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About the database ScholarIQanswers from OpenAlex & ORCID
How has S. E. Nagieva's publication output changed over time?
ScholarIQpublication output · 2022–2026
Output declined50% over the shown period — from 2 works in 2022 to 1 in 2026.
2
1
1
1
1
20222023202420252026
What are the most-cited papers on S. E. Nagieva?
ScholarIQmost cited works
Complex Diagnostics of Non-Specific Intellectual Developmental Disorder
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
International Journal of Molecular Sciences. 202212 CitationsOPEN ACCESS
Autosomal dominant intellectual disability associated with the MED13L gene
Olga Levchenko, G. E. Rudenskaya, Т. В. Маркова, Л. А. Бессонова, Andrey V. Marakhonov, S. E. Nagieva, Olga Shchagina, А. В. Лавров
Rossiyskiy Vestnik Perinatologii i Pediatrii (Russian Bulletin of Perinatology and Pediatrics). 20221 CitationsOPEN ACCESS
Unexpected extra exon skipping in the DYSF gene during restoring the reading frame by CRISPR/Cas9
Olga Levchenko, Irina Panchuk, Konstantin Kochergin‐Nikitsky, I. O. Petrova, S. E. Nagieva, Maxim Pilkin, Ivan A. Yakovlev, Svetlana Smirnikhina, R. V Deev, А. В. Лавров
S99347777. 20230 Citations
Cardiomyopathies Caused by Pathogenic Variants in the DMD Gene
S. E. Nagieva, А. В. Лавров, Svetlana Smirnikhina
S147719026. 20240 CitationsOPEN ACCESS
Clinical and genetic heterogeneity of SATB2-associated syndrome
S. E. Nagieva, Наталя Семенова, A. R. Morgul, Ж.Г. Маркова, T. I. Yanova, Nikita Vorobyov, О. С. Грознова, Maria Vorontsova, Н. А. Бодунова
Rossiyskiy Vestnik Perinatologii i Pediatrii (Russian Bulletin of Perinatology and Pediatrics). 20250 CitationsOPEN ACCESS
Related on ScholarIQ
Research Centre for Medical Genetics
Institution
Complex Diagnostics of Non-Specific Intellectual Developmental Disorder
Paper
Autosomal dominant intellectual disability associated with the MED13L gene
Paper
Unexpected extra exon skipping in the DYSF gene during restoring the reading frame by CRISPR/Cas9
Paper
Cardiomyopathies Caused by Pathogenic Variants in the DMD Gene
Paper
Clinical and genetic heterogeneity of SATB2-associated syndrome
Paper