Publications

SNP array profiling of childhood adrenocortical tumors reveals distinct pathways of tumorigenesis and highlights candidate driver genes

Authors: Enzo lalli, et al.

Journal: The journal of clinical endocrinology and metabolism, April 26 2012.

 

MAX mutations cause hereditary and sporadic pheochromocytoma and paraganglioma

Authors: Nelly Burnichon, Alberto Cascon, Francesca Schiavi, et al.

Journal: Clin Cancer Res Published OnlineFirst March 27, 2012.

 

Staging and Functional Characterization of Pheochromocytoma and Paraganglioma by 18F-Fluorodeoxyglucose (18F-FDG) Positron Emission Tomography

Authors: Henri Timmers, et al.

Journal: Journal of the National Cancer Institute, May 2 2012.

Exome sequencing identifies MAX mutations as a cause of hereditary pheochromocytoma.

Authors: Comino-Méndez I, Gracia-Aznárez FJ, Schiavi F, Landa I, Leandro-García LJ, Letón R, Honrado E, Ramos-Medina R, Caronia D, Pita G, Gómez-Graña A, de Cubas AA, Inglada-Pérez L, Maliszewska A, Taschin E, Bobisse S, Pica G, Loli P, Hernández-Lavado R, Díaz JA, Gómez-Morales M, González-Neira A, Roncador G, Rodríguez-Antona C, Benítez J, Mannelli M, Opocher G, Robledo M, Cascón A.

Journal: Nat Genet. 2011 Jun 19;43(7):663-7. doi: 10.1038/ng.861.

Towards a Virtual Research Environment for International Adrenal Cancer Research

Authors: Richard O. Sinnott, Anthony J. Stell

International Conference on Computational Science, ICCS 2011

Classifying Architectural Data Sharing Models for e-Health Collaborations

Authors: Richard Sinnott, Anthony Stell, Jipu Jiang

HealthGrid 2011

Enabling Secure, Distributed Collaborations for Adrenal Tumor Research

Authors: Anthony Stell, Richard Sinnott, Jipu Jiang

National e-Science Centre, University of Glasgow, UK

HealthGrid 2010