Marta Rusmini

830 total citations
22 papers, 467 citations indexed

About

Marta Rusmini is a scholar working on Immunology, Surgery and Molecular Biology. According to data from OpenAlex, Marta Rusmini has authored 22 papers receiving a total of 467 indexed citations (citations by other indexed papers that have themselves been cited), including 10 papers in Immunology, 8 papers in Surgery and 8 papers in Molecular Biology. Recurrent topics in Marta Rusmini's work include Congenital gastrointestinal and neural anomalies (6 papers), Immunodeficiency and Autoimmune Disorders (4 papers) and IL-33, ST2, and ILC Pathways (4 papers). Marta Rusmini is often cited by papers focused on Congenital gastrointestinal and neural anomalies (6 papers), Immunodeficiency and Autoimmune Disorders (4 papers) and IL-33, ST2, and ILC Pathways (4 papers). Marta Rusmini collaborates with scholars based in Italy, United States and Netherlands. Marta Rusmini's co-authors include Isabella Ceccherini, Francesco Caroli, Marco Gattorno, Alice Grossi, Roberta Caorsi, Roberto Ravazzolo, C. Crosti, Clara De Simone, Massimo Cugno and Pier Luigi Meroni and has published in prestigious journals such as PLoS ONE, International Journal of Molecular Sciences and Frontiers in Immunology.

In The Last Decade

Marta Rusmini

21 papers receiving 463 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Marta Rusmini Italy	12	218	130	103	85	83	22	467
Lina Tan China	14	289 1.3×	181 1.4×	88 0.9×	74 0.9×	71 0.9×	31	650
Dennis M. de Graaf United States	12	239 1.1×	274 2.1×	79 0.8×	42 0.5×	38 0.5×	20	506
Laura Nájera Spain	11	162 0.7×	42 0.3×	47 0.5×	52 0.6×	71 0.9×	29	329
Katherina Psarra Greece	12	105 0.5×	136 1.0×	51 0.5×	31 0.4×	36 0.4×	33	475
M Heslan France	8	97 0.4×	238 1.8×	51 0.5×	54 0.6×	42 0.5×	9	433
Maryam Sadr Iran	13	191 0.9×	254 2.0×	21 0.2×	84 1.0×	64 0.8×	67	580
Shunli Tang China	11	110 0.5×	215 1.7×	147 1.4×	47 0.6×	87 1.0×	24	496
Lynette Peddle Canada	16	198 0.9×	504 3.9×	98 1.0×	34 0.4×	52 0.6×	20	833
Silke Frey Germany	13	150 0.7×	359 2.8×	123 1.2×	41 0.5×	35 0.4×	20	648
Nickie Seto United States	10	205 0.9×	403 3.1×	57 0.6×	23 0.3×	88 1.1×	14	616

Countries citing papers authored by Marta Rusmini

Since Specialization

Citations

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

Fields of papers citing papers by Marta Rusmini

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Marta Rusmini

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

All Works

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20 of 20 papers shown

Grossi, Alice, Marta Rusmini, Roberto Cusano, et al.. (2023). Whole genome sequencing in ROHHAD trios proved inconclusive: what’s beyond?. Frontiers in Genetics. 14. 1031074–1031074. 4 indexed citations

Uva, Paolo, Tommaso Pippucci, Marco Seri, et al.. (2022). Exploration of Tools for the Interpretation of Human Non-Coding Variants. International Journal of Molecular Sciences. 23(21). 12977–12977. 11 indexed citations

Miano, Maurizio, Concetta Micalizzi, Michela Lupia, et al.. (2022). Sirolimus Restores Erythropoiesis and Controls Immune Dysregulation in a Child With Cartilage-Hair Hypoplasia: A Case Report. Frontiers in Immunology. 13. 893000–893000. 1 indexed citations

Rusmini, Marta, Paolo Uva, Antonio Amoroso, Manlio Tolomeo, & Andrea Cavalli. (2021). How Genetics Might Explain the Unusual Link Between Malaria and COVID-19. Frontiers in Medicine. 8. 650231–650231. 14 indexed citations

Papa, Riccardo, Marta Rusmini, Francesca Schena, et al.. (2021). Type I interferon activation in RAS-associated autoimmune leukoproliferative disease (RALD). Clinical Immunology. 231. 108837–108837. 6 indexed citations

Signa, Sara, Elena Campione, Marta Rusmini, et al.. (2019). Whole exome sequencing approach to childhood onset familial erythrodermic psoriasis unravels a novel mutation of CARD14 requiring unusual high doses of ustekinumab. Pediatric Rheumatology. 17(1). 38–38. 23 indexed citations

Nigro, Cristiana Lo, Marta Rusmini, & Isabella Ceccherini. (2019). RET in breast cancer: pathogenic implications and mechanisms of drug resistance. Cancer Drug Resistance. 2(4). 1136–1152. 14 indexed citations

Papa, Riccardo, Marta Rusmini, Stefano Volpi, et al.. (2019). FRI0568 THE USE OF NEXT GENERATION SEQUENCING PANEL IN UNDIFFERENTIATED AUTOINFLAMMATORY DISEASES IDENTIFY A SEPARATE SUBSET OF COLCHICINE-RESPONDER RECURRENT FEVERS DISTINCT FROM PFAPA SYNDROME. Annals of the Rheumatic Diseases. 78. 979–980. 2 indexed citations

Caorsi, Roberta, Marta Rusmini, Stefano Volpi, et al.. (2018). CD70 Deficiency due to a Novel Mutation in a Patient with Severe Chronic EBV Infection Presenting As a Periodic Fever. Frontiers in Immunology. 8. 2015–2015. 21 indexed citations

10.

Rocco, Maja Di, Marta Rusmini, Francesco Caroli, et al.. (2017). Novel spondyloepimetaphyseal dysplasia due to UFSP2 gene mutation. Clinical Genetics. 93(3). 671–674. 32 indexed citations

11.

Matera, Ivana, Marta Rusmini, Yiran Guo, et al.. (2016). Variants of the ACTG2 gene correlate with degree of severity and presence of megacystis in chronic intestinal pseudo-obstruction. European Journal of Human Genetics. 24(8). 1211–1215. 34 indexed citations

12.

Vanni, Irene, Simona Coco, Anna Truini, et al.. (2015). Next-Generation Sequencing Workflow for NSCLC Critical Samples Using a Targeted Sequencing Approach by Ion Torrent PGM™ Platform. International Journal of Molecular Sciences. 16(12). 28765–28782. 33 indexed citations

13.

Rusmini, Marta, Silvia Federici, Francesco Caroli, et al.. (2015). Next-generation sequencing and its initial applications for molecular diagnosis of systemic auto-inflammatory diseases. Annals of the Rheumatic Diseases. 75(8). 1550–1557. 47 indexed citations

14.

Signa, Sara, Marta Rusmini, Elena Campione, et al.. (2015). Severe erytrodermic psoriasis and arthritis as clinical presentation of a CARD14-mediated psoriasis (CAMPS). Pediatric Rheumatology. 13(S1). 1 indexed citations

15.

Rusmini, Marta, Silvia Federici, Francesco Caroli, et al.. (2015). A Next Generation Sequencing approach to the mutational screening of patients affected with systemic autoinflammatory disorders: diagnosis improvement and interpretation of complex clinical phenotypes. Pediatric Rheumatology. 13(S1).

16.

Marzano, Angelo Valerio, Isabella Ceccherini, Marco Gattorno, et al.. (2014). Association of Pyoderma Gangrenosum, Acne, and Suppurative Hidradenitis (PASH) Shares Genetic and Cytokine Profiles With Other Autoinflammatory Diseases. Medicine. 93(27). e187–e187. 96 indexed citations

17.

Rusmini, Marta, Paola Griseri, Ivana Matera, et al.. (2014). Expression Variability and Function of the RET Gene in Adult Peripheral Blood Mononuclear Cells. Journal of Cellular Physiology. 229(12). 2027–2037. 9 indexed citations

18.

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

19.

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

20.

Matera, Ivana, Marco Musso, Paola Griseri, et al.. (2013). Allele-Specific Expression at theRETLocus in Blood and Gut Tissue of Individuals Carrying Risk Alleles for Hirschsprung Disease. Human Mutation. 34(5). 754–762. 3 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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