Atypical presentation of neuronal ceroid lipofuscinosis type 8 in a sibling pair and review of the eye findings and neurological features

por Sanchez, Rossana L., Yan, Jiong, Richards, Sarah, Mierau, Gary, Wartchow, Eric P., Collins, Christin D., Shankar, Suma P.
Publicado 2016

Divergent dysregulation of gene expression in murine models of fragile X syndrome and tuberous sclerosis

por Kong, Sek Won, Sahin, Mustafa, Collins, Christin D, Wertz, Mary H, Campbell, Malcolm G, Leech, Jarrett D, Krueger, Dilja, Bear, Mark F, Kunkel, Louis M, Kohane, Isaac S
Publicado 2014

Characteristics and Predictive Value of Blood Transcriptome Signature in Males with Autism Spectrum Disorders

por Kong, Sek Won, Collins, Christin D., Shimizu-Motohashi, Yuko, Holm, Ingrid A., Campbell, Malcolm G., Lee, In-Hee, Brewster, Stephanie J., Hanson, Ellen, Harris, Heather K., Lowe, Kathryn R., Saada, Adrianna, Mora, Andrea, Madison, Kimberly, Hundley, Rachel, Egan, Jessica, McCarthy, Jillian, Eran, Ally, Galdzicki, Michal, Rappaport, Leonard, Kunkel, Louis M., Kohane, Isaac S.
Publicado 2012