Maria Pintaudi

476 total citations
9 papers, 245 citations indexed

About

Maria Pintaudi is a scholar working on Genetics, Molecular Biology and Cognitive Neuroscience. According to data from OpenAlex, Maria Pintaudi has authored 9 papers receiving a total of 245 indexed citations (citations by other indexed papers that have themselves been cited), including 7 papers in Genetics, 4 papers in Molecular Biology and 3 papers in Cognitive Neuroscience. Recurrent topics in Maria Pintaudi's work include Genetics and Neurodevelopmental Disorders (6 papers), Genomic variations and chromosomal abnormalities (4 papers) and Autism Spectrum Disorder Research (3 papers). Maria Pintaudi is often cited by papers focused on Genetics and Neurodevelopmental Disorders (6 papers), Genomic variations and chromosomal abnormalities (4 papers) and Autism Spectrum Disorder Research (3 papers). Maria Pintaudi collaborates with scholars based in Italy, Israel and France. Maria Pintaudi's co-authors include Silvia Russo, Francesca Cogliati, E. Veneselli, Margherita Marchi, M. G. Baglietto, Aglaia Vignoli, Maria Grazia Calevo, Lidia Larizza, Maria Teresa Bonati and Edvige Veneselli and has published in prestigious journals such as International Journal of Molecular Sciences, Epilepsy Research and Epilepsy & Behavior.

In The Last Decade

Maria Pintaudi

9 papers receiving 240 citations

Peers

Maria Pintaudi

GENET

MB

CN

PMH

CP

Karl-Ludvig Reichelt Norway

Alex D. Shaw Australia

Jordana Weissman United States

Tianyun Wang China

Monica B. Proud United States

Francesca Cogliati Italy

Malgorzata Lamacz United States

Qingping Zhang China

William Byerley United States

J.A.S. Vorstman Netherlands

Karl-Ludvig Reichelt Norway

Maria Pintaudi

144 ×0.7

GENET

57 ×0.6

MB

171 ×2.2

CN

55 ×1.2

PMH

18 ×0.8

CP

Citations per year, relative to Maria Pintaudi Maria Pintaudi (= 1×) peers Karl-Ludvig Reichelt

Countries citing papers authored by Maria Pintaudi

Since Specialization

Citations

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

Fields of papers citing papers by Maria Pintaudi

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Maria Pintaudi

This figure shows the co-authorship network connecting the top 25 collaborators of Maria Pintaudi. A scholar is included among the top collaborators of Maria Pintaudi 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 Maria Pintaudi. Maria Pintaudi 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:

9 of 9 papers shown

1.

Cogliati, Francesca, Maura Masciadri, Maria Teresa Bonati, et al.. (2019). Pathogenic Variants in STXBP1 and in Genes for GABAa Receptor Subunities Cause Atypical Rett/Rett-like Phenotypes. International Journal of Molecular Sciences. 20(15). 3621–3621. 25 indexed citations

2.

Pintaudi, Maria, Maria Grazia Calevo, Aglaia Vignoli, et al.. (2015). Antiepileptic drugs in Rett Syndrome. European Journal of Paediatric Neurology. 19(4). 446–452. 15 indexed citations

3.

Pintaudi, Maria, E. Veneselli, Adriana Voci, et al.. (2015). Blood oxidative stress and metallothionein expression in Rett syndrome: Probing for markers. The World Journal of Biological Psychiatry. 17(3). 198–209. 10 indexed citations

4.

Pintaudi, Maria, Maria Grazia Calevo, Aglaia Vignoli, et al.. (2010). Epilepsy in Rett syndrome: Clinical and genetic features. Epilepsy & Behavior. 19(3). 296–300. 63 indexed citations

5.

Russo, Silvia, Margherita Marchi, Francesca Cogliati, et al.. (2009). Novel mutations in the CDKL5 gene, predicted effects and associated phenotypes. Neurogenetics. 10(3). 241–250. 58 indexed citations

6.

Pintaudi, Maria, Monika Eisermann, Dorothée Ville, et al.. (2007). Can fever treat epileptic encephalopathies?. Epilepsy Research. 77(1). 44–61. 5 indexed citations

7.

Pintaudi, Maria, M. G. Baglietto, R. Gaggero, et al.. (2007). Clinical and electroencephalographic features in patients with CDKL5 mutations: Two new Italian cases and review of the literature. Epilepsy & Behavior. 12(2). 326–331. 29 indexed citations

8.

Giribaldi, Gaia, et al.. (2007). A Case of Major Form Familial Hyperekplexia: Prenatal Diagnosis and Effective Treatment With Clonazepam. Journal of Child Neurology. 22(6). 769–772. 6 indexed citations

9.

Striano, Pasquale, Michela Malacarne, Simona Cavani, et al.. (2006). Clinical phenotype and molecular characterization of 6q terminal deletion syndrome: Five new cases. American Journal of Medical Genetics Part A. 140A(18). 1944–1949. 34 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