Anna K. Naumova

3.3k total citations
59 papers, 2.0k citations indexed

About

Anna K. Naumova is a scholar working on Molecular Biology, Genetics and Physiology. According to data from OpenAlex, Anna K. Naumova has authored 59 papers receiving a total of 2.0k indexed citations (citations by other indexed papers that have themselves been cited), including 42 papers in Molecular Biology, 35 papers in Genetics and 8 papers in Physiology. Recurrent topics in Anna K. Naumova's work include Epigenetics and DNA Methylation (23 papers), Genetic Syndromes and Imprinting (20 papers) and Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities (10 papers). Anna K. Naumova is often cited by papers focused on Epigenetics and DNA Methylation (23 papers), Genetic Syndromes and Imprinting (20 papers) and Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities (10 papers). Anna K. Naumova collaborates with scholars based in Canada, United States and Japan. Anna K. Naumova's co-authors include Carmen Sapienza, Kenneth Morgan, Robert M. Plenge, Mark Leppert, Sylvie Croteau, Lynne M. Bird, Brian Hendrich, Charles E. Schwartz, Robin M. Winter and J. Fernando Arena and has published in prestigious journals such as Cell, Nucleic Acids Research and Nature Genetics.

In The Last Decade

Anna K. Naumova

59 papers receiving 2.0k citations

Peers — A (Enhanced Table)

Peers by citation overlap · career bar shows stage (early→late) cites · hero ref

Name h Career Trend Papers Cites
Anna K. Naumova Canada 24 1.3k 952 230 178 172 59 2.0k
Jürgen Horst Germany 27 1.7k 1.3× 1.1k 1.1× 330 1.4× 114 0.6× 282 1.6× 74 2.9k
Hamid Gourabi Iran 30 1.3k 1.0× 674 0.7× 255 1.1× 92 0.5× 126 0.7× 139 2.6k
David Goudie United Kingdom 25 1.2k 0.9× 663 0.7× 112 0.5× 206 1.2× 67 0.4× 69 2.6k
Bruce Bennetts Australia 31 1.3k 1.0× 1.4k 1.5× 246 1.1× 104 0.6× 325 1.9× 101 3.2k
Asaf Hellman Israel 12 1.7k 1.3× 683 0.7× 170 0.7× 107 0.6× 91 0.5× 18 1.9k
W.G. Kearns United States 23 1.0k 0.8× 948 1.0× 663 2.9× 159 0.9× 73 0.4× 97 2.2k
H H Kazazian United States 32 1.7k 1.3× 857 0.9× 273 1.2× 166 0.9× 113 0.7× 64 3.2k
Ann Nordgren Sweden 29 1.1k 0.9× 997 1.0× 391 1.7× 84 0.5× 91 0.5× 134 2.6k
Dusica Babovic‐Vuksanovic United States 27 863 0.7× 540 0.6× 144 0.6× 138 0.8× 288 1.7× 99 2.2k
Vincent Laugel France 26 1.7k 1.3× 475 0.5× 126 0.5× 123 0.7× 114 0.7× 88 2.3k

Countries citing papers authored by Anna K. Naumova

Since Specialization
Citations

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

Fields of papers citing papers by Anna K. Naumova

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Anna K. Naumova. 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 Anna K. Naumova. The network helps show where Anna K. Naumova may publish in the future.

Co-authorship network of co-authors of Anna K. Naumova

This figure shows the co-authorship network connecting the top 25 collaborators of Anna K. Naumova. A scholar is included among the top collaborators of Anna K. Naumova 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 Anna K. Naumova. Anna K. Naumova is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

20 of 20 papers shown
1.
Kimura, Tohru, et al.. (2022). Genetic variation in the Y chromosome and sex-biased DNA methylation in somatic cells in the mouse. Mammalian Genome. 34(1). 44–55. 3 indexed citations
2.
Xiao, Qian, et al.. (2020). Sex Chromosomes and Sex Phenotype Contribute to Biased DNA Methylation in Mouse Liver. Cells. 9(6). 1436–1436. 10 indexed citations
3.
Youssef, Mina, et al.. (2020). Treatment of Allergic Asthma with Fenretinide Formulation (LAU-7b) Downregulates ORMDL Sphingolipid Biosynthesis Regulator 3 (Ormdl3) Expression and Normalizes Ceramide Imbalance. Journal of Pharmacology and Experimental Therapeutics. 373(3). 476–487. 5 indexed citations
4.
Fayer, Shawn, et al.. (2016). Robertsonian translocations modify genomic distribution of γH2AFX and H3.3 in mouse germ cells. Mammalian Genome. 27(5-6). 225–236. 3 indexed citations
5.
Naumova, Anna K. & Teruko Taketo. (2016). Epigenetics in Human Reproduction and Development. WORLD SCIENTIFIC eBooks. 3 indexed citations
6.
Naumova, Anna K., et al.. (2016). The Problems of project management software implementation in construction corporations. SHILAP Revista de lepidopterología. 73. 7016–7016. 7 indexed citations
7.
Murai, Junko, Ilaria Dalla Rosa, Thomas S. Dexheimer, et al.. (2013). TDP1 repairs nuclear and mitochondrial DNA damage induced by chain-terminating anticancer and antiviral nucleoside analogs. Nucleic Acids Research. 41(16). 7793–7803. 86 indexed citations
8.
Naumova, Anna K., Abeer Al Tuwaijri, Andréanne Morin, et al.. (2013). Sex- and age-dependent DNA methylation at the 17q12-q21 locus associated with childhood asthma. Human Genetics. 132(7). 811–822. 56 indexed citations
9.
Berlivet, Soizik, Sanny Moussette, Manon Ouimet, et al.. (2012). Interaction between genetic and epigenetic variation defines gene expression patterns at the asthma-associated locus 17q12-q21 in lymphoblastoid cell lines. Human Genetics. 131(7). 1161–1171. 45 indexed citations
10.
Saferali, Aabida, Elin Grundberg, Soizik Berlivet, et al.. (2010). Cell culture-induced aberrant methylation of the imprinted IG DMR in human lymphoblastoid cell lines. Epigenetics. 5(1). 50–60. 24 indexed citations
11.
Labialle, Stéphane, Aude Villemain, Jennifer V. Schmidt, et al.. (2007). Coordinated diurnal regulation of genes from the Dlk1–Dio3 imprinted domain: implications for regulation of clusters of non-paralogous genes. Human Molecular Genetics. 17(1). 15–26. 19 indexed citations
12.
Mogil, Jeffrey S., Jennifer Ritchie, Susana G. Sotocinal, et al.. (2006). Screening for pain phenotypes: Analysis of three congenic mouse strains on a battery of nine nociceptive assays. Pain. 126(1). 24–34. 56 indexed citations
13.
Pastinen, Tomi, Robert Sladek, Scott Gurd, et al.. (2004). A survey of genetic and epigenetic variation affecting human gene expression. Physiological Genomics. 16(2). 184–193. 209 indexed citations
14.
Croteau, Sylvie, Moises Freitas‐Andrade, Fleur Huang, et al.. (2002). Inheritance patterns of maternal alleles in imprinted regions of the mouse genome at different stages of development. Mammalian Genome. 13(1). 24–29. 16 indexed citations
15.
CRUMLEY, M. JOYCE, Anna K. Naumova, Denis Morin, et al.. (2000). Report of 33 Novel AVPR2 Mutations and Analysis of 117 Families with X-Linked Nephrogenic Diabetes Insipidus. Journal of the American Society of Nephrology. 11(6). 1044–1054. 123 indexed citations
16.
Song, Young‐Han, Anna K. Naumova, Stephen A. Liebhaber, & Nancy E. Cooke. (1999). Physical and Meiotic Mapping of the Region of Human Chromosome 4q11–q13 Encompassing the Vitamin D Binding Protein DBP/Gc-Globulin and Albumin Multigene Cluster. Genome Research. 9(6). 581–587. 40 indexed citations
17.
Ørstavik, Karen Helene, Ragnhild Ørstavik, Anna K. Naumova, et al.. (1998). X Chromosome Inactivation in Carriers of Barth Syndrome. The American Journal of Human Genetics. 63(5). 1457–1463. 58 indexed citations
18.
Naumova, Anna K., Lynne M. Bird, Mark A. Smith, et al.. (1998). Genetic mapping of X-linked loci involved in skewing of X chromosome inactivation in the human. European Journal of Human Genetics. 6(6). 552–562. 60 indexed citations
19.
Naumova, Anna K., Robert M. Plenge, Lynne M. Bird, et al.. (1996). Heritability of X chromosome--inactivation phenotype in a large family.. PubMed. 58(6). 1111–9. 148 indexed citations
20.
Naumova, Anna K., Lynne M. Bird, M. E. N. Fonseca, et al.. (1995). Transmission‐ratio distortion of X chromosomes among male offspring of females with skewed X‐inactivation. Developmental Genetics. 17(3). 198–205. 22 indexed citations

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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