Julia Wallmeier

3.0k total citations · 1 hit paper
18 papers, 837 citations indexed

About

Julia Wallmeier is a scholar working on Pulmonary and Respiratory Medicine, Genetics and Pediatrics, Perinatology and Child Health. According to data from OpenAlex, Julia Wallmeier has authored 18 papers receiving a total of 837 indexed citations (citations by other indexed papers that have themselves been cited), including 13 papers in Pulmonary and Respiratory Medicine, 11 papers in Genetics and 4 papers in Pediatrics, Perinatology and Child Health. Recurrent topics in Julia Wallmeier's work include Cystic Fibrosis Research Advances (12 papers), Genetic and Kidney Cyst Diseases (11 papers) and Neonatal Respiratory Health Research (7 papers). Julia Wallmeier is often cited by papers focused on Cystic Fibrosis Research Advances (12 papers), Genetic and Kidney Cyst Diseases (11 papers) and Neonatal Respiratory Health Research (7 papers). Julia Wallmeier collaborates with scholars based in Germany, Denmark and United States. Julia Wallmeier's co-authors include Heymut Omran, Heike Olbrich, Kim G. Nielsen, Petra Pennekamp, Niki T. Loges, Margaret W. Leigh, Claudia E. Kuehni, Jane S. Lucas, Gerard W. Dougherty and Maimoona A. Zariwala and has published in prestigious journals such as The American Journal of Human Genetics, European Respiratory Journal and Nature Reviews Disease Primers.

In The Last Decade

Julia Wallmeier

18 papers receiving 830 citations

Hit Papers

Motile ciliopathies 2020 2026 2022 2024 2020 50 100 150 200
What are hit papers?

Hit papers significantly outperform the citation benchmark for their cohort. A paper qualifies if it has ≥500 total citations, achieves ≥1.5× the top-1% citation threshold for papers in the same subfield and year (this is the minimum needed to enter the top 1%, not the average within it), or reaches the top citation threshold in at least one of its specific research topics.

  1. Motile ciliopathies
    2020 204 citations Julia Wallmeier, Kim G. Nielsen et al. Nature Reviews Disease Primers profile →

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Julia Wallmeier Germany 13 504 413 275 91 77 18 837
Brian P. Hackett United States 18 504 1.0× 359 0.9× 726 2.6× 89 1.0× 77 1.0× 24 1.2k
Anne-Marie Vojtek France 6 275 0.5× 251 0.6× 188 0.7× 37 0.4× 54 0.7× 6 473
Edmond G. Lemire Canada 14 142 0.3× 202 0.5× 240 0.9× 76 0.8× 51 0.7× 42 616
Carolyn Applegate United States 17 146 0.3× 270 0.7× 328 1.2× 43 0.5× 32 0.4× 24 821
Chia‐Cheng Hung Taiwan 19 94 0.2× 181 0.4× 310 1.1× 146 1.6× 11 0.1× 38 785
Josephine Wincent Sweden 12 75 0.1× 214 0.5× 243 0.9× 66 0.7× 18 0.2× 19 467
Emilie Falconnet Switzerland 15 99 0.2× 251 0.6× 409 1.5× 91 1.0× 11 0.1× 16 672
Marie‐José H. van den Boogaard Netherlands 13 77 0.2× 616 1.5× 552 2.0× 25 0.3× 19 0.2× 19 901
Pamela Brock United States 15 59 0.1× 286 0.7× 277 1.0× 45 0.5× 12 0.2× 39 712
Anita Wischmeijer Italy 16 96 0.2× 333 0.8× 260 0.9× 96 1.1× 32 0.4× 29 622

Countries citing papers authored by Julia Wallmeier

Since Specialization
Citations

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

Fields of papers citing papers by Julia Wallmeier

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Julia Wallmeier

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

All Works

18 of 18 papers shown
1.
Raidt, Johanna, Niki T. Loges, Heike Olbrich, et al.. (2023). Primary ciliary dyskinesia. La Presse Médicale. 52(3). 104171–104171. 17 indexed citations
2.
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
3.
Raidt, Johanna, Henrike Krenz, Johannes Tebbe, et al.. (2022). Optimizing the diagnostic approach for Primary Ciliary Dyskinesia with normal ultrastructure. 4564–4564. 1 indexed citations
4.
Wallmeier, Julia, Marlene Dallmayer, & Heymut Omran. (2022). The role of cilia for hydrocephalus formation. American Journal of Medical Genetics Part C Seminars in Medical Genetics. 190(1). 47–56. 17 indexed citations
5.
Wallmeier, Julia, Hessa S. Alsaif, Gerard W. Dougherty, et al.. (2021). Mutations in TP73 cause impaired mucociliary clearance and lissencephaly. The American Journal of Human Genetics. 108(7). 1318–1329. 21 indexed citations
6.
Aprea, Isabella, Tabea Nöthe-Menchen, Gerard W. Dougherty, et al.. (2021). Motility of efferent duct cilia aids passage of sperm cells through the male reproductive system. Molecular Human Reproduction. 27(3). 45 indexed citations
7.
Hjeij, Rim, Sandra Cindrić, Heike Olbrich, et al.. (2021). Diagnosis of Primary Ciliary Dyskinesia: a multi-center experience. OA1221–OA1221. 1 indexed citations
8.
Wallmeier, Julia, Kim G. Nielsen, Claudia E. Kuehni, et al.. (2020). Motile ciliopathies. Nature Reviews Disease Primers. 6(1). 77–77. 204 indexed citations breakdown →
9.
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
10.
Emiralioğlu, Nagehan, Julia Wallmeier, Heike Olbrich, Heymut Omran, & Uğur Özçelik. (2017). DYNC2H1 mutation causes Jeune syndrome and recurrent lung infections associated with ciliopathy. The Clinical Respiratory Journal. 12(3). 1017–1020. 9 indexed citations
11.
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
12.
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
13.
Werner, Claudius, Martin Lablans, Johanna Raidt, et al.. (2015). An international registry for primary ciliary dyskinesia. European Respiratory Journal. 47(3). 849–859. 55 indexed citations
14.
Raidt, Johanna, Julia Wallmeier, Rim Hjeij, et al.. (2015). Identification of distinct ciliary beat pattern abnormalities by high-speed video microscopy in primary ciliary dyskinesia. PA510–PA510. 1 indexed citations
15.
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
16.
Werner, Claudius, Julia Wallmeier, Johanna Raidt, et al.. (2014). An international patient-registry for primary ciliary dyskinesia. Ktisis at Cyprus University of Technology (Cyprus University of Technology). 1 indexed citations
17.
Hjeij, Rim, Shubha Vij, Niki T. Loges, et al.. (2014). Mutations in CCDC11, which Encodes a Coiled-Coil Containing Ciliary Protein, Causes Situs Inversus Due to Dysmotility of Monocilia in the Left-Right Organizer. Human Mutation. 36(3). 307–318. 35 indexed citations
18.
Sommer, J. Ulrich, Heymut Omran, Heike Olbrich, et al.. (2010). ENT manifestations in patients with primary ciliary dyskinesia: prevalence and significance of otorhinolaryngologic co-morbidities. European Archives of Oto-Rhino-Laryngology. 268(3). 383–388. 91 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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