Nico Derichs

2.7k total citations · 1 hit paper
33 papers, 1.4k citations indexed

About

Nico Derichs is a scholar working on Pulmonary and Respiratory Medicine, Genetics and Surgery. According to data from OpenAlex, Nico Derichs has authored 33 papers receiving a total of 1.4k indexed citations (citations by other indexed papers that have themselves been cited), including 29 papers in Pulmonary and Respiratory Medicine, 4 papers in Genetics and 2 papers in Surgery. Recurrent topics in Nico Derichs's work include Cystic Fibrosis Research Advances (29 papers), Neonatal Respiratory Health Research (20 papers) and Tracheal and airway disorders (15 papers). Nico Derichs is often cited by papers focused on Cystic Fibrosis Research Advances (29 papers), Neonatal Respiratory Health Research (20 papers) and Tracheal and airway disorders (15 papers). Nico Derichs collaborates with scholars based in Germany, United Kingdom and United States. Nico Derichs's co-authors include Kevin W Southern, Isabelle Sermet‐Gaudelus, Terry B. White, Philip M. Farrell, Patrick R. Sosnay, Michelle S. Howenstine, Clement L. Ren, Margaret Rosenfeld, Susanna A. McColley and Michael J. Rock and has published in prestigious journals such as The FASEB Journal, The Journal of Pediatrics and Thorax.

In The Last Decade

Nico Derichs

32 papers receiving 1.4k citations

Hit Papers

Diagnosis of Cystic Fibrosis: Consensus Guidelines from t... 2017 2026 2020 2023 2017 100 200 300 400 500

Peers

Nico Derichs
Vicky A. LeGrys United States
Patrick R. Sosnay United States
John Massie Australia
Cori Daines United States
Hara Levy United States
Danieli B. Salinas United States
Khin M. Gyi United Kingdom
C Simard United States
Nico Derichs
Citations per year, relative to Nico Derichs Nico Derichs (= 1×) peers Michelle S. Howenstine

Countries citing papers authored by Nico Derichs

Since Specialization
Citations

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

Fields of papers citing papers by Nico Derichs

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Nico Derichs

This figure shows the co-authorship network connecting the top 25 collaborators of Nico Derichs. A scholar is included among the top collaborators of Nico Derichs 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 Nico Derichs. Nico Derichs 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.
Yaakov, Yasmin, Nico Derichs, Nicholas J. Simmonds, et al.. (2019). Nasal potential difference in suspected cystic fibrosis patients with 5T polymorphism. Journal of Cystic Fibrosis. 19(4). 627–631. 8 indexed citations
2.
Davies, Jane C., Silke van Koningsbruggen‐Rietschel, Pavel Dřevı́nek, et al.. (2019). GLPG1837, a CFTR potentiator, in p.Gly551Asp (G551D)-CF patients: An open-label, single-arm, phase 2a study (SAPHIRA1). Journal of Cystic Fibrosis. 18(5). 693–699. 22 indexed citations
3.
Farrell, Philip M., Terry B. White, Nico Derichs, Carlo Castellani, & Beryl J. Rosenstein. (2017). Cystic Fibrosis Diagnostic Challenges over 4 Decades: Historical Perspectives and Lessons Learned. The Journal of Pediatrics. 181. S16–S26. 23 indexed citations
4.
Taylor‐Cousar, Jennifer L., Nico Derichs, D. Elizabeth Tullis, et al.. (2017). Safety, Tolerability and early signs of efficacy with riociguat for the treatment of adult PHE508DEL homozygous cystic fibrosis patients: safety data from the RIO-CF study. Pediatric Pulmonology. 52. 1 indexed citations
5.
Sosnay, Patrick R., Terry B. White, Philip M. Farrell, et al.. (2017). Diagnosis of Cystic Fibrosis in Nonscreened Populations. The Journal of Pediatrics. 181. S52–S57.e2. 45 indexed citations
6.
Farrell, Philip M., Terry B. White, Clement L. Ren, et al.. (2017). Diagnosis of Cystic Fibrosis: Consensus Guidelines from the Cystic Fibrosis Foundation. Publisher. 3 indexed citations
7.
Cirilli, Natalia, Kevin W Southern, Roberto Buzzetti, et al.. (2017). Real life practice of sweat testing in Europe. Journal of Cystic Fibrosis. 17(3). 325–332. 19 indexed citations
8.
Farrell, Philip M., Terry B. White, Clement L. Ren, et al.. (2017). Diagnosis of Cystic Fibrosis: Consensus Guidelines from the Cystic Fibrosis Foundation. The Journal of Pediatrics. 181. S4–S15.e1. 566 indexed citations breakdown →
9.
Munck, À., Sarah Mayell, Anna Shawcross, et al.. (2015). Cystic Fibrosis Screen Positive, Inconclusive Diagnosis (CFSPID): A new designation and management recommendations for infants with an inconclusive diagnosis following newborn screening. Journal of Cystic Fibrosis. 14(6). 706–713. 123 indexed citations
10.
Beekman, Jeffrey M., Isabelle Sermet‐Gaudelus, K. De Boeck, et al.. (2014). CFTR functional measurements in human models for diagnosis, prognosis and personalized therapy. Journal of Cystic Fibrosis. 13(4). 363–372. 26 indexed citations
11.
Naehrlich, Lutz, Manfred Ballmann, Jane C. Davies, et al.. (2013). Nasal potential difference measurements in diagnosis of cystic fibrosis: An international survey. Journal of Cystic Fibrosis. 13(1). 24–28. 31 indexed citations
12.
Derichs, Nico. (2013). Targeting a genetic defect: cystic fibrosis transmembrane conductance regulator modulators in cystic fibrosis. European Respiratory Review. 22(127). 58–65. 83 indexed citations
13.
Hyde, Rebecca, Florian Länger, A. Simón, et al.. (2012). Immunochemical Analysis of Mutant CFTR in Lung Explants. Cellular Physiology and Biochemistry. 30(3). 587–595. 1 indexed citations
14.
Derichs, Nico, Byung‐Ju Jin, Yuanlin Song, Walter E. Finkbeiner, & A. S. Verkman. (2011). Hyperviscous airway periciliary and mucous liquid layers in cystic fibrosis measured by confocal fluorescence photobleaching. The FASEB Journal. 25(7). 2325–2332. 70 indexed citations
15.
Stanke, Frauke, Stephanie Tamm, B. Siebert, et al.. (2010). Functional analysis of F508del CFTR in native human colon. Biochimica et Biophysica Acta (BBA) - Molecular Basis of Disease. 1802(11). 1062–1069. 26 indexed citations
16.
Thiagarajah, Jay R., Yuanlin Song, Nico Derichs, & A. S. Verkman. (2010). Airway surface liquid depth imaged by surface laser reflectance microscopy. The Journal of General Physiology. 136(3). 353–362. 8 indexed citations
17.
Derichs, Nico, Javier Sanz, Thomas von Känel, et al.. (2010). Intestinal current measurement for diagnostic classification of patients with questionable cystic fibrosis: validation and reference data. Thorax. 65(7). 594–599. 105 indexed citations
18.
Wilschanski, Michael, Veronika Skalická, Patrick Lebecque, et al.. (2009). Phenotypic characterisation of patients with intermediate sweat chloride values: towards validation of the European diagnostic algorithm for cystic fibrosis. Thorax. 64(8). 683–691. 53 indexed citations
19.
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
20.
Dördelmann, Michael, Gunnar A. Rau, Daniela Bartels, et al.. (2008). Evaluation of portal venous gas detected by ultrasound examination for diagnosis of necrotising enterocolitis. Archives of Disease in Childhood Fetal & Neonatal. 94(3). F183–F187. 44 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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