Jorge Amigo

2.0k total citations
51 papers, 1.4k citations indexed

About

Jorge Amigo is a scholar working on Genetics, Molecular Biology and Pathology and Forensic Medicine. According to data from OpenAlex, Jorge Amigo has authored 51 papers receiving a total of 1.4k indexed citations (citations by other indexed papers that have themselves been cited), including 35 papers in Genetics, 33 papers in Molecular Biology and 4 papers in Pathology and Forensic Medicine. Recurrent topics in Jorge Amigo's work include Genetic Associations and Epidemiology (15 papers), Forensic and Genetic Research (11 papers) and Genomics and Rare Diseases (9 papers). Jorge Amigo is often cited by papers focused on Genetic Associations and Epidemiology (15 papers), Forensic and Genetic Research (11 papers) and Genomics and Rare Diseases (9 papers). Jorge Amigo collaborates with scholars based in Spain, Saudi Arabia and United States. Jorge Amigo's co-authors include Ángel Carracedo, Christopher Phillips, Antonio Salas, Tomás F. Pena, Juan C. Pichel, M.V. Lareu, Diego Villar, Nuria Pescador, Luis del Peso and Alberto Gómez‐Carballa and has published in prestigious journals such as Nucleic Acids Research, Bioinformatics and Gastroenterology.

In The Last Decade

Jorge Amigo

50 papers receiving 1.4k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Jorge Amigo Spain 21 797 662 159 108 95 51 1.4k
Jeroen F. J. Laros Netherlands 21 1.2k 1.5× 772 1.2× 251 1.6× 154 1.4× 58 0.6× 48 1.9k
Eugene Kulesha United Kingdom 13 1.4k 1.7× 432 0.7× 131 0.8× 68 0.6× 27 0.3× 13 1.8k
Lira Mamanova United Kingdom 11 878 1.1× 599 0.9× 226 1.4× 113 1.0× 70 0.7× 16 1.4k
Stefano Castellana Italy 16 616 0.8× 259 0.4× 109 0.7× 57 0.5× 41 0.4× 73 952
Frida Belinky United States 15 838 1.1× 212 0.3× 144 0.9× 80 0.7× 20 0.2× 20 1.2k
Fuli Yu United States 22 694 0.9× 756 1.1× 176 1.1× 28 0.3× 51 0.5× 41 1.5k
Paul L. Auer United States 17 716 0.9× 466 0.7× 184 1.2× 29 0.3× 50 0.5× 42 1.4k
Daniel E. Newburger United States 12 2.1k 2.6× 365 0.6× 192 1.2× 37 0.3× 98 1.0× 15 2.4k
Artem Tarasov Germany 4 1.0k 1.3× 330 0.5× 214 1.3× 92 0.9× 18 0.2× 7 1.6k
Brad Marshall United States 4 954 1.2× 209 0.3× 146 0.9× 64 0.6× 23 0.2× 4 1.4k

Countries citing papers authored by Jorge Amigo

Since Specialization
Citations

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

Fields of papers citing papers by Jorge Amigo

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Jorge Amigo

This figure shows the co-authorship network connecting the top 25 collaborators of Jorge Amigo. A scholar is included among the top collaborators of Jorge Amigo 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 Jorge Amigo. Jorge Amigo 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.
Bartolomé, Carolina, Ana L. García‐Pérez, Karine Monceau, et al.. (2024). Prevalence and population genetic analyses of parasites in invasive Vespa velutina and native Hymenoptera. Journal of Invertebrate Pathology. 207. 108203–108203.
2.
Ceballos, Francisco C., Pablo Serrano‐Lorenzo, Laura Bermejo‐Guerrero, et al.. (2024). Clinical and Genetic Analysis of Patients With TK2 Deficiency. Neurology Genetics. 10(2). e200138–e200138. 4 indexed citations
3.
Bonjoch, Laia, Ceres Fernández–Rozadilla, Jorge Amigo, et al.. (2023). BMPR2 as a Novel Predisposition Gene for Hereditary Colorectal Polyposis. Gastroenterology. 165(1). 162–172.e5. 10 indexed citations
4.
Brea‐Fernández, Alejandro, Jorge Amigo, Montse Fernández‐Prieto, et al.. (2022). Trio-based exome sequencing reveals a high rate of the de novo variants in intellectual disability. European Journal of Human Genetics. 30(8). 938–945. 13 indexed citations
5.
Fernández–Rozadilla, Ceres, Jorge Amigo, José Cameselle‐Teijeiro, et al.. (2021). Exome sequencing of early-onset patients supports genetic heterogeneity in colorectal cancer. Scientific Reports. 11(1). 11135–11135. 7 indexed citations
6.
Puente, M. de la, Catarina Xavier, Jorge Amigo, et al.. (2020). Broadening the Applicability of a Custom Multi-Platform Panel of Microhaplotypes: Bio-Geographical Ancestry Inference and Expanded Reference Data. Frontiers in Genetics. 11. 581041–581041. 20 indexed citations
7.
Bartolomé, Carolina, Beatriz Sobrino, Jorge Amigo, et al.. (2020). Longitudinal analysis on parasite diversity in honeybee colonies: new taxa, high frequency of mixed infections and seasonal patterns of variation. Scientific Reports. 10(1). 10454–10454. 25 indexed citations
8.
Puente, M. de la, Christopher Phillips, Catarina Xavier, et al.. (2019). Building a custom large-scale panel of novel microhaplotypes for forensic identification using MiSeq and Ion S5 massively parallel sequencing systems. Forensic Science International Genetics. 45. 102213–102213. 61 indexed citations
9.
Salas, Antonio, Jacobo Pardo‐Seco, Ruth Barral‐Arca, et al.. (2018). Whole Exome Sequencing Identifies New Host Genomic Susceptibility Factors in Empyema Caused by Streptococcus pneumoniae in Children: A Pilot Study. Genes. 9(5). 240–240. 10 indexed citations
10.
Cacheiro, Pilar, Andrés Ordóñez‐Ugalde, Beatriz Quintáns, et al.. (2017). Evaluating the Calling Performance of a Rare Disease NGS Panel for Single Nucleotide and Copy Number Variants. Molecular Diagnosis & Therapy. 21(3). 303–313. 6 indexed citations
11.
Pichel, Juan C., et al.. (2016). SparkBWA: Speeding Up the Alignment of High-Throughput DNA Sequencing Data. PLoS ONE. 11(5). e0155461–e0155461. 74 indexed citations
12.
Álvarez‐Mora, María Isabel, Rosa Calvo, Irene Madrigal, et al.. (2016). Comprehensive molecular testing in patients with high functioning autism spectrum disorder. Mutation research. Fundamental and molecular mechanisms of mutagenesis. 784-785. 46–52. 22 indexed citations
13.
Suárez‐Rama, Jose Javier, Manuel Arrojo, Beatriz Sobrino, et al.. (2015). Resequencing and association analysis of coding regions at twenty candidate genes suggest a role for rare risk variation at AKAP9 and protective variation at NRXN1 in schizophrenia susceptibility. Journal of Psychiatric Research. 66-67. 38–44. 14 indexed citations
14.
Phillips, Christopher, Jorge Amigo, Ángel Carracedo, & M.V. Lareu. (2015). Tetra-allelic SNPs: Informative forensic markers compiled from public whole-genome sequence data. Forensic Science International Genetics. 19. 100–106. 39 indexed citations
15.
Allegue, Catarina, Mónica Coll, Jesús Matés, et al.. (2015). Genetic Analysis of Arrhythmogenic Diseases in the Era of NGS: The Complexity of Clinical Decision-Making in Brugada Syndrome. PLoS ONE. 10(7). e0133037–e0133037. 42 indexed citations
16.
Gómez‐Carballa, Alberto, Jacobo Pardo‐Seco, Jorge Amigo, Federico Martinón‐Torres, & Antonio Salas. (2015). Mitogenomes from The 1000 Genome Project Reveal New Near Eastern Features in Present-Day Tuscans. PLoS ONE. 10(3). e0119242–e0119242. 13 indexed citations
17.
Pardo‐Seco, Jacobo, Jorge Amigo, Wenceslao González–Manteiga, & Antonio Salas. (2013). A Generalized Model to Estimate the Statistical Power in Mitochondrial Disease Studies Involving 2×k Tables. PLoS ONE. 8(9). e73567–e73567. 11 indexed citations
18.
Amigo, Jorge, Antonio Salas, & Christopher Phillips. (2011). ENGINES: exploring single nucleotide variation in entire human genomes. BMC Bioinformatics. 12(1). 105–105. 29 indexed citations
19.
Chang, Chia Lin, et al.. (2010). Adaptive selection of an incretin gene in Eurasian populations. Genome Research. 21(1). 21–32. 12 indexed citations
20.
Amigo, Jorge, et al.. (2008). The SNPforID browser: an online tool for query and display of frequency data from the SNPforID project. International Journal of Legal Medicine. 122(5). 435–440. 37 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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