Cornelis P Lanting (C P Lanting, Cris P Lanting)

Publication Activity (10 Years)

Years Active: 2021-2024
Publications (10 Years): 9

Top Topics

Diabetic Retinopathy

Systematic Review

Top Venues

European archives of oto-rhino-laryngology : official journal of the European Federation of Oto-Rhino-Laryngological Societies (EUFOS) : affiliated with the German Society for Oto-Rhino-Laryngology - Head and Neck Surgery

This page only lists publications with an associated author ORCID identifier.

Publications

A V M Burger, C W Duinkerken, Klaske E van Sluis, Jan Paul de Boer, Arash Navran, Cornelis P Lanting, Katarzyna Jóźwiak, Wouter A Dreschler, A J M Balm, C L Zuur
Treatment-related hearing loss in weekly versus triweekly cisplatin chemoradiation for head and neck cancer. European archives of oto-rhino-laryngology : official journal of the European Federation of Oto-Rhino-Laryngological Societies (EUFOS) : affiliated with the German Society for Oto-Rhino-Laryngology - Head and Neck Surgery (2024)
M L A Fehrmann, Frederick J A Meijer, Emmanuel A M Mylanus, Ronald J E Pennings, Cornelis P Lanting, Wendy J Huinck
Evaluating cochlear implant outcomes in DFNA9 subjects: a comprehensive study on cerebral white matter lesions and vestibular abnormalities. European archives of oto-rhino-laryngology : official journal of the European Federation of Oto-Rhino-Laryngological Societies (EUFOS) : affiliated with the German Society for Oto-Rhino-Laryngology - Head and Neck Surgery (2024)
Hedwig M Velde, Xanne J J Huizenga, Helger G Yntema, Lonneke Haer-Wigman, Andy J Beynon, Jaap Oostrik, Sjoert A H Pegge, Hannie Kremer, Cornelis P Lanting, Ronald J E Pennings
Genotype and Phenotype Analyses of a Novel WFS1 Variant (c.2512C>T p.(Pro838Ser)) Associated with DFNA6/14/38. Genes 14 (2) (2023)
Hedwig M Velde, Xanne J J Huizenga, Helger G Yntema, Lonneke Haer-Wigman, Andy J Beynon, Jaap Oostrik, Sjoert A H Pegge, Hannie Kremer, Cornelis P Lanting, Ronald J E Pennings
Genotype and Phenotype Analyses of a Novel WFS1 Variant (c.2512C>T p.(Pro838Ser)) Associated with DFNA6/14/38. Genes 14 (2) (2023)
Hedwig M Velde, Xanne J J Huizenga, Helger G Yntema, Lonneke Haer-Wigman, Andy J Beynon, Jaap Oostrik, Sjoert A H Pegge, Hannie Kremer, Cornelis P Lanting, Ronald J E Pennings
Genotype and Phenotype Analyses of a Novel WFS1 Variant (c.2512C>T p.(Pro838Ser)) Associated with DFNA6/14/38. Genes 14 (2) (2023)
Sybren M M Robijn, Jeroen J Smits, Kadriye Sezer, Patrick L M Huygen, Andy J Beynon, Erwin van Wijk, Hannie Kremer, Erik de Vrieze, Cornelis P Lanting, Ronald J E Pennings
Genotype-Phenotype Correlations of Pathogenic COCH Variants in DFNA9: A HuGE Systematic Review and Audiometric Meta-Analysis. Biomolecules 12 (2) (2022)
Hedwig M Velde, Janine Reurink, Sebastian Held, Catherina H Z Li, Suzanne Yzer, Jaap Oostrik, Jack Weeda, Lonneke Haer-Wigman, Helger G Yntema, Susanne Roosing, Laurenz J B Pauleikhoff, Clemens A Lange, Laura Whelan, Adrian Dockery, Julia Zhu, David J Keegan, Gwyneth Jane Farrar, Hannie Kremer, Cornelis P Lanting, Markus Damme, Ronald J E Pennings
Usher syndrome type IV: clinically and molecularly confirmed by novel ARSG variants. Human genetics 141 (11) (2022)
Jeroen J Smits, Suzanne E de Bruijn, Cornelis P Lanting, Jaap Oostrik, Luke O'Gorman, Tuomo Mantere, null null, Frans P M Cremers, Susanne Roosing, Helger G Yntema, Erik de Vrieze, Ronny Derks, Alexander Hoischen, Sjoert A H Pegge, Kornelia Neveling, Ronald J E Pennings, Hannie Kremer
Correction to: Exploring the missing heritability in subjects with hearing loss, enlarged vestibular aqueducts, and a single or no pathogenic SLC26A4 variant. Human genetics (2021)
Jeroen J Smits, Suzanne E de Bruijn, Cornelis P Lanting, Jaap Oostrik, Luke O'Gorman, Tuomo Mantere, null null, Frans P M Cremers, Susanne Roosing, Helger G Yntema, Erik de Vrieze, Ronny Derks, Alexander Hoischen, Sjoert A H Pegge, Kornelia Neveling, Ronald J E Pennings, Hannie Kremer
Exploring the missing heritability in subjects with hearing loss, enlarged vestibular aqueducts, and a single or no pathogenic SLC26A4 variant. Human genetics (2021)