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Issue Date	Title	Author(s)
2011	A white mass behind the tympanic membrane: adenoma of the middle ear with neuroendocrine differentiation	Verhage-Damen, G.W.; Engen-van Grunsven, I.A. van; Schans, E.J. van der; Kunst, H.P.M.
2011	Retrosigmoidale neurotomie van de nervus vestibularis als behandeling van invaliderende vertigo. Een case report.	Neeskens, L.J.; Honings, J.; Lavieille, J.P.; Kunst, H.P.M.
2011	A new locus for otosclerosis, OTSC10, maps to chromosome 1q41-44	Schrauwen, I.; Weegerink, N.J.D.; Fransen, E.; Claes, C.; Pennings, R.J.E.; Cremers, C.W.R.J.; Huygen, P.L.M.; Kunst, H.P.M.; Camp, G. van
2011	Variable degrees of hearing impairment in a Dutch DFNX4 (DFN6) family.	Weegerink, N.J.D.; Huygen, P.L.M.; Schraders, M.; Kremer, H.; Pennings, R.J.; Kunst, H.P.
2011	Disruption of Teashirt Zinc Finger Homeobox 1 Is Associated with Congenital Aural Atresia in Humans.	Feenstra, I.; Vissers, L.E.L.M.; Pennings, R.J.E.; Nillesen, W.M.; Pfundt, R.; Kunst, H.P.; Admiraal, R.J.; Veltman, J.A.; Ravenswaaij-Arts, C.M.A. van; Brunner, H.G.; Cremers, C.W.R.J.
2011	Progressive sensorineural hearing loss and normal vestibular function in a Dutch DFNB7/11 family with a novel mutation in TMC1	Heer, A.M. de; Collin, R.W.J.; Huygen, P.L.M.; Schraders, M.; Oostrik, J.; Rouwette, M.; Kunst, H.P.M.; Kremer, J.M.J.; Cremers, C.W.R.J.
2011	Phenotypes of two Dutch DFNA3 families with mutations in GJB2	Weegerink, N.J.D.; Pennings, R.J.E.; Huygen, P.L.M.; Hoefsloot, L.H.; Cremers, C.W.R.J.; Kunst, H.P.M.
2011	Congenital stapes ankylosis associated with another ossicular chain anomaly: surgical results in 30 ears	Thomeer, H.G.X.M.; Kunst, H.P.M.; Cremers, C.W.R.J.
2011	Causes of permanent childhood hearing impairment	Korver, A.M.; Admiraal, R.J.C.; Kant, S.G.; Dekker, F.W.; Wever, C.; Kunst, H.P.M.; Frijns, J.H.; Oudesluys-Murphy, A.M.
2011	Phenotype of the first otosclerosis family linked to OTSC10	Weegerink, N.J.D.; Schrauwen, I.; Huygen, P.L.M.; Pennings, R.J.E.; Cremers, C.W.R.J.; Camp, G. van; Kunst, H.P.M.
2011	Proximal symphalangism, hyperopia, conductive hearing impairment, and the NOG gene: 2 new mutations	Thomeer, H.G.X.M.; Admiraal, R.J.C.; Hoefsloot, L.H.; Kunst, H.P.M.; Cremers, C.W.R.J.
2011	Endolymphatic sac tumors: clinical outcome and management in a series of 9 cases	Timmer, F.C.A.; Neeskens, L.J.; Hoogen, F.J.A. van den; Slootweg, P.J.; Dunnebier, E.A.; Pauw, B.H.; Mulder, J.J.S.; Cremers, C.W.R.J.; Kunst, D.
2011	Ear and hearing problems in relation to karyotype in children with Turner syndrome	Verver, E.J.; Freriks, K.; Thomeer, H.G.X.M.; Huygen, P.L.M.; Pennings, R.J.E.; Alfen-van der Velden, A.A.E.M. van; Timmers, H.J.L.M.; Otten, B.J.; Cremers, C.W.R.J.; Kunst, H.P.M.
2011	Next-generation sequencing identifies mutations of SMPX, which encodes the small muscle protein, X-linked, as a cause of progressive hearing impairment	Schraders, M.; Haas, S.A.; Weegerink, N.J.D.; Oostrik, J.; Hu, H.; Hoefsloot, L.H.; Kannan, S.; Huygen, P.L.M.; Pennings, R.J.E.; Admiraal, R.J.C.; Kalscheuer, V.M.M.; Kunst, H.P.M.; Kremer, J.M.J.
2011	SDHAF2 (PGL2-SDH5) and hereditary head and neck paraganglioma	Kunst, H.P.M.; Rutten, M.H.; Monnink, J.P. de; Hoefsloot, L.H.; Timmers, H.J.L.M.; Marres, H.A.M.; Jansen, J.C.; Kremer, J.M.J.; Bayley, J.P.M.; Cremers, C.W.R.J.
2011	Genotype-Phenotype Correlation in DFNB8/10 Families with TMPRSS3 Mutations	Weegerink, N.J.D.; Schraders, M.; Oostrik, J.; Huygen, P.L.M.; Strom, T.M.; Granneman, S.; Pennings, R.J.E.; Venselaar, H.; Hoefsloot, L.H.; Elting, M.; Cremers, C.W.R.J.; Admiraal, R.J.C.; Kremer, J.M.J.; Kunst, H.P.M.
2011	Standardized multidisciplinary evaluation yields significant previously undiagnosed morbidity in adult women with Turner syndrome	Freriks, K.; Timmermans, J.; Beerendonk, C.C.M.; Verhaak, C.M.; Netea-Maier, R.T.; Otten, B.J.; Braat, D.D.M.; Smeets, D.F.C.M.; Kunst, D.; Hermus, A.R.M.M.; Timmers, H.J.L.M.
2010	Facial nerve palsy in aviation facial baroparesis.	Rutten, M.H.; Kunst, H.P.M.
2010	Mutations in PTPRQ are a cause of autosomal-recessive nonsyndromic hearing impairment DFNB84 and associated with vestibular dysfunction.	Schraders, M.; Oostrik, J.; Huygen, P.L.M.; Strom, T.M.; Wijk, E. van; Kunst, H.P.M.; Hoefsloot, L.H.; Cremers, C.W.R.J.; Admiraal, R.J.C.; Kremer, J.M.J.
2010	Isolated congenital stapes ankylosis: surgical results in a consecutive series of 39 ears.	Thomeer, H.G.X.M.; Kunst, H.P.M.; Cremers, C.W.R.J.
2010	Autosomal dominant optic neuropathy and sensorineual hearing loss associated with a novel mutation of WFS1	Hogewind, B.F.T.; Pennings, R.J.E.; Hol, F.A.; Kunst, H.P.M.; Hoefsloot, E.H.; Cruysberg, J.R.M.; Cremers, C.W.R.J.
2010	Homozygosity mapping reveals mutations of GRXCR1 as a cause of autosomal-recessive nonsyndromic hearing impairment.	Schraders, M.; Lee, K.; Oostrik, J.; Huygen, P.L.M.; Ali, G.; Hoefsloot, L.H.; Veltman, J.A.; Cremers, F.P.M.; Basit, S.; Ansar, M.; Cremers, C.W.R.J.; Kunst, H.P.M.; Ahmad, W.; Admiraal, R.J.C.; Leal, S.M.; Kremer, J.M.J.
2010	Newborn hearing screening vs later hearing screening and developmental outcomes in children with permanent childhood hearing impairment.	Korver, A.M.; Konings, S.; Dekker, F.W.; Beers, M. van; Wever, C.; Frijns, J.H.; Oudesluys-Murphy, A.M.; Cremers, C.W.R.J.; Kunst, H.P.M.; Admiraal, R.J.C.
2010	SDHAF2 mutations in familial and sporadic paraganglioma and phaeochromocytoma.	Bayley, J.P.M.; Kunst, H.P.M.; Cascon, A.; Sampietro, M.L.; Gaal, J.; Korpershoek, E.; Hinojar-Gutierrez, A.; Timmers, H.J.L.M.; Hoefsloot, L.H.; Hermsen, M.A.; Suarez, C.; Hussain, A.K.; Vriends, A.H.; Hes, F.J.; Jansen, J.C.; Tops, C.M.; Corssmit, E.P.; Knijff, P. de; Lenders, J.W.M.; Cremers, C.W.R.J.; Devilee, P.; Dinjens, W.N.; Krijger, R.R. de; Robledo, M.
2009	SDH5, a gene required for flavination of succinate dehydrogenase, is mutated in paraganglioma.	Hao, H.X.; Khalimonchuk, O.; Schraders, M.; Dephoure, N.; Bayley, J.P.M.; Kunst, H.P.M.; Devilee, P.; Cremers, C.W.R.J.; Schiffman, J.D.; Bentz, B.G.; Gygi, S.P.; Winge, D.R.; Kremer, H.; Rutter, J.
2009	The first Dutch SDHB founder deletion in paraganglioma – pheochromocytoma patients	Bayley, J.P.M.; Grimbergen, A.E.; Bunderen, P.A. van; Wielen, M. van der; Kunst, H.P.M.; Lenders, J.W.M.; Jansen, J.C.; Dullaart, R.P.; Devilee, P.; Corssmit, E.P.; Vriends, A.H.; Losekoot, M.; Weiss, M.M.
2008	Etiologie, diagnose en therapeutische mogelijkheden bij invaliderende Morbus Meniere	Crins, T.; Kunst, H.P.M.
2008	Squamous cell carcinoma of the temporal bone: results and management.	Kunst, H.P.M.; Lavieille, J.P.; Marres, H.A.M.
2007	Audiological evaluation of affected members from a Dutch DFNA8/12 (TECTA) family	Plantinga, R.F.; Cremers, C.W.R.J.; Huygen, P.L.M.; Kunst, H.P.M.; Bosman, A.J.
2006	A novel TECTA mutation in a Dutch DFNA8/12 family confirms genotype-phenotype correlation	Plantinga, R.F.; Brouwer, A.P.M. de; Huygen, P.L.M.; Kunst, H.P.M.; Kremer, H.; Cremers, C.W.R.J.
2006	Sub-alar batten grafts as treatment for nasal valve incompetence; description of technique and functional evaluation.	Andre, R.F.; D'Souza, A.R.; Kunst, H.P.M.; Vuyk, H.D.
2005	Management of carcinoma of the temporal bone.	Lavieille, J.; Delande, C.; Kunst, H.P.M.; Deveze, A.; Magnan, J.
2005	Fine mapping of autosomal dominant nonsyndromic hearing impairment DFNA21 to chromosome 6p24.1-22.3.	Brouwer, A.P.M. de; Kunst, H.P.M.; Krebsova, A.; Asseldonk, K. van; Reis, A.; Snoeckx, R.L.; Camp, G. van; Cremers, C.W.R.J.; Cremers, F.P.M.; Kremer, J.M.J.
2004	Audiological characteristics of some affected members of a Dutch DFNA13/COL11A2 family.	Leenheer, E. de; Bosman, A.J.; Kunst, H.P.M.; Huygen, P.L.M.; Cremers, C.W.R.J.
1999	Autosomal dominant inherited non-syndromic sensorineural hearing impairment : phenotype and genotype correlations of DFNA2-DFNA13-DFNA14-DFNA21	Kunst, H.P.M.
1997	Autosomaal dominant non-syndromaal gehoorverlies	Marres, H.A.M.; Kunst, H.P.M.; Huygen, P.L.M.; Cremers, C.W.R.J.
1997	Non-syndromal autosomal dominant hearing loss.	Marres, H.A.M.; Kunst, H.P.M.; Huygen, P.L.M.; Cremers, C.W.R.J.
1997	Inherited nonsyndromic hearing loss: an audiovestibular study in a large family with autosomal dominant progressive hearing loss related to DFNA2	Marres, H.A.M.; Ewijk, M. van; Huygen, P.L.M.; Kunst, H.P.M.; Camp, G. van; Coucke, P.J.; Willems, P.; Cremers, C.W.R.J.
1997	Linkage analysis of progressive hearing loss in five extended families maps the DFNA2 gene to a 1.25-Mb region on chromosome 1p	Camp, G. van; Coucke, P.J.; Kunst, H.P.M.; Schatteman, I.; Velzen, D. van; Marres, H.A.M.; Ewijk, M. van; Declau, F.; Hauwe, P. van; Meyers, J.; Kenyon, J.; Smith, S.D.; Smith, R.J.H.; Djelantik, B.; Cremers, C.W.R.J.; Heyning, P. van de; Willems, P.
1996	Autosomaal dominant non-syndromaal gehoorverlies.	Marres, H.A.M.; Kunst, H.P.M.; Huygen, P.L.M.; Cremers, C.W.R.J.
1996	Non-syndromic autosomal dominant progressive sensorineural hearing loss. Audiological analysis on a pedigree linked to DFNA2.	Kunst, H.P.M.; Marres, H.A.M.; Huygen, P.L.M.; Coucke, P.J.; Willems, P.; Cremers, C.W.R.J.