Е. Н. Толмачева

421 citations

31 papers · 240 indexed · h-index 9

Co-authors: И. Н. Лебедев А. А. Кашеварова N. A. Skryabin Е. А. Саженова Nikitina Tv Л. П. Назаренко Pamela Magini Claudio Graziano
Topics: Prenatal Screening and Diagnostics (15 papers)Epigenetics and DNA Methylation (10 papers)Genomic variations and chromosomal abnormalities (10 papers)
Cited by: Pediatrics, Perinatology and Child Health Genetics Molecular Biology
Journals: Scientific Reports Gene Human Reproduction
Partner nations: Russia United Kingdom Italy

In The Last Decade

Е. Н. Толмачева

28 papers receiving 235 citations

Peers

Countries citing papers authored by Е. Н. Толмачева

Since Specialization

Citations

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

Fields of papers citing papers by Е. Н. Толмачева

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Е. Н. Толмачева. 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. Н. Толмачева. The network helps show where Е. Н. Толмачева may publish in the future.

Co-authorship network of co-authors of Е. Н. Толмачева

This figure shows the co-authorship network connecting the top 25 collaborators of Е. Н. Толмачева. A scholar is included among the top collaborators of Е. Н. Толмачева 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 Е. Н. Толмачева. Е. Н. Толмачева 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	Identification of differentially methylated genes in first-trimester placentas with trisomy 16 2022 ·Scientific Reports ·Е. Н. Толмачева,(unknown),Nikitina Tv,(unknown),Е. А. Саженова,(unknown),(unknown),(unknown),(unknown),Л. А. Таширева,А. А. Кашеварова,И. Н. Лебедев	2
3	Skewed X-Chromosome Inactivation as a Possible Marker of X-Linked CNV in Women with Pregnancy Loss 2022 ·Cytogenetic and Genome Research ·(unknown),Е. Н. Толмачева,А. А. Кашеварова,Е. А. Саженова,Nikitina Tv,(unknown),(unknown),(unknown),(unknown),(unknown),N. A. Skryabin,В. А. Степанов,И. Н. Лебедев	2
4	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
5	Method of targeted bisulfite massive parallel sequencing of the human LINE-1 retrotransposon promoter 2021 ·MethodsX ·(unknown),(unknown),(unknown),Е. Н. Толмачева,(unknown),(unknown),(unknown),(unknown),И. Н. Лебедев	1
6	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
7	Aneuploidy and DNA Methylation as Mirrored Features of Early Human Embryo Development 2020 ·Genes ·Е. Н. Толмачева,(unknown),И. Н. Лебедев	11
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	Karyotype evaluation of repeated abortions in primary and secondary recurrent pregnancy loss 2020 ·Journal of Assisted Reproduction and Genetics ·Nikitina Tv,Е. А. Саженова,(unknown),Е. Н. Толмачева,(unknown),И. Н. Лебедев	23
10	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
11	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
12	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
13	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
14	Epigenetic effects of trisomy 16 in human placenta 2013 ·Molecular Biology ·Е. Н. Толмачева,А. А. Кашеварова,N. A. Skryabin,И. Н. Лебедев	9
15	Skewed X-chromosome inactivation in human embryos with mosaic trisomy 16 2011 ·Russian Journal of Genetics ·Е. Н. Толмачева,А. А. Кашеварова,(unknown),V. N. Kharkov,И. Н. Лебедев	2
16	[Epigenetic aspects of early lymphogenic metastasis in breast cancer]. 2011 ·PubMed ·(unknown),И. Н. Лебедев,Е. Н. Толмачева,С. В. Вторушин,(unknown),(unknown)	1
17	[Methylation profiling of the cell cycle regulating genes in placenta of human embryos with chromosomal mosaicism]. 2011 ·PubMed ·А. А. Кашеварова,Е. Н. Толмачева,Е. А. Саженова,(unknown),И. Н. Лебедев	0
18	Epigenetic inactivation of the RB1 gene as a factor of genomic instability: A possible contribution to etiology of chromosomal mosaicism during human embryo development 2008 ·Russian Journal of Genetics ·Е. Н. Толмачева,А. А. Кашеварова,(unknown),Е. А. Саженова,И. Н. Лебедев	6
19	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
20	Polymorphism of Trinucleotide Repeats at Loci FRAXA and FRAXE in the Population of Tomsk 2002 ·Russian Journal of Genetics ·Е. Н. Толмачева,(unknown)	2

About Е. Н. Толмачева

Е. Н. Толмачева is a scholar working on Pediatrics, Perinatology and Child Health, Genetics and Molecular Biology, having authored 31 papers that have together received 240 indexed citations. Recurring topics across this work include Prenatal Screening and Diagnostics (15 papers), Epigenetics and DNA Methylation (10 papers) and Genomic variations and chromosomal abnormalities (10 papers). The work is most often cited by research in Pediatrics, Perinatology and Child Health (95 citations), Genetics (117 citations) and Molecular Biology (145 citations). Е. Н. Толмачева has collaborated with scholars based in Russia, United Kingdom and Italy. Frequent co-authors include И. Н. Лебедев, А. А. Кашеварова, N. A. Skryabin, Е. А. Саженова, Nikitina Tv, Л. П. Назаренко, Pamela Magini, Claudio Graziano, G. Cara Romeo and Vaidutis Kučinskas. Their work appears in journals such as Scientific Reports, Gene and Human Reproduction.

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