Carla Lintas

5.5k total citations
52 papers, 1.7k citations indexed

About

Carla Lintas is a scholar working on Genetics, Molecular Biology and Cognitive Neuroscience. According to data from OpenAlex, Carla Lintas has authored 52 papers receiving a total of 1.7k indexed citations (citations by other indexed papers that have themselves been cited), including 29 papers in Genetics, 22 papers in Molecular Biology and 17 papers in Cognitive Neuroscience. Recurrent topics in Carla Lintas's work include Genetics and Neurodevelopmental Disorders (21 papers), Autism Spectrum Disorder Research (17 papers) and Genomic variations and chromosomal abnormalities (10 papers). Carla Lintas is often cited by papers focused on Genetics and Neurodevelopmental Disorders (21 papers), Autism Spectrum Disorder Research (17 papers) and Genomic variations and chromosomal abnormalities (10 papers). Carla Lintas collaborates with scholars based in Italy, United States and Czechia. Carla Lintas's co-authors include Antonio M. Persico, Roberto Sacco, Barbara Manzi, Krassimira Garbett, Károly Mirnics, Philip J. Ebert, Amanda Mitchell, R. Seed, Susan K. Murphy and Jessica Johnson and has published in prestigious journals such as Proceedings of the National Academy of Sciences, PLoS ONE and International Journal of Molecular Sciences.

In The Last Decade

Carla Lintas

46 papers receiving 1.7k citations

Peers

Carla Lintas

GENET

PMH

Shiro Suda Japan

Philip J. Ebert United States

John T. Morgan United States

Ashfaq M. Sheikh United States

Daniel Braunschweig United States

Jacob Ellegood Canada

Aubin Michalon Switzerland

Krassimira Garbett United States

Emma L. Meaburn United Kingdom

Hanna E. Stevens United States

Shiro Suda Japan

Carla Lintas

501 ×0.7

GENET

739 ×1.1

450 ×0.7

151 ×0.5

320 ×2.0

PMH

Citations per year, relative to Carla Lintas Carla Lintas (= 1×) peers Shiro Suda

Countries citing papers authored by Carla Lintas

Since Specialization

Citations

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

Fields of papers citing papers by Carla Lintas

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Carla Lintas

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

Tabolacci, Claudio, Angela Caruso, Martina Micai, et al.. (2025). Biogenic Amine Metabolism and Its Genetic Variations in Autism Spectrum Disorder: A Comprehensive Overview. Biomolecules. 15(4). 539–539.

Bottillo, Irene, Luigi Laino, Alessia Azzarà, et al.. (2024). A pathogenic variant in the FLCN gene presenting with pure dementia: is autophagy at the intersection between neurodegeneration and cancer?. Frontiers in Neuroscience. 17. 1304080–1304080.

Azzarà, Alessia, et al.. (2024). Exome Profiling Suggests Combined Effect of Myeloperoxidase, Toll-Like Receptors, and Metallopeptidase in Hidradenitis Suppurativa. Biomedicines. 12(11). 2498–2498.

Zoccante, Leonardo, et al.. (2024). Effectiveness of Equine-Assisted Activities and Therapies for Children with Autism Spectrum Disorder: An Update. Children. 11(12). 1494–1494.

Azzarà, Alessia, Carla Lintas, Fabio Pilato, et al.. (2023). Melkersson–Rosenthal Syndrome and Migraine: A New Phenotype Associated with SCN1A Variants?. Genes. 14(7). 1482–1482. 1 indexed citations

Tabolacci, Claudio, Daniela De Vita, Antonio Facchiano, et al.. (2023). Phytochemicals as Immunomodulatory Agents in Melanoma. International Journal of Molecular Sciences. 24(3). 2657–2657. 12 indexed citations

Lintas, Carla, Angelo Facchiano, Alessia Azzarà, et al.. (2023). Deletion of a Single Lysine Residue at Position 292 of CAMK2A Disrupts Protein Function, Causing Severe Epileptic Encephalopathy and Intellectual Disability. Genes. 14(7). 1353–1353. 3 indexed citations

Buccarelli, Mariachiara, Stefania Rossi, Maria Elena Pisanu, et al.. (2023). BRAF Mutations in Melanoma: Biological Aspects, Therapeutic Implications, and Circulating Biomarkers. Cancers. 15(16). 4026–4026. 74 indexed citations

Lintas, Carla, Alessia Azzarà, Chiara Gregorj, et al.. (2023). Maternal Epigenetic Dysregulation as a Possible Risk Factor for Neurodevelopmental Disorders. Genes. 14(3). 585–585. 4 indexed citations

10.

Azzarà, Alessia, et al.. (2022). Genetic variants determine intrafamilial variability of SARS-CoV-2 clinical outcomes in 19 Italian families. PLoS ONE. 17(10). e0275988–e0275988. 5 indexed citations

11.

Tabolacci, Claudio, Martina Cordella, Sabrina Mariotti, et al.. (2021). Melanoma Cell Resistance to Vemurafenib Modifies Inter-Cellular Communication Signals. Biomedicines. 9(1). 79–79. 13 indexed citations

12.

Castronovo, Paola, Marco Baccarin, Arianna Ricciardello, et al.. (2019). Phenotypic spectrum of NRXN1 mono‐ and bi‐allelic deficiency: A systematic review. Clinical Genetics. 97(1). 125–137. 38 indexed citations

13.

Cordella, Martina, Claudio Tabolacci, Stefania Rossi, et al.. (2019). Theophylline induces differentiation and modulates cytoskeleton dynamics and cytokines secretion in human melanoma-initiating cells. Life Sciences. 230. 121–131. 14 indexed citations

14.

Lintas, Carla, Ignazio S. Piras, Stefano Gabriele, et al.. (2016). Recurrent 15q11.2 BP1‐BP2 microdeletions and microduplications in the etiology of neurodevelopmental disorders. American Journal of Medical Genetics Part B Neuropsychiatric Genetics. 171(8). 1088–1098. 34 indexed citations

15.

Lintas, Carla, Ignazio S. Piras, Roberto Sacco, et al.. (2015). Xp22.33p22.12 Duplication in a Patient with Intellectual Disability and Dysmorphic Facial Features. Molecular Syndromology. 6(5). 236–241. 10 indexed citations

16.

Sacco, Roberto, Carla Lintas, & Antonio M. Persico. (2015). Autism genetics: Methodological issues and experimental design. Science China Life Sciences. 58(10). 946–957.

17.

Gentile, Ivan, Laura Altieri, Carla Lintas, et al.. (2013). Urinary polyomavirus infections in neurodevelopmental disorders. Open Journal of Psychiatry. 3(2). 18–25. 5 indexed citations

18.

Muratore, Christina, Nathaniel Hodgson, Malav Trivedi, et al.. (2013). Age-Dependent Decrease and Alternative Splicing of Methionine Synthase mRNA in Human Cerebral Cortex and an Accelerated Decrease in Autism. PLoS ONE. 8(2). e56927–e56927. 56 indexed citations

19.

Lintas, Carla, Francesco Guidi, Barbara Manzi, et al.. (2011). Lack of Infection with XMRV or Other MLV-Related Viruses in Blood, Post-Mortem Brains and Paternal Gametes of Autistic Individuals. PLoS ONE. 6(2). e16609–e16609. 18 indexed citations

20.

Lintas, Carla, Marco Cappa, Donatella Comparcola, Valério Nobili, & Alessandra Fierabracci. (2007). An 8-year-old boy with autoimmune hepatitis and Candida onychosis as the first symptoms of autoimmune polyglandular syndrome (APS1): identification of a new homozygous mutation in the autoimmune regulator gene (aire). European Journal of Pediatrics. 167(8). 949–953. 13 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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