Niki T. Loges

8.5k citations

42 papers · 2.0k indexed · h-index 22

Genetics top 2%
Pulmonary and Respiratory Medicine top 2%
Molecular Biology top 10%
Cell Biology top 5%
Pediatrics, Perinatology and Child Health top 5%

Co-authors: Heymut Omran Heike Olbrich Petra Pennekamp Claudius Werner Gerard W. Dougherty Julia Wallmeier Johanna Raidt Manfred Fliegauf
Topics: Genetic and Kidney Cyst Diseases (25 papers)Cystic Fibrosis Research Advances (24 papers)Neonatal Respiratory Health Research (11 papers)
Cited by: Genetics Pulmonary and Respiratory Medicine Reproductive Medicine
Journals: Nature Genetics Development American Journal of Respiratory and Critical Care Medicine
Partner nations: Germany United States Switzerland

In The Last Decade

Niki T. Loges

39 papers receiving 2.0k citations

Peers

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

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20 of 20 papers shown

#	Work	Indexed citations
1	Primary Ciliary Dyskinesia Associated Disease-Causing Variants in CCDC39 and CCDC40 Cause Axonemal Absence of Inner Dynein Arm Heavy Chains DNAH1, DNAH6, and DNAH7 2024 ·Cells ·(unknown),Inga M. Höben,Alexander Wolter,Niki T. Loges,Heike Olbrich,Isabella Aprea,Bernd Dworniczak,Johanna Raidt,Heymut Omran	2
2	Pathogenic variants inCFAP46,CFAP54,CFAP74andCFAP221cause primary ciliary dyskinesia with a defective C1d projection of the central apparatus 2024 ·European Respiratory Journal ·Kai Wohlgemuth,(unknown),(unknown),Niki T. Loges,Johanna Raidt,(unknown),Sandra Cindrić,(unknown),(unknown),(unknown),Gerard W. Dougherty,Heike Olbrich,Petra Pennekamp,Bernd Dworniczak,Heymut Omran	1
3	Primary ciliary dyskinesia 2023 ·La Presse Médicale ·Johanna Raidt,Niki T. Loges,Heike Olbrich,Julia Wallmeier,Petra Pennekamp,Heymut Omran	17
4	Limitations of Nasal Nitric Oxide Measurement for Diagnosis of Primary Ciliary Dyskinesia with Normal Ultrastructure 2022 ·Annals of the American Thoracic Society ·Johanna Raidt,Henrike Krenz,Johannes Tebbe,Jörg Große-Onnebrink,Heike Olbrich,Niki T. Loges,(unknown),(unknown),Christina Keßler,Julia Wallmeier,Bernd Dworniczak,Petra Pennekamp,Martin Dugas,Claudius Werner,Heymut Omran	21
5	Defects in the cytoplasmic assembly of axonemal dynein arms cause morphological abnormalities and dysmotility in sperm cells leading to male infertility 2021 ·PLoS Genetics ·Isabella Aprea,Johanna Raidt,Inga M. Höben,Niki T. Loges,Tabea Nöthe-Menchen,Petra Pennekamp,Heike Olbrich,Thomas Kaiser,(unknown),Frank Tüttelmann,Judit Horváth,Maria Schubert,Claudia Krallmann,Sabine Kliesch,Heymut Omran	58
6	Generation of induced pluripotent stem cell lines from a Crisponi/Cold induced sweating syndrome type 1 individual 2020 ·Stem Cell Research ·(unknown),Niki T. Loges,Yvonne Nitschke,Inga M. Höben,Albrecht Röpke,Laura Crisponi,Heymut Omran,Frank Rutsch,Insa Buers	1
7	SPEF2- and HYDIN -Mutant Cilia Lack the Central Pair–associated Protein SPEF2, Aiding Primary Ciliary Dyskinesia Diagnostics 2019 ·American Journal of Respiratory Cell and Molecular Biology ·Sandra Cindrić,Gerard W. Dougherty,Heike Olbrich,Rim Hjeij,Niki T. Loges,Israel Amirav,(unknown),June K. Marthin,Kim G. Nielsen,Sivagurunathan Sutharsan,Johanna Raidt,Claudius Werner,Petra Pennekamp,Bernd Dworniczak,Heymut Omran	49
8	Severe pulmonary disease in an adult primary ciliary dyskinesia population in Brazil 2019 ·Scientific Reports ·(unknown),Fernando Augusto Lima Marson,Rodrigo Abensur Athanazio,Naomi Kondo Nakagawa,Mariângela Macchione,Niki T. Loges,Heymut Omran,Samia Zahi Rached,Carmen Sílvia Bertuzzo,Rafaël Stelmach,Paulo Hilário Nascimento Saldiva,José Dirceu Ribeiro,Marcus Herbert Jones,Thaís Mauad	16
9	Mutation of serine/threonine protein kinase 36 ( STK36 ) causes primary ciliary dyskinesia with a central pair defect 2017 ·Human Mutation ·Christine Edelbusch,Sandra Cindrić,Gerard W. Dougherty,Niki T. Loges,Heike Olbrich,Joseph Rivlin,Julia Wallmeier,Petra Pennekamp,Israel Amirav,Heymut Omran	49
10	Systematic Analysis ofCCNOVariants in a Defined Population: Implications for Clinical Phenotype and Differential Diagnosis 2016 ·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	62
11	Loss-of-Function GAS8 Mutations Cause Primary Ciliary Dyskinesia and Disrupt the Nexin-Dynein Regulatory Complex 2015 ·The American Journal of Human Genetics ·Heike Olbrich,(unknown),Niki T. Loges,Claudius Werner,Kim G. Nielsen,June K. Marthin,(unknown),Julia Wallmeier,Petra Pennekamp,Tabea Menchen,Christine Edelbusch,Gerard W. Dougherty,Oliver Schwartz,Hölger Thiele,Janine Altmüller,(unknown),Heymut Omran	84
12	Ciliary beat pattern and frequency in genetic variants of primary ciliary dyskinesia 2014 ·European Respiratory Journal ·Johanna Raidt,Julia Wallmeier,Rim Hjeij,(unknown),Petra Pennekamp,Niki T. Loges,Heike Olbrich,Karsten Häffner,Gerard W. Dougherty,Heymut Omran,Claudius Werner	123
13	Lethal phenotype of mice carrying aSept11null mutation 2011 ·Biological Chemistry ·(unknown),Kirstin Sandrock,Ingrid Bartsch,(unknown),Heymut Omran,Niki T. Loges,Barbara Zieger	17
14	Immunofluorescence Staining of Ciliated Respiratory Epithelial Cells 2009 ·Methods in cell biology ·Heymut Omran,Niki T. Loges	25
15	Deletions and Point Mutations of LRRC50 Cause Primary Ciliary Dyskinesia Due to Dynein Arm Defects 2009 ·The American Journal of Human Genetics ·Niki T. Loges,Heike Olbrich,Anita Becker-Heck,Karsten Häffner,(unknown),(unknown),Miriam Schmidts,Andreas Kispert,Maimoona A. Zariwala,Margaret W. Leigh,Michael R. Knowles,Hanswalter Zentgraf,Horst Seithe,Gudrun Nürnberg,Peter Nürnberg,Richard Reinhardt,Heymut Omran	144
16	Initiation and maturation of cilia-generated flow in newborn and postnatal mouse airway 2009 ·American Journal of Physiology-Lung Cellular and Molecular Physiology ·Richard Francis,Bishwanath Chatterjee,Niki T. Loges,Hanswalter Zentgraf,Heymut Omran,Cecilia Lo	39
17	Further Evidence for a Somatic KRAS Mutation in a Pilocytic Astrocytoma 2007 ·Neuropediatrics ·(unknown),(unknown),Niki T. Loges,Heike Olbrich,Cornelia Klein,T. Schäfer,Wolfram Scheurlen,Wolfgang Roggendorf,Cornelius Weiller,C. Niemeyer,Rudolf Korinthenberg,Stefan M. Pfister,Heymut Omran	51
18	Primary ciliary dyskinesia associated with normal axoneme ultrastructure is caused by DNAH11 mutations 2007 ·Human Mutation ·Georg C. Schwabe,Katrin Hoffmann,Niki T. Loges,(unknown),Colette Rossier,(unknown),Heike Olbrich,Manfred Fliegauf,Mike Failly,Uta Liebers,Mirella Collura,Gerhard Gaedicke,Stefan Mundlos,U. Wahn,Jean‐Louis Blouin,B. Niggemann,Heymut Omran,Stylianos E. Antonarakis,Lucia Bartoloni	163
19	DNAH5 Mutations are a Common Cause of Primary Ciliary Dyskinesia with Outer Dynein Arm Defects 2006 ·American Journal of Respiratory and Critical Care Medicine ·(unknown),Heike Olbrich,Judit Horváth,Maimoona A. Zariwala,Manfred Fliegauf,Niki T. Loges,Johannes H. Wildhaber,Peadar G. Noone,Marcus P. Kennedy,Stylianos E. Antonarakis,Jean-Louis Blouin,Lucia Bartoloni,Thomas Nüßlein,Peter Ahrens,Matthias Griese,Heiner Kuhl,Ralf Sudbrak,Michael R. Knowles,Richard Reinhardt,Heymut Omran	214
20	Mutations in ACY1, the Gene Encoding Aminoacylase 1, Cause a Novel Inborn Error of Metabolism 2006 ·The American Journal of Human Genetics ·Jörn Oliver Sass,(unknown),Heike Olbrich,Udo F. H. Engelke,Judit Horváth,Manfred Fliegauf,Niki T. Loges,Susanne Schweitzer‐Krantz,(unknown),(unknown),Andreas Kispert,Andrea Superti‐Furga,Ron A. Wevers,Heymut Omran	63

About Niki T. Loges

Niki T. Loges is a scholar working on Genetics, Pulmonary and Respiratory Medicine and Pediatrics, Perinatology and Child Health, having authored 42 papers that have together received 2.0k indexed citations. Recurring topics across this work include Genetic and Kidney Cyst Diseases (25 papers), Cystic Fibrosis Research Advances (24 papers) and Neonatal Respiratory Health Research (11 papers). The work is most often cited by research in Genetics (1.1k citations), Pulmonary and Respiratory Medicine (991 citations) and Reproductive Medicine (134 citations). Niki T. Loges has collaborated with scholars based in Germany, United States and Switzerland. Frequent 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. Their work appears in journals such as Nature Genetics, Development and American Journal of Respiratory and Critical Care Medicine.

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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