Dolores González‐Morón

517 total citations
19 papers, 346 citations indexed

About

Dolores González‐Morón is a scholar working on Molecular Biology, Genetics and Cellular and Molecular Neuroscience. According to data from OpenAlex, Dolores González‐Morón has authored 19 papers receiving a total of 346 indexed citations (citations by other indexed papers that have themselves been cited), including 11 papers in Molecular Biology, 7 papers in Genetics and 5 papers in Cellular and Molecular Neuroscience. Recurrent topics in Dolores González‐Morón's work include Genomics and Rare Diseases (6 papers), Mitochondrial Function and Pathology (6 papers) and Genetic Neurodegenerative Diseases (5 papers). Dolores González‐Morón is often cited by papers focused on Genomics and Rare Diseases (6 papers), Mitochondrial Function and Pathology (6 papers) and Genetic Neurodegenerative Diseases (5 papers). Dolores González‐Morón collaborates with scholars based in Argentina, United States and Switzerland. Dolores González‐Morón's co-authors include Marcelo Kauffman, Orlando Garcea, Ricardo Alonso, Patricia Vega, Marta Córdoba, Hernán Amartino, D. Consalvo, Silvia Kochen, Bartolomé Bejarano and Luciana D’Alessio and has published in prestigious journals such as PLoS ONE, The American Journal of the Medical Sciences and Epilepsy Research.

In The Last Decade

Dolores González‐Morón

19 papers receiving 340 citations

Peers — A (Enhanced Table)

Peers by citation overlap · career bar shows stage (early→late) cites · hero ref

Name h Career Trend Papers Cites
Dolores González‐Morón Argentina 10 129 119 105 70 43 19 346
R.S. Kandt United States 10 107 0.8× 195 1.6× 66 0.6× 57 0.8× 95 2.2× 12 571
Sinan Çomu Türkiye 8 87 0.7× 165 1.4× 14 0.1× 91 1.3× 39 0.9× 15 404
Sheena Chew United States 10 70 0.5× 147 1.2× 49 0.5× 46 0.7× 166 3.9× 17 414
Adam Mp 6 113 0.9× 180 1.5× 27 0.3× 37 0.5× 30 0.7× 286 388
Ardinger Hh United States 6 124 1.0× 192 1.6× 27 0.3× 37 0.5× 30 0.7× 287 402
Arzu Çoban Türkiye 10 26 0.2× 81 0.7× 121 1.2× 34 0.5× 165 3.8× 27 378
Bean Ljh 6 113 0.9× 180 1.5× 27 0.3× 37 0.5× 29 0.7× 285 386
Raquel Samões Portugal 12 42 0.3× 105 0.9× 117 1.1× 22 0.3× 91 2.1× 44 363
Neven Maksemous Australia 12 134 1.0× 121 1.0× 20 0.2× 89 1.3× 81 1.9× 28 362
Marc D’Hooghe Belgium 12 63 0.5× 337 2.8× 24 0.2× 95 1.4× 45 1.0× 18 580

Countries citing papers authored by Dolores González‐Morón

Since Specialization
Citations

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

Fields of papers citing papers by Dolores González‐Morón

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Dolores González‐Morón. 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 Dolores González‐Morón. The network helps show where Dolores González‐Morón may publish in the future.

Co-authorship network of co-authors of Dolores González‐Morón

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

All Works

19 of 19 papers shown
1.
González‐Morón, Dolores, et al.. (2020). A Family with Late‐Onset and Predominant Choreic Niemann Pick Type C: A Treatable Piece in the Etiological Puzzle of Choreas. Movement Disorders Clinical Practice. 7(3). 332–334. 3 indexed citations
2.
Vega, Patricia, Luca Marsili, Dolores González‐Morón, et al.. (2020). The odyssey of complex neurogenetic disorders: From undetermined to positive. American Journal of Medical Genetics Part C Seminars in Medical Genetics. 184(4). 876–884. 10 indexed citations
3.
4.
Cohen, Leila, Dolores González‐Morón, Hernán Amartino, et al.. (2019). Argentinian clinical genomics in a leukodystrophies and genetic leukoencephalopathies cohort: Diagnostic yield in our first 9 years. Annals of Human Genetics. 84(1). 11–28. 6 indexed citations
5.
González‐Morón, Dolores, et al.. (2018). Holmes Tremor‐Like Phenotype in DYT1 Dystonia. Movement Disorders Clinical Practice. 5(2). 206–208. 1 indexed citations
6.
Córdoba, Marta, et al.. (2018). Whole exome sequencing in neurogenetic odysseys: An effective, cost- and time-saving diagnostic approach. PLoS ONE. 13(2). e0191228–e0191228. 56 indexed citations
7.
Vega, Patricia, Carlos Ciraolo, Silvia Christiansen, et al.. (2018). Identification of a somatic mutation in the RHEB gene through high depth and ultra-high depth next generation sequencing in a patient with Hemimegalencephaly and drug resistant Epilepsy. European Journal of Medical Genetics. 62(11). 103571–103571. 20 indexed citations
8.
Alonso, Ricardo, Dolores González‐Morón, & Orlando Garcea. (2018). Optical coherence tomography as a biomarker of neurodegeneration in multiple sclerosis: A review. Multiple Sclerosis and Related Disorders. 22. 77–82. 66 indexed citations
9.
González‐Morón, Dolores, D. Consalvo, Marcelo A. Martí, et al.. (2017). Germline and somatic mutations in cortical malformations: Molecular defects in Argentinean patients with neuronal migration disorders. PLoS ONE. 12(9). e0185103–e0185103. 14 indexed citations
10.
Nemirovsky, Sergio I., Marta Córdoba, Patricia Vega, et al.. (2015). Whole Genome Sequencing Reveals a De Novo SHANK3 Mutation in Familial Autism Spectrum Disorder. PLoS ONE. 10(2). e0116358–e0116358. 39 indexed citations
11.
Córdoba, Marta, Dolores González‐Morón, Patricia Vega, et al.. (2015). Neurogenetics in Argentina: diagnostic yield in a personalized research based clinic. Genetics Research. 97. e10–e10. 13 indexed citations
12.
González‐Morón, Dolores, et al.. (2013). [The broad phenotypic spectrum of SCA-3: hereditary spastic paraplegia].. PubMed. 73(6). 552–4. 4 indexed citations
13.
González‐Morón, Dolores, et al.. (2013). Progressive external ophthalmoplegia (PEO) due to a mutation in the C10orf2 (PEO1) gene mimicking a myasthenic crisis. BMJ Case Reports. 2013. bcr2013010181–bcr2013010181. 5 indexed citations
14.
González‐Morón, Dolores, et al.. (2013). Huntington’s disease masquerading as spinocerebellar ataxia. BMJ Case Reports. 2013. bcr2012008380–bcr2012008380. 7 indexed citations
15.
Kauffman, Marcelo, Dolores González‐Morón, D. Consalvo, et al.. (2012). Diagnosis of mitochondrial disorders applying massive pyrosequencing. Molecular Biology Reports. 39(6). 6655–6660. 3 indexed citations
16.
Kauffman, Marcelo, Dolores González‐Morón, Orlando Garcea, & Andrés Villa. (2011). TNFSFR1A R92Q mutation, autoinflammatory symptoms and multiple sclerosis in a cohort from Argentina. Molecular Biology Reports. 39(1). 117–121. 12 indexed citations
17.
Bejarano, Bartolomé, Mariangela Bianco, Dolores González‐Morón, et al.. (2011). Computational classifiers for predicting the short-term course of Multiple sclerosis. BMC Neurology. 11(1). 67–67. 48 indexed citations
18.
Kauffman, Marcelo, Dolores González‐Morón, D. Consalvo, & Silvia Kochen. (2011). Cerebrotendinous Xanthomatosis Revealed in Drug-Resistant Epilepsy Diagnostic Workup. The American Journal of the Medical Sciences. 343(4). 332–333. 8 indexed citations
19.
Kauffman, Marcelo, et al.. (2009). Serotonin transporter gene variation and refractory mesial temporal epilepsy with hippocampal sclerosis. Epilepsy Research. 85(2-3). 231–234. 25 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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