Valerio Conti

3.5k total citations
50 papers, 935 citations indexed

About

Valerio Conti is a scholar working on Genetics, Molecular Biology and Pulmonary and Respiratory Medicine. According to data from OpenAlex, Valerio Conti has authored 50 papers receiving a total of 935 indexed citations (citations by other indexed papers that have themselves been cited), including 17 papers in Genetics, 13 papers in Molecular Biology and 8 papers in Pulmonary and Respiratory Medicine. Recurrent topics in Valerio Conti's work include Genetics and Neurodevelopmental Disorders (13 papers), Epilepsy research and treatment (6 papers) and Genomics and Rare Diseases (5 papers). Valerio Conti is often cited by papers focused on Genetics and Neurodevelopmental Disorders (13 papers), Epilepsy research and treatment (6 papers) and Genomics and Rare Diseases (5 papers). Valerio Conti collaborates with scholars based in Italy, United States and France. Valerio Conti's co-authors include Renzo Guerrini, Elena Parrini, William B. Dobyns, Davide Mei, Carla Marini, Aldamaria Puliti, Aristea S. Galanopoulou, Massimo Mantegazza, Simona Balestrini and Fabio Benfenati and has published in prestigious journals such as Physiological Reviews, SHILAP Revista de lepidopterología and Neurology.

In The Last Decade

Valerio Conti

48 papers receiving 905 citations

Peers

Valerio Conti

GENET

CMN

PMH

PPCH

Zsolt Horváth Hungary

Afshin Saffari Germany

Mizue Iai Japan

Robert W. Pyzalski United States

Damien Ferraro United States

Mélanie Morin‐Brureau France

Jing Luo China

Jennifer Stanley United States

Katherine Holland‐Bouley United States

Chiara Pastori Italy

Zsolt Horváth Hungary

Valerio Conti

694 ×1.9

98 ×0.3

GENET

564 ×3.0

CMN

102 ×0.5

PMH

35 ×0.4

PPCH

Citations per year, relative to Valerio Conti Valerio Conti (= 1×) peers Zsolt Horváth

Countries citing papers authored by Valerio Conti

Since Specialization

Citations

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

Fields of papers citing papers by Valerio Conti

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Valerio Conti

This figure shows the co-authorship network connecting the top 25 collaborators of Valerio Conti. A scholar is included among the top collaborators of Valerio Conti 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 Valerio Conti. Valerio Conti is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

Sort: Min cites: Since: Top N: Style:

20 of 20 papers shown

Riva, Antonella, et al.. (2025). SLC35A2-Related Brain Disorders: Genetics, Pathophysiology, and Therapeutic Insights. International Journal of Molecular Sciences. 26(23). 11560–11560.

Falace, Antonio, Emmanuelle Buhler, Š. Bauer, et al.. (2025). Mosaic expression of SLC35A2 pathogenetic variants impairs neuronal migration and dendritogenesis in the developing cortex. Human Molecular Genetics. 34(24). 2019–2026. 1 indexed citations

Lenge, Matteo, Simona Balestrini, Antonio Napolitano, et al.. (2024). Morphometric network-based abnormalities correlate with psychiatric comorbidities and gene expression in PCDH19-related developmental and epileptic encephalopathy. Translational Psychiatry. 14(1). 35–35. 2 indexed citations

Conti, Valerio, Lorenzo Peruzzi, Fabrizio Bartolucci, et al.. (2024). Chromosome numbers for the Italian flora: 15. SHILAP Revista de lepidopterología. 18. 167–177. 1 indexed citations

Caporalini, Chiara, Mirko Scagnet, Laura Giunti, et al.. (2023). Myxoid glioneuronal tumor: Histopathologic, neuroradiologic, and molecular features in a single center series. Neoplasia. 37. 100885–100885. 8 indexed citations

Costa, Anna‐Maria, Valerio Conti, Laura Roli, et al.. (2022). Prospective Evaluation of Ghrelin and Des-Acyl Ghrelin Plasma Levels in Children with Newly Diagnosed Epilepsy: Evidence for Reduced Ghrelin-to-Des-Acyl Ghrelin Ratio in Generalized Epilepsies. Journal of Personalized Medicine. 12(4). 527–527. 8 indexed citations

Galardi, Francesca, Francesca De Luca, Chiara Biagioni, et al.. (2021). Circulating tumor cells and palbociclib treatment in patients with ER-positive, HER2-negative advanced breast cancer: results from a translational sub-study of the TREnd trial. Breast Cancer Research. 23(1). 38–38. 25 indexed citations

Bacci, Giacomo Maria, et al.. (2020). Atypical Ocular Coloboma in Tuberous Sclerosis-2: Report of Two Novel Cases. Journal of Neuro-Ophthalmology. 41(3). e363–e365. 1 indexed citations

Virgilio, Armando De, Andrea Costantino, Claudia Ebm, et al.. (2020). High definition three-dimensional exoscope (VITOM 3D) for microsurgery training: a preliminary experience. European Archives of Oto-Rhino-Laryngology. 277(9). 2589–2595. 21 indexed citations

10.

Cellini, Elena, Annalisa Vetro, Valerio Conti, et al.. (2019). Multiple genomic copy number variants associated with periventricular nodular heterotopia indicate extreme genetic heterogeneity. European Journal of Human Genetics. 27(6). 909–918. 21 indexed citations

11.

Guerrini, Renzo, Elena Parrini, Alessandro Esposito, Anna Fassio, & Valerio Conti. (2019). Lesional and non-lesional epilepsies: A blurring genetic boundary. European Journal of Paediatric Neurology. 24. 24–29. 5 indexed citations

12.

Parrini, Elena, Valerio Conti, William B. Dobyns, & Renzo Guerrini. (2016). Genetic Basis of Brain Malformations. Molecular Syndromology. 7(4). 220–233. 121 indexed citations

13.

Waśniewska, Małgorzata, Antonio Balsamo, Mariella Valenzise, et al.. (2013). Increased large artery intima media thickness in adolescents with either classical or non-classical congenital adrenal hyperplasia.. Archivio istituzionale della ricerca (Alma Mater Studiorum Università di Bologna). 36(1). 12–5. 30 indexed citations

14.

Puliti, Aldamaria, Pia Rossi, Gianluca Caridi, et al.. (2011). Albuminuria and Glomerular Damage in Mice Lacking the Metabotropic Glutamate Receptor 1. American Journal Of Pathology. 178(3). 1257–1269. 25 indexed citations

15.

Conti, Valerio, Carla Marini, Simone Gana, et al.. (2011). Corpus callosum agenesis, severe mental retardation, epilepsy, and dyskinetic quadriparesis due to a novel mutation in the homeodomain of ARX. American Journal of Medical Genetics Part A. 155(4). 892–897. 13 indexed citations

16.

Puliti, Aldamaria, et al.. (2010). A top-down linguistic approach to the analysis of genomic sequences: The metabotropic glutamate receptors 1 and 5 in human and in mouse as a case study. Journal of Theoretical Biology. 270(1). 134–142. 1 indexed citations

17.

Puliti, Aldamaria, Cosmeri Rizzato, Valerio Conti, et al.. (2010). Low-copy repeats on chromosome 22q11.2 show replication timing switches, DNA flexibility peaks and stress inducible asynchrony, sharing instability features with fragile sites. Mutation research. Fundamental and molecular mechanisms of mutagenesis. 686(1-2). 74–83. 9 indexed citations

18.

Conti, Valerio, et al.. (2010). Contractions in the second polyA tract of ARX are rare, non‐pathogenic polymorphisms. American Journal of Medical Genetics Part A. 155(1). 164–167. 1 indexed citations

19.

Musante, Veronica, Elisa Neri, Marco Feligioni, et al.. (2008). Presynaptic mGlu1 and mGlu5 autoreceptors facilitate glutamate exocytosis from mouse cortical nerve endings. Neuropharmacology. 55(4). 474–482. 46 indexed citations

20.

Behnam, Babak, et al.. (2006). Expression of Tsga10 sperm tail protein in embryogenesis and neural development: From cilium to cell division. Biochemical and Biophysical Research Communications. 344(4). 1102–1110. 36 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.

Explore authors with similar magnitude of impact