Julia Wallmeier

3.0k citations

18 papers · 837 indexed · 1 hit paper · h-index 13

Impact in

Pulmonary and Respiratory Medicine top 5%
- Cystic Fibrosis Research Advances
- Neonatal Respiratory Health Research
- Tracheal and airway disorders
Genetics top 5%
- Genetic and Kidney Cyst Diseases

Papers in ⓘ

Pulmonary and Respiratory Medicine 13
- Cystic Fibrosis Research Advances 12
- Neonatal Respiratory Health Research 7
- Tracheal and airway disorders 3
- Medical Imaging and Pathology Studies 1
Genetics 11
- Genetic and Kidney Cyst Diseases 11

Co-authors: Heymut Omran (17 shared papers)Heike Olbrich (13 shared papers)Kim G. Nielsen (3 shared papers)Petra Pennekamp (11 shared papers)Niki T. Loges (11 shared papers)Margaret W. Leigh (2 shared papers)Claudia E. Kuehni (3 shared papers)Jane S. Lucas (3 shared papers)
Journals: Human Mutation (3 papers)The American Journal of Human Genetics (2 papers)European Respiratory Journal (2 papers)Annals of the American Thoracic Society (1 paper)Molecular Human Reproduction (1 paper)
Partner nations: Germany United States Denmark

In The Last Decade

Julia Wallmeier

18 papers receiving 830 citations

Hit Papers

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Motile ciliopathies 2020 · 204 citations

Peers

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-authors

The 25 scholars most cited alongside Julia Wallmeier, linked wherever they have co-authored with each other. Click a name or a connecting line to browse the papers they share.

Border = papers with Julia Wallmeier Line = papers co-authored together Julia Wallmeier links everyone, so they are left out of the graph.

All Works

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18 of 18 papers shown

#	Work
1	Motile ciliopathies Nature Reviews Disease Primers ·Julia Wallmeier, Kim G. Nielsen, Claudia E. Kuehni, Jane S. Lucas, Margaret W. Leigh, Maimoona A. Zariwala, Heymut Omran Hit paper breakdown →	2020	204
2	Ciliary beat pattern and frequency in genetic variants of primary ciliary dyskinesia European Respiratory Journal ·Johanna Raidt, Julia Wallmeier, Rim Hjeij, Jörg Große Onnebrink, Petra Pennekamp, Niki T. Loges, Heike Olbrich, Karsten Häffner, Gerard W. Dougherty, Heymut Omran, Claudius Werner	2014	123
3	ENT manifestations in patients with primary ciliary dyskinesia: prevalence and significance of otorhinolaryngologic co-morbidities European Archives of Oto-Rhino-Laryngology ·J. Ulrich Sommer, Kerstin Schäfer, Heymut Omran, Heike Olbrich, Julia Wallmeier, Andreas Blum, Karl Hörmann, Boris A. Stuck	2010	91
4	Loss-of-Function GAS8 Mutations Cause Primary Ciliary Dyskinesia and Disrupt the Nexin-Dynein Regulatory Complex The American Journal of Human Genetics ·Heike Olbrich, Carolin Cremers, Niki T. Loges, Claudius Werner, Kim G. Nielsen, June K. Marthin, Maria C. Philipsen, Julia Wallmeier, Petra Pennekamp, Tabea Menchen, Christine Edelbusch, Gerard W. Dougherty, Oliver Schwartz, Hölger Thiele, Janine Altmüller, Frank Rommelmann, Heymut Omran	2015	84
5	Systematic Analysis ofCCNOVariants in a Defined Population: Implications for Clinical Phenotype and Differential Diagnosis Human Mutation ·Israel Amirav, Julia Wallmeier, Niki T. Loges, Tabea Menchen, Petra Pennekamp, Huda Mussaffi, Revital Abitbul, Avraham Avital, Lea Bentur, Gerard W. Dougherty, Nael Elias, Moran Lavie, Heike Olbrich, Claudius Werner, Chris Kintner, Heymut Omran	2016	62
6	An international registry for primary ciliary dyskinesia European Respiratory Journal ·Claudius Werner, Martin Lablans, Maximilian Ataian, Johanna Raidt, Julia Wallmeier, Jörg Große-Onnebrink, Claudia E. Kuehni, Eric G. Haarman, Margaret W. Leigh, Alexandra L. Quittner, Jane S. Lucas, Claire Hogg, Michał Witt, Kostas Ν. Priftis, Panayiotis K. Yiallouros, Kim G. Nielsen, Francesca Santamaria, Frank Ückert, Heymut Omran	2015	55
7	Mutation of serine/threonine protein kinase 36 ( STK36 ) causes primary ciliary dyskinesia with a central pair defect Human Mutation ·Christine Edelbusch, Sandra Cindrić, Gerard W. Dougherty, Niki T. Loges, Heike Olbrich, Joseph Rivlin, Julia Wallmeier, Petra Pennekamp, Israel Amirav, Heymut Omran	2017	49
8	Motility of efferent duct cilia aids passage of sperm cells through the male reproductive system Molecular Human Reproduction ·Isabella Aprea, Tabea Nöthe-Menchen, Gerard W. Dougherty, Johanna Raidt, Niki T. Loges, Thomas Kaiser, Julia Wallmeier, Heike Olbrich, Timo Strünker, Sabine Kliesch, Petra Pennekamp, Heymut Omran	2021	45
9	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 ·Vijayashankaranarayanan Narasimhan, Rim Hjeij, Shubha Vij, Niki T. Loges, Julia Wallmeier, Cordula Koerner‐Rettberg, Claudius Werner, Surin Kumar Thamilselvam, Adrian Boey, Semil P. Choksi, Petra Pennekamp, Sudipto Roy, Heymut Omran	2014	35
10	Limitations of Nasal Nitric Oxide Measurement for Diagnosis of Primary Ciliary Dyskinesia with Normal Ultrastructure Annals of the American Thoracic Society ·Johanna Raidt, Henrike Krenz, Johannes Tebbe, Jörg Große-Onnebrink, Heike Olbrich, Niki T. Loges, Luisa Biebach, Christian Schmalstieg, Christina Keßler, Julia Wallmeier, Bernd Dworniczak, Petra Pennekamp, Martin Dugas, Claudius Werner, Heymut Omran	2022	21
11	Mutations in TP73 cause impaired mucociliary clearance and lissencephaly The American Journal of Human Genetics ·Julia Wallmeier, Diana Bracht, Hessa S. Alsaif, Gerard W. Dougherty, Heike Olbrich, Sandra Cindrić, Mark Dzietko, Christoph M. Heyer, Norbert Teig, Charlotte Thiels, Eissa Faqeih, Aqeela AlHashim, Sameena Khan, Ibrahim Mogarri, Mohammed Almannai, Wadha Al Otaibi, Fowzan S. Alkuraya, Cordula Koerner‐Rettberg, Heymut Omran	2021	21
12	Primary ciliary dyskinesia La Presse Médicale ·Johanna Raidt, Niki T. Loges, Heike Olbrich, Julia Wallmeier, Petra Pennekamp, Heymut Omran	2023	17
13	The role of cilia for hydrocephalus formation American Journal of Medical Genetics Part C Seminars in Medical Genetics ·Julia Wallmeier, Marlene Dallmayer, Heymut Omran	2022	17
14	DYNC2H1 mutation causes Jeune syndrome and recurrent lung infections associated with ciliopathy The Clinical Respiratory Journal ·Nagehan Emiralioğlu, Julia Wallmeier, Heike Olbrich, Heymut Omran, Uğur Özçelik	2017	9
15	An international patient-registry for primary ciliary dyskinesia Ktisis at Cyprus University of Technology (Cyprus University of Technology) ·Claudius Werner, Julia Wallmeier, Johanna Raidt, Claudia E. Kuehni, M.W. Leigh, Panayiotis K. Yiallouros, Jane S. Lucas, Martin Lablans, Frank Ueckert, Heyder Omran	2014	1
16	Optimizing the diagnostic approach for Primary Ciliary Dyskinesia with normal ultrastructure Johanna Raidt, Henrike Krenz, Johannes Tebbe, Jörg Große-Onnebrink, Heike Olbrich, Niki T. Loges, Luisa Biebach, Christian Schmalstieg, Christina Keßler, Julia Wallmeier, Bernd Dworniczak, Petra Pennekamp, Martin Dugas, Carsten Werner, Heymut Omran	2022	1
17	Identification of distinct ciliary beat pattern abnormalities by high-speed video microscopy in primary ciliary dyskinesia Johanna Raidt, Julia Wallmeier, Rim Hjeij, Jörg Große Onnebrink, Heike Olbrich, Niki T. Loges, Petra Pennekamp, Gerard W. Dougherty, Karsten Häffner, Heymut Omran, Claudius Werner	2015	1
18	Diagnosis of Primary Ciliary Dyskinesia: a multi-center experience Rim Hjeij, Sandra Cindrić, Heike Olbrich, Petra Pennekamp, Niki T. Loges, Gerard W. Dougherty, Julia Wallmeier, Johanna Raidt, Heymut Omran	2021	1

About Julia Wallmeier

Julia Wallmeier is a scholar working on Pulmonary and Respiratory Medicine, Genetics, Pediatrics, Perinatology and Child Health, Cellular and Molecular Neuroscience and Reproductive Medicine, having authored 18 papers that have together received 837 indexed citations. Recurring topics across this work include Cystic Fibrosis Research Advances (12 papers), Genetic and Kidney Cyst Diseases (11 papers), Neonatal Respiratory Health Research (7 papers), Cerebrospinal fluid and hydrocephalus (3 papers), Tracheal and airway disorders (3 papers), Fetal and Pediatric Neurological Disorders (2 papers), Epigenetics and DNA Methylation (2 papers) and Medical Imaging and Pathology Studies (1 paper). The work is most often cited by research in Pulmonary and Respiratory Medicine (504 citations), Genetics (413 citations), Otorhinolaryngology (33 citations), Cell Biology (77 citations) and Pediatrics, Perinatology and Child Health (91 citations). Julia Wallmeier has collaborated with scholars based in Germany, United States and Denmark. Frequent 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. Their work appears in journals such as Human Mutation, The American Journal of Human Genetics, European Respiratory Journal, Annals of the American Thoracic Society and Molecular Human Reproduction.

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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