Jasmin Lisfeld

1.2k total citations
12 papers, 231 citations indexed

About

Jasmin Lisfeld is a scholar working on Genetics, Molecular Biology and Pathology and Forensic Medicine. According to data from OpenAlex, Jasmin Lisfeld has authored 12 papers receiving a total of 231 indexed citations (citations by other indexed papers that have themselves been cited), including 6 papers in Genetics, 5 papers in Molecular Biology and 5 papers in Pathology and Forensic Medicine. Recurrent topics in Jasmin Lisfeld's work include Lymphoma Diagnosis and Treatment (5 papers), Genomics and Rare Diseases (3 papers) and Viral-associated cancers and disorders (3 papers). Jasmin Lisfeld is often cited by papers focused on Lymphoma Diagnosis and Treatment (5 papers), Genomics and Rare Diseases (3 papers) and Viral-associated cancers and disorders (3 papers). Jasmin Lisfeld collaborates with scholars based in Germany, Austria and Switzerland. Jasmin Lisfeld's co-authors include Wolfram Klapper, Birgit Burkhardt, Ilske Oschlies, Reiner Siebert, Michael Baudis, Itziar Salaverría, África García‐Orad, Monika Szczepanowski, Susanne Bens and Idoia Martín‐Guerrero and has published in prestigious journals such as SHILAP Revista de lepidopterología, British Journal of Haematology and Human Mutation.

In The Last Decade

Jasmin Lisfeld

12 papers receiving 229 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Jasmin Lisfeld Germany 7 179 89 82 44 42 12 231
Ana Batlle Spain 7 151 0.8× 38 0.4× 115 1.4× 29 0.7× 38 0.9× 15 248
Gina M. Kavanagh United Kingdom 8 171 1.0× 173 1.9× 112 1.4× 120 2.7× 34 0.8× 10 338
Mahsa Khanlari United States 9 103 0.6× 26 0.3× 114 1.4× 12 0.3× 36 0.9× 28 205
Renee H. Grau United States 5 55 0.3× 66 0.7× 29 0.4× 30 0.7× 23 0.5× 7 258
Arantza Onaindía Spain 7 153 0.9× 83 0.9× 73 0.9× 41 0.9× 24 0.6× 11 202
Marie-Hélène Delfau France 7 150 0.8× 65 0.7× 114 1.4× 23 0.5× 8 0.2× 14 213
Dominique Penther France 7 73 0.4× 33 0.4× 67 0.8× 19 0.4× 6 0.1× 13 219
Kseniya Petrova‐Drus United States 7 80 0.4× 25 0.3× 54 0.7× 9 0.2× 13 0.3× 20 183
L. Gusdorf France 8 60 0.3× 58 0.7× 25 0.3× 69 1.6× 7 0.2× 20 273
Aysche Landmann Germany 7 80 0.4× 33 0.4× 29 0.4× 25 0.6× 42 1.0× 10 360

Countries citing papers authored by Jasmin Lisfeld

Since Specialization
Citations

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

Fields of papers citing papers by Jasmin Lisfeld

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Jasmin Lisfeld

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

All Works

12 of 12 papers shown
1.
Lisfeld, Jasmin, Christopher M. Grochowski, Alex Hastie, et al.. (2024). A combination of long- and short-read genomics reveals frequent p-arm breakpoints within chromosome 21 complex genomic rearrangements. SHILAP Revista de lepidopterología. 2. 101863–101863. 2 indexed citations
2.
Harms, Frederike L., et al.. (2023). INPP4A-related genetic and phenotypic spectrum and functional relevance of subcellular targeting of INPP4A isoforms. Neurogenetics. 24(2). 79–93. 3 indexed citations
3.
Harms, Frederike L., Deike Weiss, Jasmin Lisfeld, Malik Alawi, & Kerstin Kutsche. (2023). A deep intronic variant in DNM1 in a patient with developmental and epileptic encephalopathy creates a splice acceptor site and affects only transcript variants including exon 10a. Neurogenetics. 24(3). 171–180. 3 indexed citations
4.
Lisfeld, Jasmin, et al.. (2022). Autosomal dominantly inherited myopathy likely caused by the TNNT1 variant p.(Asp65Ala). Human Mutation. 43(9). 1224–1233. 1 indexed citations
5.
Ven, Amelie T. van der, Jessika Johannsen, Fanny Kortüm, et al.. (2021). Prevalence and clinical prediction of mitochondrial disorders in a large neuropediatric cohort. Clinical Genetics. 100(6). 766–770. 8 indexed citations
6.
Blohm, Martin, Fanny Kortüm, Tatjana Bierhals, et al.. (2021). Whole-Exome Sequencing in Critically Ill Neonates and Infants: Diagnostic Yield and Predictability of Monogenic Diagnosis. Neonatology. 118(4). 454–461. 18 indexed citations
7.
Fuchs, Sigrid, et al.. (2021). The acrocentric part of der(Y)t(Y;acro)(q12;p1?2) contains D15Z1 sequences in the majority of cases. Human Genome Variation. 8(1). 32–32. 1 indexed citations
8.
Burkhardt, Birgit, Martin Zimmermann, Edita Kabíčková, et al.. (2016). Impact of Fc gamma-receptor polymorphisms on the response to rituximab treatment in children and adolescents with mature B cell lymphoma/leukemia. Annals of Hematology. 95(9). 1503–1512. 16 indexed citations
9.
Kontny, Udo, Ilske Oschlies, Willi Woessmann, et al.. (2014). Non‐anaplastic peripheral T‐cell lymphoma in children and adolescents – a retrospective analysis of the NHL‐BFM study group. British Journal of Haematology. 168(6). 835–844. 29 indexed citations
10.
Martín‐Guerrero, Idoia, Itziar Salaverría, Birgit Burkhardt, et al.. (2013). Recurrent loss of heterozygosity in 1p36 associated with TNFRSF14 mutations in IRF4 translocation negative pediatric follicular lymphomas. Haematologica. 98(8). 1237–1241. 49 indexed citations
11.
Oschlies, Ilske, Jasmin Lisfeld, Laurence Lamant, et al.. (2012). ALK-positive anaplastic large cell lymphoma limited to the skin: clinical, histopathological and molecular analysis of 6 pediatric cases. A report from the ALCL99 study. Haematologica. 98(1). 50–56. 80 indexed citations
12.
Salaverría, Itziar, Idoia Martín‐Guerrero, Birgit Burkhardt, et al.. (2012). High resolution copy number analysis of IRF4 translocation‐positive diffuse large B‐cell and follicular lymphomas. Genes Chromosomes and Cancer. 52(2). 150–155. 21 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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