Arvis Sulovari

4.5k citations
21 papers · 1.1k indexed · 2 hit papers · h-index 13
Topics
Genomic variations and chromosomal abnormalities (7 papers)Chromosomal and Genetic Variations (7 papers)Genomics and Phylogenetic Studies (5 papers)

In The Last Decade

Arvis Sulovari

21 papers receiving 1.1k citations

Hit Papers

Characterizing the Major Structural Variant Alleles of th...20192026202120232019202250100150200250

Peers

Arvis Sulovari
Comparison fields: 5 of 96
  • Molecular Biology 726
  • Genetics 552
  • Plant Science 223
  • Cancer Research 106
  • Cellular and Molecular Neuroscience 104
Replace Alex Plocik with:
Alex Plocik United States
Ian C. Gray United Kingdom
Seungtai Yoon United States
Hao He China
Jasmine M. McCammon United States
Obah A. Ojarikre United Kingdom
Yoshihide Hayashizaki Japan
Aurélie Lardenois France
Elena Raimondi Italy
Magali Hennion France
Arvis Sulovari relative to Alex Plocik United States Alex Plocik's profile →
Citations per field
00.5×6.0×
Alex Plocik · 1×
Citations per year

Countries citing papers authored by Arvis Sulovari

Since Specialization
Citations

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

Fields of papers citing papers by Arvis Sulovari

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Arvis Sulovari

This figure shows the co-authorship network connecting the top 25 collaborators of Arvis Sulovari. A scholar is included among the top collaborators of Arvis Sulovari 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 Arvis Sulovari. Arvis Sulovari 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
#WorkIndexed citations
1 10
2 16
3
Segmental duplications and their variation in a complete human genomebreakdown →
152
4 15
5 17
6 7
7 11
8 35
9 81
10 4
11
Characterizing the Major Structural Variant Alleles of the Human Genomebreakdown →
269
12 44
13 166
14 5
15 91
16 37
17 9
18 5
19 6
20 75

About Arvis Sulovari

Arvis Sulovari is a scholar working on Biological Psychiatry, Genetics and Plant Science, having authored 21 papers that have together received 1.1k indexed citations. Recurring topics across this work include Genomic variations and chromosomal abnormalities (7 papers), Chromosomal and Genetic Variations (7 papers) and Genomics and Phylogenetic Studies (5 papers). The work is most often cited by research in Genetics (552 citations), Molecular Biology (726 citations) and Cancer Research (106 citations). Arvis Sulovari has collaborated with scholars based in United States, Germany and Italy. Frequent co-authors include Evan E. Eichler, Bradley P. Coe, Dawei Li, Peter A. Audano, Stuart Cantsilieris, Melanie Sorensen, Tychele N. Turner, Amy B. Wilfert, Vincent Magrini and Ankeeta Shah. Their work appears in journals such as Science, Cell and Proceedings of the National Academy of Sciences.

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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