Sign in
Author
|
Conference
|
Journal
|
Organization
|
Year
|
DOI
Look for results that meet for the following criteria:
since
equal to
before
between
and
Search in all fields of study
Limit my searches in the following fields of study
Agriculture Science
Arts & Humanities
Biology
Chemistry
Computer Science
Economics & Business
Engineering
Environmental Sciences
Geosciences
Material Science
Mathematics
Medicine
Physics
Social Science
Multidisciplinary
Co-authors
(122)
Cor W. R. J. Cremers
30
Patrick L. M. Huygen
19
Henri A. M. Marres
12
Guy Van Camp
11
Ronald J. E. Pennings
6
Journals
(23)
ANN OTOL RHINOL LARYNGOL
3
JARO
3
AMER J HUM GENET
3
ARCH OTOLAR-HEAD NECK SURGERY
2
OTOL NEUROTOL
2
Keywords
(70)
Embed
Subscribe
Academic
Authors
Henricus P. M. Kunst
Henricus P. M. Kunst,University Medical Center St Radboud Nijmegen,Anatomy,Genetics & Genealogy,Physiology
Edit
Henricus P. M. Kunst
University Medical Center St Radboud Nijmegen
Publications:
36
|
Citations:
209
Fields:
Anatomy
,
Genetics & Genealogy
,
Physiology
View FAQ about top research areas and Fields of study
Collaborated with
122 co-authors
from 1997 to 2011
|
Cited by
753 authors
Cumulative
Annual
Sort by:
Publications
(36)
BibTeX
|
RIS
|
RefWorks
Download
Genotype–Phenotype Correlation in DFNB8/10 Families with TMPRSS3 Mutations
Nicole J. D. Weegerink
,
Margit Schraders
,
Jaap Oostrik
,
Patrick L. M. Huygen
,
Tim M. Strom
,
Susanne Granneman
,
Ronald J. E. Pennings
,
Hanka Venselaar
,
Lies H. Hoefsloot
,
Mariet Elting
,
Cor W. R. J. Cremers
,
Ronald J. C. Admiraal
Henricus P. M. Kunst
http://academic.research.microsoft.com/io.ashx?type=5&id=48407983&selfId1=11406963&selfId2=0&maxNumber=12&query=
Journal:
Jaro-journal of The Association for Research in Otolaryngology - JARO
, pp. 1-14, 2011
SDHAF2 (PGL2SDH5) and hereditary head and neck paraganglioma
H. P. M. Kunst
,
M. H. Rutten
,
J. P. de Monnink
,
L. H. Hoefsloot
,
H. J. L. M. Timmers
,
H. A. M. Marres
,
J. C. Jansen
,
J. M. J. Kremer
,
J. P. M. Bayley
,
C. W. R. J. Cremers
Journal:
Clinical Cancer Research - CLIN CANCER RES
, pp. 247-254, 2011
Disruption of Teashirt Zinc Finger Homeobox 1 Is Associated with Congenital Aural Atresia in Humans
I. Feenstra
,
L. E. L. M. Vissers
,
R. J. E. Pennings
,
W. M. Nillesen
,
R. Pfundt
,
H. P. Kunst
,
R. J. Admiraal
,
J. A. Veltman
,
C. M. A. van Ravenswaaij-Arts
,
H. G. Brunner
,
C. W. R. J. Cremers
Journal:
American Journal of Human Genetics - AMER J HUM GENET
, pp. 813-819, 2011
Progressive Sensorineural Hearing Loss and Normal Vestibular Function in a Dutch DFNB7/11 Family with a Novel Mutation in TMC1
Anne-Martine R. de Heer
,
Rob W. J. Collin
,
Patrick L. M. Huygen
,
Margit Schraders
,
Jaap Oostrik
,
Myrthe Rouwette
,
Henricus P. M. Kunst
,
Hannie Kremer
,
Cor W. R. J. Cremers
Journal:
Audiology and Neuro-otology - AUDIOL NEURO-OTOL
, vol. 16, no. 2, pp. 93-105, 2011
A new locus for otosclerosis, OTSC10, maps to chromosome 1q41-44
I. Schrauwen
,
N. J. D. Weegerink
,
E. Fransen
,
C. Claes
,
R. J. E. Pennings
,
C. W. R. J. Cremers
,
P. L. M. Huygen
,
H. P. M. Kunst
,
G. van Camp
Journal:
Clinical Genetics - CLIN GENET
, pp. 495-497, 2011
Sort by:
Citations
(209 times by 172 publications)
Gipc3 mutations associated with audiogenic seizures and sensorineural hearing loss in mouse and human
(
Citations: 1
)
Nikoletta Charizopoulou
,
Andrea Lelli
,
Margit Schraders
,
Kausik Ray
,
Michael S. Hildebrand
,
Arabandi Ramesh
,
C. R. Srikumari Srisailapathy
,
Jaap Oostrik
,
Ronald J. C. Admiraal
,
Harold R. Neely
,
Joseph R. Latoche
,
Richard J. H. Smith
http://academic.research.microsoft.com/io.ashx?type=5&id=53381775&selfId1=11406963&selfId2=0&maxNumber=12&query=
Journal:
Nature Communications
, vol. 2, pp. 201-201, 2011
Genotype–Phenotype Correlation in DFNB8/10 Families with TMPRSS3 Mutations
Nicole J. D. Weegerink
,
Margit Schraders
,
Jaap Oostrik
,
Patrick L. M. Huygen
,
Tim M. Strom
,
Susanne Granneman
,
Ronald J. E. Pennings
,
Hanka Venselaar
,
Lies H. Hoefsloot
,
Mariet Elting
,
Cor W. R. J. Cremers
,
Ronald J. C. Admiraal
Henricus P. M. Kunst
http://academic.research.microsoft.com/io.ashx?type=5&id=48407983&selfId1=11406963&selfId2=0&maxNumber=12&query=
Journal:
Jaro-journal of The Association for Research in Otolaryngology - JARO
, pp. 1-14, 2011
Family-based designs for genome-wide association studies
Yoichiro Kamatani
,
Mark Lathrop
,
Jurg Ott
Journal:
Nature Reviews Genetics - NAT REV GENET
, vol. 12, no. 7, pp. 465-474, 2011
Homozygosity Mapping Reveals Mutations of GRXCR1 as a Cause of Autosomal-Recessive Nonsyndromic Hearing Impairment
(
Citations: 7
)
Margit Schraders
,
Kwanghyuk Lee
,
Jaap Oostrik
,
Patrick L. M. Huygen
,
Ghazanfar Ali
,
Lies H. Hoefsloot
,
Joris A. Veltman
,
Frans P. M. Cremers
,
Sulman Basit
,
Muhammad Ansar
,
Cor W. R. J. Cremers
,
Henricus P. M. Kunst
http://academic.research.microsoft.com/io.ashx?type=5&id=36196472&selfId1=11406963&selfId2=0&maxNumber=12&query=
Journal:
American Journal of Human Genetics - AMER J HUM GENET
, vol. 86, no. 2, pp. 138-147, 2010
Wolfram syndrome: important implications for pediatricians and pediatric endocrinologists
(
Citations: 3
)
Sharath Kumar
Journal:
Pediatric Diabetes - PEDIATR DIABETES
, vol. 11, no. 1, pp. 28-37, 2010
Comments