Marco Brumat

7.9k total citations
6 papers, 95 citations indexed

About

Marco Brumat is a scholar working on Sensory Systems, Molecular Biology and Nutrition and Dietetics. According to data from OpenAlex, Marco Brumat has authored 6 papers receiving a total of 95 indexed citations (citations by other indexed papers that have themselves been cited), including 4 papers in Sensory Systems, 3 papers in Molecular Biology and 2 papers in Nutrition and Dietetics. Recurrent topics in Marco Brumat's work include Hearing, Cochlea, Tinnitus, Genetics (4 papers), Genomics and Phylogenetic Studies (3 papers) and Biochemical Analysis and Sensing Techniques (2 papers). Marco Brumat is often cited by papers focused on Hearing, Cochlea, Tinnitus, Genetics (4 papers), Genomics and Phylogenetic Studies (3 papers) and Biochemical Analysis and Sensing Techniques (2 papers). Marco Brumat collaborates with scholars based in Italy, United Kingdom and Sweden. Marco Brumat's co-authors include Giorgia Girotto, Paolo Gasparini, Anna Morgan, Massimiliano Cocca, Massimo Mezzavilla, Maria Pina Concas, Dragana Vuckovic, Umberto Ambrosetti, Mariateresa Di Stazio and Martina La Bianca and has published in prestigious journals such as Gene, British Journal of Haematology and European Journal of Human Genetics.

In The Last Decade

Marco Brumat

6 papers receiving 95 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Marco Brumat Italy	6	47	30	29	16	14	6	95
Radka Kremlíková Pourová Czechia	8	45 1.0×	50 1.7×	82 2.8×	15 0.9×	23 1.6×	18	168
Stefania Lenarduzzi Italy	7	61 1.3×	64 2.1×	22 0.8×	11 0.7×	26 1.9×	17	132
Beatrice Spedicati Italy	6	27 0.6×	21 0.7×	16 0.6×	8 0.5×	8 0.6×	22	74
Thomas Jaworek United States	5	47 1.0×	73 2.4×	27 0.9×	8 0.5×	10 0.7×	7	122
Faezeh Mojahedi Iran	6	35 0.7×	82 2.7×	64 2.2×	4 0.3×	10 0.7×	8	160
Mariet Elting Netherlands	4	65 1.4×	39 1.3×	11 0.4×	30 1.9×	28 2.0×	4	96
Allen C. Simpson United States	3	69 1.5×	57 1.9×	18 0.6×	9 0.6×	20 1.4×	5	92
Christina Canavati Israel	4	29 0.6×	30 1.0×	18 0.6×	7 0.4×	11 0.8×	5	64
María Eugenia Foncuberta Argentina	5	48 1.0×	99 3.3×	18 0.6×	8 0.5×	6 0.4×	8	134
Ryan J. Carlson United States	3	51 1.1×	25 0.8×	7 0.2×	16 1.0×	18 1.3×	7	67

Countries citing papers authored by Marco Brumat

Since Specialization

Citations

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

Fields of papers citing papers by Marco Brumat

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Marco Brumat

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

All Works

Sort: Min cites: Since: Top N: Style:

6 of 6 papers shown

1.

Stazio, Mariateresa Di, Anna Morgan, Marco Brumat, et al.. (2020). New age-related hearing loss candidate genes in humans: an ongoing challenge. Gene. 742. 144561–144561. 8 indexed citations

2.

Nkya, Siana, Helen Rooks, Josephine Mgaya, et al.. (2020). F cell numbers are associated with an X‐linked genetic polymorphism and correlate with haematological parameters in patients with sickle cell disease. British Journal of Haematology. 191(5). 888–896. 10 indexed citations

3.

Cocca, Massimiliano, Caterina Barbieri, Maria Pina Concas, et al.. (2019). A bird’s-eye view of Italian genomic variation through whole-genome sequencing. European Journal of Human Genetics. 28(4). 435–444. 25 indexed citations

4.

Girotto, Giorgia, Anna Morgan, Navaneethakrishnan Krishnamoorthy, et al.. (2019). Next Generation Sequencing and Animal Models Reveal SLC9A3R1 as a New Gene Involved in Human Age-Related Hearing Loss. Frontiers in Genetics. 10. 142–142. 8 indexed citations

5.

Vuckovic, Dragana, Massimo Mezzavilla, Massimiliano Cocca, et al.. (2018). Whole-genome sequencing reveals new insights into age-related hearing loss: cumulative effects, pleiotropy and the role of selection. European Journal of Human Genetics. 26(8). 1167–1179. 19 indexed citations

6.

Morgan, Anna, Stefania Lenarduzzi, Stefania Cappellani, et al.. (2018). Genomic Studies in a Large Cohort of Hearing Impaired Italian Patients Revealed Several New Alleles, a Rare Case of Uniparental Disomy (UPD) and the Importance to Search for Copy Number Variations. Frontiers in Genetics. 9. 681–681. 25 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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