Aline Cano

1.0k total citations
27 papers, 485 citations indexed

About

Aline Cano is a scholar working on Molecular Biology, Clinical Biochemistry and Rheumatology. According to data from OpenAlex, Aline Cano has authored 27 papers receiving a total of 485 indexed citations (citations by other indexed papers that have themselves been cited), including 13 papers in Molecular Biology, 12 papers in Clinical Biochemistry and 7 papers in Rheumatology. Recurrent topics in Aline Cano's work include Metabolism and Genetic Disorders (12 papers), Mitochondrial Function and Pathology (7 papers) and Folate and B Vitamins Research (5 papers). Aline Cano is often cited by papers focused on Metabolism and Genetic Disorders (12 papers), Mitochondrial Function and Pathology (7 papers) and Folate and B Vitamins Research (5 papers). Aline Cano collaborates with scholars based in France, United Kingdom and Belgium. Aline Cano's co-authors include B. Chabrol, Véronique Paquis‐Flucklinger, B. Vialettes, Sylvie Bannwarth, Cécile Rouzier, Annabelle Chaussenot, Pierre Labauge, Samira Ait El Mkadem, Alain Fouilhoux and Caroline Ovaert and has published in prestigious journals such as Diabetes Care, Annals of Neurology and International Journal of Molecular Sciences.

In The Last Decade

Aline Cano

26 papers receiving 471 citations

Peers

Countries citing papers authored by Aline Cano

Since Specialization

Citations

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

Fields of papers citing papers by Aline Cano

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Aline Cano

This figure shows the co-authorship network connecting the top 25 collaborators of Aline Cano. A scholar is included among the top collaborators of Aline Cano 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 Aline Cano. Aline Cano 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	French recommendations for the management of glycogen storage disease type III 2023 ·European journal of medical research ·(unknown), Aline Cano, V. Decostre, Roseline Froissart, F. Maillot, (unknown), François Petit, (unknown), Karim Wahbi, (unknown), Pascal Laforêt, Philippe Labrune	3
2	Executive functions in preschool children with moderate hyperphenylalaninemia and phenylketonuria: a prospective study 2023 ·Orphanet Journal of Rare Diseases ·(unknown), Aline Cano, B. Chabrol, Arnaud Roy	4
3	Dilated-Left Ventricular Non-Compaction Cardiomyopathy in a Pediatric Case with SPEG Compound Heterozygous Variants 2022 ·International Journal of Molecular Sciences ·(unknown), (unknown), (unknown), Aline Cano, (unknown), Stéphane Zaffran	1
4	Very long‐term outcomes in 23 patients with cblA type methylmalonic acidemia 2022 ·Journal of Inherited Metabolic Disease ·Cécilia Marelli, Alain Fouilhoux, Jean‐François Benoist, Pascale de Lonlay, (unknown), Anaïs Brassier, Aline Cano, B. Chabrol, (unknown), Manuel Schiff, Cécile Acquaviva, Elaine Murphy, Aude Servais, Robin Lachmann	3
5	Novel partial loss-of-function variants in the tyrosyl-tRNA synthetase 1 (YARS1) gene involved in multisystem disease 2021 ·European Journal of Medical Genetics ·(unknown), (unknown), (unknown), (unknown), (unknown), F. Blanc, Patrice Bourgeois, (unknown), Aline Cano, (unknown), Clémence Delteil, Caroline Lacoste, Marie Loosveld, A. Maues de Paula, (unknown), Véronique Secq, Nicolas Lévy, Catherine Badens, Alexandre Fabre	5
6	Cerliponase alfa changes the natural history of children with neuronal ceroid lipofuscinosis type 2: The first French cohort 2020 ·European Journal of Paediatric Neurology ·(unknown), Aline Cano, (unknown), Samia Pichard, Didier Scavarda, Isabelle Desguerre, Stéphane Auvin, B. Chabrol	13
7	A new mutation in the mitochondrial tRNAPro gene associated with early-onset neuromuscular phenotype and ragged-red fibers 2016 ·Neuromuscular Disorders ·(unknown), Sylvie Bannwarth, Annabelle Chaussenot, Aline Cano, Konstantina Fragaki, Samira Ait-El-Mkadem, Cécile Rouzier, A. Maues de Paula, B. Chabrol, Véronique Paquis‐Flucklinger	4
8	Efficacy and safety of i.v. sodium benzoate in urea cycle disorders: a multicentre retrospective study 2016 ·Orphanet Journal of Rare Diseases ·(unknown), Manuel Schiff, Alain Fouilhoux, Aline Cano, Dries Dobbelaere, Anaïs Brassier, Karine Mention, Jean‐Baptiste Arnoux, François Feillet, B. Chabrol, Nathalie Guffon, Caroline Elie, Pascale de Lonlay	30
9	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
10	Assessment of quality of life of the children and parents affected by inborn errors of metabolism with restricted diet: preliminary results of a cross-sectional study 2013 ·Health and Quality of Life Outcomes ·Alexandre Fabre, Karine Baumstarck, Aline Cano, Anderson Loundou, Julie Berbis, B. Chabrol, Pascal Auquier	36
11	Atypical pyridoxine-dependent epilepsy due to a pseudoexon in ALDH7A1 2012 ·Molecular Genetics and Metabolism ·Mathieu Milh, Ana Pop, Warsha A. Kanhai, Nathalie Villeneuve, Aline Cano, Eduard A. Struys, Gajja S. Salomons, B. Chabrol, Cornelis Jakobs	9
12	Maternal phenylketonuria: low phenylalaninemia might increase the risk of intra uterine growth retardation 2012 ·Journal of Inherited Metabolic Disease ·(unknown), Emmanuel Nowak, Murielle Assoun, Karine Mention, Aline Cano, Alain Fouilhoux, François Feillet, Hélène Ogier, Emmanuel Oger, L de Parscau	34
13	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
14	Mouvements anormaux dans les encéphalopathies néonatales 2011 ·Mathieu Milh, Aline Cano, B. Chabrol	0
15	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
16	Multiple Distal Pulmonary Arterial Thromboses Revealed by Lung Scintigraphy in a Patient With Homocystinuria and Normal Multidetector CT Pulmonary Angiography 2008 ·Clinical Nuclear Medicine ·Laurent Tessonnier, Eric Guedj, Aline Cano, Serge Cammilleri, Andréea Dragulescu, B. Chabrol, O. Mundler	1
17	Carnitine Membrane Transporter Deficiency: A Rare Treatable Cause of Cardiomyopathy and Anemia 2007 ·Pediatric Cardiology ·Aline Cano, Caroline Ovaert, Christine Vianey‐Saban, B. Chabrol	16
18	Aortic dilatation in Cockayne syndrome 2007 ·American Journal of Medical Genetics Part A ·Caroline Ovaert, Aline Cano, B. Chabrol	7
19	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
20	Comparative study between European and American species of Polistes using sera from European sensitized subjects 1995 ·Clinical & Experimental Allergy ·F Sánchez, M. Blanca, Javier Fernández, Alfonso Miranda, (unknown), Marı́a José Torres, Aline Cano, J.J. Garcı́a, C. Juárez	17

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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