David Hewett‐Emmett

Carbonic anhydrase II deficiency identified as the primary defect in the autosomal recessive syndrome of osteopetrosis with renal tubular acidosis and cerebral calcification.

William S. Sly, David Hewett‐Emmett, Michael P. Whyte et al. · Proceedings of the National Academy of Sciences · 1983 · 618 citations · Full text

Electrolyte Disorder, Carbonic Anhydrase Ii, Pathology +16

Functional Diversity, Conservation, and Convergence in the Evolution of the α-, β-, and γ-Carbonic Anhydrase Gene Families

David Hewett‐Emmett, Richard E. Tashian · Molecular Phylogenetics and Evolution · 1996 · 606 citations

Biology, Biosynthesis, Phylogenetics +15

Rates of Nucleotide Substitution in Primates and Rodents and the Generation–Time Effect Hypothesis

Wen‐Hsiung Li, Darrell L. Ellsworth, Julia Krushkal et al. · Molecular Phylogenetics and Evolution · 1996 · 340 citations

Biology, Nucleotide Substitution, Molecular Ecology +12

Carbonic Anhydrase II Deficiency in 12 Families with the Autosomal Recessive Syndrome of Osteopetrosis with Renal Tubular Acidosis and Cerebral Calcification

William S. Sly, Michael P. Whyte, Vasantha Sundaram et al. · New England Journal of Medicine · 1985 · 324 citations

High Polymorphism at the Human Melanocortin 1 Receptor Locus

Brinda K. Rana, David Hewett‐Emmett, Jin Li et al. · Genetics · 1999 · 284 citations · Full text