Niki T. Loges

Klinik und Poliklinik für Kinder- und Jugendmedizin — Germany

Biochemistry, Genetics and Molecular Biology · Life Sciences

48h-index8.5kcitations110works5.32yr avg
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Research Topics

Genetic and Kidney Cyst Diseases(57), Cystic Fibrosis Research Advances(56), Neonatal Respiratory Health Research(26), Protist diversity and phylogeny(17), Tracheal and airway disorders(15)

Publications109 total

Rezessiv vererbter Mangel an sekretorischem WFDC2 (HE4) verursacht Nasenpolypen und Bronchiektasen
Klinische Pädiatrie·2025
A range of 30–62% of functioning multiciliated airway cells is sufficient to maintain ciliary airway clearance
Klinische Pädiatrie·2025
Pathogenic variants in CFAP46, CFAP54, CFAP74, and CFAP221 cause Primary Ciliary Dyskinesia with a defective C1d projection of the central apparatus
Klinische Pädiatrie·2025
Pathogenic variants in<i>CFAP46</i>,<i>CFAP54</i>,<i>CFAP74</i>and<i>CFAP221</i>cause primary ciliary dyskinesia with a defective C1d projection of the central apparatus
European Respiratory Journal·2024· 12 citedOpen Access
Late Breaking Abstract - Recessively inherited deficiency of secreted WFDC2 (HE4) causes nasal polyposis and bronchiectasis
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·2024· 12 citedOpen Access
A range of 30–62% of functioning multiciliated airway cells is sufficient to maintain ciliary airway clearance
European Respiratory Journal·2024· 10 citedOpen Access
Recessively Inherited Deficiency of Secreted WFDC2 (HE4) Causes Nasal Polyposis and Bronchiectasis
American Journal of Respiratory and Critical Care Medicine·2024· 14 citedOpen Access
Pathogene NEK10-Varianten verursachen PCD mit unauffälliger Ultrastruktur und schwerem pulmonalen Phänotyp
Klinische Pädiatrie·2024
Primary ciliary dyskinesia
La Presse Médicale·2023· 53 cited
Caffeine Citrate Increases Ciliary Beat Frequency in Human Respiratory Epithelial Cells
Preprints.org·2023· 1 citedOpen Access
Genetische und diagnostische Charakterisierung einer großen israelischen PCD-Kohorte – Notwendigkeit der geografischen Anpassungen der aktuellen diagnostischen Leitlinien?
Klinische Pädiatrie·2023
Pathogenic gene variants in CCDC39, CCDC40, RSPH1, RSPH9, HYDIN, and SPEF2 cause defects of sperm flagella composition and male infertility
Frontiers in Genetics·2023· 29 citedOpen Access
Optimizing the diagnostic approach for Primary Ciliary Dyskinesia with normal ultrastructure
10.01 - Respiratory infections and bronchiectasis·2022· 1 cited
Limitations of Nasal Nitric Oxide Measurement for Diagnosis of Primary Ciliary Dyskinesia with Normal Ultrastructure
Annals of the American Thoracic Society·2022· 30 cited
Diagnosis of Primary Ciliary Dyskinesia: a multi-center experience
2021· 1 cited
The international primary ciliary dyskinesia (PCD) registry reports genotype/phenotype-correlations
2021· 2 cited
Mutations of DNAH11 in patients with primary ciliary dyskinesia with normal ciliary ultrastructure
UNC Libraries·2021· 17 citedOpen Access
Defects in the cytoplasmic assembly of axonemal dynein arms cause morphological abnormalities and dysmotility in sperm cells leading to male infertility
PLoS Genetics·2021· 83 citedOpen Access
Motility of efferent duct cilia aids passage of sperm cells through the male reproductive system
Molecular Human Reproduction·2021· 64 citedOpen Access
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Frequent Co-authors

Heymut Omran(50), Heike Olbrich(43), Petra Pennekamp(25), Claudius Werner(24), Gerard W. Dougherty(22), Johanna Raidt(18), Julia Wallmeier(17), Rim Hjeij(16), Miriam Schmidts(13), Maimoona A. Zariwala(12), Michael R. Knowles(12), Israel Amirav(12), Margaret W. Leigh(11), Kim G. Nielsen(10), Hannah M. Mitchison(10), Manfred Fliegauf(8), Eddie M.K. Chung(8), Tabea Nöthe-Menchen(8), Richard Reinhardt(7), June K. Marthin(7)