Jesper Eisfeldt

2.0k total citations
50 papers, 349 citations indexed

About

Jesper Eisfeldt is a scholar working on Genetics, Molecular Biology and Plant Science. According to data from OpenAlex, Jesper Eisfeldt has authored 50 papers receiving a total of 349 indexed citations (citations by other indexed papers that have themselves been cited), including 30 papers in Genetics, 28 papers in Molecular Biology and 10 papers in Plant Science. Recurrent topics in Jesper Eisfeldt's work include Genomic variations and chromosomal abnormalities (20 papers), Genomics and Rare Diseases (12 papers) and Chromosomal and Genetic Variations (10 papers). Jesper Eisfeldt is often cited by papers focused on Genomic variations and chromosomal abnormalities (20 papers), Genomics and Rare Diseases (12 papers) and Chromosomal and Genetic Variations (10 papers). Jesper Eisfeldt collaborates with scholars based in Sweden, United States and Finland. Jesper Eisfeldt's co-authors include Anna Lindstrand, Daniel Nilsson, Maria Pettersson, Adam Ameur, Claudia M.B. Carvalho, Lars Feuk, Elisabeth Syk Lundberg, Emma Tham, Magnus Nordenskjöld and Gustaf Mårtensson and has published in prestigious journals such as Nature Communications, Nature Genetics and SHILAP Revista de lepidopterología.

In The Last Decade

Jesper Eisfeldt

46 papers receiving 348 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Jesper Eisfeldt Sweden 12 191 166 60 55 33 50 349
Robert J. Hardwick United Kingdom 6 270 1.4× 268 1.6× 125 2.1× 47 0.9× 47 1.4× 8 494
Sjors Middelkamp Netherlands 8 349 1.8× 167 1.0× 90 1.5× 70 1.3× 32 1.0× 12 499
Corinne Fasquelle Belgium 11 193 1.0× 225 1.4× 136 2.3× 41 0.7× 17 0.5× 18 450
Marco Garieri Switzerland 10 278 1.5× 156 0.9× 105 1.8× 29 0.5× 52 1.6× 12 435
Detlef Trost France 10 224 1.2× 124 0.7× 40 0.7× 23 0.4× 48 1.5× 20 346
Anna Jauch Germany 10 200 1.0× 137 0.8× 32 0.5× 91 1.7× 33 1.0× 11 319
Chureerat Phokaew Thailand 9 282 1.5× 67 0.4× 58 1.0× 61 1.1× 18 0.5× 21 367
Laura A. Crinnion United Kingdom 13 274 1.4× 160 1.0× 50 0.8× 45 0.8× 22 0.7× 26 413
Fatih Z Boyar United States 8 194 1.0× 169 1.0× 40 0.7× 69 1.3× 70 2.1× 18 342
Nadja Kokalj-Vokač Slovenia 11 276 1.4× 176 1.1× 55 0.9× 73 1.3× 51 1.5× 19 406

Countries citing papers authored by Jesper Eisfeldt

Since Specialization
Citations

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

Fields of papers citing papers by Jesper Eisfeldt

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Jesper Eisfeldt

This figure shows the co-authorship network connecting the top 25 collaborators of Jesper Eisfeldt. A scholar is included among the top collaborators of Jesper Eisfeldt 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 Jesper Eisfeldt. Jesper Eisfeldt 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.
Eisfeldt, Jesper, et al.. (2025). Toward clinical long-read genome sequencing for rare diseases. Nature Genetics. 57(6). 1334–1343. 5 indexed citations
2.
Eisfeldt, Jesper, et al.. (2024). Detecting transposable elements in long-read genomes using sTELLeR. Bioinformatics. 40(11). 3 indexed citations
3.
Swolin‐Eide, Diana, Anna Hammarsjö, Jesper Eisfeldt, et al.. (2024). Structural Variants in COL1A1 and COL1A2 in Osteogenesis Imperfecta. American Journal of Medical Genetics Part A. 197(3). e63935–e63935. 1 indexed citations
4.
Eisfeldt, Jesper, Kassahun Desalegn Bilcha, Carl‐Fredrik Wahlgren, et al.. (2024). Uncommon Variants in FLG2 and NOD2 Are Associated with Atopic Dermatitis in the Ethiopian Population. SHILAP Revista de lepidopterología. 4(4). 100284–100284. 2 indexed citations
5.
Axelsson, Tomas, et al.. (2024). Diagnostic and prognostic genomic aberrations in upper tract urothelial carcinoma can be identified in focal barbotage samples. British Journal of Urology. 135(5). 792–801. 2 indexed citations
6.
Eisfeldt, Jesper, Edward J. Higginbotham, Jennifer Howe, et al.. (2024). Resolving complex duplication variants in autism spectrum disorder using long-read genome sequencing. Genome Research. 34(11). 1763–1773. 3 indexed citations
7.
Pettersson, Maria, Dora Dias‐Santagata, Daniel Nilsson, et al.. (2023). Case report: Extending the spectrum of clinical and molecular findings in FOXC1 haploinsufficiency syndrome. Frontiers in Genetics. 14. 1174046–1174046. 5 indexed citations
8.
Hård, Joanna, Jeff E. Mold, Jesper Eisfeldt, et al.. (2023). Long-read whole-genome analysis of human single cells. Nature Communications. 14(1). 5164–5164. 25 indexed citations
9.
Nilsson, Daniel, Håkan Thonberg, Emma Tham, et al.. (2023). Transposable element insertions in 1000 Swedish individuals. PLoS ONE. 18(7). e0289346–e0289346. 1 indexed citations
10.
Gustafsson, Charlotte, Jesper Eisfeldt, Marcin Kierczak, et al.. (2022). Linked-read whole-genome sequencing resolves common and private structural variants in multiple myeloma. Blood Advances. 6(17). 5009–5023. 2 indexed citations
11.
Taylan, Fulya, Symeon Tournis, Jesper Eisfeldt, et al.. (2022). Mosaic Deletions of Known Genes Explain Skeletal Dysplasias With High and Low Bone Mass. JBMR Plus. 6(8). e10660–e10660.
12.
Natarajan, Karthick, Jesper Eisfeldt, Maria Hammond, et al.. (2021). Single-cell multimodal analysis in a case with reduced penetrance of Progranulin-Frontotemporal Dementia. Acta Neuropathologica Communications. 9(1). 132–132. 4 indexed citations
13.
Pettersson, Maria, Christopher M. Grochowski, Josephine Wincent, et al.. (2020). Cytogenetically visible inversions are formed by multiple molecular mechanisms. Human Mutation. 41(11). 1979–1998. 11 indexed citations
14.
Thutkawkorapin, Jessada, Jesper Eisfeldt, Emma Tham, & Daniel Nilsson. (2020). pyCancerSig: subclassifying human cancer with comprehensive single nucleotide, structural and microsatellite mutational signature deconstruction from whole genome sequencing. BMC Bioinformatics. 21(1). 128–128. 5 indexed citations
15.
16.
Zhang, Chaofan, Juliana F. Mazzeu, Jesper Eisfeldt, et al.. (2020). Novel pathogenic genomic variants leading to autosomal dominant and recessive Robinow syndrome. American Journal of Medical Genetics Part A. 185(12). 3593–3600. 14 indexed citations
17.
Eisfeldt, Jesper, Gustaf Mårtensson, Adam Ameur, Daniel Nilsson, & Anna Lindstrand. (2019). Discovery of Novel Sequences in 1,000 Swedish Genomes. Molecular Biology and Evolution. 37(1). 18–30. 18 indexed citations
18.
Eisfeldt, Jesper, Maria Pettersson, Francesco Vezzi, et al.. (2019). Comprehensive structural variation genome map of individuals carrying complex chromosomal rearrangements. PLoS Genetics. 15(2). e1007858–e1007858. 30 indexed citations
19.
Pettersson, Maria, Raquel Vaz, Anna Hammarsjö, et al.. (2018). Alu-Alu mediated intragenic duplications in IFT81 and MATN3 are associated with skeletal dysplasias. Human Mutation. 39(10). 1456–1467. 11 indexed citations
20.
García, Miguel, Szilveszter Juhos, Maria Larsson, et al.. (2018). CAW - Cancer Analysis Workflow to process normal/tumor WGS data. European Journal of Human Genetics. 26. 702–702. 1 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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