| A seventh locus for otosclerosis, OTSC7, maps to chromosome 6q13–16.1 M Thys, K Van Den Bogaert, V Iliadou, K Vanderstraeten, N Dieltjens, ... European journal of human genetics 15 (3), 362-368, 2007 | 81 | 2007 |
| Missense mutations in POU4F3 cause autosomal dominant hearing impairment DFNA15 and affect subcellular localization and DNA binding RWJ Collin, R Chellappa, RJ Pauw, G Vriend, J Oostrik, W Van Drunen, ... Human mutation 29 (4), 545-554, 2008 | 74 | 2008 |
| Antiactin-targeted immunoliposomes ameliorate tissue plasminogen activator-induced hemorrhage after focal embolic stroke M Asahi, R Rammohan, T Sumii, X Wang, RJ Pauw, V Weissig, ... Journal of Cerebral Blood Flow & Metabolism 23 (8), 895-899, 2003 | 56 | 2003 |
| Mid-frequency DFNA8/12 hearing loss caused by a synonymous TECTA mutation that affects an exonic splice enhancer RWJ Collin, AMR de Heer, J Oostrik, RJ Pauw, RF Plantinga, PL Huygen, ... European journal of human genetics 16 (12), 1430-1436, 2008 | 48 | 2008 |
| Single-stage mastoid obliteration in cholesteatoma surgery and recurrent and residual disease rates: a systematic review HFE van der Toom, MP van der Schroeff, RJ Pauw JAMA Otolaryngology–Head & Neck Surgery 144 (5), 440-446, 2018 | 46 | 2018 |
| Implementation of the “EAONO/JOS definitions and classification of middle ear cholesteatoma”–from STAM to STAMCO P Merkus, FA Ten Tije, M Stam, FML Tan, RJ Pauw Journal of International Advanced Otology 13 (2), 272-274, 2017 | 37 | 2017 |
| Identification of a novel COCH mutation, G87W, causing autosomal dominant hearing impairment (DFNA9) RWJ Collin, RJ Pauw, J Schoots, PLM Huygen, LH Hoefsloot, ... American Journal of Medical Genetics Part A 140 (16), 1791-1794, 2006 | 35 | 2006 |
| Audiometric characteristics of a Dutch family linked to DFNA15 with a novel mutation (p. L289F) in POU4F3 RJ Pauw, FJW van Drunen, RWJ Collin, PLM Huygen, H Kremer, ... Archives of Otolaryngology–Head & Neck Surgery 134 (3), 294-300, 2008 | 34 | 2008 |
| Phenotype description of a novel DFNA9/COCH mutation, I109T RJ Pauw, PLM Huygen, RWJ Collin, JRM Cruysberg, LH Hoefsloot, ... Annals of Otology, Rhinology & Laryngology 116 (5), 349-357, 2007 | 32 | 2007 |
| A retrospective analysis and comparison of the STAM and STAMCO classification and EAONO/JOS cholesteatoma staging system in predicting surgical treatment outcomes of middle ear … HFE van der Toom, MP Van der Schroeff, JMH Janssen, AM Westzaan, ... Otology & Neurotology 41 (4), e468-e474, 2020 | 23 | 2020 |
| Clinical characteristics of a Dutch DFNA9 family with a novel COCH mutation, G87W RJ Pauw, RWJ Collin, PLM Huygen, LH Hoefsloot, H Kremer, ... Audiology and Neurotology 12 (2), 77-84, 2007 | 21 | 2007 |
| Flat Threshold and Mid-Frequency Hearing Impairment in a Dutch DFNA8/12 Family with a Novel Mutation in TECTA Some Evidence for Protection of the Inner Ear AR De Heer, RJ Pauw, PLM Huygen, RWJ Collin, H Kremer, C Cremers Audiology and Neurotology 14 (3), 153-162, 2009 | 20 | 2009 |
| Evaluation of the modified Pittsburgh classification for predicting the disease‐free survival outcome of squamous cell carcinoma of the external auditory canal CH Nabuurs, W Kievit, N Labbé, CR Leemans, CFGM Smit, ... Head & Neck 42 (12), 3609-3622, 2020 | 18 | 2020 |
| Comparison of FAIR perfusion kinetics with DSC‐MRI and functional histology in a model of transient ischemia J Schepers, WB Veldhuis, RJ Pauw, JW de Groot, MJP van Osch, ... Magnetic Resonance in Medicine: An Official Journal of the International …, 2004 | 18 | 2004 |
| Audiometric profiles associated with genetic non-syndromal hearing impairment: a review and phenotype analysis PLM Huygen, RJ Pauw, C Cremers I. A M., editor editors. Genes, Hearing and Deafness. London: Informa …, 2007 | 16 | 2007 |
| Vestibular impairment in a Dutch DFNA15 family with an L289F mutation in POU4F3 FJW Van Drunen, RJ Pauw, RWJ Collin, H Kremer, PLM Huygen, ... Audiology and Neurotology 14 (5), 303-307, 2009 | 15 | 2009 |
| Treatment outcome of the bony obliteration tympanoplasty versus nonobliterative techniques in cholesteatoma surgery: a retrospective analysis HFE van der Toom, MP van der Schroeff, M Metselaar, A van Linge, ... Otology & Neurotology 42 (9), 1366-1374, 2021 | 14 | 2021 |
| The phenotype of the first otosclerosis family linked to OTSC5 RJ Pauw, EMR De Leenheer, K Van Den Bogaert, PLM Huygen, ... Otology & Neurotology 27 (3), 308-315, 2006 | 12 | 2006 |
| Vertical corneal striae in families with autosomal dominant hearing loss: DFNA9/COCH AMLC Bischoff, RJ Pauw, PLM Huygen, AL Aandekerk, H Kremer, ... American Journal of Ophthalmology 143 (5), 847-852. e6, 2007 | 11 | 2007 |
| Phenotype Analysis of an Australian DFNA9 Family with the I109N COCH Mutation RJ Pauw, PLM Huygen, GM Colditz, WRJ Cremers Annals of Otology, Rhinology & Laryngology 120 (6), 414-421, 2011 | 9 | 2011 |
