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Niki T. Loges

Observed names: Loges, N., Loges, N.T., Loges, Niki T, Loges, Niki T., Loges, Niki Tomas, N Loges, N T Loges, N. Loges, N. T. Loges, N.T. Loges, NT Loges, Niki Loges, Niki Loges T. Loges, Niki T Loges, Niki Tomas Loges, Niki Tomas Loges (7585775), Niki T. Loges
Observed institutions: University of North Carolina at Chapel Hill, University of Geneva, University of Freiburg, The University of Melbourne, Princeton University, University of Münster, Concord Repatriation General Hospital, The Royal Free Hospital, University Medical Center Freiburg, University Hospital Münster, University Hospital of Geneva, University Children's Hospital Zurich, Max Planck Institute for Molecular Genetics, Klinik für Neuropädiatrie und Muskelerkrankungen, Ludwig-Maximilians-Universität München, Ruhr University Bochum
ORCID: 0000-0002-1534-2105
Observed ORCID: 0000-0002-1534-2105
OpenAlex ID: A5087055286
Ktu/PF13 is required for cytoplasmic pre-assembly of axonemal dyneins
2008 · Heymut Omran, Daisuke Kobayashi, et al. · Nature · 370
DNAH5 Mutations are a Common Cause of Primary Ciliary Dyskinesia with Outer Dynein Arm Defects
2006 · Nada Hornef, Heike Olbrich, et al. · American Journal of Respiratory and Critical Care Medicine · 353
CCDC39 is required for assembly of inner dynein arms and the dynein regulatory complex and for normal ciliary motility in humans and dogs
2010 · Anne-Christine Merveille, Erica E Davis, et al. · Nature Genetics · 350
The coiled-coil domain containing protein CCDC40 is essential for motile cilia function and left-right axis formation
2010 · Anita Becker-Heck, Irene E Zohn, et al. · Nature Genetics · 334
Recessive HYDIN Mutations Cause Primary Ciliary Dyskinesia without Randomization of Left-Right Body Asymmetry
2012 · Heike Olbrich, Miriam Schmidts, et al. · The American Journal of Human Genetics · 295
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Mutations in CCNO result in congenital mucociliary clearance disorder with reduced generation of multiple motile cilia
2014 · Julia Wallmeier, Dalal A Al-Mutairi, et al. · Nature Genetics · 292
DYX1C1 is required for axonemal dynein assembly and ciliary motility
2013 · UK10K, Aarti Tarkar, et al. · Nature Genetics · 279
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Mutations in axonemal dynein assembly factor DNAAF3 cause primary ciliary dyskinesia
2012 · Hannah M Mitchison, Miriam Schmidts, et al. · Nature Genetics · 273
DNAI2 Mutations Cause Primary Ciliary Dyskinesia with Defects in the Outer Dynein Arm
2008 · Niki Tomas Loges, Heike Olbrich, et al. · The American Journal of Human Genetics · 264
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MCIDAS mutations result in a mucociliary clearance disorder with reduced generation of multiple motile cilia
2014 · Mieke Boon, Julia Wallmeier, et al. · Nature Communications · 261
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CCDC103 mutations cause primary ciliary dyskinesia by disrupting assembly of ciliary dynein arms
2012 · Jennifer R Panizzi, Anita Becker-Heck, et al. · Nature Genetics · 248
Primary ciliary dyskinesia associated with normal axoneme ultrastructure is caused by DNAH11 mutations
2007 · Georg C. Schwabe, Katrin Hoffmann, et al. · Human Mutation · 241
Mutations of DNAH11 in patients with primary ciliary dyskinesia with normal ciliary ultrastructure
2011 · Michael R Knowles, Margaret W Leigh, et al. · Thorax · 227
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The nexin-dynein regulatory complex subunit DRC1 is essential for motile cilia function in algae and humans
2013 · Maureen Wirschell, Heike Olbrich, et al. · Nature Genetics · 222
Deletions and Point Mutations of LRRC50 Cause Primary Ciliary Dyskinesia Due to Dynein Arm Defects
2009 · Niki Tomas Loges, Heike Olbrich, et al. · The American Journal of Human Genetics · 213
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De Novo Mutations in FOXJ1 Result in a Motile Ciliopathy with Hydrocephalus and Randomization of Left/Right Body Asymmetry
2019 · Julia Wallmeier, Diana Frank, et al. · The American Journal of Human Genetics · 212
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Zebrafish Ciliopathy Screen Plus Human Mutational Analysis Identifies C21orf59 and CCDC65 Defects as Causing Primary Ciliary Dyskinesia
2013 · Christina Austin-Tse, Jan Halbritter, et al. · The American Journal of Human Genetics · 202
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Ciliary beat pattern and frequency in genetic variants of primary ciliary dyskinesia
2014 · Johanna Raidt, Julia Wallmeier, et al. · European Respiratory Journal · 198
ZMYND10 Is Mutated in Primary Ciliary Dyskinesia and Interacts with LRRC6
2013 · Maimoona A. Zariwala, Heon Yung Gee, et al. · The American Journal of Human Genetics · 197
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Mutations in CCDC 39 and CCDC 40 are the Major Cause of Primary Ciliary Dyskinesia with Axonemal Disorganization and Absent Inner Dynein Arms
2012 · Dinu Antony, Anita Becker-Heck, et al. · Human Mutation · 189
Mutations of DNAI1 in Primary Ciliary Dyskinesia
2006 · Maimoona A. Zariwala, Margaret W. Leigh, et al. · American Journal of Respiratory and Critical Care Medicine · 186
CCDC151 Mutations Cause Primary Ciliary Dyskinesia by Disruption of the Outer Dynein Arm Docking Complex Formation
2014 · Rim Hjeij, Alexandros Onoufriadis, et al. · The American Journal of Human Genetics · 173
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ARMC4 Mutations Cause Primary Ciliary Dyskinesia with Randomization of Left/Right Body Asymmetry
2013 · Rim Hjeij, Anna Lindstrand, et al. · The American Journal of Human Genetics · 160
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Mutations in PIH1D3 Cause X-Linked Primary Ciliary Dyskinesia with Outer and Inner Dynein Arm Defects
2016 · Tamara Paff, Niki T. Loges, et al. · The American Journal of Human Genetics · 151
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Mutations in SPAG1 Cause Primary Ciliary Dyskinesia Associated with Defective Outer and Inner Dynein Arms
2013 · Michael R. Knowles, Lawrence E. Ostrowski, et al. · The American Journal of Human Genetics · 148
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Works count: 129
Citation count: 8,564
H-index: 49
I10-index: 69
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