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

por Suhl, Joshua A., Warren, Stephen T.
Publicado 2015

Identification of consensus binding sites clarifies FMRP binding determinants

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

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

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

A catalog of hemizygous variation in 127 22q11 deletion patients

por 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
Publicado 2016