Steven J. H. Bom - Concepedia

Author

Steven J. H. Bom

Radboud University Nijmegen ORCID

Also Known As

S J H Bom, S. J. H. Bom, S.J.H. Bom, STEVEN J H BOM, Steven J. Bom, Steven J. H Bom, Steven J. H. Bom, Steven J.H. Bom

Publications

540

Citations

H-Index

Concepts

All Affiliations

Radboud University Nijmegen Radboud University Medical Center Canisius-Wilhelmina Ziekenhuis University of Antwerp Deventer Ziekenhuis

About

Steven J. H. Bom is an author at Radboud University Nijmegen specializing in medicine, genetics, and hearing loss.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	5	5	177
2	Arts	3	3	129
3	Health Sciences	3	3	62
4	Biology	1	1	18
5	Hearing Sciences	1	1	16

Steven J. H. Bom

Publications

436

Citations

H-Index

Page 1

	Year	Citations
Mutations in the WFS1 gene that cause low-frequency sensorineural hearing loss are small non-inactivating mutations Kim Cryns, Markus Pfister, Ronald J. E. Pennings, Human Genetics Wfs1 GeneGenetic DisorderGeneticsAudiologyArts	2002	90
Progressive Cochleovestibular Impairment Caused by a Point Mutation in the <i>COCH</i> Gene at DFNA9 Steven J. H. Bom, Martijn H. Kemperman, Y.J.M. de Kok, The Laryngoscope	1999	48
Vestibular Deterioration Precedes Hearing Deterioration in the P51S COCH Mutation (DFNA9): An Analysis in 74 Mutation Carriers Anne M.L.C. Bischoff, P.L.M. Huygen, Martijn H. Kemperman, Otology & Neurotology	2005	46
Speech Recognition Scores Related to Age and Degree of Hearing Impairment in DFNA2/KCNQ4 and DFNA9/COCH Steven J. H. Bom, Els De Leenheer, F. X. Lemaire, Archives of Otolaryngology - Head and Neck Surgery	2001	42
Progression of Low-Frequency Sensorineural Hearing Loss (DFNA6/14-WFS1) Ronald J. E. Pennings, Steven J. H. Bom, Kim Cryns, Archives of Otolaryngology - Head and Neck Surgery	2003	42
Familial Progressive Vestibulocochlear Dysfunction Caused by a COCH Mutation (DFNA9) W. I. M. Verhagen, Steven J. H. Bom, P.L.M. Huygen, Archives of Neurology	2000	28
Hereditary cochleovestibular dysfunction due to a COCH gene mutation (DFNA9): a follow-up study of a family W. I. M. Verhagen, Steven J. H. Bom, Erik Fransén, Clinical Otolaryngology Balance DisordersGeneticsGenetic EpidemiologyPathologyPro51ser Mutation	2001	27
Cross-Sectional Analysis of Hearing Threshold in Relation to Age in a Large Family with Cochleovestibular Impairment Thoroughly Genotyped for DFNA9/<i>COCH</i> Steven J. H. Bom, Martijn H. Kemperman, Mirjam W.J. Luijendijk, Annals of Otology Rhinology & Laryngology	2003	24
Non-Syndromal Autosomal Dominant Hearing Impairment: Ongoing Phenotypical Characterization of Genotypes Steven J. H. Bom, Henricus P. M. Kunst, P.L.M. Huygen, British Journal of Audiology GeneticsGenetic EpidemiologyAuditory ScienceOngoing Phenotypical CharacterizationAudiology	1999	23
Percutaneous bone-anchored hearing implant surgery: linear incision technique with tissue preservation versus linear incision technique with tissue reduction E. H. H. van der Stee, Ruben M. Strijbos, Steven J. H. Bom, European Archives of Oto-Rhino-Laryngology Tissue ReductionHealth SciencesSoft Tissue SurgeryTissue PreservationMedicine	2018	19

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