Amber Hogart

Affiliations: 
University of California, Davis, Davis, CA 
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"Amber Hogart"
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Publications

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Hogart A, Lichtenberg J, Ajay SS, et al. (2012) Genome-wide DNA methylation profiles in hematopoietic stem and progenitor cells reveal overrepresentation of ETS transcription factor binding sites. Genome Research. 22: 1407-18
Hogart A, Wu D, LaSalle JM, et al. (2010) The comorbidity of autism with the genomic disorders of chromosome 15q11.2-q13. Neurobiology of Disease. 38: 181-91
Hogart A, La Salle JM. (2010) Epigenetic dysregulation of 15q11-13 GABAA receptor genes in autism The Neurochemical Basis of Autism: From Molecules to Minicolumns. 113-127
Hogart A, Leung KN, Wang NJ, et al. (2009) Chromosome 15q11-13 duplication syndrome brain reveals epigenetic alterations in gene expression not predicted from copy number. Journal of Medical Genetics. 46: 86-93
Hogart A, Patzel KA, LaSalle JM. (2008) Gender influences monoallelic expression of ATP10A in human brain. Human Genetics. 124: 235-42
Yasui DH, Peddada S, Bieda MC, et al. (2007) Integrated epigenomic analyses of neuronal MeCP2 reveal a role for long-range interaction with active genes. Proceedings of the National Academy of Sciences of the United States of America. 104: 19416-21
Hogart A, Nagarajan RP, Patzel KA, et al. (2007) 15q11-13 GABAA receptor genes are normally biallelically expressed in brain yet are subject to epigenetic dysregulation in autism-spectrum disorders. Human Molecular Genetics. 16: 691-703
Nagarajan RP, Hogart AR, Gwye Y, et al. (2006) Reduced MeCP2 expression is frequent in autism frontal cortex and correlates with aberrant MECP2 promoter methylation. Epigenetics : Official Journal of the Dna Methylation Society. 1: e1-11
LaSalle JM, Hogart A, Thatcher KN. (2005) Rett syndrome: a Rosetta stone for understanding the molecular pathogenesis of autism. International Review of Neurobiology. 71: 131-65
Samaco RC, Hogart A, LaSalle JM. (2005) Epigenetic overlap in autism-spectrum neurodevelopmental disorders: MECP2 deficiency causes reduced expression of UBE3A and GABRB3. Human Molecular Genetics. 14: 483-92
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