Norma B. Romero

14.3k citations

193 papers · 7.6k indexed · h-index 46

Genetics top 0.5%
- Neurogenetic and Muscular Disorders Research 32
Clinical Biochemistry top 0.5%
- Metabolism and Genetic Disorders 21
Cell Biology top 0.5%
- Cellular transport and secretion 33
Cardiology and Cardiovascular Medicine top 0.5%
- Cardiomyopathy and Myosin Studies 62
Molecular Biology top 0.5%
- Muscle Physiology and Disorders 88
- Mitochondrial Function and Pathology 31
- Nuclear Structure and Function 23
Cellular and Molecular Neuroscience
- Genetic Neurodegenerative Diseases 30

Co-authors: Michel Fardeau Pascale Guicheney B. Eymard B. Estournet Jocelyn Laporte Thomas Voit Pascal Laforêt France Leturcq
Cited by: Genetics Clinical Biochemistry Cell Biology
Journals: Cell (1 paper)Journal of Clinical Investigation (3 papers)Nature Genetics (2 papers)
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

The 25 scholars most cited alongside Norma B. Romero, 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 Norma B. Romero Line = papers co-authored together Norma B. Romero links everyone, so they are left out of the graph.

All Works

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20 of 20 papers shown

#	Work
1	Severe Respiratory and Swallowing Disorders in Infantile-Onset Multisystem Neurologic, Endocrine, and Pancreatic Disease Type 1 Neurology Genetics ·Édouard Berling,Philippe Latour,Klervie Loiselet,Clément Guémy,Léo Vidoni,Norma B. Romero,Emmanuelle Lacène,Teresinha Evangelista,Tanya Stojkovic	2024	0
2	Functional benefit of CRISPR-Cas9-induced allele deletion for RYR1 dominant mutation Molecular Therapy — Nucleic Acids ·Mathilde Beaufils,Margaux Melka,Julie Brocard,Benoît Clément,Nagi Debbah,Kamel Mamchaoui,Norma B. Romero,Anne Frédérique Dalmas-Laurent,Susana Quijano‐Roy,Julien Fauré,John Rendu,Isabelle Marty	2024	1
3	Clinical and functional characterization of a long survivor congenital titinopathy patient with a novel metatranscript-only titin variant Acta Neuropathologica Communications ·Nastasia Cardone,Melissa Moula,R. Baelde,Ariane Biquand,Marcello Villanova,Corinne Métay,Chiara Fiorillo,Serena Baratto,Luciano Merlini,Patrizia Sabatelli,Norma B. Romero,Frédéric Relaix,François‐Jérôme Authier,Valentina Taglietti,Marco Savarese,Josine de Winter,Coen A. C. Ottenheijm,Isabelle Richard,Edoardo Malfatti	2023	3
4	Caveolae and Bin1 form ring-shaped platforms for T-tubule initiation eLife ·Eline Lemerle,Jeanne Lainé,Marion Benoist,Gilles Moulay,Anne Bigot,C. Labasse,A. Madelaine,Alexis Canette,Perrine Aubin,Jean‐Michel Vallat,Norma B. Romero,Marc Bitoun,Vincent Mouly,Isabelle Marty,Bruno Cadot,Laura Picas,Stéphane Vassilopoulos	2023	13
5	Caveolinopathy: Clinical, histological, and muscle imaging features and follow‐up in a multicenter retrospective cohort European Journal of Neurology ·Édouard Berling,Camille Verebi,Nadia Venturelli,Stéphane Vassilopoulos,Anthony Béhin,Céline Tard,Maud Michaud,Rocío N. Villar‐Quiles,Savine Vicart,Marion Masingue,Robert‐Yves Carlier,Norma B. Romero,Emmanuelle Lacène,France Leturcq,B. Eymard,Pascal Laforêt,Tanya Stojkovic	2023	4
6	Benefits of therapy by dynamin-2-mutant-specific silencing are maintained with time in a mouse model of dominant centronuclear myopathy Molecular Therapy — Nucleic Acids ·Delphine Trochet,Bernard Prudhon,Lylia Mekzine,Mégane Lemaître,Maud Beuvin,Laura Julien,Sofia Benkhelifa‐Ziyyat,Mai Thao Bui,Norma B. Romero,Marc Bitoun	2022	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 Stem Cell Research ·Joshua S. Clayton,Carolin K. Scriba,Norma B. Romero,Edoardo Malfatti,Safaa Saker,Thierry Larmonier,Kristen L. Nowak,Gianina Ravenscroft,Nigel G. Laing,Rhonda L. Taylor	2021	6
8	In vivo RyR1 reduction in muscle triggers a core-like myopathy Acta Neuropathologica Communications ·Laurent Pelletier,Anne Petiot,Julie Brocard,Benoı̂t Giannesini,Diane Giovannini,Colline Sanchez,Lauriane Travard,Mathilde Chivet,Mathilde Beaufils,Candice Kutchukian,David Bendahan,Daniel Metzger,Clara Franzini Armstrong,Norma B. Romero,John Rendu,Vincent Jacquemond,Julien Fauré,Isabelle Marty	2020	15
9	A new congenital multicore titinopathy associated with fast myosin heavy chain deficiency 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	2020	9
10	Lamin-Related Congenital Muscular Dystrophy Alters Mechanical Signaling and Skeletal Muscle Growth International Journal of Molecular Sciences ·Daniel J. Owens,Julien Messéant,Sophie Moog,Mark Viggars,Arnaud Ferry,Kamel Mamchaoui,Emmanuelle Lacène,Norma B. Romero,Astrid Brull,Gisèle Bonne,Gillian Butler‐Browne,Catherine Coirault	2020	21
11	Physiological impact and disease reversion for the severe form of centronuclear myopathy linked to dynamin JCI Insight ·Xènia Massana-Muñoz,Christine Kretz,Roberto Silva‐Rojas,Julien Ochala,Alexia Menuet,Norma B. Romero,Belinda S. Cowling,Jocelyn Laporte	2020	21
12	Dynamin-2 mutations linked to Centronuclear Myopathy impair actin-dependent trafficking in muscle cells Scientific Reports ·Arlek M. González‐Jamett,Ximena Báez‐Matus,María José Olivares,Fernando Hinostroza,María José Guerra Palmero,Jacqueline Vásquez-Navarrete,Mai Thao Bui,Pascale Guicheney,Norma B. Romero,Jorge A. Bevilacqua,Marc Bitoun,Pablo Caviedes,Ana M. Cárdenas	2017	28
13	An Integrated Diagnosis Strategy for Congenital Myopathies 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	2013	43
14	Expression of myogenic regulatory factors and myo-endothelial remodeling in sporadic inclusion body myositis 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	2012	31
15	Congenital myopathy-causing tropomyosin mutations induce thin filament dysfunction via distinct physiological mechanisms Human Molecular Genetics ·Julien Ochala,David S. Gokhin,I. Pénisson-Besnier,Susana Quijano-Roy,Nicolas Monnier,Joël Lunardi,Norma B. Romero,Velia M. Fowler	2012	36
16	Novel molecular diagnostic approaches for X-linked centronuclear (myotubular) myopathy reveal intronic mutations Neuromuscular Disorders ·Valérie Tosch,Nasim Vasli,Christine Kretz,Anne-Sophie Nicot,Claire Gasnier,Nicolas Dondaine,Denis Oriot,Magalie Barth,Hugues Puissant,Norma B. Romero,Carsten G. Bönnemann,Betty Heller,Gilles Duval,Valérie Biancalana,Jocelyn Laporte	2010	26
17	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
18	Dynamin 2 mutations associated with human diseases impair clathrin-mediated receptor endocytosis 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	2009	67
19	Apoptosis in mitochondrial myopathies is linked to mitochondrial proliferation Brain ·Karine Auré,G. Fayet,Jean Paul Leroy,Emmanuelle Lacène,Norma B. Romero,Anne Lombès	2006	62
20	Deficiency of dystrophin-associated proteins in Duchenne muscular dystrophy patients lacking COOH-terminal domains of dystrophin. 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	1993	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), Cellular transport and secretion (33 papers), Neurogenetic and Muscular Disorders Research (32 papers), Mitochondrial Function and Pathology (31 papers), Genetic Neurodegenerative Diseases (30 papers), Nuclear Structure and Function (23 papers) and Metabolism and Genetic Disorders (21 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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