Genome-wide association analysis identifies a susceptibility locus for sporadic vestibular schwannoma at 9p21

Autor: Katherine V Sadler, John Bowes, Charlie F Rowlands, Cristina Perez-Becerril, C Mwee van der Meer, Andrew T King, Scott A Rutherford, Omar N Pathmanaban, Charlotte Hammerbeck-Ward, Simon K W Lloyd, Simon R Freeman, Ricky Williams, Cathal John Hannan, Daniel Lewis, Steve Eyre, D Gareth Evans, Miriam J Smith

Publikováno v: Sadler, K, Bowes, J, Rowlands, C, Perez-Becerril, C, van der Meer, C M, King, A T, Rutherford, S A, Pathmanaban, O, Hammerbeck-ward, C, Lloyd, S K W, Freeman, S, Williams, R, Hannan, C J, Lewis, D, Eyre, S, Evans, D G & Smith, M J 2022, ' Genome-wide association analysis identifies a susceptibility locus for sporadic vestibular schwannoma at 9p21 ', Brain. https://doi.org/10.1093/brain/awac478

Vestibular schwannomas are benign nerve sheath tumours that arise on the vestibulocochlear nerves. Vestibular schwannomas are known to occur in the context of tumour predisposition syndromes NF2-related and LZTR1-related schwannomatosis. However, the

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::56e6e7c9057bbb14c32811fc35e8e63c
https://uom.elsevierpure.com/en/publications/79199585-efc4-4ec3-bcac-4c50a72be735

1199P Identification of patient specific immune therapy treatment sensitivity by ex vivo testing

Autor: F. Grillet, Kuan Yan, W. Vader, D. C. H. van der Meer, J. Overkamp, A. Jariani, C. de Kroon, L. Daszkiewicz, Leo S. Price, Judith R. Kroep

Publikováno v: Annals of Oncology. 31:S788

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::8170e3a9db715287027977f065737101
https://doi.org/10.1016/j.annonc.2020.08.093

Verslag jaarvergadering Vereniging voor Gezondheidsrecht 2008

Autor: H. C. B. van der Meer

Publikováno v: Tijdschrift voor Gezondheidsrecht. 32:343-349

Op vrijdag 18 april 2008 vond in Congrescentrum Figi te Zeist de jaarvergadering 2008 plaats van de Vereniging voor Gezondheidsrecht.

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::057f5ce9d6b826e7c536d6b2cbd71c6d
https://doi.org/10.1007/bf03081523

Genetic testing in hereditary non-polyposis colorectal cancer families with a MSH2, MLH1, or MSH6 mutation

Autor: Hans F. A. Vasen, J. T. Wijnen, C. Tops, Anja Wagner, Aad Tibben, J. G. M. Klijn, C. A. Van Der Meer, Martinus F. Niermeijer, K Zwinderman, Hanne Meijers-Heijboer, M Kets

Publikováno v: Journal of medical genetics, 39(11), 833-837. BMJ Publishing Group
Journal of Medical Genetics, 39, 833-837. BMJ Publishing Group
Journal of Medical Genetics, 39, 833-7
Journal of Medical Genetics, 39, 11, pp. 833-7

About 5% of colorectal cancers are associated with the autosomal dominantly inherited cancer susceptibility syndrome hereditary non-polyposis colorectal cancer (HNPCC).1,2 HNPCC is characterised by a high risk of developing colorectal cancer and endo

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::69001ce53af807830d45137c93cd4baa
https://doi.org/10.1136/jmg.39.11.833

Psychological impact of receiving a BRCA1/BRCA2 test result

Autor: L, Lodder, P G, Frets, R W, Trijsburg, E J, Meijers-Heijboer, J G, Klijn, H J, Duivenvoorden, A, Tibben, A, Wagner, C A, van der Meer, A M, van den Ouweland, M F, Niermeijer

Publikováno v: American journal of medical genetics. 98(1)

Mutation analysis for autosomal dominant hereditary breast/ovarian cancer genes (BRCA1/BRCA2) became an important technique for women at risk of carrying these mutations. Healthy female mutation carriers have a high lifetime risk for breast and/or ov

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=pmid________::2af4e017a164d4d2d1750c4964dc3fdf
https://pubmed.ncbi.nlm.nih.gov/11426450