Ellen D. Renner

7.3k total citations
46 papers, 2.4k citations indexed

About

Ellen D. Renner is a scholar working on Immunology, Genetics and Dermatology. According to data from OpenAlex, Ellen D. Renner has authored 46 papers receiving a total of 2.4k indexed citations (citations by other indexed papers that have themselves been cited), including 34 papers in Immunology, 8 papers in Genetics and 5 papers in Dermatology. Recurrent topics in Ellen D. Renner's work include Immunodeficiency and Autoimmune Disorders (26 papers), Immune Cell Function and Interaction (16 papers) and T-cell and B-cell Immunology (16 papers). Ellen D. Renner is often cited by papers focused on Immunodeficiency and Autoimmune Disorders (26 papers), Immune Cell Function and Interaction (16 papers) and T-cell and B-cell Immunology (16 papers). Ellen D. Renner collaborates with scholars based in Germany, United States and Switzerland. Ellen D. Renner's co-authors include Bernd H. Belohradsky, Annette Jansson, Jordan S. Orange, Steven M. Holland, Bodo Grimbacher, B. H. Belohradsky, Joie Davis, Jennifer M. Puck, Brian Kim and Dmytro Kobuley and has published in prestigious journals such as Nature Medicine, PLoS ONE and Clinical Infectious Diseases.

In The Last Decade

Ellen D. Renner

45 papers receiving 2.3k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Ellen D. Renner Germany 21 1.4k 504 469 399 339 46 2.4k
Ali Akbar Amirzargar Iran 26 1.2k 0.8× 312 0.6× 269 0.6× 379 0.9× 202 0.6× 106 2.3k
Yukio Sakiyama Japan 26 905 0.7× 495 1.0× 489 1.0× 256 0.6× 270 0.8× 118 2.4k
Joyce Eskdale United Kingdom 26 1.8k 1.3× 452 0.9× 232 0.5× 490 1.2× 176 0.5× 46 3.0k
Ikuya Tsuge Japan 24 1.6k 1.1× 290 0.6× 382 0.8× 199 0.5× 191 0.6× 87 3.0k
Linna Ding United States 18 1.2k 0.9× 266 0.5× 270 0.6× 268 0.7× 225 0.7× 33 2.2k
Arnold I. Levinson United States 27 1.2k 0.9× 320 0.6× 330 0.7× 267 0.7× 153 0.5× 89 2.4k
Jan Marsal Sweden 22 2.0k 1.5× 415 0.8× 494 1.1× 110 0.3× 244 0.7× 48 3.0k
Jaime Darce United States 12 1.9k 1.4× 1.0k 2.0× 360 0.8× 398 1.0× 121 0.4× 13 3.2k
Fabio Almerigogna Italy 23 1.8k 1.3× 364 0.7× 145 0.3× 187 0.5× 276 0.8× 61 2.9k
Nathalie Schmitt United States 25 3.3k 2.4× 469 0.9× 248 0.5× 363 0.9× 136 0.4× 42 4.1k

Countries citing papers authored by Ellen D. Renner

Since Specialization
Citations

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

Fields of papers citing papers by Ellen D. Renner

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Ellen D. Renner. 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 Ellen D. Renner. The network helps show where Ellen D. Renner may publish in the future.

Co-authorship network of co-authors of Ellen D. Renner

This figure shows the co-authorship network connecting the top 25 collaborators of Ellen D. Renner. A scholar is included among the top collaborators of Ellen D. Renner 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 Ellen D. Renner. Ellen D. Renner 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.
Faßhauer, Maria, Horst von Bernuth, Monika Bullinger, et al.. (2024). A patient empowerment program for primary immunodeficiency improves quality of life in children and adolescents. Immunotherapy. 16(12). 813–819.
2.
Effner, Renate, Maria Nordengrün, Anton Lechner, et al.. (2024). Staphylococcus aureus Serine protease-like protein A (SplA) induces IL-8 by keratinocytes and synergizes with IL-17A. Cytokine. 180. 156634–156634. 5 indexed citations
3.
Fieten, Karin B., José María Maya‐Manzano, Beate Rückert, et al.. (2023). Environmental exposure and sensitization patterns in a Swiss alpine pediatric cohort. World Allergy Organization Journal. 16(12). 100847–100847. 2 indexed citations
4.
Rinaldi, Arturo, Anita Dreher, Ge Tan, et al.. (2021). Electrical impedance spectroscopy for the characterization of skin barrier in atopic dermatitis. Allergy. 76(10). 3066–3079. 46 indexed citations
5.
Renner, Ellen D., et al.. (2021). Inborn Error of Immunity or Atopic Dermatitis: When to be Concerned and How to Investigate. The Journal of Allergy and Clinical Immunology In Practice. 9(4). 1501–1507. 13 indexed citations
6.
Hagl, Beate, Carolin Kröner, Ekaterini Paschos, et al.. (2020). Retained primary teeth in STAT3 hyper-IgE syndrome: early intervention in childhood is essential. Orphanet Journal of Rare Diseases. 15(1). 244–244. 11 indexed citations
7.
Hagl, Beate, Silvia Thoene, Sophie Bonnal, et al.. (2018). Somatic alterations compromised molecular diagnosis of DOCK8 hyper-IgE syndrome caused by a novel intronic splice site mutation. Scientific Reports. 8(1). 16719–16719. 5 indexed citations
8.
Hiller, Julia, Beate Hagl, Renate Effner, et al.. (2017). STAT1 Gain-of-Function and Dominant Negative STAT3 Mutations Impair IL-17 and IL-22 Immunity Associated with CMC. Journal of Investigative Dermatology. 138(3). 711–714. 22 indexed citations
9.
Stentzel, Sebastian, et al.. (2017). Reduced Immunoglobulin (Ig) G Response to Staphylococcus aureus in STAT3 Hyper-IgE Syndrome. Clinical Infectious Diseases. 64(9). 1279–1282. 11 indexed citations
10.
Mertsch, Pontus, Nikolaus Kneidinger, Sandhya Matthes, et al.. (2017). Perception of climate change in patients with chronic lung disease. PLoS ONE. 12(10). e0186632–e0186632. 7 indexed citations
11.
Herbst, Martin, Roel P. Gazendam, Julie Sawalle‐Belohradsky, et al.. (2015). Chronic Candida albicans Meningitis in a 4-Year-Old Girl with a Homozygous Mutation in the CARD9 Gene (Q295X). The Pediatric Infectious Disease Journal. 34(9). 999–1002. 44 indexed citations
12.
Mizesko, Melissa, Pinaki P. Banerjee, Linda Monaco-Shawver, et al.. (2013). Defective actin accumulation impairs human natural killer cell function in patients with dedicator of cytokinesis 8 deficiency. Journal of Allergy and Clinical Immunology. 131(3). 840–848. 93 indexed citations
13.
Nijman, Isaäc J., Joris M. van Montfrans, Marlous Hoogstraat, et al.. (2013). Targeted next-generation sequencing: A novel diagnostic tool for primary immunodeficiencies. Journal of Allergy and Clinical Immunology. 133(2). 529–534.e1. 95 indexed citations
14.
Schimke, Lena F., Nikolaus Rieber, Stacey Rylaarsdam, et al.. (2013). A Novel Gain-of-Function IKBA Mutation Underlies Ectodermal Dysplasia with Immunodeficiency and Polyendocrinopathy. Journal of Clinical Immunology. 33(6). 1088–1099. 43 indexed citations
15.
Boztug, Heidrun, Ellen D. Renner, Michael H. Albert, et al.. (2012). Clinical and Immunological Correction of DOCK8 Deficiency by Allogeneic Hematopoietic Stem Cell Transplantation Following a Reduced Toxicity Conditioning Regimen. Pediatric Hematology and Oncology. 29(7). 585–594. 26 indexed citations
16.
Pannicke, Ulrich, Ellen D. Renner, Gundula Notheis, et al.. (2010). Successful Long-Term Correction of Autosomal Recessive Hyper-IgE Syndrome due to DOCK8 Deficiency by Hematopoietic Stem Cell Transplantation. Klinische Pädiatrie. 222(6). 351–355. 52 indexed citations
17.
Yeganeh, Mehdi, Philipp Henneke, Nima Rezaei, et al.. (2008). Toll-Like Receptor Stimulation Induces Higher TNF-α Secretion in Peripheral Blood Mononuclear Cells from Patients with Hyper IgE Syndrome. International Archives of Allergy and Immunology. 146(3). 190–194. 9 indexed citations
18.
Renner, Ellen D., F. Hoffmann, Veit Hornung, et al.. (2005). No Indication for a Defect in Toll-Like Receptor Signaling in Patients with Hyper-IgE Syndrome. Journal of Clinical Immunology. 25(4). 321–328. 12 indexed citations
19.
Renner, Ellen D., Jennifer M. Puck, Steven M. Holland, et al.. (2004). Autosomal recessive hyperimmunoglobulin E syndrome: a distinct disease entity. The Journal of Pediatrics. 144(1). 93–99. 197 indexed citations
20.
Renner, Ellen D., B. H. Belohradsky, & Bodo Grimbacher. (2002). Hyper-IgE-Syndrom. Monatsschrift Kinderheilkunde. 150(10). 1168–1179. 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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