Julia Etzler

693 total citations
12 papers, 481 citations indexed

About

Julia Etzler is a scholar working on Molecular Biology, Genetics and Pathology and Forensic Medicine. According to data from OpenAlex, Julia Etzler has authored 12 papers receiving a total of 481 indexed citations (citations by other indexed papers that have themselves been cited), including 8 papers in Molecular Biology, 5 papers in Genetics and 3 papers in Pathology and Forensic Medicine. Recurrent topics in Julia Etzler's work include Acute Myeloid Leukemia Research (3 papers), Genetics and Neurodevelopmental Disorders (3 papers) and Genetic factors in colorectal cancer (3 papers). Julia Etzler is often cited by papers focused on Acute Myeloid Leukemia Research (3 papers), Genetics and Neurodevelopmental Disorders (3 papers) and Genetic factors in colorectal cancer (3 papers). Julia Etzler collaborates with scholars based in Austria, United States and Germany. Julia Etzler's co-authors include Katharina Wimmer, Ludwine Messiaen, Xavier Roca, A. R. Rao, Christa Fonatsch, Adrian R. Krainer, Tom Callens, Steven Gallinger, Melchior Lauten and Sabine M. Hölter and has published in prestigious journals such as Scientific Reports, International Journal of Molecular Sciences and International Journal of Biological Macromolecules.

In The Last Decade

Julia Etzler

12 papers receiving 478 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Julia Etzler Austria 8 241 198 144 103 101 12 481
Karim Labrèche France 8 120 0.5× 211 1.1× 122 0.8× 52 0.5× 147 1.5× 10 508
Elena Lualdi Italy 7 147 0.6× 355 1.8× 77 0.5× 141 1.4× 48 0.5× 9 568
Shuji Momose Japan 14 201 0.8× 201 1.0× 47 0.3× 208 2.0× 48 0.5× 46 521
Marija Velickovic Australia 12 72 0.3× 192 1.0× 94 0.7× 128 1.2× 101 1.0× 18 516
Valère Cacheux France 10 159 0.7× 175 0.9× 46 0.3× 121 1.2× 72 0.7× 19 526
Yiu Wah Fan China 10 97 0.4× 159 0.8× 155 1.1× 101 1.0× 41 0.4× 11 445
Domenico Trombetta Italy 12 83 0.3× 358 1.8× 247 1.7× 266 2.6× 54 0.5× 36 731
Lynn M. Nycum United States 10 122 0.5× 277 1.4× 83 0.6× 123 1.2× 58 0.6× 12 584
Shelley Idziaszczyk United Kingdom 8 194 0.8× 242 1.2× 60 0.4× 321 3.1× 35 0.3× 13 803
Jacquelyn J. Roth United States 13 93 0.4× 229 1.2× 88 0.6× 53 0.5× 49 0.5× 25 473

Countries citing papers authored by Julia Etzler

Since Specialization
Citations

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

Fields of papers citing papers by Julia Etzler

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Julia Etzler

This figure shows the co-authorship network connecting the top 25 collaborators of Julia Etzler. A scholar is included among the top collaborators of Julia Etzler 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 Julia Etzler. Julia Etzler 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.
Derdak, Sophia, Julia Etzler, Sigismund Huck, et al.. (2024). Generation and Characterization of a Human Neuronal In Vitro Model for Rett Syndrome Using a Direct Reprogramming Method. Stem Cells and Development. 33(5-6). 128–142. 1 indexed citations
2.
Steinkellner, Hannes, Prakasha Kempaiah, Julia Etzler, et al.. (2022). TAT-MeCP2 protein variants rescue disease phenotypes in human and mouse models of Rett syndrome. International Journal of Biological Macromolecules. 209(Pt A). 972–983. 4 indexed citations
3.
Nguyen, Chi Huu, Hubert Hackl, Heinz Sill, et al.. (2021). Downregulation of MTSS1 in acute myeloid leukemia is associated with a poor prognosis, chemotherapy resistance, and disease aggressiveness. Leukemia. 35(10). 2827–2839. 13 indexed citations
4.
Steinkellner, Hannes, Julia Etzler, Prakasha Kempaiah, et al.. (2019). An electrochemiluminescence based assay for quantitative detection of endogenous and exogenously applied MeCP2 protein variants. Scientific Reports. 9(1). 7929–7929. 4 indexed citations
5.
Nguyen, Chi Huu, Julia Etzler, Michael Fuchs, et al.. (2019). CGRP Signaling via CALCRL Increases Chemotherapy Resistance and Stem Cell Properties in Acute Myeloid Leukemia. International Journal of Molecular Sciences. 20(23). 5826–5826. 22 indexed citations
6.
Steinkellner, Hannes, Julia Etzler, Bernhard Gmeiner, & Franco Laccone. (2015). Detection of Survival Motor Neuron Protein in Buccal Cells Through Electrochemiluminescence-Based Assay. Assay and Drug Development Technologies. 13(3). 167–173. 6 indexed citations
7.
Heller, Gerwin, Julia Etzler, Hubert Hackl, et al.. (2015). EVI1 promotes tumor growth via transcriptional repression of MS4A3. Journal of Hematology & Oncology. 8(1). 28–28. 24 indexed citations
8.
Steinkellner, Hannes, Julia Etzler, Jürgen Neesen, et al.. (2014). Identification and molecular characterisation of a homozygous missense mutation in the ADAMTS10 gene in a patient with Weill–Marchesani syndrome. European Journal of Human Genetics. 23(9). 1186–1191. 11 indexed citations
9.
Kratz, Christian P., Sabine M. Hölter, Julia Etzler, et al.. (2009). Rhabdomyosarcoma in patients with constitutional mismatch-repair-deficiency syndrome. Journal of Medical Genetics. 46(6). 418–420. 44 indexed citations
10.
Wimmer, Katharina & Julia Etzler. (2008). Constitutional mismatch repair-deficiency syndrome: have we so far seen only the tip of an iceberg?. Human Genetics. 124(2). 105–122. 195 indexed citations
11.
Wimmer, Katharina, Xavier Roca, Tom Callens, et al.. (2007). Extensive in silico analysis of NF1 splicing defects uncovers determinants for splicing outcome upon 5′ splice-site disruption. Human Mutation. 28(6). 599–612. 103 indexed citations
12.
Etzler, Julia, Andreas Peyrl, Andrea Zaťková, et al.. (2007). RNA-based mutation analysis identifies an unusual MSH6 splicing defect and circumvents PMS2 pseudogene interference. Human Mutation. 29(2). 299–305. 54 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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2026