Norma B. Romero

14.3k citations

193 papers · 7.6k indexed · h-index 46

Molecular Biology top 0.5%
Cardiology and Cardiovascular Medicine top 0.5%
Cell Biology top 0.5%
Cellular and Molecular Neuroscience top 1%
Genetics top 0.5%

Co-authors: Michel Fardeau Pascale Guicheney B. Eymard B. Estournet Jocelyn Laporte Thomas Voit Pascal Laforêt France Leturcq
Topics: Muscle Physiology and Disorders (88 papers)Cardiomyopathy and Myosin Studies (62 papers)Cellular transport and secretion (33 papers)
Cited by: Genetics Clinical Biochemistry Cell Biology
Journals: Cell Journal of Clinical Investigation Nature Genetics
Partner nations: France United States Italy

In The Last Decade

Norma B. Romero

185 papers receiving 7.4k citations

Peers

Countries citing papers authored by Norma B. Romero

Since Specialization

Citations

This map shows the geographic impact of Norma B. Romero'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 Norma B. Romero with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Norma B. Romero more than expected).

Fields of papers citing papers by Norma B. Romero

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Norma B. Romero. 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 Norma B. Romero. The network helps show where Norma B. Romero may publish in the future.

Co-authorship network of co-authors of Norma B. Romero

This figure shows the co-authorship network connecting the top 25 collaborators of Norma B. Romero. A scholar is included among the top collaborators of Norma B. Romero based on the total number of citations received by their joint publications. Widths of edges represent the number of papers authors have co-authored together. Node borders signify the number of papers an author published with Norma B. Romero. Norma B. Romero is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

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20 of 20 papers shown

#	Work	Indexed citations
1	Severe Respiratory and Swallowing Disorders in Infantile-Onset Multisystem Neurologic, Endocrine, and Pancreatic Disease Type 1 2024 ·Neurology Genetics ·(unknown),Philippe Latour,(unknown),(unknown),(unknown),Norma B. Romero,Emmanuelle Lacène,Teresinha Evangelista,Tanya Stojkovic	0
2	Functional benefit of CRISPR-Cas9-induced allele deletion for RYR1 dominant mutation 2024 ·Molecular Therapy — Nucleic Acids ·(unknown),(unknown),Julie Brocard,(unknown),(unknown),Kamel Mamchaoui,Norma B. Romero,(unknown),Susana Quijano‐Roy,Julien Fauré,John Rendu,Isabelle Marty	1
3	Clinical and functional characterization of a long survivor congenital titinopathy patient with a novel metatranscript-only titin variant 2023 ·Acta Neuropathologica Communications ·(unknown),(unknown),(unknown),(unknown),Marcello Villanova,Corinne Métay,Chiara Fiorillo,(unknown),Luciano Merlini,Patrizia Sabatelli,Norma B. Romero,Frédéric Relaix,François‐Jérôme Authier,Valentina Taglietti,Marco Savarese,(unknown),Coen A. C. Ottenheijm,Isabelle Richard,Edoardo Malfatti	3
4	Caveolae and Bin1 form ring-shaped platforms for T-tubule initiation 2023 ·eLife ·(unknown),Jeanne Lainé,Marion Benoist,Gilles Moulay,Anne Bigot,C. Labasse,(unknown),Alexis Canette,(unknown),Jean‐Michel Vallat,Norma B. Romero,Marc Bitoun,Vincent Mouly,Isabelle Marty,Bruno Cadot,Laura Picas,Stéphane Vassilopoulos	13
5	Caveolinopathy: Clinical, histological, and muscle imaging features and follow‐up in a multicenter retrospective cohort 2023 ·European Journal of Neurology ·(unknown),(unknown),(unknown),Stéphane Vassilopoulos,Anthony Béhin,Céline Tard,Maud Michaud,(unknown),Savine Vicart,Marion Masingue,Robert‐Yves Carlier,Norma B. Romero,Emmanuelle Lacène,France Leturcq,B. Eymard,Pascal Laforêt,Tanya Stojkovic	4
6	Benefits of therapy by dynamin-2-mutant-specific silencing are maintained with time in a mouse model of dominant centronuclear myopathy 2022 ·Molecular Therapy — Nucleic Acids ·Delphine Trochet,Bernard Prudhon,(unknown),(unknown),Maud Beuvin,Laura Julien,Sofia Benkhelifa‐Ziyyat,Mai Thao Bui,Norma B. Romero,Marc Bitoun	2
7	Generation of two isogenic induced pluripotent stem cell lines from a 4-month-old severe nemaline myopathy patient with a heterozygous dominant c.553C > A (p.Arg183Ser) variant in the ACTA1 gene 2021 ·Stem Cell Research ·Joshua S. Clayton,Carolin K. Scriba,Norma B. Romero,Edoardo Malfatti,(unknown),(unknown),Kristen L. Nowak,Gianina Ravenscroft,Nigel G. Laing,Rhonda L. Taylor	6
8	In vivo RyR1 reduction in muscle triggers a core-like myopathy 2020 ·Acta Neuropathologica Communications ·Laurent Pelletier,Anne Petiot,Julie Brocard,Benoı̂t Giannesini,(unknown),(unknown),(unknown),Mathilde Chivet,(unknown),(unknown),David Bendahan,Daniel Metzger,(unknown),Norma B. Romero,John Rendu,Vincent Jacquemond,Julien Fauré,Isabelle Marty	15
9	A new congenital multicore titinopathy associated with fast myosin heavy chain deficiency 2020 ·Annals of Clinical and Translational Neurology ·Aurélien Perrin,Corinne Métay,Marcello Villanova,Robert‐Yves Carlier,Elena Pegoraro,Raúl Juntas‐Morales,Tanya Stojkovic,Isabelle Richard,Pascale Richard,Norma B. Romero,Henk Granzier,M. Kœnig,Edoardo Malfatti,Mireille Cossée	9
10	Lamin-Related Congenital Muscular Dystrophy Alters Mechanical Signaling and Skeletal Muscle Growth 2020 ·International Journal of Molecular Sciences ·Daniel J. Owens,(unknown),Sophie Moog,(unknown),Arnaud Ferry,Kamel Mamchaoui,Emmanuelle Lacène,Norma B. Romero,Astrid Brull,Gisèle Bonne,Gillian Butler‐Browne,Catherine Coirault	21
11	Physiological impact and disease reversion for the severe form of centronuclear myopathy linked to dynamin 2020 ·JCI Insight ·(unknown),Christine Kretz,(unknown),Julien Ochala,(unknown),Norma B. Romero,Belinda S. Cowling,Jocelyn Laporte	21
12	Dynamin-2 mutations linked to Centronuclear Myopathy impair actin-dependent trafficking in muscle cells 2017 ·Scientific Reports ·Arlek M. González‐Jamett,(unknown),(unknown),(unknown),María José Guerra Palmero,(unknown),Mai Thao Bui,Pascale Guicheney,Norma B. Romero,Jorge A. Bevilacqua,Marc Bitoun,Pablo Caviedes,Ana M. Cárdenas	28
13	An Integrated Diagnosis Strategy for Congenital Myopathies 2013 ·PLoS ONE ·Johann Böhm,Nasim Vasli,Edoardo Malfatti,Stéphanie Le Gras,Claire Feger,Bernard Jost,Nicole Monnier,Julie Brocard,Hatice Karasoy,Marion Gérard,Maggie C. Walter,Peter Reilich,Valérie Biancalana,Christine Kretz,Nadia Messaddeq,Isabelle Marty,Joël Lunardi,Norma B. Romero,Jocelyn Laporte	43
14	Expression of myogenic regulatory factors and myo-endothelial remodeling in sporadic inclusion body myositis 2012 ·Neuromuscular Disorders ·Julia Wanschitz,O. Dubourg,Emmanuelle Lacène,Michael B. Fischer,Romana Höftberger,Herbert Budka,Norma B. Romero,B. Eymard,S. Herson,Gillian Butler‐Browne,Thomas Voït,Olivier Benvéniste	31
15	Congenital myopathy-causing tropomyosin mutations induce thin filament dysfunction via distinct physiological mechanisms 2012 ·Human Molecular Genetics ·Julien Ochala,David S. Gokhin,I. Pénisson-Besnier,Susana Quijano-Roy,(unknown),Joël Lunardi,Norma B. Romero,Velia M. Fowler	36
16	Novel molecular diagnostic approaches for X-linked centronuclear (myotubular) myopathy reveal intronic mutations 2010 ·Neuromuscular Disorders ·Valérie Tosch,Nasim Vasli,Christine Kretz,Anne-Sophie Nicot,(unknown),Nicolas Dondaine,Denis Oriot,Magalie Barth,(unknown),Norma B. Romero,Carsten G. Bönnemann,(unknown),(unknown),Valérie Biancalana,Jocelyn Laporte	26
17	Recessive RYR1 mutations cause unusual congenital myopathy with prominent nuclear internalization and large areas of myofibrillar disorganization 2010 ·Neuropathology and Applied Neurobiology ·Jorge A. Bevilacqua,Nicole Monnier,Marc Bitoun,B. Eymard,Ana Ferreiro,Soledad Monges,(unknown),(unknown),A. Laquérrière,Kristl G. Claeys,Isabelle Marty,Michel Fardeau,Pascale Guicheney,Joël Lunardi,Norma B. Romero	75
18	Dynamin 2 mutations associated with human diseases impair clathrin-mediated receptor endocytosis 2009 ·Human Mutation ·Marc Bitoun,Anne‐Cécile Durieux,Bernard Prudhon,Jorge A. Bevilacqua,Adrien Herlédan,Vehary Sakanyan,Andoni Urtizberea,Luis Cartier,Norma B. Romero,Pascale Guicheney	67
19	Apoptosis in mitochondrial myopathies is linked to mitochondrial proliferation 2006 ·Brain ·Karine Auré,G. Fayet,(unknown),Emmanuelle Lacène,Norma B. Romero,Anne Lombès	62
20	Deficiency of dystrophin-associated proteins in Duchenne muscular dystrophy patients lacking COOH-terminal domains of dystrophin. 1993 ·Journal of Clinical Investigation ·Kiichiro Matsumura,F.M.S. Tomé,Victor Ionâşescu,James M. Ervasti,Richard D. Anderson,Norma B. Romero,Dávid Simon,Dominique Récan,J.‐C. Kaplan,Michel Fardeau	60

About Norma B. Romero

Norma B. Romero is a scholar working on Cell Biology, Genetics and Clinical Biochemistry, having authored 193 papers that have together received 7.6k indexed citations. Recurring topics across this work include Muscle Physiology and Disorders (88 papers), Cardiomyopathy and Myosin Studies (62 papers) and Cellular transport and secretion (33 papers). The work is most often cited by research in Genetics (1.2k citations), Clinical Biochemistry (706 citations) and Cell Biology (1.7k citations). Norma B. Romero has collaborated with scholars based in France, United States and Italy. Frequent co-authors include Michel Fardeau, Pascale Guicheney, B. Eymard, B. Estournet, Jocelyn Laporte, Thomas Voit, Pascal Laforêt, France Leturcq, Martin Brockington and Marc Bitoun. Their work appears in journals such as Cell, Journal of Clinical Investigation and Nature Genetics.

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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