A. Caño

538 total citations
19 papers, 366 citations indexed

About

A. Caño is a scholar working on Molecular Biology, Clinical Biochemistry and Epidemiology. According to data from OpenAlex, A. Caño has authored 19 papers receiving a total of 366 indexed citations (citations by other indexed papers that have themselves been cited), including 12 papers in Molecular Biology, 8 papers in Clinical Biochemistry and 3 papers in Epidemiology. Recurrent topics in A. Caño's work include Mitochondrial Function and Pathology (8 papers), Metabolism and Genetic Disorders (8 papers) and ATP Synthase and ATPases Research (6 papers). A. Caño is often cited by papers focused on Mitochondrial Function and Pathology (8 papers), Metabolism and Genetic Disorders (8 papers) and ATP Synthase and ATPases Research (6 papers). A. Caño collaborates with scholars based in France, Spain and United States. A. Caño's co-authors include B. Chabrol, Véronique Paquis‐Flucklinger, Vincent Procaccio, Cécile Rouzier, Arnaud Chevrollier, Jean Pouget, Konstantina Fragaki, Annie Verschueren, Sylvie Bannwarth and Annabelle Chaussenot and has published in prestigious journals such as Brain, Human Reproduction and Molecular Genetics and Metabolism.

In The Last Decade

A. Caño

19 papers receiving 363 citations

Peers — A (Enhanced Table)

Peers by citation overlap · career bar shows stage (early→late) cites · hero ref

Name	h						Papers	Cites
A. Caño France	7	250	133	76	70	44	19	366
Marianna Bugiani Italy	9	600 2.4×	343 2.6×	98 1.3×	69 1.0×	48 1.1×	10	720
Hiroko Shimbo Japan	12	192 0.8×	101 0.8×	40 0.5×	51 0.7×	73 1.7×	33	315
Virginie Guillet France	10	483 1.9×	139 1.0×	134 1.8×	39 0.6×	17 0.4×	11	581
Hannah E. Steele United Kingdom	9	180 0.7×	53 0.4×	77 1.0×	51 0.7×	30 0.7×	14	275
Heiko Brennenstuhl Germany	11	180 0.7×	99 0.7×	47 0.6×	19 0.3×	74 1.7×	25	315
Hye-Won Hyun South Korea	11	195 0.8×	25 0.2×	89 1.2×	72 1.0×	23 0.5×	13	334
Anna Marcé‐Grau Spain	10	139 0.6×	52 0.4×	63 0.8×	24 0.3×	48 1.1×	19	284
Valentina Del Dotto Italy	11	518 2.1×	189 1.4×	38 0.5×	24 0.3×	20 0.5×	16	575
Mathieu Lachance Canada	5	227 0.9×	47 0.4×	78 1.0×	49 0.7×	22 0.5×	8	321
Jack J. Collier United Kingdom	5	248 1.0×	93 0.7×	30 0.4×	23 0.3×	23 0.5×	6	344

Countries citing papers authored by A. Caño

Since Specialization

Citations

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

Fields of papers citing papers by A. Caño

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of A. Caño

This figure shows the co-authorship network connecting the top 25 collaborators of A. Caño. A scholar is included among the top collaborators of A. Caño 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 A. Caño. A. Caño is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

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19 of 19 papers shown

Caño, A., Bertrand Roquelaure, Patrice Bourgeois, et al.. (2020). Mutations in NBAS and SCYL1, genetic causes of recurrent liver failure in children: Three case reports and a literature review. Archives de Pédiatrie. 27(3). 155–159. 13 indexed citations

Cacciagli, Pierre, A. Caño, Michèle Roussel, et al.. (2020). The phenotype caused by recessive variations in SLC25A22: Report of a new case and literature review. Archives de Pédiatrie. 28(1). 87–92. 4 indexed citations

Caño, A., et al.. (2020). Clinical phenotype associated with TANGO2 gene mutation. Archives de Pédiatrie. 28(1). 80–86. 13 indexed citations

Caño, A., et al.. (2015). Rachitisme carentiel compliquant une maladie de Chanarin-Dorfman. Archives de Pédiatrie. 22(4). 414–417. 2 indexed citations

Caño, A., C. Halbert, Julien Mancini, et al.. (2012). Épilepsie et cytopathies mitochondriales : étude rétrospective de 53 enfants épileptiques. Archives de Pédiatrie. 19(8). 794–802. 2 indexed citations

Rouzier, Cécile, Sylvie Bannwarth, Annabelle Chaussenot, et al.. (2012). Reply: MFN2 mutations cause compensatory mitochondrial DNA proliferation. Brain. 135(8). e220–e220. 2 indexed citations

Rouzier, Cécile, Valérie Serre, Annabelle Chaussenot, et al.. (2012). Reply: MFN2, a new gene responsible for mitochondrial DNA depletion. Brain. 135(8). e224–e224. 2 indexed citations

Rouzier, Cécile, Sylvie Bannwarth, Annabelle Chaussenot, et al.. (2011). The MFN2 gene is responsible for mitochondrial DNA instability and optic atrophy 'plus' phenotype. Brain. 135(1). 23–34. 176 indexed citations

Boutron, Audrey, Cécile Acquaviva, Christine Vianey‐Saban, et al.. (2011). Comprehensive cDNA study and quantitative analysis of mutant HADHA and HADHB transcripts in a French cohort of 52 patients with mitochondrial trifunctional protein deficiency. Molecular Genetics and Metabolism. 103(4). 341–348. 42 indexed citations

10.

Caño, A., et al.. (2008). Le syndrome de déficit en transporteur du glucose de type 1 (GLUT-1). Revue Neurologique. 164(11). 896–901. 6 indexed citations

11.

Moreno, Edgardo, Iria Fernández-Silva, Iban Eduardo, et al.. (2008). Agronomical, genetical and developmental characterization of fs6.4: a Quantitative Trait Locus controlling melon fruit shape.. 101–108. 2 indexed citations

12.

Caño, A., et al.. (2008). Le syndrome de déficit en GLUT-1 ou maladie de De Vivo : à propos d’un cas. Archives de Pédiatrie. 15(8). 1296–1299. 1 indexed citations

13.

Caño, A., Cécile Rouzier, Sophie Monnot, et al.. (2007). Identification of novel mutations in WFS1 and genotype–phenotype correlation in Wolfram syndrome. American Journal of Medical Genetics Part A. 143A(14). 1605–1612. 60 indexed citations

14.

Monnot, Sophie, B. Chabrol, A. Caño, et al.. (2005). Syndrome de Leigh avec déficit en cytochrome c oxydase lié à une mutation homozygote du gène SURF1. Archives de Pédiatrie. 12(5). 568–571. 4 indexed citations

15.

Bosdure, E., A. Caño, Bertrand Roquelaure, et al.. (2004). Oxcarbazépine et syndrome DRESS : un cas pédiatrique révélé par une hépatite fulminante. Archives de Pédiatrie. 11(9). 1073–1077. 27 indexed citations

16.

Caño, A., et al.. (2001). [Partial benign crises in adolescence].. PubMed. 16(7). 329–30. 1 indexed citations

17.

Tarı́n, Juan J. & A. Caño. (1995). Potential health hazards of assisted human reproduction: Effects of manipulations in vitro of human oocytes and embryos on the birthweight of the resultant babies. Human Reproduction. 10(6). 1322–1324. 5 indexed citations

18.

Roquer, Jaume, et al.. (1995). [Spinal cord ischemia indicating aneurysm of the abdominal aorta. Report of three cases].. PubMed. 10(5). 201–4. 3 indexed citations

19.

Baños, V., et al.. (1991). [Enterococcus faecalis bacteremia].. PubMed. 97(4). 133–6. 1 indexed citations

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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