Ewa Rutkiewicz

401 total citations
12 papers, 268 citations indexed

About

Ewa Rutkiewicz is a scholar working on Pulmonary and Respiratory Medicine, Molecular Biology and Genetics. According to data from OpenAlex, Ewa Rutkiewicz has authored 12 papers receiving a total of 268 indexed citations (citations by other indexed papers that have themselves been cited), including 11 papers in Pulmonary and Respiratory Medicine, 3 papers in Molecular Biology and 3 papers in Genetics. Recurrent topics in Ewa Rutkiewicz's work include Cystic Fibrosis Research Advances (11 papers), Neonatal Respiratory Health Research (7 papers) and Genetic and Kidney Cyst Diseases (3 papers). Ewa Rutkiewicz is often cited by papers focused on Cystic Fibrosis Research Advances (11 papers), Neonatal Respiratory Health Research (7 papers) and Genetic and Kidney Cyst Diseases (3 papers). Ewa Rutkiewicz collaborates with scholars based in Poland, Germany and Switzerland. Ewa Rutkiewicz's co-authors include Andrzej Pogorzelski, Michał Witt, Ewa Ziętkiewicz, Katarzyna Voelkel, Zuzanna Bukowy‐Bieryłło, Barbara Klimek, Maciej Geremek, James F. Martin, Lucy Morgan and Maria Barcikowska and has published in prestigious journals such as PLoS ONE, Neurology and American Journal of Respiratory Cell and Molecular Biology.

In The Last Decade

Ewa Rutkiewicz

12 papers receiving 266 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Ewa Rutkiewicz Poland 8 171 108 106 31 23 12 268
Maciej Geremek Poland 10 113 0.7× 122 1.1× 110 1.0× 5 0.2× 15 0.7× 17 268
B. Kerem Israel 9 187 1.1× 55 0.5× 237 2.2× 8 0.3× 21 0.9× 12 456
Katsuya Hirata Japan 9 142 0.8× 40 0.4× 107 1.0× 9 0.3× 89 3.9× 40 314
Karen K. Deal United States 7 128 0.7× 70 0.6× 289 2.7× 19 0.6× 165 7.2× 12 450
Molly B. Sheridan United States 8 98 0.6× 137 1.3× 118 1.1× 5 0.2× 25 1.1× 11 281
A Joannard France 9 28 0.2× 41 0.4× 98 0.9× 27 0.9× 24 1.0× 34 208
Nada Quercia Canada 8 39 0.2× 95 0.9× 148 1.4× 5 0.2× 14 0.6× 17 256
Abeer Al Tuwaijri Saudi Arabia 12 49 0.3× 131 1.2× 230 2.2× 6 0.2× 30 1.3× 23 368
Giselda Maria Kalil de Cabello Brazil 12 77 0.5× 80 0.7× 57 0.5× 46 1.5× 18 0.8× 26 301
Angeliki Balassopoulou Greece 10 161 0.9× 59 0.5× 53 0.5× 18 0.6× 33 1.4× 16 328

Countries citing papers authored by Ewa Rutkiewicz

Since Specialization
Citations

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

Fields of papers citing papers by Ewa Rutkiewicz

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Ewa Rutkiewicz

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

All Works

12 of 12 papers shown
1.
Ziętkiewicz, Ewa, Zuzanna Bukowy‐Bieryłło, Patrycja Daca‐Roszak, et al.. (2019). CFAP300 : Mutations in Slavic Patients with Primary Ciliary Dyskinesia and a Role in Ciliary Dynein Arms Trafficking. American Journal of Respiratory Cell and Molecular Biology. 61(4). 440–449. 18 indexed citations
2.
Ziętkiewicz, Ewa, Ewa Rutkiewicz, Andrzej Pogorzelski, et al.. (2014). CFTR Mutations Spectrum and the Efficiency of Molecular Diagnostics in Polish Cystic Fibrosis Patients. PLoS ONE. 9(2). e89094–e89094. 20 indexed citations
3.
Ziętkiewicz, Ewa, Zuzanna Bukowy‐Bieryłło, Katarzyna Voelkel, et al.. (2012). Mutations in Radial Spoke Head Genes and Ultrastructural Cilia Defects in East-European Cohort of Primary Ciliary Dyskinesia Patients. PLoS ONE. 7(3). e33667–e33667. 37 indexed citations
4.
Bukowy‐Bieryłło, Zuzanna, Ewa Ziętkiewicz, Niki T. Loges, et al.. (2012). RPGR mutations might cause reduced orientation of respiratory cilia. Pediatric Pulmonology. 48(4). 352–363. 65 indexed citations
5.
Ziętkiewicz, Ewa, Katarzyna Voelkel, Ewa Rutkiewicz, et al.. (2010). Population specificity of the DNAI1 gene mutation spectrum in primary ciliary dyskinesia (PCD). Respiratory Research. 11(1). 174–174. 27 indexed citations
6.
Rutkiewicz, Ewa, et al.. (2007). Carrier status for 3 most frequentCFTR mutations in Polish PCD/KS patients: lack of association with the primary ciliary dyskinesia phenotype. Journal of Applied Genetics. 48(1). 85–88. 3 indexed citations
7.
Golańska, Ewa, Ewa Rutkiewicz, Maria Styczyńska, et al.. (2004). Polymorphisms within the prion (PrP) and prion-like protein (Doppel) genes in AD. Neurology. 62(2). 313–315. 35 indexed citations
8.
Walkowiak, Jarosław, Karl‐Heinz Herzig, Michał Witt, et al.. (2001). Analysis of exocrine pancreatic function in cystic fibrosis: one mild CFTR mutation does not exclude pancreatic insufficiency. European Journal of Clinical Investigation. 31(9). 796–801. 39 indexed citations
9.
Pogorzelski, Andrzej, et al.. (2001). Effect of genotype on selected clinical features of Polish cystic fibrosis adults.. PubMed. 42(3). 367–77. 2 indexed citations
10.
Pogorzelski, Andrzej, et al.. (2000). Partial CFTR genotyping and characterisation of cystic fibrosis patients with myocardial fibrosis and necrosis. Clinical Genetics. 57(1). 56–60. 16 indexed citations
11.
Witt, Michał, et al.. (1999). [Frequency of mutations and genotypes of the CFTR gene in cystic fibrosis adults in Poland].. PubMed. 67(3-4). 137–41. 5 indexed citations
12.

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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