Freja K. Ekman

580 total citations
7 papers, 402 citations indexed

About

Freja K. Ekman is a scholar working on Molecular Biology, Cellular and Molecular Neuroscience and Oncology. According to data from OpenAlex, Freja K. Ekman has authored 7 papers receiving a total of 402 indexed citations (citations by other indexed papers that have themselves been cited), including 7 papers in Molecular Biology, 2 papers in Cellular and Molecular Neuroscience and 2 papers in Oncology. Recurrent topics in Freja K. Ekman's work include CRISPR and Genetic Engineering (5 papers), RNA Interference and Gene Delivery (2 papers) and Genetic Neurodegenerative Diseases (2 papers). Freja K. Ekman is often cited by papers focused on CRISPR and Genetic Engineering (5 papers), RNA Interference and Gene Delivery (2 papers) and Genetic Neurodegenerative Diseases (2 papers). Freja K. Ekman collaborates with scholars based in United States, Portugal and India. Freja K. Ekman's co-authors include Thomas Gaj, David V. Schaffer, David S. Ojala, Prajit Limsirichai, Leah C. Byrne, Maroof M. Adil, Paola A. Lopez, Gonçalo Rodrigues, Jennifer A. Doudna and Brett T. Staahl and has published in prestigious journals such as Nucleic Acids Research, Nature Communications and Blood.

In The Last Decade

Freja K. Ekman

7 papers receiving 397 citations

Peers

Freja K. Ekman

MB

GENET

CMN

NEURO

GENET

M. Alejandra Zeballos C. United States

Ryan J. Marina United States

Aslam Abbasi Akhtar United States

Julian Halmai United States

Raygene Martier Netherlands

Jana Miniarikova Netherlands

Kana Hosoki Japan

Lorelei Stoica United States

Ejona Rusha Germany

Jonna Saarimäki‐Vire Finland

M. Alejandra Zeballos C. United States

Freja K. Ekman

315 ×0.9

MB

105 ×0.8

GENET

39 ×0.5

CMN

55 ×0.9

NEURO

54 ×1.1

GENET

Citations per year, relative to Freja K. Ekman Freja K. Ekman (= 1×) peers M. Alejandra Zeballos C.

Countries citing papers authored by Freja K. Ekman

Since Specialization

Citations

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

Fields of papers citing papers by Freja K. Ekman

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Freja K. Ekman

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

All Works

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7 of 7 papers shown

1.

Ekman, Freja K., Sridhar Selvaraj, Eric Soupène, et al.. (2025). Engineering synthetic signaling receptors to enable erythropoietin-free erythropoiesis. Nature Communications. 16(1). 1140–1140. 1 indexed citations

2.

Ekman, Freja K., Sridhar Selvaraj, Jason Gotlib, M. Kyle Cromer, & Matthew H. Porteus. (2024). Targeting the JAK2-V617F Mutation in Polycythemia Vera Using CRISPR/AAV6 Genome Editing. Blood. 144(Supplement 1). 4524–4524. 2 indexed citations

3.

Selvaraj, Sridhar, Sébastien Viel, Sriram Vaidyanathan, et al.. (2023). High-efficiency transgene integration by homology-directed repair in human primary cells using DNA-PKcs inhibition. Nature Biotechnology. 42(5). 731–744. 40 indexed citations

4.

Ekman, Freja K., David S. Ojala, Maroof M. Adil, et al.. (2019). CRISPR-Cas9-Mediated Genome Editing Increases Lifespan and Improves Motor Deficits in a Huntington’s Disease Mouse Model. Molecular Therapy — Nucleic Acids. 17. 829–839. 106 indexed citations

5.

Adil, Maroof M., Thomas Gaj, Antara Rao, et al.. (2018). hPSC-Derived Striatal Cells Generated Using a Scalable 3D Hydrogel Promote Recovery in a Huntington Disease Mouse Model. Stem Cell Reports. 10(5). 1481–1491. 39 indexed citations

6.

Gaj, Thomas, David S. Ojala, Freja K. Ekman, et al.. (2017). In vivo genome editing improves motor function and extends survival in a mouse model of ALS. Science Advances. 3(12). eaar3952–eaar3952. 142 indexed citations

7.

Gaj, Thomas, Brett T. Staahl, Gonçalo Rodrigues, et al.. (2017). Targeted gene knock-in by homology-directed genome editing using Cas9 ribonucleoprotein and AAV donor delivery. Nucleic Acids Research. 45(11). e98–e98. 72 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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