Format
Sort by
Items per page

Send to

Choose Destination

Search results

Items: 13

1.

Self-reported pregnancy exposures and placental DNA methylation in the MARBLES prospective autism sibling study.

Schmidt RJ, Schroeder DI, Crary-Dooley FK, Barkoski JM, Tancredi DJ, Walker CK, Ozonoff S, Hertz-Picciotto I, LaSalle JM.

Environ Epigenet. 2016 Dec;2(4). pii: dvw024. doi: 10.1093/eep/dvw024. Epub 2016 Dec 1.

2.

Placental methylome analysis from a prospective autism study.

Schroeder DI, Schmidt RJ, Crary-Dooley FK, Walker CK, Ozonoff S, Tancredi DJ, Hertz-Picciotto I, LaSalle JM.

Mol Autism. 2016 Dec 15;7:51. doi: 10.1186/s13229-016-0114-8. eCollection 2016.

3.

Early Developmental and Evolutionary Origins of Gene Body DNA Methylation Patterns in Mammalian Placentas.

Schroeder DI, Jayashankar K, Douglas KC, Thirkill TL, York D, Dickinson PJ, Williams LE, Samollow PB, Ross PJ, Bannasch DL, Douglas GC, LaSalle JM.

PLoS Genet. 2015 Aug 4;11(8):e1005442. doi: 10.1371/journal.pgen.1005442. eCollection 2015 Aug.

4.

Methylation and gene expression responses to ethanol feeding and betaine supplementation in the cystathionine beta synthase-deficient mouse.

Medici V, Schroeder DI, Woods R, LaSalle JM, Geng Y, Shibata NM, Peerson J, Hodzic E, Dayal S, Tsukamoto H, Kharbanda KK, Tillman B, French SW, Halsted CH.

Alcohol Clin Exp Res. 2014 Jun;38(6):1540-9. doi: 10.1111/acer.12405. Epub 2014 Apr 14.

5.

How has the study of the human placenta aided our understanding of partially methylated genes?

Schroeder DI, LaSalle JM.

Epigenomics. 2013 Dec;5(6):645-54. doi: 10.2217/epi.13.62.

6.

The human placenta methylome.

Schroeder DI, Blair JD, Lott P, Yu HO, Hong D, Crary F, Ashwood P, Walker C, Korf I, Robinson WP, LaSalle JM.

Proc Natl Acad Sci U S A. 2013 Apr 9;110(15):6037-42. doi: 10.1073/pnas.1215145110. Epub 2013 Mar 25.

7.

Role of DNMT3B in the regulation of early neural and neural crest specifiers.

Martins-Taylor K, Schroeder DI, LaSalle JM, Lalande M, Xu RH.

Epigenetics. 2012 Jan 1;7(1):71-82. doi: 10.4161/epi.7.1.18750. Epub 2012 Jan 1.

8.

15q11.2-13.3 chromatin analysis reveals epigenetic regulation of CHRNA7 with deficiencies in Rett and autism brain.

Yasui DH, Scoles HA, Horike S, Meguro-Horike M, Dunaway KW, Schroeder DI, Lasalle JM.

Hum Mol Genet. 2011 Nov 15;20(22):4311-23. doi: 10.1093/hmg/ddr357. Epub 2011 Aug 12.

9.

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

Schroeder DI, Lott P, Korf I, LaSalle JM.

Genome Res. 2011 Oct;21(10):1583-91. doi: 10.1101/gr.119131.110. Epub 2011 Jul 22.

10.

Neuron-specific impairment of inter-chromosomal pairing and transcription in a novel model of human 15q-duplication syndrome.

Meguro-Horike M, Yasui DH, Powell W, Schroeder DI, Oshimura M, Lasalle JM, Horike S.

Hum Mol Genet. 2011 Oct 1;20(19):3798-810. doi: 10.1093/hmg/ddr298. Epub 2011 Jul 1.

11.

MeCP2 is required for global heterochromatic and nucleolar changes during activity-dependent neuronal maturation.

Singleton MK, Gonzales ML, Leung KN, Yasui DH, Schroeder DI, Dunaway K, LaSalle JM.

Neurobiol Dis. 2011 Jul;43(1):190-200. doi: 10.1016/j.nbd.2011.03.011. Epub 2011 Mar 21.

12.

Multiple transcription start sites for FOXP2 with varying cellular specificities.

Schroeder DI, Myers RM.

Gene. 2008 Apr 30;413(1-2):42-8. doi: 10.1016/j.gene.2008.01.015. Epub 2008 Jan 29.

PMID:
18316164
13.

An abundance of bidirectional promoters in the human genome.

Trinklein ND, Aldred SF, Hartman SJ, Schroeder DI, Otillar RP, Myers RM.

Genome Res. 2004 Jan;14(1):62-6.

Supplemental Content

Loading ...
Support Center