Francesca Lantieri

3.3k total citations
46 papers, 954 citations indexed

About

Francesca Lantieri is a scholar working on Surgery, Genetics and Immunology. According to data from OpenAlex, Francesca Lantieri has authored 46 papers receiving a total of 954 indexed citations (citations by other indexed papers that have themselves been cited), including 17 papers in Surgery, 15 papers in Genetics and 12 papers in Immunology. Recurrent topics in Francesca Lantieri's work include Congenital gastrointestinal and neural anomalies (13 papers), Digestive system and related health (6 papers) and Immune Cell Function and Interaction (5 papers). Francesca Lantieri is often cited by papers focused on Congenital gastrointestinal and neural anomalies (13 papers), Digestive system and related health (6 papers) and Immune Cell Function and Interaction (5 papers). Francesca Lantieri collaborates with scholars based in Italy, United States and Netherlands. Francesca Lantieri's co-authors include Isabella Ceccherini, Paola Griseri, Marcella Devoto, Giuseppe Murdaca, Roberto Ravazzolo, Francesco Puppo, Tiziana Bachetti, Francesca Puppo, Håkon Håkonarson and Josephine Elia and has published in prestigious journals such as PLoS ONE, International Journal of Molecular Sciences and British Journal of Cancer.

In The Last Decade

Francesca Lantieri

45 papers receiving 936 citations

Peers — A (Enhanced Table)

Peers by citation overlap · career bar shows stage (early→late) cites · hero ref

Name h Career Trend Papers Cites
Francesca Lantieri Italy 21 275 198 197 166 143 46 954
Michel Toledano United States 17 204 0.7× 99 0.5× 182 0.9× 140 0.8× 184 1.3× 54 1.5k
Miriam Davis United States 13 110 0.4× 330 1.7× 221 1.1× 121 0.7× 89 0.6× 18 892
Pieter van der Vlies Netherlands 20 178 0.6× 196 1.0× 590 3.0× 235 1.4× 168 1.2× 34 1.3k
Catherine Keohane Ireland 21 211 0.8× 235 1.2× 340 1.7× 281 1.7× 55 0.4× 64 1.8k
Yunyuan Li Canada 14 97 0.4× 210 1.1× 260 1.3× 97 0.6× 56 0.4× 32 858
Karen M. Chisholm United States 20 110 0.4× 122 0.6× 584 3.0× 222 1.3× 121 0.8× 68 1.4k
Kai Shu China 18 131 0.5× 112 0.6× 259 1.3× 124 0.7× 27 0.2× 100 1.0k
Ana Silva Portugal 24 110 0.4× 284 1.4× 560 2.8× 242 1.5× 106 0.7× 110 1.9k
Gökçe Törüner United States 19 101 0.4× 126 0.6× 581 2.9× 213 1.3× 376 2.6× 86 1.4k
Kristina Allen‐Brady United States 22 269 1.0× 76 0.4× 440 2.2× 93 0.6× 622 4.3× 80 1.4k

Countries citing papers authored by Francesca Lantieri

Since Specialization
Citations

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

Fields of papers citing papers by Francesca Lantieri

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Francesca Lantieri

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

All Works

20 of 20 papers shown
1.
Mattioli, Francesca, et al.. (2023). Deprescribing Strategies: A Prospective Study on Proton Pump Inhibitors. Journal of Clinical Medicine. 12(8). 3029–3029. 1 indexed citations
2.
Conteduca, Giuseppina, Marina Grasso, Maurizio Cecconi, et al.. (2023). Molecular Analysis and Reclassification of NSD1 Gene Variants in a Cohort of Patients with Clinical Suspicion of Sotos Syndrome. Genes. 14(2). 295–295. 9 indexed citations
3.
Ciliberti, Rosagemma, et al.. (2022). A Survey on Undergraduate Medical Students’ Perception of COVID-19 Vaccination. Vaccines. 10(9). 1464–1464. 4 indexed citations
4.
Murdaca, Giuseppe, Francesca Lantieri, Simona Pigozzi, et al.. (2018). HLA-G expression in gastric carcinoma: clinicopathological correlations and prognostic impact. Archiv für Pathologische Anatomie und Physiologie und für Klinische Medicin. 473(4). 425–433. 38 indexed citations
5.
Musso, Natale R., Francesco Orlandini, Franco Rabbia, et al.. (2015). Prevalence of erectile dysfunction in a cohort of Italian hypertensive subjects. Clinical and Experimental Hypertension. 38(2). 143–149. 8 indexed citations
6.
Lantieri, Francesca, et al.. (2015). Effectiveness of psychological support in patients undergoing primary total hip or knee arthroplasty: a controlled cohort study. Journal of Orthopaedics and Traumatology. 17(2). 137–147. 28 indexed citations
7.
8.
Prato, Alessio Pini, Valentina Rossi, Manuela Mosconi, et al.. (2013). A prospective observational study of associated anomalies in Hirschsprung’s disease. Orphanet Journal of Rare Diseases. 8(1). 184–184. 23 indexed citations
9.
Rusmini, Marta, Paola Griseri, Francesca Lantieri, et al.. (2013). Correction: Induction of RET Dependent and Independent Pro-Inflammatory Programs in Human Peripheral Blood Mononuclear Cells from Hirschsprung Patients. PLoS ONE. 8(4). 6 indexed citations
10.
Rusmini, Marta, Paola Griseri, Francesca Lantieri, et al.. (2013). Induction of RET Dependent and Independent Pro-Inflammatory Programs in Human Peripheral Blood Mononuclear Cells from Hirschsprung Patients. PLoS ONE. 8(3). e59066–e59066. 41 indexed citations
11.
Jannot, Anne‐Sophie, Jeanne Amiel, Anna Pelet, et al.. (2012). Male and female differential reproductive rate could explain parental transmission asymmetry of mutation origin in Hirschsprung disease. European Journal of Human Genetics. 20(9). 917–920. 8 indexed citations
12.
Lantieri, Francesca, Francesco Caroli, Isabella Ceccherini, & Paola Griseri. (2012). The involvement of the RET variant G691S in medullary thyroid carcinoma enlightened by a meta‐analysis study. International Journal of Cancer. 132(12). 2808–2819. 26 indexed citations
13.
14.
Lantieri, Francesca, Joseph Glessner, Håkon Håkonarson, Josephine Elia, & Marcella Devoto. (2010). Analysis of GWAS top hits in ADHD suggests association to two polymorphisms located in genes expressed in the cerebellum. American Journal of Medical Genetics Part B Neuropsychiatric Genetics. 153B(6). 1127–1133. 30 indexed citations
15.
Lantieri, Francesca, Min A. Jhun, Jungsun Park, Taesung Park, & Marcella Devoto. (2009). Comparative analysis of different approaches for dealing with candidate regions in the context of a genome-wide association study. BMC Proceedings. 3(S7). S93–S93. 5 indexed citations
16.
Elia, Josephine, Mario Capasso, Francesca Lantieri, et al.. (2009). Candidate gene analysis in an on-going genome-wide association study of attention-deficit hyperactivity disorder: suggestive association signals in ADRA1A. Psychiatric Genetics. 19(3). 134–141. 28 indexed citations
17.
18.
Lantieri, Francesca, Halfdan Rydbeck, Paola Griseri, Isabella Ceccherini, & Marcella Devoto. (2007). Incorporating prior biological information in linkage studies increases power and limits multiple testing. BMC Proceedings. 1(S1). S89–S89. 3 indexed citations
19.
Lantieri, Francesca, Paola Griseri, & Isabella Ceccherini. (2006). Molecular mechanisms ofRET‐induced Hirschsprung pathogenesis. Annals of Medicine. 38(1). 11–19. 30 indexed citations
20.
Torre, Gabriella Della, Barbara Pasini, Simona Frigerio, et al.. (2001). CDKN2A and CDK4 mutation analysis in Italian melanoma-prone families: functional characterization of a novel CDKN2A germ line mutation. British Journal of Cancer. 85(6). 836–844. 41 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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