Anna Maierhofer

1.2k total citations
11 papers, 264 citations indexed

About

Anna Maierhofer is a scholar working on Molecular Biology, Genetics and Genetics. According to data from OpenAlex, Anna Maierhofer has authored 11 papers receiving a total of 264 indexed citations (citations by other indexed papers that have themselves been cited), including 7 papers in Molecular Biology, 4 papers in Genetics and 3 papers in Genetics. Recurrent topics in Anna Maierhofer's work include Epigenetics and DNA Methylation (6 papers), DNA Repair Mechanisms (4 papers) and Acute Myeloid Leukemia Research (3 papers). Anna Maierhofer is often cited by papers focused on Epigenetics and DNA Methylation (6 papers), DNA Repair Mechanisms (4 papers) and Acute Myeloid Leukemia Research (3 papers). Anna Maierhofer collaborates with scholars based in Germany, United States and Australia. Anna Maierhofer's co-authors include Thomas Haaf, Julia Flunkert, George M. Martin, Steve Horvath, Junko Oshima, Tobias Müller, Marcus Dittrich, Indrajit Nanda, Nady El Hajj and Yvonne Böttcher and has published in prestigious journals such as Blood, PLoS ONE and Scientific Reports.

In The Last Decade

Anna Maierhofer

11 papers receiving 262 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 Maierhofer Germany 9 215 75 46 40 28 11 264
Haojiang Lu Sweden 9 161 0.7× 47 0.6× 43 0.9× 17 0.4× 24 0.9× 15 390
Jon Alderson United Kingdom 4 420 2.0× 67 0.9× 113 2.5× 29 0.7× 38 1.4× 6 534
Mônica M. França Brazil 14 255 1.2× 236 3.1× 50 1.1× 13 0.3× 33 1.2× 28 541
Sara Di Persio Germany 12 332 1.5× 148 2.0× 36 0.8× 12 0.3× 49 1.8× 20 519
Dale McAninch Australia 14 185 0.9× 71 0.9× 81 1.8× 25 0.6× 103 3.7× 22 419
Daniel Petkovich United States 3 198 0.9× 53 0.7× 24 0.5× 55 1.4× 17 0.6× 3 255
Vibha Patil Australia 4 251 1.2× 46 0.6× 36 0.8× 22 0.6× 21 0.8× 6 296
Rinho Kim United States 4 205 1.0× 67 0.9× 17 0.4× 21 0.5× 18 0.6× 5 242
Yexing Xian China 9 184 0.9× 40 0.5× 48 1.0× 10 0.3× 7 0.3× 14 293
Deepika Puri India 7 135 0.6× 27 0.4× 26 0.6× 13 0.3× 10 0.4× 14 189

Countries citing papers authored by Anna Maierhofer

Since Specialization
Citations

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

Fields of papers citing papers by Anna Maierhofer

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Anna Maierhofer

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

All Works

11 of 11 papers shown
1.
Maierhofer, Anna, Nikita Mehta, Ryan A. Chisholm, et al.. (2023). The clinical and genomic landscape of patients with DDX41 variants identified during diagnostic sequencing. Blood Advances. 7(23). 7346–7357. 9 indexed citations
2.
Maierhofer, Anna, Lucy C. Fox, Stephan Hütter, et al.. (2022). Detection of Novel Occult Germline Multi-Exon Deletions in Patients with DDX41 Familial Predisposition to Myeloid Malignancy. Blood. 140(Supplement 1). 8676–8677. 1 indexed citations
3.
Petkov, Stoyan, Anna Maierhofer, Thomas Haaf, et al.. (2021). A piggyBac-based platform for genome editing and clonal rhesus macaque iPSC line derivation. Scientific Reports. 11(1). 15439–15439. 9 indexed citations
4.
Maierhofer, Anna, Constance Baer, Christian Pohlkamp, et al.. (2020). Putative Germline Variants in the Predisposition Genes DDX41, ETV6 and GATA2 investigated in 1,228 Patients with Sporadic AML or MDS. Blood. 136(Supplement 1). 17–18. 1 indexed citations
5.
Maierhofer, Anna, Julia Flunkert, Junko Oshima, et al.. (2019). Epigenetic signatures of Werner syndrome occur early in life and are distinct from normal epigenetic aging processes. Aging Cell. 18(5). e12995–e12995. 26 indexed citations
6.
Flunkert, Julia, Anna Maierhofer, Marcus Dittrich, et al.. (2018). Genetic and epigenetic changes in clonal descendants of irradiated human fibroblasts. Experimental Cell Research. 370(2). 322–332. 20 indexed citations
7.
Jansch, Charline, Katharina Günther, Jonas Waider, et al.. (2018). Generation of a human induced pluripotent stem cell (iPSC) line from a 51-year-old female with attention-deficit/hyperactivity disorder (ADHD) carrying a duplication of SLC2A3. Stem Cell Research. 28. 136–140. 11 indexed citations
8.
Haertle, Larissa, Anna Maierhofer, H Lehnen, et al.. (2017). Hypermethylation of the non-imprinted maternal MEG3 and paternal MEST alleles is highly variable among normal individuals. PLoS ONE. 12(8). e0184030–e0184030. 9 indexed citations
9.
Maierhofer, Anna, Julia Flunkert, Junko Oshima, et al.. (2017). Accelerated epigenetic aging in Werner syndrome. Aging. 9(4). 1143–1152. 110 indexed citations
10.
Maierhofer, Anna, Julia Flunkert, Marcus Dittrich, et al.. (2017). Analysis of global DNA methylation changes in primary human fibroblasts in the early phase following X-ray irradiation. PLoS ONE. 12(5). e0177442–e0177442. 20 indexed citations
11.
Pfeiffer, Susanne, Anna Maierhofer, Yvonne Böttcher, et al.. (2016). Hypoxia-inducible factor 3A gene expression and methylation in adipose tissue is related to adipose tissue dysfunction. Scientific Reports. 6(1). 27969–27969. 48 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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