Els De Leenheer - Concepedia

Author

Els De Leenheer

Also Known As

De Leenheer, Els, E De Leenheer, E M R De Leenheer, E. De Leenheer, E.M.R De Leenheer, E.M.R. De Leenheer, E.M.R. de Leenheer, Els De Leenheer, Els M De Leenheer, Els M R De Leenheer

107

Publications

2.4K

Citations

H-Index

Concepts

All Affiliations

Ghent University Hospital Radboud University Nijmegen Radboud University Medical Center Ghent University University of Antwerp

About

Els De Leenheer is an author at Ghent University Hospital specializing in medicine, hearing loss, and audiology.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	11	11	396
2	Arts	7	7	225
3	Health Sciences	6	6	218
4	Education	1	1	51
5	Language Studies	1	1	14

Els De Leenheer

Publications

1.6K

Citations

H-Index

Page 1

	Year	Citations
Hearing in Children with Congenital Cytomegalovirus Infection: Results of a Longitudinal Study Julie Goderis, Annelies Keymeulen, Koenraad Smets, The Journal of Pediatrics Congenital Cytomegalovirus InfectionPediatric OtolaryngologyPediatric AudiologyAudiologyPediatrics	2016	117
KCNQ4 K+ channels tune mechanoreceptors for normal touch sensation in mouse and man Matthias Heidenreich, Stefan G. Lechner, Vitya Vardanyan, Nature Neuroscience Haptic FeedbackKcnq4 K+ ChannelsNeurophysiologyPhysiologyHaptic Technology	2011	111
DNA Diagnostics of Hereditary Hearing Loss: A Targeted Resequencing Approach Combined with a Mutation Classification System Manou Sommen, Isabelle Schrauwen, Geert Vandeweyer, Human Mutation Cnv AnalysisSyndromic Hearing LossGeneticsMolecular BiologyPathology	2016	108
A Novel Mutation Identified in the <i>DFNA5</i> Gene in a Dutch Family: A Clinical and Genetic Evaluation Anne M.L.C. Bischoff, Mirjam W.J. Luijendijk, P.L.M. Huygen, Audiology and Neurotology	2003	84
Osteogenesis imperfecta: the audiological phenotype lacks correlation with the genotype Freya Swinnen, Paul Coucke, Anne M. De Paepe, Orphanet Journal of Rare Diseases	2011	64
Novel pathogenic COL11A1/COL11A2 variants in Stickler syndrome detected by targeted NGS and exome sequencing Frederic Acke, Fransiska Malfait, Olivier Vanakker, Molecular Genetics and Metabolism Targeted NgsAutoimmune DiseaseMedicinePathogenesisImmunology	2014	56
A mutational hot spot in theKCNQ4 gene responsible for autosomal dominant hearing impairment Guy Van Camp, Paul Coucke, Jiro Akita, Human Mutation	2002	51
The impact of cleft lip and/or palate on parental quality of life: A pilot study Elise De Cuyper, Frederick Dochy, Els De Leenheer, International Journal of Pediatric Otorhinolaryngology Pilot StudyCleft LipParental CareChild Well-beingEarly Childhood Development	2019	51
Otosclerosis: a genetically heterogeneous disease involving at least three different genes K Van Den Bogaert, Paul Govaerts, Els De Leenheer, Bone Genetic DiseasesDisease MechanismDisease EtiologyGenetic DisorderGenetics	2002	50
Longitudinal and Cross-Sectional Phenotype Analysis in a New, Large Dutch DFNA2/<i>KCNQ4</i> Family Els De Leenheer, P.L.M. Huygen, Paul Coucke, Annals of Otology Rhinology & Laryngology	2002	50

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