Catherine Brunel‐Guitton

1.4k citations

28 papers · 621 indexed · h-index 14

Co-authors: Florin Sasarman Eric A. Shoubridge Hana Antonická Timothy Wai Grant A. Mitchell Pierre Allard David Brossier Geneviève Du Pont‐Thibodeau
Topics: Metabolism and Genetic Disorders (14 papers)Mitochondrial Function and Pathology (8 papers)Folate and B Vitamins Research (5 papers)
Cited by: Clinical Biochemistry Molecular Biology Biochemistry
Journals: SHILAP Revista de lepidopterologíaAnnals of Neurology Human Molecular Genetics
Partner nations: Canada United States France

In The Last Decade

Catherine Brunel‐Guitton

26 papers receiving 619 citations

Peers

Countries citing papers authored by Catherine Brunel‐Guitton

Since Specialization

Citations

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

Fields of papers citing papers by Catherine Brunel‐Guitton

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Catherine Brunel‐Guitton. 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 Catherine Brunel‐Guitton. The network helps show where Catherine Brunel‐Guitton may publish in the future.

Co-authorship network of co-authors of Catherine Brunel‐Guitton

This figure shows the co-authorship network connecting the top 25 collaborators of Catherine Brunel‐Guitton. A scholar is included among the top collaborators of Catherine Brunel‐Guitton 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 Catherine Brunel‐Guitton. Catherine Brunel‐Guitton 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	The MMACHC variant c.158T>C: Mild clinical and biochemical phenotypes and marked hydroxocobalamin response in cblC patients 2024 ·Molecular Genetics and Metabolism ·Tanguy Demaret,Karine Bédard,(unknown),David Watkins,Pierre Allard,(unknown),(unknown),Catherine Brunel‐Guitton,David S. Rosenblatt,Grant A. Mitchell	0
2	Use of dexamethasone in acute rhabdomyolysis in LPIN1 deficiency 2023 ·Molecular Genetics and Metabolism Reports ·Mehdi Yeganeh,(unknown),Catherine Jones,Gloria Y. F. Ho,Kathryn Selby,Jean‐Pierre Chanoine,Sylvia Stöckler,Ramona Salvarinova,Gabriella Horváth,Catherine Brunel‐Guitton	1
3	Congenital lactic acidosis, cerebral cysts and pulmonary hypertension in an infant with FOXRED1 related complex I deficiency 2019 ·Molecular Genetics and Metabolism Reports ·(unknown),Bojana Rakić,Catherine Brunel‐Guitton,Glenda Hendson,Renkui Bai,Michael A. Sargent,Pascal M. Lavoie,Millan S. Patel,Sylvia Stöckler‐Ipsiroglu	7
4	Fulminant Necrotizing Enterocolitis and Multiple Organ Dysfunction in a Toddler with Mitochondrial DNA Depletion Syndrome-13 2019 ·Journal of Pediatric Intensive Care ·(unknown),François Proulx,Catherine Brunel‐Guitton,Luc L. Oligny,Nelson Piché,Grant A. Mitchell,Jean Sébastien Joyal	3
5	Muscle problems in juvenile-onset acid maltase deficiency (Pompe disease) 2019 ·Paediatrics & Child Health ·(unknown),Hugh J. McMillan,Tony Rupar,Catherine Brunel‐Guitton,Pranesh Chakraborty,John J. Mitchell,Johannes Roth,Mark A. Tarnopolsky,Lesley Turner,Craig Campbell	1
6	Acute pediatric hyperammonemia: current diagnosis and management strategies 2018 ·SHILAP Revista de lepidopterología ·(unknown),David Brossier,Catherine Brunel‐Guitton,(unknown),Geneviève Du Pont‐Thibodeau,Philippe Jouvet	47
7	Premature Ovarian Failure in French Canadian Leigh Syndrome 2017 ·The Journal of Pediatrics ·(unknown),Charles Morin,Catherine Brunel‐Guitton,Grant A. Mitchell,Guy Van Vliet,Céline Huot	13
8	Recessive Mutations in NDUFA2 Cause Mitochondrial Leukoencephalopathy 2017 ·Annals of Neurology ·(unknown),(unknown),Martine Tétreault,Luan T. Tran,(unknown),Myriam Srour,(unknown),Catherine Brunel‐Guitton,Jacek Majewski,Long Long,(unknown),Michael J. Gambello,Cas Simons,Adeline Vanderver,Geneviève Bernard	0
9	Glutaric Aciduria Type 3: Three Unrelated Canadian Cases, with Different Routes of Ascertainment 2017 ·JIMD Reports ·Paula J. Waters,Thomas M. Kitzler,Annette Feigenbaum,Michael T. Geraghty,Osama Y. Al-Dirbashi,Patrick Bhérer,Christiane Auray‐Blais,Serge Gravel,(unknown),Komudi Siriwardena,Yannis Trakadis,Catherine Brunel‐Guitton,Walla Al‐Hertani	12
10	Atypical juvenile presentation of GM2 gangliosidosis AB in a patient compound-heterozygote for c.259G > T and c.164C > T mutations in the GM2A gene 2017 ·Molecular Genetics and Metabolism Reports ·(unknown),Catherine Brunel‐Guitton,Anne Lortie,France Gauvin,Carlos R. Morales,Grant A. Mitchell,Alexey V. Pshezhetsky	13
11	Recessive mutations in NDUFA2 cause mitochondrial leukoencephalopathy 2017 ·Clinical Genetics ·(unknown),(unknown),Martine Tétreault,Luan T. Tran,(unknown),Myriam Srour,John J. Mitchell,Catherine Brunel‐Guitton,Jacek Majewski,(unknown),Stephanie Keller,Michael J. Gambello,Cas Simons,Adeline Vanderver,Geneviève Bernard	12
12	LPIN1 deficiency with severe recurrent rhabdomyolysis and persistent elevation of creatine kinase levels due to chromosome 2 maternal isodisomy 2015 ·SHILAP Revista de lepidopterología ·Inge A. Meijer,Florin Sasarman,(unknown),Elsa Rossignol,Michel Vanasse,(unknown),Grant A. Mitchell,Catherine Brunel‐Guitton	19
13	A Highly Diverse Portrait: Heterogeneity of Neuropsychological Profiles in cblC Defect 2015 ·JIMD Reports ·Jenny Bellerose,(unknown),Karine Bédard,Catherine Brunel‐Guitton,Grant A. Mitchell,Luis H. Ospina,Miriam H. Beauchamp	9
14	Normal Cerebrospinal Fluid Pyridoxal 5′-Phosphate Level in a PNPO-Deficient Patient with Neonatal-Onset Epileptic Encephalopathy 2015 ·JIMD Reports ·(unknown),Stéphane Camuzeaux,Anne‐Marie Laberge,Pierre Allard,Catherine Brunel‐Guitton,Paola Diadori,Elsa Rossignol,Keith Hyland,Peter T. Clayton,Philippa B. Mills,Grant A. Mitchell	17
15	An N-terminal formyl methionine on COX 1 is required for the assembly of cytochrome c oxidase 2015 ·Human Molecular Genetics ·Reetta Hinttala,Florin Sasarman,Takashi Nishimura,Hana Antonická,Catherine Brunel‐Guitton,Jeremy Schwartzentruber,Somayyeh Fahiminiya,Jacek Majewski,Denis Faubert,Elsebet Østergaard,Jan Smeıtınk,Eric A. Shoubridge	21
16	Mitochondrial Diseases and Cardiomyopathies 2015 ·Canadian Journal of Cardiology ·Catherine Brunel‐Guitton,(unknown),Florin Sasarman	41
17	Inborn errors of cytoplasmic triglyceride metabolism 2014 ·Journal of Inherited Metabolic Disease ·Jiang Wei Wu,Hao Yang,Shu Pei Wang,Krishnakant G. Soni,Catherine Brunel‐Guitton,Grant A. Mitchell	27
18	Late-onset nonketotic hyperglycinemia caused by a novel homozygous missense mutation in the GLDC gene 2011 ·Molecular Genetics and Metabolism ·Catherine Brunel‐Guitton,Brett Casey,Marion B. Coulter-Mackie,Hilary Vallance,(unknown),Sylvia Stöckler‐Ipsiroglu,Saadet Mercimek‐Mahmutoglu	19
19	LRPPRC and SLIRP Interact in a Ribonucleoprotein Complex That Regulates Posttranscriptional Gene Expression in Mitochondria 2010 ·Molecular Biology of the Cell ·Florin Sasarman,Catherine Brunel‐Guitton,Hana Antonická,Timothy Wai,Eric A. Shoubridge	215
20	Enzyme replacement therapy in pediatric patients with Gaucher disease: What should we use as maintenance dosage? 2008 ·Molecular Genetics and Metabolism ·Catherine Brunel‐Guitton,Georges‐Étienne Rivard,Jacques Galipeau,Nathalie Alos,Marie‐Claude Miron,(unknown),Grant A. Mitchell,Guy Lapierre,Marie Lambert	4

About Catherine Brunel‐Guitton

Catherine Brunel‐Guitton is a scholar working on Clinical Biochemistry, Biochemistry and Rheumatology, having authored 28 papers that have together received 621 indexed citations. Recurring topics across this work include Metabolism and Genetic Disorders (14 papers), Mitochondrial Function and Pathology (8 papers) and Folate and B Vitamins Research (5 papers). The work is most often cited by research in Clinical Biochemistry (203 citations), Molecular Biology (454 citations) and Biochemistry (47 citations). Catherine Brunel‐Guitton has collaborated with scholars based in Canada, United States and France. Frequent co-authors include Florin Sasarman, Eric A. Shoubridge, Hana Antonická, Timothy Wai, Grant A. Mitchell, Pierre Allard, David Brossier, Geneviève Du Pont‐Thibodeau, Philippe Jouvet and Philippe M. Campeau. Their work appears in journals such as SHILAP Revista de lepidopterología, Annals of Neurology and Human Molecular 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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