Germán Morís

4.4k total citations
58 papers, 1.2k citations indexed

About

Germán Morís is a scholar working on Neurology, Molecular Biology and Cellular and Molecular Neuroscience. According to data from OpenAlex, Germán Morís has authored 58 papers receiving a total of 1.2k indexed citations (citations by other indexed papers that have themselves been cited), including 21 papers in Neurology, 17 papers in Molecular Biology and 12 papers in Cellular and Molecular Neuroscience. Recurrent topics in Germán Morís's work include Parkinson's Disease Mechanisms and Treatments (11 papers), RNA regulation and disease (9 papers) and Peripheral Neuropathies and Disorders (6 papers). Germán Morís is often cited by papers focused on Parkinson's Disease Mechanisms and Treatments (11 papers), RNA regulation and disease (9 papers) and Peripheral Neuropathies and Disorders (6 papers). Germán Morís collaborates with scholars based in Spain, United States and Italy. Germán Morís's co-authors include Juan Carlos García‐Moncó, Victoria Álvarez, Eliécer Coto, Manuel Menéndez‐González, Lucía Cardo, Lorena Benavente, René Ribacoba, Ana I. Corao, Marta Díaz and Lorena de Mena and has published in prestigious journals such as SHILAP Revista de lepidopterología, Neurology and Scientific Reports.

In The Last Decade

Germán Morís

55 papers receiving 1.2k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Germán Morís Spain 20 409 377 292 219 207 58 1.2k
Brahim Tabarki Saudi Arabia 24 567 1.4× 327 0.9× 155 0.5× 258 1.2× 240 1.2× 89 1.8k
Viviana Nociti Italy 27 503 1.2× 287 0.8× 214 0.7× 247 1.1× 65 0.3× 78 2.1k
William E. Karnes United States 21 240 0.6× 456 1.2× 173 0.6× 224 1.0× 186 0.9× 50 2.0k
R. Rand Allingham United States 40 1.3k 3.3× 550 1.5× 225 0.8× 158 0.7× 287 1.4× 129 5.0k
Carlo Fusco Italy 21 565 1.4× 270 0.7× 276 0.9× 72 0.3× 258 1.2× 118 1.8k
Anna Paola Batocchi Italy 26 387 0.9× 555 1.5× 160 0.5× 192 0.9× 62 0.3× 54 1.9k
Yair M. Gozal United States 20 370 0.9× 380 1.0× 129 0.4× 173 0.8× 109 0.5× 48 1.2k
Katrin Frauenknecht Germany 22 451 1.1× 244 0.6× 165 0.6× 66 0.3× 115 0.6× 57 1.2k
Eroboghene E. Ubogu United States 27 314 0.8× 574 1.5× 545 1.9× 103 0.5× 62 0.3× 72 2.0k
Naoyuki Tanuma Japan 25 381 0.9× 177 0.5× 182 0.6× 89 0.4× 81 0.4× 66 1.7k

Countries citing papers authored by Germán Morís

Since Specialization
Citations

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

Fields of papers citing papers by Germán Morís

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Germán Morís

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

All Works

20 of 20 papers shown
1.
Morís, Germán, et al.. (2025). Clinical features of phantom limb pain in patients with lower limb amputation in a Spanish population. Neurología (English Edition). 40(3). 279–289.
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Domínguez‐González, Cristina, Laura Bermejo‐Guerrero, Germán Morís, et al.. (2022). Metrics of progression and prognosis in untreated adults with thymidine kinase 2 deficiency: An observational study. Neuromuscular Disorders. 32(9). 728–735. 5 indexed citations
5.
Domínguez‐González, Cristina, Roberto Fernández‐Torrón, U. Moore, et al.. (2022). Muscle MRI characteristic pattern for late-onset TK2 deficiency diagnosis. Journal of Neurology. 269(7). 3550–3562. 9 indexed citations
6.
Álvarez‐Argüelles, Marta Elena, et al.. (2018). Neuroinvasion of influenza A/H3N2: a fatal case in an immunocompetent adult. Journal of NeuroVirology. 25(2). 275–279. 8 indexed citations
7.
Morís, Germán, Silvia Arboleya, Leonardo Mancabelli, et al.. (2018). Fecal microbiota profile in a group of myasthenia gravis patients. Scientific Reports. 8(1). 14384–14384. 53 indexed citations
8.
Morís, Germán, et al.. (2017). Involuntary movements of pelvic stump. Clinical Case Reports. 5(5). 640–641. 3 indexed citations
9.
Cardo, Lucía, Eliécer Coto, René Ribacoba, et al.. (2014). MiRNA Profile in the Substantia Nigra of Parkinson’s Disease and Healthy Subjects. Journal of Molecular Neuroscience. 54(4). 830–836. 65 indexed citations
10.
Morís, Germán. (2014). Inflammatory bowel disease: An increased risk factor for neurologic complications. World Journal of Gastroenterology. 20(5). 1228–1228. 75 indexed citations
11.
Cardo, Lucía, Eliécer Coto, Lorena de Mena, et al.. (2014). Alpha-synuclein transcript isoforms in three different brain regions from Parkinson's disease and healthy subjects in relation to the SNCA rs356165/rs11931074 polymorphisms. Neuroscience Letters. 562. 45–49. 34 indexed citations
12.
Cardo, Lucía, Eliécer Coto, René Ribacoba, et al.. (2014). The screening of the 3′UTR sequence of LRRK2 identified an association between the rs66737902 polymorphism and Parkinson’s disease. Journal of Human Genetics. 59(6). 346–348. 15 indexed citations
13.
Morís, Germán, et al.. (2013). Two cases of neurosarcoidosis with atypical manifestations. European Journal of Internal Medicine. 24. e253–e253. 1 indexed citations
14.
Mena, Lorena de, Lluı́s Samaranch, Eliécer Coto, et al.. (2012). Mutational Screening of PARKIN Identified a 3′ UTR Variant (rs62637702) Associated with Parkinson’s Disease. Journal of Molecular Neuroscience. 50(2). 264–269. 10 indexed citations
15.
Miar, Ana, Victoria Álvarez, Ana I. Corao, et al.. (2011). Lack of association between protocadherin 11-X/Y (PCDH11X and PCDH11Y) polymorphisms and late onset Alzheimer's disease. Brain Research. 1383. 252–256. 15 indexed citations
16.
Sánchez-Ferrero, Elena, Eliécer Coto, Ana I. Corao, et al.. (2011). Mitochondrial DNA polymorphisms/haplogroups in hereditary spastic paraplegia. Journal of Neurology. 259(2). 246–250. 4 indexed citations
17.
Mata, Ignácio F., Owen A. Ross, Jennifer M. Kachergus, et al.. (2006). LRRK2 mutations are a common cause of Parkinson's disease in Spain. European Journal of Neurology. 13(4). 391–394. 45 indexed citations
18.
Morís, Germán, et al.. (2001). SUNCT Syndrome and Seborrheic Dermatitis Associated with Craneosynostosis. Cephalalgia. 21(2). 157–159. 27 indexed citations
19.
Álvarez, Rubén, Victoria Álvarez, Carlos Lahoz, et al.. (1999). Angiotensin converting enzyme and endothelial nitric oxide synthase DNA polymorphisms and late onset Alzheimer's disease. Journal of Neurology Neurosurgery & Psychiatry. 67(6). 733–736. 83 indexed citations
20.
Morís, Germán, et al.. (1998). The Distinctive Headache of the Occipital Condyle Syndrome: A Report of Four Cases. Headache The Journal of Head and Face Pain. 38(4). 308–311. 20 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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