David Ellinghaus

29.8k total citations · 1 hit paper
41 papers, 2.0k citations indexed

About

David Ellinghaus is a scholar working on Genetics, Molecular Biology and Epidemiology. According to data from OpenAlex, David Ellinghaus has authored 41 papers receiving a total of 2.0k indexed citations (citations by other indexed papers that have themselves been cited), including 27 papers in Genetics, 19 papers in Molecular Biology and 10 papers in Epidemiology. Recurrent topics in David Ellinghaus's work include Inflammatory Bowel Disease (13 papers), Genetic Associations and Epidemiology (11 papers) and Liver Disease Diagnosis and Treatment (5 papers). David Ellinghaus is often cited by papers focused on Inflammatory Bowel Disease (13 papers), Genetic Associations and Epidemiology (11 papers) and Liver Disease Diagnosis and Treatment (5 papers). David Ellinghaus collaborates with scholars based in Germany, Denmark and United States. David Ellinghaus's co-authors include Ute Willhoeft, Stefan Kurtz, André Franke, Britt‐Sabina Petersen, Stefan Schreiber, Michael Nothnagel, Michael Krawczak, Marc P. Hoeppner, Lars Wienbrandt and Jie Huang and has published in prestigious journals such as Nucleic Acids Research, Nature Communications and SHILAP Revista de lepidopterología.

In The Last Decade

David Ellinghaus

40 papers receiving 2.0k citations

Hit Papers

align trajectories

What are hit papers?

Hit papers significantly outperform the citation benchmark for their cohort. A paper qualifies if it has ≥500 total citations, achieves ≥1.5× the top-1% citation threshold for papers in the same subfield and year (this is the minimum needed to enter the top 1%, not the average within it), or reaches the top citation threshold in at least one of its specific research topics.

LTRharvest, an efficient and flexible software for de novo detection of LTR retrotransposons

2008 955 citations David Ellinghaus et al. profile →

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
David Ellinghaus Germany	18	1.1k	702	658	145	144	41	2.0k
Jie Xu United States	27	1.4k 1.3×	462 0.7×	554 0.8×	148 1.0×	195 1.4×	117	2.6k
Hiroshi Imai Japan	35	2.6k 2.5×	412 0.6×	950 1.4×	77 0.5×	276 1.9×	154	4.1k
Rolf H. A. M. Vossen Netherlands	23	1.4k 1.4×	289 0.4×	497 0.8×	92 0.6×	69 0.5×	50	2.2k
Joel A. Malek Qatar	30	1.9k 1.8×	825 1.2×	766 1.2×	86 0.6×	76 0.5×	77	3.2k
Miguel Pignatelli Spain	25	2.1k 2.0×	288 0.4×	590 0.9×	143 1.0×	142 1.0×	32	3.1k
Miria Ricchetti France	23	1.4k 1.4×	215 0.3×	340 0.5×	136 0.9×	88 0.6×	44	1.9k
Sun Shim Choi South Korea	27	1.3k 1.2×	187 0.3×	336 0.5×	140 1.0×	146 1.0×	75	2.3k
Yukiko Yamazaki Japan	38	2.7k 2.5×	758 1.1×	1.3k 2.0×	52 0.4×	138 1.0×	100	3.9k
Steve Hoffmann Germany	25	2.7k 2.5×	318 0.5×	580 0.9×	144 1.0×	207 1.4×	63	3.6k
Eric Haugen United States	25	3.7k 3.5×	668 1.0×	1.7k 2.6×	203 1.4×	112 0.8×	37	5.1k

Countries citing papers authored by David Ellinghaus

Since Specialization

Citations

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

Fields of papers citing papers by David Ellinghaus

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of David Ellinghaus

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

All Works

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20 of 20 papers shown

Schulte-Schrepping, Jonas, Florian Tran, Jan Taubenheim, et al.. (2025). P0092 Advancing precision medicine in IBD: Systematic evaluation of single-cell transcriptomics protocols for intestinal biopsies. Journal of Crohn s and Colitis. 19(Supplement_1). i460–i461. 1 indexed citations

Weiß, Stefan, et al.. (2024). Legal aspects of privacy-enhancing technologies in genome-wide association studies and their impact on performance and feasibility. Genome biology. 25(1). 154–154. 3 indexed citations

Wacker, Eike Matthias, Florian Uellendahl-Werth, Olaf Wolkenhauer, et al.. (2023). Whole blood RNA sequencing identifies transcriptional differences between primary sclerosing cholangitis and ulcerative colitis. JHEP Reports. 6(2). 100988–100988. 2 indexed citations

Ellinghaus, David. (2023). COVID-19 host genetics and ABO blood group susceptibility. SHILAP Revista de lepidopterología. 1. e10–e10. 1 indexed citations

Jung, Eun Suk, David Ellinghaus, Frauke Degenhardt, et al.. (2023). Genome-wide association analysis reveals the associations of NPHP4, TYW1-AUTS2 and SEMA6D for Behçet's disease and HLA-B*46:01 for its intestinal involvement. Digestive and Liver Disease. 56(6). 994–1001. 4 indexed citations

Xiong, Ying, Susanna Kullberg, Lori Garman, et al.. (2023). Sex differences in the genetics of sarcoidosis across European and African ancestry populations. Frontiers in Medicine. 10. 1132799–1132799. 7 indexed citations

Wienbrandt, Lars & David Ellinghaus. (2022). EagleImp : fast and accurate genome-wide phasing and imputation in a single tool. Bioinformatics. 38(22). 4999–5006. 2 indexed citations

Moitinho‐Silva, Lucas, Frauke Degenhardt, Elke Rodríguez, et al.. (2022). Host genetic factors related to innate immunity, environmental sensing and cellular functions are associated with human skin microbiota. Nature Communications. 13(1). 6204–6204. 39 indexed citations

Ellinghaus, David. (2022). How genetic risk contributes to autoimmune liver disease. Seminars in Immunopathology. 44(4). 397–410. 26 indexed citations

10.

Uellendahl-Werth, Florian, Markus Wolfien, André Franke, Olaf Wolkenhauer, & David Ellinghaus. (2020). A benchmark of hemoglobin blocking during library preparation for mRNA-Sequencing of human blood samples. Scientific Reports. 10(1). 5630–5630. 4 indexed citations

11.

Yadav, Pankaj, David Ellinghaus, Sandra Freitag‐Wolf, et al.. (2017). Genetic Factors Interact With Tobacco Smoke to Modify Risk for Inflammatory Bowel Disease in Humans and Mice. Gastroenterology. 153(2). 550–565. 60 indexed citations

12.

Ellinghaus, Eva, David Ellinghaus, Susanna Nikolaus, et al.. (2017). Genome-wide association analysis for chronic venous disease identifies EFEMP1 and KCNH8 as susceptibility loci. Scientific Reports. 7(1). 45652–45652. 45 indexed citations

13.

Dankowski, Theresa, Torsten Schröder, Steffen Möller, et al.. (2016). Male-specific association between MT-ND4 11719 A/G polymorphism and ulcerative colitis: a mitochondria-wide genetic association study. BMC Gastroenterology. 16(1). 118–118. 20 indexed citations

14.

Förster, Michael, Silke Szymczak, David Ellinghaus, et al.. (2015). Vy-PER: eliminating false positive detection of virus integration events in next generation sequencing data. Scientific Reports. 5(1). 11534–11534. 29 indexed citations

15.

Ellinghaus, David, Jörn Bethune, Britt‐Sabina Petersen, & André Franke. (2014). The genetics of Crohn’s disease and ulcerative colitis –status quoand beyond. Scandinavian Journal of Gastroenterology. 50(1). 13–23. 67 indexed citations

16.

Skiecevičienė, Jurgita, Gediminas Kiudelis, Eva Ellinghaus, et al.. (2013). Replication Study of Ulcerative Colitis Risk Loci in a Lithuanian–Latvian Case–Control Sample. Inflammatory Bowel Diseases. 19(11). 2349–2355. 11 indexed citations

17.

Förster, Michael, Peter Forster, Abdou ElSharawy, et al.. (2012). From next-generation sequencing alignments to accurate comparison and validation of single-nucleotide variants: the pibase software. Nucleic Acids Research. 41(1). e16–e16. 18 indexed citations

18.

Huang, Jie, David Ellinghaus, André Franke, Bryan Howie, & Yun Li. (2012). 1000 Genomes-based imputation identifies novel and refined associations for the Wellcome Trust Case Control Consortium phase 1 Data. European Journal of Human Genetics. 20(7). 801–805. 91 indexed citations

19.

Ellinghaus, David, Stefan Schreiber, André Franke, & Michael Nothnagel. (2009). Current software for genotype imputation. Human Genomics. 3(4). 371–80. 15 indexed citations

20.

Nothnagel, Michael, David Ellinghaus, Stefan Schreiber, Michael Krawczak, & André Franke. (2008). A comprehensive evaluation of SNP genotype imputation. Human Genetics. 125(2). 163–171. 111 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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