M. J. Barceló

1.3k total citations
36 papers, 951 citations indexed

About

M. J. Barceló is a scholar working on Genetics, Molecular Biology and Surgery. According to data from OpenAlex, M. J. Barceló has authored 36 papers receiving a total of 951 indexed citations (citations by other indexed papers that have themselves been cited), including 26 papers in Genetics, 19 papers in Molecular Biology and 15 papers in Surgery. Recurrent topics in M. J. Barceló's work include Neurogenetic and Muscular Disorders Research (21 papers), RNA modifications and cancer (13 papers) and Congenital Anomalies and Fetal Surgery (12 papers). M. J. Barceló is often cited by papers focused on Neurogenetic and Muscular Disorders Research (21 papers), RNA modifications and cancer (13 papers) and Congenital Anomalies and Fetal Surgery (12 papers). M. J. Barceló collaborates with scholars based in Spain, Palestinian Territory and United States. M. J. Barceló's co-authors include Montserrat Baiget, Eduardo F. Tizzano, Sara Larriba, Ivon Cuscó, Lluís Bassas, A. Mata, Francesc Vigués, Lluís Bassas, Laura Alías and Rebeca Martínez‐Hernández and has published in prestigious journals such as Neurology, Scientific Reports and Journal of Bacteriology.

In The Last Decade

M. J. Barceló

35 papers receiving 941 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
M. J. Barceló Spain 17 680 535 294 132 88 36 951
Bärbel Brunswig‐Spickenheier Germany 16 259 0.4× 140 0.3× 68 0.2× 103 0.8× 52 0.6× 25 598
Huitao Xu China 10 492 0.7× 222 0.4× 127 0.4× 231 1.8× 17 0.2× 10 731
Yunchuan Ding United Kingdom 10 413 0.6× 173 0.3× 206 0.7× 85 0.6× 4 0.0× 12 785
Mehrdad Noruzinia Iran 15 443 0.7× 80 0.1× 25 0.1× 122 0.9× 219 2.5× 71 810
Behnam Ebrahimi United States 14 274 0.4× 83 0.2× 97 0.3× 88 0.7× 10 0.1× 34 764
H. Li China 12 189 0.3× 40 0.1× 61 0.2× 97 0.7× 67 0.8× 38 578
Min Ding China 12 295 0.4× 137 0.3× 37 0.1× 169 1.3× 46 0.5× 26 623
Yuta Ito Japan 13 131 0.2× 97 0.2× 53 0.2× 37 0.3× 12 0.1× 53 554
Lihua Sun China 18 231 0.3× 65 0.1× 52 0.2× 97 0.7× 377 4.3× 43 802

Countries citing papers authored by M. J. Barceló

Since Specialization
Citations

This map shows the geographic impact of M. J. 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 M. J. Barceló 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. Barceló more than expected).

Fields of papers citing papers by M. J. Barceló

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

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

This figure shows the co-authorship network connecting the top 25 collaborators of M. J. Barceló. A scholar is included among the top collaborators of M. J. 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 M. J. Barceló. M. J. Barceló 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.
Peris, Pilar, M. J. Barceló, P. Aguado, et al.. (2024). Bisphosphonate drug holidays in osteoporosis according to fracture risk profile. Osteoporosis International. 36(2). 245–254. 2 indexed citations
2.
Barceló, M. J., et al.. (2019). Semen miRNAs Contained in Exosomes as Non-Invasive Biomarkers for Prostate Cancer Diagnosis. Scientific Reports. 9(1). 13772–13772. 107 indexed citations
3.
Alías, Laura, Sara Bernal, M. J. Barceló, et al.. (2011). Accuracy of Marker Analysis, Quantitative Real-Time Polymerase Chain Reaction, and Multiple Ligation-Dependent Probe Amplification to Determine SMN2 Copy Number in Patients with Spinal Muscular Atrophy. Genetic Testing and Molecular Biomarkers. 15(9). 587–594. 27 indexed citations
4.
Also‐Rallo, Eva, Laura Alías, Rebeca Martínez‐Hernández, et al.. (2011). Treatment of spinal muscular atrophy cells with drugs that upregulate SMN expression reveals inter- and intra-patient variability. European Journal of Human Genetics. 19(10). 1059–1065. 25 indexed citations
5.
Alías, Laura, Eva Also‐Rallo, Rebeca Martínez‐Hernández, et al.. (2011). Evaluation of fetal nuchal translucency in 98 pregnancies at risk for severe spinal muscular atrophy: possible relevance of the SMN2 copy number. The Journal of Maternal-Fetal & Neonatal Medicine. 25(8). 1246–1249. 9 indexed citations
6.
Martínez‐Hernández, Rebeca, Eva Also‐Rallo, Laura Alías, et al.. (2010). Ultrasound evaluation of fetal movements in pregnancies at risk for severe spinal muscular atrophy. Neuromuscular Disorders. 21(2). 97–101. 13 indexed citations
7.
Alías, Laura, Sara Bernal, Pablo Fuentes‐Prior, et al.. (2008). Mutation update of spinal muscular atrophy in Spain: molecular characterization of 745 unrelated patients and identification of four novel mutations in the SMN1 gene. Human Genetics. 125(1). 29–39. 131 indexed citations
8.
Gámez, Josep, Laura Alías, Marc Corbera‐Bellalta, et al.. (2007). Investigation of the role of SMN1 and SMN2 haploinsufficiency as a risk factor for Hirayama's disease: Clinical, neurophysiological and genetic characteristics in a Spanish series of 13 patients. Clinical Neurology and Neurosurgery. 109(10). 844–848. 12 indexed citations
9.
Alías, Laura, et al.. (2007). Evidence of a segregation ratio distortion of SMN1 alleles in spinal muscular atrophy. European Journal of Human Genetics. 15(10). 1090–1093. 5 indexed citations
10.
Barceló, M. J., et al.. (2006). Two independent mutations of the SMN1 gene in the same spinal muscular atrophy family branch: Lessons for carrier diagnosis. Genetics in Medicine. 8(4). 259–262. 3 indexed citations
11.
Barceló, M. J., Manel Baena, Adoración Venceslá, et al.. (2005). Rapid identification of female haemophilia A carriers with deletions in the factor VIII gene by quantitative Real-Time PCR analysis. Thrombosis and Haemostasis. 94(9). 661–664. 11 indexed citations
12.
Cuscó, Ivon, M. J. Barceló, Ricard Rojas‐García, et al.. (2005). SMN2 copy number predicts acute or chronic spinal muscular atrophy but does not account for intrafamilial variability in siblings. Journal of Neurology. 253(1). 21–25. 86 indexed citations
13.
Altés, Albert, M. J. Barceló, Ángel F. Remacha, et al.. (2004). Prevalence of the C282Y, H63D, and S65C Mutations of the HFE Gene in 1,146 Newborns from a Region of Northern Spain. Genetic Testing. 8(4). 407–410. 26 indexed citations
14.
Cuscó, Ivon, Eva López, Carolina Soler‐Botija, et al.. (2003). A genetic and phenotypic analysis in Spanish spinal muscular atrophy patients with c.399_402del AGAG, the most frequently found subtle mutation in the SMN1 gene. Human Mutation. 22(2). 136–143. 38 indexed citations
15.
Rı́o, E. del, et al.. (2002). [Interest in the study of genetic variants of the promoter region of the UGT1A1 gene in neonatal jaundice].. PubMed. 56(2). 139–43. 7 indexed citations
16.
Tizzano, Eduardo F., et al.. (2002). Should gamete donors be tested for spinal muscular atrophy?. Fertility and Sterility. 77(2). 409–411. 11 indexed citations
17.
Cuscó, Ivon, M. J. Barceló, Elisabeth del Río, et al.. (2001). Characterisation of SMN hybrid genes in Spanish SMA patients: de novo, homozygous and compound heterozygous cases. Human Genetics. 108(3). 222–229. 36 indexed citations
18.
Remacha, Ángel F., et al.. (1996). The deoxyuridine suppression test in HIV‐1 positive patients: the role of azydothymidine (AZT). European Journal Of Haematology. 56(4). 208–212. 1 indexed citations
19.
Remacha, Ángel F., et al.. (1992). Congenital intrinsic factor deficiency in a Spanish patient. Annals of Hematology. 64(4). 202–204. 4 indexed citations
20.
Remacha, Ángel F., et al.. (1990). The deoxyuridine suppression test in peripheral lymphocytes. European Journal Of Haematology. 44(3). 196–200. 3 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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