Nino Spataro

505 total citations
16 papers, 247 citations indexed

About

Nino Spataro is a scholar working on Molecular Biology, Genetics and Neurology. According to data from OpenAlex, Nino Spataro has authored 16 papers receiving a total of 247 indexed citations (citations by other indexed papers that have themselves been cited), including 9 papers in Molecular Biology, 6 papers in Genetics and 4 papers in Neurology. Recurrent topics in Nino Spataro's work include Genomics and Rare Diseases (4 papers), Genetic Associations and Epidemiology (3 papers) and Parkinson's Disease Mechanisms and Treatments (2 papers). Nino Spataro is often cited by papers focused on Genomics and Rare Diseases (4 papers), Genetic Associations and Epidemiology (3 papers) and Parkinson's Disease Mechanisms and Treatments (2 papers). Nino Spataro collaborates with scholars based in Spain, Germany and United States. Nino Spataro's co-authors include Elena Bosch, Arcadi Navarro, Juan Antonio Rodríguez, Urko M. Marigorta, David A. Hughes, Jordi Clarimón, Laura Cervera‐Carles, Francesc Calafell, Alberto Lleó and Ferrán Casals and has published in prestigious journals such as Bioinformatics, PLoS ONE and Human Molecular Genetics.

In The Last Decade

Nino Spataro

15 papers receiving 245 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Nino Spataro Spain	9	107	85	59	33	33	16	247
M. Reza Jabalameli United Kingdom	10	147 1.4×	82 1.0×	66 1.1×	30 0.9×	46 1.4×	18	312
Jenny Blechingberg Denmark	10	294 2.7×	67 0.8×	41 0.7×	27 0.8×	26 0.8×	18	388
Manuela Pendziwiat Germany	12	204 1.9×	103 1.2×	48 0.8×	18 0.5×	42 1.3×	21	379
Mika H. Martikainen Finland	13	205 1.9×	47 0.6×	130 2.2×	42 1.3×	61 1.8×	34	418
Leire Abalde-Atristain United States	6	211 2.0×	47 0.6×	45 0.8×	13 0.4×	25 0.8×	10	267
Pengcheng Shu China	10	360 3.4×	56 0.7×	13 0.2×	23 0.7×	60 1.8×	30	485
Abigail L. Pfaff Australia	11	178 1.7×	57 0.7×	84 1.4×	21 0.6×	17 0.5×	33	276
Max van Min Netherlands	5	152 1.4×	66 0.8×	15 0.3×	27 0.8×	50 1.5×	7	217
Miranda C. Dyson United Kingdom	6	114 1.1×	21 0.2×	83 1.4×	8 0.2×	112 3.4×	7	273
Ilaria D’Amato Italy	6	236 2.2×	39 0.5×	27 0.5×	85 2.6×	47 1.4×	8	320

Countries citing papers authored by Nino Spataro

Since Specialization

Citations

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

Fields of papers citing papers by Nino Spataro

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Nino Spataro

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

All Works

Sort: Min cites: Since: Top N: Style:

16 of 16 papers shown

Trujillo‐Quintero, Juan Pablo, Anna Brunet‐Vega, Nino Spataro, et al.. (2025). A Novel RHEB Germline Variant Associated With Intellectual Disability and Epilepsy: Expanding the Spectrum of mTORopathies. Clinical Genetics. 108(2). 218–223.

Spataro, Nino, Elisabeth Gabau, Juan Pablo Trujillo‐Quintero, et al.. (2024). Case report: Identification of a novel variant p.Gly215Arg in the CHN1 gene causing Moebius syndrome. Frontiers in Genetics. 15. 1291063–1291063. 1 indexed citations

Spataro, Nino, Juan Pablo Trujillo‐Quintero, Elisabeth Gabau, et al.. (2023). High Performance of a Dominant/X-Linked Gene Panel in Patients with Neurodevelopmental Disorders. Genes. 14(3). 708–708. 3 indexed citations

Spataro, Nino, et al.. (2022). Elimination of lipaemic interference by high-speed centrifugation. Biochemia Medica. 33(1). 10703–10703. 1 indexed citations

Gabau, Elisabeth, Carme Brun i Gasca, Steven Laurie, et al.. (2021). New genes involved in Angelman syndrome-like: Expanding the genetic spectrum. PLoS ONE. 16(10). e0258766–e0258766. 14 indexed citations

Tirado-Muñoz, Judit, et al.. (2020). Alcohol Induced Depression: Clinical, Biological and Genetic Features. Journal of Clinical Medicine. 9(8). 2668–2668. 9 indexed citations

Farré, Xavier, Nino Spataro, Frédéric Haziza, Jordi Rambla, & Arcadi Navarro. (2019). Genome-phenome explorer (GePhEx): a tool for the visualization and interpretation of phenotypic relationships supported by genetic evidence. Bioinformatics. 36(3). 890–896. 3 indexed citations

Malhotra, Sunny, Melissa Sorosina, Jordi Río, et al.. (2017). NLRP3 polymorphisms and response to interferon-beta in multiple sclerosis patients. Multiple Sclerosis Journal. 24(11). 1507–1510. 8 indexed citations

Dols‐Icardo, Oriol, Alberto García‐Redondo, Ricardo Rojas‐García, et al.. (2017). Analysis of known amyotrophic lateral sclerosis and frontotemporal dementia genes reveals a substantial genetic burden in patients manifesting both diseases not carrying the C9orf72 expansion mutation. Journal of Neurology Neurosurgery & Psychiatry. 89(2). 162–168. 42 indexed citations

10.

Rodríguez, Juan Antonio, Urko M. Marigorta, David A. Hughes, et al.. (2017). Antagonistic pleiotropy and mutation accumulation influence human senescence and disease. Nature Ecology & Evolution. 1(3). 55–55. 68 indexed citations

11.

Spataro, Nino, Juan Antonio Rodríguez, Arcadi Navarro, & Elena Bosch. (2016). Properties of human disease genes and the role of genes linked to Mendelian disorders in complex disease aetiology. Human Molecular Genetics. 26(3). ddw405–ddw405. 30 indexed citations

12.

Spataro, Nino, Laura Cervera‐Carles, Roger Anglada, et al.. (2016). Detection of genomic rearrangements from targeted resequencing data in Parkinson's disease patients. Movement Disorders. 32(1). 165–169. 15 indexed citations

13.

Engelken, Johannes, Guadalupe Espadas, Francesco M. Mancuso, et al.. (2015). Signatures of Evolutionary Adaptation in Quantitative Trait Loci Influencing Trace Element Homeostasis in Liver. Molecular Biology and Evolution. 33(3). 738–754. 18 indexed citations

14.

Spataro, Nino, Francesc Calafell, Laura Cervera‐Carles, et al.. (2014). Mendelian genes for Parkinson's disease contribute to the sporadic forms of the disease†. Human Molecular Genetics. 24(7). 2023–2034. 26 indexed citations

15.

Spataro, Nino, et al.. (2013). Draft Genome Sequence of Aeromonas molluscorum Strain 848T ^T , Isolated from Bivalve Molluscs. Genome Announcements. 1(3). 5 indexed citations

16.

Farfán, Maribel, et al.. (2013). Draft Genome Sequence of the Aeromonas diversa Type Strain. Genome Announcements. 1(3). 4 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.

Explore authors with similar magnitude of impact