LaSalle JM - Search Results

1

Autism and Cancer Share Risk Genes, Pathways, and Drug Targets.

Crawley JN, Heyer WD, LaSalle JM. Crawley JN, et al. Among authors: lasalle jm. Trends Genet. 2016 Mar;32(3):139-146. doi: 10.1016/j.tig.2016.01.001. Epub 2016 Jan 29. Trends Genet. 2016. PMID: 26830258 Free PMC article. Review.

2

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

Samaco RC, Hogart A, LaSalle JM. Samaco RC, et al. Among authors: lasalle jm. Hum Mol Genet. 2005 Feb 15;14(4):483-92. doi: 10.1093/hmg/ddi045. Epub 2004 Dec 22. Hum Mol Genet. 2005. PMID: 15615769 Free PMC article.

3

Homologous pairing of 15q11-13 imprinted domains in brain is developmentally regulated but deficient in Rett and autism samples.

Thatcher KN, Peddada S, Yasui DH, Lasalle JM. Thatcher KN, et al. Among authors: lasalle jm. Hum Mol Genet. 2005 Mar 15;14(6):785-97. doi: 10.1093/hmg/ddi073. Epub 2005 Feb 2. Hum Mol Genet. 2005. PMID: 15689352

4

Reduced MeCP2 expression is frequent in autism frontal cortex and correlates with aberrant MECP2 promoter methylation.

Nagarajan RP, Hogart AR, Gwye Y, Martin MR, LaSalle JM. Nagarajan RP, et al. Among authors: lasalle jm. Epigenetics. 2006 Oct-Dec;1(4):e1-11. doi: 10.4161/epi.1.4.3514. Epigenetics. 2006. PMID: 17486179 Free PMC article.

5

Immunologic and neurodevelopmental susceptibilities of autism.

Pessah IN, Seegal RF, Lein PJ, LaSalle J, Yee BK, Van De Water J, Berman RF. Pessah IN, et al. Neurotoxicology. 2008 May;29(3):532-45. doi: 10.1016/j.neuro.2008.02.006. Epub 2008 Feb 23. Neurotoxicology. 2008. PMID: 18394707 Free PMC article. Review.

6

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

Hogart A, Wu D, LaSalle JM, Schanen NC. Hogart A, et al. Among authors: lasalle jm. Neurobiol Dis. 2010 May;38(2):181-91. doi: 10.1016/j.nbd.2008.08.011. Epub 2008 Sep 18. Neurobiol Dis. 2010. PMID: 18840528 Free PMC article. Review.

7

Reciprocal co-regulation of EGR2 and MECP2 is disrupted in Rett syndrome and autism.

Swanberg SE, Nagarajan RP, Peddada S, Yasui DH, LaSalle JM. Swanberg SE, et al. Among authors: lasalle jm. Hum Mol Genet. 2009 Feb 1;18(3):525-34. doi: 10.1093/hmg/ddn380. Epub 2008 Nov 10. Hum Mol Genet. 2009. PMID: 19000991 Free PMC article.

8

Evolving role of MeCP2 in Rett syndrome and autism.

LaSalle JM, Yasui DH. LaSalle JM, et al. Epigenomics. 2009 Oct;1(1):119-30. doi: 10.2217/epi.09.13. Epigenomics. 2009. PMID: 20473347 Free PMC article. Review.

9

A genomic point-of-view on environmental factors influencing the human brain methylome.

LaSalle JM. LaSalle JM. Epigenetics. 2011 Jul;6(7):862-9. doi: 10.4161/epi.6.7.16353. Epub 2011 Jul 1. Epigenetics. 2011. PMID: 21617367 Free PMC article. Review.

10

Large-scale methylation domains mark a functional subset of neuronally expressed genes.

Schroeder DI, Lott P, Korf I, LaSalle JM. Schroeder DI, et al. Among authors: lasalle jm. Genome Res. 2011 Oct;21(10):1583-91. doi: 10.1101/gr.119131.110. Epub 2011 Jul 22. Genome Res. 2011. PMID: 21784875 Free PMC article.

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