Peer victimization and suicidal ideation

Autor: Geel, M. van, Vedder, P.H., Martin, C., Preedy, V.R., Patel, V.B.

Publikováno v: Handbook of anger, aggression, and violence. Springer International Publishing
Handbook of anger, aggression, and violence

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=dedup_wf_001::d09f2d276b31b1063b69c253150e2289
https://doi.org/10.1007/978-3-030-98711-4_80-1

Does cyberbullying predict internalizing problems and conduct problems when controlled for traditional bullying?

Autor: Geel, M. van, Vedder, P.H.

Publikováno v: Scandinavian Journal of Psychology, 61(2), 307-311
Scandinavian Journal of Psychology

In this study, relations between cybervictimization and internalizing and conduct problems were analyzed while controlling for traditional victimization. A sample of 701 emerging adults in secondary vocational education completed self‐reports about

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c9ca4293cda8fb05ed33944be90f2f67
https://doi.org/10.1111/sjop.12601

Intergroup contact and prejudice between Dutch majority and Muslim minority youth in the Netherlands

Autor: Vedder, P., Wenink, E.G., Geel, M. van, Van, Geel M.

Publikováno v: Cultural Diversity & Ethnic Minority Psychology
Cultural Diversity & Ethnic Minority Psychology, 23(4), 477-485

Objectives: This study deals with three relatively understudied issues in intergroup contact: negative contact, mediating mechanisms, and the minority perspective. Both direct and extended positive and negative contact experiences are included in the

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b69e29dc2846fb5a39f6fa63117a1e59
https://pubmed.ncbi.nlm.nih.gov/28301182

Complete allele information in the diagnosis of facioscapulohumeral muscular dystrophy by triple DNA analysis

Autor: Kievit, P. de, Geel, M. van, Wielen, M.J.R. van der, Bakker, E., Padberg, G.W.A.M., Frants, R.R., Maarel, S.M. van der

Publikováno v: Annals of Neurology, 50, 6, pp. 816--9
Annals of Neurology, 50, 816--9

Item does not contain fulltext Facioscapulohumeral muscular dystrophy is caused by partial deletion of the D4Z4 repeat array on chromosome 4q35. Genetic diagnosis is based on sizing of this repeat array, which is complicated by cross-hybridization of

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=dedup_wf_001::37d21268777dc5a0c0c63c8228f472d7
https://hdl.handle.net/2066/185593

Identification of the first gene (FRG1) from the FSHD region on human chromosome 4q35

Autor: Deutekom, J.C.T. van, Lemmers, R.J.L.F., Grewal, P.K., Geel, M. van, Romberg, S., Dauwerse, H.G., Wright, T.J., Padberg, G.W., Hofker, M.H., Hewitt, J.E., Frants, R.R.

Publikováno v: Human Molecular Genetics, 5, 5, pp. 581-590
Human Molecular Genetics, 5, 581-590. Oxford univ press united kingdom
Human Molecular Genetics, 5, 581-590

Contains fulltext : 24067___.PDF (Publisher’s version ) (Open Access)

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=dedup_wf_001::0f05ee2d895d54924910a7bb259c5386
https://hdl.handle.net/2066/24067