Baerbel Keller

4.2k total citations
32 papers, 1.0k citations indexed

About

Baerbel Keller is a scholar working on Immunology, Genetics and Pulmonary and Respiratory Medicine. According to data from OpenAlex, Baerbel Keller has authored 32 papers receiving a total of 1.0k indexed citations (citations by other indexed papers that have themselves been cited), including 31 papers in Immunology, 5 papers in Genetics and 4 papers in Pulmonary and Respiratory Medicine. Recurrent topics in Baerbel Keller's work include Immunodeficiency and Autoimmune Disorders (29 papers), Immune Cell Function and Interaction (24 papers) and T-cell and B-cell Immunology (17 papers). Baerbel Keller is often cited by papers focused on Immunodeficiency and Autoimmune Disorders (29 papers), Immune Cell Function and Interaction (24 papers) and T-cell and B-cell Immunology (17 papers). Baerbel Keller collaborates with scholars based in Germany, Israel and Switzerland. Baerbel Keller's co-authors include Klaus Warnatz, Hermann Eibel, Sigune Goldacker, Mirzokhid Rakhmanov, Sylvia Gutenberger, Christian Foerster, Susanne Unger, Polina Stepensky, Nadine Voelxen and Hans‐Hartmut Peter and has published in prestigious journals such as Proceedings of the National Academy of Sciences, Nature Communications and The Journal of Experimental Medicine.

In The Last Decade

Baerbel Keller

31 papers receiving 1.0k citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Baerbel Keller Germany	18	915	274	150	118	92	32	1.0k
Moritz Braun Germany	6	757 0.8×	212 0.8×	127 0.8×	121 1.0×	82 0.9×	9	860
Mirzokhid Rakhmanov Germany	7	703 0.8×	222 0.8×	91 0.6×	115 1.0×	54 0.6×	15	789
Catharina Schuetz Germany	15	504 0.6×	223 0.8×	85 0.6×	60 0.5×	129 1.4×	51	784
Sylvia Gutenberger Germany	9	610 0.7×	204 0.7×	96 0.6×	106 0.9×	52 0.6×	13	713
Patricia Lugar United States	11	528 0.6×	116 0.4×	86 0.6×	70 0.6×	81 0.9×	26	831
Barbara H. Barendregt Netherlands	14	389 0.4×	147 0.5×	94 0.6×	50 0.4×	93 1.0×	18	674
A. David B. Webster United Kingdom	18	702 0.8×	295 1.1×	198 1.3×	164 1.4×	108 1.2×	20	1.0k
Elizabeth Garabedian United States	16	506 0.6×	258 0.9×	75 0.5×	89 0.8×	108 1.2×	35	843
Torsten Witte Germany	19	708 0.8×	113 0.4×	52 0.3×	66 0.6×	91 1.0×	50	965
Yen-Shing Ng United States	9	1.2k 1.3×	292 1.1×	303 2.0×	34 0.3×	83 0.9×	9	1.5k

Countries citing papers authored by Baerbel Keller

Since Specialization

Citations

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

Fields of papers citing papers by Baerbel Keller

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Baerbel Keller

This figure shows the co-authorship network connecting the top 25 collaborators of Baerbel Keller. A scholar is included among the top collaborators of Baerbel Keller 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 Baerbel Keller. Baerbel Keller 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

Andrieux, Geoffroy, Andrea Maul‐Pavicic, Sigune Goldacker, et al.. (2025). CD21low B cells reveal a unique glycosylation pattern with hypersialylation and hyperfucosylation. Frontiers in Immunology. 16. 1512279–1512279.

Rodríguez‐Ubreva, Javier, Josep Calafell-Segura, Baerbel Keller, et al.. (2024). COVID-19 progression and convalescence in common variable immunodeficiency patients show dysregulated adaptive immune responses and persistent type I interferon and inflammasome activation. Nature Communications. 15(1). 10344–10344. 1 indexed citations

Keller, Baerbel, Shlomit Kfir‐Erenfeld, Frederike A. Hartl, et al.. (2023). Combined Immunodeficiency Caused by a Novel Nonsense Mutation in LCK. Journal of Clinical Immunology. 44(1). 4–4. 4 indexed citations

Keller, Baerbel & Klaus Warnatz. (2023). T-bethighCD21low B cells: the need to unify our understanding of a distinct B cell population in health and disease. Current Opinion in Immunology. 82. 102300–102300. 18 indexed citations

Unger, Susanne, Baerbel Keller, Mirzokhid Rakhmanov, et al.. (2021). Bronchoalveolar Lavage Fluid Reflects a TH1-CD21low B-Cell Interaction in CVID-Related Interstitial Lung Disease. Frontiers in Immunology. 11. 616832–616832. 17 indexed citations

Rojas‐Restrepo, Jessica, Andrés Caballero-Oteyza, Manfred Fliegauf, et al.. (2021). Establishing the Molecular Diagnoses in a Cohort of 291 Patients With Predominantly Antibody Deficiency by Targeted Next-Generation Sequencing: Experience From a Monocentric Study. Frontiers in Immunology. 12. 786516–786516. 23 indexed citations

Voll, Reinhard, et al.. (2020). Naive- and Memory-like CD21low B Cell Subsets Share Core Phenotypic and Signaling Characteristics in Systemic Autoimmune Disorders. The Journal of Immunology. 205(8). 2016–2025. 30 indexed citations

Krüger, Renate, Ulrich Baumann, Stephan Borte, et al.. (2019). Impaired polysaccharide responsiveness without agammaglobulinaemia in three patients with hypomorphic mutations in Bruton Tyrosine Kinase—No detection by newborn screening for primary immunodeficiencies. Scandinavian Journal of Immunology. 91(1). e12811–e12811. 6 indexed citations

Stepensky, Polina, Baerbel Keller, Oded Shamriz, et al.. (2018). T+ NK+ IL-2 Receptor γ Chain Mutation: a Challenging Diagnosis of Atypical Severe Combined Immunodeficiency. Journal of Clinical Immunology. 38(4). 527–536. 12 indexed citations

10.

Breuer, Oded, Hagit Daum, Malena Cohen‐Cymberknoh, et al.. (2017). Autosomal dominant gain of function STAT1 mutation and severe bronchiectasis. Respiratory Medicine. 126. 39–45. 20 indexed citations

11.

Keller, Baerbel, et al.. (2017). Preferential Reduction of Circulating Innate Lymphoid Cells Type 2 in Patients with Common Variable Immunodeficiency with Secondary Complications Is Part of a Broader Immune Dysregulation. Journal of Clinical Immunology. 37(8). 759–769. 5 indexed citations

12.

Unger, Susanne, Maximilian Seidl, Pauline A. van Schouwenburg, et al.. (2017). The TH1 phenotype of follicular helper T cells indicates an IFN-γ–associated immune dysregulation in patients with CD21low common variable immunodeficiency. Journal of Allergy and Clinical Immunology. 141(2). 730–740. 95 indexed citations

13.

Nabhani, Schafiq, Hagit Miskin, Carina Levin, et al.. (2017). STAT3 gain-of-function mutations associated with autoimmune lymphoproliferative syndrome like disease deregulate lymphocyte apoptosis and can be targeted by BH3 mimetic compounds. Clinical Immunology. 181. 32–42. 33 indexed citations

14.

Keller, Baerbel, Irina Zaidman, O. Sascha Yousefi, et al.. (2016). Early onset combined immunodeficiency and autoimmunity in patients with loss-of-function mutation in LAT. The Journal of Experimental Medicine. 213(7). 1185–1199. 44 indexed citations

15.

Stepensky, Polina, Baerbel Keller, Oded Shamriz, et al.. (2016). Deep intronic mis-splicing mutation in JAK3 gene underlies T − B + NK − severe combined immunodeficiency phenotype. Clinical Immunology. 163. 91–95. 13 indexed citations

16.

NaserEddin, Adeeb, Oded Shamriz, Baerbel Keller, et al.. (2015). Enteroviral Infection in a Patient with BLNK Adaptor Protein Deficiency. Journal of Clinical Immunology. 35(4). 356–360. 14 indexed citations

17.

Stepensky, Polina, Baerbel Keller, Mary Buchta, et al.. (2013). Deficiency of caspase recruitment domain family, member 11 (CARD11), causes profound combined immunodeficiency in human subjects. Journal of Allergy and Clinical Immunology. 131(2). 477–485.e1. 121 indexed citations

18.

Warnatz, Klaus, Baerbel Keller, Mary Buchta, et al.. (2013). Human CARD11 deficiency causes profound combined immunodeficiency (P3325). The Journal of Immunology. 190(Supplement_1). 175.10–175.10. 1 indexed citations

19.

Foerster, Christian, Nadine Voelxen, Mirzokhid Rakhmanov, et al.. (2010). B Cell Receptor-Mediated Calcium Signaling Is Impaired in B Lymphocytes of Type Ia Patients with Common Variable Immunodeficiency. The Journal of Immunology. 184(12). 7305–7313. 56 indexed citations

20.

Rakhmanov, Mirzokhid, Baerbel Keller, Sylvia Gutenberger, et al.. (2009). Circulating CD21 ^low B cells in common variable immunodeficiency resemble tissue homing, innate-like B cells. Proceedings of the National Academy of Sciences. 106(32). 13451–13456. 261 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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