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Paper Details

Divergent dysregulation of gene expression in murine models of fragile X syndrome and tuberous sclerosis.
Mol Autism
16
2014
ASD, Fmr1, Fmr1-, Fragile X syndrome, Tsc2 heterozygous (+/-), Tsc2+/-, autism spectrum disorder, blood, fragile X syndrome, gene sets, genes, genetic syndromes, genome, mice, monogenic disorders, phosphatidylinositol, tuberous sclerosis
Author NameAffiliation
Sek Won KongBoston Children's Hospital, Harvard Medical School
Sek Won KongCenter for Biomedical Informatics, Harvard Medical School
Mustafa SahinBoston Children's Hospital, Harvard Medical School
Christin D CollinsHoward Hughes Medical Institute, Boston Children's Hospital, Harvard Medical School
Mary H WertzBoston Children's Hospital, Harvard Medical School
Malcolm G CampbellCenter for Biomedical Informatics, Harvard Medical School
Jarrett D LeechBoston Children's Hospital, Harvard Medical School
Dilja D KruegerHoward Hughes Medical Institute, The Picower Institute for Learning and Memory, Massachusetts Institute of Technology
Mark F BearHoward Hughes Medical Institute, The Picower Institute for Learning and Memory, Massachusetts Institute of Technology
Louis M KunkelHoward Hughes Medical Institute, Boston Children's Hospital, Harvard Medical School
Isaac S KohaneBoston Children's Hospital, Harvard Medical School
Isaac S KohaneCenter for Biomedical Informatics, Harvard Medical School
Isaac S KohaneBoston Children's Hospital, Harvard Medical School
Isaac S KohaneCenter for Biomedical Informatics, Harvard Medical School
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Datasets

Release 1.2