N. A. Skryabin

549 total citations
46 papers, 371 citations indexed

About

N. A. Skryabin is a scholar working on Genetics, Molecular Biology and Pediatrics, Perinatology and Child Health. According to data from OpenAlex, N. A. Skryabin has authored 46 papers receiving a total of 371 indexed citations (citations by other indexed papers that have themselves been cited), including 29 papers in Genetics, 21 papers in Molecular Biology and 20 papers in Pediatrics, Perinatology and Child Health. Recurrent topics in N. A. Skryabin's work include Prenatal Screening and Diagnostics (20 papers), Genomic variations and chromosomal abnormalities (14 papers) and Genetics and Neurodevelopmental Disorders (10 papers). N. A. Skryabin is often cited by papers focused on Prenatal Screening and Diagnostics (20 papers), Genomic variations and chromosomal abnormalities (14 papers) and Genetics and Neurodevelopmental Disorders (10 papers). N. A. Skryabin collaborates with scholars based in Russia, United Kingdom and Italy. N. A. Skryabin's co-authors include И. Н. Лебедев, А. А. Кашеварова, Е. Н. Толмачева, Л. П. Назаренко, Е. А. Саженова, Nikitina Tv, Pamela Magini, Claudio Graziano, G. Cara Romeo and Evgeny V. Denisov and has published in prestigious journals such as SHILAP Revista de lepidopterología, Scientific Reports and International Journal of Molecular Sciences.

In The Last Decade

N. A. Skryabin

40 papers receiving 359 citations

Peers

Countries citing papers authored by N. A. Skryabin

Since Specialization

Citations

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

Fields of papers citing papers by N. A. Skryabin

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by N. A. Skryabin. 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 N. A. Skryabin. The network helps show where N. A. Skryabin may publish in the future.

Co-authorship network of co-authors of N. A. Skryabin

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

#	Work	Indexed citations
1	Prevalence of CNVs on the X chromosome in patients with neurodevelopmental disorders 2025 ·Molecular Cytogenetics ·Е. Н. Толмачева, А. А. Кашеварова, (unknown), (unknown), (unknown), Л. П. Назаренко, (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), N. A. Skryabin, И. Н. Лебедев	0
2	Embryoid bodies as a model system for exploring early human embryonic development 2025 ·Journal of Assisted Reproduction and Genetics ·(unknown), Evgeny V. Denisov, И. Н. Лебедев, N. A. Skryabin	1
3	Variability of the mitochondrial genome in young Yakut patients with breast cancer 2024 ·SHILAP Revista de lepidopterología ·(unknown), (unknown), М. В. Голубенко, (unknown), (unknown), Polina Gervas, N. A. Skryabin	1
4	An Unusual Presentation of Novel Missense Variant in PAX6 Gene: NM_000280.4:c.341A>G, p.(Asn114Ser) 2023 ·Current Issues in Molecular Biology ·Tatyana A. Vasilyeva, (unknown), (unknown), Andrey V. Marakhonov, Nikolai S. Prokhorov, (unknown), N. A. Skryabin, Sergey I. Kutsev, Р. А. Зинченко	2
5	Analysis of mutations spectrum in the ATP7B gene in patients with Wilson disease using massively parallel sequencing 2022 ·Russian Clinical Laboratory Diagnostics ·(unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), N. A. Skryabin	1
6	NLRP7 variants in spontaneous abortions with multilocus imprinting disturbances from women with recurrent pregnancy loss 2021 ·Journal of Assisted Reproduction and Genetics ·Е. А. Саженова, Nikitina Tv, (unknown), (unknown), (unknown), (unknown), (unknown), N. A. Skryabin, (unknown), (unknown), В. А. Степанов, И. Н. Лебедев	3
7	Differential DNA Methylation of the IMMP2L Gene in Families with Maternally Inherited 7q31.1 Microdeletions is Associated with Intellectual Disability and Developmental Delay 2021 ·Cytogenetic and Genome Research ·(unknown), N. A. Skryabin, А. А. Кашеварова, Е. Н. Толмачева, (unknown), (unknown), (unknown), (unknown), Veniamin Fishman, (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), Л. П. Назаренко, И. Н. Лебедев	9
8	Delineation of Clinical Manifestations of the Inherited Xq24 Microdeletion Segregating with sXCI in Mothers: Two Novel Cases with Distinct Phenotypes Ranging from UBE2A Deficiency Syndrome to Recurrent Pregnancy Loss 2020 ·Cytogenetic and Genome Research ·Е. Н. Толмачева, А. А. Кашеварова, Л. П. Назаренко, (unknown), N. A. Skryabin, (unknown), Nikitina Tv, Е. А. Саженова, (unknown), (unknown), (unknown), Victor Tarabykin, И. Н. Лебедев	11
9	46,XY,r(8)/45,XY,−8 Mosaicism as a Possible Mechanism of the Imprinted Birk-Barel Syndrome: A Case Study 2020 ·Genes ·А. А. Кашеварова, Nikitina Tv, (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), N. A. Skryabin, Л. П. Назаренко, И. Н. Лебедев	3
10	Runs of homozygosity in spontaneous abortions from families with recurrent pregnancy loss 2019 ·Vavilov Journal of Genetics and Breeding ·N. A. Skryabin, (unknown), Nikitina Tv, (unknown), (unknown), (unknown), (unknown), А. А. Кашеварова, И. Н. Лебедев	0
11	Generation of four iPSC lines from two siblings with a microdeletion at the CNTN6 gene and intellectual disability 2019 ·Stem Cell Research ·(unknown), Inna E. Pristyazhnyuk, (unknown), N. M. Matveeva, Nikitina Tv, (unknown), N. A. Skryabin, А. А. Кашеварова, (unknown), Л. П. Назаренко, И. Н. Лебедев, O. L. Serov	2
12	Karyotype of the blastocoel fluid demonstrates low concordance with both trophectoderm and inner cell mass 2018 ·Fertility and Sterility ·Olga Tšuiko, (unknown), Tatjana Jatsenko, N. A. Skryabin, (unknown), (unknown), (unknown), (unknown), (unknown), Andres Salumets, Ants Kurg, И. Н. Лебедев	48
13	Compound phenotype in a girl with r(22), concomitant microdeletion 22q13.32-q13.33 and mosaic monosomy 22 2018 ·Molecular Cytogenetics ·А. А. Кашеварова, (unknown), (unknown), Olga Plotnikova, N. A. Skryabin, Nikitina Tv, (unknown), (unknown), (unknown), Е. Н. Толмачева, (unknown), (unknown), Л. П. Назаренко, И. Н. Лебедев	12
14	Induced pluripotent stem cell line, ICAGi001-A, derived from human skin fibroblasts of a patient with 2p25.3 deletion and 2p25.3-p23.3 inverted duplication 2018 ·Stem Cell Research ·(unknown), Inna E. Pristyazhnyuk, Nikitina Tv, (unknown), (unknown), N. A. Skryabin, А. А. Кашеварова, (unknown), (unknown), (unknown), Л. П. Назаренко, (unknown), (unknown), И. Н. Лебедев, O. L. Serov	2
15	Genomic structural variations for cardiovascular and metabolic comorbidity 2017 ·Scientific Reports ·М. С. Назаренко, (unknown), И. Н. Лебедев, N. A. Skryabin, (unknown), М. В. Голубенко, (unknown), (unknown), О. Л. Барбараш, В. П. Пузырев	27
16	Comparative Cytogenetic Analysis of Spontaneous Abortions in Recurrent and Sporadic Pregnancy Losses 2016 ·PubMed ·Nikitina Tv, Е. А. Саженова, Е. Н. Толмачева, (unknown), А. А. Кашеварова, N. A. Skryabin, (unknown), (unknown), (unknown), И. Н. Лебедев	26
17	A de novo microtriplication at 4q21.21‐q21.22 in a patient with a vascular malignant hemangioma, elongated sigmoid colon, developmental delay, and absence of speech 2016 ·American Journal of Medical Genetics Part A ·И. Н. Лебедев, Л. П. Назаренко, N. A. Skryabin, (unknown), А. А. Кашеварова	5
18	Single gene microdeletions and microduplication of 3p26.3 in three unrelated families: CNTN6 as a new candidate gene for intellectual disability 2014 ·Molecular Cytogenetics ·А. А. Кашеварова, Л. П. Назаренко, (unknown), N. A. Skryabin, (unknown), (unknown), Е. Н. Толмачева, (unknown), Pamela Magini, Claudio Graziano, G. Cara Romeo, Shelagh Joss, Zeynep Tümer, И. Н. Лебедев	43
19	Array-based comparative genomic hybridization (ARRAY-CGH) in analysis of chromosomalaberrations and CNV in blighted ovum pregnancies 2013 ·Journal of obstetrics and women s diseases ·И. Н. Лебедев, А. А. Кашеварова, N. A. Skryabin, (unknown), (unknown), (unknown), (unknown), (unknown), (unknown)	2
20	Array CGH analysis of a cohort of Russian patients with intellectual disability 2013 ·Gene ·А. А. Кашеварова, Л. П. Назаренко, N. A. Skryabin, (unknown), (unknown), Е. Н. Толмачева, Е. А. Саженова, Pamela Magini, Claudio Graziano, G. Cara Romeo, Vaidutis Kučinskas, И. Н. Лебедев	33

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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