The Meiotic Recombination Activator PRDM9 Trimethylates Both H3K36 and H3K4 at Recombination Hotspots In Vivo

Por Powers, Natalie R., Parvanov, Emil D., Baker, Christopher L., Walker, Michael, Petkov, Petko M., Paigen, Kenneth
Publicado no PLoS Genet (2016)

Alleles of a Polymorphic ETV6 Binding Site in DCDC2 Confer Risk of Reading and Language Impairment

Por Powers, Natalie R., Eicher, John D., Butter, Falk, Kong, Yong, Miller, Laura L., Ring, Susan M., Mann, Matthias, Gruen, Jeffrey R.
Publicado em 2013

Alleles of a Polymorphic ETV6 Binding Site in DCDC2 Confer Risk of Reading and Language Impairment

Por Powers, Natalie R., Eicher, John D., Butter, Falk, Kong, Yong, Miller, Laura L., Ring, Susan M., Mann, Matthias, Gruen, Jeffrey R.
Publicado em 2014

A Dyslexia-Associated Variant in DCDC2 Changes Gene Expression

Por Meng, Haiying, Powers, Natalie R., Tang, Ling, Cope, Natalie A., Zhang, Ping-Xia, Fuleihan, Ramsay, Gibson, Christopher, Page, Grier P., Gruen, Jeffrey R.
Publicado em 2010

Associations of Prenatal Nicotine Exposure and the Dopamine Related Genes ANKK1 and DRD2 to Verbal Language

Por Eicher, John D., Powers, Natalie R., Cho, Kelly, Miller, Laura L., Mueller, Kathryn L., Ring, Susan M., Tomblin, J. Bruce, Gruen, Jeffrey R.
Publicado em 2013

The regulatory element READ1 epistatically influences reading and language, with both deleterious and protective alleles

Por Powers, Natalie R, Eicher, John D, Miller, Laura L, Kong, Yong, Smith, Shelley D, Pennington, Bruce F, Willcutt, Erik G, Olson, Richard K, Ring, Susan M, Gruen, Jeffrey R
Publicado no J Med Genet (2016)

Characterization of the DYX2 locus on chromosome 6p22 with reading disability, language impairment, and IQ

Por Eicher, John D., Powers, Natalie R., Miller, Laura L., Mueller, Kathryn L., Mascheretti, Sara, Marino, Cecilia, Willcutt, Erik G., DeFries, John C., Olson, Richard K., Smith, Shelley D., Pennington, Bruce F., Tomblin, J. Bruce, Ring, Susan M., Gruen, Jeffrey R.
Publicado em 2014