A. Hogart

发表

Genome-wide DNA methylation profiles in hematopoietic stem and progenitor cells reveal overrepresentation of ETS transcription factor binding sites

S. S. Ajay, E. H. Margulies, D. Bodine, 2012, Genome research.

Gender influences monoallelic expression of ATP10A in human brain

J. LaSalle, Katherine A. Patzel, A. Hogart, 2008, Human Genetics.

The comorbidity of autism with the genomic disorders of chromosome 15q11.2-q13

N. C. Schanen, J. LaSalle, A. Hogart, 2010, Neurobiology of Disease.

factor binding sites progenitor cells reveal overrepresentation of ETS transcription Genome-wide DNA methylation profiles in hematopoietic stem and Material Supplemental

S. S. Ajay, E. H. Margulies, D. Bodine, 2012 .

Rett syndrome: a Rosetta stone for understanding the molecular pathogenesis of autism.

J. LaSalle, A. Hogart, Karen N Thatcher, 2005, International review of neurobiology.

Chromosome 15q11–13 duplication syndrome brain reveals epigenetic alterations in gene expression not predicted from copy number

Jennette D. Driscoll, N. C. Schanen, J. LaSalle, 2008, Journal of Medical Genetics.

Integrated epigenomic analyses of neuronal MeCP2 reveal a role for long-range interaction with active genes

M. Bieda, P. Farnham, J. LaSalle, 2007, Proceedings of the National Academy of Sciences.

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

J. LaSalle, D. Yasui, Katherine A. Patzel, 2007, Human molecular genetics.

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

Rodney C Samaco, Rodney C. Samaco, J. LaSalle, 2005, Human molecular genetics.

Epigenetic Dysregulation of 15q11-13 GABAA Receptor Genes in Autism

J. LaSalle, A. Hogart, Amber Hogart, 2010 .

Reduced MeCP2 Expression is Frequent in Autism Frontal Cortex and Correlates with Aberrant MECP2 Promoter Methylation

J. LaSalle, Michelle R. Martin, A. Hogart, 2006, Epigenetics.

15 q 11-13 GABAA receptor genes are normally biallelically expressed in brain yet are subject to epigenetic dysregulation in autism-spectrum disorders

J. LaSalle, D. Yasui, Katherine A. Patzel, 2007 .

Analysis of novel and recurrent mutations responsible for the tricho-rhino-phalangeal syndromes

D. Wells, A. Hogart, M. Hilton, 2002, Journal of Human Genetics.