Luca Trotta

809 total citations
14 papers, 197 citations indexed

About

Luca Trotta is a scholar working on Molecular Biology, Immunology and Neurology. According to data from OpenAlex, Luca Trotta has authored 14 papers receiving a total of 197 indexed citations (citations by other indexed papers that have themselves been cited), including 5 papers in Molecular Biology, 4 papers in Immunology and 3 papers in Neurology. Recurrent topics in Luca Trotta's work include Hearing, Cochlea, Tinnitus, Genetics (3 papers), Immunodeficiency and Autoimmune Disorders (3 papers) and Parkinson's Disease Mechanisms and Treatments (3 papers). Luca Trotta is often cited by papers focused on Hearing, Cochlea, Tinnitus, Genetics (3 papers), Immunodeficiency and Autoimmune Disorders (3 papers) and Parkinson's Disease Mechanisms and Treatments (3 papers). Luca Trotta collaborates with scholars based in Italy, Finland and United States. Luca Trotta's co-authors include Francesca Sironi, Stefano Goldwurm, Domenico Coviello, Gianni Pezzoli, Paola Primignani, Ilaria Guella, Rosanna Asselta, Stefano Duga, Margherita Canesi and Giulia Soldà and has published in prestigious journals such as Blood, Neurobiology of Aging and The Laryngoscope.

In The Last Decade

Luca Trotta

13 papers receiving 197 citations

Peers

Luca Trotta

NEURO

CMN

NEURO

I. M. Khidiyatova Russia

Ricardo Romero‐Guevara Italy

Kwang Woo Ko United States

Hongjun Song United States

Jenna Glatzer United States

Dana Šafka Brožková Czechia

Fatih Semerci United States

Diego Lopergolo Italy

Jiachen Bu China

Ave Eesmaa Finland

I. M. Khidiyatova Russia

Luca Trotta

124 ×1.6

29 ×0.4

NEURO

40 ×0.9

36 ×0.8

CMN

37 ×1.0

NEURO

Citations per year, relative to Luca Trotta Luca Trotta (= 1×) peers I. M. Khidiyatova

Countries citing papers authored by Luca Trotta

Since Specialization

Citations

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

Fields of papers citing papers by Luca Trotta

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Luca Trotta

This figure shows the co-authorship network connecting the top 25 collaborators of Luca Trotta. A scholar is included among the top collaborators of Luca Trotta 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 Luca Trotta. Luca Trotta 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

Dong, Liang, Bingtai Lu, Xiaoqiong Gu, et al.. (2025). Intracellular concentration of ADA2 is a marker for monocyte differentiation and activation. Frontiers of Medicine. 19(2). 359–375. 1 indexed citations

Trotta, Luca, Angelo Corso Faini, Licia Peruzzi, et al.. (2023). Relevance of next generation sequencing (NGS) data re-analysis in the diagnosis of monogenic diseases leading to organ failure. BMC Medical Genomics. 16(1). 303–303.

Tuovinen, Elina, Juha Grönholm, Tiina Öhman, et al.. (2020). Novel Hemizygous IL2RG p.(Pro58Ser) Mutation Impairs IL-2 Receptor Complex Expression on Lymphocytes Causing X-Linked Combined Immunodeficiency. Journal of Clinical Immunology. 40(3). 503–514. 13 indexed citations

Rajamäki, Kristiina, Salla Keskitalo, Mikko Seppänen, et al.. (2018). Haploinsufficiency of A20 impairs protein–protein interactome and leads into caspase-8-dependent enhancement of NLRP3 inflammasome activation. RMD Open. 4(2). e000740–e000740. 26 indexed citations

Trotta, Luca, Anna Norberg, Mervi Taskinen, et al.. (2018). Diagnostics of rare disorders: whole-exome sequencing deciphering locus heterogeneity in telomere biology disorders. Orphanet Journal of Rare Diseases. 13(1). 139–139. 10 indexed citations

Trotta, Luca, Timo Hautala, Sari Hämäläinen, et al.. (2016). Enrichment of rare variants in population isolates: single AICDA mutation responsible for hyper-IgM syndrome type 2 in Finland. European Journal of Human Genetics. 24(10). 1473–1478. 13 indexed citations

Taskinen, Mervi, Satu Mustjoki, Kirsi Jahnukainen, et al.. (2015). Large Granular Lymphocyte Infiltration in the Bone Marrow in Children and Young Adults May Suggest Primary Immune Deficiency. Blood. 126(23). 1024–1024. 1 indexed citations

Trotta, Luca, Ilaria Guella, Giulia Soldà, et al.. (2011). SNCA and MAPT genes: Independent and joint effects in Parkinson disease in the Italian population. Parkinsonism & Related Disorders. 18(3). 257–262. 38 indexed citations

Trotta, Luca, Paola Primignani, Pierangela Castorina, et al.. (2010). GJB2 and MTRNR1 contributions in children with hearing impairment from Northern Cameroon. International Journal of Audiology. 50(2). 133–138. 14 indexed citations

10.

Guella, Ilaria, Anna Pistocchi, Rosanna Asselta, et al.. (2010). Mutational screening and zebrafish functional analysis of GIGYF2 as a Parkinson-disease gene. Neurobiology of Aging. 32(11). 1994–2005. 19 indexed citations

11.

Sironi, Francesca, Luca Trotta, Angelo Antonini, et al.. (2009). α-Synuclein multiplication analysis in Italian familial Parkinson disease. Parkinsonism & Related Disorders. 16(3). 228–231. 27 indexed citations

12.

Primignani, Paola, Luca Trotta, Pierangela Castorina, et al.. (2009). Analysis of the GJB2 and GJB6 Genes in Italian Patients with Nonsyndromic Hearing Loss: Frequencies, Novel Mutations, Genotypes, and Degree of Hearing Loss. Genetic Testing and Molecular Biomarkers. 13(2). 209–217. 26 indexed citations

13.

Guella, I., Anna Pistocchi, Rosanna Asselta, et al.. (2009). Mutational screening and Zebrafish functional analysis of Gigyf2 as a Parkinson-disease gene. 2 indexed citations

14.

Primignani, Paola, Luca Trotta, Pierangela Castorina, et al.. (2007). A New De Novo Missense Mutation in Connexin 26 in a Sporadic Case of Nonsyndromic Deafness. The Laryngoscope. 117(5). 821–824. 7 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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