citations), Molecular Biology (2.5k citations), Nutrition and Dietetics (506 citations) and Cell Biology (492 citations). Ana Ferreiro has collaborated with scholars based in France, United States and United Kingdom. Frequent co-authors include Pascale Guicheney, Sandrine Arbogast, Michel Fardeau, Pascale Richard, Claire Chauveau, John Rowell, Carsten G. Bönnemann, Heinz Jungbluth, B. Estournet and Norma B. Romero. Their work appears in journals such as Neuromuscular Disorders, Annals of Neurology, Human Mutation, Neurology and Neuropediatrics.

Rankless uses publication and citation data sourced from OpenAlex, an open and comprehensive bibliographic database. While OpenAlex provides broad and valuable coverage of the global research landscape, it—like all bibliographic datasets—has inherent limitations. These include incomplete records, variations in author disambiguation, differences in journal indexing, and delays in data updates. As a result, some metrics and network relationships displayed in Rankless may not fully capture the entirety of a scholar's output or impact.

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