M.J. Trujillo

724 total citations
24 papers, 500 citations indexed

About

M.J. Trujillo is a scholar working on Molecular Biology, Pediatrics, Perinatology and Child Health and Ophthalmology. According to data from OpenAlex, M.J. Trujillo has authored 24 papers receiving a total of 500 indexed citations (citations by other indexed papers that have themselves been cited), including 13 papers in Molecular Biology, 5 papers in Pediatrics, Perinatology and Child Health and 4 papers in Ophthalmology. Recurrent topics in M.J. Trujillo's work include Retinal Development and Disorders (9 papers), Prenatal Screening and Diagnostics (5 papers) and Retinal Diseases and Treatments (4 papers). M.J. Trujillo is often cited by papers focused on Retinal Development and Disorders (9 papers), Prenatal Screening and Diagnostics (5 papers) and Retinal Diseases and Treatments (4 papers). M.J. Trujillo collaborates with scholars based in Spain, Colombia and Canada. M.J. Trujillo's co-authors include Carmen Ayuso, Marta Rodríguez de Alba, Isabel Lorda‐Sánchez, María González‐González, Joaquín Diaz-Recasens, Keith Warriner, Carmen Viana Ramos, Carmen Ramos, Blanca Garcı́a-Sandoval and Dan Diego‐Álvarez and has published in prestigious journals such as SHILAP Revista de lepidopterología, Neurology and Human Reproduction.

In The Last Decade

M.J. Trujillo

24 papers receiving 467 citations

Peers

M.J. Trujillo
Ariel Kantor United Kingdom
Chuan Chen China
K. S. Lavappa United States
A. Lefèvre France
Qingran Kong China
Yuanfang Zhu China
Kei Tominaga Japan
Kazue Nishioka Japan
Ariel Kantor United Kingdom
M.J. Trujillo
Citations per year, relative to M.J. Trujillo M.J. Trujillo (= 1×) peers Ariel Kantor

Countries citing papers authored by M.J. Trujillo

Since Specialization
Citations

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

Fields of papers citing papers by M.J. Trujillo

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by M.J. Trujillo. 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 M.J. Trujillo. The network helps show where M.J. Trujillo may publish in the future.

Co-authorship network of co-authors of M.J. Trujillo

This figure shows the co-authorship network connecting the top 25 collaborators of M.J. Trujillo. A scholar is included among the top collaborators of M.J. Trujillo 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 M.J. Trujillo. M.J. Trujillo 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.
2.
Trujillo, M.J., et al.. (2021). Asistencia a clase virtual en directo como factor de éxito académico en estudios de posgrado a distancia. Minerva Digital Library (Universidad EAN). 9(1). 1 indexed citations
3.
4.
Gamundi, María José, Imma Hernán, M.J. Trujillo, et al.. (2007). High prevalence of mutations in peripherin/RDS in autosomal dominant macular dystrophies in a Spanish population.. PubMed. 13. 1031–7. 26 indexed citations
5.
Lorda‐Sánchez, Isabel, Dan Diego‐Álvarez, Carmen Ayuso, et al.. (2005). Trisomy 2 due to a 3:1 segregation in an abortion studied by QF‐PCR and CGH. Prenatal Diagnosis. 25(10). 934–938. 18 indexed citations
6.
Diego‐Álvarez, Dan, Maria García‐Hoyos, M.J. Trujillo, et al.. (2005). Application of quantitative fluorescent PCR with short tandem repeat markers to the study of aneuploidies in spontaneous miscarriages. Human Reproduction. 20(5). 1235–1243. 45 indexed citations
7.
García‐Hoyos, Maria, Diego Cantalapiedra, Pilar Esteve, et al.. (2004). Evaluation of SFRP1 as a candidate for human retinal dystrophies.. PubMed. 10. 426–31. 22 indexed citations
8.
Lorda‐Sánchez, Isabel, M.J. Trujillo, Pilar Gómez‐Garre, et al.. (2003). Turner phenotype in a girl with a 45,X/46,XX/47,XX,+18 mosaicism. American Journal of Medical Genetics Part A. 121A(1). 20–24. 6 indexed citations
9.
González‐González, María, M.J. Trujillo, Marta Rodríguez de Alba, et al.. (2003). Huntington disease–unaffected fetus diagnosed from maternal plasma using QF‐PCR. Prenatal Diagnosis. 23(3). 232–234. 67 indexed citations
10.
González‐González, María, M.J. Trujillo, Marta Rodríguez de Alba, & Carmen Viana Ramos. (2003). Early Huntington disease prenatal diagnosis by maternal semiquantitative fluorescent-PCR. Neurology. 60(7). 1214–1215. 31 indexed citations
11.
González‐González, María, M.J. Trujillo, Marta Rodríguez de Alba, et al.. (2002). Prenatal detection of a cystic fibrosis mutation in fetal DNA from maternal plasma. Prenatal Diagnosis. 22(10). 946–948. 107 indexed citations
12.
Trujillo, M.J., et al.. (2001). Allergy to calcitonin. Allergy. 56(8). 801–801. 4 indexed citations
13.
Trujillo, M.J., et al.. (2000). Mutación Asp-190-Tyr en el gen de la rodopsina en una familia española afectada de retinosis pigmentaria autosómica dominante. Medicina Clínica. 115(18). 699–703. 1 indexed citations
14.
Trujillo, M.J., Blanca Garcı́a-Sandoval, Isabel Lorda‐Sánchez, et al.. (2000). Ser186Pro mutation of RHO gene in a Spanish autosomal dominant retinitis pigmentosa (ADRP) family. Ophthalmic Genetics. 21(4). 251–256. 1 indexed citations
15.
Lorda‐Sánchez, Isabel, Raúl Sanz, M.J. Trujillo, et al.. (2000). Choroideremia, sensorineural deafness, and primary ovarian failure in a woman with a balanced X-4 translocation. Ophthalmic Genetics. 21(3). 185–189. 29 indexed citations
16.
Lorda‐Sánchez, Isabel, M.J. Trujillo, Ascensión Giménez, et al.. (1999). Retinitis pigmentosa, mental retardation, marked short stature, and brachydactyly in two sibs. Ophthalmic Genetics. 20(2). 127–131. 4 indexed citations
17.
Cuevas, José M., et al.. (1999). Identification of three novel mutations in the MYO7A gene. Human Mutation. 14(2). 181–181. 15 indexed citations
18.
Ayuso, Carmen, Blanca Garcı́a-Sandoval, M.J. Trujillo, et al.. (1996). G106R rhodopsin mutation is also present in Spanish ADRP patients. Ophthalmic Genetics. 17(3). 95–101. 9 indexed citations
19.
Ayuso, Carmen, M.J. Trujillo, Mercedes Robledo, et al.. (1996). Novel rhodopsin mutation in an autosomal dominant retinitis pigmentosa family: phenotypic variation in both heterozygote and homozygote Val137Met mutant patients. Human Genetics. 98(1). 51–54. 20 indexed citations
20.
Trujillo, M.J., et al.. (1995). Polymorphic variations in peripherin-RDS gene in the Spanish population.. PubMed. 38(4). 225–7. 1 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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