F. Crary

Mice with an isoform-ablating Mecp2 exon 1 mutation recapitulate the neurologic deficits of Rett syndrome.

Michael L. Gonzales, J. Vincent, M. Golub, 2014, Human molecular genetics.

A Prader–Willi locus lncRNA cloud modulates diurnal genes and energy expenditure

P. Tsang, R. Ach, J. LaSalle, 2013, Human molecular genetics.

The human placenta methylome

Wendy P Robinson, I. Korf, D. Schroeder, 2013, Proceedings of the National Academy of Sciences.

R-loop formation at Snord116 mediates topotecan inhibition of Ube3a-antisense and allele-specific chromatin decondensation

Peter Tsang, Michael L. Gonzales, N. Yamada, 2013, Proceedings of the National Academy of Sciences.

Mice with an isoform-ablating Mecp2 exon 1 mutation recapitulate the neurologic deficits of Rett syndrome.

Michael L. Gonzales, J. Vincent, M. Golub, 2014, Human molecular genetics.