А. А. Кашеварова

531 citations

51 papers · 287 indexed · h-index 10

Co-authors: И. Н. Лебедев Е. Н. Толмачева N. A. Skryabin Е. А. Саженова Л. П. Назаренко Nikitina Tv Pamela Magini Claudio Graziano
Topics: Genomic variations and chromosomal abnormalities (22 papers)Prenatal Screening and Diagnostics (21 papers)Pluripotent Stem Cells Research (12 papers)
Cited by: Genetics Pediatrics, Perinatology and Child Health Molecular Biology
Journals: Scientific Reports Gene Human Reproduction
Partner nations: Russia United Kingdom Italy

In The Last Decade

А. А. Кашеварова

41 papers receiving 280 citations

Peers

Countries citing papers authored by А. А. Кашеварова

Since Specialization

Citations

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

Fields of papers citing papers by А. А. Кашеварова

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by А. А. Кашеварова. 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 А. А. Кашеварова. The network helps show where А. А. Кашеварова may publish in the future.

Co-authorship network of co-authors of А. А. Кашеварова

This figure shows the co-authorship network connecting the top 25 collaborators of А. А. Кашеварова. A scholar is included among the top collaborators of А. А. Кашеварова 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 А. А. Кашеварова. А. А. Кашеварова 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	Copy number variations in spontaneous abortions: a meta-analysis 2025 ·Journal of Assisted Reproduction and Genetics ·(unknown),А. А. Кашеварова,И. Н. Лебедев	0
3	Design of iPSC-based cell model to study the functions of the <i>UBE2A</i> gene 2024 ·Genes and Cells ·(unknown),(unknown),(unknown),(unknown),(unknown),(unknown),(unknown),(unknown),(unknown),А. А. Кашеварова,(unknown),Elena Zerkalenkova,Maria A. Lagarkova,И. Н. Лебедев,Alexandra N. Bogomazova	0
4	Guidelines of the Russian Society of Medical Geneticists for Chromosomal Microarray Analysis 2023 ·Nauchno-prakticheskii zhurnal «Medicinskaia genetika» ·(unknown),(unknown),(unknown),Olga Malysheva,(unknown),(unknown),(unknown),(unknown),А. А. Кашеварова	2
5	Generation of Induced Pluripotent Stem Cell Line iTAF15Xsk4 from Fibroblasts of a Patient with Microdeletion at Xq24 2023 ·Russian Journal of Developmental Biology ·Inna E. Pristyazhnyuk,(unknown),Nikitina Tv,А. А. Кашеварова,(unknown),(unknown),(unknown),Л. П. Назаренко,И. Н. Лебедев,(unknown)	0
6	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
7	Prenatal Diagnosis of Small Supernumerary Marker Chromosome 10 by Array-Based Comparative Genomic Hybridization and Microdissected Chromosome Sequencing 2021 ·Biomedicines ·И. Н. Лебедев,Т. В. Карамышева,Eugeny A. Elisaphenko,Alex Makunin,(unknown),(unknown),(unknown),(unknown),(unknown),(unknown),(unknown),А. А. Кашеварова,Л. П. Назаренко,Н. Б. Рубцов	6
8	LINE-1 retrotransposon methylation in chorionic villi of first trimester miscarriages with aneuploidy 2020 ·Journal of Assisted Reproduction and Genetics ·(unknown),Е. Н. Толмачева,(unknown),(unknown),(unknown),(unknown),(unknown),(unknown),Е. А. Саженова,Nikitina Tv,А. А. Кашеварова,И. Н. Лебедев	4
9	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
10	Establishment of an induced pluripotent stem cell line (ICGi025-A) from fibroblasts of a patient with 46,XY,r(8)/45,XY,–8 mosaicism 2020 ·Stem Cell Research ·(unknown),Nikitina Tv,(unknown),(unknown),А. А. Кашеварова,(unknown),(unknown),(unknown),(unknown),(unknown),Л. П. Назаренко,И. Н. Лебедев,(unknown)	3
11	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
12	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
13	Induced pluripotent stem cell line, IMGTi003-A, derived from skin fibroblasts of an intellectually disabled patient with ring chromosome 13 2018 ·Stem Cell Research ·Nikitina Tv,(unknown),А. А. Кашеварова,(unknown),(unknown),(unknown),(unknown),Inna E. Pristyazhnyuk,(unknown),O. L. Serov,И. Н. Лебедев	5
14	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
15	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
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	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
19	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
20	Session 05: Embryology 2007 ·Human Reproduction ·Е. Н. Толмачева,А. А. Кашеварова,И. Н. Лебедев,Е. А. Саженова,(unknown),(unknown),(unknown),(unknown),(unknown),(unknown),Kazuhiko Yumoto,Yutaka Ueno,Sarah Jane Flaherty,Yasuyuki Mio,(unknown),(unknown),(unknown)	3

About А. А. Кашеварова

А. А. Кашеварова is a scholar working on Genetics, Pediatrics, Perinatology and Child Health and Molecular Biology, having authored 51 papers that have together received 287 indexed citations. Recurring topics across this work include Genomic variations and chromosomal abnormalities (22 papers), Prenatal Screening and Diagnostics (21 papers) and Pluripotent Stem Cells Research (12 papers). The work is most often cited by research in Genetics (162 citations), Pediatrics, Perinatology and Child Health (108 citations) and Molecular Biology (180 citations). А. А. Кашеварова has collaborated with scholars based in Russia, United Kingdom and Italy. Frequent co-authors include И. Н. Лебедев, Е. Н. Толмачева, N. A. Skryabin, Е. А. Саженова, Л. П. Назаренко, Nikitina Tv, Pamela Magini, Claudio Graziano, G. Cara Romeo and Vaidutis Kučinskas. Their work appears in journals such as Scientific Reports, Gene and Human Reproduction.

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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