J. Oostrik: search on Z-Library

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1

Brain-to-Brain Synchrony and Learning Outcomes Vary by Student–Teacher Dynamics: Evidence from a Real-world Classroom Electroencephalography Study

Bevilacqua, Dana, Davidesco, Ido, Wan, Lu, Oostrik, Matthias, Chaloner, Kim, Rowland, Jess, Ding, Mingzhou, Poeppel, David, Dikker, Suzanne

Journal:

Journal of Cognitive Neuroscience

Year:

2018

Language:

english

File:

PDF, 1.53 MB

english, 2018

2

Brain-to-Brain Synchrony Tracks Real-World Dynamic Group Interactions in the Classroom

Dikker, Suzanne, Wan, Lu, Davidesco, Ido, Kaggen, Lisa, Oostrik, Matthias, McClintock, James, Rowland, Jess, Michalareas, Georgios, Van Bavel, Jay J., Ding, Mingzhou, Poeppel, David

Journal:

Current Biology

Year:

2017

Language:

english

File:

PDF, 1.56 MB

english, 2017

3

Crowdsourcing neuroscience: inter-brain coupling during face-to-face interactions outside the laboratory

Dikker, Suzanne, Michalareas, Georgios, Oostrik, Matthias, Serafimaki, Amalia, Kahraman, Hasibe Melda, Struiksma, Marijn E., Poeppel, David

Journal:

Year:

2020

File:

PDF, 1.48 MB

2020

4

Progressive hearing loss and vestibular dysfunction caused by a homozygous nonsense mutation in CLIC5

Seco, Celia Zazo, Oonk, Anne MM, Domínguez-Ruiz, María, Draaisma, Jos MT, Gandía, Marta, Oostrik, Jaap, Neveling, Kornelia, Kunst, Henricus PM, Hoefsloot, Lies H, del Castillo, Ignacio, Pennings, Rona

Journal:

European Journal of Human Genetics

Year:

2015

Language:

english

File:

PDF, 1.08 MB

english, 2015

5

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

6

Involvement of DFNB59 mutations in autosomal recessive nonsyndromic hearing impairment

Rob W.J. Collin, Ersan Kalay, Jaap Oostrik, Refik Çaylan, Bernd Wollnik, Selçuk Arslan, Anneke I. den Hollander, Yelda Birinci, Peter Lichtner, Tim M. Strom, Bayram Toraman, Lies H. Hoefsloot, Cor W.R

Journal:

Year:

2007

Language:

english

File:

PDF, 311 KB

english, 2007

7

Missense mutations in POU4F3 cause autosomal dominant hearing impairment DFNA15 and affect subcellular localization and DNA binding

Rob W.J. Collin, Ramesh Chellappa, Robert-Jan Pauw, Gert Vriend, Jaap Oostrik, Wendy van Drunen, Patrick L. Huygen, Ronald Admiraal, Lies H. Hoefsloot, Frans P.M. Cremers, Mengqing Xiang, Cor W.R.J. C

Journal:

Year:

2008

Language:

english

File:

PDF, 396 KB

english, 2008

8

A novel locus for autosomal recessive nonsyndromic hearing impairment,DFNB63,maps to chromosome 11q13.2–q13.4

E. Kalay, R. Caylan, A. F. Kıroglu, T. Yasar, R. W. J. Collin, J. G. A. M. Heister, J. Oostrik, C. W. R. J. Cremers, H. G. Brunner, A. Karaguzel, H. Kremer

Journal:

Journal of Molecular Medicine

Year:

2007

Language:

english

File:

PDF, 308 KB

english, 2007

9

Genotype–Phenotype Correlation in DFNB8/10 Families withTMPRSS3Mutations

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. Cr

Journal:

Journal of the Association for Research in Otolaryngology

Year:

2011

Language:

english

File:

PDF, 1003 KB

english, 2011

10

Mid-frequency DFNA8/12 hearing loss caused by a synonymous TECTA mutation that affects an exonic splice enhancer

Collin, Rob W J, de Heer, Anne-Martine R, Oostrik, Jaap, Pauw, Robert-Jan, Plantinga, Rutger F, Huygen, Patrick L, Admiraal, Ronald, de Brouwer, Arjan P M, Strom, Tim M, Cremers, Cor W R J

Journal:

European Journal of Human Genetics

Year:

2008

Language:

english

File:

PDF, 282 KB

english, 2008

11

Homozygosity Mapping Reveals Mutations of GRXCR1 as a Cause of Autosomal-Recessive Nonsyndromic Hearing Impairment

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

Journal:

The American Journal of Human Genetics

Year:

2010

Language:

english

File:

PDF, 915 KB

english, 2010

12

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

13

Next-Generation Sequencing Identifies Mutations of SMPX, which Encodes the Small Muscle Protein, X-Linked, as a Cause of Progressive Hearing Impairment

Margit Schraders, Stefan A. Haas, Nicole J.D. Weegerink, Jaap Oostrik, Hao Hu, Lies H. Hoefsloot, Sriram Kannan, Patrick L.M. Huygen, Ronald J.E. Pennings, Ronald J.C. Admiraal, Vera M. Kalscheuer, He

Journal:

The American Journal of Human Genetics

Year:

2011

Language:

english

File:

PDF, 587 KB

english, 2011

14

Mutations of ESRRB Encoding Estrogen-Related Receptor Beta Cause Autosomal-Recessive Nonsyndromic Hearing Impairment DFNB35

Rob W.J. Collin, Ersan Kalay, Muhammad Tariq, Theo Peters, Bert van der Zwaag, Hanka Venselaar, Jaap Oostrik, Kwanghyuk Lee, Zubair M. Ahmed, Refik Çaylan, Yun Li, Henk A. Spierenburg, Erol Eyupoglu,

Journal:

The American Journal of Human Genetics

Year:

2008

Language:

english

File:

PDF, 2.04 MB

english, 2008

15

Audiometric characteristics of a Dutch family with Muckle-Wells syndrome

N.J.D. Weegerink, M. Schraders, J. Leijendeckers, K. Slieker, P.L.M. Huygen, L. Hoefsloot, J. Oostrik, R.J.E. Pennings, A. Simon, A. Snik, H. Kremer, H.P.M. Kunst

Journal:

Hearing Research

Year:

2011

Language:

english

File:

PDF, 685 KB

english, 2011

16

Involvement of lipooligosaccharides of Haemophilus influenzae and Neisseria meningitidis in defensin-enhanced bacterial adherence to epithelial cells

Annelies D Gorter, Jaap Oostrik, Peter van der Ley, Pieter S Hiemstra, Jacob Dankert, Loek van Alphen

Journal:

Microbial Pathogenesis

Year:

2003

Language:

english

File:

PDF, 212 KB

english, 2003

17

A Mutation in CABP2, Expressed in Cochlear Hair Cells, Causes Autosomal-Recessive Hearing Impairment

Isabelle Schrauwen, Sarah Helfmann, Akira Inagaki, Friederike Predoehl, Mohammad Amin Tabatabaiefar, Maria Magdalena Picher, Manou Sommen, Celia Zazo Seco, Jaap Oostrik, Hannie Kremer, Annelies Dheede

Journal:

The American Journal of Human Genetics

Year:

2012

Language:

english

File:

PDF, 600 KB

english, 2012

18

Mutations in OTOGL, Encoding the Inner Ear Protein Otogelin-like, Cause Moderate Sensorineural Hearing Loss

Kemal O. Yariz, Duygu Duman, Celia Zazo Seco, Julia Dallman, Mingqian Huang, Theo A. Peters, Asli Sirmaci, Na Lu, Margit Schraders, Isaac Skromne, Jaap Oostrik, Oscar Diaz-Horta, Juan I. Young, Suna T

Journal:

The American Journal of Human Genetics

Year:

2012

Language:

english

File:

PDF, 1.19 MB

english, 2012

19

Mutations of the Gene Encoding Otogelin Are a Cause of Autosomal-Recessive Nonsyndromic Moderate Hearing Impairment

Margit Schraders, Laura Ruiz-Palmero, Ersan Kalay, Jaap Oostrik, Francisco J. del Castillo, Orhan Sezgin, Andy J. Beynon, Tim M. Strom, Ronald J.E. Pennings, Celia Zazo Seco, Anne M.M. Oonk, Henricus

Journal:

The American Journal of Human Genetics

Year:

2012

Language:

english

File:

PDF, 652 KB

english, 2012

20

Progressive hereditary hearing impairment caused by a MYO6 mutation resembles presbyacusis

Oonk, A.M.M., Leijendeckers, J.M., Lammers, E.M., Weegerink, N.J.D., Oostrik, J., Beynon, A.J., Huygen, P.L.M., Kunst, H.P.M., Kremer, H., Snik, A.F.M., Pennings, R.J.E.

Journal:

Hearing Research

Year:

2013

Language:

english

File:

PDF, 1.36 MB

english, 2013

21

Clinical aspects of an autosomal dominantly inherited hearing impairment linked to the DFNA60 locus on chromosome 2q23.1–2q23.3

van Beelen, E., Schraders, M., Huygen, P.L.M., Oostrik, J., Plantinga, R.F., van Drunen, W., Collin, R.W.J., Kooper, D.P., Pennings, R.J.E., Cremers, C.W.R.J., Kremer, H., Kunst, H.P.M.

Journal:

Hearing Research

Year:

2013

Language:

english

File:

PDF, 670 KB

english, 2013

22

Vrijheid versus rechtvaardigheid

Hans Oostrik,Marion van Hattum

Journal:

Year:

2012

Language:

dutch

File:

PDF, 563 KB

dutch, 2012

23

Het handwerk onderzocht

Journal:

Year:

2014

Language:

dutch

File:

PDF, 1.93 MB

dutch, 2014

24

A canonical splice site mutation in GIPC3 causes sensorineural hearing loss in a large Pakistani family

Siddiqi, Saima, Ismail, Muhammad, Oostrik, Jaap, Munawar, Saba, Mansoor, Atika, Kremer, Hannie, Qamar, Raheel, Schraders, Margit

Journal:

Journal of Human Genetics

Year:

2014

Language:

english

File:

PDF, 812 KB

english, 2014

25

Novel mutation in AAA domain of BCS1L causing Bjornstad syndrome

Siddiqi, Saima, Siddiq, Saadat, Mansoor, Atika, Oostrik, Jaap, Ahmad, Nafees, Kazmi, Syed Ali Raza, Kremer, Hannie, Qamar, Raheel, Schraders, Margit

Journal:

Journal of Human Genetics

Year:

2013

Language:

english

File:

PDF, 962 KB

english, 2013

26

Democratische wortels

Spierts, Marcel, Oostrik, Hans

Journal:

Year:

2014

Language:

dutch

File:

PDF, 156 KB

dutch, 2014

27

Progressive Sensorineural Hearing Loss and Normal Vestibular Function in a Dutch DFNB7/11 Family with a Novel Mutation in TMC1

de Heer, Anne-Martine R., Collin, Rob W.J., Huygen, Patrick L.M., Schraders, Margit, Oostrik, Jaap, Rouwette, Myrthe, Kunst, Henricus P.M., Kremer, Hannie, Cremers, Cor W.R.J.

Journal:

Audiology & Neuro-Otology

Year:

2011

Language:

english

File:

PDF, 517 KB

english, 2011

28

Audiometric and Vestibular Features in a Second Dutch DFNA20/26 Family with a Novel Mutation in ACTG1

de Heer, A.-M. R., Huygen, P. L. M., Collin, R. W. J., Oostrik, J., Kremer, H., Cremers, W. R. J.

Journal:

Annals of Otology, Rhinology & Laryngology

Year:

2009

Language:

english

File:

PDF, 989 KB

english, 2009

29

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

30

Gipc3 mutations associated with audiogenic seizures and sensorineural hearing loss in mouse and human

Charizopoulou, Nikoletta, Lelli, Andrea, Schraders, Margit, Ray, Kausik, Hildebrand, Michael S., Ramesh, Arabandi, Srisailapathy, C. R. Srikumari, Oostrik, Jaap, Admiraal, Ronald J. C., Neely, Harold

Journal:

Nature Communications

Year:

2011

Language:

english

File:

PDF, 1.10 MB

english, 2011

31

A homozygous FITM2 mutation causes a deafness-dystonia syndrome with motor regression and signs of ichthyosis and sensory neuropathy

Zazo Seco, Celia, Castells-Nobau, Anna, Joo, Seol-hee, Schraders, Margit, Foo, Jia Nee, van der Voet, Monique, Velan, S. Sendhil, Nijhof, Bonnie, Oostrik, Jaap, de Vrieze, Erik, Katana, Radoslaw, Mans

Journal:

Disease Models & Mechanisms

Year:

2017

Language:

english

File:

PDF, 5.68 MB

english, 2017

32

Broadening the phenotype of DFNB28: Mutations in TRIOBP are associated with moderate, stable hereditary hearing impairment

Wesdorp, Mieke, van de Kamp, Jiddeke M., Hensen, Erik F., Schraders, Margit, Oostrik, Jaap, Yntema, Helger G., Feenstra, Ilse, Admiraal, Ronald J.C., Kunst, Henricus P.M., Tekin, Mustafa, Kanaan, Moie

Journal:

Hearing Research

Year:

2017

Language:

english

File:

PDF, 425 KB

english, 2017

33

Gallery Artists

Beck, Robert, Bornstein, Jennifer, Dikker, Suzanne, Oostrik, Matthias, Garvey, Greg, Ottiger, Nicole, Philbrick, Jane, Scott, Jill

Journal:

Year:

2014

Language:

english

File:

PDF, 2.96 MB

english, 2014

34

Heterozygous missense variants of LMX1A lead to nonsyndromic hearing impairment and vestibular dysfunction

Wesdorp, Mieke, de Koning Gans, Pia A. M., Schraders, Margit, Oostrik, Jaap, Huynen, Martijn A., Venselaar, Hanka, Beynon, Andy J., van Gaalen, Judith, Piai, Vitória, Voermans, Nicol, van Rossum, Mich

Journal:

Year:

2018

Language:

english

File:

PDF, 1.68 MB

english, 2018

35

Genetic Spectrum of Autosomal Recessive Non-Syndromic Hearing Loss in Pakistani Families

Shafique, Sobia, Siddiqi, Saima, Schraders, Margit, Oostrik, Jaap, Ayub, Humaira, Bilal, Ammad, Ajmal, Muhammad, Seco, Celia Zazo, Strom, Tim M., Mansoor, Atika, Mazhar, Kehkashan, Shah, Syed Tahir A.

Journal:

Year:

2014

Language:

english

File:

PDF, 1.07 MB

english, 2014

36

MPZL2 , Encoding the Epithelial Junctional Protein Myelin Protein Zero-like 2, Is Essential for Hearing in Man and Mouse

Wesdorp, Mieke, Murillo-Cuesta, Silvia, Peters, Theo, Celaya, Adelaida M., Oonk, Anne, Schraders, Margit, Oostrik, Jaap, Gomez-Rosas, Elena, Beynon, Andy J., Hartel, Bas P., Okkersen, Kees, Koenen, Ha

Journal:

The American Journal of Human Genetics

Year:

2018

Language:

english

File:

PDF, 2.51 MB

english, 2018

37

Klant, schuldhulpverlener en schuldeiser hebben voordeel bij Schuldenknooppunt

Oostrik, Marianne

Journal:

Year:

2020

File:

PDF, 291 KB

2020

38

A RIPOR2 in-frame deletion is a frequent and highly penetrant cause of adult-onset hearing loss

de Bruijn, Suzanne E, Smits, Jeroen J, Liu, Chang, Lanting, Cornelis P, Beynon, Andy J, Blankevoort, JoÃ«lle, Oostrik, Jaap, Koole, Wouter, de Vrieze, Erik, Cremers, Cor W R J, Cremers, Frans P M, Roo

Journal:

Journal of Medical Genetics

Year:

2020

File:

PDF, 1.62 MB

2020