Prevalence of Common HFE and SERPINA1 Mutations in Patients with Hepatocellular Carcinoma in a Moroccan Population

A novel MHC class I–like gene is mutated in patients with hereditary haemochromatosis

John N. Feder, Andreas Gnirke, Zenta Tsuchihashi et al. · Nature Genetics · 1996 · 3.7K citations

Life Sciences, Genetics, Molecular Genetics +12

Global prevalence of putative haemochromatosis mutations.

Alison T. Merryweather‐Clarke, J. J. Pointon, Jeremy D. Shearman et al. · Journal of Medical Genetics · 1997 · 794 citations · Full text

Life Sciences, Genetics, Molecular Genetics +12

Risk of Cirrhosis and Primary Liver Cancer in Alpha₁-Antitrypsin Deficiency

Sten Eriksson, Joyce Carlson, Ramón Vélez · New England Journal of Medicine · 1986 · 584 citations

Medicine, Oncology, Pathology +17

Clinical Features and History of the Destructive Lung Disease Associated with Alpha-1-Antitrypsin Deficiency of Adults with Pulmonary Symptoms

Mark Brantly, L Paul, Barbara H. Miller et al. · American Review of Respiratory Disease · 1988 · 302 citations

Medicine, Clinical Sciences, Internal Medicine +11

A population-based study of the biochemical and clinical expression of the H63D hemochromatosis mutation

Peter Gochee, Lawrie W. Powell, Digby J Cullen et al. · Gastroenterology · 2002 · 257 citations · Full text

Medicine, Genetics, Molecular Genetics +8