Sam Martin

Polymorphisms in the initiators of RET signalling pathway and susceptibility to sporadic Medullary Thyroid Carcinoma Running Title : Association of RET , ARTN and GFR α 1 with sMTC

B. Ponder, P. Pharoah, R. Luben, 2005 .

Polymorphisms in the initiators of RET (rearranged during transfection) signaling pathway and susceptibility to sporadic medullary thyroid carcinoma.

B. Ponder, P. Pharoah, A. Dunning, 2005, The Journal of clinical endocrinology and metabolism.

Molecular characterisation and structural analysis of an interferon homologue in sea bass (Dicentrarchus labrax L.).

S. Costantini, F. Buonocore, G. Scapigliati, 2009, Molecular immunology.

COL2A1 exon 2 mutations: relevance to the Stickler and Wagner syndromes

J. Yates, D. Baguley, Sam Martin, 2000, The British journal of ophthalmology.

A novel activating mutation in the RET tyrosine kinase domain mediates neoplastic transformation.

B. Ponder, M. Pierotti, S. Hodgson, 2006, Molecular endocrinology.

Extensive Local Gene Duplication and Functional Divergence among Paralogs in Atlantic Salmon

W. Jordan, D. Hazlerigg, S. Sumner, 2014, Genome biology and evolution.

Stickler syndrome: further mutations in COL11A1 and evidence for additional locus heterogeneity

J. Yates, Sam Martin, John D. Scott, 1999, European Journal of Human Genetics.