Fiona Blanco‐Kelly

2.8k total citations
70 papers, 1.6k citations indexed

About

Fiona Blanco‐Kelly is a scholar working on Molecular Biology, Ophthalmology and Genetics. According to data from OpenAlex, Fiona Blanco‐Kelly has authored 70 papers receiving a total of 1.6k indexed citations (citations by other indexed papers that have themselves been cited), including 50 papers in Molecular Biology, 24 papers in Ophthalmology and 23 papers in Genetics. Recurrent topics in Fiona Blanco‐Kelly's work include Retinal Development and Disorders (35 papers), Retinal Diseases and Treatments (19 papers) and Ocular Disorders and Treatments (9 papers). Fiona Blanco‐Kelly is often cited by papers focused on Retinal Development and Disorders (35 papers), Retinal Diseases and Treatments (19 papers) and Ocular Disorders and Treatments (9 papers). Fiona Blanco‐Kelly collaborates with scholars based in Spain, United States and United Kingdom. Fiona Blanco‐Kelly's co-authors include Carmen Ayuso, Marta Cortón, Almudena Ávila‐Fernández, José M. Millán, Elena Aller, Rosa Riveiro-Álvarez, Blanca Garcı́a-Sandoval, Teresa Jaijo, Ascensión Gimenez-Pardo and María José Trujillo-Tiebas and has published in prestigious journals such as PLoS ONE, Circulation Research and Scientific Reports.

In The Last Decade

Fiona Blanco‐Kelly

67 papers receiving 1.6k citations

Peers

Countries citing papers authored by Fiona Blanco‐Kelly

Since Specialization

Citations

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

Fields of papers citing papers by Fiona Blanco‐Kelly

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Fiona Blanco‐Kelly. 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 Fiona Blanco‐Kelly. The network helps show where Fiona Blanco‐Kelly may publish in the future.

Co-authorship network of co-authors of Fiona Blanco‐Kelly

This figure shows the co-authorship network connecting the top 25 collaborators of Fiona Blanco‐Kelly. A scholar is included among the top collaborators of Fiona Blanco‐Kelly 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 Fiona Blanco‐Kelly. Fiona Blanco‐Kelly 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	Apolipoprotein E-ε2 and Resistance to Atherosclerosis in Midlife: The PESA Observational Study 2024 ·Circulation Research ·(unknown), (unknown), Juan Carlos Silla-Castro, Sergio Callejas, Belén Oliva, (unknown), Inés García‐Lunar, (unknown), José M. Ordovás, Pilar Martı́n, Fiona Blanco‐Kelly, Carmen Ayuso, Enrique Lara‐Pezzi, Antonio Fernández‐Ortíz, Ana García‐Álvarez, Ana Dopazo, Fátima Sánchez‐Cabo, Borja Ibáñez, Marta Cortés‐Canteli, Valentı́n Fuster	4
2	Clinical and genetic analysis further delineates the phenotypic spectrum of ALDH1A3-related anophthalmia and microphthalmia 2023 ·European Journal of Human Genetics ·Yeşim Kesim, Fabiola Ceroni, (unknown), Fiona Blanco‐Kelly, Carmen Ayuso, Kathy Williamson, Véronique Paquis‐Flucklinger, Dorine A. Bax, Julie Plaisancié, Claudine Rieubland, (unknown), Marta Cortón, Nicolas Chassaing, Patrick Calvas, Nicola Ragge	2
3	The enduring enigma of sporadic chorea: A single center case series 2023 ·Tremor and Other Hyperkinetic Movements ·Pedro Ruiz, (unknown), Cici Feliz, (unknown), Almudena Fernández, Fiona Blanco‐Kelly, (unknown), Javier del Val, (unknown)	0
4	Biallelic intragenic tandem duplication of CPLANE1 in Joubert syndrome: A case report 2023 ·Clinical Genetics ·Francisco Martínez‐Granero, (unknown), (unknown), (unknown), Marta Rodríguez de Alba, Fiona Blanco‐Kelly, Raquel Escutia Romero, Pablo Mínguez, Carmen Ayuso, Isabel Lorda‐Sánchez, Marta Cortón, Berta Almoguera	1
5	Prioritization of New Candidate Genes for Rare Genetic Diseases by a Disease-Aware Evaluation of Heterogeneous Molecular Networks 2023 ·International Journal of Molecular Sciences ·(unknown), Marta Del Pozo‐Valero, Irene Perea‐Romero, Fiona Blanco‐Kelly, (unknown), Marta Cortón, Carmen Ayuso, Pablo Mínguez	1
6	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
7	Novel homozygous mutations in the transcription factor NRL cause non-syndromic retinitis pigmentosa 2022 ·PubMed Central ·Mohammed E. El‐Asrag, Marta Cortón, Martin McKibbin, Almudena Ávila‐Fernández, Moin Mohamed, Fiona Blanco‐Kelly, Carmel Toomes, Chris F. Inglehearn, Carmen Ayuso, Manir Ali	8
8	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
9	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
10	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
11	Genetics and epidemiology of aniridia: Updated guidelines for genetic study 2021 ·Archivos de la Sociedad Española de Oftalmología (English Edition) ·Fiona Blanco‐Kelly, (unknown), Manuela Villamar, (unknown), (unknown), Miguel A. Moreno‐Pelayo, Carmen Ayuso, Marta Cortón	10
12	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
13	Implication of non-coding PAX6 mutations in aniridia 2018 ·Human Genetics ·Julie Plaisancié, (unknown), Patrícia Locosque Ramos, (unknown), Véronique Gaston, Hélène Dollfus, (unknown), J.‐C. Kaplan, Lucas Fares‐Taie, Fiona Blanco‐Kelly, Cristina Villaverde, Christine Francannet, Alice Goldenberg, Ignacio Arroyo, Jean‐Michel Rozet, Carmen Ayuso, Nicolas Chassaing, Patrick Calvas, Marta Cortón	34
14	Generation of a human iPSC line from a patient with congenital glaucoma caused by mutation in CYP1B1 gene 2018 ·Stem Cell Research ·(unknown), Dunja Lukovic, Ana Artero‐Castro, Marian León, (unknown), Radka Kaneva, Pavla Jendelová, Fiona Blanco‐Kelly, Carmen Ayuso, Marta Cortón, Slaven Erceg	5
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
16	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
17	Application of Whole Exome Sequencing in Six Families with an Initial Diagnosis of Autosomal Dominant Retinitis Pigmentosa: Lessons Learned 2015 ·PLoS ONE ·Berta Almoguera, Jiankang Li, Patrícia José, Yichuan Liu, Michael March, Renata Pellegrino, Ryan Golhar, Marta Cortón, Fiona Blanco‐Kelly, María Isabel López-Molina, Blanca Garcı́a-Sandoval, Yiran Guo, Lifeng Tian, Xuanzhu Liu, Liping Guan, Jianguo Zhang, Brendan J. Keating, Xun Xu, Håkon Håkonarson, Carmen Ayuso	16
18	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
19	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
20	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

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