CNS cancer

Cancer risk in 348 French MSH2 or MLH1 gene carriers
Y Parc, C Boisson, G Thomas, S Olschwang

Journal of Medical Genetics Mar 2003, 40 (3) 208-213; DOI: 10.1136/jmg.40.3.208
A molecular analysis of individuals with neurofibromatosis type 1 (NF1) and optic pathway gliomas (OPGs), and an assessment of genotype–phenotype correlations
Saba Sharif, Meena Upadhyaya, Rosalie Ferner, Elisa Majounie, Andrew Shenton, Michael Baser, Nalin Thakker, D Gareth Evans

Journal of Medical Genetics Apr 2011, 48 (4) 256-260; DOI: 10.1136/jmg.2010.081760
Cranial meningiomas in 411 neurofibromatosis type 2 (NF2) patients with proven gene mutations: clear positional effect of mutations, but absence of female severity effect on age at onset
Miriam J Smith, Jenny E Higgs, Naomi L Bowers, Dorothy Halliday, Joan Paterson, James Gillespie, Susan M Huson, Simon R Freeman, Simon Lloyd, Scott A Rutherford, Andrew T King, Andrew J Wallace, Richard T Ramsden, D Gareth R Evans

Journal of Medical Genetics Apr 2011, 48 (4) 261-265; DOI: 10.1136/jmg.2010.085241
Age associated increase in the prevalence of chromosome 22q loss of heterozygosity in histological subsets of benign meningioma
M E Baser, T Y Poussaint

Journal of Medical Genetics Mar 2006, 43 (3) 285-287; DOI: 10.1136/jmg.2005.035162
A PDGFRA promoter polymorphism, which disrupts the binding of ZNF148, is associated with primitive neuroectodermal tumours and ependymomas
C De Bustos, A Smits, B Strömberg, V P Collins, M Nistér, G Afink

Journal of Medical Genetics Jan 2005, 42 (1) 31-37; DOI: 10.1136/jmg.2004.024034
Molecular genetic analysis of the NF2 gene in young patients with unilateral vestibular schwannomas
A Mohyuddin, W J Neary, A Wallace, C L Wu, S Purcell, H Reid, R T Ramsden, A Read, G Black, D G R Evans

Journal of Medical Genetics May 2002, 39 (5) 315-322; DOI: 10.1136/jmg.39.5.315
Mental retardation and cardiovascular malformations in NF1 microdeleted patients point to candidate genes in 17q11.2
M Venturin, P Guarnieri, F Natacci, M Stabile, R Tenconi, M Clementi, C Hernandez, P Thompson, M Upadhyaya, L Larizza, P Riva

Journal of Medical Genetics Jan 2004, 41 (1) 35-41; DOI: 10.1136/jmg.2003.014761
Over-representation of PPARγ sequence variants in sporadic cases of glioblastoma multiforme: preliminary evidence for common low penetrance modifiers for brain tumour risk in the general population
Xiao-Ping Zhou, Wendy M Smith, Oliver Gimm, Elisabetta Mueller, Xin Gao, Pasha Sarraf, Thomas W Prior, Christoph Plass, Andreas von Deimling, Peter McL Black, Allan J Yates, Charis Eng

Journal of Medical Genetics Jun 2000, 37 (6) 410-414; DOI: 10.1136/jmg.37.6.410
Rhabdomyosarcoma in patients with constitutional mismatch-repair-deficiency syndrome
C P Kratz, S Holter, J Etzler, M Lauten, A Pollett, C M Niemeyer, S Gallinger, K Wimmer

Journal of Medical Genetics Jun 2009, 46 (6) 418-420; DOI: 10.1136/jmg.2008.064212
Rare TP53 genetic variant associated with glioma risk and outcome
Kathleen M Egan, L Burton Nabors, Jeffrey J Olson, Alvaro N Monteiro, James E Browning, Melissa H Madden, Reid C Thompson

Journal of Medical Genetics Jul 2012, 49 (7) 420-421; DOI: 10.1136/jmedgenet-2012-100941

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