Lia Santulli

539 total citations
14 papers, 347 citations indexed

About

Lia Santulli is a scholar working on Genetics, Neurology and Psychiatry and Mental health. According to data from OpenAlex, Lia Santulli has authored 14 papers receiving a total of 347 indexed citations (citations by other indexed papers that have themselves been cited), including 8 papers in Genetics, 5 papers in Neurology and 5 papers in Psychiatry and Mental health. Recurrent topics in Lia Santulli's work include Epilepsy research and treatment (5 papers), Genetics and Neurodevelopmental Disorders (5 papers) and Genomic variations and chromosomal abnormalities (4 papers). Lia Santulli is often cited by papers focused on Epilepsy research and treatment (5 papers), Genetics and Neurodevelopmental Disorders (5 papers) and Genomic variations and chromosomal abnormalities (4 papers). Lia Santulli collaborates with scholars based in Italy, United Kingdom and Switzerland. Lia Santulli's co-authors include Salvatore Striano, Antonietta Coppola, Pasquale Striano, Simona Balestrini, Federico Zara, Carlo Nobile, Carlo Minetti, Pantaleo Romanelli, Roberto Michelucci and Luigi Del Gaudio and has published in prestigious journals such as Neurology, Epilepsia and Pharmacological Research.

In The Last Decade

Lia Santulli

13 papers receiving 326 citations

Peers

Lia Santulli

GENET

PMH

NEURO

CMN

Dora Steel United Kingdom

Nelide Romeo Italy

Amedeo Bianchi Italy

Kristien Verhaert Belgium

J.F. de Rijk-van Andel Netherlands

Jennifer J. Rilstone Canada

Inês Carrilho Portugal

Francesco Sasanelli Italy

Fatima Jaffer United Kingdom

João Ramalheira Portugal

Dora Steel United Kingdom

Lia Santulli

107 ×0.8

GENET

105 ×0.8

PMH

46 ×0.5

NEURO

111 ×1.2

CMN

131 ×1.7

Citations per year, relative to Lia Santulli Lia Santulli (= 1×) peers Dora Steel

Countries citing papers authored by Lia Santulli

Since Specialization

Citations

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

Fields of papers citing papers by Lia Santulli

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Lia Santulli

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

All Works

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14 of 14 papers shown

Stülpnagel, Celina von, Till Hartlieb, Ingo Borggräfe, et al.. (2018). Chewing induced reflex seizures (“eating epilepsy”) and eye closure sensitivity as a common feature in pediatric patients with SYNGAP1 mutations: Review of literature and report of 8 cases. Seizure. 65. 131–137. 27 indexed citations

Bernardo, Pia, Francesca Madia, Lia Santulli, et al.. (2016). 17q21.31 microdeletion syndrome: Description of a case further contributing to the delineation of Koolen-de Vries syndrome. Brain and Development. 38(7). 663–668. 7 indexed citations

Coppola, Antonietta, Lia Santulli, Simona Balestrini, et al.. (2016). Psychiatric comorbidities in patients from seven families with autosomal dominant cortical tremor, myoclonus, and epilepsy. Epilepsy & Behavior. 56. 38–43. 20 indexed citations

Santulli, Lia, Antonietta Coppola, Simona Balestrini, & Salvatore Striano. (2016). The challenges of treating epilepsy with 25 antiepileptic drugs. Pharmacological Research. 107. 211–219. 70 indexed citations

Striano, Pasquale, Lia Santulli, Ida Manna, et al.. (2015). DEPDC5 mutations are not a frequent cause of familial temporal lobe epilepsy. Epilepsia. 56(10). e168–71. 26 indexed citations

Dazzo, Emanuela, Lia Santulli, Annio Posar, et al.. (2014). Autosomal dominant lateral temporal epilepsy (ADLTE): Novel structural and single-nucleotide LGI1 mutations in families with predominant visual auras. Epilepsy Research. 110. 132–138. 15 indexed citations

Coppola, Antonietta, P. Ruosi, Lia Santulli, et al.. (2013). Neurological features and long-term follow-up in 15q11.2-13.1 duplication. European Journal of Medical Genetics. 56(11). 614–618. 17 indexed citations

Coppola, Antonietta, Irene Bagnasco, Monica Traverso, et al.. (2013). Different electroclinical picture of generalized epilepsy in two families with 15q13.3 microdeletion. Epilepsia. 54(5). e69–73. 12 indexed citations

Ferraro, Fausto, et al.. (2013). Spontaneous Intracranial Hypotension and Epidural Blood Patch: A Report Involving Seven Cases. Anaesthesia and Intensive Care. 41(3). 393–396. 1 indexed citations

10.

Fanciulli, Manuela, Lia Santulli, Chiara Barozzi, et al.. (2012). LGI1 microdeletion in autosomal dominant lateral temporal epilepsy. Neurology. 78(17). 1299–1303. 24 indexed citations

11.

Striano, Salvatore, et al.. (2012). The gelastic seizures-hypothalamic hamartoma syndrome: Facts, hypotheses, and perspectives. Epilepsy & Behavior. 24(1). 7–13. 49 indexed citations

12.

Coppola, Antonietta, Lia Santulli, Luigi Del Gaudio, et al.. (2011). Natural history and long-term evolution in families with autosomal dominant cortical tremor, myoclonus, and epilepsy. Epilepsia. 52(7). 1245–1250. 38 indexed citations

13.

Striano, Pasquale, Lia Santulli, Emanuela Leonardi, et al.. (2011). Familial temporal lobe epilepsy with psychic auras associated with a novel LGI1 mutation. Neurology. 76(13). 1173–1176. 39 indexed citations

14.

Coppola, Antonietta, Pasquale Striano, Stefania Gimelli, et al.. (2009). A de novo 11p12-p15.4 duplication in a patient with pharmacoresistant epilepsy, mental retardation, and dysmorphisms. Brain and Development. 32(3). 248–252. 2 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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