M.P. Botella

743 total citations
7 papers, 135 citations indexed

About

M.P. Botella is a scholar working on Molecular Biology, Pediatrics, Perinatology and Child Health and Rheumatology. According to data from OpenAlex, M.P. Botella has authored 7 papers receiving a total of 135 indexed citations (citations by other indexed papers that have themselves been cited), including 3 papers in Molecular Biology, 2 papers in Pediatrics, Perinatology and Child Health and 2 papers in Rheumatology. Recurrent topics in M.P. Botella's work include RNA regulation and disease (2 papers), Prenatal Substance Exposure Effects (2 papers) and Autoimmune Neurological Disorders and Treatments (1 paper). M.P. Botella is often cited by papers focused on RNA regulation and disease (2 papers), Prenatal Substance Exposure Effects (2 papers) and Autoimmune Neurological Disorders and Treatments (1 paper). M.P. Botella collaborates with scholars based in Spain, United Kingdom and United States. M.P. Botella's co-authors include Blanca Gener, Miguel Del Campo, Luis A. Pérez‐Jurado, Gemma Aznar‐Laín, Guillermo Antiñolo, Benjamín Rodríguez‐Santiago, Elisabeth Gabau, Maria Rigau, Marta Codina‐Solà and Javier Santoyo‐López and has published in prestigious journals such as Human Mutation, Frontiers in Genetics and American Journal of Medical Genetics.

In The Last Decade

M.P. Botella

6 papers receiving 132 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
M.P. Botella Spain	5	80	79	33	10	8	7	135
Huidan Wu China	8	65 0.8×	68 0.9×	28 0.8×	5 0.5×	5 0.6×	13	126
Ada J. S. Chan Canada	5	103 1.3×	158 2.0×	29 0.9×	14 1.4×	10 1.3×	7	212
Craig Chinault United States	6	98 1.2×	94 1.2×	30 0.9×	7 0.7×	17 2.1×	6	189
Bärbel Felder Germany	3	87 1.1×	74 0.9×	24 0.7×	6 0.6×	5 0.6×	3	127
Emily Hansen‐Kiss United States	5	89 1.1×	46 0.6×	36 1.1×	9 0.9×	7 0.9×	9	150
Thuong Ha Australia	6	77 1.0×	47 0.6×	20 0.6×	16 1.6×	3 0.4×	13	136
Yoko Hiraki Japan	10	97 1.2×	131 1.7×	14 0.4×	10 1.0×	5 0.6×	17	219
Jasmin Morandell Austria	5	132 1.6×	77 1.0×	46 1.4×	21 2.1×	3 0.4×	7	177
Jason Carmichael United States	5	61 0.8×	58 0.7×	11 0.3×	14 1.4×	5 0.6×	6	103
Souad Gherbi France	8	103 1.3×	50 0.6×	18 0.5×	13 1.3×	8 1.0×	11	199

Countries citing papers authored by M.P. Botella

Since Specialization

Citations

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

Fields of papers citing papers by M.P. Botella

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of M.P. Botella

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

All Works

Sort: Min cites: Since: Top N: Style:

7 of 7 papers shown

1.

Villate, Olatz, Jesús Ibarluzea, Eladio A. Velasco, et al.. (2018). Functional Analyses of a Novel Splice Variant in the CHD7 Gene, Found by Next Generation Sequencing, Confirm Its Pathogenicity in a Spanish Patient and Diagnose Him with CHARGE Syndrome. Frontiers in Genetics. 9. 7–7. 14 indexed citations

2.

Codina‐Solà, Marta, Benjamín Rodríguez‐Santiago, Javier Santoyo‐López, et al.. (2015). Integrated analysis of whole-exome sequencing and transcriptome profiling in males with autism spectrum disorders. Molecular Autism. 6(1). 21–21. 89 indexed citations

3.

Rice, Gillian, Martin A.M. Reijns, Gabriella Forte, et al.. (2013). Synonymous Mutations inRNASEH2ACreate Cryptic Splice Sites Impairing RNase H2 Enzyme Function in Aicardi-Goutières Syndrome. Human Mutation. 34(8). 1066–1070. 13 indexed citations

4.

Botella, M.P., et al.. (2010). Generalized epileptic seizures in an infant due to passive exposure to cocaine. Anales del Sistema Sanitario de Navarra. 32(3). 453–6.

5.

Aguilera, Sergio, et al.. (2009). Síndrome opsoclono-mioclono-atáxico paraneoplásico. Anales del Sistema Sanitario de Navarra. 32(1). 3 indexed citations

6.

Vasudevan, Pradeep, Sixto García‐Miñáur, M.P. Botella, et al.. (2005). Microcephaly-lymphoedema-chorioretinal dysplasia: three cases to delineate the facial phenotype and review of the literature. Clinical Dysmorphology. 14(3). 109–116. 12 indexed citations

7.

García‐Miñáur, Sixto & M.P. Botella. (2000). Further case of aminopterin syndrome sine aminopterin in a Spanish child. American Journal of Medical Genetics. 95(4). 320–324. 4 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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