Isabel Llano‐Rivas

1.3k total citations
18 papers, 286 citations indexed

About

Isabel Llano‐Rivas is a scholar working on Genetics, Molecular Biology and Nephrology. According to data from OpenAlex, Isabel Llano‐Rivas has authored 18 papers receiving a total of 286 indexed citations (citations by other indexed papers that have themselves been cited), including 14 papers in Genetics, 11 papers in Molecular Biology and 2 papers in Nephrology. Recurrent topics in Isabel Llano‐Rivas's work include Genomics and Rare Diseases (3 papers), Genetic Syndromes and Imprinting (3 papers) and Renal and related cancers (3 papers). Isabel Llano‐Rivas is often cited by papers focused on Genomics and Rare Diseases (3 papers), Genetic Syndromes and Imprinting (3 papers) and Renal and related cancers (3 papers). Isabel Llano‐Rivas collaborates with scholars based in Spain, United Kingdom and Japan. Isabel Llano‐Rivas's co-authors include Gloria Fraga, Gema Ariceta, Patricia Ruíz, Roser Torrá, Elisabet Ars, Mónica Furlano, Juan Alberto Piñero‐Fernández, Blanca Gener, Iván Vargas and Gemma Bullich and has published in prestigious journals such as Journal of Biological Chemistry, Kidney International and PLoS Genetics.

In The Last Decade

Isabel Llano‐Rivas

15 papers receiving 286 citations

Peers

Isabel Llano‐Rivas

GENET

NEPHR

NEURO

ONCOL

Katsuyoshi Kanemoto Japan

Paula Martin Finland

Jaume Crespí Spain

Erich J. Goebel United States

Veronica Moran United Kingdom

Andrea Alonso United States

Cassio Menezes Raposo do Amaral Brazil

Sigrid Tinschert Germany

Rakesh Kumar Verma India

Gabriele Krüger Germany

Katsuyoshi Kanemoto Japan

Isabel Llano‐Rivas

203 ×1.2

66 ×0.5

GENET

147 ×1.8

NEPHR

7 ×0.3

NEURO

16 ×0.6

ONCOL

Citations per year, relative to Isabel Llano‐Rivas Isabel Llano‐Rivas (= 1×) peers Katsuyoshi Kanemoto

Countries citing papers authored by Isabel Llano‐Rivas

Since Specialization

Citations

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

Fields of papers citing papers by Isabel Llano‐Rivas

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Isabel Llano‐Rivas. 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 Isabel Llano‐Rivas. The network helps show where Isabel Llano‐Rivas may publish in the future.

Co-authorship network of co-authors of Isabel Llano‐Rivas

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

All Works

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18 of 18 papers shown

Nunes‐Xavier, Caroline E., Sonia Bañuelos, Fabio Cavaliere, et al.. (2025). Genotype-phenotype characterization and functional reconstitution of pathogenic β-catenin variants from CTNNB1 syndrome patients. PLoS Genetics. 21(10). e1011907–e1011907.

Pereda, Arrate, et al.. (2023). Incidental finding at methylation-specific multiplex ligation-dependent probe amplification (MS-MLPA): how to proceed?. Frontiers in Genetics. 14. 1274056–1274056. 1 indexed citations

Villate, Olatz, et al.. (2022). RNA Analysis and Clinical Characterization of a Novel Splice Variant in the NSD1 Gene Causing Familial Sotos Syndrome. Frontiers in Pediatrics. 10. 827802–827802.

Pybus, Marc, Gemma Bullich, Mónica Furlano, et al.. (2021). Clinical utility of genetic testing in early-onset kidney disease: seven genes are the main players. Nephrology Dialysis Transplantation. 37(4). 687–696. 47 indexed citations

Infante, Arantza, Blanca Gener, Miguél Vázquez, et al.. (2021). Reiterative infusions of MSCs improve pediatric osteogenesis imperfecta eliciting a pro‐osteogenic paracrine response: TERCELOI clinical trial. Clinical and Translational Medicine. 11(1). e265–e265. 31 indexed citations

Hoz, Ana B. de la, Olatz Villate, Isabel Llano‐Rivas, et al.. (2020). Targeted Next-Generation Sequencing in Patients with Suggestive X-Linked Intellectual Disability. Genes. 11(1). 51–51. 18 indexed citations

Pereda, Arrate, et al.. (2020). Novel Variant in PLAG1 in a Familial Case with Silver–Russell Syndrome Suspicion. Genes. 11(12). 1461–1461. 10 indexed citations

Sagasta, Amaia, et al.. (2020). Prenatal and foetal autopsy findings in glutaric aciduria type II. Birth Defects Research. 112(19). 1738–1749.

Llano‐Rivas, Isabel, et al.. (2019). P87-F Severe congenital myopathy related to a novel mutation in the titin gene. A case report. Clinical Neurophysiology. 130(7). e92–e93. 1 indexed citations

10.

Bullich, Gemma, Iván Vargas, Patricia Ruíz, et al.. (2018). A kidney-disease gene panel allows a comprehensive genetic diagnosis of cystic and glomerular inherited kidney diseases. Kidney International. 94(2). 363–371. 86 indexed citations

11.

Martínez‐Fernández, M.L., et al.. (2015). Delineation of the clinically recognizable 17q22 contiguous gene deletion syndrome in a patient carrying the smallest microdeletion known to date. American Journal of Medical Genetics Part A. 167(9). 2034–2041. 4 indexed citations

12.

Brems, Hilde, Mayu Suzuki, Mitsuhiro Kanamori, et al.. (2015). Interaction between a Domain of the Negative Regulator of the Ras-ERK Pathway, SPRED1 Protein, and the GTPase-activating Protein-related Domain of Neurofibromin Is Implicated in Legius Syndrome and Neurofibromatosis Type 1. Journal of Biological Chemistry. 291(7). 3124–3134. 46 indexed citations

13.

Pangrazio, Alessandra, Manuela Oppo, Maria Consuelo Valentini, et al.. (2013). Exome sequencing identifies CTSK mutations in patients originally diagnosed as intermediate osteopetrosis. Bone. 59. 122–126. 26 indexed citations

14.

Llano‐Rivas, Isabel, et al.. (2011). Discondrosteosis de Leri-Weill. Mutación en gen SHOX y expresividad variable. Anales de Pediatría. 74(6). 405–408. 1 indexed citations

15.

Llano‐Rivas, Isabel, et al.. (2011). A novel mutation in the IRF6 gene associated with facial asymmetry in a family affected with Van der Woude Syndrome. Pediatric Dermatology. 29(6). 768–770. 6 indexed citations

16.

Llano‐Rivas, Isabel, et al.. (2011). Incontinencia pigmenti. Cuatro pacientes con diferentes manifestaciones clínicas. Anales de Pediatría. 76(3). 156–160. 7 indexed citations

17.

Llano‐Rivas, Isabel, et al.. (2007). Mortalidad perinatal por defectos estructurales congénitos: Un estudio de sitio. Perinatología y Reproducción Humana. 21(4). 185–192. 1 indexed citations

18.

Aguinaga‐Ríos, Mónica, et al.. (2002). Polidactilia preaxial en recién nacidos expuestos a ácido valproico durante el embarazo: presentación de dos casos. Perinatología y Reproducción Humana. 16(4). 180–186. 1 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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