Begoña Atarés

3.1k total citations · 1 hit paper
12 papers, 2.4k citations indexed

About

Begoña Atarés is a scholar working on Neurology, Molecular Biology and Neurology. According to data from OpenAlex, Begoña Atarés has authored 12 papers receiving a total of 2.4k indexed citations (citations by other indexed papers that have themselves been cited), including 9 papers in Neurology, 8 papers in Molecular Biology and 7 papers in Neurology. Recurrent topics in Begoña Atarés's work include Neurological diseases and metabolism (9 papers), Prion Diseases and Protein Misfolding (6 papers) and Parkinson's Disease Mechanisms and Treatments (3 papers). Begoña Atarés is often cited by papers focused on Neurological diseases and metabolism (9 papers), Prion Diseases and Protein Misfolding (6 papers) and Parkinson's Disease Mechanisms and Treatments (3 papers). Begoña Atarés collaborates with scholars based in Spain, Netherlands and India. Begoña Atarés's co-authors include J.J. Zarranz, Juan Carlos Gómez‐Esteban, Elena Lezcano, Janet Hoenicka, Javier Alegre‐Abarrategui, Justo Garcı́a de Yébenes, Olga Rodriguez, Teodoro del Ser, Verónica Llorens and Raquel Ros and has published in prestigious journals such as Neurology, Annals of Neurology and Movement Disorders.

In The Last Decade

Begoña Atarés

12 papers receiving 2.4k citations

Hit Papers

align trajectories

What are hit papers?

Hit papers significantly outperform the citation benchmark for their cohort. A paper qualifies if it has ≥500 total citations, achieves ≥1.5× the top-1% citation threshold for papers in the same subfield and year (this is the minimum needed to enter the top 1%, not the average within it), or reaches the top citation threshold in at least one of its specific research topics.

The new mutation, E46K, of α‐synuclein causes parkinson and Lewy body dementia

2003 2.1k citations J.J. Zarranz, Javier Alegre‐Abarrategui et al. Annals of Neurology profile →

Peers

Countries citing papers authored by Begoña Atarés

Since Specialization

Citations

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

Fields of papers citing papers by Begoña Atarés

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Begoña Atarés

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

All Works

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12 of 12 papers shown

#	Work	Indexed citations
1	Molecularly determined total tumour load in lymph nodes of stage I–II colon cancer patients correlates with high-risk factors. A multicentre prospective study 2016 ·Archiv für Pathologische Anatomie und Physiologie und für Klinische Medicin ·Ibán Aldecoa, Begoña Atarés, (unknown), Laia Bernet, (unknown), Teresa Pereda, (unknown), (unknown), (unknown), Kepa Elorriaga, (unknown), (unknown), Núria Planell, José Palacios, Antoni Castells, Xavier Matías‐Guiu, Míriam Cuatrecasas	20
2	Coexistence of protease sensitive and resistant prion protein in 129VV homozygous sporadic Creutzfeldt–Jakob disease: a case report 2012 ·Journal of Medical Case Reports ·Ana Belén Rodríguez-Martínez, Adolfo López de Munaín, Isidró Ferrer, J.J. Zarranz, Begoña Atarés, Nuria T. Villagrá, José M. Arteagoitia, Joseba M. Garrido, Ramón A. Juste	14
3	A NovelPRNP Y218NMutation in Gerstmann-Sträussler-Scheinker Disease With Neurofibrillary Degeneration 2010 ·Journal of Neuropathology & Experimental Neurology ·Ainhoa Alzualde, Begoña Indakoetxea, Isidró Ferrer, Fermín Moreno, Myriam Barandiarán, Ana Gorostidi, Ainara Estanga, Irune Ruiz, Miguel Calero, Fred W. van Leeuwen, Begoña Atarés, Ramón A. Juste, Ana Belén Rodríguez-Martínez, Adolfo López de Munaín	37
4	A novel form of human disease with a protease-sensitive prion protein and heterozygosity methionine/valine at codon 129: Case report 2010 ·BMC Neurology ·Ana Belén Rodríguez-Martínez, Joseba M. Garrido, J.J. Zarranz, José M. Arteagoitia, Marian M. de Pancorbo, Begoña Atarés, (unknown), Isidró Ferrer, Ramón A. Juste	25
5	Somatic mosaicism in a case of apparently sporadic Creutzfeldt‐Jakob disease carrying a de novo D178N mutation in the PRNP gene 2010 ·American Journal of Medical Genetics Part B Neuropsychiatric Genetics ·Ainhoa Alzualde, Fermín Moreno, Pablo Martínez‐Lage, Isidró Ferrer, Ana Gorostidi, David Otaegui, Lorea Blázquez, Begoña Atarés, Sergio Cardoso, Marian M. de Pancorbo, Ramón A. Juste, Ana Belén Rodríguez-Martínez, Begoña Indakoetxea, Adolfo López de Munaín	26
6	Tau‐predominant–associated pathology in a sporadic late‐onset Hallervorden–Spatz syndrome 2005 ·Movement Disorders ·J.J. Zarranz, Juan Carlos Gómez‐Esteban, Begoña Atarés, Elena Lezcano, (unknown)	9
7	A novel mutation (K317M) in the MAPT gene causes FTDP and motor neuron disease 2005 ·Neurology ·J.J. Zarranz, Isidró Ferrer, E. Lezcano, (unknown), (unknown), Begoña Atarés, Berta Puig, Juan Carlos Gómez‐Esteban, (unknown), (unknown), (unknown), Manel Fernández, (unknown), Ana Belén Rodríguez-Martínez, Marian M. de Pancorbo, Pau Pástor, Jordi Pérez‐Tur	77
8	Familial Prion Diseases in the Basque Country (Spain) 2004 ·Neuroepidemiology ·J.J. Zarranz, (unknown), Begoña Atarés, José M. Arteagoitia, (unknown), (unknown), Manuel Fernández Martínez, (unknown), (unknown), (unknown), Agustín Ibáñez, Elena Lezcano, J.F. Martí-Massó, (unknown), Miguel Urtasun, (unknown), (unknown), Fernando Velasco, (unknown)	8
9	Parkinson's disease‐like presentation of multiple system atrophy with poor response to STN stimulation: A clinicopathological case report 2004 ·Movement Disorders ·Elena Lezcano, Juan Carlos Gómez‐Esteban, J.J. Zarranz, (unknown), Begoña Atarés, G. Bilbao, J. Garibi, (unknown)	32
10	The new mutation, E46K, of α‐synuclein causes parkinson and Lewy body dementia breakdown → 2003 ·Annals of Neurology ·J.J. Zarranz, Javier Alegre‐Abarrategui, Juan Carlos Gómez‐Esteban, Elena Lezcano, Raquel Ros, Israel Ampuero, Lídice Vidal, Janet Hoenicka, Olga Rodriguez, Begoña Atarés, Verónica Llorens, (unknown), Teodoro del Ser, David G. Muñoz, Justo Garcı́a de Yébenes	2133
11	Value of Limited Necropsy in HIV-positive Patients 2001 ·Pathology - Research and Practice ·Isabel Guerra, (unknown), Joseba Portu, Begoña Atarés, (unknown), (unknown)	17
12	Dementia, Amyotrophy, and Periodic Complexes on the Electroencephalogram 2001 ·Archives of Neurology ·Juan Carlos Gómez‐Esteban, Begoña Atarés, J.J. Zarranz, Fernando Velasco, (unknown)	4

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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