Cécile Rouzier

2.0k citations

42 papers · 842 indexed · h-index 16

Clinical Biochemistry top 2%
- Metabolism and Genetic Disorders 13
Cell Biology top 10%
- Endoplasmic Reticulum Stress and Disease 6
Physiology top 10%
Molecular Biology
- Mitochondrial Function and Pathology 24
- ATP Synthase and ATPases Research 9
- RNA modifications and cancer 7
- RNA regulation and disease 4
- Coenzyme Q10 studies and effects 3
Genetics
- Genomics and Rare Diseases 4

Co-authors: Véronique Paquis‐Flucklinger Annabelle Chaussenot Sylvie Bannwarth B. Chabrol Konstantina Fragaki Vincent Procaccio A. Caño J.-F. Pellissier
Cited by: Clinical Biochemistry Cell Biology Physiology
Journals: Brain (3 papers)The Journal of Clinical Endocrinology & Metabolism (1 paper)Annals of Neurology (1 paper)
Partner nations: France United Kingdom Slovakia

In The Last Decade

Cécile Rouzier

39 papers receiving 833 citations

Peers

Countries citing papers authored by Cécile Rouzier

Since Specialization

Citations

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

Fields of papers citing papers by Cécile Rouzier

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network

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

All Works

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20 of 20 papers shown

#	Work
1	UQCRC2-related mitochondrial complex III deficiency, about 7 patients Mitochondrion ·Claire Bansept,Pauline Gaignard,Élise Lebigot,Didier Eyer,Geoffroy Delplancq,Célia Hoebeke,K. Mazodier,Anaïs Ledoyen,Cécile Rouzier,Konstantina Fragaki,Samira Ait‐El‐Mkadem Saadi,Christophe Philippe,Ange‐Line Bruel,Laurence Faivre,François Feillet,Marie‐Thérèse Abi Wardé	2022	7
2	Splicing variants in NARS2 are associated with milder phenotypes and intra-familial variability European Journal of Medical Genetics ·Samira Ait‐El‐Mkadem Saadi,Elsa Kaphan,Amaya Morales Jaurrieta,Konstantina Fragaki,Annabelle Chaussenot,Sylvie Bannwarth,A. Maues de Paula,Véronique Paquis‐Flucklinger,Cécile Rouzier	2022	3
3	Psycho-social impact of predictive genetic testing in hereditary heart diseases (PREDICT Study) Archives of Cardiovascular Diseases Supplements ·Céline Bordet,Sandrine Brice,Carole Maupain,Estelle Gandjbakhch,Bertrand Isidor,Aurélien Palmyre,A. Moerman,Annick Toutain,Sylvie Odent,Anne‐Claire Bréhin,Laureline Faivre,(unknown),Élise Schaefer,Karine Nguyen,D. Dupin Deguine,Cécile Rouzier,Pascale Richard,Sophie Tézenas du Montcel,Marcela Gargiulo,Philippe Charron	2020	3
4	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 Molecular Genetics and Metabolism Reports ·Konstantina Fragaki,Annabelle Chaussenot,Valérie Serre,Cécile Acquaviva,Sylvie Bannwarth,Cécile Rouzier,B. Chabrol,Véronique Paquis‐Flucklinger	2019	12
5	Targeted next generation sequencing with an extended gene panel does not impact variant detection in mitochondrial diseases BMC Medical Genetics ·Morgane Plutino,Annabelle Chaussenot,Cécile Rouzier,Samira Ait-El-Mkadem,Konstantina Fragaki,Véronique Paquis‐Flucklinger,Sylvie Bannwarth	2018	19
6	Myopathy with MTCYB mutation mimicking Multiple Acyl-CoA Dehydrogenase Deficiency Revue Neurologique ·Elsa Kaphan,Hanna Bou Ali,Marguerite Gastaldi,Cécile Acquaviva,Christine Vianey‐Saban,Cécile Rouzier,Konstantina Fragaki,Sylvie Bannwarth,Véronique Paquis‐Flucklinger,Norma B. Romero,Anthony Béhin,Anne Lombès,Claude Jardel,Odile Rigal,Pascal Laforêt	2018	4
7	A Broad Test Based on Fluorescent-Multiplex PCR for Noninvasive Prenatal Diagnosis of Cystic Fibrosis Fetal Diagnosis and Therapy ·Claire Guissart,Frédéric Tran Mau‐Them,Vanessa Debant,Victoria Viart,Charlotte Dubucs,Victoria L. Pritchard,Cécile Rouzier,Amandine Boureau‐Wirth,Emmanuelle Haquet,Jacques Puechberty,Éric Bieth,Philippe Khau Van Kien,Marie‐Pierre Bréchard,Caroline Raynal,Anne Girardet,Mireille Claustres,M. Kœnig,Marie‐Claire Vincent	2018	9
8	Non-invasive prenatal diagnosis (NIPD) of cystic fibrosis: an optimized protocol using MEMO fluorescent PCR to detect the p.Phe508del mutation Journal of Cystic Fibrosis ·Claire Guissart,Charlotte Dubucs,Caroline Raynal,Anne Girardet,Frédéric Tran Mau‐Them,Vanessa Debant,Cécile Rouzier,Amandine Boureau‐Wirth,Emmanuelle Haquet,Jacques Puechberty,Éric Bieth,D. Dupin Deguine,Philippe Khau Van Kien,Marie‐Pierre Bréchard,Victoria L. Pritchard,M. Kœnig,Mireille Claustres,M.-C. Vincent	2016	12
9	Coenzyme Q10 defects may be associated with a deficiency of Q10-independent mitochondrial respiratory chain complexes Biological Research ·Konstantina Fragaki,Annabelle Chaussenot,Jean‐François Benoist,Samira Ait-El-Mkadem,Sylvie Bannwarth,Cécile Rouzier,Charlotte Cochaud,Véronique Paquis‐Flucklinger	2016	16
10	A false positive newborn screening result due to a complex allele carrying two frequent CF-causing variants Journal of Cystic Fibrosis ·Anne Bergougnoux,Amandine Boureau‐Wirth,Cécile Rouzier,Jean-Pierre Altiéri,F. Verneau,Lise Larrieu,M. Kœnig,Mireille Claustres,Caroline Raynal	2016	12
11	Syndrome de Wolfram familial Archives de Pédiatrie ·M. Bessahraoui,V. Paquis,Cécile Rouzier,K. Bouziane-Nedjadi,M. Naceur,S. Niar,A. Zennaki,G. Boudraa,M. Touhami	2014	1
12	Extragestational βHCG Secretion Due to an Isolated Lung Epithelioid Trophoblastic Tumor: Microsatellite Genotyping of Tumoral Cells Confirmed Their Placental Origin and Oriented Specific Chemotherapy The Journal of Clinical Endocrinology & Metabolism ·Patrick Fénichel,Cécile Rouzier,Catherine Butori,P. Chevallier,Anne-Gaelle Poullot,Antoine Thyss,Jérôme Mouroux	2014	12
13	Quantitative multiplex PCR of short fluorescent fragments for the detection of large intragenic POLG rearrangements in a large French cohort 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	2013	28
14	Fatal heart failure associated with CoQ10 and multiple OXPHOS deficiency in a child with propionic acidemia Mitochondrion ·Konstantina Fragaki,Aline Cano,Jean‐François Benoist,Odile Rigal,Annabelle Chaussenot,Cécile Rouzier,Sylvie Bannwarth,C. Caruba,B. Chabrol,Véronique Paquis‐Flucklinger	2011	31
15	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
16	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	98
17	LMNA , ZMPSTE24 , and LBR Are Not Mutated in Scleroderma Genetic Testing and Molecular Biomarkers ·Caroline Gaudy‐Marqueste,Amandine Boyer,Claire Navarro,Cécile Rouzier,Jean Robert Harley,Pierre‐Jean Weiller,Jean‐Jacques Grob,Nicolas Lévy,Annachiara De Sandre‐Giovannoli	2009	2
18	Detection of the TMPRSS2-ETS fusion gene in prostate carcinomas: retrospective analysis of 55 formalin-fixed and paraffin-embedded samples with clinical data Cancer Genetics and Cytogenetics ·Cécile Rouzier,Juliette Haudebourg,Xavier Carpentier,Laure Valério,J. Amiel,Jean‐François Michiels,Florence Pédeutour	2008	22
19	Identification of novel mutations in WFS1 and genotype–phenotype correlation in Wolfram syndrome American Journal of Medical Genetics Part A ·A. Caño,Cécile Rouzier,Sophie Monnot,B. Chabrol,J. Conrath,Philippe Lecomte,B Delobel,Pascal Boileau,René Valéro,Vincent Procaccio,Véronique Paquis‐Flucklinger,(unknown),(unknown)	2007	60
20	Lactose intake and lactase activity: two risk factors for senile and diabetic cataract. I. Birlouez-Aragon,L. Stevenin,Cécile Rouzier,M. Brivet	1990	1

About Cécile Rouzier

Cécile Rouzier is a scholar working on Clinical Biochemistry, Molecular Biology and Cell Biology, having authored 42 papers that have together received 842 indexed citations. Recurring topics across this work include Mitochondrial Function and Pathology (24 papers), Metabolism and Genetic Disorders (13 papers), ATP Synthase and ATPases Research (9 papers), RNA modifications and cancer (7 papers), Endoplasmic Reticulum Stress and Disease (6 papers), Genomics and Rare Diseases (4 papers), RNA regulation and disease (4 papers) and Coenzyme Q10 studies and effects (3 papers). The work is most often cited by research in Clinical Biochemistry (206 citations), Cell Biology (200 citations) and Physiology (45 citations). Cécile Rouzier has collaborated with scholars based in France, United Kingdom and Slovakia. Frequent co-authors include Véronique Paquis‐Flucklinger, Annabelle Chaussenot, Sylvie Bannwarth, B. Chabrol, Konstantina Fragaki, Vincent Procaccio, A. Caño, J.-F. Pellissier, Samira Ait-El-Mkadem and Jean Pouget. Their work appears in journals such as Brain, The Journal of Clinical Endocrinology & Metabolism and Annals of Neurology.

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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