Ilya Kanivets

458 total citations
39 papers, 162 citations indexed

About

Ilya Kanivets is a scholar working on Molecular Biology, Genetics and Pediatrics, Perinatology and Child Health. According to data from OpenAlex, Ilya Kanivets has authored 39 papers receiving a total of 162 indexed citations (citations by other indexed papers that have themselves been cited), including 17 papers in Molecular Biology, 13 papers in Genetics and 11 papers in Pediatrics, Perinatology and Child Health. Recurrent topics in Ilya Kanivets's work include Metabolism and Genetic Disorders (8 papers), Prenatal Screening and Diagnostics (8 papers) and Genetics and Neurodevelopmental Disorders (6 papers). Ilya Kanivets is often cited by papers focused on Metabolism and Genetic Disorders (8 papers), Prenatal Screening and Diagnostics (8 papers) and Genetics and Neurodevelopmental Disorders (6 papers). Ilya Kanivets collaborates with scholars based in Russia, United States and United Kingdom. Ilya Kanivets's co-authors include Ekaterina Zakharova, Fedor A. Konovalov, Galina Baydakova, Е. Л. Дадали, E. N. Yakusheva, Sergey I. Kutsev, Svetlana Mikhaylova, Nataliya V. Melnikova, Alexei D. Kolotii and Vladimir L. Katanaev and has published in prestigious journals such as SHILAP Revista de lepidopterología, PLoS ONE and International Journal of Molecular Sciences.

In The Last Decade

Ilya Kanivets

29 papers receiving 161 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Ilya Kanivets Russia 7 91 61 29 26 19 39 162
Rodolphe Dard France 6 113 1.2× 63 1.0× 27 0.9× 21 0.8× 12 0.6× 19 233
Deepa Krishnakumar United Kingdom 7 65 0.7× 36 0.6× 30 1.0× 18 0.7× 7 0.4× 15 187
Huifang Yan China 9 108 1.2× 79 1.3× 23 0.8× 7 0.3× 10 0.5× 23 201
Bryan Sayson Canada 7 70 0.8× 48 0.8× 29 1.0× 12 0.5× 7 0.4× 8 160
Özkan Özdemir Türkiye 7 100 1.1× 47 0.8× 24 0.8× 9 0.3× 8 0.4× 22 173
Nuria García Segarra Switzerland 7 78 0.9× 45 0.7× 57 2.0× 10 0.4× 5 0.3× 10 148
Ramona Salvarinova Canada 8 109 1.2× 40 0.7× 80 2.8× 13 0.5× 7 0.4× 18 202
Anne Dieux‐Coëslier France 7 99 1.1× 39 0.6× 25 0.9× 24 0.9× 3 0.2× 12 156
Bregje Jaeger Netherlands 9 80 0.9× 16 0.3× 95 3.3× 26 1.0× 10 0.5× 22 216
Thipwimol Tim‐Aroon Thailand 8 102 1.1× 68 1.1× 20 0.7× 17 0.7× 6 0.3× 49 228

Countries citing papers authored by Ilya Kanivets

Since Specialization
Citations

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

Fields of papers citing papers by Ilya Kanivets

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Ilya Kanivets

This figure shows the co-authorship network connecting the top 25 collaborators of Ilya Kanivets. A scholar is included among the top collaborators of Ilya Kanivets 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 Ilya Kanivets. Ilya Kanivets 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.
2.
Дадали, Е. Л., et al.. (2023). Four Novel Disease-Causing Variants in the NOTCH3 Gene in Russian Patients with CADASIL. Genes. 14(9). 1715–1715.
3.
Marakhonov, Andrey V., Magdalena Přechová, Fedor A. Konovalov, et al.. (2021). Mutation in PHACTR1 associated with multifocal epilepsy with infantile spasms and hypsarrhythmia. Clinical Genetics. 99(5). 673–683. 6 indexed citations
4.
Kanivets, Ilya, et al.. (2021). The role of fetal chromosomal aberrations in the genesis of recurrent and sporadic miscarriage. Voprosy ginekologii akušerstva i perinatologii. 20(1). 34–39. 2 indexed citations
5.
Kanivets, Ilya, et al.. (2021). SNP-Based Chromosomal Microarray Analysis for Detecting DNA Copy Number Variations in Fetuses with a Thickened Nuchal Fold. Sovremennye tehnologii v medicine. 13(6). 72–72. 2 indexed citations
6.
Kanivets, Ilya, et al.. (2021). Congenital cerebral palsy: genetic cause and nosological integrity. SHILAP Revista de lepidopterología. 15(3-4). 65–77. 4 indexed citations
7.
Дадали, Е. Л., et al.. (2021). Clinical and genetic characteristics of distal arthrogryposis caused by mutations in the PIEZO2 gene. SHILAP Revista de lepidopterología. 11(2). 48–55. 1 indexed citations
8.
Гундорова, П., et al.. (2021). BH4-deficient hyperphenylalaninemia in Russia. PLoS ONE. 16(4). e0249608–e0249608. 11 indexed citations
9.
Рыжкова, О. П., et al.. (2020). Spastic paraplegias types 11 and 15. SHILAP Revista de lepidopterología. 14(4). 29–38. 1 indexed citations
10.
Kanivets, Ilya, et al.. (2020). Infantile parkinsonism-dystonia, type 1 (case report). 1(4). 232–241.
11.
12.
Konovalov, Fedor A., et al.. (2020). Case Report: Complicated Molecular Diagnosis of MECP2 Gene Structural Rearrangement in a Proband with Rett Syndrome. Journal of Autism and Developmental Disorders. 51(6). 2159–2163.
13.
Vasilyeva, Tatyana A., Andrey V. Marakhonov, Н.В. Петрова, et al.. (2020). A sporadic case of congenital aniridia caused by pericentric inversion inv(11)(p13q14) associated with a 977 kb deletion in the 11p13 region. BMC Medical Genomics. 13(S8). 130–130. 4 indexed citations
14.
Дадали, Е. Л., et al.. (2020). Clinical and genetic characteristics of epilepsy caused by mutations in the PCDH19 gene (OMIM: 300088). S S Korsakov Journal of Neurology and Psychiatry. 120(1). 55–55. 4 indexed citations
15.
Kanivets, Ilya, et al.. (2019). Genetic Aspects of Pathogenesis of Congenital Spastic Cerebral Paralysis. SHILAP Revista de lepidopterología. 4(3). 28–39. 3 indexed citations
16.
Kanivets, Ilya, et al.. (2019). Cell-free-fetal DNA: an experience of population screening for chromosome pathology in Russia. Voprosy ginekologii akušerstva i perinatologii. 18(3). 46–51. 3 indexed citations
17.
Zakharova, Ekaterina, et al.. (2019). Case report: a rare case of Hunter syndrome (type II mucopolysaccharidosis) in a girl. BMC Medical Genetics. 20(1). 66–66. 13 indexed citations
18.
Кулеш, А. А., et al.. (2019). CADASIL syndrome: differential diagnosis with multiple sclerosis. S S Korsakov Journal of Neurology and Psychiatry. 119(10). 128–128.
19.
Дадали, Е. Л., et al.. (2016). HEREDITARY DISEASES AND SYNDROMES ACCOMPANIED BY FEBRILE CONVULSIONS: CLINICAL AND GENETIC CHARACTERISTICS AND DIAGNOSTIC PROCEDURES. SHILAP Revista de lepidopterología. 11(2). 33–41. 6 indexed citations
20.
Kanivets, Ilya, et al.. (2014). Association of non-invasive prenatal testing and chromosomal microarray analysis for prenatal diagnostics. Gynecological Endocrinology. 30(sup1). 13–16. 5 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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