Julius Wehrle

1.5k total citations
29 papers, 411 citations indexed

About

Julius Wehrle is a scholar working on Hematology, Molecular Biology and Genetics. According to data from OpenAlex, Julius Wehrle has authored 29 papers receiving a total of 411 indexed citations (citations by other indexed papers that have themselves been cited), including 13 papers in Hematology, 12 papers in Molecular Biology and 10 papers in Genetics. Recurrent topics in Julius Wehrle's work include Acute Myeloid Leukemia Research (10 papers), Myeloproliferative Neoplasms: Diagnosis and Treatment (8 papers) and Cancer Genomics and Diagnostics (8 papers). Julius Wehrle is often cited by papers focused on Acute Myeloid Leukemia Research (10 papers), Myeloproliferative Neoplasms: Diagnosis and Treatment (8 papers) and Cancer Genomics and Diagnostics (8 papers). Julius Wehrle collaborates with scholars based in Germany, Switzerland and Austria. Julius Wehrle's co-authors include Heike L. Pahl, Thalia S. Seeger, Nikolas von Bubnoff, Albert Gründer, Monika Gothwal, Sven Schwemmers, Dietmar Pfeifer, Marie Follo, Rainer Claus and Justus Duyster and has published in prestigious journals such as The Journal of Experimental Medicine, SHILAP Revista de lepidopterología and Blood.

In The Last Decade

Julius Wehrle

27 papers receiving 408 citations

Peers

Julius Wehrle
Julius Wehrle
Citations per year, relative to Julius Wehrle Julius Wehrle (= 1×) peers Carmen Azqueta

Countries citing papers authored by Julius Wehrle

Since Specialization
Citations

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

Fields of papers citing papers by Julius Wehrle

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Julius Wehrle

This figure shows the co-authorship network connecting the top 25 collaborators of Julius Wehrle. A scholar is included among the top collaborators of Julius Wehrle 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 Julius Wehrle. Julius Wehrle 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.
Boerries, Melanie, Alexandra Nieters, Gerhard Kindle, et al.. (2024). Information Mode–Dependent Success Rates of Obtaining German Medical Informatics Initiative–Compliant Broad Consent in the Emergency Department: Single-Center Prospective Observational Study. JMIR Medical Informatics. 12. e65646–e65646. 1 indexed citations
2.
Benning, Leo, et al.. (2023). Factors influencing the occurrence of ambulatory care sensitive conditions in the emergency department - a single-center cross-sectional study. Frontiers in Medicine. 10. 1256447–1256447. 1 indexed citations
3.
Rassner, Michael, Marie Follo, Stefanie Jilg, et al.. (2023). Development of Highly Sensitive Digital Droplet PCR for Detection of cKIT Mutations in Circulating Free DNA That Mediate Resistance to TKI Treatment for Gastrointestinal Stromal Tumor (GIST). International Journal of Molecular Sciences. 24(6). 5411–5411. 1 indexed citations
4.
Ranganathan, Lavanya, Samuel Bandara, Stephanie J. Yaung, et al.. (2023). Early Prediction of Treatment Response By Circulating Tumor DNA Profiling in Patients with Diffuse Large B-Cell Lymphoma Receiving CAR T-Cell Therapy. Blood. 142(Supplement 1). 2987–2987. 2 indexed citations
5.
Kiefer, Jurij, Johannes Zeller, Peter Bronsert, et al.. (2022). Genotyping of Circulating Free DNA Enables Monitoring of Tumor Dynamics in Synovial Sarcomas. Cancers. 14(9). 2078–2078. 12 indexed citations
6.
Wehrle, Julius, Rainer Claus, Justus Duyster, et al.. (2021). Bisulfite-free epigenomics and genomics of single cells through methylation-sensitive restriction. Communications Biology. 4(1). 153–153. 21 indexed citations
7.
Schwemmers, Sven, et al.. (2020). The transcription factor NFE2 enhances expression of the hematopoietic master regulators SCL/TAL1 and GATA2. Experimental Hematology. 87. 42–47.e1. 5 indexed citations
8.
Wehrle, Julius, Gabriele Ihorst, Konrad Aumann, et al.. (2020). Prevalence and characteristics of myeloproliferative neoplasms with concomitant monoclonal gammopathy. Leukemia Research. 98. 106454–106454. 4 indexed citations
9.
Becker, Heiko, Dietmar Pfeifer, Gabriele Ihorst, et al.. (2020). Monosomal karyotype and chromosome 17p loss or TP53 mutations in decitabine-treated patients with acute myeloid leukemia. Annals of Hematology. 99(7). 1551–1560. 11 indexed citations
10.
Peeken, Jan C., Jonas S. Jutzi, Julius Wehrle, et al.. (2018). Epigenetic regulation of NFE2 overexpression in myeloproliferative neoplasms. Blood. 131(18). 2065–2073. 35 indexed citations
11.
Scheller, Elisa, Lena V. Schumacher, Jessica Peter, et al.. (2018). Brain Aging and APOE ε4 Interact to Reveal Potential Neuronal Compensation in Healthy Older Adults. Frontiers in Aging Neuroscience. 10. 74–74. 20 indexed citations
12.
Rothenberg‐Thurley, Maja, Katarzyna Szarc vel Szic, Alexandra Nieters, et al.. (2017). Progression of Mds to Aml Features Gain of Single Driver Mutations with Consequent Changes in Clonal Composition and Occurrence of Multiple Clones with Mutations in Identical Genes. Haematologica.
13.
Wehrle, Julius, Rainer Claus, Heiko Becker, et al.. (2017). The oligodendrocyte lineage transcription factor 2 (OLIG2) is epigenetically regulated in acute myeloid leukemia. Experimental Hematology. 55. 76–85.e3. 3 indexed citations
14.
Pastor, Victoria, Shinsuke Hirabayashi, Axel Karow, et al.. (2016). Mutational landscape in children with myelodysplastic syndromes is distinct from adults: specific somatic drivers and novel germline variants. Leukemia. 31(3). 759–762. 55 indexed citations
15.
Gothwal, Monika, Julius Wehrle, Konrad Aumann, et al.. (2016). A novel role for nuclear factor-erythroid 2 in erythroid maturation by modulation of mitochondrial autophagy. Haematologica. 101(9). 1054–1064. 12 indexed citations
16.
Wehrle, Julius, Heike L. Pahl, & Nikolas von Bubnoff. (2014). Ponatinib: A Third-Generation Inhibitor for the Treatment of CML. Recent results in cancer research. 201. 99–107. 17 indexed citations
17.
Krohn, Alexander, Theresa D. Ahrens, Till Plönes, et al.. (2014). Tumor Cell Heterogeneity in Small Cell Lung Cancer (SCLC): Phenotypical and Functional Differences Associated with Epithelial-Mesenchymal Transition (EMT) and DNA Methylation Changes. PLoS ONE. 9(6). e100249–e100249. 52 indexed citations
18.
Wehrle, Julius, Thalia S. Seeger, Sven Schwemmers, et al.. (2013). Transcription factor nuclear factor erythroid-2 mediates expression of the cytokine interleukin 8, a known predictor of inferior outcome in patients with myeloproliferative neoplasms. Haematologica. 98(7). 1073–1080. 23 indexed citations
19.
Jutzi, Jonas S., Ruzhica Bogeska, Gorica Nikoloski, et al.. (2013). MPN patients harbor recurrent truncating mutations in transcription factor NF-E2. The Journal of Experimental Medicine. 210(5). 1003–1019. 49 indexed citations
20.
Peeken, Jan C., Thalia S. Seeger, Julius Wehrle, et al.. (2013). Overexpression Of The Histone Demethylase JMJD1C In Polycythemia Vera Contributes To NF-E2 Overexpression Via Epigenetic Dysregulation and An Auto-Regulatory Loop. Blood. 122(21). 1602–1602. 2 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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