Single-Nucleotide Mutations in FMR1 Reveal Novel Functions and Regulatory Mechanisms of the Fragile X Syndrome Protein FMRP

by Suhl, Joshua A., Warren, Stephen T.
Published 2015

Reactivation of FMR1 by CRISPR/Cas9-Mediated Deletion of the Expanded CGG-Repeat of the Fragile X Chromosome

by Xie, Nina, Gong, He, Suhl, Joshua A., Chopra, Pankaj, Wang, Tao, Warren, Stephen T.
Published 2016

Identification of consensus binding sites clarifies FMRP binding determinants

by Anderson, Bart R., Chopra, Pankaj, Suhl, Joshua A., Warren, Stephen T., Bassell, Gary J.
Published 2016

A catalog of hemizygous variation in 127 22q11 deletion patients

by Hestand, Matthew S, Nowakowska, Beata A, Vergaelen, Elfi, Van Houdt, Jeroen, Dehaspe, Luc, Suhl, Joshua A, Del-Favero, Jurgen, Mortier, Geert, Zackai, Elaine, Swillen, Ann, Devriendt, Koenraad, Gur, Raquel E, McDonald-McGinn, Donna M, Warren, Stephen T, Emanuel, Beverly S, Vermeesch, Joris R
Published 2016