Andrew Read

A gene (PEX) with homologies to endopeptidases is mutated in patients with X–linked hypophosphatemic rickets

Fiona Francis, Steffen Hennig, Bernd Korn et al. · Nature Genetics · 1995 · 1.1K citations

Genetic Disorder, Genetics, X–linked Hypophosphatemic Rickets +3

SOX10 mutations in patients with Waardenburg-Hirschsprung disease

Véronique Pingault, Nadège Bondurand, Kirsten Kuhlbrodt et al. · Nature Genetics · 1998 · 817 citations

Mendelian Disorder, Genetic Disorder, Medicine +7

Waardenburg's syndrome patients have mutations in the human homologue of the Pax-3 paired box gene

Mayada Tassabehji, Andrew Read, Valerie Newton et al. · Nature · 1992 · 694 citations · Full text

Developmental Biology, Mendelian Disorder, Genetic Disorder +10

Waardenburg syndrome type 2 caused by mutations in the human microphthalmia (MITF) gene

Mayada Tassabehji, Valeria E. Newton, Andrew Read · Nature Genetics · 1994 · 667 citations

Developmental Biology, Disease Mechanism, Mendelian Disorder +8

FURTHER EXPERIENCE OF VITAMIN SUPPLEMENTATION FOR PREVENTION OF NEURAL TUBE DEFECT RECURRENCES

R. W. Smithells, Mary J. Seller, R Harris et al. · The Lancet · 1983 · 507 citations

Medicine, Neurology, Nutritional Neuroscience