David Hewett‐Emmett

Author

David Hewett‐Emmett

The University of Texas Health Science Center at Houston

Also Known As

D Hewett-Emmett, D. HEWETT-EMMETT, D. HEWETT‐EMMETT, D. Hewett-Emmett, DAVID HEWETT-EMMETT, DAVID HEWETT‐EMMETT, David Hewett-Emmett, David Hewett‐Emmett, Hewett-Emmett, D

Publications

5.6K

Citations

H-Index

118

Concepts

All Affiliations

The University of Texas Health Science Center at Houston University of Michigan Wayne State University The University of Texas at Austin

About

David Hewett‐Emmett is an author at The University of Texas Health Science Center at Houston specializing in medicine, genetics, and natural sciences.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	25	38	3.4K
2	Natural Sciences	19	24	2K
3	Public Health	7	7	342
4	Health Sciences	3	3	739
5	Engineering	1	1	14

David Hewett‐Emmett

Publications

5.1K

Citations

H-Index

Page 1

	Year	Citations
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, Proceedings of the National Academy of Sciences Electrolyte DisorderCarbonic Anhydrase IiPathologyCerebral CalcificationOsteoporosis	1983	618
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 BiologyBiosynthesisPhylogeneticsMolecular EcologyFunctional Diversity	1996	606
Rates of Nucleotide Substitution in Primates and Rodents and the Generation–Time Effect Hypothesis Wen‐Hsiung Li, Darrell L. Ellsworth, Julia Krushkal, Molecular Phylogenetics and Evolution BiologyNucleotide SubstitutionMolecular EcologyMedicineMammalogy	1996	340
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, New England Journal of Medicine	1985	324
High Polymorphism at the Human Melanocortin 1 Receptor Locus Brinda K. Rana, David Hewett‐Emmett, Jin Li, Genetics	1999	284
Phylogenetic origins and adaptive evolution of avian and mammalian haemoglobin genes John Czelusniak, Morris Goodman, David Hewett‐Emmett, Nature PhylogeneticsMammalian Haemoglobin GenesNatural SciencesGeneticsEvolutionary Biology	1982	187
Investigating single nucleotide polymorphism (SNP) density in the human genome and its implications for molecular evolution Zhongming Zhao, Yun‐Xin Fu, David Hewett‐Emmett, Gene Genome-wide Association StudyHaplotype DeterminationAllelic VariantSingle Nucleotide PolymorphismGenotype-phenotype Association	2003	180
Origins of u.s. Hispanics: Implications for Diabetes Craig L. Hanis, David Hewett‐Emmett, Terry Bertin, Diabetes Care	1991	175
Molecular evolution of trichromacy in primates David M. Hunt, Kanwaljit S. Dulai, Jill A. Cowing, Vision Research GeneticsEvolutionary BiologyMolecular GeneticsPrimate SystematicsMedicine	1998	156
Weak male-driven molecular evolution in rodents. Bill H. Chang, Lawrence C. Shimmin, Song‐Kun Shyue, Proceedings of the National Academy of Sciences SpermatogenesisExperimental EvolutionFertilityAlpha MGenetics	1994	122

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