Alejandro Leal

721 total citations
22 papers, 453 citations indexed

About

Alejandro Leal is a scholar working on Cellular and Molecular Neuroscience, Molecular Biology and Genetics. According to data from OpenAlex, Alejandro Leal has authored 22 papers receiving a total of 453 indexed citations (citations by other indexed papers that have themselves been cited), including 9 papers in Cellular and Molecular Neuroscience, 7 papers in Molecular Biology and 5 papers in Genetics. Recurrent topics in Alejandro Leal's work include Hereditary Neurological Disorders (9 papers), Neurological diseases and metabolism (4 papers) and Genetic Neurodegenerative Diseases (4 papers). Alejandro Leal is often cited by papers focused on Hereditary Neurological Disorders (9 papers), Neurological diseases and metabolism (4 papers) and Genetic Neurodegenerative Diseases (4 papers). Alejandro Leal collaborates with scholars based in Costa Rica, Germany and United States. Alejandro Leal's co-authors include Bernd Rautenstrauß, Ramiro Barrantes, André Reis, Thomas E. Ichim, Neil H Riordan, Annette M. Marleau, Amit N. Patel, Constantin A Dasanu, Erik J. Woods and Fabio Solano and has published in prestigious journals such as Nucleic Acids Research, PLoS ONE and The American Journal of Human Genetics.

In The Last Decade

Alejandro Leal

21 papers receiving 443 citations

Peers

Alejandro Leal
Katja Piltti United States
Natalia Lowry United States
I. Snoeck Netherlands
Sarah Wynn United Kingdom
Alejandro Leal
Citations per year, relative to Alejandro Leal Alejandro Leal (= 1×) peers Javier Ganz

Countries citing papers authored by Alejandro Leal

Since Specialization
Citations

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

Fields of papers citing papers by Alejandro Leal

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Alejandro Leal

This figure shows the co-authorship network connecting the top 25 collaborators of Alejandro Leal. A scholar is included among the top collaborators of Alejandro Leal 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 Alejandro Leal. Alejandro Leal 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.
Krey, Ilona, Rami Abou Jamra, Tobias Bartolomaeus, et al.. (2021). Prenatal phenotype of PNKP-related primary microcephaly associated with variants affecting both the FHA and phosphatase domain. European Journal of Human Genetics. 30(1). 101–110. 2 indexed citations
2.
Ruiz-Narváez, Edward, Ana Baylín, Jorge Azofeifa, Alejandro Leal, & Luis Rosero‐Bixby. (2021). Diet and Leukocyte Telomere Length in a Population with Extended Longevity: The Costa Rican Longevity and Healthy Aging Study (CRELES). Nutrients. 13(8). 2585–2585. 11 indexed citations
3.
Leal, Alejandro, et al.. (2020). Mutational survivorship bias: The case of PNKP. PLoS ONE. 15(12). e0237682–e0237682. 6 indexed citations
4.
Rosero‐Bixby, Luis, David H. Rehkopf, William H. Dow, et al.. (2019). Correlates of longitudinal leukocyte telomere length in the Costa Rican Longevity Study of Healthy Aging (CRELES): On the importance of DNA collection and storage procedures. PLoS ONE. 14(10). e0223766–e0223766. 14 indexed citations
5.
Leal, Alejandro, et al.. (2019). DNA repair deficiency in neuropathogenesis: when all roads lead to mitochondria. Translational Neurodegeneration. 8(1). 14–14. 20 indexed citations
6.
Leal, Alejandro, Arif B. Ekici, Steffen Uebe, et al.. (2018). The polynucleotide kinase 3′-phosphatase gene (PNKP) is involved in Charcot-Marie-Tooth disease (CMT2B2) previously related to MED25. Neurogenetics. 19(4). 215–225. 27 indexed citations
7.
8.
Smogavec, Mateja, Juliane Hoyer, Damien Lederer, et al.. (2016). Eight further individuals with intellectual disability and epilepsy carrying bi-allelic CNTNAP2 aberrations allow delineation of the mutational and phenotypic spectrum. Journal of Medical Genetics. 53(12). 820–827. 41 indexed citations
9.
Leal, Alejandro, et al.. (2014). ENSEÑANZA Y APRENDIZAJE DE LA NATURALEZA DE LA CIENCIA, LA TECNOLOGÍA Y LA SOCIEDAD (NdCyTS) EN PROFESORES UNIVERSITARIOS DE LA FACULTAD DE CIENCIAS DE LA EDUCACIÓN DE LA UNIVERSIDAD DEL TOLIMA.
10.
Leal, Alejandro. (2014). Genetics of hereditary motor and sensory neuropathy and the Costa Rican contribution. Revista de Biología Tropical. 1(2). 475–475. 1 indexed citations
11.
Leal, Alejandro, et al.. (2014). A Costa Rican family affected with Charcot-Marie-Tooth disease due to the myelin protein zero (MPZ) p.Thr124Met mutation shares the Belgian haplotype. Revista de Biología Tropical. 62(4). 1285–1285. 4 indexed citations
12.
Ichim, Thomas E., Doru T Alexandrescu, Fabio Solano, et al.. (2009). Mesenchymal stem cells as anti-inflammatories: Implications for treatment of Duchenne muscular dystrophy. Cellular Immunology. 260(2). 75–82. 122 indexed citations
13.
Cháves, Gerardo, Adrián García‐Rodríguez, Alejandra Núñez‐de la Mora, & Alejandro Leal. (2009). A new species of dink frog (Anura: Eleutherodactylidae: Diasporus) from Cordillera de Talamanca, Costa Rica. Zootaxa. 2088(1). 10 indexed citations
14.
Leal, Alejandro, et al.. (2008). Immune effects of mesenchymal stem cells: Implications for Charcot–Marie–Tooth disease. Cellular Immunology. 253(1-2). 11–15. 11 indexed citations
15.
Berghoff, Martin, Alejandro Leal, Bernal Morera-Brenes, et al.. (2008). Late onset autosomal dominant Charcot–Marie–Tooth 2 neuropathy in a Costa Rican family. Neurological Research. 31(3). 283–288. 3 indexed citations
16.
Berghoff, Martin, Alejandro Leal, Bernal Morera-Brenes, et al.. (2004). Clinical and electrophysiological characteristics of autosomal recessive axonal Charcot-Marie-Tooth disease (ARCMT2B) that maps to chromosome 19q13.3. Neuromuscular Disorders. 14(5). 301–306. 14 indexed citations
17.
Leal, Alejandro, Sabine Endele, Kathrin Huehne, et al.. (2003). A novel myosin heavy chain gene in human chromosome 19q13.3. Gene. 312. 165–171. 53 indexed citations
18.
Leal, Alejandro, Martin Berghoff, Gerardo Del Valle, et al.. (2003). Charcot-Marie-Tooth disease: a novel Tyr145Ser mutation in the myelin protein zero ( MPZ , P0 ) gene causes different phenotypes in homozygous and heterozygous carriers within one family. Neurogenetics. 4(4). 191–197. 14 indexed citations
19.
Leal, Alejandro, Bernal Morera-Brenes, Gerardo Del Valle, et al.. (2001). A Second Locus for an Axonal Form of Autosomal Recessive Charcot-Marie-Tooth Disease Maps to Chromosome 19q13.3. The American Journal of Human Genetics. 68(1). 269–274. 49 indexed citations
20.
Garavello, Júlio César, Odete Rocha, Evaldo Luiz Gaeta Espíndola, Arnola C. Rietzler, & Alejandro Leal. (1998). Diversity of fauna in the interdunal lakes of "Lencois Maranhenses": II- The ichthyofauna. Anais da Academia Brasileira de Ciências. 70(4). 797–803. 4 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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