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1

Predictive Value of Panoramic Radiography for Injury of Inferior Alveolar Nerve After Mandibular Third Molar Surgery

Su, Naichuan, van Wijk, Arjen, Berkhout, Erwin, Sanderink, Gerard, De Lange, Jan, Wang, Hang, van der Heijden, Geert J.M.G.

Journal:

Journal of Oral and Maxillofacial Surgery

Year:

2017

Language:

english

File:

PDF, 1.32 MB

english, 2017

2

Daytime triglyceride variability in men and women with different levels of triglyceridemia

Boudewijn Klop, Jeffrey S. Cohn, Antonie J.H.H.M. van Oostrom, Jeroen P.H. van Wijk, Erwin Birnie, Manuel Castro Cabezas

Journal:

Clinica Chimica Acta

Year:

2011

Language:

english

File:

PDF, 189 KB

english, 2011

3

Nonsyndromic Hearing Loss Caused by USH1G Mutations

Maria Oonk, Anne Marthe, van Huet, Ramon A. C., Leijendeckers, Joop M., Oostrik, Jaap, Venselaar, Hanka, van Wijk, Erwin, Beynon, Andy, Kunst, Henricus P. M., Hoyng, Carel B., Kremer, Hannie, Schrader

Journal:

Year:

2015

Language:

english

File:

PDF, 597 KB

english, 2015

4

Microscopic Residues of Bone from Dissolving Human Remains in Acids

Vermeij, Erwin, Zoon, Peter, van Wijk, Mayonne, Gerretsen, Reza

Journal:

Journal of Forensic Sciences

Year:

2015

Language:

english

File:

PDF, 925 KB

english, 2015

5

Mutations in the lipoma HMGIC fusion partner-like 5 (LHFPL5) gene cause autosomal recessive nonsyndromic hearing loss

Ersan Kalay, Yun Li, Abdullah Uzumcu, Oya Uyguner, Rob W. Collin, Refik Caylan, Melike Ulubil-Emiroglu, Ferry F.J. Kersten, Gunter Hafiz, Erwin van Wijk, Hulya Kayserili, Edyta Rohmann, Janine Wagenst

Journal:

Year:

2006

Language:

english

File:

PDF, 487 KB

english, 2006

6

Identification and molecular modelling of a mutation in the motor head domain of myosin VIIA in a family with autosomal dominant hearing impairment (DFNA11)

Mirjam W. J. Luijendijk, Erwin van Wijk, Anne M. L. C. Bischoff, Elmar Krieger, Patrick L. M. Huygen, Ronald J. E. Pennings, Han G. Brunner, Cor W. R. J. Cremers, Frans P. M. Cremers, Hannie Kremer

Journal:

Year:

2004

Language:

english

File:

PDF, 579 KB

english, 2004

7

OFD1 Is Mutated in X-Linked Joubert Syndrome and Interacts with LCA5-Encoded Lebercilin

Karlien L.M. Coene, Ronald Roepman, Dan Doherty, Bushra Afroze, Hester Y. Kroes, Stef J.F. Letteboer, Lock H. Ngu, Bartlomiej Budny, Erwin van Wijk, Nicholas T. Gorden, Malika Azhimi, Christel Thauvin

Journal:

The American Journal of Human Genetics

Year:

2009

Language:

english

File:

PDF, 2.74 MB

english, 2009

8

Mutations in PTPRQ Are a Cause of Autosomal-Recessive Nonsyndromic Hearing Impairment DFNB84 and Associated with Vestibular Dysfunction

Margit Schraders, Jaap Oostrik, Patrick L.M. Huygen, Tim M. Strom, Erwin van Wijk, Henricus P.M. Kunst, Lies H. Hoefsloot, Cor W.R.J. Cremers, Ronald J.C. Admiraal, Hannie Kremer

Journal:

The American Journal of Human Genetics

Year:

2010

Language:

english

File:

PDF, 657 KB

english, 2010

9

Direct interaction of the Usher syndrome 1G protein SANS and myomegalin in the retina

Nora Overlack, Dilek Kilic, Katharina Bauß, Tina Märker, Hannie Kremer, Erwin van Wijk, Uwe Wolfrum

Journal:

Biochimica et Biophysica Acta (BBA) - Molecular Cell Research

Year:

2011

Language:

english

File:

PDF, 2.51 MB

english, 2011

10

The mitotic spindle protein SPAG5/Astrin connects to the Usher protein network postmitotically

Ferry FJ Kersten, Erwin van Wijk, Lisette Hetterschijt, Katharina Bauβ, Theo A Peters, Mariam G Aslanyan, Bert van der Zwaag, Uwe Wolfrum, Jan EE Keunen, Ronald Roepman, Hannie Kremer

Journal:

Year:

2012

Language:

english

File:

PDF, 1.55 MB

english, 2012

11

Modulation of intercellular communication between smooth muscle cells by growth factors and cytokines

Anne Mensink, Abraham Brouwer, Erwin H. Van den Burg, Saskia Geurts, Wim M.F. Jongen, Catriona M.M. Lakemond, Irma Meijerman, Thea Van der Wijk

Journal:

European Journal of Pharmacology

Year:

1996

Language:

english

File:

PDF, 878 KB

english, 1996

12

Identification of 51 Novel Exons of the Usher Syndrome Type 2A (USH2A) Gene That Encode Multiple Conserved Functional Domains and That Are Mutated in Patients with Usher Syndrome Type II

Erwin van Wijk, Ronald J.E. Pennings, Heleen te Brinke, Annemarie Claassen, Helger G. Yntema, Lies H. Hoefsloot, Frans P.M. Cremers, Cor. W.R.J. Cremers, Hannie Kremer

Journal:

The American Journal of Human Genetics

Year:

2004

Language:

english

File:

PDF, 595 KB

english, 2004

13

Analysis of protein-protein interaction between late cornified envelope proteins and corneodesmosin

Bergboer, Judith G. M., Dulak, Maria G., van Vlijmen-Willems, Ivonne M. J. J., Jonca, Nathalie, van Wijk, Erwin, Hendriks, Wiljan J. A. J., Zeeuwen, Patrick L. J. M., Schalkwijk, Joost

Journal:

Experimental Dermatology

Year:

2014

Language:

english

File:

PDF, 363 KB

english, 2014

14

The pros and cons of vertebrate animal models for functional and therapeutic research on inherited retinal dystrophies

Slijkerman, Ralph W.N., Song, Fei, Astuti, Galuh D.N., Huynen, Martijn A., van Wijk, Erwin, Stieger, Knut, Collin, Rob W.J.

Journal:

Progress in Retinal and Eye Research

Year:

2015

Language:

english

File:

PDF, 13.15 MB

english, 2015

15

CNNM2 Mutations Cause Impaired Brain Development and Seizures in Patients with Hypomagnesemia

Arjona, Francisco J., de Baaij, Jeroen H. F., Schlingmann, Karl P., Lameris, Anke L. L., van Wijk, Erwin, Flik, Gert, Regele, Sabrina, Korenke, G. Christoph, Neophytou, Birgit, Rust, Stephan, Reintjes

Journal:

Year:

2014

Language:

english

File:

PDF, 8.28 MB

english, 2014

16

Active Transport and Diffusion Barriers Restrict Joubert Syndrome-Associated ARL13B/ARL-13 to an Inv-like Ciliary Membrane Subdomain

Cevik, Sebiha, Sanders, Anna A. W. M., Van Wijk, Erwin, Boldt, Karsten, Clarke, Lara, van Reeuwijk, Jeroen, Hori, Yuji, Horn, Nicola, Hetterschijt, Lisette, Wdowicz, Anita, Mullins, Andrea, Kida, Kata

Journal:

Year:

2013

Language:

english

File:

PDF, 2.64 MB

english, 2013

17

Novel and recurrent CIB2 variants, associated with nonsyndromic deafness, do not affect calcium buffering and localization in hair cells

Seco, Celia Zazo, Giese, Arnaud P, Shafique, Sobia, Schraders, Margit, Oonk, Anne M M, Grossheim, Mike, Oostrik, Jaap, Strom, Tim, Hegde, Rashmi, van Wijk, Erwin, Frolenkov, Gregory I, Azam, Maleeha,

Journal:

European Journal of Human Genetics

Year:

2015

Language:

english

File:

PDF, 1.67 MB

english, 2015

18

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

Pierrache, Laurence H.M., Hartel, Bas P., van Wijk, Erwin, Meester-Smoor, Magda A., Cremers, Frans P.M., de Baere, Elfride, de Zaeytijd, Julie, van Schooneveld, Mary J., Cremers, Cor W.R.J., Dagnelie,

Journal:

Year:

2016

Language:

english

File:

PDF, 601 KB

english, 2016

19

Cochleovestibular and Ocular Features in a Dutch DFNA11 Family

Bischoff, Anne M. L. C., Pennings, Ronald J. E., Huygen, Patrick L. M., Luijendijk, Mirjam W., van Wijk, Erwin, Cruysberg, Johannes R. M., Kremer, Hannie, Cremers, Cor W. R. J.

Journal:

Otology & Neurotology

Year:

2006

Language:

english

File:

PDF, 327 KB

english, 2006

20

Identification of a homozygous nonsense mutation inKIAA0556in a consanguineous family displaying Joubert syndrome

Roosing, Susanne, Rosti, Rasim O., Rosti, Basak, de Vrieze, Erik, Silhavy, Jennifer L., van Wijk, Erwin, Wakeling, Emma, Gleeson, Joseph G.

Journal:

Year:

2016

Language:

english

File:

PDF, 2.67 MB

english, 2016

21

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

Hartel, Bas P., Löfgren, Maria, Huygen, Patrick L.M., Guchelaar, Iris, Lo-A-Njoe Kort, Nicole, Sadeghi, Andre M., van Wijk, Erwin, Tranebjærg, Lisbeth, Kremer, Hannie, Kimberling, William J., Cremers,

Journal:

Hearing Research

Year:

2016

Language:

english

File:

PDF, 520 KB

english, 2016

22

Comment on “Usherʼs Syndrome

Hartel, Bas P., Pennings, Ronald J.E., van Wijk, Erwin

Journal:

Otology & Neurotology

Year:

2016

Language:

english

File:

PDF, 38 KB

english, 2016

23

Genetic and clinical characterization of Pakistani families with Bardet-Biedl syndrome extends the genetic and phenotypic spectrum

Maria, Maleeha, Lamers, Ideke J. C., Schmidts, Miriam, Ajmal, Muhammad, Jaffar, Sulman, Ullah, Ehsan, Mustafa, Bilal, Ahmad, Shakeel, Nazmutdinova, Katia, Hoskins, Bethan, van Wijk, Erwin, Koster-Kamp

Journal:

Scientific Reports

Year:

2016

Language:

english

File:

PDF, 728 KB

english, 2016

24

Living with transversal upper limb reduction deficiency: limitations experienced by young adults during their transition to adulthood

Lankhorst, Ilse M. F., Baars, Erwin C. T., Wijk, Iris van, Janssen, Wim G. M., Poelma, Margriet J., van der Sluis, Corry K.

Journal:

Disability & Rehabilitation

Year:

2017

Language:

english

File:

PDF, 918 KB

english, 2017

25

A Dutch Family With Hearing Loss Linked to the DFNA20/26 Locus

Kemperman, Martijn H., De Leenheer, Els M. R., Huygen, Patrick L. M., van Wijk, Erwin, van Duijnhoven, Gerard, Cremers, Frans P. M., Kremer, Hannie, Cremers, Cor W. R. J.

Journal:

Archives of Otolaryngology - Head and Neck Surgery

Year:

2004

Language:

english

File:

PDF, 150 KB

english, 2004

26

Whole-exome sequencing reveals POC5 as a novel gene associated with autosomal recessive retinitis pigmentosa

Weisz Hubshman, Monika, Broekman, Sanne, van Wijk, Erwin, Cremers, Frans, Abu-Diab, Alaa, Samer, Khateb, Tzur, Shay, Lagovsky, Irena, Smirin-Yosef, Pola, Sharon, Dror, Haer-Wigman, Lonneke, Banin, Eya

Journal:

Human Molecular Genetics

Year:

2017

Language:

english

File:

PDF, 927 KB

english, 2017

27

C2orf71a/pcare1 is important for photoreceptor outer segment morphogenesis and visual function in zebrafish

Corral-Serrano, Julio C., Messchaert, Muriël, Dona, Margo, Peters, Theo A., Kamminga, Leonie M., van Wijk, Erwin, Collin, Rob W. J.

Journal:

Scientific Reports

Year:

2018

Language:

english

File:

PDF, 3.23 MB

english, 2018

28

Eyes shut homolog is important for the maintenance of photoreceptor morphology and visual function in zebrafish

Messchaert, Muriël, Dona, Margo, Broekman, Sanne, Peters, Theo A., Corral-Serrano, Julio C., Slijkerman, Ralph W. N., van Wijk, Erwin, Collin, Rob W. J., Neuhauss, Stephan C.F.

Journal:

Year:

2018

Language:

english

File:

PDF, 7.18 MB

english, 2018

29

Association of Whirlin with Ca v 1.3 (α 1D ) Channels in Photoreceptors, Defining a Novel Member of the Usher Protein Network

Kersten, Ferry F. J., van Wijk, Erwin, van Reeuwijk, Jeroen, van der Zwaag, Bert, Märker, Tina, Peters, Theo A., Katsanis, Nicholas, Wolfrum, Uwe, Keunen, Jan E. E., Roepman, Ronald, Kremer, Hannie

Journal:

Investigative Ophthalmology & Visual Science

Year:

2010

Language:

english

File:

PDF, 492 KB

english, 2010

30

Poor Splice-Site Recognition in a Humanized Zebrafish Knockin Model for the Recurrent Deep-Intronic c.7595-2144A>G Mutation in USH2A

Slijkerman, Ralph, Goloborodko, Alexander, Broekman, Sanne, de Vrieze, Erik, Hetterschijt, Lisette, Peters, Theo, Gerits, Milou, Kremer, Hannie, van Wijk, Erwin

Journal:

Year:

2018

Language:

english

File:

PDF, 1.21 MB

english, 2018

31

SLC41A1 is essential for magnesium homeostasis in vivo

Arjona, Francisco J., Latta, Femke, Mohammed, Sami G., Thomassen, Michael, van Wijk, Erwin, Bindels, René J. M., Hoenderop, Joost G. J., de Baaij, Jeroen H. F.

Journal:

Pflügers Archiv European Journal of Physiology

Year:

2018

Language:

english

File:

PDF, 3.36 MB

english, 2018

32

Modeling ZNF408 -Associated FEVR in Zebrafish Results in Abnormal Retinal Vasculature

Karjosukarso, Dyah W., Ali, Zaheer, Peters, Theo A., Zhang, Jia Qi Cheng, Hoogendoorn, Anita D M., Garanto, Alejandro, van Wijk, Erwin, Jensen, Lasse D., Collin, Rob W J.

Journal:

Investigative Opthalmology & Visual Science

Year:

2020

Language:

english

File:

PDF, 2.62 MB

english, 2020

33

How do 66 European institutional review boards approve one protocol for an international prospective observational study on traumatic brain injury? Experiences from the CENTER-TBI study

Timmers, Marjolein, van Dijck, Jeroen T. J. M., van Wijk, Roel P. J., Legrand, Valerie, van Veen, Ernest, Maas, Andrew I. R., Menon, David K., Citerio, Giuseppe, Stocchetti, Nino, Kompanje, Erwin J. O

Journal:

BMC Medical Ethics

Year:

2020

File:

PDF, 1.23 MB

2020