Rosa Riveiro-Álvarez

2.5k total citations
53 papers, 1.5k citations indexed

About

Rosa Riveiro-Álvarez is a scholar working on Molecular Biology, Ophthalmology and Genetics. According to data from OpenAlex, Rosa Riveiro-Álvarez has authored 53 papers receiving a total of 1.5k indexed citations (citations by other indexed papers that have themselves been cited), including 44 papers in Molecular Biology, 26 papers in Ophthalmology and 13 papers in Genetics. Recurrent topics in Rosa Riveiro-Álvarez's work include Retinal Development and Disorders (34 papers), Retinal Diseases and Treatments (25 papers) and RNA regulation and disease (6 papers). Rosa Riveiro-Álvarez is often cited by papers focused on Retinal Development and Disorders (34 papers), Retinal Diseases and Treatments (25 papers) and RNA regulation and disease (6 papers). Rosa Riveiro-Álvarez collaborates with scholars based in Spain, United States and Switzerland. Rosa Riveiro-Álvarez's co-authors include Carmen Ayuso, Almudena Ávila‐Fernández, Marta Cortón, Fiona Blanco‐Kelly, Jana Aguirre-Lambán, Diego Cantalapiedra, María José Trujillo-Tiebas, Elena Vallespín, Blanca Garcı́a-Sandoval and Miguel Ángel López-Martínez and has published in prestigious journals such as PLoS ONE, Scientific Reports and International Journal of Molecular Sciences.

In The Last Decade

Rosa Riveiro-Álvarez

53 papers receiving 1.5k citations

Peers

Countries citing papers authored by Rosa Riveiro-Álvarez

Since Specialization

Citations

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

Fields of papers citing papers by Rosa Riveiro-Álvarez

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Rosa Riveiro-Álvarez. 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 Rosa Riveiro-Álvarez. The network helps show where Rosa Riveiro-Álvarez may publish in the future.

Co-authorship network of co-authors of Rosa Riveiro-Álvarez

This figure shows the co-authorship network connecting the top 25 collaborators of Rosa Riveiro-Álvarez. A scholar is included among the top collaborators of Rosa Riveiro-Álvarez 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 Rosa Riveiro-Álvarez. Rosa Riveiro-Álvarez 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:

20 of 20 papers shown

#	Work	Indexed citations
1	Methylation analysis by targeted bisulfite sequencing in large for gestational age (LGA) newborns: the LARGAN cohort 2023 ·Clinical Epigenetics ·(unknown), (unknown), (unknown), (unknown), Miguel Ángel López-Martínez, Rosa Riveiro-Álvarez, Larry Wilhelm, (unknown), Cármen Garcés, Alejandro Lomniczi, Leandro Soriano‐Guillén	5
2	Aggregated Genomic Data as Cohort-Specific Allelic Frequencies can Boost Variants and Genes Prioritization in Non-Solved Cases of Inherited Retinal Dystrophies 2022 ·International Journal of Molecular Sciences ·(unknown), Irene Perea‐Romero, (unknown), Lorena de la Fuente, Raquel Escutia Romero, Almudena Ávila‐Fernández, María José Trujillo-Tiebas, Rosa Riveiro-Álvarez, Berta Almoguera, Inmaculada Martín-Mérida, Marta Del Pozo‐Valero, (unknown), Marta Cortón, Carmen Ayuso, Pablo Mínguez	3
3	Sanger sequencing is no longer always necessary based on a single-center validation of 1109 NGS variants in 825 clinical exomes 2021 ·Scientific Reports ·Ana Arteche‐López, (unknown), Raquel Escutia Romero, Rosa Riveiro-Álvarez, Miguel Ángel López-Martínez, Ascensión Gimenez-Pardo, (unknown), J. Gallego‐Merlo, (unknown), Berta Almoguera, Ana Bustamante‐Aragonés, Fiona Blanco‐Kelly, Saoud Tahsin Swafiri, Elvira Rodríguez‐Pinilla, Pablo Mínguez, (unknown), María José Trujillo-Tiebas, Carmen Ayuso	37
4	Comparison of the diagnostic yield of aCGH and genome-wide sequencing across different neurodevelopmental disorders 2021 ·npj Genomic Medicine ·Francisco Martínez‐Granero, Fiona Blanco‐Kelly, C. Sánchez-Jimeno, Almudena Ávila‐Fernández, Ana Arteche‐López, Ana Bustamante‐Aragonés, (unknown), Elvira Rodríguez‐Pinilla, Rosa Riveiro-Álvarez, Saoud Tahsin Swafiri, María José Trujillo-Tiebas, Carmen Ayuso, Marta Rodríguez de Alba, Isabel Lorda‐Sánchez, Berta Almoguera	23
5	Prioritizing variants of uncertain significance for reclassification using a rule-based algorithm in inherited retinal dystrophies 2021 ·npj Genomic Medicine ·(unknown), Almudena Ávila‐Fernández, Ana Arteche‐López, María José Trujillo-Tiebas, Rosa Riveiro-Álvarez, Berta Almoguera, Inmaculada Martín-Mérida, Marta Del Pozo‐Valero, Irene Perea‐Romero, Marta Cortón, Pablo Mínguez, Carmen Ayuso	21
6	RPE65-related retinal dystrophy: Mutational and phenotypic spectrum in 45 affected patients 2021 ·Experimental Eye Research ·Rosario López‐Rodríguez, (unknown), Fiona Blanco‐Kelly, Almudena Ávila‐Fernández, (unknown), Marta Del Pozo‐Valero, Irene Perea‐Romero, Olga Zurita, Belén Jimenez‐Rolando, Saoud Tahsin Swafiri, Rosa Riveiro-Álvarez, María José Trujillo-Tiebas, Ester Carreño, Blanca Garcı́a-Sandoval, Marta Cortón, Carmen Ayuso	15
7	Genotype–Phenotype Correlations in a Spanish Cohort of 506 Families With Biallelic ABCA4 Pathogenic Variants 2020 ·American Journal of Ophthalmology ·Marta Del Pozo‐Valero, Rosa Riveiro-Álvarez, Fiona Blanco‐Kelly, Jana Aguirre-Lambán, Inmaculada Martín-Mérida, (unknown), Saoud Tahsin Swafiri, Isabel Lorda‐Sánchez, Elvira Rodríguez‐Pinilla, María José Trujillo-Tiebas, Belén Jimenez‐Rolando, Ester Carreño, Ignacio Mahíllo, Carlo Rivolta, Marta Cortón, Almudena Ávila‐Fernández, Blanca Garcı́a-Sandoval, Carmen Ayuso	22
8	Pharmacogenetics of methylphenidate in childhood attention-deficit/hyperactivity disorder: long-term effects 2017 ·Scientific Reports ·Clara Gomez-Sanchez, Juan J. Carballo, Rosa Riveiro-Álvarez, Víctor Soto-Insuga, (unknown), Ignacio Mahíllo, Francisco Abad‐Santos, Rafael Dal‐Ré, Carmen Ayuso	17
9	Clinical Exome Sequencing Reveals <b><i>MKRN3</i></b> Pathogenic Variants in Familial and Nonfamilial Idiopathic Central Precocious Puberty 2016 ·Hormone Research in Paediatrics ·(unknown), Rosa Riveiro-Álvarez, Miguel Ángel López-Martínez, (unknown), (unknown), María José Trujillo-Tiebas, Leandro Soriano‐Guillén	27
10	Panel-based NGS Reveals Novel Pathogenic Mutations in Autosomal Recessive Retinitis Pigmentosa 2016 ·Scientific Reports ·Raquel Pérez-Carro, Marta Cortón, Iker Sánchez‐Navarro, Olga Zurita, (unknown), Rocío Sánchez-Alcudia, Stefan H. Lelieveld, Elena Aller, Miguel Ángel López-Martínez, (unknown), Patrícia José, Fiona Blanco‐Kelly, Rosa Riveiro-Álvarez, Christian Gilissen, José M. Millán, Almudena Ávila‐Fernández, Carmen Ayuso	49
11	Whole-exome sequencing reveals ZNF408 as a new gene associated with autosomal recessive retinitis pigmentosa with vitreal alterations 2015 ·Human Molecular Genetics ·Almudena Ávila‐Fernández, Raquel Pérez-Carro, Marta Cortón, María Isabel López-Molina, Laura Campello, Alejandro Garanto, Laura Fernández‐Sánchez, Lonneke Duijkers, Miguel Ángel López-Martínez, Rosa Riveiro-Álvarez, (unknown), Rocío Sánchez-Alcudia, (unknown), Noelia Reyes, Francisco García‐García, Joaquı́n Dopazo, Blanca Garcı́a-Sandoval, Rob W.J. Collin, Nicolás Cuenca, Carmen Ayuso	37
12	Contribution of Mutation Load to the Intrafamilial Genetic Heterogeneity in a Large Cohort of Spanish Retinal Dystrophies Families 2014 ·Investigative Ophthalmology & Visual Science ·Rocío Sánchez-Alcudia, Marta Cortón, Almudena Ávila‐Fernández, Olga Zurita, Sorina D. Tatu, Raquel Pérez-Carro, Patrícia José, Miguel Ángel López-Martínez, Francisco Castillo, José M. Millán, Fiona Blanco‐Kelly, Blanca Garcı́a-Sandoval, María Isabel López-Molina, Rosa Riveiro-Álvarez, Carmen Ayuso	9
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	Outcome of ABCA4 Disease-Associated Alleles in Autosomal Recessive Retinal Dystrophies 2013 ·Ophthalmology ·Rosa Riveiro-Álvarez, (unknown), Jana Zernant, Jana Aguirre-Lambán, Diego Cantalapiedra, Almudena Ávila‐Fernández, Ascensión Giménez, (unknown), Blanca Garcı́a-Sandoval, Fiona Blanco‐Kelly, Marta Cortón, Sorina D. Tatu, Patrícia José, M J Trujillo-Tiebas, Carmen Ramos, Rando Allikmets, Carmen Ayuso	61
15	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
16	Association of common genetic variants with risperidone adverse events in a Spanish schizophrenic population 2012 ·The Pharmacogenomics Journal ·Berta Almoguera, Rosa Riveiro-Álvarez, Jorge López‐Castromán, Pedro Dorado, Concepción Vaquero‐Lorenzo, José Fernández‐Piqueras, Adrián LLerena, Francisco Abad‐Santos, Enrique Baca‐García, Rafael Dal‐Ré, Carmen Ayuso	20
17	Identification of an RP1 Prevalent Founder Mutation and Related Phenotype in Spanish Patients with Early-Onset Autosomal Recessive Retinitis 2012 ·Ophthalmology ·Almudena Ávila‐Fernández, Marta Cortón, Koji M. Nishiguchi, (unknown), (unknown), Fiona Blanco‐Kelly, Rosa Riveiro-Álvarez, Blanca Garcı́a-Sandoval, Carlo Rivolta, Carmen Ayuso	41
18	ATA homozigosity in the IL-10gene promoter is a risk factor for schizophrenia in Spanish females: a case control study 2011 ·BMC Medical Genetics ·Berta Almoguera, Rosa Riveiro-Álvarez, Jorge López‐Castromán, Pedro Dorado, Rosario López‐Rodríguez, Pablo Fernández‐Navarro, Enrique Baca‐García, José Fernández‐Piqueras, Rafael Dal‐Ré, Francisco Abad‐Santos, Adrián LLerena, Carmen Ayuso	14
19	Overview of the mutation spectrum in familial exudative vitreoretinopathy and Norrie disease with identification of 21 novel variants in FZD4, LRP5, and NDP 2010 ·Human Mutation ·Konstantinos Nikopoulos, Hanka Venselaar, Rob W.J. Collin, Rosa Riveiro-Álvarez, F. Nienke Boonstra, Johanna M. M. Hooymans, Arijit Mukhopadhyay, Deborah Shears, (unknown), Ilse J. de Wijs, Anthonie J. van Essen, Rolf H. Sijmons, M. A. D. Tilanus, (unknown), Carmen Ayuso, (unknown), Frans P.M. Cremers	121
20	Microarray-based mutation analysis of the ABCA4 gene in Spanish patients with Stargardt disease: evidence of a prevalent mutated allele. 2006 ·PubMed ·Diana Valverde, Rosa Riveiro-Álvarez, Sara Bernal, (unknown), Montserrat Baiget, Rafael Navarro, Carmen Ayuso	44

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.

Explore authors with similar magnitude of impact