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

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

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20 of 20 papers shown

#	Work	Indexed citations
1	Epigenetic signatures relating to disease-associated genotypic burden in familial risk of bipolar disorder 2022 ·Translational Psychiatry ·(unknown), Bronwyn J. Overs, Gloria Roberts, Claudio Toma, Oliver J. Watkeys, Melissa J. Green, Kerrie D. Pierce, Howard J. Edenberg, Holly C. Wilcox, Emma K. Stapp, Melvin G. McInnis, Leslie A. Hulvershorn, John I. Nürnberger, Peter R. Schofield, Philip B. Mitchell, Janice M. Fullerton	7
2	Cortical mediation of relationships between dopamine receptor D2 and cognition is absent in youth at risk of bipolar disorder 2021 ·Psychiatry Research Neuroimaging ·Bronwyn J. Overs, Rhoshel Lenroot, Gloria Roberts, Melissa J. Green, Claudio Toma, Dušan Pavlović, Kerrie D. Pierce, Peter R. Schofield, Philip B. Mitchell, Janice M. Fullerton	9
3	Diverse phenotypic measurements of wellbeing: Heritability, temporal stability and the variance explained by polygenic scores 2020 ·Genes Brain & Behavior ·Javad Jamshidi, Leanne M. Williams, Peter R. Schofield, Haeme R. P. Park, (unknown), (unknown), Richard A. Bryant, Claudio Toma, Janice M. Fullerton, Justine M. Gatt	20
4	Exploration of experiences with and understanding of polygenic risk scores for bipolar disorder 2020 ·Journal of Affective Disorders ·(unknown), Tatiane Yanes, Bettina Meiser, Rajneesh Kaur, Janice M. Fullerton, Kristine Barlow‐Stewart, Peter R. Schofield, Claudio Toma, Holly L. Peay, Philip B. Mitchell	16
5	Genetic Variation across Phenotypic Severity of Autism 2020 ·Trends in Genetics ·Claudio Toma	17
6	Truncating variant burden in high-functioning autism and pleiotropic effects of LRP1 across psychiatric phenotypes 2019 ·Journal of Psychiatry and Neuroscience ·Bàrbara Torrico, Alex D. Shaw, Roberto Mosca, (unknown), Amaia Hervás, Noèlia Fernàndez‐Castillo, Patrick Aloy, Mónica Bayés, Janice M. Fullerton, Bru Cormand, Claudio Toma	21
7	An examination of multiple classes of rare variants in extended families with bipolar disorder 2018 ·Translational Psychiatry ·Claudio Toma, Alex D. Shaw, Richard J. N. Allcock, Anna Heath, Kerrie D. Pierce, Philip B. Mitchell, Peter R. Schofield, Janice M. Fullerton	28
8	Comprehensive cross-disorder analyses of CNTNAP2 suggest it is unlikely to be a primary risk gene for psychiatric disorders 2018 ·PLoS Genetics ·Claudio Toma, Kerrie D. Pierce, Alex D. Shaw, Anna Heath, Philip B. Mitchell, Peter R. Schofield, Janice M. Fullerton	31
9	Mutation Spectrum in the CACNA1A Gene in 49 Patients with Episodic Ataxia 2017 ·Scientific Reports ·Cèlia Sintas, (unknown), Noèlia Fernàndez‐Castillo, Roser Corominas, Marta Vila‐Pueyo, Claudio Toma, Ester Cuenca-León, Isabel Barroeta, (unknown), Vı́ctor Volpini, Alfons Macaya, Bru Cormand	37
10	Traumatic Stress Interacts With Bipolar Disorder Genetic Risk to Increase Risk for Suicide Attempts 2017 ·Journal of the American Academy of Child & Adolescent Psychiatry ·Holly C. Wilcox, Janice M. Fullerton, Anne L. Glowinski, Kelly S. Benke, Masoud Kamali, Leslie A. Hulvershorn, Emma K. Stapp, Howard J. Edenberg, Gloria Roberts, Neera Ghaziuddin, (unknown), Christine Brucksch, Andrew Frankland, Claudio Toma, Alex D. Shaw, Elizabeth Kastelic, Leslie Miller, Melvin G. McInnis, Philip B. Mitchell, John I. Nürnberger	32
11	The involvement of serotonin polymorphisms in autistic spectrum symptomatology 2014 ·Psychiatric Genetics ·Amaia Hervás, Claudio Toma, (unknown), Marta Ribasès, Marta Morgade Salgado, Mónica Bayés, (unknown), Bru Cormand, (unknown), Silvina Guijarro, María J. Arranz	6
12	Rare variants analysis of neurexin-1β in autism reveals a novel start codon mutation affecting protein levels at synapses 2013 ·Psychiatric Genetics ·(unknown), Amaia Hervás, Claudio Toma, (unknown), Bru Cormand, Amalia Martı́nez-Mir, Francisco G. Scholl	11
13	Characterisation of two deletions involving NPC1 and flanking genes in Niemann–Pick Type C disease patients 2012 ·Molecular Genetics and Metabolism ·Laura Rodríguez‐Pascau, Claudio Toma, Judit Macías‐Vidal, Mónica Cozar, Bru Cormand, (unknown), María Josep Coll, Daniel Grinberg, Lluı̈sa Vilageliu	14
14	Neurotransmitter systems and neurotrophic factors in autism: association study of 37 genes suggests involvement of DDC 2012 ·The World Journal of Biological Psychiatry ·Claudio Toma, Amaia Hervás, (unknown), Marta Morgade Salgado, (unknown), Elisabet Vilella, (unknown), (unknown), Ivon Cuscó, (unknown), Luis A. Pérez‐Jurado, (unknown), Yolanda de Diego‐Otero, (unknown), Josep Antoni Ramos‐Quiroga, Marta Ribasès, Mónica Bayés, Bru Cormand	35
15	Using 3D scan architecture. 2011 ·Journal of horticulture, forestry and biotechnology ·(unknown), (unknown), Claudio Toma, (unknown), (unknown)	1
16	Cerebral Folate Deficiency Syndromes in Childhood 2011 ·Archives of Neurology ·Belén Pérez‐Dueñas, Aída Ormazábal, Claudio Toma, Bàrbara Torrico, Bru Cormand, Mercedes Serrano, Cristina Sierra, Elisa De Grandis, (unknown), Àngels García‐Cazorla, Jaime Campistol, Juan M. Pascual, Rafael Artuch	48
17	Tyrosine hydroxylase deficiency in three Greek patients with a common ancestral mutation 2010 ·Movement Disorders ·Roser Pons, Mercedes Serrano, Aída Ormazábal, Claudio Toma, Àngels García‐Cazorla, Estela Área-Gómez, Marta Ribasès, Emmanuel Kanavakis, (unknown), Aristeidis Giannakopoulos, (unknown), Sotiris Youroukos, Bru Cormand, Rafael Artuch	17
18	Copy number variation and association analysis of SHANK3 as a candidate gene for autism in the IMGSAC collection 2009 ·European Journal of Human Genetics ·Nuala Sykes, Claudio Toma, (unknown), Emanuela V. Volpi, Inês Sousa, Alistair T. Pagnamenta, Raffaella Tancredi, Agatino Battaglia, Elena Maestrini, Anthony Bailey, Anthony P. Monaco	54
19	The dyslexia-associated gene KIAA0319 encodes highly N- and O-glycosylated plasma membrane and secreted isoforms 2007 ·Human Molecular Genetics ·Antonio Velayos‐Baeza, Claudio Toma, Silvia Paracchini, Anthony P. Monaco	50
20	SLC25A12 and CMYA3 gene variants are not associated with autism in the IMGSAC multiplex family sample 2005 ·European Journal of Human Genetics ·Francesca Blasi, Elena Bacchelli, Simona Carone, Claudio Toma, Anthony P. Monaco, Anthony Bailey, Elena Maestrini	38

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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