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S. E. Nagieva

ResearcherPublications, citations & collaboration network

S. E. Nagieva is a researcher indexed in ScholarIQ from OpenAlex & ORCID.

How many works does S. E. Nagieva have?

ScholarIQindexed works

S. E. Nagieva has 6 works in the ScholarIQ index. The count is the OpenAlex total, not the number of papers listed on this page.

How many citations does S. E. Nagieva have?

ScholarIQcitation count

S. E. Nagieva has 13 citations in the OpenAlex counts ScholarIQ stores.

What is the h-index of S. E. Nagieva?

ScholarIQh-index

S. E. Nagieva has an h-index of 1 in OpenAlex.

What is the i10-index of S. E. Nagieva?

ScholarIQi10-index

S. E. Nagieva has an i10-index of 1 in OpenAlex.

What is the ORCID of S. E. Nagieva?

ScholarIQorcid

The ORCID for S. E. Nagieva is on the source record.

What is the OpenAlex record for S. E. Nagieva?

ScholarIQopenalex

The OpenAlex for S. E. Nagieva is on the source record.

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
Biosystems. 20230 Citations
Cardiomyopathies Caused by Pathogenic Variants in the DMD Gene
S. E. Nagieva, А. В. Лавров, Svetlana Smirnikhina
Kardiologiia. 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

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