Thomas Fernandez

11.6k total citations
55 papers, 1.9k citations indexed

About

Thomas Fernandez is a scholar working on Cognitive Neuroscience, Clinical Psychology and Genetics. According to data from OpenAlex, Thomas Fernandez has authored 55 papers receiving a total of 1.9k indexed citations (citations by other indexed papers that have themselves been cited), including 33 papers in Cognitive Neuroscience, 22 papers in Clinical Psychology and 17 papers in Genetics. Recurrent topics in Thomas Fernandez's work include Autism Spectrum Disorder Research (26 papers), Obsessive-Compulsive Spectrum Disorders (19 papers) and Genetics and Neurodevelopmental Disorders (12 papers). Thomas Fernandez is often cited by papers focused on Autism Spectrum Disorder Research (26 papers), Obsessive-Compulsive Spectrum Disorders (19 papers) and Genetics and Neurodevelopmental Disorders (12 papers). Thomas Fernandez collaborates with scholars based in United States, Canada and Brazil. Thomas Fernandez's co-authors include Jeffrey S. Bedwell, Marge Lenane, Jay N. Giedd, Rob Nicolson, Ralph E. Hoffman, Brian Pittman, Neal Jeffries, Jonathan D. Blumenthal, Judith L. Rapoport and Charles G. Gross and has published in prestigious journals such as Science, Nucleic Acids Research and Nature Communications.

In The Last Decade

Thomas Fernandez

50 papers receiving 1.8k citations

Peers

Thomas Fernandez

PMH

GENET

Martine Hoogman Netherlands

Elysa J. Marco United States

Simon Maier Germany

Masumi Inagaki Japan

S. J. M. C. Palmen Netherlands

Aaron L. Goldman United States

Marieke Langen Netherlands

Sara Bulgheroni Italy

Christine Wu Nordahl United States

Wouter Staal Netherlands

Martine Hoogman Netherlands

Thomas Fernandez

1.2k ×1.4

1.1k ×1.8

PMH

200 ×0.4

180 ×0.6

GENET

159 ×0.6

Citations per year, relative to Thomas Fernandez Thomas Fernandez (= 1×) peers Martine Hoogman

Countries citing papers authored by Thomas Fernandez

Since Specialization

Citations

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

Fields of papers citing papers by Thomas Fernandez

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Thomas Fernandez

This figure shows the co-authorship network connecting the top 25 collaborators of Thomas Fernandez. A scholar is included among the top collaborators of Thomas Fernandez 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 Thomas Fernandez. Thomas Fernandez 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

Olfson, Emily, Carolina Cappi, Gwyneth Zai, et al.. (2025). Characterizing Rare DNA Copy-Number Variants in Pediatric Obsessive-Compulsive Disorder. Journal of the American Academy of Child & Adolescent Psychiatry.

Chawarska, Katarzyna, Thomas Fernandez, Fred Volkmar, et al.. (2025). Motor stereotypies in toddlers with and without autism: A transdiagnostic dimension. Journal of Child Psychology and Psychiatry. 67(1). 104–114.

Fitzpatrick, Sarah E., Erika L. Nurmi, Thomas Fernandez, et al.. (2024). Review: Child Psychiatry in the Era of Genomics: The Promise of Translational Genetics Research for the Clinic. PubMed. 3(2). 157–170. 2 indexed citations

Olfson, Emily, Luís C. Farhat, Wenzhong Liu, et al.. (2024). Rare de novo damaging DNA variants are enriched in attention-deficit/hyperactivity disorder and implicate risk genes. Nature Communications. 15(1). 5870–5870. 2 indexed citations

Hedderly, Tammy, Clare Mitchell, Nirit Soffer‐Dudek, et al.. (2024). Intense Imagery Movements May Lead to Maladaptive Daydreaming: A Case Series and Literature Review. Movement Disorders Clinical Practice. 11(6). 716–719. 2 indexed citations

Farhat, Luís C., et al.. (2024). The genetics of trichotillomania and excoriation disorder: A systematic review. Comprehensive Psychiatry. 133. 152506–152506.

Costa, Daniel L., Thomas Fernandez, James J. Crowley, et al.. (2023). Clinical characteristics of probands with obsessive-compulsive disorder from simplex and multiplex families. Psychiatry Research. 331. 115627–115627. 1 indexed citations

Fernandez, Thomas, Catherine Sullivan, Emily Olfson, et al.. (2023). Primary complex motor stereotypies are associated with de novo damaging DNA coding mutations that identify KDM5B as a risk gene. PLoS ONE. 18(10). e0291978–e0291978. 2 indexed citations

Jang, Yeongjun, Liana Fasching, Taejeong Bae, et al.. (2023). Efficient reconstruction of cell lineage trees for cell ancestry and cancer. Nucleic Acids Research. 51(10). e57–e57. 1 indexed citations

10.

Fasching, Liana, Yeongjun Jang, Simone Tomasi, et al.. (2021). Early developmental asymmetries in cell lineage trees in living individuals. Science. 371(6535). 1245–1248. 35 indexed citations

11.

Murphy, Tanya K., Thomas Fernandez, Barbara J. Coffey, et al.. (2017). Extended-Release Guanfacine Does Not Show a Large Effect on Tic Severity in Children with Chronic Tic Disorders. Journal of Child and Adolescent Psychopharmacology. 27(9). 762–770. 48 indexed citations

12.

Fernandez, Thomas, et al.. (2017). Motor Stereotypies: A Pathophysiological Review. Frontiers in Neuroscience. 11. 171–171. 55 indexed citations

13.

Lennington, Jessica B., Gianfilippo Coppola, Yuko Kataoka-Sasaki, et al.. (2014). Transcriptome Analysis of the Human Striatum in Tourette Syndrome. Biological Psychiatry. 79(5). 372–382. 135 indexed citations

14.

Gupta, Abha R., Michelle Pirruccello, Feng Cheng, et al.. (2014). Rare deleterious mutations of the gene EFR3A in autism spectrum disorders. Molecular Autism. 5(1). 31–31. 21 indexed citations

15.

Pauls, David L., Thomas Fernandez, Carol A. Mathews, Matthew W. State, & Jeremiah M. Scharf. (2014). The inheritance of Tourette Disorder: A review. Journal of Obsessive-Compulsive and Related Disorders. 3(4). 380–385. 44 indexed citations

16.

Hoffman, Ralph E., Kun Wu, Brian Pittman, et al.. (2013). Transcranial Magnetic Stimulation of Wernicke’s and Right Homologous Sites to Curtail “Voices”: A Randomized Trial. Biological Psychiatry. 73(10). 1008–1014. 62 indexed citations

17.

Fernandez, Thomas, Thomas M. Morgan, Nicole R. Davis, et al.. (2008). Disruption of Contactin 4 (CNTN4) Results in Developmental Delay and Other Features of 3p Deletion Syndrome. The American Journal of Human Genetics. 82(6). 1385–1385. 45 indexed citations

18.

Nicolson, Rob, Dolores Malaspina, Jay N. Giedd, et al.. (1999). Obstetrical Complications and Childhood-Onset Schizophrenia. American Journal of Psychiatry. 156(10). 1650–1652. 20 indexed citations

19.

Evett, Matthew P. & Thomas Fernandez. (1998). Numeric Mutation: Improved Search in Genetic Programming. The Florida AI Research Society. 106–109. 3 indexed citations

20.

Evett, Matthew P. & Thomas Fernandez. (1998). Numeric Mutation Improves the Discovery of Numeric Constants in Genetic Programming. 8 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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