E. K. Ginter

1.8k total citations
47 papers, 1.2k citations indexed

About

E. K. Ginter is a scholar working on Molecular Biology, Genetics and Genetics. According to data from OpenAlex, E. K. Ginter has authored 47 papers receiving a total of 1.2k indexed citations (citations by other indexed papers that have themselves been cited), including 14 papers in Molecular Biology, 11 papers in Genetics and 5 papers in Genetics. Recurrent topics in E. K. Ginter's work include Nutrition, Genetics, and Disease (5 papers), Cystic Fibrosis Research Advances (5 papers) and BRCA gene mutations in cancer (4 papers). E. K. Ginter is often cited by papers focused on Nutrition, Genetics, and Disease (5 papers), Cystic Fibrosis Research Advances (5 papers) and BRCA gene mutations in cancer (4 papers). E. K. Ginter collaborates with scholars based in Russia, United States and Slovakia. E. K. Ginter's co-authors include Björn Dahlbäck, Kenneth A. Bauer, Rogier M. Bertina, Joseph P. Miletich, Frits R. Rosendaal, Nikolay P. Bochkov, Mammen Chandy, David A. Lane, Uri Seligsohn and Pier Mannuccio Mannucci and has published in prestigious journals such as Science, International Journal of Molecular Sciences and The American Journal of Human Genetics.

In The Last Decade

E. K. Ginter

43 papers receiving 1.2k citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
E. K. Ginter Russia	13	617	405	269	232	155	47	1.2k
Marie‐Christine Mowinckel Norway	14	278 0.5×	125 0.3×	70 0.3×	70 0.3×	63 0.4×	29	824
Inger Hagen Norway	18	721 1.2×	21 0.1×	243 0.9×	66 0.3×	68 0.4×	39	1.1k
Joan D. Beckman United States	13	209 0.3×	42 0.1×	337 1.3×	35 0.2×	274 1.8×	31	754
Francesca Marino Italy	16	119 0.2×	20 0.0×	145 0.5×	271 1.2×	16 0.1×	49	821
Maria Lombardi Netherlands	17	245 0.4×	4 0.0×	329 1.2×	246 1.1×	263 1.7×	45	1.1k
Morihiko Takeda Japan	17	132 0.2×	5 0.0×	632 2.3×	249 1.1×	42 0.3×	37	1.2k
Renato Vanacore Italy	18	61 0.1×	9 0.0×	400 1.5×	44 0.2×	163 1.1×	37	1.2k
Jina Yun South Korea	17	42 0.1×	25 0.1×	389 1.4×	16 0.1×	29 0.2×	68	1.1k
R. M. Bannerman United States	25	525 0.9×	6 0.0×	314 1.2×	33 0.1×	488 3.1×	67	1.6k
Milena Braga‐Basaria United States	12	57 0.1×	6 0.0×	254 0.9×	55 0.2×	43 0.3×	21	1.2k

Countries citing papers authored by E. K. Ginter

Since Specialization

Citations

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

Fields of papers citing papers by E. K. Ginter

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by E. K. Ginter. 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 E. K. Ginter. The network helps show where E. K. Ginter may publish in the future.

Co-authorship network of co-authors of E. K. Ginter

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

All Works

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20 of 20 papers shown

Marakhonov, Andrey V., et al.. (2024). Genetic Landscape and Clinical Features of Hyperphenylalaninemia in North Ossetia-Alania: High Frequency of P281L and P211T Genetic Variants in the PAH Gene. International Journal of Molecular Sciences. 25(9). 4598–4598. 2 indexed citations

Marakhonov, Andrey V., et al.. (2024). The Study of the Inheritance Mechanisms of Myotonic Dystrophy Type 1 (DM1) in Families from the Republic of North Ossetia-Alania. International Journal of Molecular Sciences. 25(17). 9734–9734. 2 indexed citations

Vasilyeva, Tatyana A., Andrey V. Marakhonov, A. A. Voskresenskaya, et al.. (2023). Epidemiology of PAX6 Gene Pathogenic Variants and Expected Prevalence of PAX6-Associated Congenital Aniridia across the Russian Federation: A Nationwide Study. Genes. 14(11). 2041–2041. 2 indexed citations

Kashirskaya, N., Н.В. Петрова, А. И. Хавкин, et al.. (2023). International experience in the primary prevention of cystic fibrosis (part one). Experimental and Clinical Gastroenterology. 150–159.

Kashirskaya, N., Н.В. Петрова, А. И. Хавкин, et al.. (2023). International experience in the primary prevention of cystic fibrosis (part two). Experimental and Clinical Gastroenterology. 160–170. 2 indexed citations

Петрова, Н.В., Andrey V. Marakhonov, Tatyana A. Vasilyeva, et al.. (2023). Hereditary etiology of non-syndromic sensorineural hearing loss in the Republic of North Ossetia–Alania. PeerJ. 11. e14514–e14514. 2 indexed citations

Ginter, E. K., et al.. (2022). Epidemiology of hereditary eye disease in the populations of Russian Federation. Russian Journal of Clinical Ophthalmology. 22(2). 69–79. 3 indexed citations

Volchkov, Pavel, E. K. Ginter, Vera L. Izhevskaya, et al.. (2021). Human embryo genome editing: an interdisciplinary approach. Annals of the Russian academy of medical sciences. 76(1). 86–92.

Зинченко, Р. А., et al.. (2019). Main methodological approaches to the identification and diagnosis of monogenic hereditary diseases and problems in the organization of medical care and unified preventive programs. Problems of Social Hygiene Public Health and History of Medicine. 27(5). 865–877. 4 indexed citations

10.

Петрова, Н.В., N. Kashirskaya, Tatyana A. Vasilyeva, et al.. (2016). High prevalence of W1282x mutation in cystic fibrosis patients from Karachay-Cherkessia. Journal of Cystic Fibrosis. 15(3). e28–e32. 16 indexed citations

11.

Simko, Vlado & E. K. Ginter. (2014). Understanding cholesterol: high is bad but too low may also be risky – is low cholesterol associated with cancer?. Bratislavské lekárske listy/Bratislava medical journal. 115(2). 59–65. 7 indexed citations

12.

Kostyuk, Svetlana V., Elena M. Malinovskaya, Christian Dani, et al.. (2012). Extracellular DNA oxidation stimulates activation of NRF2 and reduces the production of ROS in human mesenchymal stem cells. Expert Opinion on Biological Therapy. 12(sup1). S85–S97. 36 indexed citations

13.

Tverskaya, Svetlana, et al.. (2009). Genetic analysis of autosomal recessive osteopetrosis in Chuvashiya: the unique splice site mutation in TCIRG1 gene spread by the founder effect. European Journal of Human Genetics. 17(5). 664–672. 31 indexed citations

14.

Plotnikova, Olga, Fyodor A. Kondrashov, Peter K. Vlasov, et al.. (2007). Conversion and Compensatory Evolution of the γ-Crystallin Genes and Identification of a Cataractogenic Mutation That Reverses the Sequence of the Human CRYGD Gene to an Ancestral State. The American Journal of Human Genetics. 81(1). 32–43. 33 indexed citations

15.

Tjulandin, S., et al.. (2007). High incidence of mutations in BRCA1 and BRCA2 genes in ovarian cancer. Bulletin of Experimental Biology and Medicine. 144(1). 83–85. 5 indexed citations

16.

Казанцева, А. В., Andrey Goltsov, Р. А. Зинченко, et al.. (2006). Human Hair Growth Deficiency Is Linked to a Genetic Defect in the Phospholipase Gene LIPH. Science. 314(5801). 982–985. 134 indexed citations

17.

Krajcovicová-Kudlácková, M, P Blažiček, Viera Spustová, Martina Valachovičová, & E. K. Ginter. (2004). Cardiovascular risk factors in young Gypsy population.. PubMed. 105(7-8). 256–9. 41 indexed citations

18.

Гарькавцева, Р Ф, et al.. (2003). Spectrum of Mutations in BRCA1 Gene in Hereditary Forms of Breast and Ovarian Cancer in Russian Families. Bulletin of Experimental Biology and Medicine. 136(3). 276–278. 21 indexed citations

19.

Verlingue, C., Bernard Mercier, E. K. Ginter, et al.. (1995). Complete screening of mutations in the coding sequence of the CFTR gene in a sample of CF patients from Russia: Identification of three novel alleles. Human Mutation. 5(3). 205–209. 7 indexed citations

20.

Ginter, E. K., et al.. (1994). Emery‐Dreifuss syndrome: Genetic and clinical varieties. American Journal of Medical Genetics. 50(3). 228–233. 10 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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