Claudio Toma

5.4k total citations
41 papers, 1.0k citations indexed

About

Claudio Toma is a scholar working on Genetics, Molecular Biology and Cognitive Neuroscience. According to data from OpenAlex, Claudio Toma has authored 41 papers receiving a total of 1.0k indexed citations (citations by other indexed papers that have themselves been cited), including 24 papers in Genetics, 16 papers in Molecular Biology and 13 papers in Cognitive Neuroscience. Recurrent topics in Claudio Toma's work include Genetics and Neurodevelopmental Disorders (15 papers), Autism Spectrum Disorder Research (11 papers) and Genomics and Rare Diseases (7 papers). Claudio Toma is often cited by papers focused on Genetics and Neurodevelopmental Disorders (15 papers), Autism Spectrum Disorder Research (11 papers) and Genomics and Rare Diseases (7 papers). Claudio Toma collaborates with scholars based in Spain, Australia and United States. Claudio Toma's co-authors include Bru Cormand, Anthony P. Monaco, Janice M. Fullerton, Amaia Hervás, Bàrbara Torrico, Silvia Paracchini, Antonio Velayos‐Baeza, Elena Maestrini, Peter R. Schofield and Marta Morgade Salgado and has published in prestigious journals such as PLoS ONE, Scientific Reports and Biological Psychiatry.

In The Last Decade

Claudio Toma

40 papers receiving 989 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Claudio Toma Spain 21 527 359 359 153 151 41 1.0k
Hagit Flusser Israel 20 255 0.5× 533 1.5× 306 0.9× 124 0.8× 156 1.0× 46 1.3k
Myriam Srour Canada 20 653 1.2× 703 2.0× 197 0.5× 320 2.1× 154 1.0× 88 1.9k
Maria T. Acosta United States 20 253 0.5× 386 1.1× 333 0.9× 163 1.1× 273 1.8× 63 1.3k
Teresa Temudo Portugal 16 413 0.8× 299 0.8× 263 0.7× 128 0.8× 291 1.9× 51 1.0k
Francesca Darra Italy 24 522 1.0× 365 1.0× 285 0.8× 285 1.9× 819 5.4× 86 1.6k
Lan Xiong Canada 24 298 0.6× 263 0.7× 436 1.2× 139 0.9× 340 2.3× 58 1.5k
Andrés Moreno-De-Luca United States 14 472 0.9× 298 0.8× 285 0.8× 101 0.7× 269 1.8× 24 1.1k
Margaret A Pericak‐Vance United States 15 480 0.9× 433 1.2× 414 1.2× 306 2.0× 114 0.8× 33 1.2k
Zoran Brkanac United States 24 675 1.3× 755 2.1× 272 0.8× 332 2.2× 76 0.5× 32 1.6k
Jonathan Picker United States 24 1.3k 2.4× 1.0k 2.8× 670 1.9× 223 1.5× 145 1.0× 47 2.1k

Countries citing papers authored by Claudio Toma

Since Specialization
Citations

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

Fields of papers citing papers by Claudio Toma

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Claudio Toma

This figure shows the co-authorship network connecting the top 25 collaborators of Claudio Toma. A scholar is included among the top collaborators of Claudio Toma 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 Claudio Toma. Claudio Toma 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.
Overs, Bronwyn J., Gloria Roberts, Claudio Toma, et al.. (2022). Epigenetic signatures relating to disease-associated genotypic burden in familial risk of bipolar disorder. Translational Psychiatry. 12(1). 310–310. 7 indexed citations
2.
Overs, Bronwyn J., Rhoshel Lenroot, Gloria Roberts, et al.. (2021). Cortical mediation of relationships between dopamine receptor D2 and cognition is absent in youth at risk of bipolar disorder. Psychiatry Research Neuroimaging. 309. 111258–111258. 9 indexed citations
3.
Jamshidi, Javad, Leanne M. Williams, Peter R. Schofield, et al.. (2020). Diverse phenotypic measurements of wellbeing: Heritability, temporal stability and the variance explained by polygenic scores. Genes Brain & Behavior. 19(8). e12694–e12694. 20 indexed citations
4.
Yanes, Tatiane, Bettina Meiser, Rajneesh Kaur, et al.. (2020). Exploration of experiences with and understanding of polygenic risk scores for bipolar disorder. Journal of Affective Disorders. 265. 342–350. 16 indexed citations
5.
Toma, Claudio. (2020). Genetic Variation across Phenotypic Severity of Autism. Trends in Genetics. 36(4). 228–231. 17 indexed citations
6.
Torrico, Bàrbara, Alex D. Shaw, Roberto Mosca, et al.. (2019). Truncating variant burden in high-functioning autism and pleiotropic effects of LRP1 across psychiatric phenotypes. Journal of Psychiatry and Neuroscience. 44(5). 350–359. 21 indexed citations
7.
Toma, Claudio, Alex D. Shaw, Richard J. N. Allcock, et al.. (2018). An examination of multiple classes of rare variants in extended families with bipolar disorder. Translational Psychiatry. 8(1). 65–65. 28 indexed citations
8.
Toma, Claudio, Kerrie D. Pierce, Alex D. Shaw, et al.. (2018). Comprehensive cross-disorder analyses of CNTNAP2 suggest it is unlikely to be a primary risk gene for psychiatric disorders. PLoS Genetics. 14(12). e1007535–e1007535. 31 indexed citations
9.
Sintas, Cèlia, Noèlia Fernàndez‐Castillo, Roser Corominas, et al.. (2017). Mutation Spectrum in the CACNA1A Gene in 49 Patients with Episodic Ataxia. Scientific Reports. 7(1). 2514–2514. 37 indexed citations
10.
Wilcox, Holly C., Janice M. Fullerton, Anne L. Glowinski, et al.. (2017). Traumatic Stress Interacts With Bipolar Disorder Genetic Risk to Increase Risk for Suicide Attempts. Journal of the American Academy of Child & Adolescent Psychiatry. 56(12). 1073–1080. 32 indexed citations
11.
Hervás, Amaia, Claudio Toma, Marta Ribasès, et al.. (2014). The involvement of serotonin polymorphisms in autistic spectrum symptomatology. Psychiatric Genetics. 24(4). 158–163. 6 indexed citations
12.
Hervás, Amaia, et al.. (2013). Rare variants analysis of neurexin-1β in autism reveals a novel start codon mutation affecting protein levels at synapses. Psychiatric Genetics. 23(6). 262–266. 11 indexed citations
13.
Rodríguez‐Pascau, Laura, Claudio Toma, Judit Macías‐Vidal, et al.. (2012). Characterisation of two deletions involving NPC1 and flanking genes in Niemann–Pick Type C disease patients. Molecular Genetics and Metabolism. 107(4). 716–720. 14 indexed citations
14.
Toma, Claudio, Amaia Hervás, Marta Morgade Salgado, et al.. (2012). Neurotransmitter systems and neurotrophic factors in autism: association study of 37 genes suggests involvement of DDC. The World Journal of Biological Psychiatry. 14(7). 516–527. 35 indexed citations
15.
Toma, Claudio, et al.. (2011). Using 3D scan architecture.. Journal of horticulture, forestry and biotechnology. 15(2). 52–56. 1 indexed citations
16.
Pérez‐Dueñas, Belén, Aída Ormazábal, Claudio Toma, et al.. (2011). Cerebral Folate Deficiency Syndromes in Childhood. Archives of Neurology. 68(5). 615–21. 48 indexed citations
17.
Pons, Roser, Mercedes Serrano, Aída Ormazábal, et al.. (2010). Tyrosine hydroxylase deficiency in three Greek patients with a common ancestral mutation. Movement Disorders. 25(8). 1086–1090. 17 indexed citations
18.
Sykes, Nuala, Claudio Toma, Emanuela V. Volpi, et al.. (2009). Copy number variation and association analysis of SHANK3 as a candidate gene for autism in the IMGSAC collection. European Journal of Human Genetics. 17(10). 1347–1353. 54 indexed citations
19.
Velayos‐Baeza, Antonio, Claudio Toma, Silvia Paracchini, & Anthony P. Monaco. (2007). The dyslexia-associated gene KIAA0319 encodes highly N- and O-glycosylated plasma membrane and secreted isoforms. Human Molecular Genetics. 17(6). 859–871. 50 indexed citations
20.
Blasi, Francesca, Elena Bacchelli, Simona Carone, et al.. (2005). SLC25A12 and CMYA3 gene variants are not associated with autism in the IMGSAC multiplex family sample. European Journal of Human Genetics. 14(1). 123–126. 38 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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