Manel Baena

462 total citations
17 papers, 346 citations indexed

About

Manel Baena is a scholar working on Hematology, Molecular Biology and Genetics. According to data from OpenAlex, Manel Baena has authored 17 papers receiving a total of 346 indexed citations (citations by other indexed papers that have themselves been cited), including 9 papers in Hematology, 8 papers in Molecular Biology and 3 papers in Genetics. Recurrent topics in Manel Baena's work include Hemophilia Treatment and Research (9 papers), Blood Coagulation and Thrombosis Mechanisms (7 papers) and Cancer-related gene regulation (4 papers). Manel Baena is often cited by papers focused on Hemophilia Treatment and Research (9 papers), Blood Coagulation and Thrombosis Mechanisms (7 papers) and Cancer-related gene regulation (4 papers). Manel Baena collaborates with scholars based in Spain, Brazil and United Kingdom. Manel Baena's co-authors include Montserrat Baiget, Montserrat Domènech, Orland Dı́ez, Carmen Alonso, Edgard Verdura, Lidia González‐Quereda, Eduardo F. Tizzano, Jonàs Juan‐Mateu, A. Nascimento and C. Ortez and has published in prestigious journals such as Blood, PLoS ONE and International Journal of Molecular Sciences.

In The Last Decade

Manel Baena

16 papers receiving 340 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Manel Baena Spain 10 275 121 68 45 34 17 346
Lutz-Peter Berg United Kingdom 11 148 0.5× 40 0.3× 85 1.3× 12 0.3× 36 1.1× 15 281
Giulia Pianigiani Italy 10 283 1.0× 26 0.2× 97 1.4× 22 0.5× 46 1.4× 17 347
Q. Tian Wang United States 10 427 1.6× 134 1.1× 15 0.2× 16 0.4× 15 0.4× 13 484
Goranka Tanačković Switzerland 9 430 1.6× 51 0.4× 21 0.3× 15 0.3× 64 1.9× 16 498
J.J. Wasmuth United States 7 122 0.4× 58 0.5× 53 0.8× 10 0.2× 35 1.0× 10 206
Colleen M. Carlston United States 8 122 0.4× 112 0.9× 28 0.4× 14 0.3× 20 0.6× 13 234
Margaret K. R. Donovan United States 10 275 1.0× 107 0.9× 17 0.3× 25 0.6× 12 0.4× 10 399
Emine İkbal Atlı Türkiye 8 119 0.4× 46 0.4× 51 0.8× 8 0.2× 51 1.5× 48 212
Alessandra Splendore Brazil 11 172 0.6× 227 1.9× 48 0.7× 7 0.2× 58 1.7× 16 392
Anand Saggar United Kingdom 8 280 1.0× 231 1.9× 14 0.2× 11 0.2× 26 0.8× 15 415

Countries citing papers authored by Manel Baena

Since Specialization
Citations

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

Fields of papers citing papers by Manel Baena

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Manel Baena

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

All Works

17 of 17 papers shown
1.
Bernal, Sara, Laura Alías, Manel Baena, et al.. (2021). High Mutational Heterogeneity, and New Mutations in the Human Coagulation Factor V Gene. Future Perspectives for Factor V Deficiency Using Recombinant and Advanced Therapies. International Journal of Molecular Sciences. 22(18). 9705–9705. 9 indexed citations
2.
Baena, Manel, et al.. (2016). Carotid Stenosis and Anaesthesia. 1(1).
3.
Juan‐Mateu, Jonàs, Lidia González‐Quereda, Maria José Rodríguez, et al.. (2015). DMD Mutations in 576 Dystrophinopathy Families: A Step Forward in Genotype-Phenotype Correlations. PLoS ONE. 10(8). e0135189–e0135189. 109 indexed citations
4.
Barón‐Franco, Bosco, et al.. (2013). Improvement of the prescription in polymedicated elderly. 15(5). 339–343. 2 indexed citations
5.
Venceslá, Adoración, Manel Baena, Rosario Garrido, et al.. (2012). F8 gene dosage defects in atypical patients with severe haemophilia A. Haemophilia. 18(5). 708–713. 5 indexed citations
6.
Venceslá, Adoración, María Román, Ihosvany Fernández Bello, et al.. (2010). Clinical and genetic findings in five female patients with haemophilia A: Identification of a novel missense mutation, p.Phe2127Ser. Thrombosis and Haemostasis. 104(10). 718–723. 12 indexed citations
7.
Belvís, R., Eduardo F. Tizzano, Joan Martí‐Fàbregas, et al.. (2009). Mutations in the NKX2-5 gene in patients with stroke and patent foramen ovale. Clinical Neurology and Neurosurgery. 111(7). 574–578. 14 indexed citations
8.
Venceslá, Adoración, Pablo Fuentes‐Prior, Manel Baena, et al.. (2008). Severe haemophilia A in a female resulting from an inherited gross deletion and a de novo codon deletion in the F8 gene. Haemophilia. 14(5). 1094–1098. 10 indexed citations
9.
Venceslá, Adoración, María Ángeles Corral-Rodríguez, Manel Baena, et al.. (2008). Identification of 31 novel mutations in the F8 gene in Spanish hemophilia A patients: structural analysis of 20 missense mutations suggests new intermolecular binding sites. Blood. 111(7). 3468–3478. 12 indexed citations
10.
Venceslá, Adoración, et al.. (2008). Application of intron 9 and intron 25 dinucleotide repeats of the factor VIII gene for carrier diagnosis in haemophilia A. Haemophilia. 14(3). 489–493. 7 indexed citations
11.
Venceslá, Adoración, Manel Baena, María Teresa Calvo, et al.. (2005). First report of two independent point factor VIII mutations in a family with haemophilia A: a wordof caution for carrier diagnosis. Thrombosis and Haemostasis. 94(9). 675–677. 6 indexed citations
12.
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
13.
Tizzano, Eduardo F., et al.. (2005). Utility of a (GT)n dinucleotide repeat in intron 1 of the factor 8 gene for haemophilia A carrier diagnosis. Haemophilia. 11(2). 142–144. 9 indexed citations
14.
Campos, Berta, Orland Dı́ez, Montserrat Domènech, et al.. (2003). RNA analysis of eightBRCA1andBRCA2unclassified variants identified in breast/ovarian cancer families from Spain. Human Mutation. 22(4). 337–337. 35 indexed citations
15.
Campos, Berta, Orland Dı́ez, Montserrat Domènech, et al.. (2001). BRCA2 mutation analysis of 87 Spanish breast/ovarian cancer families. Annals of Oncology. 12(12). 1699–1703. 12 indexed citations
16.
Vega, Ana, Berta Campos, Brigitte Bressac–de Paillerets, et al.. (2001). The R71GBRCA1is a founder Spanish mutation and leads to aberrant splicing of the transcript. Human Mutation. 17(6). 520–521. 92 indexed citations
17.
Pericay, Carles, Orland Dı́ez, Berta Campos, et al.. (2001). Características clinicopatológicas y evolución clínica de pacientes con cáncer de mama y mutaciones en los genes BRCA1 o BRCA2. Medicina Clínica. 117(5). 161–166. 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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