Niki T. Loges

8.5k total citations
42 papers, 2.0k citations indexed

About

Niki T. Loges is a scholar working on Pulmonary and Respiratory Medicine, Genetics and Molecular Biology. According to data from OpenAlex, Niki T. Loges has authored 42 papers receiving a total of 2.0k indexed citations (citations by other indexed papers that have themselves been cited), including 26 papers in Pulmonary and Respiratory Medicine, 26 papers in Genetics and 17 papers in Molecular Biology. Recurrent topics in Niki T. Loges's work include Genetic and Kidney Cyst Diseases (25 papers), Cystic Fibrosis Research Advances (24 papers) and Neonatal Respiratory Health Research (11 papers). Niki T. Loges is often cited by papers focused on Genetic and Kidney Cyst Diseases (25 papers), Cystic Fibrosis Research Advances (24 papers) and Neonatal Respiratory Health Research (11 papers). Niki T. Loges collaborates with scholars based in Germany, United States and Switzerland. Niki T. Loges's co-authors include Heymut Omran, Heike Olbrich, Petra Pennekamp, Claudius Werner, Gerard W. Dougherty, Julia Wallmeier, Johanna Raidt, Manfred Fliegauf, Miriam Schmidts and Judit Horváth and has published in prestigious journals such as Nature Genetics, Development and American Journal of Respiratory and Critical Care Medicine.

In The Last Decade

Niki T. Loges

39 papers receiving 2.0k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Niki T. Loges Germany 22 1.1k 991 807 218 217 42 2.0k
Petra Pennekamp Germany 22 1.1k 1.0× 500 0.5× 1.1k 1.4× 218 1.0× 192 0.9× 51 2.1k
Miriam Schmidts Germany 19 931 0.8× 367 0.4× 990 1.2× 251 1.2× 164 0.8× 49 1.8k
Marie Legendre France 23 583 0.5× 503 0.5× 741 0.9× 104 0.5× 97 0.4× 82 1.6k
Manfred Fliegauf Germany 27 2.0k 1.8× 666 0.7× 2.0k 2.4× 450 2.1× 398 1.8× 47 3.3k
Michał Witt Poland 25 671 0.6× 607 0.6× 690 0.9× 46 0.2× 158 0.7× 87 1.7k
Karsten Häffner Germany 15 571 0.5× 413 0.4× 508 0.6× 75 0.3× 122 0.6× 33 1.1k
Tatsuro Ikeuchi Japan 28 869 0.8× 340 0.3× 1.4k 1.7× 232 1.1× 271 1.2× 106 2.6k
Bénédicte Duriez France 17 724 0.6× 291 0.3× 698 0.9× 69 0.3× 111 0.5× 25 1.5k
Årindam Majumdar United States 21 671 0.6× 448 0.5× 2.3k 2.9× 579 2.7× 379 1.7× 27 2.9k
Shalini N. Jhangiani United States 25 801 0.7× 128 0.1× 1.1k 1.3× 142 0.7× 115 0.5× 80 2.0k

Countries citing papers authored by Niki T. Loges

Since Specialization
Citations

This map shows the geographic impact of Niki T. Loges'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 Niki T. Loges with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Niki T. Loges more than expected).

Fields of papers citing papers by Niki T. Loges

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Niki T. Loges. 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 Niki T. Loges. The network helps show where Niki T. Loges may publish in the future.

Co-authorship network of co-authors of Niki T. Loges

This figure shows the co-authorship network connecting the top 25 collaborators of Niki T. Loges. A scholar is included among the top collaborators of Niki T. Loges 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 Niki T. Loges. Niki T. Loges 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.
Höben, Inga M., Alexander Wolter, Niki T. Loges, et al.. (2024). Primary Ciliary Dyskinesia Associated Disease-Causing Variants in CCDC39 and CCDC40 Cause Axonemal Absence of Inner Dynein Arm Heavy Chains DNAH1, DNAH6, and DNAH7. Cells. 13(14). 1200–1200. 2 indexed citations
2.
Raidt, Johanna, Niki T. Loges, Heike Olbrich, et al.. (2023). Primary ciliary dyskinesia. La Presse Médicale. 52(3). 104171–104171. 17 indexed citations
3.
Raidt, Johanna, Henrike Krenz, Johannes Tebbe, et al.. (2022). Limitations of Nasal Nitric Oxide Measurement for Diagnosis of Primary Ciliary Dyskinesia with Normal Ultrastructure. Annals of the American Thoracic Society. 19(8). 1275–1284. 21 indexed citations
4.
Aprea, Isabella, Johanna Raidt, Inga M. Höben, et al.. (2021). Defects in the cytoplasmic assembly of axonemal dynein arms cause morphological abnormalities and dysmotility in sperm cells leading to male infertility. PLoS Genetics. 17(2). e1009306–e1009306. 58 indexed citations
5.
Buers, Insa, Niki T. Loges, Yvonne Nitschke, et al.. (2020). Crisponi syndrome/cold-induced sweating syndrome type 2: Reprogramming of CS/CISS2 individual derived fibroblasts into three clones of one iPSC line. Stem Cell Research. 46. 101855–101855.
6.
Cindrić, Sandra, Gerard W. Dougherty, Heike Olbrich, et al.. (2019). SPEF2- and HYDIN -Mutant Cilia Lack the Central Pair–associated Protein SPEF2, Aiding Primary Ciliary Dyskinesia Diagnostics. American Journal of Respiratory Cell and Molecular Biology. 62(3). 382–396. 49 indexed citations
7.
Marthin, June K., Morten Dunø, Heymut Omran, et al.. (2019). Genetic profile, nasal Nitric Oxide and age at diagnosis in 60 Danish PCD patients. PA5004–PA5004. 1 indexed citations
8.
Edelbusch, Christine, Sandra Cindrić, Gerard W. Dougherty, et al.. (2017). Mutation of serine/threonine protein kinase 36 ( STK36 ) causes primary ciliary dyskinesia with a central pair defect. Human Mutation. 38(8). 964–969. 49 indexed citations
9.
Amirav, Israel, Julia Wallmeier, Niki T. Loges, et al.. (2016). Systematic Analysis ofCCNOVariants in a Defined Population: Implications for Clinical Phenotype and Differential Diagnosis. Human Mutation. 37(4). 396–405. 62 indexed citations
10.
Olbrich, Heike, Niki T. Loges, Claudius Werner, et al.. (2015). Loss-of-Function GAS8 Mutations Cause Primary Ciliary Dyskinesia and Disrupt the Nexin-Dynein Regulatory Complex. The American Journal of Human Genetics. 97(4). 546–554. 84 indexed citations
11.
Raidt, Johanna, Julia Wallmeier, Rim Hjeij, et al.. (2014). Ciliary beat pattern and frequency in genetic variants of primary ciliary dyskinesia. European Respiratory Journal. 44(6). 1579–1588. 123 indexed citations
12.
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
13.
Sandrock, Kirstin, et al.. (2011). Lethal phenotype of mice carrying aSept11null mutation. Biological Chemistry. 392(8-9). 779–781. 17 indexed citations
14.
Omran, Heymut & Niki T. Loges. (2009). Immunofluorescence Staining of Ciliated Respiratory Epithelial Cells. Methods in cell biology. 91. 123–133. 25 indexed citations
15.
Loges, Niki T., Heike Olbrich, Anita Becker-Heck, et al.. (2009). Deletions and Point Mutations of LRRC50 Cause Primary Ciliary Dyskinesia Due to Dynein Arm Defects. The American Journal of Human Genetics. 85(6). 883–889. 144 indexed citations
16.
Loges, Niki T., Heike Olbrich, Cornelia Klein, et al.. (2007). Further Evidence for a Somatic KRAS Mutation in a Pilocytic Astrocytoma. Neuropediatrics. 38(2). 61–63. 51 indexed citations
17.
Schwabe, Georg C., Katrin Hoffmann, Niki T. Loges, et al.. (2007). Primary ciliary dyskinesia associated with normal axoneme ultrastructure is caused by DNAH11 mutations. Human Mutation. 29(2). 289–298. 163 indexed citations
18.
Olbrich, Heike, Judit Horváth, Maimoona A. Zariwala, et al.. (2006). DNAH5 Mutations are a Common Cause of Primary Ciliary Dyskinesia with Outer Dynein Arm Defects. American Journal of Respiratory and Critical Care Medicine. 174(2). 120–126. 214 indexed citations
19.
Sass, Jörn Oliver, Heike Olbrich, Udo F. H. Engelke, et al.. (2006). Mutations in ACY1, the Gene Encoding Aminoacylase 1, Cause a Novel Inborn Error of Metabolism. The American Journal of Human Genetics. 78(3). 401–409. 63 indexed citations
20.
Olbrich, Heike, Judit Horváth, Andrea Fekete, et al.. (2006). Axonemal Localization of the Dynein Component DNAH5 Is Not Altered in Secondary Ciliary Dyskinesia. Pediatric Research. 59(3). 418–422. 27 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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