Maureen Boxer

Genetic defects of the UDP-glucuronosyltransferase-1 (UGT1) gene that cause familial non-haemolytic unconjugated hyperbilirubinaemias

Douglas J. Clarke, Nabil Moghrabi, Gemma Monaghan et al. · Clinica Chimica Acta · 1997 · 139 citations

Life Sciences, Genetics, Molecular Genetics +14

Family history of severe cardiovascular disease in Marfan syndrome is associated with increased aortic diameter and decreased survival

David I. Silverman, Jonathon Gray, Mary J. Roman et al. · Journal of the American College of Cardiology · 1995 · 107 citations · Full text

Medicine, Cardiology, Genetics +14

A molecular genetic service for diagnosing individuals with familial hypercholesterolaemia (FH) in the United Kingdom

Karen E. Heath, Steve E. Humphries, Helen Middleton‐Price et al. · European Journal of Human Genetics · 2001 · 107 citations

Life Sciences, Genetics, Molecular Genetics +11

Genetic analysis of microsomal epoxide hydrolase in patients with carbamazepine hypersensitivity

Victoria J. Green, Munir Pirmohamed, Neil R. Kitteringham et al. · Biochemical Pharmacology · 1995 · 88 citations

Life Sciences, Genetics, Pharmacology +7

Identification of an A-to-G Missense Mutation in Exon 2 of the UGT1 Gene Complex That Causes Crigler-Najjar Syndrome Type 2

Nabil Moghrabi, Douglas J. Clarke, Maureen Boxer et al. · Genomics · 1993 · 83 citations

Life Sciences, Genetics, Molecular Genetics +9