Ferguson, Betsy M.

Evolutionary and biomedical insights from the rhesus macaque genome.

Gibbs, R. A., Rogers, J., Katze, M. G., Bumgarner, R., Weinstock, G. M., Mardis, E. R., Remington, K. A., Strausberg, R. L., Venter, J. C., Wilson, R. K., et al. (2007) · Science

Genomics and Phylogenetic StudiesChromosomal and Genetic Variations

Cited by 1,403

X-linked anhidrotic (hypohidrotic) ectodermal dysplasia is caused by mutation in a novel transmembrane protein

Kere, J., Srivastava, A. K., Montonen, O., Zonana, J., Thomas, N., Ferguson, B., Munoz, F., Morgan, D., Clarke, A., Baybayan, P., et al. (1996) · Nature Genetics

dental development and anomaliesHair Growth and Disorders

Cited by 749

A novel X-linked disorder of immune deficiency and hypohidrotic ectodermal dysplasia is allelic to incontinentia pigmenti and due to mutations in IKK-gamma (NEMO)

Zonana, J., Elder, M. E., Schneider, L. C., Orlow, S. J., Moss, C., Golabi, M., Shapira, S. K., Farndon, P. A., Wara, D. W., Emmal, S. A., et al. (2000) · The American Journal of Human Genetics

Immunodeficiency and Autoimmune Disordersdental development and anomalies

Cited by 521

Mutations in the human homologue of mouse dl cause autosomal recessive and dominant hypohidrotic ectodermal dysplasia

Monreal, A. W., Ferguson, B. M., Headon, D. J., Street, S. L., Overbeek, P. A., & Zonana, J. (1999) · Nature Genetics

dental development and anomaliesHair Growth and Disorders

Cited by 397

Gene defect in ectodermal dysplasia implicates a death domain adapter in development

Headon, D. J., Emmal, S. A., Ferguson, B. M., Tucker, A. S., Justice, M. J., Sharpe, P. T., Zonana, J., & Overbeek, P. A. (2001) · Nature

dental development and anomaliesHair Growth and Disorders

Cited by 378

Edar/Eda interactions regulate enamel knot formation in tooth morphogenesis.

Tucker, A. S., Headon, D. J., Schneider, P., Ferguson, B. M., Overbeek, P., Tschopp, J., & Sharpe, P. T. (2000) · Development

dental development and anomaliesDevelopmental Biology and Gene Regulation

Cited by 211

A novel non-human primate model of Pelizaeus-Merzbacher disease

Sherman, L. S., Su, W., Johnson, A. L., Peterson, S. M., Cullin, C., Lavinder, T., Ferguson, B., & Lewis, A. D. (2021) · Neurobiology of Disease

Hereditary Neurological DisordersMultiple Sclerosis Research Studies

Cited by 15