Sylvie Bannwarth

3.9k total citations
62 papers, 2.0k citations indexed

About

Sylvie Bannwarth is a scholar working on Molecular Biology, Clinical Biochemistry and Genetics. According to data from OpenAlex, Sylvie Bannwarth has authored 62 papers receiving a total of 2.0k indexed citations (citations by other indexed papers that have themselves been cited), including 58 papers in Molecular Biology, 22 papers in Clinical Biochemistry and 7 papers in Genetics. Recurrent topics in Sylvie Bannwarth's work include Mitochondrial Function and Pathology (36 papers), Metabolism and Genetic Disorders (22 papers) and ATP Synthase and ATPases Research (14 papers). Sylvie Bannwarth is often cited by papers focused on Mitochondrial Function and Pathology (36 papers), Metabolism and Genetic Disorders (22 papers) and ATP Synthase and ATPases Research (14 papers). Sylvie Bannwarth collaborates with scholars based in France, United States and Canada. Sylvie Bannwarth's 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 Aı̈cha Daher and has published in prestigious journals such as Journal of Biological Chemistry, Nature Communications and Bioinformatics.

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-authorship network of co-authors of Sylvie Bannwarth

This figure shows the co-authorship network connecting the top 25 collaborators of Sylvie Bannwarth. A scholar is included among the top collaborators of Sylvie Bannwarth 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 Sylvie Bannwarth. Sylvie Bannwarth 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	Splicing variants in NARS2 are associated with milder phenotypes and intra-familial variability 2022 ·European Journal of Medical Genetics ·(unknown), Elsa Kaphan, (unknown), Konstantina Fragaki, Annabelle Chaussenot, Sylvie Bannwarth, A. Maues de Paula, Véronique Paquis‐Flucklinger, Cécile Rouzier	3
2	A novel variant m.8561C>T in the overlapping region of MT-ATP6 and MT-ATP8 in a child with early-onset severe neurological signs 2019 ·Molecular Genetics and Metabolism Reports ·Konstantina Fragaki, Annabelle Chaussenot, Valérie Serre, Cécile Acquaviva, Sylvie Bannwarth, Cécile Rouzier, B. Chabrol, Véronique Paquis‐Flucklinger	12
3	Petite Integration Factor 1 (PIF1) helicase deficiency increases weight gain in Western diet-fed female mice without increased inflammatory markers or decreased glucose clearance 2019 ·PLoS ONE ·Frances Belmonte, Nikolaos Dedousis, Ian Sipula, (unknown), Aatur D. Singhi, Yanxia Chu, Yingze Zhang, Sylvie Bannwarth, Véronique Paquis‐Flucklinger, Lea Harrington, Sruti Shiva, Michael J. Jurczak, Robert M. O’Doherty, Brett A. Kaufman	6
4	Targeted next generation sequencing with an extended gene panel does not impact variant detection in mitochondrial diseases 2018 ·BMC Medical Genetics ·Morgane Plutino, Annabelle Chaussenot, Cécile Rouzier, Samira Ait-El-Mkadem, Konstantina Fragaki, Véronique Paquis‐Flucklinger, Sylvie Bannwarth	19
5	Coenzyme Q10 defects may be associated with a deficiency of Q10-independent mitochondrial respiratory chain complexes 2016 ·Biological Research ·Konstantina Fragaki, Annabelle Chaussenot, Jean‐François Benoist, Samira Ait-El-Mkadem, Sylvie Bannwarth, Cécile Rouzier, Charlotte Cochaud, Véronique Paquis‐Flucklinger	16
6	Quantitative multiplex PCR of short fluorescent fragments for the detection of large intragenic POLG rearrangements in a large French cohort 2013 ·European Journal of Human Genetics ·Cécile Rouzier, Annabelle Chaussenot, Valérie Serre, Konstantina Fragaki, Sylvie Bannwarth, Samira Ait-El-Mkadem, Shahram Attarian, Elsa Kaphan, Aline Cano, Émilien Delmont, Sabrina Sacconi, Bénédicte Mousson de Camaret, Marlène Rio, Anne-Sophie Lèbre, Claude Jardel, Romain Deschamps, Christian Richelme, Jean Pouget, B. Chabrol, Véronique Paquis‐Flucklinger	28
7	Fatal heart failure associated with CoQ10 and multiple OXPHOS deficiency in a child with propionic acidemia 2011 ·Mitochondrion ·Konstantina Fragaki, Aline Cano, Jean‐François Benoist, Odile Rigal, Annabelle Chaussenot, Cécile Rouzier, Sylvie Bannwarth, (unknown), B. Chabrol, Véronique Paquis‐Flucklinger	31
8	Neurologic features and genotype‐phenotype correlation in Wolfram syndrome 2010 ·Annals of Neurology ·Annabelle Chaussenot, Sylvie Bannwarth, Cécile Rouzier, B. Vialettes, Samira Ait El Mkadem, B. Chabrol, Aline Cano, Pierre Labauge, Véronique Paquis‐Flucklinger	98
9	Rapid Identification of Unknown Heteroplasmic Mitochondrial DNA Mutations with Mismatch-Specific Surveyor Nuclease 2009 ·Methods in molecular biology ·Sylvie Bannwarth, Vincent Procaccio, Véronique Paquis‐Flucklinger	6
10	TRBP Control of PACT-Induced Phosphorylation of Protein Kinase R Is Reversed by Stress 2008 ·Molecular and Cellular Biology ·Aı̈cha Daher, (unknown), Madhurima Singh, Carlos E Melendez-Peña, Sylvie Bannwarth, Antoine H.F.M. Peters, Éliane Meurs, Robert E. Braun, Rekha C. Patel, Anne Gatignol	103
11	Autosomal dominant transmission of diabetes and congenital hearing impairment secondary to a missense mutation in the WFS1 gene 2008 ·Diabetic Medicine ·René Valéro, Sylvie Bannwarth, (unknown), Véronique Paquis‐Flucklinger, B. Vialettes	36
12	Detection of Low Levels of the Mitochondrial tRNALeu(UUR) 3243A>G Mutation in Blood Derived from Patients with Diabetes 2006 ·Molecular Diagnosis & Therapy ·Vincent Procaccio, Nicolas Neckelmann, Véronique Paquis‐Flucklinger, Sylvie Bannwarth, Richard Jimenez, Antonio Dávila, Jason C. Poole, Douglas C. Wallace	7
13	Rapid identification of unknown heteroplasmic mutations across the entire human mitochondrial genome with mismatch-specific Surveyor Nuclease 2006 ·Nature Protocols ·Sylvie Bannwarth, Vincent Procaccio, Véronique Paquis‐Flucklinger	29
14	Surveyor™ Nuclease: A new strategy for a rapid identification of heteroplasmic mitochondrial DNA mutations in patients with respiratory chain defects 2005 ·Human Mutation ·Sylvie Bannwarth, Vincent Procaccio, Véronique Paquis‐Flucklinger	59
15	Wolfram syndrome in French population: Characterization of novel mutations and polymorphisms in theWFS1 gene 2004 ·Human Mutation ·Fabienne Giuliano, Sylvie Bannwarth, Sophie Monnot, Aline Cano, B. Chabrol, B. Vialettes, Bruno Delobel, (unknown), (unknown)	46
16	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 2003 ·Journal of Biological Chemistry ·Dominique Dorin, Marion Bonnet, Sylvie Bannwarth, Anne Gatignol, Éliane Meurs, Catherine Vaquero	80
17	Additive Activity between the Trans -Activation Response RNA-Binding Protein, TRBP2, and Cyclin T1 on HIV Type 1 Expression and Viral Production in Murine Cells 2003 ·AIDS Research and Human Retroviruses ·(unknown), Aı̈cha Daher, Sylvie Bannwarth, Johannes Voortman, Keith Peden, John Hiscott, Andrew J. Mouland, Richard Benarous, Anne Gatignol	15
18	Characterization of TRBP1 and TRBP2 2000 ·Journal of Biomedical Science ·Mariela Duarte, Kenneth Graham, Aı̈cha Daher, (unknown), Sylvie Bannwarth, Emmanuel Ségéral, Kuan‐Teh Jeang, Anne Gatignol	23
19	Cloning, Mapping, and Genomic Organization of the LSLCL Gene, Encoding a New Lymphocytic Secreted Mucin-like Protein with a C-Type Lectin Domain: A New Model of Exon Shuffling 1999 ·Genomics ·Sylvie Bannwarth, Valérie Giordanengo, Josiane Grosgeorge, Claude Turc‐Carel, Jean‐Claude Lefebvre	6
20	Molecular Cloning of a New Secreted Sulfated Mucin-like Protein With a C-type Lectin Domain That Is Expressed in Lymphoblastic Cells 1998 ·Journal of Biological Chemistry ·Sylvie Bannwarth, Valérie Giordanengo, (unknown), Jean‐Claude Lefebvre	20

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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