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Author Details

Carol L Freund
the Center for Genetics and Health Policy, Vanderbilt University Medical School
1990
14
11
PMIDPaper TitleJournal TitlePublished Year
15152432Natural settings trials--improving the introduction of clinical genetic tests.J Law Med Ethics2004
14993088Evaluating pharmacogenetic tests: a case example.Arch Pediatr Adolesc Med2004
14672521Pharmacogenomics and children: meeting the ethical challenges.Am J Pharmacogenomics2003
12421098Emerging ethical issues in pharmacogenomics: from research to clinical practice.Am J Pharmacogenomics2002
11731243Vsx1, a rapidly evolving paired-like homeobox gene expressed in cone bipolar cells.Mech Dev2001
9792858A range of clinical phenotypes associated with mutations in CRX, a photoreceptor transcription-factor gene.Am J Hum Genet1998
9537410De novo mutations in the CRX homeobox gene associated with Leber congenital amaurosis.Nat Genet1998
9804150Retinal degenerations with truncation mutations in the cone-rod homeobox (CRX) gene.Invest Ophthalmol Vis Sci1998
9390563Cone-rod dystrophy due to mutations in a novel photoreceptor-specific homeobox gene (CRX) essential for maintenance of the photoreceptor.Cell1997
9149946A differential hybridization scheme to identify photoreceptor-specific genes.Genome Res1997
8845848A ubiquitin C-terminal hydrolase gene on the proximal short arm of the X chromosome: implications for X-linked retinal disorders.Hum Mol Genet1996
8875254Transcription factor genes and the developing eye: a genetic perspective.Hum Mol Genet1996
1898742Sequence of the clathrin heavy chain from Saccharomyces cerevisiae and requirement of the COOH terminus for clathrin function.J Cell Biol1991
2407603Genetic instability of clathrin-deficient strains of Saccharomyces cerevisiae.Genetics1990
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Collaborators

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The University of Hong Kong
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