Hanna Davies

2.1k total citations
13 papers, 856 citations indexed

About

Hanna Davies is a scholar working on Molecular Biology, Genetics and Immunology. According to data from OpenAlex, Hanna Davies has authored 13 papers receiving a total of 856 indexed citations (citations by other indexed papers that have themselves been cited), including 6 papers in Molecular Biology, 6 papers in Genetics and 3 papers in Immunology. Recurrent topics in Hanna Davies's work include Genomic variations and chromosomal abnormalities (4 papers), Epigenetics and DNA Methylation (3 papers) and Immunotherapy and Immune Responses (2 papers). Hanna Davies is often cited by papers focused on Genomic variations and chromosomal abnormalities (4 papers), Epigenetics and DNA Methylation (3 papers) and Immunotherapy and Immune Responses (2 papers). Hanna Davies collaborates with scholars based in Sweden, Poland and United States. Hanna Davies's co-authors include Jan P. Dumanski, Lars A. Forsberg, Vilmantas Giedraitis, Chiara Rasi, Cecilia M. Lindgren, Lars Lind, Lars Lannfelt, Erik Ingelsson, Eva Tiensuu Janson and Martin Ingelsson and has published in prestigious journals such as Science, Nature Genetics and Scientific Reports.

In The Last Decade

Hanna Davies

12 papers receiving 845 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Hanna Davies Sweden 8 447 348 148 106 99 13 856
Aurélien A. Sérandour France 13 945 2.1× 271 0.8× 135 0.9× 145 1.4× 77 0.8× 22 1.2k
Andrea Piunti United States 21 1.7k 3.9× 212 0.6× 278 1.9× 174 1.6× 90 0.9× 34 2.0k
Emilie Lalonde Canada 17 550 1.2× 329 0.9× 246 1.7× 100 0.9× 66 0.7× 30 1.0k
Bénédicte Delaval France 19 896 2.0× 409 1.2× 74 0.5× 168 1.6× 28 0.3× 27 1.2k
Hogune Im United States 13 776 1.7× 85 0.2× 61 0.4× 56 0.5× 58 0.6× 32 890
Beatriz Aranda-Orgillés United States 13 1.1k 2.5× 117 0.3× 147 1.0× 260 2.5× 142 1.4× 17 1.3k
Ana-Teresa Maia United Kingdom 15 703 1.6× 276 0.8× 235 1.6× 174 1.6× 76 0.8× 26 1.3k
Renée Beekman Netherlands 12 583 1.3× 190 0.5× 193 1.3× 156 1.5× 253 2.6× 20 1.1k
Ruth Barber United Kingdom 13 496 1.1× 157 0.5× 161 1.1× 154 1.5× 497 5.0× 20 1.3k

Countries citing papers authored by Hanna Davies

Since Specialization
Citations

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

Fields of papers citing papers by Hanna Davies

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Hanna Davies

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

All Works

13 of 13 papers shown
1.
Rychlicka-Buniowska, Edyta, Daniil Sarkisyan, Bożena Bruhn‐Olszewska, et al.. (2025). Loss of Y chromosome in Alzheimer’s patients co-occurs with somatic mutations beyond CHIP drivers. Life Science Alliance. 9(2). e202503533–e202503533.
2.
Jąkalski, Marcin, Bożena Bruhn‐Olszewska, Edyta Rychlicka-Buniowska, et al.. (2025). DNA methylation patterns contribute to changes of cellular differentiation pathways in leukocytes with LOY from patients with Alzheimer´s disease. Cellular and Molecular Life Sciences. 82(1). 93–93. 1 indexed citations
3.
Mattisson, Jonas, Jonatan Halvardson, Hanna Davies, et al.. (2024). Loss of chromosome Y in regulatory T cells. BMC Genomics. 25(1). 243–243. 15 indexed citations
4.
Chojnowska, Katarzyna, Michał Bieńkowski, Anna Kostecka, et al.. (2023). Size matters: the impact of nucleus size on results from spatial transcriptomics. Journal of Translational Medicine. 21(1). 270–270. 6 indexed citations
5.
Mattisson, Jonas, Marcus Danielsson, Maria Hammond, et al.. (2021). Leukocytes with chromosome Y loss have reduced abundance of the cell surface immunoprotein CD99. Scientific Reports. 11(1). 15160–15160. 26 indexed citations
6.
Rydzanicz, Małgorzata, Paweł Olszewski, Darek Kedra, et al.. (2020). Variable degree of mosaicism for tetrasomy 18p in phenotypically discordant monozygotic twins—Diagnostic implications. Molecular Genetics & Genomic Medicine. 9(1). e1526–e1526. 5 indexed citations
7.
Danielsson, Marcus, Jonatan Halvardson, Hanna Davies, et al.. (2019). Longitudinal changes in the frequency of mosaic chromosome Y loss in peripheral blood cells of aging men varies profoundly between individuals. European Journal of Human Genetics. 28(3). 349–357. 46 indexed citations
8.
Dumanski, Jan P., Chiara Rasi, Peyman Björklund, et al.. (2017). A MUTYH germline mutation is associated with small intestinal neuroendocrine tumors. Endocrine Related Cancer. 24(8). 427–443. 49 indexed citations
9.
Dumanski, Jan P., Jean‐Charles Lambert, Chiara Rasi, et al.. (2016). Mosaic Loss of Chromosome Y in Blood Is Associated with Alzheimer Disease. The American Journal of Human Genetics. 98(6). 1208–1219. 158 indexed citations
10.
Pekár, Gyula, Hanna Davies, Lars A. Forsberg, et al.. (2015). Biobanking multifocal breast carcinomas: sample adequacy with regard to histology andDNAcontent. Histopathology. 68(3). 411–421. 2 indexed citations
11.
Dumanski, Jan P., Chiara Rasi, Mikael Lönn, et al.. (2014). Smoking is associated with mosaic loss of chromosome Y. Science. 347(6217). 81–83. 154 indexed citations
12.
Forsberg, Lars A., Chiara Rasi, Hanna Davies, et al.. (2014). Mosaic loss of chromosome Y in peripheral blood is associated with shorter survival and higher risk of cancer. Nature Genetics. 46(6). 624–628. 287 indexed citations
13.
Eggeling, Ferdinand von, Hanna Davies, Lee Lomas, et al.. (2000). Tissue-Specific Microdissection Coupled with ProteinChip ® Array Technologies: Applications in Cancer Research. BioTechniques. 29(5). 1066–1070. 107 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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