Juana Barceló

3.0k total citations · 1 hit paper
13 papers, 2.4k citations indexed

About

Juana Barceló is a scholar working on Molecular Biology, Cellular and Molecular Neuroscience and Neurology. According to data from OpenAlex, Juana Barceló has authored 13 papers receiving a total of 2.4k indexed citations (citations by other indexed papers that have themselves been cited), including 10 papers in Molecular Biology, 7 papers in Cellular and Molecular Neuroscience and 3 papers in Neurology. Recurrent topics in Juana Barceló's work include Genetic Neurodegenerative Diseases (7 papers), Mitochondrial Function and Pathology (4 papers) and Cancer therapeutics and mechanisms (2 papers). Juana Barceló is often cited by papers focused on Genetic Neurodegenerative Diseases (7 papers), Mitochondrial Function and Pathology (4 papers) and Cancer therapeutics and mechanisms (2 papers). Juana Barceló collaborates with scholars based in Canada, United States and Portugal. Juana Barceló's co-authors include Robert G. Korneluk, Catherine Tsilfidis, Catherine Neville, Mani S. Mahadevan, Kim O'Hoy, Chris T. Amemiya, Bé Wieringa, Luc A. Sabourin, Gary Shutler and S. Leblond and has published in prestigious journals such as Science, Proceedings of the National Academy of Sciences and Nature Genetics.

In The Last Decade

Juana Barceló

13 papers receiving 2.4k citations

Hit Papers

Myotonic Dystrophy Mutation: an Unstable CTG Repeat in th... 1992 2026 2003 2014 1992 400 800 1.2k
What are hit papers?

Hit papers significantly outperform the citation benchmark for their cohort. A paper qualifies if it has ≥500 total citations, achieves ≥1.5× the top-1% citation threshold for papers in the same subfield and year (this is the minimum needed to enter the top 1%, not the average within it), or reaches the top citation threshold in at least one of its specific research topics.

  1. Myotonic Dystrophy Mutation: an Unstable CTG Repeat in the 3′ Untranslated region of the Gene
    1992 1.3k citations Mani S. Mahadevan, Catherine Tsilfidis et al. Science profile →

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Juana Barceló Canada 10 2.1k 1.6k 537 291 217 13 2.4k
Brigit E. Riley United States 12 1.3k 0.6× 393 0.2× 311 0.6× 124 0.4× 15 0.1× 16 1.7k
Karen Sitney United States 9 679 0.3× 264 0.2× 538 1.0× 83 0.3× 18 0.1× 11 1.4k
Alexandre Mezghrani France 17 1.2k 0.6× 408 0.3× 54 0.1× 82 0.3× 98 0.5× 27 1.7k
Alexander Reuter Germany 17 670 0.3× 137 0.1× 197 0.4× 91 0.3× 76 0.4× 25 1.3k
John M. Jenco United States 9 1.1k 0.5× 248 0.2× 284 0.5× 100 0.3× 34 0.2× 11 1.6k
Gregor Schaffar Germany 11 1.3k 0.6× 703 0.4× 192 0.4× 73 0.3× 20 0.1× 15 1.6k
Takahiro Fujimoto Japan 23 716 0.3× 154 0.1× 84 0.2× 124 0.4× 57 0.3× 61 1.3k
Jenny Carmichael United Kingdom 10 952 0.5× 728 0.5× 232 0.4× 118 0.4× 10 0.0× 15 1.2k
Lynn Bedford United Kingdom 18 1.1k 0.5× 165 0.1× 197 0.4× 126 0.4× 21 0.1× 21 1.6k
Jennifer J. Carlisle Michel United States 14 1.7k 0.8× 164 0.1× 39 0.1× 96 0.3× 283 1.3× 14 2.0k

Countries citing papers authored by Juana Barceló

Since Specialization
Citations

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

Fields of papers citing papers by Juana Barceló

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Juana Barceló

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

All Works

13 of 13 papers shown
1.
Marques, C. Joana, Duarte Pignatelli, Juana Barceló, et al.. (2009). Mutational Characterization of Steroid 21-Hydroxylase Gene in Portuguese patients with Congenital Adrenal Hyperplasia. Experimental and Clinical Endocrinology & Diabetes. 118(8). 505–512. 9 indexed citations
2.
Vögler, Oliver, Juana Barceló, Catalina Ribas, & Pablo V. Escribá. (2008). Membrane interactions of G proteins and other related proteins. Biochimica et Biophysica Acta (BBA) - Biomembranes. 1778(7-8). 1640–1652. 93 indexed citations
3.
Oliveira, João Paulo, Susana Ferreira, Juana Barceló, et al.. (2008). Effect of single‐nucleotide polymorphisms of the 5′ untranslated region of the human α‐galactosidase gene on enzyme activity, and their frequencies in Portuguese caucasians. Journal of Inherited Metabolic Disease. 31(S2). 247–253. 12 indexed citations
4.
Pommier, Yves, Juana Barceló, V. Ashutosh Rao, et al.. (2006). Repair of Topoisomerase I‐Mediated DNA Damage. Progress in nucleic acid research and molecular biology. 81. 179–229. 233 indexed citations
5.
Zhang, Hongliang, Juana Barceló, Glenda Kohlhagen, et al.. (2001). Human mitochondrial topoisomerase I. Proceedings of the National Academy of Sciences. 98(19). 10608–10613. 167 indexed citations
6.
Rajcan‐Separovic, Evica, Juana Barceló, & Robert G. Korneluk. (1998). Fluorescence in situ hybridization analysis of the replication properties of the myotonic dystrophy protein kinase (DMPK) gene region. Cytogenetic and Genome Research. 82(3-4). 247–250. 1 indexed citations
7.
Cheng, Suzanne, Juana Barceló, & Robert G. Korneluk. (1996). Characterization of large CTG repeat expansions in myotonic dystrophy alleles using PCR. Human Mutation. 7(4). 304–310. 29 indexed citations
8.
Neville, Catherine, et al.. (1994). High resolution genetic analysis suggests one ancestral predisposing haplotype for the origin of the myotonic dystrophy mutation. Human Molecular Genetics. 3(1). 45–51. 77 indexed citations
9.
Soria, José Manuel, David V.C. Brito, Juana Barceló, et al.. (1994). Severe Homozygous Protein C Deficiency: Identification of a Splice Site Missense Mutation (184, Q → H) in Exon 7 of the Protein C Gene. Thrombosis and Haemostasis. 72(1). 65–69. 6 indexed citations
10.
Barceló, Juana, Mani S. Mahadevan, Catherine Tsilfidis, Alex MacKenzie, & Robert G. Korneluk. (1993). Intergenerational stability of the myotonic dystrophy protomutation. Human Molecular Genetics. 2(6). 705–709. 67 indexed citations
11.
O'Hoy, Kim, Catherine Tsilfidis, Mani S. Mahadevan, et al.. (1993). Reduction in Size of the Myotonic Dystrophy Trinucleotide Repeat Mutation During Transmission. Science. 259(5096). 809–812. 87 indexed citations
12.
Tsilfidis, Catherine, Alex MacKenzie, Gabrielle Mettler, Juana Barceló, & Robert G. Korneluk. (1992). Correlation between CTG trinucleotide repeat length and frequency of severe congenital myotonic dystrophy. Nature Genetics. 1(3). 192–195. 274 indexed citations
13.
Mahadevan, Mani S., Catherine Tsilfidis, Luc A. Sabourin, et al.. (1992). Myotonic Dystrophy Mutation: an Unstable CTG Repeat in the 3′ Untranslated region of the Gene. Science. 255(5049). 1253–1255. 1340 indexed citations breakdown →

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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