Katja Hilbert

617 total citations
21 papers, 406 citations indexed

About

Katja Hilbert is a scholar working on Molecular Biology, Genetics and Immunology and Allergy. According to data from OpenAlex, Katja Hilbert has authored 21 papers receiving a total of 406 indexed citations (citations by other indexed papers that have themselves been cited), including 12 papers in Molecular Biology, 11 papers in Genetics and 5 papers in Immunology and Allergy. Recurrent topics in Katja Hilbert's work include Connective tissue disorders research (9 papers), Cell Adhesion Molecules Research (5 papers) and Fibroblast Growth Factor Research (3 papers). Katja Hilbert is often cited by papers focused on Connective tissue disorders research (9 papers), Cell Adhesion Molecules Research (5 papers) and Fibroblast Growth Factor Research (3 papers). Katja Hilbert collaborates with scholars based in Germany, Switzerland and United States. Katja Hilbert's co-authors include Bernhard Zabel, Andreas Winterpacht, Andrea Superti‐Furga, Jürgen W. Spranger, Heinz Decker, Hugo Segerer, J. Spranger, Thorsten Schweikardt, H Stöß and Andreas Zankl and has published in prestigious journals such as Nature Communications, The American Journal of Human Genetics and Frontiers in Immunology.

In The Last Decade

Katja Hilbert

20 papers receiving 401 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Katja Hilbert Germany 11 218 178 63 56 43 21 406
Darwin J. Prockop United States 9 216 1.0× 191 1.1× 77 1.2× 123 2.2× 55 1.3× 10 504
K.B.C. Apparao United States 10 163 0.7× 216 1.2× 65 1.0× 76 1.4× 11 0.3× 13 1.1k
Melinda Jen United States 10 132 0.6× 48 0.3× 24 0.4× 60 1.1× 52 1.2× 31 441
Melanie Timmen Germany 10 183 0.8× 47 0.3× 31 0.5× 44 0.8× 19 0.4× 18 301
Robert Lawrence United Kingdom 10 192 0.9× 236 1.3× 302 4.8× 58 1.0× 18 0.4× 16 880
Merry Z. C. Ruan United States 9 282 1.3× 101 0.6× 35 0.6× 281 5.0× 14 0.3× 15 603
Mingli Feng United States 5 208 1.0× 53 0.3× 32 0.5× 12 0.2× 16 0.4× 5 402
M Larrègue France 15 252 1.2× 173 1.0× 30 0.5× 49 0.9× 105 2.4× 117 736
Vincent Gâtinois France 11 269 1.2× 279 1.6× 36 0.6× 28 0.5× 12 0.3× 28 600
Ana Coelho Sweden 9 126 0.6× 111 0.6× 98 1.6× 10 0.2× 22 0.5× 14 302

Countries citing papers authored by Katja Hilbert

Since Specialization
Citations

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

Fields of papers citing papers by Katja Hilbert

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Katja Hilbert

This figure shows the co-authorship network connecting the top 25 collaborators of Katja Hilbert. A scholar is included among the top collaborators of Katja Hilbert 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 Katja Hilbert. Katja Hilbert 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.
Hilbert, Katja, Till Birkner, Theda Ulrike Patricia Bartolomaeus, et al.. (2025). CFTR modulator therapy drives microbiome restructuring through improved host physiology in cystic fibrosis: the IMMProveCF phase IV trial. Nature Communications. 16(1). 10111–10111.
2.
Islan, Germán A., Katja Hilbert, Paul M. Schneider, et al.. (2025). mRNA-LNP vaccine strategies: Effects of adjuvants on non-parenchymal liver cells and tolerance. Molecular Therapy — Methods & Clinical Development. 33(1). 101427–101427. 1 indexed citations
3.
Jarquín‐Díaz, Víctor Hugo, Katja Hilbert, Daniel Pfirrmann, et al.. (2023). Resilience and stability of the CF- intestinal and respiratory microbiome during nutritional and exercise intervention. BMC Microbiology. 23(1). 44–44. 5 indexed citations
4.
Gröndahl, Britta, et al.. (2022). Long-Term, CD4+ Memory T Cell Response to SARS-CoV-2. Frontiers in Immunology. 13. 800070–800070. 10 indexed citations
5.
Ferretti, Pamela, Claudius U. Meyer, Katja Hilbert, et al.. (2022). Meconium Microbiome of Very Preterm Infants across Germany. mSphere. 7(1). e0080821–e0080821. 22 indexed citations
6.
Cacicedo, Maximiliano L., Katja Hilbert, Nigel Horscroft, et al.. (2022). Phenylalanine hydroxylase mRNA rescues the phenylketonuria phenotype in mice. Frontiers in Bioengineering and Biotechnology. 10. 993298–993298. 22 indexed citations
7.
Gröndahl, Britta, Katja Hilbert, Wolfgang Kohnen, et al.. (2020). Containment of a Large SARS-CoV-2 Outbreak Among Healthcare Workers in a Pediatric Intensive Care Unit. The Pediatric Infectious Disease Journal. 39(11). e336–e339. 8 indexed citations
8.
Lausch, Ekkehart, Katja Hilbert, Valérie Cormier‐Daire, et al.. (2009). Mutations in MMP9 and MMP13 Determine the Mode of Inheritance and the Clinical Spectrum of Metaphyseal Anadysplasia. The American Journal of Human Genetics. 85(3). 420–420. 1 indexed citations
9.
Lausch, Ekkehart, Katja Hilbert, Valérie Cormier‐Daire, et al.. (2009). Mutations in MMP9 and MMP13 Determine the Mode of Inheritance and the Clinical Spectrum of Metaphyseal Anadysplasia. The American Journal of Human Genetics. 85(2). 168–178. 49 indexed citations
10.
Szczałuba, Krzysztof, Katja Hilbert, Ewa Obersztyn, et al.. (2005). Du Pan syndrome phenotype caused by heterozygous pathogenic mutations in CDMP1 gene. American Journal of Medical Genetics Part A. 138A(4). 379–383. 26 indexed citations
11.
Zankl, Andreas, Luitgard M. Neumann, Peter G. J. Nikkels, et al.. (2005). Dominant negative mutations in the C-propeptide of COL2A1 cause platyspondylic lethal skeletal dysplasia, torrance type, and define a novel subfamily within the type 2 collagenopathies. American Journal of Medical Genetics Part A. 133A(1). 61–67. 39 indexed citations
12.
Zankl, Andreas, Bernhard Zabel, Katja Hilbert, et al.. (2004). Spondyloperipheral dysplasia is caused by truncating mutations in the C‐propeptide of COL2A1. American Journal of Medical Genetics Part A. 129A(2). 144–148. 29 indexed citations
13.
Enklaar, Thorsten, Monika Oswald, Katja Hilbert, et al.. (2000). Mtr1, a Novel Biallelically Expressed Gene in the Center of the Mouse Distal Chromosome 7 Imprinting Cluster, is a Member of the Trp Gene Family. Genomics. 67(2). 179–187. 35 indexed citations
14.
Spranger, J., et al.. (1998). Hypochondroplasie, Achondroplasie und thanatophore Dysplasie als Folge von Mutationen des Fibroblastenwachstumsfaktorrezeptor-3-Gens (FGFR3). Monatsschrift Kinderheilkunde. 146(7). 687–691. 4 indexed citations
15.
Hilbert, Katja, et al.. (1997). Human fibroblast growth factor receptor 3 gene (FGFR3): genomic sequence and primer set information for gene analysis. Human Genetics. 100(2). 215–219. 24 indexed citations
16.
Zabel, Bernhard, Katja Hilbert, H Stöß, et al.. (1996). A specific collagen type II gene (COL2A1) mutation presenting as spondyloperipheral dysplasia. American Journal of Medical Genetics. 63(1). 123–128. 35 indexed citations
17.
Zabel, Bernhard, Katja Hilbert, H Stöß, et al.. (1996). A specific collagen type II gene (COL2A1) mutation presenting as spondyloperipheral dysplasia. American Journal of Medical Genetics. 63(1). 123–128. 1 indexed citations
18.
Wildhardt, G., et al.. (1996). Two different PAX3 gene mutations causing Waardenburg syndrome type I. Molecular and Cellular Probes. 10(3). 229–231. 9 indexed citations
19.
Winterpacht, Andreas, Katja Hilbert, Ulrike Schwarze, & Bernhard Zabel. (1995). Non-radioactive multiplex-SSCP analysis: detection of a new type II procollagen gene (COL2A1) mutation. Human Genetics. 95(4). 437–9. 10 indexed citations
20.
Bahn, Andrew, et al.. (1995). Selection of a precore mutant after vertical transmission of different hepatitis B virus variants is correlated with fulminant hepatitis in infants. Journal of Medical Virology. 47(4). 336–341. 21 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.

Explore authors with similar magnitude of impact

Breakdown of academic impact, for papers by Darwin J. Prockop Breakdown of academic impact, for papers by K.B.C. Apparao Breakdown of academic impact, for papers by Melinda Jen Breakdown of academic impact, for papers by Melanie Timmen Breakdown of academic impact, for papers by Robert Lawrence Breakdown of academic impact, for papers by Merry Z. C. Ruan Breakdown of academic impact, for papers by Mingli Feng Breakdown of academic impact, for papers by M Larrègue Breakdown of academic impact, for papers by Vincent Gâtinois Breakdown of academic impact, for papers by Ana Coelho
Rankless by CCL
2026