Anna Stittrich

577 total citations
11 papers, 285 citations indexed

About

Anna Stittrich is a scholar working on Immunology, Genetics and Genetics. According to data from OpenAlex, Anna Stittrich has authored 11 papers receiving a total of 285 indexed citations (citations by other indexed papers that have themselves been cited), including 7 papers in Immunology, 5 papers in Genetics and 3 papers in Genetics. Recurrent topics in Anna Stittrich's work include Immunodeficiency and Autoimmune Disorders (5 papers), Genomics and Rare Diseases (2 papers) and Genomic variations and chromosomal abnormalities (2 papers). Anna Stittrich is often cited by papers focused on Immunodeficiency and Autoimmune Disorders (5 papers), Genomics and Rare Diseases (2 papers) and Genomic variations and chromosomal abnormalities (2 papers). Anna Stittrich collaborates with scholars based in Germany, United States and Austria. Anna Stittrich's co-authors include Gustavo Glusman, Jared C. Roach, Joseph G. Vockley, John E. Niederhuber, Dale L. Bodian, Terry Farrah, Wendy S.W. Wong, Jakob M. Goldmann, Christian Gilissen and Alexander Hoischen and has published in prestigious journals such as Nature Genetics, Frontiers in Immunology and Frontiers in Genetics.

In The Last Decade

Anna Stittrich

9 papers receiving 282 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Anna Stittrich Germany 6 141 123 44 38 30 11 285
Maria Paola Recalcati Italy 11 240 1.7× 191 1.6× 49 1.1× 13 0.3× 22 0.7× 21 378
Julie Scuffins United States 5 215 1.5× 123 1.0× 31 0.7× 41 1.1× 14 0.5× 10 348
Jakob M. Goldmann Netherlands 6 184 1.3× 180 1.5× 90 2.0× 13 0.3× 6 0.2× 7 355
Jean P. Pfotenhauer United States 8 156 1.1× 211 1.7× 16 0.4× 9 0.2× 20 0.7× 9 438
Alison Yeung Australia 11 283 2.0× 130 1.1× 38 0.9× 8 0.2× 11 0.4× 19 385
Xena Giada Pappalardo Italy 8 58 0.4× 170 1.4× 29 0.7× 24 0.6× 24 0.8× 32 263
Srinivasan Muthuswamy India 9 95 0.7× 140 1.1× 30 0.7× 18 0.5× 26 0.9× 29 391
Vanessa Rangel Miller United States 8 129 0.9× 113 0.9× 35 0.8× 7 0.2× 10 0.3× 10 249
Cíntia Fridman Brazil 15 455 3.2× 308 2.5× 16 0.4× 35 0.9× 24 0.8× 57 653
Imma Rost Germany 9 212 1.5× 157 1.3× 21 0.5× 20 0.5× 6 0.2× 24 322

Countries citing papers authored by Anna Stittrich

Since Specialization
Citations

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

Fields of papers citing papers by Anna Stittrich

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Anna Stittrich

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

All Works

11 of 11 papers shown
1.
2.
Körholz, Julia, Hye Sun Kuehn, Franziska Taube, et al.. (2024). IKAROS—how many feathers have you lost: mild and severe phenotypes in IKZF1 deficiency. Frontiers in Pediatrics. 12. 1345730–1345730.
3.
Meyer, Oliver, Carmen Scheibenbogen, Leif G. Hanitsch, et al.. (2023). Clinical and immunological characterisation of patients with common variable immunodeficiency related immune thrombocytopenia. Clinical and Experimental Medicine. 23(8). 5423–5432. 3 indexed citations
4.
Thee, Stephanie, V. Wahn, Nadine Unterwalder, et al.. (2023). Screening Newborns for Low T Cell Receptor Excision Circles (TRECs) Fails to Detect Immunodeficiency, Centromeric Instability, and Facial Anomalies Syndrome. The Journal of Allergy and Clinical Immunology In Practice. 11(9). 2872–2883. 3 indexed citations
5.
Paniskaki, Krystallenia, Moritz Anft, Constantin J. Thieme, et al.. (2022). Severe Acute Respiratory Syndrome Coronavirus 2 Cross-Reactive B and T Cell Responses in Kidney Transplant Patients. Transplantation Proceedings. 54(6). 1455–1464. 3 indexed citations
6.
Roch, Toralf, Ulrik Stervbo, Anna Stittrich, et al.. (2021). Robust hepatitis B vaccine-reactive T cell responses in failed humoral immunity. Molecular Therapy — Methods & Clinical Development. 21. 288–298. 7 indexed citations
7.
Steiner, Sophie, Jelka Hartwig, Franziska Sotzny, et al.. (2020). Autoimmunity-Related Risk Variants in PTPN22 and CTLA4 Are Associated With ME/CFS With Infectious Onset. Frontiers in Immunology. 11. 578–578. 38 indexed citations
8.
Hanitsch, Leif G., Kirsten Wittke, Anna Stittrich, Hans‐Dieter Volk, & Carmen Scheibenbogen. (2019). Interstitial Lung Disease Frequently Precedes CVID Diagnosis. Journal of Clinical Immunology. 39(8). 849–851. 9 indexed citations
9.
Goldmann, Jakob M., Wendy S.W. Wong, Michele Pinelli, et al.. (2016). Parent-of-origin-specific signatures of de novo mutations. Nature Genetics. 48(8). 935–939. 196 indexed citations
10.
Stittrich, Anna, J. R. Ashworth, Mude Shi, et al.. (2016). Genomic architecture of inflammatory bowel disease in five families with multiple affected individuals. Human Genome Variation. 3(1). 15060–15060. 11 indexed citations
11.
Glusman, Gustavo, Varsha Dhankani, Max Robinson, et al.. (2015). Identification of copy number variants in whole-genome data using Reference Coverage Profiles. Frontiers in Genetics. 6. 45–45. 15 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