| Year |
Citation |
Score |
| 2012 |
Hogart A, Lichtenberg J, Ajay SS, Anderson S, Margulies EH, Bodine DM. Genome-wide DNA methylation profiles in hematopoietic stem and progenitor cells reveal overrepresentation of ETS transcription factor binding sites. Genome Research. 22: 1407-18. PMID 22684279 DOI: 10.1101/Gr.132878.111 |
0.481 |
|
| 2011 |
Hogart A, Lichtenberg J, Ajay S, Margulies E, Bodine DM. Genome-Wide DNA Methylation Profiling of Hematopoietic Stem and Progenitor Cells Reveals Over-Representation of ETS Transcrition Factor Binding Sites Blood. 118: 211-211. DOI: 10.1182/Blood.V118.21.211.211 |
0.484 |
|
| 2010 |
Hogart A, Wu D, LaSalle JM, Schanen NC. The comorbidity of autism with the genomic disorders of chromosome 15q11.2-q13. Neurobiology of Disease. 38: 181-91. PMID 18840528 DOI: 10.1016/J.Nbd.2008.08.011 |
0.647 |
|
| 2010 |
Hogart A, La Salle JM. Epigenetic dysregulation of 15q11-13 GABAA receptor genes in autism The Neurochemical Basis of Autism: From Molecules to Minicolumns. 113-127. DOI: 10.1007/978-1-4419-1272-5_8 |
0.434 |
|
| 2009 |
Hogart A, Leung KN, Wang NJ, Wu DJ, Driscoll J, Vallero RO, Schanen NC, LaSalle JM. Chromosome 15q11-13 duplication syndrome brain reveals epigenetic alterations in gene expression not predicted from copy number. Journal of Medical Genetics. 46: 86-93. PMID 18835857 DOI: 10.1136/Jmg.2008.061580 |
0.718 |
|
| 2009 |
Hogart A, Ajay SS, Abaan HO, Anderson SM, Margulies EH, Bodine DM. Genome-Wide DNA Methylation Patterns Reveal Specific Signatures for HSC, CMP and Erythroblasts. Blood. 114: 391-391. DOI: 10.1182/Blood.V114.22.391.391 |
0.484 |
|
| 2008 |
Hogart A, Patzel KA, LaSalle JM. Gender influences monoallelic expression of ATP10A in human brain. Human Genetics. 124: 235-42. PMID 18726118 DOI: 10.1007/S00439-008-0546-0 |
0.692 |
|
| 2007 |
Yasui DH, Peddada S, Bieda MC, Vallero RO, Hogart A, Nagarajan RP, Thatcher KN, Farnham PJ, Lasalle JM. 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. PMID 18042715 DOI: 10.1073/Pnas.0707442104 |
0.623 |
|
| 2007 |
Hogart A, Nagarajan RP, Patzel KA, Yasui DH, Lasalle JM. 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. PMID 17339270 DOI: 10.1093/Hmg/Ddm014 |
0.744 |
|
| 2006 |
Nagarajan RP, Hogart AR, Gwye Y, Martin MR, LaSalle JM. 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. PMID 17486179 DOI: 10.4161/epi.1.4.3514 |
0.7 |
|
| 2005 |
LaSalle JM, Hogart A, Thatcher KN. Rett syndrome: a Rosetta stone for understanding the molecular pathogenesis of autism. International Review of Neurobiology. 71: 131-65. PMID 16512349 DOI: 10.1016/S0074-7742(05)71006-0 |
0.705 |
|
| 2005 |
Samaco RC, Hogart A, LaSalle JM. Epigenetic overlap in autism-spectrum neurodevelopmental disorders: MECP2 deficiency causes reduced expression of UBE3A and GABRB3. Human Molecular Genetics. 14: 483-92. PMID 15615769 DOI: 10.1093/Hmg/Ddi045 |
0.747 |
|
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