Claudia Bianchini

1.3k total citations
10 papers, 257 citations indexed

About

Claudia Bianchini is a scholar working on Genetics, Molecular Biology and Computational Mechanics. According to data from OpenAlex, Claudia Bianchini has authored 10 papers receiving a total of 257 indexed citations (citations by other indexed papers that have themselves been cited), including 5 papers in Genetics, 3 papers in Molecular Biology and 2 papers in Computational Mechanics. Recurrent topics in Claudia Bianchini's work include Genetics and Neurodevelopmental Disorders (4 papers), Genomics and Rare Diseases (3 papers) and Fluid Dynamics and Turbulent Flows (2 papers). Claudia Bianchini is often cited by papers focused on Genetics and Neurodevelopmental Disorders (4 papers), Genomics and Rare Diseases (3 papers) and Fluid Dynamics and Turbulent Flows (2 papers). Claudia Bianchini collaborates with scholars based in Italy, Germany and United States. Claudia Bianchini's co-authors include Bruno Facchini, Renzo Guerrini, Elena Parrini, Livio Tarchi, Davide Mei, Tiziana Pisano, Stefania Bigoni, Martino Montomoli, Francesco Mari and Carmen Barba and has published in prestigious journals such as SHILAP Revista de lepidopterología, Journal of Medical Genetics and Human Mutation.

In The Last Decade

Claudia Bianchini

10 papers receiving 252 citations

Peers

Claudia Bianchini

GENET

PMH

Heather Quiriarte United States

Lars Torsten Larsson Sweden

Seong-Hoon Jeong South Korea

О. Беличенко Russia

Rachid Fahmi United States

Connor R. Ferguson United States

Timo Frett Germany

P. A. Colloton United States

L. E. Warren United States

Lisa Gillinder Australia

Heather Quiriarte United States

Claudia Bianchini

216 ×1.9

GENET

19 ×0.2

PMH

36 ×0.5

0 ×0.0

2 ×0.0

Citations per year, relative to Claudia Bianchini Claudia Bianchini (= 1×) peers Heather Quiriarte

Countries citing papers authored by Claudia Bianchini

Since Specialization

Citations

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

Fields of papers citing papers by Claudia Bianchini

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Claudia Bianchini

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

All Works

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10 of 10 papers shown

Barbato, Alessandro, Michele Sacchini, Sara Bargiacchi, et al.. (2024). Endocrinological features and epileptic encephalopathy in COX deficiency due to SCO1 mutations: case series and review of literature. Endocrine Connections. 13(10). 2 indexed citations

Panza, N., Claudia Bianchini, Valentina Cetica, et al.. (2023). Bilateral temporal lobe dysplasia and seizure onset associated with biallelic CNTNAP2 variants. Epilepsia Open. 9(1). 417–423. 2 indexed citations

Mei, Davide, et al.. (2023). Autism and mild epilepsy associated with a de novo missense pathogenic variant in the GTPase effector domain of DNM1. American Journal of Medical Genetics Part C Seminars in Medical Genetics. 3 indexed citations

Darra, Francesca, Elena Parrini, Claudia Bianchini, et al.. (2021). Migrating Focal Seizures and Myoclonic Status in ARV1- Related Encephalopathy. Neurology Genetics. 7(3). e593–e593. 6 indexed citations

Heyne, Henrike, Mykyta Artomov, Florian Battke, et al.. (2019). Targeted gene sequencing in 6994 individuals with neurodevelopmental disorder with epilepsy. Genetics in Medicine. 21(11). 2496–2503. 36 indexed citations

Parrini, Elena, Carla Marini, Davide Mei, et al.. (2016). Diagnostic Targeted Resequencing in 349 Patients with Drug-Resistant Pediatric Epilepsies Identifies Causative Mutations in 30 Different Genes. Human Mutation. 38(2). 216–225. 122 indexed citations

Parrini, Elena, Davide Mei, Maria Antonietta Pisanti, et al.. (2015). Familial periventricular nodular heterotopia, epilepsy and Melnick–Needles Syndrome caused by a single FLNA mutation with combined gain-of-function and loss-of-function effects. Journal of Medical Genetics. 52(6). 405–412. 14 indexed citations

Andreini, Antonio, Claudia Bianchini, & Alessandro Innocenti. (2014). Large Eddy Simulation of a Bluff Body Stabilized Lean Premixed Flame. SHILAP Revista de lepidopterología. 2014. 1–18. 16 indexed citations

Bianchini, Claudia, et al.. (2011). Numerical and Experimental Investigation of Turning Flow Effects on Innovative Pin Fin Arrangements for Trailing Edge Cooling Configurations. Journal of Turbomachinery. 134(2). 46 indexed citations

10.

Andreini, Antonio, et al.. (2011). Assessment of Numerical Tools for the Evaluation of the Acoustic Impedance of Multi-Perforated Plates. Volume 2: Combustion, Fuels and Emissions, Parts A and B. 1065–1077. 10 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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