Claudio Toma

5.4k citations
41 papers · 1.0k indexed · h-index 21
Topics
Genetics and Neurodevelopmental Disorders (15 papers)Autism Spectrum Disorder Research (11 papers)Genomics and Rare Diseases (7 papers)

In The Last Decade

Claudio Toma

40 papers receiving 989 citations

Peers

Claudio Toma
Comparison fields: 5 of 90
  • Genetics 527
  • Molecular Biology 359
  • Cognitive Neuroscience 359
  • Cellular and Molecular Neuroscience 153
  • Psychiatry and Mental health 151
Replace Maria T. Acosta with:
Maria T. Acosta United States
Hagit Flusser Israel
Andrés Moreno-De-Luca United States
Myriam Srour Canada
Lan Xiong Canada
Teresa Temudo Portugal
Jonathan Picker United States
Zoran Brkanac United States
Sampath Arepalli United States
Margaret A Pericak‐Vance United States
Claudio Toma relative to Maria T. Acosta United States Maria T. Acosta's profile →
Citations per field
00.5×1.5×2.1×
Maria T. Acosta · 1×
Citations per year

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
#WorkIndexed citations
1 7
2 9
3 20
4 16
5 17
6 21
7 28
8 31
9 37
10 32
11 6
12 11
13 14
14 35
15
Using 3D scan architecture.
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16 48
17 17
18 54
19 50
20 38

About Claudio Toma

Claudio Toma is a scholar working on Genetics, Cognitive Neuroscience and Clinical Biochemistry, having authored 41 papers that have together received 1.0k indexed citations. Recurring topics across this work include Genetics and Neurodevelopmental Disorders (15 papers), Autism Spectrum Disorder Research (11 papers) and Genomics and Rare Diseases (7 papers). The work is most often cited by research in Genetics (527 citations), Cognitive Neuroscience (359 citations) and Psychiatry and Mental health (151 citations). Claudio Toma has collaborated with scholars based in Spain, Australia and United States. Frequent 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. Their work appears in journals such as PLoS ONE, Scientific Reports and Biological Psychiatry.

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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