Elena Vallespín

2.7k total citations
53 papers, 944 citations indexed

About

Elena Vallespín is a scholar working on Molecular Biology, Genetics and Ophthalmology. According to data from OpenAlex, Elena Vallespín has authored 53 papers receiving a total of 944 indexed citations (citations by other indexed papers that have themselves been cited), including 40 papers in Molecular Biology, 18 papers in Genetics and 17 papers in Ophthalmology. Recurrent topics in Elena Vallespín's work include Retinal Development and Disorders (17 papers), Retinal Diseases and Treatments (13 papers) and Genomic variations and chromosomal abnormalities (8 papers). Elena Vallespín is often cited by papers focused on Retinal Development and Disorders (17 papers), Retinal Diseases and Treatments (13 papers) and Genomic variations and chromosomal abnormalities (8 papers). Elena Vallespín collaborates with scholars based in Spain, United States and Netherlands. Elena Vallespín's co-authors include Carmen Ayuso, Diego Cantalapiedra, Rosa Riveiro-Álvarez, Jana Aguirre-Lambán, Almudena Ávila‐Fernández, María José Trujillo-Tiebas, Julián Nevado, Pablo Lapunzina, Ángela del Pozo and María Palomares‐Bralo and has published in prestigious journals such as PLoS ONE, Scientific Reports and International Journal of Molecular Sciences.

In The Last Decade

Elena Vallespín

51 papers receiving 924 citations

Peers

Countries citing papers authored by Elena Vallespín

Since Specialization

Citations

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

Fields of papers citing papers by Elena Vallespín

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Elena Vallespín

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

All Works

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20 of 20 papers shown

#	Work	Indexed citations
1	OPA1 Dominant Optic Atrophy: Diagnostic Approach in the Pediatric Population 2023 ·Current Issues in Molecular Biology ·(unknown), (unknown), (unknown), (unknown), Ángela del Pozo, (unknown), Fernando Santos‐Simarro, (unknown), (unknown), Elena Vallespín, Susana Noval	3
2	Whole Exome Sequencing of 20 Spanish Families: Candidate Genes for Non-Syndromic Pediatric Cataracts 2023 ·International Journal of Molecular Sciences ·(unknown), (unknown), (unknown), Rocío Mena, Carmen Rodríguez Jiménez, (unknown), (unknown), (unknown), (unknown), Ángela del Pozo, (unknown), (unknown), (unknown), (unknown), (unknown), M Gómez-Cano, (unknown), Susana Noval, Elena Vallespín	4
3	Next-Generation Sequencing Screening of 43 Families with Non-Syndromic Early-Onset High Myopia: A Clinical and Genetic Study 2022 ·International Journal of Molecular Sciences ·(unknown), (unknown), Susana Noval, (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), Ángela del Pozo, Fernando Santos‐Simarro, Elena Vallespín	3
4	mTOR mutations in Smith‐Kingsmore syndrome: Four additional patients and a review 2017 ·Clinical Genetics ·Gema Gordo, Jair Tenorio, Pedro Arias, Fernando Santos‐Simarro, Sixto García‐Miñáur, J.C. Moreno, Julián Nevado, Elena Vallespín, Lara Rodríguez‐Laguna, (unknown), Irene Dapía, María Palomares‐Bralo, Ángela del Pozo, Kristina Ibáñez, Juan Carlos Silla-Castro, Eva Barroso, Víctor L. Ruiz‐Pérez, Víctor Martínez‐Glez, Pablo Lapunzina	29
5	La secuenciación masiva (NGS) como método diagnóstico en la enfermedad de Stargardt 2017 ·Archivos de la Sociedad Española de Oftalmología ·Belén Jimenez‐Rolando, Susana Noval, (unknown), Eva Díaz, Ángela del Pozo, (unknown), Juan Carlos Silla-Castro, (unknown), Rubén Martín‐Arenas, Elena Vallespín	4
6	A new variant in PHKA2 is associated with glycogen storage disease type IXa 2017 ·Molecular Genetics and Metabolism Reports ·(unknown), Fernando Santos‐Simarro, Ángel Campos‐Barros, C. Camarena, (unknown), Elena Vallespín, Ángela del Pozo, Rocío Mena, Pablo Lapunzina, Sonia Rodríguez‐Nóvoa	16
7	In-frame Variants in FLNA Proximal Rod 1 Domain Associate With a Predominant Cardiac Valvular Phenotype 2017 ·Revista Española de Cardiología (English Edition) ·Luís Fernández, Jair Tenorio, (unknown), Elena Vallespín, María Palomares‐Bralo, Sixto García‐Miñáur, Fernando Santos‐Simarro, Pedro Arias, (unknown), (unknown), (unknown), (unknown), Jorge Solı́s, (unknown), (unknown), Laura Rodríguez, Julián Nevado, Víctor Martínez‐Glez, Karen E. Heath, Pablo Lapunzina	4
8	The syndrome of central hypothyroidism and macroorchidism: IGSF1 controls TRHR and FSHB expression by differential modulation of pituitary TGFβ and Activin pathways 2017 ·Scientific Reports ·(unknown), Raquel Barrio, Montserrat García-Lavandeira, (unknown), Adela Escudero, Esther Díaz‐Rodriguez, Darya Gorbenko del Blanco, (unknown), Yolanda B. de Rijke, Elena Vallespín, Julián Nevado, Pablo Lapunzina, Vilborg Matre, Patricia M. Hinkle, Anita C. S. Hokken‐Koelega, María P. De Miguel, José Cameselle‐Teijeiro, Manuel Nistal, Clara V. Álvarez, J.C. Moreno	28
9	The impact of next-generation sequencing on the DNA methylation–based translational cancer research 2015 ·Translational research ·Javier Soto, Carlos Rodríguez‐Antolín, Elena Vallespín, Javier de Castro, Inmaculada Ibañez de Cáceres	46
10	Array CGH Analysis of Paired Blood and Tumor Samples from Patients with Sporadic Wilms Tumor 2015 ·PLoS ONE ·(unknown), Lara Rodríguez‐Laguna, M. Carmen Crespo, Elena Vallespín, María Palomares‐Bralo, Rubén Martín‐Arenas, (unknown), Paulo Antônio Silvestre de Faria, (unknown), Purificación García‐Miguel, Pablo Lapunzina, Fernando Regla Vargas, Héctor N. Seuánez, Víctor Martínez‐Glez	7
11	Familial imbalance in 16p13.11 leads to a dosage compensation rearrangement in an unaffected carrier 2014 ·BMC Medical Genetics ·Alicia Delicado, Luís Fernández, María Torres, Julián Nevado, Fe Amalia García‐Santiago, R. Rodríguez, Elena Mansilla, María Palomares‐Bralo, Fernando Santos‐Simarro, Elena Vallespín, María Ángeles Mori, Pablo Lapunzina	3
12	Customized high resolution CGH‐array for clinical diagnosis reveals additional genomic imbalances in previous well‐defined pathological samples 2013 ·American Journal of Medical Genetics Part A ·Elena Vallespín, María Palomares‐Bralo, M. A. Mori, Rubén Martín‐Arenas, Sixto García‐Miñáur, Luís Fernández, María Torres, Fe Amalia García‐Santiago, Elena Mansilla, Fernando Santos, (unknown), M. Carmen Crespo, (unknown), Víctor Martínez‐Glez, Alicia Delicado, Pablo Lapunzina, Julián Nevado	27
13	Involvement of LCA5 in Leber Congenital Amaurosis and Retinitis Pigmentosa in the Spanish Population 2013 ·Ophthalmology ·Marta Cortón, Almudena Ávila‐Fernández, Elena Vallespín, María Isabel López-Molina, Berta Almoguera, (unknown), Sorina D. Tatu, Muhammad Imran Khan, Fiona Blanco‐Kelly, Rosa Riveiro-Álvarez, Marı́a Brión, Blanca Garcı́a-Sandoval, Frans P.M. Cremers, Ãngel Carracedo, Carmen Ayuso	14
14	High frequency of CRB1 mutations as cause of Early-Onset Retinal Dystrophies in the Spanish population 2013 ·Orphanet Journal of Rare Diseases ·Marta Cortón, Sorina D. Tatu, Almudena Ávila‐Fernández, Elena Vallespín, (unknown), Diego Cantalapiedra, Fiona Blanco‐Kelly, Rosa Riveiro-Álvarez, Sara Bernal, Blanca Garcı́a-Sandoval, Montserrat Baiget, Carmen Ayuso	60
15	Heterogeneous growth patterns in carriers of chromosome 7p12.2 imbalances affecting GRB10 2012 ·American Journal of Medical Genetics Part A ·Thomas Eggermann, Matthias Begemann, (unknown), María Palomares‐Bralo, Elena Vallespín, Luís Fernández, (unknown), Sabrina Spengler, Sixto García‐Miñaúr	7
16	Uveal melanoma in a 19-month-old child 2011 ·Journal of American Association for Pediatric Ophthalmology and Strabismus ·Anna Grabowska, (unknown), Jesús Peralta, M. Asencio Durán, Miguel Ángel García‐Cabezas, (unknown), Julián Nevado, Elena Vallespín, Jesús Solera, (unknown), (unknown)	9
17	Molecular characterization of an atypical inv dup del 8q. Proposal of a mechanism of formation 2011 ·American Journal of Medical Genetics Part A ·Laura Rodríguez, Julián Nevado, Elena Vallespín, María Palomares‐Bralo, (unknown), María Clara Bonaglia, Alicia Delicado, (unknown)	4
18	Foetal sex determination in maternal blood from the seventh week of gestation and its role in diagnosing haemophilia in the foetuses of female carriers 2008 ·Haemophilia ·Ana Bustamante‐Aragonés, Marta Rodríguez de Alba, Cristina González-González, María José Trujillo-Tiebas, Dan Diego‐Álvarez, Elena Vallespín, (unknown), Carmen Ayuso, Carmen Viana Ramos	50
19	Frequency of ABCA4 mutations in 278 Spanish controls: an insight into the prevalence of autosomal recessive Stargardt disease 2008 ·British Journal of Ophthalmology ·Rosa Riveiro-Álvarez, Jana Aguirre-Lambán, Miguel Ángel López-Martínez, María José Trujillo-Tiebas, Diego Cantalapiedra, Elena Vallespín, (unknown), Carmen Ramos, Carmen Ayuso	36
20	Gene symbol: ABCA4. Disease: Macular dystrophy. 2008 ·PubMed ·Jana Aguirre-Lambán, Rosa Riveiro-Álvarez, Diego Cantalapiedra, Elena Vallespín, (unknown), (unknown), M J Trujillo-Tiebas	3

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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