Dmitri Tentler

2.8k total citations · 1 hit paper
29 papers, 1.5k citations indexed

About

Dmitri Tentler is a scholar working on Molecular Biology, Genetics and Oncology. According to data from OpenAlex, Dmitri Tentler has authored 29 papers receiving a total of 1.5k indexed citations (citations by other indexed papers that have themselves been cited), including 21 papers in Molecular Biology, 8 papers in Genetics and 5 papers in Oncology. Recurrent topics in Dmitri Tentler's work include RNA modifications and cancer (7 papers), Nuclear Structure and Function (5 papers) and Genetics and Neurodevelopmental Disorders (5 papers). Dmitri Tentler is often cited by papers focused on RNA modifications and cancer (7 papers), Nuclear Structure and Function (5 papers) and Genetics and Neurodevelopmental Disorders (5 papers). Dmitri Tentler collaborates with scholars based in Russia, Sweden and United Kingdom. Dmitri Tentler's co-authors include Niklas Dahl, Birgit Carlsson, Gil Tchernia, Irma Dianzani, Thiébaut-Noël Willig, Sarah E. Ball, Peter Gustavsson, Hans Matsson, Björn Andersson and Narla Mohandas and has published in prestigious journals such as Proceedings of the National Academy of Sciences, Nature Genetics and Biochemical and Biophysical Research Communications.

In The Last Decade

Dmitri Tentler

28 papers receiving 1.5k citations

Hit Papers

align trajectories

What are hit papers?

Hit papers significantly outperform the citation benchmark for their cohort. A paper qualifies if it has ≥500 total citations, achieves ≥1.5× the top-1% citation threshold for papers in the same subfield and year (this is the minimum needed to enter the top 1%, not the average within it), or reaches the top citation threshold in at least one of its specific research topics.

The gene encoding ribosomal protein S19 is mutated in Diamond-Blackfan anaemia

1999 594 citations Peter Gustavsson, Björn Andersson et al. Nature Genetics profile →

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Dmitri Tentler Russia	18	1.1k	305	216	180	144	29	1.5k
Seiya Mizuno Japan	20	755 0.7×	270 0.9×	232 1.1×	144 0.8×	53 0.4×	101	1.4k
Raymond A. Poot Netherlands	23	2.4k 2.1×	531 1.7×	162 0.8×	139 0.8×	209 1.5×	34	2.7k
Kirsty Sawicka United States	16	807 0.7×	203 0.7×	123 0.6×	57 0.3×	189 1.3×	20	1.3k
Peri Tate United Kingdom	16	1.9k 1.7×	728 2.4×	137 0.6×	238 1.3×	225 1.6×	21	2.3k
Stephanie E. Kong United States	14	1.3k 1.1×	166 0.5×	296 1.4×	114 0.6×	103 0.7×	15	1.6k
Yufang Zheng China	24	989 0.9×	255 0.8×	289 1.3×	156 0.9×	180 1.3×	64	1.7k
Claudio Passananti Italy	25	1.2k 1.1×	269 0.9×	336 1.6×	102 0.6×	111 0.8×	66	1.6k
Sabine Lagger Austria	17	924 0.8×	306 1.0×	139 0.6×	44 0.2×	81 0.6×	23	1.2k
Dan Liang United States	14	1.8k 1.6×	287 0.9×	255 1.2×	70 0.4×	215 1.5×	25	2.3k
Jernej Murn United States	14	967 0.9×	220 0.7×	108 0.5×	91 0.5×	125 0.9×	27	1.2k

Countries citing papers authored by Dmitri Tentler

Since Specialization

Citations

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

Fields of papers citing papers by Dmitri Tentler

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Dmitri Tentler

This figure shows the co-authorship network connecting the top 25 collaborators of Dmitri Tentler. A scholar is included among the top collaborators of Dmitri Tentler 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 Dmitri Tentler. Dmitri Tentler 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

Vishnyakov, Innokentii E., Tatiana Efimova, Alexandra Daks, et al.. (2024). Effect of infection by Mycoplasma arginini and Mycoplasma salivarium on the oncogenic properties of lung cancer cell line A549. Biochemical and Biophysical Research Communications. 736. 150878–150878.

Aksenov, Nikolai D., et al.. (2022). Alpha-actnin-4 (ACTN4) selectively affects the DNA double-strand breaks repair in non-small lung carcinoma cells. Biology Direct. 17(1). 40–40. 4 indexed citations

Krishna, Vagolu Siva, et al.. (2019). 5-Chloro-2-thiophenyl-1,2,3-triazolylmethyldihydroquinolines as dual inhibitors of Mycobacterium tuberculosis and influenza virus: Synthesis and evaluation. Bioorganic & Medicinal Chemistry Letters. 29(18). 2664–2669. 11 indexed citations

Tentler, Dmitri, et al.. (2019). Role of ACTN4 in Tumorigenesis, Metastasis, and EMT. Cells. 8(11). 1427–1427. 55 indexed citations

Fedorova, Olga, Alexandra Daks, Varvara Petrova, et al.. (2018). Novel isatin-derived molecules activate p53 via interference with Mdm2 to promote apoptosis. Cell Cycle. 17(15). 1917–1930. 26 indexed citations

Lezina, Larissa, Vasilisa Aksenova, Т. А. Иванова, et al.. (2014). KMTase Set7/9 is a critical regulator of E2F1 activity upon genotoxic stress. Cell Death and Differentiation. 21(12). 1889–1899. 47 indexed citations

Lezina, Larissa, Alexey V. Antonov, Т. А. Иванова, et al.. (2013). miR-16 and miR-26a target checkpoint kinases Wee1 and Chk1 in response to p53 activation by genotoxic stress. Cell Death and Disease. 4(12). e953–e953. 67 indexed citations

Aksenova, Vasilisa, Nickolai A. Barlev, Veronika Borutinskaitė, et al.. (2010). Proteomic analysis of ACTN4-interacting proteins reveals it’s a putative involvement in mRNA metabolism. Biochemical and Biophysical Research Communications. 397(2). 192–196. 15 indexed citations

Tentler, Dmitri, et al.. (2007). Extra‐cellular matrix proteins induce re‐distribution of α‐actinin‐1 and α‐actinin‐4 in A431 cells. Cell Biology International. 31(4). 360–365. 17 indexed citations

10.

Babakov, Vladimir, et al.. (2007). RelA/NF-κB transcription factor associates with α-actinin-4. Experimental Cell Research. 314(5). 1030–1038. 46 indexed citations

11.

Coppola, Giovanni, Sang-Hyun Choi, Miguel M. Santos, et al.. (2006). Gene expression profiling in frataxin deficient mice: Microarray evidence for significant expression changes without detectable neurodegeneration. Neurobiology of Disease. 22(2). 302–311. 40 indexed citations

12.

Tentler, Dmitri, Maria Johansson, Maria Råstam, et al.. (2003). A candidate region for Asperger syndrome defined by two 17p breakpoints. European Journal of Human Genetics. 11(2). 189–195. 24 indexed citations

13.

Tentler, Dmitri, Göran Brandberg, Catalina Betancur, et al.. (2001). A balanced reciprocal translocation t(5;7)(q14;q32) associated with autistic disorder: Molecular analysis of the chromosome 7 breakpoint. American Journal of Medical Genetics. 105(8). 729–736. 16 indexed citations

14.

Tentler, Dmitri, et al.. (2000). A microdeletion in 19q13.2 associated with mental retardation, skeletal malformations, and Diamond-Blackfan anaemia suggests a novel contiguous gene syndrome. Journal of Medical Genetics. 37(2). 128–131. 19 indexed citations

15.

Schueler, Mary G., Anne W. Higgins, Ramaiah Nagaraja, et al.. (2000). Large-Insert Clone/STS Contigs in Xq11–q12, Spanning Deletions in Patients with Androgen Insensitivity and Mental Retardation. Genomics. 66(1). 104–109. 12 indexed citations

16.

Gustavsson, Peter, Björn Andersson, M Pettersson, et al.. (1999). The gene encoding ribosomal protein S19 is mutated in Diamond-Blackfan anaemia. Nature Genetics. 21(2). 169–175. 594 indexed citations breakdown →

17.

Tentler, Dmitri, Petter Gustavsson, Jaakko Leisti, et al.. (1999). Deletion including the oligophrenin-1 gene associated with enlarged cerebral ventricles, cerebellar hypoplasia, seizures and ataxia. European Journal of Human Genetics. 7(5). 541–548. 42 indexed citations

18.

Gustavsson, Petter, Emanuela Garelli, Simon Ball, et al.. (1999). IDENTIFICATION OF MICRODELETIONS SPANNING THE DIAMOND-BLACKFAN ANEMIA (DBA) LOCUS ON 19Q13 AND EVIDENCE FOR GENETIC HETEROGENEITY. Pediatric Research. 45(6). 941–941. 3 indexed citations

19.

Laporte, Jocelyn, F Blondeau, Dmitri Tentler, et al.. (1998). Characterization of the Myotubularin Dual Specificity Phosphatase Gene Family from Yeast to Human. Human Molecular Genetics. 7(11). 1703–1712. 97 indexed citations

20.

Gustavsson, Peter, Emanuela Garelli, Sarah E. Ball, et al.. (1998). Identification of Microdeletions Spanning the Diamond-Blackfan Anemia Locus on 19q13 and Evidence for Genetic Heterogeneity. The American Journal of Human Genetics. 63(5). 1388–1395. 57 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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