Magdalena Beneyto

1.4k citations

48 papers · 965 indexed · h-index 18

Sensory Systems top 1%
- Hearing, Cochlea, Tinnitus, Genetics 14
Ophthalmology top 5%
- Retinal Diseases and Treatments 3
- Ocular Oncology and Treatments 3
Neurology top 10%
Molecular Biology top 10%
- Retinal Development and Disorders 12
- RNA and protein synthesis mechanisms 4
- Congenital heart defects research 3
- Retinoids in leukemia and cellular processes 3
Otorhinolaryngology top 10%
Oncology
- Cancer-related Molecular Pathways 3

Co-authors: Carmén Nájera José M. Millán Carmen Ayuso Elena Aller Montserrat Baiget Félix Prieto Herminio Pérez-Garrigues Teresa Jaijo
Cited by: Sensory Systems Ophthalmology Neurology
Journals: The American Journal of Human Genetics (1 paper)Investigative Ophthalmology & Visual Science (2 papers)Journal of Medical Genetics (3 papers)
Partner nations: Spain United States Italy

In The Last Decade

Magdalena Beneyto

48 papers receiving 950 citations

Peers

Countries citing papers authored by Magdalena Beneyto

Since Specialization

Citations

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

Fields of papers citing papers by Magdalena Beneyto

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Magdalena Beneyto. 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 Magdalena Beneyto. The network helps show where Magdalena Beneyto may publish in the future.

Co-authorship network

The 25 scholars most cited alongside Magdalena Beneyto, linked wherever they have co-authored with each other. Click a name or a connecting line to browse the papers they share.

Border = papers with Magdalena Beneyto Line = papers co-authored together Magdalena Beneyto links everyone, so they are left out of the graph.

All Works

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20 of 20 papers shown

#	Work
1	Manejo del absceso de la glándula tiroides Acta Otorrinolaringológica Española ·Javier García Callejo,Jaume Redondo Martínez,Miguel Civera,José Verdú Colomina,Veronica Zoghbi,Magdalena Beneyto	2018	1
2	Hipo. Actitud en otorrinolaringología en pacientes que consultan. Aproximación diagnóstica y terapéutica Acta Otorrinolaringológica Española ·Francisco Javier García Callejo,Jaume Redondo Martínez,Tomàs Pérez‐Carbonell,Rafael Monzó Gandía,Magdalena Beneyto,Inés Rincón Piedrahita	2016	2
3	Cavernomatosis múltiple familiar: descripción de una nueva mutación Neurología ·Ana Simón Gozalbo,Magdalena Beneyto,David Rodríguez‐Luna,R.M. Vilar Ventura,Antonio Belenguer,D. Geffner Sclarsky	2010	1
4	Severe and moderate hemophilia A: identification of 38 new genetic alterations Haematologica ·Pilar Casaña,N. Cabrera,Ana Rosa Cid,Saturnino Haya,Magdalena Beneyto,Carmen Espinós,Vicente Cortina,M. A. Dasi,J Aznar	2008	17
5	El asesoramiento genético en los déficits visuales y auditivos Archivos de la Sociedad Española de Oftalmología ·Jesús Millán,Elena Aller,Teresa Jaijo,Elena Grau,Magdalena Beneyto,Carmén Nájera	2008	4
6	Screening of theUSH1GGene among Spanish Patients with Usher Syndrome. Lack of Mutations and Evidence of a Minor Role in the Pathogenesis of the Syndrome Ophthalmic Genetics ·Elena Aller,Teresa Jaijo,Magdalena Beneyto,Carmén Nájera,Constantino Morera,Herminio Pérez-Garrigues,Carmen Ayuso,José M. Millán	2007	10
7	Identification of 14 novel mutations in the long isoform of USH2A in Spanish patients with Usher syndrome type II Journal of Medical Genetics ·Elena Aller,Teresa Jaijo,Magdalena Beneyto,Carmén Nájera,Silvestre Oltra,Carmen Ayuso,Montserrat Baiget,Miguel Carballo,Guillermo Antiñolo,Diana Valverde,Felipe Moreno,C Vilela,Diego Collado,Herminio Pérez-Garrigues,Amparo Návea,José M. Millán	2006	67
8	Mutation profile of the MYO7A gene in Spanish patients with Usher syndrome type I Human Mutation ·Teresa Jaijo,Elena Aller,Silvestre Oltra,Magdalena Beneyto,Carmén Nájera,Carmen Ayuso,Montserrat Baiget,Miguel Carballo,Guillermo Antiñolo,Diana Valverde,Felipe Moreno,C Vilela,Herminio Pérez-Garrigues,Amparo Návea,José M. Millán	2006	38
9	Mutation screening of USH3 gene (clarin‐1) in Spanish patients with Usher syndrome: low prevalence and phenotypic variability Clinical Genetics ·Elena Aller,Teresa Jaijo,Silvestre Oltra,Jorge L. Alió del Barrio,Francisco Galán,Carmén Nájera,Magdalena Beneyto,J.M. Millán	2004	25
10	Mutations in Myosin VIIA (MYO7A) and Usherin (USH2A) in Spanish patients with usher syndrome types I and II, respectively Human Mutation ·Carmén Nájera,Magdalena Beneyto,José Blanca,Elena Aller,Ana Fontcuberta,José M. Millán,Carmen Ayuso	2002	47
11	A Common Ancestral Origin of the Frequent and Widespread 2299delG USH2A Mutation The American Journal of Human Genetics ·Bo Dreyer,Lisbeth Tranebjærg,Vigdis Brox,Thomas Rosenberg,Claes Möller,Magdalena Beneyto,Michael D. Weston,William J. Kimberling,Øivind Nilssen	2001	67
12	Mutation analysis of the RPGR gene reveals novel mutations in south European patients with X-linked retinitis pigmentosa European Journal of Human Genetics ·Maria Giuseppina Miano,Francesco Testa,Maria Strazzullo,Mariajosè Trujillo,Carmelilia De Bernardo,Barbara Grammatico,Francesca Simonelli,Massimo Mangino,Isabella Torrente,Giulio Ruberto,Magdalena Beneyto,Guillermo Antiñolo,E. Rinaldi,Cesare Danesino,V. Ventruto,Michele D’Urso,Carmen Ayuso,M. Baiget,Alfredo Ciccodicola	1999	29
13	Identification of three novel mutations in the MYO7A gene Human Mutation ·José M. Cuevas,C. Espin�s,J.M. Mill�n,F. S�nchez,M.J. Trujillo,Carmen Ayuso,Magdalena Beneyto,C. N�jera	1999	15
14	Epidemiology of Usher Syndrome in Valencia and Spain Public Health Genomics ·Carmen Espinós,José M. Millán,Magdalena Beneyto,Carmén Nájera	1998	37
15	Putative association of a mutant ROM1 allele with retinitis pigmentosa Human Genetics ·Amalia Martı́nez-Mir,Concha Vilela,Mónica Bayés,Diana Valverde,Liliana Daín,Magdalena Beneyto,Marina De Marco,Montserrat Baiget,Daniel Grinberg,Susana Balcells,Roser Gonzàlez‐Duarte,Lluı̈sa Vilageliu	1997	7
16	Clinical and genetic aspects of two Spanish families with autosomal dominant retinitis pigmentosa (ADRP) Ophthalmic Genetics ·Concha Vilela,Magdalena Beneyto,Rosabel Bosch,José M. Millán,Marina De Marco,Miguel Vallet,Luís Garcia Alonso,Isidro Tormos,Carmén Nájera,Beatriz Vails,Nuria Paricio,Félix Prieto	1996	1
17	Mutations in the human peripherin/RDS gene associated with autosomal dominant retinitis pigmentosa Human Mutation ·Gunnar Grüning,José M. Millán,Moritz Meins,Magdalena Beneyto,Manuel Caballero,Eckart Apfelstedt-Sylla,Rosabel Bosch,Eberhart Zrenner,Félix Prieto,Andreas Gal	1994	29
18	Gene localization in a family with X‐linked syndromal mental retardation (Prieto syndrome) American Journal of Medical Genetics ·Anke Watty,Félix Prieto,Magdalena Beneyto,M. Neugebauer,Andreas Gal	1991	15
19	Chromosome 5 abnormalities in acute lymphoblastic leukemia Cancer Genetics and Cytogenetics ·Francesc Palau,Félix Prieto,Lourdes Badı́a,Magdalena Beneyto,Isana Benet	1991	6
20	11q23 abnormalities in children with acute nonlymphocytic leukemia (M4–M5) Cancer Genetics and Cytogenetics ·Félix Prieto,Francesc Palau,Lourdes Badı́a,Magdalena Beneyto,Maria Luz Perez-Sirvent,Angeles Orts,Victoria Castel	1990	37

About Magdalena Beneyto

Magdalena Beneyto is a scholar working on Sensory Systems, Ophthalmology and Otorhinolaryngology, having authored 48 papers that have together received 965 indexed citations. Recurring topics across this work include Hearing, Cochlea, Tinnitus, Genetics (14 papers), Retinal Development and Disorders (12 papers), RNA and protein synthesis mechanisms (4 papers), Retinal Diseases and Treatments (3 papers), Congenital heart defects research (3 papers), Retinoids in leukemia and cellular processes (3 papers), Cancer-related Molecular Pathways (3 papers) and Ocular Oncology and Treatments (3 papers). The work is most often cited by research in Sensory Systems (328 citations), Ophthalmology (168 citations) and Neurology (116 citations). Magdalena Beneyto has collaborated with scholars based in Spain, United States and Italy. Frequent co-authors include Carmén Nájera, José M. Millán, Carmen Ayuso, Elena Aller, Montserrat Baiget, Félix Prieto, Herminio Pérez-Garrigues, Teresa Jaijo, Guillermo Antiñolo and Silvestre Oltra. Their work appears in journals such as The American Journal of Human Genetics, Investigative Ophthalmology & Visual Science and Journal of Medical Genetics.

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