Ulrike Laabs

460 total citations
7 papers, 347 citations indexed

About

Ulrike Laabs is a scholar working on Pulmonary and Respiratory Medicine, Genetics and Speech and Hearing. According to data from OpenAlex, Ulrike Laabs has authored 7 papers receiving a total of 347 indexed citations (citations by other indexed papers that have themselves been cited), including 6 papers in Pulmonary and Respiratory Medicine, 2 papers in Genetics and 2 papers in Speech and Hearing. Recurrent topics in Ulrike Laabs's work include Cystic Fibrosis Research Advances (6 papers), Tracheal and airway disorders (3 papers) and Dysphagia Assessment and Management (2 papers). Ulrike Laabs is often cited by papers focused on Cystic Fibrosis Research Advances (6 papers), Tracheal and airway disorders (3 papers) and Dysphagia Assessment and Management (2 papers). Ulrike Laabs collaborates with scholars based in Germany, Netherlands and United States. Ulrike Laabs's co-authors include Henk J. Veeze, Frauke Mekus, Burkhard Tümmler, Manfred Ballmann, Jan Bijman, Inez Bronsveld, Dicky Halley, Hugo R. de Jonge, G. Mastella and Helmut Ellemunter and has published in prestigious journals such as Journal of Clinical Investigation, Gastroenterology and Gene.

In The Last Decade

Ulrike Laabs

7 papers receiving 345 citations

Peers

Ulrike Laabs

PRM

MB

GENET

MM

PHYSI

Frauke Mekus Germany

Ron Gibson United States

Joy Lemm United States

Chandra L. Shrestha United States

Cameron B. Morrison United States

Erica A. Roesch United States

Adelina Amorim Portugal

Katherine L. Tuggle United States

Lela Olds United States

B Strunge Denmark

Frauke Mekus Germany

Ulrike Laabs

436 ×1.6

PRM

114 ×1.4

MB

67 ×1.7

GENET

14 ×0.4

MM

37 ×1.0

PHYSI

Citations per year, relative to Ulrike Laabs Ulrike Laabs (= 1×) peers Frauke Mekus

Countries citing papers authored by Ulrike Laabs

Since Specialization

Citations

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

Fields of papers citing papers by Ulrike Laabs

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Ulrike Laabs

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

All Works

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7 of 7 papers shown

1.

Stanke, Frauke, Tim Becker, Vinod Kumar, et al.. (2010). Genes that determine immunology and inflammation modify the basic defect of impaired ion conductance in cystic fibrosis epithelia. Journal of Medical Genetics. 48(1). 24–31. 55 indexed citations

2.

Stanke, Frauke, Manfred Ballmann, Inez Bronsveld, et al.. (2008). Diversity of the basic defect of homozygous CFTR mutation genotypes in humans. Journal of Medical Genetics. 45(1). 47–54. 30 indexed citations

3.

Kong, Kok‐Fai, Suriya Jayawardena, Lutz Wiehlmann, et al.. (2005). Characterization of poxB, a chromosomal-encoded Pseudomonas aeruginosa oxacillinase. Gene. 358. 82–92. 38 indexed citations

4.

Mekus, Frauke, Ulrike Laabs, Henk J. Veeze, & Burkhard Tümmler. (2003). Genes in the vicinity of CFTR modulate the cystic fibrosis phenotype in highly concordant or discordant F508del homozygous sib pairs. Human Genetics. 112(1). 1–11. 34 indexed citations

5.

Bronsveld, Inez, Frauke Mekus, Jan Bijman, et al.. (2001). Chloride conductance and genetic background modulate the cystic fibrosis phenotype of ΔF508 homozygous twins and siblings. Journal of Clinical Investigation. 108(11). 1705–1715. 111 indexed citations

6.

Bronsveld, Inez, Frauke Mekus, Jan Bijman, et al.. (2001). Chloride conductance and genetic background modulate the cystic fibrosis phenotype of ΔF508 homozygous twins and siblings. Journal of Clinical Investigation. 108(11). 1705–1715. 9 indexed citations

7.

Bronsveld, Inez, Frauke Mekus, Jan Bijman, et al.. (2000). Residual chloride secretion in intestinal tissue of ΔF508 homozygous twins and siblings with cystic fibrosis. Gastroenterology. 119(1). 32–40. 70 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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