15q11-13 GABA A receptor genes are normally biallelically expressed in brain yet are subject to epigenetic dysregulation in autism-spectrum disorders

By Hogart Amber   Nagarajan Raman P.   Patzel Katherine A.   Yasui Dag H.   LaSalle Janine M.  

Human Molecular Genetics, Vol. 16, Iss. 6, 2007-03 ,pp. : 691-703

Oxford University Press

Access to resources Recommend Favorite

Multiple pathways regulate MeCP2 expression in normal brain development and exhibit defects in autism-spectrum disorders

By Samaco Rodney C.   Nagarajan Raman P.   Braunschweig Daniel   LaSalle Janine M.  

Human Molecular Genetics, Vol. 13, Iss. 6, 2004-03 ,pp. : 629-639

Oxford University Press

Access to resources Recommend Favorite

Truncating mutations in NRXN2 and NRXN1 in autism spectrum disorders and schizophrenia

By Gauthier Julie   Siddiqui Tabrez   Huashan Peng   Yokomaku Daisaku   Hamdan Fadi   Champagne Nathalie   Lapointe Mathieu   Spiegelman Dan   Noreau Anne   Lafrenière Ronald   Fathalli Ferid   Joober Ridha   Krebs Marie-Odile   DeLisi Lynn   Mottron Laurent   Fombonne Éric   Michaud Jacques   Drapeau Pierre   Carbonetto Salvatore   Craig Ann   Rouleau Guy  

Human Genetics, Vol. 130, Iss. 4, 2011-10 ,pp. : 563-573

Springer Publishing Company

Access to resources Recommend Favorite

A common molecular basis for rearrangement disorders on chromosome 22q11

By Edelmann Lisa   Pandita Raj K.   Spiteri Elizabeth   Funke Birgit   Goldberg Rosalie   Palanisamy Nallasivam  

Human Molecular Genetics, Vol. 8, Iss. 7, 1999-07 ,pp. : 1157-1167

Oxford University Press

Access to resources Recommend Favorite

Epigenetic overlap in autism-spectrum neurodevelopmental disorders: MECP2 deficiency causes reduced expression of UBE3A and GABRB3

By Samaco Rodney C.   Hogart Amber   LaSalle Janine M.  

Human Molecular Genetics, Vol. 14, Iss. 4, 2005-02 ,pp. : 483-492

Oxford University Press

Access to resources Recommend Favorite