Inmaculada Martín-Mérida

614 total citations
15 papers, 251 citations indexed

About

Inmaculada Martín-Mérida is a scholar working on Molecular Biology, Genetics and Ophthalmology. According to data from OpenAlex, Inmaculada Martín-Mérida has authored 15 papers receiving a total of 251 indexed citations (citations by other indexed papers that have themselves been cited), including 13 papers in Molecular Biology, 9 papers in Genetics and 6 papers in Ophthalmology. Recurrent topics in Inmaculada Martín-Mérida's work include Retinal Development and Disorders (9 papers), Retinal Diseases and Treatments (5 papers) and Genomics and Rare Diseases (4 papers). Inmaculada Martín-Mérida is often cited by papers focused on Retinal Development and Disorders (9 papers), Retinal Diseases and Treatments (5 papers) and Genomics and Rare Diseases (4 papers). Inmaculada Martín-Mérida collaborates with scholars based in Spain, United Kingdom and United States. Inmaculada Martín-Mérida's co-authors include Carmen Ayuso, Marta Cortón, Almudena Ávila‐Fernández, Fiona Blanco‐Kelly, Blanca Garcı́a-Sandoval, Marta Del Pozo‐Valero, Ana Arteche‐López, María José Trujillo-Tiebas, Pablo Mínguez and Rosa Riveiro-Álvarez and has published in prestigious journals such as PLoS ONE, Scientific Reports and International Journal of Molecular Sciences.

In The Last Decade

Inmaculada Martín-Mérida

14 papers receiving 246 citations

Peers

Countries citing papers authored by Inmaculada Martín-Mérida

Since Specialization

Citations

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

Fields of papers citing papers by Inmaculada Martín-Mérida

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Inmaculada Martín-Mérida. 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 Inmaculada Martín-Mérida. The network helps show where Inmaculada Martín-Mérida may publish in the future.

Co-authorship network of co-authors of Inmaculada Martín-Mérida

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

All Works

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15 of 15 papers shown

#	Work	Indexed citations
1	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
2	Five years’ experience of the clinical exome sequencing in a Spanish single center 2022 ·Scientific Reports ·Ana Arteche‐López, (unknown), (unknown), Berta Almoguera, (unknown), Inmaculada Martín-Mérida, (unknown), (unknown), (unknown), (unknown), (unknown), Fiona Blanco‐Kelly, Saoud Tahsin Swafiri, (unknown), (unknown), Carmen Ayuso	0
3	Allelic overload and its clinical modifier effect in Bardet-Biedl syndrome 2022 ·npj Genomic Medicine ·Irene Perea‐Romero, (unknown), Fiona Blanco‐Kelly, Iker Sánchez‐Navarro, (unknown), (unknown), Isabel Lorda‐Sánchez, Saoud Tahsin Swafiri, Almudena Ávila‐Fernández, Inmaculada Martín-Mérida, María José Trujillo-Tiebas, Ester Carreño, Belén Jimenez‐Rolando, Blanca Garcı́a-Sandoval, Pablo Mínguez, Marta Cortón, Diana Valverde, Carmen Ayuso	13
4	Impact of Next Generation Sequencing in Unraveling the Genetics of 1036 Spanish Families With Inherited Macular Dystrophies 2022 ·Investigative Ophthalmology & Visual Science ·Marta Del Pozo‐Valero, Rosa Riveiro-Álvarez, Inmaculada Martín-Mérida, Fiona Blanco‐Kelly, Saoud Tahsin Swafiri, Isabel Lorda‐Sánchez, María José Trujillo-Tiebas, Ester Carreño, Belén Jimenez‐Rolando, Blanca Garcı́a-Sandoval, Marta Cortón, Almudena Ávila‐Fernández, Carmen Ayuso	13
5	An evaluation of pipelines for DNA variant detection can guide a reanalysis protocol to increase the diagnostic ratio of genetic diseases 2022 ·npj Genomic Medicine ·Raquel Escutia Romero, Lorena de la Fuente, Marta Del Pozo‐Valero, Rosa Riveiro-Álvarez, María José Trujillo-Tiebas, Inmaculada Martín-Mérida, Almudena Ávila‐Fernández, (unknown), Irene Perea‐Romero, (unknown), (unknown), (unknown), Berta Almoguera, Marta Cortón, Carmen Ayuso, Pablo Mínguez	9
6	NGS and phenotypic ontology-based approaches increase the diagnostic yield in syndromic retinal diseases 2021 ·Human Genetics ·Irene Perea‐Romero, Fiona Blanco‐Kelly, Iker Sánchez‐Navarro, Isabel Lorda‐Sánchez, Saoud Tahsin Swafiri, (unknown), Inmaculada Martín-Mérida, María José Trujillo-Tiebas, Rosario López‐Rodríguez, Marta Rodríguez de Alba, (unknown), Raquel Escutia Romero, Mathieu Quinodoz, Håkon Håkonarson, (unknown), Pablo Mínguez, Marta Cortón, Carlo Rivolta, Carmen Ayuso	12
7	Homozygous females for a X-linked RPGR-ORF15 mutation in an Iranian family with retinitis pigmentosa 2021 ·Experimental Eye Research ·(unknown), Marta Del Pozo‐Valero, Inmaculada Martín-Mérida, Masoud Reza Manaviat, Carmen Ayuso, (unknown)	3
8	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
9	Apparent but unconfirmed digenism in an Iranian consanguineous family with syndromic Retinal Disease 2021 ·Experimental Eye Research ·(unknown), Marta Del Pozo‐Valero, Inmaculada Martín-Mérida, Irene Perea‐Romero, Masoud Reza Manaviat, Carmen Ayuso, (unknown)	1
10	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
11	Expanded Phenotypic Spectrum of Retinopathies Associated with Autosomal Recessive and Dominant Mutations in PROM1 2019 ·American Journal of Ophthalmology ·Marta Del Pozo‐Valero, Inmaculada Martín-Mérida, Belén Jimenez‐Rolando, Ana Arteche‐López, Almudena Ávila‐Fernández, Fiona Blanco‐Kelly, Rosa Riveiro-Álvarez, Caroline Van Cauwenbergh, Elfride De Baere, Carlo Rivolta, Blanca Garcı́a-Sandoval, Marta Cortón, Carmen Ayuso	18
12	Genomic Landscape of Sporadic Retinitis Pigmentosa 2019 ·Ophthalmology ·Inmaculada Martín-Mérida, Almudena Ávila‐Fernández, Marta Del Pozo‐Valero, Fiona Blanco‐Kelly, Olga Zurita, Raquel Pérez-Carro, Domingo Aguilera‐Garcia, Rosa Riveiro-Álvarez, Ana Arteche‐López, María José Trujillo-Tiebas, Saoud Tahsin Swafiri, Elvira Rodríguez‐Pinilla, Isabel Lorda‐Sánchez, Blanca Garcı́a-Sandoval, Marta Cortón, Carmen Ayuso	52
13	Unravelling the pathogenic role and genotype-phenotype correlation of the USH2A p.(Cys759Phe) variant among Spanish families 2018 ·PLoS ONE ·Raquel Pérez-Carro, Fiona Blanco‐Kelly, (unknown), Gema García‐García, Elena Aller, Blanca Garcı́a-Sandoval, Pablo Mínguez, Marta Cortón, Ignacio Mahíllo, Inmaculada Martín-Mérida, Almudena Ávila‐Fernández, José M. Millán, Carmen Ayuso	14
14	Toward the Mutational Landscape of Autosomal Dominant Retinitis Pigmentosa: A Comprehensive Analysis of 258 Spanish Families 2018 ·Investigative Ophthalmology & Visual Science ·Inmaculada Martín-Mérida, Domingo Aguilera‐Garcia, Patrícia José, Fiona Blanco‐Kelly, Olga Zurita, Berta Almoguera, Blanca Garcı́a-Sandoval, Almudena Ávila‐Fernández, Ana Arteche‐López, Pablo Mínguez, Miguel Carballo, Marta Cortón, Carmen Ayuso	50
15	Analysis of the PRPF31 Gene in Spanish Autosomal Dominant Retinitis Pigmentosa Patients: A Novel Genomic Rearrangement 2017 ·Investigative Ophthalmology & Visual Science ·Inmaculada Martín-Mérida, Rocío Sánchez-Alcudia, Patrícia José, Fiona Blanco‐Kelly, Raquel Pérez-Carro, (unknown), Berta Almoguera, Blanca Garcı́a-Sandoval, María Isabel López-Molina, Almudena Ávila‐Fernández, Miguel Carballo, Marta Cortón, Carmen Ayuso	20

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