A unique form of autosomal dominant cataract explained by gene conversion between β-crystallin B2 and its pseudogene

Por Vanita, Sarhadi, V., Reis, A., Jung, M., Singh, D., Sperling, K., Singh, J. R., Burger, J.
Publicado em 2001

A low frequency variant within the GWAS locus of MTNR1B affects fasting glucose concentrations: Genetic risk is modulated by obesity

Por Been, L. F., Hatfield, J. L., Shankar, A., Aston, C. E., Ralhan, S., Wander, G. S., Mehra, N. K., Singh, J. R., Mulvihill, J. J., Sanghera, D. K.
Publicado em 2011