Publications by authors named "Amber Hogart"

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Genome-wide DNA methylation profiles in hematopoietic stem and progenitor cells reveal overrepresentation of ETS transcription factor binding sites.
Amber Hogart, Jens Lichtenberg, Subramanian S Ajay, Stacie Anderson,

Genome Res· August 2012

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The comorbidity of autism with the genomic disorders of chromosome 15q11.2-q13.
Amber Hogart, David Wu, Janine M LaSalle, N Carolyn Schanen

Neurobiol Dis· May 2010

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Gender influences monoallelic expression of ATP10A in human brain.
Amber Hogart, Katherine A Patzel, Janine M LaSalle

Hum Genet· October 2008

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Reduced MeCP2 expression is frequent in autism frontal cortex and correlates with aberrant MECP2 promoter methylation.
Raman P Nagarajan, Amber R Hogart, Ynnez Gwye, Michelle R Martin, Janine M LaSalle

Epigenetics· January 2008

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Integrated epigenomic analyses of neuronal MeCP2 reveal a role for long-range interaction with active genes.
Dag H Yasui, Sailaja Peddada, Mark C Bieda, Roxanne O Vallero, Amber Hogart

Proc Natl Acad Sci U S A· December 2007

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15q11-13 GABAA receptor genes are normally biallelically expressed in brain yet are subject to epigenetic dysregulation in autism-spectrum disorders.
Amber Hogart, Raman P Nagarajan, Katherine A Patzel, Dag H Yasui, Janine M Lasalle

Hum Mol Genet· March 2007

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Rett syndrome: a Rosetta stone for understanding the molecular pathogenesis of autism.
Janine M LaSalle, Amber Hogart, Karen N Thatcher

Int Rev Neurobiol· March 2006

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Epigenetic overlap in autism-spectrum neurodevelopmental disorders: MECP2 deficiency causes reduced expression of UBE3A and GABRB3.
Rodney C Samaco, Amber Hogart, Janine M LaSalle

Hum Mol Genet· February 2005

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Analysis of novel and recurrent mutations responsible for the tricho-rhino-phalangeal syndromes.
Matthew J Hilton, Jacob M Sawyer, Laura Gutiérrez, Amber Hogart, Ting C Kung

J Hum Genet· November 2002

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