Sylvie Bannwarth

3.9k citations

62 papers · 2.1k · h-index 27

Impact in

Virology top 2%
- HIV Research and Treatment
Clinical Biochemistry top 1%
- Metabolism and Genetic Disorders

Papers in

Molecular Biology 55
- Mitochondrial Function and Pathology 36
- ATP Synthase and ATPases Research 11
- RNA and protein synthesis mechanisms 7
- RNA regulation and disease 7
- RNA Research and Splicing 6
- RNA modifications and cancer 6
Clinical Biochemistry 15
- Metabolism and Genetic Disorders 15

Co-authors: Anne Gatignol (11 shared papers)Véronique Paquis‐Flucklinger (42 shared papers)Annabelle Chaussenot (22 shared papers)Cécile Rouzier (23 shared papers)Vincent Procaccio (12 shared papers)Konstantina Fragaki (26 shared papers)B. Chabrol (13 shared papers)Damian F. J. Purcell (5 shared papers)
Journals: Mitochondrion (5 papers)Brain (4 papers)Journal of Biological Chemistry (4 papers)Human Mutation (3 papers)Clinical Genetics (2 papers)
Partner nations: France United States Canada

In The Last Decade

Sylvie Bannwarth

61 papers receiving 2.0k citations

Peers

Countries citing papers authored by Sylvie Bannwarth

Since Specialization

Citations

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

Fields of papers citing papers by Sylvie Bannwarth

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Sylvie Bannwarth. 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 Sylvie Bannwarth. The network helps show where Sylvie Bannwarth may publish in the future.

Co-authors

The 25 scholars most cited alongside Sylvie Bannwarth, 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 Sylvie Bannwarth Line = papers co-authored together Sylvie Bannwarth 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 62 papers — load more, or switch the sort, to bring in the rest.

#	Work
1	The MFN2 gene is responsible for mitochondrial DNA instability and optic atrophy 'plus' phenotype Brain ·Cécile Rouzier, Sylvie Bannwarth, Annabelle Chaussenot, Arnaud Chevrollier, Annie Verschueren, Nathalie Bonello‐Palot, Konstantina Fragaki, A. Caño, Jean Pouget, J.-F. Pellissier, Vincent Procaccio, B. Chabrol, Véronique Paquis‐Flucklinger	2011	176
2	HIV-1 TAR RNA: The Target of Molecular Interactions Between the Virus and its Host Current HIV Research ·Sylvie Bannwarth, Anne Gatignol	2005	161
3	Astrocyte Infection by HIV-1: Mechanisms of Restricted Virus Replication, and Role in the Pathogenesis of HIV-1-Associated Dementia Current HIV Research ·Paul R. Gorry, Chi L. Ong, Janine Thorpe, Sylvie Bannwarth, Katherine A. Thompson, Anne Gatignol, Steve Wesselingh, Damian F. J. Purcell	2003	154
4	TRBP Control of PACT-Induced Phosphorylation of Protein Kinase R Is Reversed by Stress Molecular and Cellular Biology ·Aı̈cha Daher, Ghislaine Laraki, Madhurima Singh, Carlos E Melendez-Peña, Sylvie Bannwarth, Antoine H.F.M. Peters, Éliane Meurs, Robert E. Braun, Rekha C. Patel, Anne Gatignol	2008	104
5	Neurologic features and genotype‐phenotype correlation in Wolfram syndrome Annals of Neurology ·Annabelle Chaussenot, Sylvie Bannwarth, Cécile Rouzier, B. Vialettes, Samira Ait El Mkadem, B. Chabrol, Aline Cano, Pierre Labauge, Véronique Paquis‐Flucklinger	2010	100
6	Two Dimerization Domains in the Trans-activation Response RNA-binding Protein (TRBP) Individually Reverse the Protein Kinase R Inhibition of HIV-1 Long Terminal Repeat Expression Journal of Biological Chemistry ·Aı̈cha Daher, M. Longuet, Dominique Dorin, Florence Bois, Emmanuel Ségéral, Sylvie Bannwarth, Pier-Luigi Battisti, Damian F. J. Purcell, Richard Benarous, Catherine Vaquero, Éliane Meurs, Anne Gatignol	2001	86
7	The TAR RNA-binding Protein, TRBP, Stimulates the Expression of TAR-containing RNAs in Vitro and in VivoIndependently of Its Ability to Inhibit the dsRNA-dependent Kinase PKR Journal of Biological Chemistry ·Dominique Dorin, Marion Bonnet, Sylvie Bannwarth, Anne Gatignol, Éliane Meurs, Catherine Vaquero	2003	80
8	Low TRBP Levels Support an Innate Human Immunodeficiency Virus Type 1 Resistance in Astrocytes by Enhancing the PKR Antiviral Response Journal of Virology ·Chi L. Ong, Janine Thorpe, Paul R. Gorry, Sylvie Bannwarth, Anthony Jaworowski, Jane L. Howard, Sean W. L. Chung, Shahan Campbell, Helen S. Christensen, Guerline Clerzius, Andrew J. Mouland, Anne Gatignol, Damian F. J. Purcell	2005	70
9	Screening of CHCHD10 in a French cohort confirms the involvement of this gene in frontotemporal dementia with amyotrophic lateral sclerosis patients Neurobiology of Aging ·Annabelle Chaussenot, Isabelle Le Ber, Samira Ait-El-Mkadem, Agnès Camuzat, Anne de Septenville, Sylvie Bannwarth, Emmanuelle C. Genin, Valérie Serre, Gaëlle Augé, Alexis Brice, Jean Pouget, Véronique Paquis‐Flucklinger	2014	68
10	Mitochondrial defect in muscle precedes neuromuscular junction degeneration and motor neuron death in CHCHD10S59L/+ mouse Acta Neuropathologica ·Emmanuelle C. Genin, Blandine Madji Hounoum, Sylvie Bannwarth, Konstantina Fragaki, Sandra Lacas‐Gervais, Alessandra Mauri-Crouzet, Françoise Lespinasse, Julien Neveu, Baptiste Ropert, Gaëlle Augé, Charlotte Cochaud, Cynthia Lefebvre-Omar, Stéphanie Bigou, Aude Chiot, Fanny Mochel, Séverine Boillée, Christian S. Lobsiger, Delphine Bohl, Jean‐Ehrland Ricci, Véronique Paquis‐Flucklinger	2019	67
11	Surveyor™ Nuclease: A new strategy for a rapid identification of heteroplasmic mitochondrial DNA mutations in patients with respiratory chain defects Human Mutation ·Sylvie Bannwarth, Vincent Procaccio, Véronique Paquis‐Flucklinger	2005	59
12	A novel CISD2 mutation associated with a classical Wolfram syndrome phenotype alters Ca2+ homeostasis and ER-mitochondria interactions Human Molecular Genetics ·Cécile Rouzier, David Moore, Cécile Delorme, Sandra Lacas‐Gervais, Samira Ait-El-Mkadem, Konstantina Fragaki, Florence Burté, Valérie Serre, Sylvie Bannwarth, Annabelle Chaussenot, Martin Catala, Patrick Yu‐Wai‐Man, Véronique Paquis‐Flucklinger	2017	53
13	Small Interfering RNAs against the TAR RNA Binding Protein, TRBP, a Dicer Cofactor, Inhibit Human Immunodeficiency Virus Type 1 Long Terminal Repeat Expression and Viral Production Journal of Virology ·Helen S. Christensen, Aı̈cha Daher, Kaitlin J. Soye, Lisa B. Frankel, Marina R. Alexander, Sébastien Lainé, Sylvie Bannwarth, Chi L. Ong, Sean W. L. Chung, Shahan Campbell, Damian F. J. Purcell, Anne Gatignol	2007	51
14	Wolfram syndrome in French population: Characterization of novel mutations and polymorphisms in theWFS1 gene Human Mutation ·Fabienne Giuliano, Sylvie Bannwarth, Sophie Monnot, Aline Cano, B. Chabrol, B. Vialettes, Bruno Delobel, (unknown), (unknown)	2004	46
15	Cloning and Expression of cDNA for a Human Gal(β1‐3)GalNAc α2,3‐Sialyltransferase from the CEM T‐Cell Line European Journal of Biochemistry ·Valérie Giordanengo, Sylvie Bannwarth, C. Laffont, Vincent Van Miecem, Anne Harduin‐Lepers, Philippe Delannoy, Jean‐Claude Lefebvre	1997	44
16	Autosomal dominant transmission of diabetes and congenital hearing impairment secondary to a missense mutation in the WFS1 gene Diabetic Medicine ·René Valéro, Sylvie Bannwarth, Sergio Adrián Barreto Román, Véronique Paquis‐Flucklinger, B. Vialettes	2008	38
17	Molecular analysis of ANT1, TWINKLE and POLG in patients with multiple deletions or depletion of mitochondrial DNA by a dHPLC-based assay European Journal of Human Genetics ·Mourad Naïmi, Sylvie Bannwarth, Vincent Procaccio, Jean Pouget, Claude Desnuelle, Jean‐François Pellissier, Agnès Rötig, Arnold Münnich, Patrick Calvas, Christian Richelme, Philippe Jonveaux, Giovanni Castelnovo, (unknown), M. Clanet, Douglas C. Wallace, Véronique Paquis‐Flucklinger	2006	38
18	The severity of phenotype linked to SUCLG1 mutations could be correlated with residual amount of SUCLG1 protein Journal of Medical Genetics ·Cécile Rouzier, Sandie Le Guédard-Méreuze, Konstantina Fragaki, Valérie Serre, Julie Miro, Sylvie Tuffery‐Giraud, Annabelle Chaussenot, Sylvie Bannwarth, C. Caruba, Elsebet Østergaard, (unknown), Christian Richelme, Caroline Espil, B. Chabrol, Véronique Paquis‐Flucklinger	2010	37
19	Mutation update and uncommon phenotypes in a French cohort of 96 patients with WFS1‐related disorders Clinical Genetics ·Annabelle Chaussenot, Cécile Rouzier, M.P. Quéré, Morgane Plutino, Samira Ait-El-Mkadem, Sylvie Bannwarth, M. Barth, Hélène Dollfus, Perrine Charles, Marc Nicolino, B. Chabrol, B. Vialettes, Véronique Paquis‐Flucklinger	2014	35
20	eKLIPse: a sensitive tool for the detection and quantification of mitochondrial DNA deletions from next-generation sequencing data Genetics in Medicine ·David Goudenège, Céline Bris, Virginie Hoffmann, Valérie Desquiret‐Dumas, Claude Jardel, Benoît Rucheton, Sylvie Bannwarth, Véronique Paquis‐Flucklinger, Anne Sophie Lebre, Estelle Colin, Patrizia Amati‐Bonneau, Dominique Bonneau, Pascal Reynier, Guy Lenaers, Vincent Procaccio	2018	32

About Sylvie Bannwarth

Sylvie Bannwarth is a scholar working on Molecular Biology, Clinical Biochemistry, Virology, Genetics and Immunology, having authored 62 papers that have together received 2.1k indexed citations. Recurring topics across this work include Mitochondrial Function and Pathology (36 papers), Metabolism and Genetic Disorders (15 papers), ATP Synthase and ATPases Research (11 papers), RNA and protein synthesis mechanisms (7 papers), RNA regulation and disease (7 papers), RNA Research and Splicing (6 papers), HIV Research and Treatment (6 papers) and RNA modifications and cancer (6 papers). The work is most often cited by research in Virology (319 citations), Clinical Biochemistry (265 citations), Molecular Biology (1.4k citations), Neurology (142 citations) and Cell Biology (242 citations). Sylvie Bannwarth has collaborated with scholars based in France, United States and Canada. Frequent co-authors include Anne Gatignol, Véronique Paquis‐Flucklinger, Annabelle Chaussenot, Cécile Rouzier, Vincent Procaccio, Konstantina Fragaki, B. Chabrol, Damian F. J. Purcell, Éliane Meurs and B. Vialettes. Their work appears in journals such as Mitochondrion, Brain, Journal of Biological Chemistry, Human Mutation and Clinical 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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Sylvie Bannwarth

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