Javier Garcı́a-Planells

768 total citations
23 papers, 459 citations indexed

About

Javier Garcı́a-Planells is a scholar working on Molecular Biology, Cellular and Molecular Neuroscience and Genetics. According to data from OpenAlex, Javier Garcı́a-Planells has authored 23 papers receiving a total of 459 indexed citations (citations by other indexed papers that have themselves been cited), including 14 papers in Molecular Biology, 8 papers in Cellular and Molecular Neuroscience and 6 papers in Genetics. Recurrent topics in Javier Garcı́a-Planells's work include Genetic Neurodegenerative Diseases (7 papers), Mitochondrial Function and Pathology (6 papers) and Prenatal Screening and Diagnostics (5 papers). Javier Garcı́a-Planells is often cited by papers focused on Genetic Neurodegenerative Diseases (7 papers), Mitochondrial Function and Pathology (6 papers) and Prenatal Screening and Diagnostics (5 papers). Javier Garcı́a-Planells collaborates with scholars based in Spain, United States and Belgium. Javier Garcı́a-Planells's co-authors include Francesc Palau, Juan J. Vílchez, Ana Cuesta, Teresa Sevilla, Éric Leguern, Ignacio Marı́n, Laia Pedrola, María José Chumillas, F. Mayordomo and Nuria Paricio and has published in prestigious journals such as Nature Genetics, SHILAP Revista de lepidopterología and PLoS ONE.

In The Last Decade

Javier Garcı́a-Planells

21 papers receiving 445 citations

Peers

Countries citing papers authored by Javier Garcı́a-Planells

Since Specialization

Citations

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

Fields of papers citing papers by Javier Garcı́a-Planells

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Javier Garcı́a-Planells. 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 Javier Garcı́a-Planells. The network helps show where Javier Garcı́a-Planells may publish in the future.

Co-authorship network of co-authors of Javier Garcı́a-Planells

This figure shows the co-authorship network connecting the top 25 collaborators of Javier Garcı́a-Planells. A scholar is included among the top collaborators of Javier Garcı́a-Planells 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 Javier Garcı́a-Planells. Javier Garcı́a-Planells 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	Population-based genetic carrier screening. A consensus statement from the Spanish societies: AEGH, AEDP, ASEBIR, SEAGEN, SEF and SEGCD 2024 ·European Journal of Human Genetics ·(unknown), Anna Abulí, (unknown), Juan José Guillén, Joaquı́n Rueda, Javier Garcı́a-Planells, Fernando Santos‐Simarro, (unknown), (unknown), (unknown), Encarna Guillén‐Navarro	0
2	Homozygous Pro1066Arg MYBPC3 Pathogenic Variant in a 26Mb Region of Homozygosity Associated with Severe Hypertrophic Cardiomyopathy in a Patient of an Apparent Non-Consanguineous Family 2022 ·Life ·Raquel Rodríguez‐López, Javier Garcı́a-Planells, (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), Juan Martínez-León, Rafael Salguero‐Bodes	2
3	Cribado y diagnóstico prenatal de anomalías genéticas: recomendaciones de consenso SEGO, SEQC^ML, AEDP 2020 ·SHILAP Revista de lepidopterología ·Belén Prieto García, B. Adiego, Javier Suela, (unknown), Belén Santacruz, Javier Garcı́a-Planells, M. M. Gil, Concepción González, (unknown)	0
4	Prenatal screening and diagnosis of genetic abnormalities: SEGO, SEQC^ML, AEDP consensus recommendations 2020 ·SHILAP Revista de lepidopterología ·Belén Prieto García, B. Adiego, Javier Suela, (unknown), Belén Santacruz, Javier Garcı́a-Planells, M. M. Gil, Concepción González, (unknown)	1
5	Earlier relapse detection after allogeneic haematopoietic stem cell transplantation by chimerism assays: Digital PCR versus quantitative real-time PCR of insertion/deletion polymorphisms 2019 ·PLoS ONE ·(unknown), (unknown), Manuel Barrios, Greta Carmona‐Antoñanzas, Javier Garcı́a-Planells, (unknown), (unknown), Antonio Jiménez‐Velasco	29
6	A Multiomics Study To Unravel the Effects of Developmental Exposure to Endosulfan in Rats: Molecular Explanation for Sex-Dependent Effects 2019 ·ACS Chemical Neuroscience ·Sonia Tarazona, Elena Bernabeu, (unknown), Belén Gómez‐Giménez, Javier Garcı́a-Planells, P.E.G. Leonards, Stephan Jung, Ana Conesa, Vicente Felipo, Marta Llansola	9
7	Documento de consenso sobre la implementación de la secuenciación masiva de nueva generación en el diagnóstico genético de la predisposición hereditaria al cáncer 2018 ·Medicina Clínica ·José Luís Soto, Ignacio Blanco, Orland Dı́ez, Javier Garcı́a-Planells, (unknown), Gert Matthijs, Mercedes Robledo, Erika Souche, Conxi Lázaro	8
8	Consensus document on the implementation of next generation sequencing in the genetic diagnosis of hereditary cancer 2018 ·Medicina Clínica (English Edition) ·José Luís Soto, Ignacio Blanco, Orland Dı́ez, Javier Garcı́a-Planells, (unknown), Gert Matthijs, Mercedes Robledo, Erika Souche, Conxi Lázaro	7
9	Recomendaciones para el uso de microarrays en el diagnóstico prenatal 2017 ·Medicina Clínica ·Javier Suela, I. López, (unknown), (unknown), (unknown), Lluı́s Armengol, E. Antolín, Elena Garrido, María José Trujillo-Tiebas, Jordi Rosell, Javier Garcı́a-Planells, Juan C. Cigudosa	9
10	Recommendations for the use of microarrays in prenatal diagnosis 2017 ·Medicina Clínica (English Edition) ·Javier Suela, I. López, (unknown), (unknown), (unknown), Lluı́s Armengol, E. Antolín, Elena Garrido, María José Trujillo-Tiebas, Jordi Rosell, Javier Garcı́a-Planells, Juan C. Cigudosa	8
11	Recommendations of good practices for the genetic diagnosis of myotonic dystrophy 2011 ·Medicina Clínica ·Javier Garcı́a-Planells, Jesús Molano, Salud Borrego	1
12	Recomendaciones de buenas prácticas para el diagnóstico genético de la distrofia miotónica 2010 ·Medicina Clínica ·Javier Garcı́a-Planells, Jesús Molano, Salud Borrego	2
13	Ancient origin of the CAG expansion causing Huntington disease in a Spanish population 2005 ·Human Mutation ·Javier Garcı́a-Planells, J A Burguera, (unknown), José M. Millán, D. Ginestar, Francesc Palau, Carmen Espinós	17
14	The gene encoding ganglioside-induced differentiation-associated protein 1 is mutated in axonal Charcot-Marie-Tooth type 4A disease 2001 ·Nature Genetics ·Ana Cuesta, Laia Pedrola, Teresa Sevilla, Javier Garcı́a-Planells, María José Chumillas, F. Mayordomo, Éric Leguern, Ignacio Marı́n, Juan J. Vílchez, Francesc Palau	262
15	Genotype and phenotype analysis of Friedreich's ataxia compound heterozygous patients 2000 ·Human Genetics ·Mirna Castro, Javier Garcı́a-Planells, Eugènia Monrós, Joaquı́n Cañizares, Rafael P. Vázquez‐Manrique, Juan J. Vílchez, Miguel Urtasun, Miguel Lucas, Guillermo Navarro, Guillermo Izquierdo, María Dolores Moltó, Francesc Palau	46
16	Dnop56, a Drosophila gene homologous to the yeast nucleolar NOP56 gene 2000 ·Genetica ·Javier Garcı́a-Planells, Nuria Paricio, Francesc Palau, R. de Frutos	3
17	GEM, a cluster of repetitive sequences in the Drosophila subobscura genome 1999 ·Gene ·(unknown), Javier Garcı́a-Planells, Carlos Alberto Ruiz, Gemma Marfany, Nuria Paricio, (unknown), Rosa de Llanos	14
18	Genetics of the SCA6 gene in a large family segregating an autosomal dominant “pure” cerebellar ataxia 1999 ·Journal of Medical Genetics ·Javier Garcı́a-Planells, Ana Cuesta, Juan J. Vílchez, Francisco Martı́nez, F. Prieto, Francesc Palau	9
19	Déjérine-Sottas neuropathy associated with de novo S79P mutation of the peripheral myelin protein 22 (PMP22) gene 1998 ·Human Mutation ·S Bort, Teresa Sevilla, Javier Garcı́a-Planells, David Blesa, Nuria Paricio, Juan J. Vílchez, Félix Prieto, Francesc Palau	8
20	Molecular Evolution of P Transposable Elements in the Genus Drosophila. II. The obscura Species Group 1998 ·Journal of Molecular Evolution ·Javier Garcı́a-Planells, Nuria Paricio, J. B. Clark, Rosa de Llanos, Margaret G. Kidwell	9

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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