L Heredero

491 total citations
8 papers, 98 citations indexed

About

L Heredero is a scholar working on Genetics, Pediatrics, Perinatology and Child Health and Molecular Biology. According to data from OpenAlex, L Heredero has authored 8 papers receiving a total of 98 indexed citations (citations by other indexed papers that have themselves been cited), including 3 papers in Genetics, 2 papers in Pediatrics, Perinatology and Child Health and 1 paper in Molecular Biology. Recurrent topics in L Heredero's work include Genomics and Rare Diseases (2 papers), Prenatal Screening and Diagnostics (2 papers) and Congenital limb and hand anomalies (1 paper). L Heredero is often cited by papers focused on Genomics and Rare Diseases (2 papers), Prenatal Screening and Diagnostics (2 papers) and Congenital limb and hand anomalies (1 paper). L Heredero collaborates with scholars based in Cuba, Germany and Netherlands. L Heredero's co-authors include Suzana Gispert, Alejandro Hernández, María Luisa Gómez Dorronsoro, Georg Auburger, Astrid Lunkes, J. Beckmann, Guillermo Hernández Orozco, Ana M. Bertoli, Renata Sánchez and Javier Valdés-Hernández and has published in prestigious journals such as Genomics, Journal of Medical Genetics and Human Genetics.

In The Last Decade

L Heredero

7 papers receiving 87 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
L Heredero Cuba 6 29 29 17 16 15 8 98
Taisuke Okada Japan 6 30 1.0× 23 0.8× 6 0.4× 16 1.0× 2 0.1× 18 172
Martin Delatycki Australia 4 19 0.7× 8 0.3× 20 1.2× 11 0.7× 17 1.1× 7 98
Jean‐Michel Pinoit France 7 40 1.4× 13 0.4× 8 0.5× 24 1.5× 27 1.8× 15 147
Zhang Ping China 7 30 1.0× 15 0.5× 7 0.4× 23 1.4× 17 1.1× 11 144
Claire De Barace France 6 28 1.0× 12 0.4× 29 1.7× 25 1.6× 33 2.2× 6 160
Melissa Wesson United States 6 29 1.0× 52 1.8× 21 1.2× 25 1.6× 17 1.1× 10 131
Ahmed N. Sahly Saudi Arabia 8 29 1.0× 18 0.6× 9 0.5× 14 0.9× 22 1.5× 14 96
Jean‐Baptiste Le Pichon United States 8 42 1.4× 16 0.6× 17 1.0× 23 1.4× 48 3.2× 13 160
Masanobu Uchigata Japan 7 33 1.1× 16 0.6× 11 0.6× 42 2.6× 9 0.6× 14 105
Francis T. Hunter United States 4 21 0.7× 22 0.8× 18 1.1× 74 4.6× 7 0.5× 8 155

Countries citing papers authored by L Heredero

Since Specialization
Citations

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

Fields of papers citing papers by L Heredero

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of L Heredero

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

All Works

8 of 8 papers shown
1.
2.
3.
Heutink, Peter, L Heredero, B. A. Oostra, et al.. (1996). Genetic aspects of polydactyly.. PubMed. 28(4). 171–5. 1 indexed citations
4.
Gispert, Suzana, et al.. (1995). Frequency of Delta-F508 Mutation and XV2C/KM19 Haplotypes in Cuban Cystic Fibrosis Families. Human Heredity. 45(1). 55–57. 29 indexed citations
5.
Hernández, Alejandro, Suzana Gispert, Astrid Lunkes, et al.. (1995). Genetic mapping of the spinocerebellar ataxia 2 (SCA2) locus on chromosome 12q23–q24.1. Genomics. 25(2). 433–435. 33 indexed citations
6.
Heredero, L, et al.. (1986). Diagnostico precoz de fenilcetonuria en cuba. (informe preliminar). Revista cubana de pediatría. 58(1). 27–33. 1 indexed citations
7.
Horn, Anton, et al.. (1986). Maternal serum alpha-fetoprotein screening for neural tube defects and other disorders using an ultramicro-ELISA. Human Genetics. 73(1). 60–63. 5 indexed citations
8.
Martı́nez, Gustavo A., et al.. (1977). Haemoglobin Porto Alegre in a Cuban family.. Journal of Medical Genetics. 14(6). 422–425. 6 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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2026