Daria Grafodatskaya

3.5k citations
24 papers · 1.9k indexed · 1 hit paper · h-index 16
Topics
Epigenetics and DNA Methylation (10 papers)Genetic Syndromes and Imprinting (7 papers)Genetics and Neurodevelopmental Disorders (6 papers)

In The Last Decade

Daria Grafodatskaya

24 papers receiving 1.9k citations

Hit Papers

Discovery of cross-reactive probes and polymorphic CpGs i...20132026201720212013250500750

Peers

Daria Grafodatskaya
Comparison fields: 5 of 99
  • Molecular Biology 1.5k
  • Genetics 717
  • Pediatrics, Perinatology and Child Health 371
  • Cognitive Neuroscience 192
  • Cancer Research 169
Replace Lavinia Gordon with:
Lavinia Gordon Australia
Manuela Volta Italy
Hans T. Björnsson United States
Sanaa Choufani Canada
H. Eka D. Suchiman Netherlands
Anna Maria Di Blasio Italy
Arthur S. Aylsworth United States
Nady El Hajj Germany
Mordechai Shohat Israel
Tiffany Morris United Kingdom
Daria Grafodatskaya relative to Lavinia Gordon Australia Lavinia Gordon's profile →
Citations per field
00.5×1.5×2.4×
Lavinia Gordon · 1×
Citations per year

Countries citing papers authored by Daria Grafodatskaya

Since Specialization
Citations

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

Fields of papers citing papers by Daria Grafodatskaya

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Daria Grafodatskaya

This figure shows the co-authorship network connecting the top 25 collaborators of Daria Grafodatskaya. A scholar is included among the top collaborators of Daria Grafodatskaya 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 Daria Grafodatskaya. Daria Grafodatskaya 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
#WorkIndexed citations
1 3
2 3
3 7
4 24
5 2
6 36
7 18
8 68
9
Discovery of cross-reactive probes and polymorphic CpGs in the Illumina Infinium HumanMethylation450 microarraybreakdown →
983
10
A specific DNA methylation signature associated with NSD1+/- mutations in Sotos syndrome reveals a significant genome-wide loss of DNA methylation (DNAm) targeting CGs in regulatory regions of key developmental genes
1
11 21
12 46
13 89
14 17
15 16
16 61
17 208
18 159
19 83
20 20

About Daria Grafodatskaya

Daria Grafodatskaya is a scholar working on Genetics, Cancer Research and Molecular Biology, having authored 24 papers that have together received 1.9k indexed citations. Recurring topics across this work include Epigenetics and DNA Methylation (10 papers), Genetic Syndromes and Imprinting (7 papers) and Genetics and Neurodevelopmental Disorders (6 papers). The work is most often cited by research in Genetics (717 citations), Molecular Biology (1.5k citations) and Pediatrics, Perinatology and Child Health (371 citations). Daria Grafodatskaya has collaborated with scholars based in Canada, United States and United Kingdom. Frequent co-authors include Rosanna Weksberg, Sanaa Choufani, Darci T. Butcher, Y. Ann Chen, Mathieu Lemire, Steven Gallinger, Brent W. Zanke, Thomas J. Hudson, Brian Hon‐Yin Chung and Péter Szatmári. Their work appears in journals such as PLoS ONE, Genome Research and Human Molecular Genetics.

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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