Vitaly Voloshin

Dr. Vitaly Voloshin

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Research Focus & Metrics

Academic Career Length

21Years (2006-Present)

(Calculated once Scilit publication data is synced: current year − year of first publication + 1)

Representative Publications

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15 May 2006 in Discrete Applied Mathematics
Verified
Journal Article
Closed access
VVVitaly Voloshin
Vitaly Voloshin
HVHeinz-Jürgen Voss
Heinz-Jürgen Voss

14 August 2023
Verified
Book Chapter
Open access
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MGMiruna Giurgiu
Miruna Giurgiu
RKRobert Kaltenbach
Robert Kaltenbach
FAFranziska Ahrend
Franziska Ahrend
SWSummer Weeks
Summer Weeks
HCHolly Clifton
Holly Clifton
AKAlexander Kofman
Alexander Kofman
MiRNA-mRNA interaction depends on multiple factors such as 3UTR isoforms, the cell and tissue-specific expression levels of RNA-binding proteins, the sequence context around the mRNA target site, and other mechanisms. Genetic polymorphisms within miRNAs and their target sites appear to be among the most important ones because they influence the mode and outcome of miRNA-mRNA interaction universally and irreversibly. SNP disruption of miRNAs and their binding sites, as well as conformational changes preventing the access of the miRNA to its target site, are adopted as the most credible mechanistic explanations of SNP-mediated effects. The occurrence of multiple SNPs within the same miRNA-binding site implies their combinatorial mode of action. The presence of the repetitive (homologous) binding sites for the same miRNA on its mRNA target may both enhance the miRNA targeting and provide for the backup target site instead of the one disrupted by SNP, thus rescuing the miRNA functionality. While being underexplored, the multiple genetic polymorphisms within the miRNA-binding sites, as well as homologous miRNA-binding sites, may be considered as additional factors influencing miRNA-mediated regulation of gene expression.

21 August 2021 in Symmetry
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Journal Article
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Gyorgy DosaGyorgy Dosa
Gyorgy Dosa
NNNicholas Newman
Nicholas Newman
ZTZsolt Tuza
Zsolt Tuza
VVVitaly Voloshin
Vitaly Voloshin
In this paper, we investigate partitions of highly symmetrical discrete structures called cycloids. In general, a mixed hypergraph has two types of hyperedges. The vertices are colored in such a way that each C-edge has two vertices of the same color, and each D-edge has two vertices of distinct colors. In our case, a mixed cycloid is a mixed hypergraph whose vertices can be arranged in a cyclic order, and every consecutive p vertices form a C-edge, and every consecutive q vertices form a D-edge in the ordering. We completely determine the maximum number of colors that can be used for any p≥3 and any q≥2. We also develop an algorithm that generates a coloring with any number of colors between the minimum and maximum. Finally, we discuss the colorings of mixed cycloids when the maximum number of colors coincides with its upper bound, which is the largest cardinality of a set of vertices containing no C-edge.

10 April 2021 in Mathematics
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Journal Article
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NNNicholas Newman
Nicholas Newman
VVVitaly Voloshin
Vitaly Voloshin
In colorings of some block designs, the vertices of blocks can be thought of as hyperedges of a hypergraph H that can be placed on a circle and colored according to some rules that are related to colorings of circular mixed hypergraphs. A mixed hypergraph H is called circular if there exists a host cycle on the vertex set X such that every edge (C- or D-) induces a connected subgraph of this cycle. We propose an algorithm to color the (r,r)-uniform, complete, circular, mixed hypergraphs for all feasible values with no gaps. In doing so, we show χ(H)=2 and χ¯(H)=n−s or n−s−1 where s is the sieve number.

26 February 2026 in Axioms
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Journal Article
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JAJulian Allagan
Julian Allagan
VVVitaly Voloshin
Vitaly Voloshin
GMGabrielle Christina Morgan
Gabrielle Christina Morgan
The bichromatic triangle polynomial PG(k) counts vertex k-colorings in which every triangle uses exactly two colors. We develop a transfer matrix framework for three canonical families of 2-trees: book graphs Bn, 1-fans Fn1, and triangulated ladders TLm. In each case, PG(k) satisfies a second-order linear recurrence with an explicit closed form; for TLm this yields a Chebyshev representation, while for Fn1 the binary specialization gives PFn1(2)=2Fn+1. A spectral identity α2=r+ links the dominant characteristic roots of the fan and ladder recurrences, implying identical exponential growth rates when indexed by vertex count, whereas book graphs grow strictly faster for k≥4. In fact, this correspondence is exact: for all k≥2, the triangulated ladder polynomial coincides with that of a suitably indexed 1-fan. Passing to line graphs, we interpret PL(Kn)(k) as counting edge colorings of Kn that forbid both monochromatic and rainbow triangles, and we identify a sharp obstruction threshold at n≥6.

4 June 2013 in arXiv
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Preprint
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KDKefeng Diao
Kefeng Diao
VVVitaly Voloshin
Vitaly Voloshin
KWKaishun Wang
Kaishun Wang
PZPing Zhao
Ping Zhao
Let $S$ be a finite set of positive integers. A mixed hypergraph ${\cal H}$ is a one-realization of $S$ if its feasible set is $S$ and each entry of its chromatic spectrum is either 0 or 1. In [P. Zhao, K. Diao, Y. Chang and K. Wang, The smallest one-realization of a given set \uppercase\expandafter{\romannumeral2}, Discrete Math. 312 (2012) 2946--2951], we determined the minimum number of vertices of a 3-uniform bi-hypergraph which is a one-realization of $S$. In this paper, we generalize this result to $r$-uniform bi-hypergraphs.