Gene Mutations in the Succinate Dehydrogenase Subunit SDHB Cause Susceptibility to Familial Pheochromocytoma and to Familial ParagangliomaDewi Astuti, Eamonn R. Maher, Charis Eng et al.|The American Journal of Human Genetics|2001Cited by 1.1k
Germline SDHD mutation in familial phaeochromocytomaDewi Astuti, Eamonn R. Maher, Fiona Douglas et al.|The Lancet|2001Cited by 251
Epigenetic analysis of <i>HIC1</i> , <i>CASP8</i> , <i>FLIP</i> , <i>TSP1</i> , <i>DCR1</i> , <i>DCR2</i> , <i>DR4</i> , <i>DR5</i> , KvDMR1, <i>H19</i> and preferential 11p15.5 maternal-allele loss in von Hippel-Lindau and sporadic phaeochromocytomasC. D E Margetts, Eamonn R. Maher, Dewi Astuti et al.|Endocrine Related Cancer|2005Cited by 59
Evaluation of a functional epigenetic approach to identify promoter region methylation in phaeochromocytoma and neuroblastomaC. D E Margetts, Eamonn R. Maher, Hartmut P.H. Neumann et al.|Endocrine Related Cancer|2008Cited by 26