Ana María Cobo

1.5k total citations
28 papers, 979 citations indexed

About

Ana María Cobo is a scholar working on Molecular Biology, Cellular and Molecular Neuroscience and Neurology. According to data from OpenAlex, Ana María Cobo has authored 28 papers receiving a total of 979 indexed citations (citations by other indexed papers that have themselves been cited), including 19 papers in Molecular Biology, 15 papers in Cellular and Molecular Neuroscience and 5 papers in Neurology. Recurrent topics in Ana María Cobo's work include Genetic Neurodegenerative Diseases (13 papers), Mitochondrial Function and Pathology (9 papers) and Muscle Physiology and Disorders (4 papers). Ana María Cobo is often cited by papers focused on Genetic Neurodegenerative Diseases (13 papers), Mitochondrial Function and Pathology (9 papers) and Muscle Physiology and Disorders (4 papers). Ana María Cobo collaborates with scholars based in Spain, France and Italy. Ana María Cobo's co-authors include Juan José Poza, Montserrat Baiget, Adolfo López de Munaín, Loreto Martorell, Djamel Grid, J J Poza, Jill Dixon, Cornelia Daumer‐Haas, Martijn H. Breuning and Dagmar Wieczorek and has published in prestigious journals such as Nature Genetics, Neurology and Annals of Neurology.

In The Last Decade

Ana María Cobo

28 papers receiving 960 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Ana María Cobo Spain 14 703 393 252 193 138 28 979
Robyn Labrum United Kingdom 14 488 0.7× 400 1.0× 84 0.3× 145 0.8× 175 1.3× 21 772
Simon Hammans United Kingdom 25 1.4k 2.0× 425 1.1× 142 0.6× 59 0.3× 211 1.5× 45 1.7k
H G Harley United Kingdom 18 778 1.1× 790 2.0× 215 0.9× 80 0.4× 298 2.2× 35 1.0k
Ann Löfgren Belgium 13 722 1.0× 502 1.3× 189 0.8× 25 0.1× 126 0.9× 16 1.1k
Roland Spiegel Switzerland 12 654 0.9× 595 1.5× 140 0.6× 92 0.5× 295 2.1× 28 950
Joline Dalton United States 10 898 1.3× 817 2.1× 98 0.4× 125 0.6× 290 2.1× 18 1.1k
Barbara Leube Germany 16 269 0.4× 504 1.3× 204 0.8× 44 0.2× 492 3.6× 27 989
Roula Ghaoui Australia 10 300 0.4× 131 0.3× 115 0.5× 96 0.5× 83 0.6× 22 486
E. Peter Bosch United States 16 327 0.5× 179 0.5× 73 0.3× 53 0.3× 187 1.4× 21 688
A. Löfgren Belgium 18 1.1k 1.6× 878 2.2× 187 0.7× 18 0.1× 304 2.2× 37 1.8k

Countries citing papers authored by Ana María Cobo

Since Specialization
Citations

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

Fields of papers citing papers by Ana María Cobo

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Ana María Cobo. 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 Ana María Cobo. The network helps show where Ana María Cobo may publish in the future.

Co-authorship network of co-authors of Ana María Cobo

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

All Works

20 of 20 papers shown
1.
Savarese, Marco, Johanna Palmio, Juan José Poza, et al.. (2019). Actininopathy: A new muscular dystrophy caused by ACTN2 dominant mutations. Annals of Neurology. 85(6). 899–906. 26 indexed citations
2.
Mazón, Marı́a J., Francisco Barros, Pilar de la Peña, et al.. (2011). Screening for mutations in Spanish families with myotonia. Functional analysis of novel mutations in CLCN1 gene. Neuromuscular Disorders. 22(3). 231–243. 30 indexed citations
3.
Sacconi, Sabrina, Léonard Feasson, Jean Christophe Antoine, et al.. (2011). A novel CRYAB mutation resulting in multisystemic disease. Neuromuscular Disorders. 22(1). 66–72. 72 indexed citations
4.
Dauwerse, Johannes G., Jill Dixon, Saskia Seland, et al.. (2010). Mutations in genes encoding subunits of RNA polymerases I and III cause Treacher Collins syndrome. Nature Genetics. 43(1). 20–22. 243 indexed citations
5.
Cobo, Ana María, et al.. (2010). Clinical Repercussions of Analytical Interferences Due to Aldosterone Antagonists in Digoxin Immunoassays: An Assessment. Therapeutic Drug Monitoring. 32(2). 169–176. 3 indexed citations
6.
Cosme, Ángel, et al.. (2008). Características clínicas y moleculares de una familia con síndrome de neoplasia endocrina múltiple tipo 1. Gastroenterología y Hepatología. 31(10). 637–642. 3 indexed citations
7.
Moradin, Neda, et al.. (2008). CTG Expansion & Haplotype Analysis in DM1 Gene in Healthy Iranian Population. Canadian Journal of Neurological Sciences / Journal Canadien des Sciences Neurologiques. 35(2). 216–219. 7 indexed citations
8.
Martorell, Loreto, et al.. (2006). Prenatal diagnosis in myotonic dystrophy type 1. Thirteen years of experience: implications for reproductive counselling in DM1 families. Prenatal Diagnosis. 27(1). 68–72. 31 indexed citations
9.
Andoín, Nagore García de, et al.. (2005). A neonatal form of Steinert's myotonic dystrophy in twins after in vitro fertilization. Fertility and Sterility. 84(3). 756.e5–756.e8. 5 indexed citations
10.
Cobo, Ana María, Amets Sáenz, Juan José Poza, et al.. (2004). A Common Haplotype Associated with the Basque 2362AG-TCATCT Mutation in the Muscular Calpain-3 Gene. Human Biology. 76(5). 731–741. 12 indexed citations
11.
Donaldson, Michael, Jeffrey L. Jensen, Martin Tristani‐Firouzi, et al.. (2003). PIP(2) binding residues of Kir2.1 are common targets of mutations causing Andersen syndrome. HAL (Le Centre pour la Communication Scientifique Directe). 1 indexed citations
12.
Donaldson, Matthew R., Judy L. Jensen, Martin Tristani‐Firouzi, et al.. (2003). PIP 2 binding residues of Kir2.1 are common targets of mutations causing Andersen syndrome. Neurology. 60(11). 1811–1816. 137 indexed citations
13.
Poza, Juan José, Ana María Cobo, Miguel Urtasun, et al.. (1999). Autosomal dominant lateral temporal epilepsy: Clinical and genetic study of a large basque pedigree linked to chromosome 10q. Annals of Neurology. 45(2). 182–188. 103 indexed citations
14.
Sáenz, Amets, Juan Carlos Galán, Christophe Caloustian, et al.. (1999). Autosomal Dominant Nocturnal Frontal Lobe Epilepsy in a Spanish Family With a Ser252Phe Mutation in the CHRNA4 Gene. Archives of Neurology. 56(8). 1004–1004. 71 indexed citations
15.
Munaín, Adolfo López de, Ana María Cobo, Amets Sáenz, et al.. (1996). Frequency of intergenerational contractions of the CTG repeats in myotonic dystrophy. Genetic Epidemiology. 13(5). 483–487. 12 indexed citations
16.
Ashizawa, Tetsuo, Maria Anvret, Montserrat Baiget, et al.. (1994). Characteristics of intergenerational contractions of the CTG repeat in myotonic dystrophy.. PubMed. 54(3). 414–23. 99 indexed citations
17.
Munaín, Adolfo López de, José Ignacio Emparanza, J J Poza, et al.. (1993). Prevalence of myotonic dystrophy in Guipuzcoa (Basque Country, Spain). Neurology. 43(8). 1573–1573. 38 indexed citations
18.
Melchionda, Salvatore, Ana María Cobo, Massimo Gennarelli, et al.. (1992). Expansion of the myotonic dystrophy gene in Italian and Spanish patients.. Journal of Medical Genetics. 29(11). 789–790. 7 indexed citations
19.
Gennarelli, Massimo, Giuseppe Novelli, Ana María Cobo, Montserrat Baiget, & Bruno Dallapiccola. (1991). 3? creatine kinase (M-type) polymorphisms linked to myotonic dystrophy in Italian and Spanish populations. Human Genetics. 87(6). 654–6. 12 indexed citations
20.
Cobo, Ana María, et al.. (1960). Inhibition of gastric secretion by acid in the antrum.. PubMed. 10. 155–60. 13 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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