King, Richard A.

STrengthening the REporting of Genetic Association Studies (STREGA)— An Extension of the STROBE Statement

Little, J., Higgins, J. P. T., Ioannidis, J. P. A., Moher, D., Gagnon, F., von Elm, E., Khoury, M. J., Cohen, B., Davey-Smith, G., Grimshaw, J., et al. (2009) · PLoS Medicine

Meta-analysis and systematic reviewsGenetic Associations and Epidemiology

Cited by 811

Mutations in the human orthologue of the mouse underwhite gene (uw) underlie a new form of oculocutaneous albinism, OCA4

Newton, J. M., Cohen-Barak, O., Hagiwara, N., Gardner, J. M., Davisson, M. T., King, R. A., & Brilliant, M. H. (2001) · The American Journal of Human Genetics

melanin and skin pigmentationGenetic and rare skin diseases.

Cited by 355

Visualizing Human Leukocyte Antigen Class II Risk Haplotypes in Human Systemic Lupus Erythematosus

Graham, R. R., Ortmann, W. A., Langefeld, C. D., Jawaheer, D., Selby, S. A., Rodine, P. R., Baechler, E. C., Rohlf, K. E., Shark, K. B., Espe, K. J., et al. (2002) · The American Journal of Human Genetics

Systemic Lupus Erythematosus ResearchGenetic Associations and Epidemiology

Cited by 223

MC1R mutations modify the classic phenotype of oculocutaneous albinism type 2 (OCA2)

King, R. A., Willaert, R. K., Schmidt, R. M., Pietsch, J., Savage, S., Brott, M. J., Fryer, J. P., Summers, C. G., & Oetting, W. S. (2003) · The American Journal of Human Genetics

melanin and skin pigmentationGenetic and rare skin diseases.

Cited by 98

A frequent tyrosinase gene mutation in classic, tyrosinase-negative (type IA) oculocutaneous albinism

Giebel, L. B., Strunk, K. M., King, R. A., Hanifin, J. M., & Spritz, R. A. (1990) · Proceedings of the National Academy of Sciences

melanin and skin pigmentationGenetic and rare skin diseases.

Cited by 74