Publications by authors named "Ronald Pennings"

68Publications

Impact of cochlear implantation on the function of the three semicircular canals.

Authors:
Joost J A Stultiens Hieke W Kieft Emmanuel A M Mylanus Ronald J E Pennings Lotte Terwoert Andy J Beynon

Int J Audiol 2020 Nov 9;59(11):843-849. Epub 2020 Jul 9.

Department of Otorhinolaryngology and Head and Neck Surgery, Radboud University Medical Center, Nijmegen, The Netherlands.

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November 2020

A in-frame deletion is a frequent and highly penetrant cause of adult-onset hearing loss.

Authors:
Suzanne E de Bruijn Jeroen J Smits Chang Liu Cornelis P Lanting Andy J Beynon Joëlle Blankevoort Jaap Oostrik Wouter Koole Erik de Vrieze Cor W R J Cremers Frans P M Cremers Susanne Roosing Helger G Yntema Henricus P M Kunst Bo Zhao Ronald J E Pennings Hannie Kremer

J Med Genet 2020 Jul 6. Epub 2020 Jul 6.

Department of Human Genetics, Radboudumc, Nijmegen, The Netherlands

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July 2020

Hearing Results of Surgery for Acquired Atresia of the External Auditory Canal.

Authors:
Joost J A Stultiens Patrick L M Huygen Anne M M Oonk Emmanuel A M Mylanus Henricus P M Kunst Myrthe K S Hol Cor W R J Cremers Jef J S Mulder Ronald J E Pennings

Otol Neurotol 2019 06;40(5S Suppl 1):S43-S50

Department of Otorhinolaryngology, Donders Institute for Brain, Cognition and Behaviour, Radboud University Medical Center, Nijmegen, The Netherlands.

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June 2019

De novo and inherited loss-of-function variants of ATP2B2 are associated with rapidly progressive hearing impairment.

Authors:
Jeroen J Smits Jaap Oostrik Andy J Beynon Sarina G Kant Pia A M de Koning Gans Liselotte J C Rotteveel Jolien S Klein Wassink-Ruiter Rolien H Free Saskia M Maas Jiddeke van de Kamp Paul Merkus Wouter Koole Ilse Feenstra Ronald J C Admiraal Cornelis P Lanting Margit Schraders Helger G Yntema Ronald J E Pennings Hannie Kremer

Hum Genet 2019 Jan 8;138(1):61-72. Epub 2018 Dec 8.

Hearing and Genes, Department of Otorhinolaryngology, Head and Neck Surgery, Radboud University Medical Center, Nijmegen, The Netherlands.

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January 2019

Variants affecting diverse domains of MEPE are associated with two distinct bone disorders, a craniofacial bone defect and otosclerosis.

Authors:
Isabelle Schrauwen Hanne Valgaeren Laura Tomas-Roca Manou Sommen Umut Altunoglu Mieke Wesdorp Matthias Beyens Erik Fransen Abdul Nasir Geert Vandeweyer Anne Schepers Malika Rahmoun Ellen van Beusekom Matt J Huentelman Erwin Offeciers Ingeborg Dhooghe Alex Huber Paul Van de Heyning Diego Zanetti Els M R De Leenheer Christian Gilissen Alexander Hoischen Cor W Cremers Berit Verbist Arjan P M de Brouwer George W Padberg Ronald Pennings Hülya Kayserili Hannie Kremer Guy Van Camp Hans van Bokhoven

Genet Med 2019 05 5;21(5):1199-1208. Epub 2018 Oct 5.

Department of Human Genetics, Radboud University Medical Center, Nijmegen, The Netherlands.

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May 2019

MPZL2, Encoding the Epithelial Junctional Protein Myelin Protein Zero-like 2, Is Essential for Hearing in Man and Mouse.

Authors:
Mieke Wesdorp Silvia Murillo-Cuesta Theo Peters Adelaida M Celaya Anne Oonk Margit Schraders Jaap Oostrik Elena Gomez-Rosas Andy J Beynon Bas P Hartel Kees Okkersen Hans J P M Koenen Jack Weeda Stefan Lelieveld Nicol C Voermans Irma Joosten Carel B Hoyng Peter Lichtner Henricus P M Kunst Ilse Feenstra Suzanne E de Bruijn Ronald J C Admiraal Helger G Yntema Erwin van Wijk Ignacio Del Castillo Pau Serra Isabel Varela-Nieto Ronald J E Pennings Hannie Kremer

Am J Hum Genet 2018 07 28;103(1):74-88. Epub 2018 Jun 28.

Hearing and Genes Division, Department of Otorhinolaryngology, Radboud University Medical Center, 6500 HB Nijmegen, the Netherlands; Donders Institute for Brain, Cognition and Behavior, Radboud University Medical Center, 6500 HB Nijmegen, the Netherlands; Department of Human Genetics, Radboud University Medical Center, 6500 HB Nijmegen, the Netherlands. Electronic address:

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July 2018

Hearing Rehabilitation with Active Middle Ear Implants.

Authors:
Neil P Donnelly Ronald J E Pennings

Adv Otorhinolaryngol 2018 6;81:43-56. Epub 2018 Apr 6.

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October 2018

Heterozygous missense variants of LMX1A lead to nonsyndromic hearing impairment and vestibular dysfunction.

Authors:
Mieke Wesdorp Pia A M de Koning Gans Margit Schraders Jaap Oostrik Martijn A Huynen Hanka Venselaar Andy J Beynon Judith van Gaalen Vitória Piai Nicol Voermans Michelle M van Rossum Bas P Hartel Stefan H Lelieveld Laurens Wiel Berit Verbist Liselotte J Rotteveel Marieke F van Dooren Peter Lichtner Henricus P M Kunst Ilse Feenstra Ronald J C Admiraal Helger G Yntema Lies H Hoefsloot Ronald J E Pennings Hannie Kremer

Hum Genet 2018 May 12;137(5):389-400. Epub 2018 May 12.

Department of Otorhinolaryngology, Hearing and Genes, Radboud University Medical Center, Internal Postal Code 377, P.O. Box 9101, 6500 HB, Nijmegen, The Netherlands.

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May 2018

Risk factors for complications in cochlear implant surgery.

Authors:
Henricus J Theunisse Ronald J E Pennings Henricus P M Kunst Jef J Mulder Emmanuel A M Mylanus

Eur Arch Otorhinolaryngol 2018 Apr 10;275(4):895-903. Epub 2018 Feb 10.

Department of Otorhinolaryngology and Head and Neck Surgery, Radboud University Medical Center, Nijmegen, The Netherlands.

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April 2018

Bayesian quantification of sensory reweighting in a familial bilateral vestibular disorder (DFNA9).

Authors:
Bart B G T Alberts Luc P J Selen Wim I M Verhagen Ronald J E Pennings W Pieter Medendorp

J Neurophysiol 2018 03 13;119(3):1209-1221. Epub 2017 Dec 13.

Donders Institute for Brain, Cognition and Behaviour, Radboud University Nijmegen , Nijmegen , The Netherlands.

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March 2018

Cochlear Implantation in Patients With Usher Syndrome Type IIa Increases Performance and Quality of Life.

Authors:
Bas P Hartel Josephine W I van Nierop Wendy J Huinck Liselotte J C Rotteveel Emmanuel A M Mylanus Ad F Snik Henricus P M Kunst Ronald J E Pennings

Otol Neurotol 2017 07;38(6):e120-e127

*Department of Otorhinolaryngology †Radboud Institute for Health Sciences, Radboud University Medical Center ‡Donders Institute for Brain, Cognition and Behaviour, Radboud University Nijmegen, Nijmegen §Department of Otorhinolaryngology, Leiden University Medical Center, Leiden, the Netherlands.

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July 2017

Broadening the phenotype of DFNB28: Mutations in TRIOBP are associated with moderate, stable hereditary hearing impairment.

Authors:
Mieke Wesdorp Jiddeke M van de Kamp Erik F Hensen Margit Schraders Jaap Oostrik Helger G Yntema Ilse Feenstra Ronald J C Admiraal Henricus P M Kunst Mustafa Tekin Moien Kanaan Hannie Kremer Ronald J E Pennings

Hear Res 2017 04 12;347:56-62. Epub 2017 Jan 12.

Department of Otorhinolaryngology, Hearing & Genes, Radboud University Medical Center, Nijmegen, The Netherlands; Donders Institute for Brain, Cognition and Behaviour, Radboud University Medical Center, Nijmegen, The Netherlands.

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April 2017

The diagnostic yield of whole-exome sequencing targeting a gene panel for hearing impairment in The Netherlands.

Authors:
Celia Zazo Seco Mieke Wesdorp Ilse Feenstra Rolph Pfundt Jayne Y Hehir-Kwa Stefan H Lelieveld Steven Castelein Christian Gilissen Ilse J de Wijs Ronald Jc Admiraal Ronald Je Pennings Henricus Pm Kunst Jiddeke M van de Kamp Saskia Tamminga Arjan C Houweling Astrid S Plomp Saskia M Maas Pia Am de Koning Gans Sarina G Kant Christa M de Geus Suzanna Gm Frints Els K Vanhoutte Marieke F van Dooren Marie-José H van den Boogaard Hans Scheffer Marcel Nelen Hannie Kremer Lies Hoefsloot Margit Schraders Helger G Yntema

Eur J Hum Genet 2017 02 21;25(3):308-314. Epub 2016 Dec 21.

The Radboud Institute for Molecular Life Sciences, Radboud University Medical Center, Nijmegen, The Netherlands.

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February 2017

Antisense Oligonucleotide-based Splice Correction for USH2A-associated Retinal Degeneration Caused by a Frequent Deep-intronic Mutation.

Authors:
Radulfus Wn Slijkerman Christel Vaché Margo Dona Gema García-García Mireille Claustres Lisette Hetterschijt Theo A Peters Bas P Hartel Ronald Je Pennings José M Millan Elena Aller Alejandro Garanto Rob Wj Collin Hannie Kremer Anne-Françoise Roux Erwin Van Wijk

Mol Ther Nucleic Acids 2016 Nov 1;5(10):e381. Epub 2016 Nov 1.

Department of Otorhinolaryngology, Radboudumc, Nijmegen, the Netherlands.

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November 2016

A combination of two truncating mutations in USH2A causes more severe and progressive hearing impairment in Usher syndrome type IIa.

Authors:
Bas P Hartel Maria Löfgren Patrick L M Huygen Iris Guchelaar Nicole Lo-A-Njoe Kort Andre M Sadeghi Erwin van Wijk Lisbeth Tranebjærg Hannie Kremer William J Kimberling Cor W R J Cremers Claes Möller Ronald J E Pennings

Hear Res 2016 09 16;339:60-8. Epub 2016 Jun 16.

Department of Otorhinolaryngology, Donders Institute for Brain, Cognition and Behaviour, Radboud Institute for Molecular Life Sciences, Radboud University Medical Center, Nijmegen, The Netherlands.

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September 2016

Paediatric Cochlear Implantation in Patients with Waardenburg Syndrome.

Authors:
Josephine W I van Nierop Rebecca R Snabel Margreet Langereis Ronald J E Pennings Ronald J C Admiraal Emmanuel A M Mylanus Henricus P M Kunst

Audiol Neurootol 2016 1;21(3):187-94. Epub 2016 Jun 1.

Department of Otorhinolaryngology - Head and Neck Surgery, Radboud University Medical Center, Nijmegen, The Netherlands.

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February 2018

Comment on "Usher's Syndrome: Evaluation of the Vestibular System with Cervical and Ocular Vestibular Evoked Myogenic Potentials and the Video Head Impulse Test".

Authors:
Bas P Hartel Ronald J E Pennings Erwin van Wijk

Otol Neurotol 2016 06;37(5):608

Department of Otorhinolaryngology, Head and Neck Surgery, and Radboud Institute for Health Sciences, Radboud University Medical Center Nijmegen, The Netherlands Department of Otorhinolaryngology, Head and Neck Surgery, and Radboud Institute for Molecular Life Sciences, Radboud University Medical Center Nijmegen, The Netherlands.

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June 2016

Visual Prognosis in USH2A-Associated Retinitis Pigmentosa Is Worse for Patients with Usher Syndrome Type IIa Than for Those with Nonsyndromic Retinitis Pigmentosa.

Authors:
Laurence H M Pierrache Bas P Hartel Erwin van Wijk Magda A Meester-Smoor Frans P M Cremers Elfride de Baere Julie de Zaeytijd Mary J van Schooneveld Cor W R J Cremers Gislin Dagnelie Carel B Hoyng Arthur A Bergen Bart P Leroy Ronald J E Pennings L Ingeborgh van den Born Caroline C W Klaver

Ophthalmology 2016 May 27;123(5):1151-60. Epub 2016 Feb 27.

Department of Ophthalmology, Erasmus Medical Center, Rotterdam, The Netherlands; Department of Epidemiology, Erasmus Medical Center, Rotterdam, The Netherlands. Electronic address:

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May 2016

Allelic Mutations of KITLG, Encoding KIT Ligand, Cause Asymmetric and Unilateral Hearing Loss and Waardenburg Syndrome Type 2.

Authors:
Celia Zazo Seco Luciana Serrão de Castro Josephine W van Nierop Matías Morín Shalini Jhangiani Eva J J Verver Margit Schraders Nadine Maiwald Mieke Wesdorp Hanka Venselaar Liesbeth Spruijt Jaap Oostrik Jeroen Schoots Jeroen van Reeuwijk Stefan H Lelieveld Patrick L M Huygen María Insenser Ronald J C Admiraal Ronald J E Pennings Lies H Hoefsloot Alejandro Arias-Vásquez Joep de Ligt Helger G Yntema Joop H Jansen Donna M Muzny Gerwin Huls Michelle M van Rossum James R Lupski Miguel Angel Moreno-Pelayo Henricus P M Kunst Hannie Kremer

Am J Hum Genet 2015 Nov 29;97(5):647-60. Epub 2015 Oct 29.

Hearing & Genes Division, Department of Otorhinolaryngology, Radboud University Medical Center, Nijmegen 6525GA, the Netherlands; The Radboud Institute for Molecular Life Sciences, Radboud University Medical Center, Nijmegen 6525GA, the Netherlands; Department of Human Genetics, Radboud University Medical Center, Nijmegen 6525GA, the Netherlands. Electronic address:

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November 2015

Audiometric Characteristics of a Dutch DFNA10 Family With Mid-Frequency Hearing Impairment.

Authors:
Eline van Beelen Anne M M Oonk Joop M Leijendeckers Elisabeth H Hoefsloot Ronald J E Pennings Ilse Feenstra Hendrik-Jan Dieker Patrick L M Huygen Ad F M Snik Hannie Kremer Henricus P M Kunst

Ear Hear 2016 Jan-Feb;37(1):103-11

1Department of Otorhinolaryngology, Head and Neck Surgery, Radboud university medical center, Nijmegen, The Netherlands; 2Department of Human Genetics, Radboud university medical center, Nijmegen, The Netherlands; 3Department of Clinical Genetics, Erasmus MC, University Medical Center Rotterdam, Rotterdam, The Netherlands; 4Donders Institute for Brain, Cognition and Behavior, Radboud University, Nijmegen, The Netherlands; 5Department of Cardiology, Radboud university medical center, Nijmegen, The Netherlands; and 6Radboud Institute for Molecular Life Sciences, Radboud university medical center, Nijmegen, The Netherlands.

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September 2016