Julia Schreml

1.1k total citations
23 papers, 567 citations indexed

About

Julia Schreml is a scholar working on Molecular Biology, Surgery and Genetics. According to data from OpenAlex, Julia Schreml has authored 23 papers receiving a total of 567 indexed citations (citations by other indexed papers that have themselves been cited), including 9 papers in Molecular Biology, 7 papers in Surgery and 7 papers in Genetics. Recurrent topics in Julia Schreml's work include Neurogenetic and Muscular Disorders Research (5 papers), Body Contouring and Surgery (4 papers) and Skin and Cellular Biology Research (3 papers). Julia Schreml is often cited by papers focused on Neurogenetic and Muscular Disorders Research (5 papers), Body Contouring and Surgery (4 papers) and Skin and Cellular Biology Research (3 papers). Julia Schreml collaborates with scholars based in Germany, United Kingdom and Poland. Julia Schreml's co-authors include Brunhilde Wirth, Markus Rießland, Stephan Schreml, Simon H. Parson, Ioanna Gouni‐Berthold, Lukas Prantl, Mark Berneburg, Lutz Garbes, Raoul Heller and Thomas H. Gillingwater and has published in prestigious journals such as SHILAP Revista de lepidopterología, Scientific Reports and Human Molecular Genetics.

In The Last Decade

Julia Schreml

22 papers receiving 558 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 Schreml Germany 12 377 258 168 83 56 23 567
Tarjinder Singh United States 8 256 0.7× 81 0.3× 322 1.9× 269 3.2× 100 1.8× 16 629
Nicolas Dard France 13 358 0.9× 100 0.4× 51 0.3× 37 0.4× 135 2.4× 15 589
Navid Almadani Iran 14 352 0.9× 113 0.4× 56 0.3× 233 2.8× 20 0.4× 45 702
Charis L. Himeda United States 19 894 2.4× 135 0.5× 64 0.4× 318 3.8× 44 0.8× 25 995
Erik A. Toso United States 12 437 1.2× 90 0.3× 31 0.2× 48 0.6× 42 0.8× 18 557
Gabriel Sanchez France 15 651 1.7× 224 0.9× 43 0.3× 42 0.5× 21 0.4× 17 767
Claudio Macias-Treviño United States 6 428 1.1× 168 0.7× 26 0.2× 87 1.0× 25 0.4× 10 559
Tamar Eigler United States 11 260 0.7× 73 0.3× 72 0.4× 41 0.5× 63 1.1× 12 541
Erica Yada Japan 12 306 0.8× 71 0.3× 73 0.4× 41 0.5× 35 0.6× 17 387
Shuyi Ji China 7 616 1.6× 39 0.2× 259 1.5× 51 0.6× 31 0.6× 12 814

Countries citing papers authored by Julia Schreml

Since Specialization
Citations

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

Fields of papers citing papers by Julia Schreml

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Julia Schreml

This figure shows the co-authorship network connecting the top 25 collaborators of Julia Schreml. A scholar is included among the top collaborators of Julia Schreml 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 Schreml. Julia Schreml 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.
Schreml, Julia, Judith Fischer, Alrun Hotz, et al.. (2024). Hereditary epidermolytic palmoplantar keratosis due to a novel desmoglein‐1 mutation: A case report. SHILAP Revista de lepidopterología. 12(5). e8881–e8881.
2.
Peters, Franziska, Julia Schreml, Oliver Semler, et al.. (2024). Ehlers-Danlos Syndromes and Related Disorders: Diagnostic Challenges and the Need for an Interdisciplinary Patient Care in Germany. Dermatology. 241(2). 124–132. 1 indexed citations
3.
Hehr, Ute, et al.. (2023). Congenital ichthyosiform erythroderma with epidermolysis due to a novel frameshift mutation in KRT10. JAAD Case Reports. 35. 74–76. 1 indexed citations
4.
Bergbreiter, Astrid, Diane Bitzinger, Tobias Ettl, et al.. (2021). Recurrent necrotizing cellulitis, multi-organ autoimmune disease and humoral immunodeficiency due to a novel NFKB1 frameshift mutation. European Journal of Medical Genetics. 64(3). 104144–104144. 7 indexed citations
5.
Schiltz, Daniel, Alexandra Anker, S. Klein, et al.. (2020). Adipose Tissue in Multiple Symmetric Lipomatosis Shows Features of Brown/Beige Fat. Aesthetic Plastic Surgery. 44(3). 855–861. 6 indexed citations
6.
Berneburg, Mark, Oliver Felthaus, Lukas Prantl, et al.. (2019). Calcyphosine-like (CAPSL) is regulated in Multiple Symmetric Lipomatosis and is involved in Adipogenesis. Scientific Reports. 9(1). 8444–8444. 11 indexed citations
7.
Schiltz, Daniel, Alexandra Anker, Michael Koller, et al.. (2018). Multiple Symmetric Lipomatosis: New Classification System Based on the Largest German Patient Cohort. Plastic & Reconstructive Surgery Global Open. 6(4). e1722–e1722. 17 indexed citations
8.
Schreml, Julia & Ioanna Gouni‐Berthold. (2017). Role of Anti-PCSK9 Antibodies in the Treatment of Patients with Statin Intolerance. Current Medicinal Chemistry. 25(13). 1538–1548. 5 indexed citations
9.
Schreml, Julia & Ioanna Gouni‐Berthold. (2017). Apolipoprotein(a) Antisense Oligonucleotides: A New Treatment Option for Lowering Elevated Lipoprotein(a)?. Current Pharmaceutical Design. 23(10). 1562–1570. 14 indexed citations
10.
Schröder, Josef, Ines Schönbuchner, Julia Schreml, et al.. (2016). Erythrodermia Congenitalis Ichthyosiformis Bullosa of Brocq. Case Reports in Dermatology. 8(1). 19–21. 1 indexed citations
11.
Prantl, Lukas, Julia Schreml, Sebastian Gehmert, et al.. (2016). Transcription Profile in Sporadic Multiple Symmetric Lipomatosis Reveals Differential Expression at the Level of Adipose Tissue–Derived Stem Cells. Plastic & Reconstructive Surgery. 137(4). 1181–1190. 19 indexed citations
12.
Weiß, Katharina, Matthias Fante, Gudrun Köhl, et al.. (2016). Proton‐sensing G protein‐coupled receptors as regulators of cell proliferation and migration during tumor growth and wound healing. Experimental Dermatology. 26(2). 127–132. 53 indexed citations
13.
Vincendeau, Michelle, Julia Schreml, Armand G. Ngounou Wetie, et al.. (2015). Modulation of human endogenous retrovirus (HERV) transcription during persistent and de novo HIV-1 infection. Retrovirology. 12(1). 27–27. 52 indexed citations
14.
Somers, Eilidh, Markus Rießland, Julia Schreml, et al.. (2013). Increasing SMN levels using the histone deacetylase inhibitor SAHA ameliorates defects in skeletal muscle microvasculature in a mouse model of severe spinal muscular atrophy. Neuroscience Letters. 544. 100–104. 10 indexed citations
15.
Schreml, Julia, Burak Durmaz, Özgür Çoğulu, et al.. (2013). The missing “link”: an autosomal recessive short stature syndrome caused by a hypofunctional XYLT1 mutation. Human Genetics. 133(1). 29–39. 55 indexed citations
16.
Schreml, Julia, Markus Rießland, Lutz Garbes, et al.. (2012). Severe SMA mice show organ impairment that cannot be rescued by therapy with the HDACi JNJ-26481585. European Journal of Human Genetics. 21(6). 643–652. 60 indexed citations
17.
Kröber, Sandra, Laura Torres‐Benito, Anke Borgmann, et al.. (2012). Plastin 3 ameliorates spinal muscular atrophy via delayed axon pruning and improves neuromuscular junction functionality. Human Molecular Genetics. 22(7). 1328–1347. 101 indexed citations
18.
Garbes, Lutz, Ludwig Heesen, Irmgard Hölker, et al.. (2012). VPA response in SMA is suppressed by the fatty acid translocase CD36. Human Molecular Genetics. 22(2). 398–407. 44 indexed citations
19.
Mutsaers, Chantal A., Thomas M. Wishart, Douglas J. Lamont, et al.. (2011). Reversible molecular pathology of skeletal muscle in spinal muscular atrophy. Human Molecular Genetics. 20(22). 4334–4344. 79 indexed citations
20.
Schreml, Stephan, et al.. (2008). Neurocutaneous melanosis in association with Dandy-Walker malformation: case report and literature review. Clinical and Experimental Dermatology. 33(5). 611–614. 23 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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