Stuart Tanner

A genetic study of Wilson’s disease in the United Kingdom

Alison J. Coffey, Miranda Durkie, Stephen Hague et al. · Brain · 2013 · 353 citations · Full text

Glycogen storage disease type IX: High variability in clinical phenotype

Nicholas Beauchamp, Ann Dalton, Uma Ramaswami et al. · Molecular Genetics and Metabolism · 2007 · 123 citations

Genome-wide Association Study, Medicine, Genetics +13

Re-evaluation of the penicillamine challenge test in the diagnosis of Wilson’s disease in children

Thomas Müller, S.V. Koppikar, Rachel M. Taylor et al. · Journal of Hepatology · 2007 · 112 citations

Clinical Finding, Penicillamine Challenge Test, Clinical Epidemiology +3

Genotype Analysis for ΔF508, G551d and R553x Mutations in Children and Young Adults With Cystic Fibrosis With and Without Chronic Liver Disease

Ann Duthie, Derek G. Doherty, Carolyn Williams et al. · Hepatology · 1992 · 86 citations

Immunohistochemical analysis of Mallory bodies in Wilsonian and non-Wilsonian hepatic copper toxicosis

Thomas Müller, Cord Langner, Andrea Fuchsbichler et al. · Hepatology · 2004 · 80 citations

Immunology, Pathology, Cell Death +19