E. D. Cherstvoy

1.1k total citations
23 papers, 820 citations indexed

About

E. D. Cherstvoy is a scholar working on Molecular Biology, Genetics and Endocrinology, Diabetes and Metabolism. According to data from OpenAlex, E. D. Cherstvoy has authored 23 papers receiving a total of 820 indexed citations (citations by other indexed papers that have themselves been cited), including 9 papers in Molecular Biology, 6 papers in Genetics and 5 papers in Endocrinology, Diabetes and Metabolism. Recurrent topics in E. D. Cherstvoy's work include Thyroid Cancer Diagnosis and Treatment (5 papers), Congenital limb and hand anomalies (3 papers) and Amino Acid Enzymes and Metabolism (2 papers). E. D. Cherstvoy is often cited by papers focused on Thyroid Cancer Diagnosis and Treatment (5 papers), Congenital limb and hand anomalies (3 papers) and Amino Acid Enzymes and Metabolism (2 papers). E. D. Cherstvoy collaborates with scholars based in Belarus, Italy and Germany. E. D. Cherstvoy's co-authors include Iosif W. Lurie, G. I. Lazjuk, Bogdanova Ti, М.D. Тronko, Alfredo Fusco, Giancarlo Vecchio, G Thomas, Gennaro Chiappetta, Francesca Pentimalli and Giuseppe Viglietto and has published in prestigious journals such as The Journal of Clinical Endocrinology & Metabolism, British Journal of Cancer and Clinical Endocrinology.

In The Last Decade

E. D. Cherstvoy

23 papers receiving 790 citations

Peers

E. D. Cherstvoy

EDM

GENET

SURGE

ONCOL

Gail S. Lebovic United States

Jonathan P. Park United States

Angela Mariano Italy

Tatiana Vorontsova Italy

M J Delisle France

Ajith Kumar United Kingdom

Dagmar Arnold United States

Ayako Miyakawa Japan

Nimrod Kiss Sweden

Sumito Dateki Japan

Gail S. Lebovic United States

E. D. Cherstvoy

378 ×1.0

EDM

380 ×1.4

145 ×0.6

GENET

114 ×0.7

SURGE

226 ×1.4

ONCOL

Citations per year, relative to E. D. Cherstvoy E. D. Cherstvoy (= 1×) peers Gail S. Lebovic

Countries citing papers authored by E. D. Cherstvoy

Since Specialization

Citations

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

Fields of papers citing papers by E. D. Cherstvoy

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of E. D. Cherstvoy

This figure shows the co-authorship network connecting the top 25 collaborators of E. D. Cherstvoy. A scholar is included among the top collaborators of E. D. Cherstvoy 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. D. Cherstvoy. E. D. Cherstvoy 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

Cherstvoy, E. D., et al.. (2021). The significance of the expression of matrix metalloproteinases in the differential diagnosis of periodontal diseases. Russian Journal of Archive of Pathology. 83(3). 20–20. 2 indexed citations

Cherstvoy, E. D., et al.. (2009). βIII-tubulin at the invasive margin of colorectal cancer: possible link to invasion. Archiv für Pathologische Anatomie und Physiologie und für Klinische Medicin. 454(5). 541–548. 33 indexed citations

Cherstvoy, E. D., et al.. (2009). Tissue transglutaminase expression in celiac mucosa: an immunohistochemical study. Archiv für Pathologische Anatomie und Physiologie und für Klinische Medicin. 455(4). 363–373. 13 indexed citations

Drozd, Valentina M., et al.. (2002). Ultrasound diagnosis of radiation-induced childhood thyroid cancer in Belarus: 10 years of practical experience. International Congress Series. 1234. 221–229. 1 indexed citations

Santoro, Massimo, G Thomas, Giancarlo Vecchio, et al.. (2000). Gene rearrangement and Chernobyl related thyroid cancers. British Journal of Cancer. 82(2). 315–322. 91 indexed citations

Elisei, Rossella, Cristina Romei, Barbara Cosci, et al.. (2000). New breakpoints in both the H4 and RET genes create a variant of PTC‐1 in a post‐Chernobyl papillary thyroid carcinoma. Clinical Endocrinology. 53(1). 131–136. 12 indexed citations

Thomas, G, Helen Cook, E. D. Williams, et al.. (1999). High Prevalence of RET/PTC Rearrangements in Ukrainian and Belarussian Post-Chernobyl Thyroid Papillary Carcinomas: A Strong Correlation between RET/PTC3 and the Solid-Follicular Variant1. The Journal of Clinical Endocrinology & Metabolism. 84(11). 4232–4238. 203 indexed citations

Pacini, Furio, Tatiana Vorontsova, Eleonora Molinaro, et al.. (1997). Post-Chernobyl Thyroid Carcinoma in Belarus Children and Adolescents: Comparison with Naturally Occurring Thyroid Carcinoma in Italy and France¹. The Journal of Clinical Endocrinology & Metabolism. 82(11). 3563–3569. 161 indexed citations

Williams, Elizabeth D., E. D. Cherstvoy, B Egloff, et al.. (1996). Interaction of pathology and molecular characterization of thyroid cancers. OSTI OAI (U.S. Department of Energy Office of Scientific and Technical Information). 8 indexed citations

10.

Lurie, Iosif W., et al.. (1991). The cerebro‐reno‐digital syndromes: a new community. Clinical Genetics. 39(2). 104–113. 16 indexed citations

11.

Lazjuk, G. I., et al.. (1985). Elaboration of the phenotypic changes of the upper limbs in the Neu‐Laxova syndrome. American Journal of Medical Genetics. 20(1). 1–11. 20 indexed citations

12.

Cherstvoy, E. D., et al.. (1984). The smith-lemli-opitz syndrome. Archiv für Pathologische Anatomie und Physiologie und für Klinische Medicin. 404(4). 413–425. 29 indexed citations

13.

Lurie, Iosif W. & E. D. Cherstvoy. (1984). Renal agenesis as a diagnostic feature of the crypthophthalmos‐syndactyly syndrome. Clinical Genetics. 25(6). 528–532. 29 indexed citations

14.

Cherstvoy, E. D., et al.. (1983). The popliteal pterygium syndrome (a condition of the main anatomical structures of the lower limbs).. PubMed. 31(3). 258–62. 1 indexed citations

15.

Cherstvoy, E. D., et al.. (1980). Difficulties in classification of the short rib-polydactyly syndromes. European Journal of Pediatrics. 133(1). 57–61. 16 indexed citations

16.

Lurie, Iosif W., et al.. (1979). Aprosencephaly‐atelencephaly and the aprosencephaly (XK) syndrome. American Journal of Medical Genetics. 3(3). 303–309. 31 indexed citations

17.

Lazjuk, G. I., et al.. (1979). The Neu‐Laxova syndrome—a distinct entity. American Journal of Medical Genetics. 3(3). 261–267. 43 indexed citations

18.

Cherstvoy, E. D., et al.. (1978). Pulmonary hypoplasia, multiple ankyloses, and camptodactyly: one syndrome or some related forms?. PubMed. 33(1). 73–9. 20 indexed citations

19.

Lurie, Iosif W., et al.. (1976). Further evidence'for the autosomal‐recessive inheritance of the COFS syndrome. Clinical Genetics. 10(5). 343–346. 17 indexed citations

20.

Lazjuk, G. I., et al.. (1976). A syndrome of multiple congenital malformations including amelia and oligodactyly occurring in half‐cousins. Teratology. 13(2). 161–165. 3 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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