С. А. Кравченко

1.3k total citations
44 papers, 315 citations indexed

About

С. А. Кравченко is a scholar working on Genetics, Molecular Biology and Pediatrics, Perinatology and Child Health. According to data from OpenAlex, С. А. Кравченко has authored 44 papers receiving a total of 315 indexed citations (citations by other indexed papers that have themselves been cited), including 15 papers in Genetics, 14 papers in Molecular Biology and 4 papers in Pediatrics, Perinatology and Child Health. Recurrent topics in С. А. Кравченко's work include Genomics and Rare Diseases (4 papers), Synthesis and Characterization of Heterocyclic Compounds (3 papers) and Reproductive Biology and Fertility (3 papers). С. А. Кравченко is often cited by papers focused on Genomics and Rare Diseases (4 papers), Synthesis and Characterization of Heterocyclic Compounds (3 papers) and Reproductive Biology and Fertility (3 papers). С. А. Кравченко collaborates with scholars based in Ukraine, Russia and United Kingdom. С. А. Кравченко's co-authors include Л. А. Лившиц, P. Gourmelon, B. Le Guen, Svitlana Malyarchuk, Élisabeth Petit, Gilles Vergnaud, Limborskaia Sa, P. A. Slominsky, Э. К. Хуснутдинова and Oleg Balanovsky and has published in prestigious journals such as Radiation Research, Spectrochimica Acta Part A Molecular and Biomolecular Spectroscopy and Journal of Luminescence.

In The Last Decade

С. А. Кравченко

40 papers receiving 289 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
С. А. Кравченко Ukraine 10 116 102 53 47 46 44 315
R. Gerth Austria 10 172 1.5× 50 0.5× 54 1.0× 85 1.8× 30 0.7× 15 315
H. Priddle United Kingdom 7 212 1.8× 52 0.5× 89 1.7× 70 1.5× 14 0.3× 8 486
Ron Hadas Israel 10 214 1.8× 26 0.3× 39 0.7× 18 0.4× 39 0.8× 17 363
Daniel Laune France 10 184 1.6× 48 0.5× 24 0.5× 22 0.5× 112 2.4× 14 382
G.H. Westerveld Netherlands 10 161 1.4× 169 1.7× 41 0.8× 126 2.7× 53 1.2× 16 346
Christian Mueller Germany 10 179 1.5× 128 1.3× 13 0.2× 12 0.3× 27 0.6× 15 446
C.J. Flickinger United States 12 156 1.3× 67 0.7× 113 2.1× 185 3.9× 23 0.5× 19 365
Simon Goldbard United States 12 193 1.7× 85 0.8× 174 3.3× 32 0.7× 27 0.6× 19 521
Ji Wu China 12 395 3.4× 60 0.6× 132 2.5× 51 1.1× 16 0.3× 19 549
Angela Alme United States 7 89 0.8× 52 0.5× 30 0.6× 43 0.9× 8 0.2× 11 388

Countries citing papers authored by С. А. Кравченко

Since Specialization
Citations

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

Fields of papers citing papers by С. А. Кравченко

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by С. А. Кравченко. 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 С. А. Кравченко. The network helps show where С. А. Кравченко may publish in the future.

Co-authorship network of co-authors of С. А. Кравченко

This figure shows the co-authorship network connecting the top 25 collaborators of С. А. Кравченко. A scholar is included among the top collaborators of С. А. Кравченко 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 С. А. Кравченко. С. А. Кравченко 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
1.
Кравченко, С. А., et al.. (2020). THE FREQUENCY OF ASSOCIATED WITH THE GILBERT’S SYNDROME UGT1A1 GENE LOW-FUNCTIONAL ALLELE 7(TA) (rs8175347) IN UKRAINE. Bulletin of Problems Biology and Medicine. 2(1). 91–91.
2.
Кравченко, С. А., et al.. (2017). Features of Near-Surface Layer at Monomolecular Isotropic Adsorption: Nonequilibrium Molecular Dynamics Simulation. Ukrainian Journal of Physics. 62(8). 717–726. 1 indexed citations
3.
4.
Кравченко, С. А., et al.. (2015). ZNF527 gene rs386809049 analysis in population of ukraine. Cytology and Genetics. 49(4). 240–244. 1 indexed citations
5.
Rębała, Krzysztof, et al.. (2013). Northern Slavs from Serbia do not show a founder effect at autosomal and Y-chromosomal STRs and retain their paternal genetic heritage. Forensic Science International Genetics. 8(1). 126–131. 2 indexed citations
6.
Кравченко, С. А., et al.. (2013). Association of PvuII polymorphism in ESR1 gene with impaired ovarian reserve in patients from Ukraine. Reproductive Biology. 13(1). 96–99. 10 indexed citations
7.
Кравченко, С. А., et al.. (2012). Clinical genealogical and molecular genetic study of patients with mental retardation. Cytology and Genetics. 46(1). 47–53. 1 indexed citations
8.
Кравченко, С. А., et al.. (2009). Novel L558P Mutation of the TGFBI Gene Found in Ukrainian Families with Atypical Corneal Dystrophy. Ophthalmologica. 223(3). 207–214. 11 indexed citations
9.
Кравченко, С. А., et al.. (2009). CAG polymorphism of the androgen receptor gene in azoospermic and oligozoospermic men from Ukraine. Cytology and Genetics. 43(6). 401–405. 4 indexed citations
10.
Кравченко, С. А., et al.. (2009). Effect of the topography of silver films on the structure of surface ensembles of 11-mercaptoundecanol. Theoretical and Experimental Chemistry. 45(2). 108–113. 2 indexed citations
11.
Кравченко, С. А., et al.. (2008). A distribution of two SNPs in exon 10 of the FSHR gene among the women with a diminished ovarian reserve in Ukraine. Journal of Assisted Reproduction and Genetics. 26(1). 29–34. 42 indexed citations
12.
Кравченко, С. А., et al.. (2008). Molecular-genetics analysis of natural and stimulated ovulation impairment. Cytology and Genetics. 42(4). 272–277. 3 indexed citations
13.
Roewer, Lutz, Sascha Willuweit, Marion Nagy, et al.. (2007). Y-chromosomal STR haplotypes in Kalmyk population samples. Forensic Science International. 173(2-3). 204–209. 25 indexed citations
14.
Кравченко, С. А. & Л. А. Лившиц. (2007). Nature and origin of germline mutations in human tandem repeated loci. Biopolymers and Cell. 23(3). 188–201. 2 indexed citations
15.
Кравченко, С. А., et al.. (2005). [The use of DNA analysis for diagnostics of hereditary premature ovarian failure].. PubMed. 39(2). 59–63. 1 indexed citations
16.
Лившиц, Л. А., et al.. (2004). Association between genotype and clinical manifestation of the most spread monogenic hereditary disorders. Biopolymers and Cell. 20(1-2). 107–114. 1 indexed citations
17.
Sa, Limborskaia, Oleg Balanovsky, P. A. Slominsky, et al.. (2002). Analysis of CCR5Δ32 Geographic Distribution and Its Correlation with Some Climatic and Geographic Factors. Human Heredity. 53(1). 49–54. 22 indexed citations
18.
Лившиц, Л. А., Svitlana Malyarchuk, С. А. Кравченко, et al.. (2001). Children of Chernobyl Cleanup Workers do not Show Elevated Rates of Mutations in Minisatellite Alleles. Radiation Research. 155(1). 74–80. 64 indexed citations
19.
Remennikov, G. Ya., et al.. (1998). σ-Complexes in the pyrimidine series. 13. Reaction of 7- and 5-methoxyfuroxano-[3,4-d]pyrimidines with some C-nucleophiles. Chemistry of Heterocyclic Compounds. 34(1). 104–110. 4 indexed citations
20.
Remennikov, G. Ya., et al.. (1993). Synthesis and some conversions of 4-aryl-6-methyl-2-methoxy(phenyl)-5-nitro-1,4-dihydropyrimidines. Chemistry of Heterocyclic Compounds. 29(10). 1200–1205. 1 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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