Е. Л. Дадали

3.5k total citations
115 papers, 760 citations indexed

About

Е. Л. Дадали is a scholar working on Molecular Biology, Genetics and Cellular and Molecular Neuroscience. According to data from OpenAlex, Е. Л. Дадали has authored 115 papers receiving a total of 760 indexed citations (citations by other indexed papers that have themselves been cited), including 55 papers in Molecular Biology, 41 papers in Genetics and 36 papers in Cellular and Molecular Neuroscience. Recurrent topics in Е. Л. Дадали's work include Genetic Neurodegenerative Diseases (25 papers), Hereditary Neurological Disorders (20 papers) and Muscle Physiology and Disorders (14 papers). Е. Л. Дадали is often cited by papers focused on Genetic Neurodegenerative Diseases (25 papers), Hereditary Neurological Disorders (20 papers) and Muscle Physiology and Disorders (14 papers). Е. Л. Дадали collaborates with scholars based in Russia, United States and United Kingdom. Е. Л. Дадали's co-authors include Oleg V. Evgrafov, A. V. Polyakov, Irina Mersiyanova, V. F. Sitnikov, А. Н. Петрин, Christine Van Broeckhoven, Vincent Timmerman, Andrey V. Marakhonov, В. П. Федотов and Eva Nelis and has published in prestigious journals such as SHILAP Revista de lepidopterología, International Journal of Molecular Sciences and The American Journal of Human Genetics.

In The Last Decade

Е. Л. Дадали

89 papers receiving 732 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Е. Л. Дадали Russia 10 454 260 208 207 152 115 760
Friedmar R. Kreuz Germany 17 441 1.0× 498 1.9× 211 1.0× 129 0.6× 99 0.7× 30 923
Andrzej Kochański Poland 14 490 1.1× 287 1.1× 184 0.9× 143 0.7× 126 0.8× 73 706
Alice B. Schindler United States 15 396 0.9× 607 2.3× 128 0.6× 202 1.0× 132 0.9× 37 1.0k
Moreno Ferrarini Italy 16 353 0.8× 249 1.0× 105 0.5× 223 1.1× 168 1.1× 31 607
Tine Deconinck Belgium 17 376 0.8× 376 1.4× 149 0.7× 107 0.5× 89 0.6× 28 733
María José Chumillas Spain 12 525 1.2× 246 0.9× 229 1.1× 263 1.3× 97 0.6× 14 766
Nazha Birouk France 17 1.0k 2.2× 344 1.3× 362 1.7× 463 2.2× 263 1.7× 47 1.3k
Sandra Gill United States 11 461 1.0× 481 1.9× 117 0.6× 83 0.4× 171 1.1× 15 880
Djamel Grid France 17 710 1.6× 692 2.7× 309 1.5× 251 1.2× 272 1.8× 28 1.3k
Paul R. Kasher United Kingdom 12 178 0.4× 384 1.5× 153 0.7× 305 1.5× 96 0.6× 29 847

Countries citing papers authored by Е. Л. Дадали

Since Specialization
Citations

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

Fields of papers citing papers by Е. Л. Дадали

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Е. Л. Дадали. 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 Е. Л. Дадали. The network helps show where Е. Л. Дадали may publish in the future.

Co-authorship network of co-authors of Е. Л. Дадали

This figure shows the co-authorship network connecting the top 25 collaborators of Е. Л. Дадали. A scholar is included among the top collaborators of Е. Л. Дадали 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 Е. Л. Дадали. Е. Л. Дадали 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.
Kenis, Vladimir, et al.. (2025). Expanding the Clinical Spectrum of BCARD Syndrome Caused by Novel Biallelic Variants in the PLOD3 Gene. Clinical Genetics. 108(4). 474–478.
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Kenis, Vladimir, et al.. (2024). Presentation of Rare Phenotypes Associated with the FKBP10 Gene. Genes. 15(6). 674–674. 1 indexed citations
5.
Дадали, Е. Л., et al.. (2024). Special clinical manifestations and genetic characteristics of schaaf–Yang syndrome in Russian patients. SHILAP Revista de lepidopterología. 14(1). 42–50.
6.
Danilov, Sergei M., Pavel A. Petukhov, Valery Ilinsky, et al.. (2023). Blood ACE Phenotyping for Personalized Medicine: Revelation of Patients with Conformationally Altered ACE. Biomedicines. 11(2). 534–534. 4 indexed citations
7.
Kenis, Vladimir, et al.. (2023). Principles of the differential diagnosis of achondroplasia and pseudoachondroplasia. Pediatric Traumatology Orthopaedics and Reconstructive Surgery. 11(1). 17–28.
8.
Kenis, Vladimir, Mikhail Skoblov, Р. И. Хусаинова, et al.. (2023). Clinical and Genetic Characteristics of Calvarial Doughnut Lesions with Bone Fragility in Three Families with a Reccurent SGMS2 Gene Variant. International Journal of Molecular Sciences. 24(9). 8021–8021. 4 indexed citations
9.
Kenis, Vladimir, et al.. (2022). Сlinical and genetic characteristics of skeletal cyliopathies – short-rib thoracic dysplasia. Pediatric Traumatology Orthopaedics and Reconstructive Surgery. 10(1). 43–56. 1 indexed citations
10.
Дадали, Е. Л., et al.. (2022). Complex Diagnostics of Non-Specific Intellectual Developmental Disorder. International Journal of Molecular Sciences. 23(14). 7764–7764. 2 indexed citations
11.
Kenis, Vladimir, et al.. (2022). Differential diagnosis of myopathy and multiple epiphysal dysplasia caused by mutations in the <i>COMP</i> gene in children. SHILAP Revista de lepidopterología. 12(2). 37–46. 1 indexed citations
12.
Дадали, Е. Л., et al.. (2021). A Two-Year Clinical Description of a Patient with a Rare Type of Low-GGT Cholestasis Caused by a Novel Variant of USP53. Genes. 12(10). 1618–1618. 6 indexed citations
13.
Дадали, Е. Л., et al.. (2020). Clinical and genetic characteristics of Charcot–Marie–Tooth disease type 4D (type Lom) in Russia. SHILAP Revista de lepidopterología. 10(2). 39–45. 1 indexed citations
14.
Konovalov, Fedor A., et al.. (2018). Clinical and genetic characteristics of new allele variants of the Mowat–Wilson syndrome caused by ZEB2 gene mutations. SHILAP Revista de lepidopterología. 8(3). 28–33.
15.
Дадали, Е. Л., et al.. (2018). Early epileptic encephalopathy associated with SCN2A mutations: clinical and genetic description of eight novel patients. SHILAP Revista de lepidopterología. 8(2). 42–52. 2 indexed citations
16.
Дадали, Е. Л., et al.. (2018). Spinal muscular atrophy with lower limbs phenotype: clinical and genetic description of novel mutation in the DYNC1H1 gene. SHILAP Revista de lepidopterología. 8(2). 59–67.
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Myasnikov, R. P., Е. Л. Дадали, М. С. Харлап, et al.. (2017). CARDIOMYOPATHY IN THE FRIEDREICH ATAXIA: CLINICAL PRESENTATION AND DIAGNOSTICS OF COMPLICATIONS. Russian Journal of Cardiology. 100–106. 2 indexed citations
20.
Дадали, Е. Л., et al.. (2015). Proximal spinal muscular atrophy types I-IV: Specific features of molecular genetic diagnosis. SHILAP Revista de lepidopterología. 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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