Schizophrenia-risk variant rs6994992 in the neuregulin-1 gene on brain developmental trajectories in typically developing children

by Douet, V, Chang, L, Pritchett, A, Lee, K, Keating, B, Bartsch, H, Jernigan, T L, Dale, A, Akshoomoff, N, Murray, S, Bloss, C, Kennedy, D N, Amaral, D, Gruen, J, Kaufmann, W E, Casey, B J, Sowell, E, Ernst, T
Published 2014

Multipoint genome-wide linkage scan for nonword repetition in a multigenerational family further supports chromosome 13q as a locus for verbal trait disorders

by Truong, D. T., Shriberg, L. D., Smith, S. D., Chapman, K. L., Scheer-Cohen, A. R., DeMille, M. M. C., Adams, A. K., Nato, A. Q., Wijsman, E. M., Eicher, J. D., Gruen, J. R.
Published 2016

The DYX2 locus and neurochemical signaling genes contribute to speech sound disorder and related neurocognitive domains

by Eicher, J. D., Stein, C. M., Deng, F., Ciesla, A. A., Powers, N. R., Boada, R., Smith, S. D., Pennington, B. F., Iyengar, S. K., Lewis, B. A., Gruen, J. R.
Published 2015

Differential expression of miR-4520a is associated with gain of function mutations in Familial Mediterranean Fever (FMF)

by Latsoudis, H, Mashreghi, MF, Gruen, J, Chang, H-D, Stuhlmueller, B, Repa, A, Gergiannaki, I, Kabouraki, E, Papakosta, P, Haeupl, T, Radbruch, A, Sidiropoulos, P, Kardassis, D, Boumpas, D, Goulielmos, G
Published 2015

Genome-wide association study of shared components of reading disability and language impairment

by Eicher, J D, Powers, N R, Miller, L L, Akshoomoff, N, Amaral, D G, Bloss, C S, Libiger, O, Schork, N J, Darst, B F, Casey, B J, Chang, L, Ernst, T, Frazier, J, Kaufmann, W E, Keating, B, Kenet, T, Kennedy, D, Mostofsky, S, Murray, S S, Sowell, E R, Bartsch, H, Kuperman, J M, Brown, T T, Hagler, D J, Dale, A M, Jernigan, T L, St Pourcain, B, Davey Smith, G, Ring, S M, Gruen, J R
Published 2013