The Genetics of Reading Disability in an Often Excluded Sample: Novel Loci Suggested for Reading Disability in Rolandic Epilepsy

Por Strug, Lisa J., Addis, Laura, Chiang, Theodore, Baskurt, Zeynep, Li, Weili, Clarke, Tara, Hardison, Huntley, Kugler, Steven L., Mandelbaum, David E., Novotny, Edward J., Wolf, Steven M., Pal, Deb K.
Publicado em 2012

Centrotemporal sharp wave EEG trait in rolandic epilepsy maps to Elongator Protein Complex 4 (ELP4)

Por Strug, Lisa J, Clarke, Tara, Chiang, Theodore, Chien, Minchen, Baskurt, Zeynep, Li, Weili, Dorfman, Ruslan, Bali, Bhavna, Wirrell, Elaine, Kugler, Steven L, Mandelbaum, David E, Wolf, Steven M, McGoldrick, Patricia, Hardison, Huntley, Novotny, Edward J, Ju, Jingyue, Greenberg, David A, Russo, James J, Pal, Deb K
Publicado em 2009

A microRNA‐328 binding site in PAX6 is associated with centrotemporal spikes of rolandic epilepsy

Por Panjwani, Naim, Wilson, Michael D., Addis, Laura, Crosbie, Jennifer, Wirrell, Elaine, Auvin, Stéphane, Caraballo, Roberto H., Kinali, Maria, McCormick, David, Oren, Caroline, Taylor, Jacqueline, Trounce, John, Clarke, Tara, Akman, Cigdem I., Kugler, Steven L., Mandelbaum, David E., McGoldrick, Patricia, Wolf, Steven M., Arnold, Paul, Schachar, Russell, Pal, Deb K., Strug, Lisa J.
Publicado no Ann Clin Transl Neurol (2016)