Е. Л. Дадали

3.6k citations

117 papers · 775 · h-index 10

Impact in

Cellular and Molecular Neuroscience top 5%
- Hereditary Neurological Disorders
- Genetic Neurodegenerative Diseases
Neurology top 5%
- Neurological diseases and metabolism
- Botulinum Toxin and Related Neurological Disorders
- Amyotrophic Lateral Sclerosis Research

Papers in

Molecular Biology 53
- Muscle Physiology and Disorders 14
- RNA Research and Splicing 11
- Mitochondrial Function and Pathology 11
Genetics 38
- Connective tissue disorders research 12
- Neurogenetic and Muscular Disorders Research 11

Co-authors: Oleg V. Evgrafov (5 shared papers)A. V. Polyakov (21 shared papers)Irina Mersiyanova (4 shared papers)V. F. Sitnikov (1 shared paper)А. Н. Петрин (1 shared paper)Christine Van Broeckhoven (4 shared papers)Vincent Timmerman (4 shared papers)Olga Shchagina (22 shared papers)
Journals: Genes (11 papers)International Journal of Molecular Sciences (8 papers)Gene (2 papers)Human Mutation (2 papers)Frontiers in Pediatrics (2 papers)
Partner nations: Russia United States United Kingdom

In The Last Decade

Е. Л. Дадали

89 papers receiving 749 citations

Peers

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-authors

The 25 scholars most cited alongside Е. Л. Дадали, linked wherever they have co-authored with each other. Click a name or a connecting line to browse the papers they share.

Border = papers with Е. Л. Дадали Line = papers co-authored together Е. Л. Дадали links everyone, so they are left out of the graph.

All Works

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20 of 20 papers shown

Showing the 20 most-cited of 117 papers — load more, or switch the sort, to bring in the rest.

#	Work
1	A New Variant of Charcot-Marie-Tooth Disease Type 2 Is Probably the Result of a Mutation in the Neurofilament-Light Gene The American Journal of Human Genetics ·Irina Mersiyanova, Alexander V. Perepelov, A. V. Polyakov, V. F. Sitnikov, Е. Л. Дадали, Roman B. Oparin, А. Н. Петрин, Oleg V. Evgrafov	2000	319
2	Screening for mutations in the peripheral myelin genesPMP22,MPZ andCx32 (GJB1) in Russian Charcot-Marie-Tooth neuropathy patients Human Mutation ·Irina Mersiyanova, Sookhrat M. Ismailov, Alexandr V. Polyakov, Е. Л. Дадали, В. П. Федотов, Eva Nelis, Ann L�fgren, Vincent Timmerman, Christine Van Broeckhoven, Oleg V. Evgrafov	2000	67
3	A new locus for autosomal dominant Charcot-Marie-Tooth disease type 2 (CMT2F) maps to chromosome 7q11-q21 European Journal of Human Genetics ·ShoukhratM Ismailov, В. П. Федотов, Е. Л. Дадали, AlexanderV Polyakov, Christine Van Broeckhoven, VladimirI Ivanov, Peter De Jonghe, Vincent Timmerman, Oleg V. Evgrafov	2001	49
4	Genotype Phenotype Correlation and Variability in Microcephaly Associated With Chorioretinopathy or Familial Exudative Vitreoretinopathy Investigative Ophthalmology & Visual Science ·М. Ф. Шурыгина, Joseph M. Simonett, Maria A. Parker, Amanda Mitchell, Florin Grigorian, Jacob Lifton, Aaron Nagiel, А. А. Шпак, Е. Л. Дадали, Irina Mishina, Richard G. Weleber, Paul Yang, Mark E. Pennesi	2020	19
5	Two novel COL6A3 mutations disrupt extracellular matrix formation and lead to myopathy from Ullrich congenital muscular dystrophy and Bethlem myopathy spectrum Gene ·Andrey V. Marakhonov, Vyacheslav Tabakov, Nikolay V. Zernov, Е. Л. Дадали, И. В. Шаркова, Mikhail Skoblov	2018	17
6	HINT1 gene pathogenic variants: the most common cause of recessive hereditary motor and sensory neuropathies in Russian patients Molecular Biology Reports ·Olga Shchagina, (unknown), Aysylu Murtazina, G. N. Rudenskaya, С. С. Никитин, Е. Л. Дадали, A. V. Polyakov	2019	16
7	DES GENE MUTATION IN A FAMILY OF PROBAND WITH MYOFIBRILLARY MYOPATHY AND NON-COMPACTION CARDIOMYOPATHY, RESULTED IN CARDIAC TRANSPLANTATION Russian Journal of Cardiology ·R. P. Myasnikov, Н. В. Щербакова, О. В. Куликова, А. Н. Мешков, М. С. Харлап, А. В. Киселева, Anastasia A. Zharikova, Е. Л. Дадали, N. A. Semenova, S. N. Koretsky, О. V. Blagova, Е. А. Мершина, В. Е. Синицын, О. М. Драпкина, S. А. Boytsov	2017	13
8	Primary microcephaly case from the Karachay-Cherkess Republic poses an additional support for microcephaly and Seckel syndrome spectrum disorders BMC Medical Genomics ·Andrey V. Marakhonov, Fedor A. Konovalov, А. Х. Макаов, Tatyana A. Vasilyeva, В. В. Кадышев, В. А. Галкина, Е. Л. Дадали, Sergey I. Kutsev, Р. А. Зинченко	2018	12
9	Epidemiology of Hereditary Diseases in the Karachay-Cherkess Republic International Journal of Molecular Sciences ·Р. А. Зинченко, А. Х. Макаов, Andrey V. Marakhonov, В. А. Галкина, В. В. Кадышев, Г. И. Ельчинова, Е. Л. Дадали, Л. К. Михайлова, Н.В. Петрова, Н. Е. Петрина, Tatyana A. Vasilyeva, П. Гундорова, A. V. Polyakov, OKSANA YU . ALEXANDROVA, Sergey I. Kutsev, E. K. Ginter	2020	11
10	Genetics and treatment of early infantile epileptic encephalopathies S S Korsakov Journal of Neurology and Psychiatry ·Artem Sharkov, И. В. Шаркова, Е. Д. Белоусова, Е. Л. Дадали	2016	10
11	Ataxia with Oculomotor Apraxia Type 4 with PNKP Common “Portuguese” and Novel Mutations in Two Belarusian Families Journal of Pediatric Genetics ·G. E. Rudenskaya, Andrey V. Marakhonov, Olga Shchagina, Ekaterina Lozier, Е. Л. Дадали, (unknown), Nika Petrova, Fedor A. Konovalov	2019	9
12	The spectrum of CLCN1 gene mutations in patients with nondystrophic Thomsen’s and Becker’s myotonias Russian Journal of Genetics ·Elena A. Ivanova, Е. Л. Дадали, В. П. Федотов, С. В. Курбатов, G. N. Rudenskaya, Т Н Проскокова, A. V. Polyakov	2012	9
13	Mitochondrial DNA maintenance disorders in 102 patients from different parts of Russia: Mutational spectrum and phenotypes Mitochondrion ·Igor Bychkov, Yulia S. Itkis, Polina Tsygankova, Tatiana Krylova, Svetlana Mikhaylova, S. A. Klyushnikov, Н. Л. Печатникова, А. V. Degtyareva, Е. А. Николаева, Yury Seliverstov, С. В. Курбатов, Е. Л. Дадали, G. N. Rudenskaya, С. Н. Иллариошкин, Ekaterina Zakharova	2021	8
14	SMN1 gene point mutations in type I–IV proximal spinal muscular atrophy patients with a single copy of SMN1 Russian Journal of Genetics ·В. В. Забненкова, Е. Л. Дадали, Svetlana Artemieva, И. В. Шаркова, G. E. Rudenskaya, A. V. Polyakov	2015	8
15	Identification of a Novel de Novo Variant in the SYT2 Gene Causing a Rare Type of Distal Hereditary Motor Neuropathy Genes ·О. Л. Миронович, Е. Л. Дадали, S. A. Malmberg, Т. В. Маркова, О. П. Рыжкова, А. В. Поляков	2020	7
16	Genetic and Clinical Spectrum of GNE Myopathy in Russia Genes ·Aysylu Murtazina, С. С. Никитин, G. E. Rudenskaya, И. В. Шаркова, Artem Borovikov, Peter Sparber, Olga Shchagina, А. Л. Чухрова, О. П. Рыжкова, Olga Shatokhina, А. А. Орлова, Vasilisa Udalova, Ilya Kanivets, С. А. Коростелев, A. V. Polyakov, Е. Л. Дадали, Sergey I. Kutsev	2022	7
17	[Clinical-genetic characteristics of limb girdle-muscular dystrophy type 2A]. PubMed ·Е. Л. Дадали, O A Shagina, О. П. Рыжкова, Г. Е. Руденская, В. П. Федотов, А. В. Поляков	2010	7
18	HEREDITARY DISEASES AND SYNDROMES ACCOMPANIED BY FEBRILE CONVULSIONS: CLINICAL AND GENETIC CHARACTERISTICS AND DIAGNOSTIC PROCEDURES DOAJ (DOAJ: Directory of Open Access Journals) ·Е. Л. Дадали, Artem Sharkov, И. В. Шаркова, Ilya Kanivets, Fedor A. Konovalov, И. А. Акимова	2016	6
19	Clinical and genetic characterization of autosomal recessive stickler syndrome caused by novel compound heterozygous mutations in the COL9A3 gene Molecular Genetics & Genomic Medicine ·Т. В. Маркова, Peter Sparber, Artem Borovikov, Tatyana Nagornova, Е. Л. Дадали	2021	6
20	Complex Diagnostics of Non-Specific Intellectual Developmental Disorder International Journal of Molecular Sciences ·Olga Levchenko, Е. Л. Дадали, Л. А. Бессонова, Nina Demina, G. E. Rudenskaya, Galina Matyushchenko, Т. В. Маркова, И. В. Анисимова, Наталя Семенова, Olga Shchagina, О. П. Рыжкова, Р. А. Зинченко, В. А. Галкина, V. Yu. Voinova, S. E. Nagieva, А. В. Лавров	2022	6

About Е. Л. Дадали

Е. Л. Дадали is a scholar working on Molecular Biology, Genetics, Cellular and Molecular Neuroscience, Genetics and Pediatrics, Perinatology and Child Health, having authored 117 papers that have together received 775 indexed citations. Recurring topics across this work include Genetic Neurodegenerative Diseases (25 papers), Hereditary Neurological Disorders (20 papers), Muscle Physiology and Disorders (14 papers), Connective tissue disorders research (12 papers), RNA Research and Splicing (11 papers), Neurogenetic and Muscular Disorders Research (11 papers), Mitochondrial Function and Pathology (11 papers) and Neurological diseases and metabolism (9 papers). The work is most often cited by research in Cellular and Molecular Neuroscience (441 citations), Neurology (181 citations), Neurology (180 citations), Cell Biology (139 citations) and Genetics (70 citations). Е. Л. Дадали has collaborated with scholars based in Russia, United States and United Kingdom. Frequent co-authors include Oleg V. Evgrafov, A. V. Polyakov, Irina Mersiyanova, V. F. Sitnikov, А. Н. Петрин, Christine Van Broeckhoven, Vincent Timmerman, Olga Shchagina, Andrey V. Marakhonov and В. П. Федотов. Their work appears in journals such as Genes, International Journal of Molecular Sciences, Gene, Human Mutation and Frontiers in Pediatrics.

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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Е. Л. Дадали

Impact in

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In The Last Decade

Е. Л. Дадали

Peers

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Fields of papers citing papers by Е. Л. Дадали

All Works

About Е. Л. Дадали

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