| Year |
Citation |
Score |
| 2016 |
Schmidt RJ, Schroeder DI, Crary-Dooley FK, Barkoski JM, Tancredi DJ, Walker CK, Ozonoff S, Hertz-Picciotto I, LaSalle JM. Self-reported pregnancy exposures and placental DNA methylation in the MARBLES prospective autism sibling study. Environmental Epigenetics. 2. PMID 28781890 DOI: 10.1093/Eep/Dvw024 |
0.313 |
|
| 2015 |
Schroeder DI, Jayashankar K, Douglas KC, Thirkill TL, York D, Dickinson PJ, Williams LE, Samollow PB, Ross PJ, Bannasch DL, Douglas GC, LaSalle JM. Early Developmental and Evolutionary Origins of Gene Body DNA Methylation Patterns in Mammalian Placentas. Plos Genetics. 11: e1005442. PMID 26241857 DOI: 10.1371/Journal.Pgen.1005442 |
0.434 |
|
| 2013 |
Schroeder DI, LaSalle JM. How has the study of the human placenta aided our understanding of partially methylated genes? Epigenomics. 5: 645-54. PMID 24283879 DOI: 10.2217/Epi.13.62 |
0.538 |
|
| 2013 |
Schroeder DI, Blair JD, Lott P, Yu HO, Hong D, Crary F, Ashwood P, Walker C, Korf I, Robinson WP, LaSalle JM. The human placenta methylome. Proceedings of the National Academy of Sciences of the United States of America. 110: 6037-42. PMID 23530188 DOI: 10.1073/Pnas.1215145110 |
0.509 |
|
| 2012 |
Martins-Taylor K, Schroeder DI, LaSalle JM, Lalande M, Xu RH. Role of DNMT3B in the regulation of early neural and neural crest specifiers. Epigenetics : Official Journal of the Dna Methylation Society. 7: 71-82. PMID 22207353 DOI: 10.4161/Epi.7.1.18750 |
0.388 |
|
| 2011 |
Yasui DH, Scoles HA, Horike S, Meguro-Horike M, Dunaway KW, Schroeder DI, Lasalle JM. 15q11.2-13.3 chromatin analysis reveals epigenetic regulation of CHRNA7 with deficiencies in Rett and autism brain. Human Molecular Genetics. 20: 4311-23. PMID 21840925 DOI: 10.1093/Hmg/Ddr357 |
0.327 |
|
| 2011 |
Schroeder DI, Lott P, Korf I, LaSalle JM. Large-scale methylation domains mark a functional subset of neuronally expressed genes. Genome Research. 21: 1583-91. PMID 21784875 DOI: 10.1101/Gr.119131.110 |
0.514 |
|
| 2011 |
Singleton MK, Gonzales ML, Leung KN, Yasui DH, Schroeder DI, Dunaway K, LaSalle JM. MeCP2 is required for global heterochromatic and nucleolar changes during activity-dependent neuronal maturation. Neurobiology of Disease. 43: 190-200. PMID 21420494 DOI: 10.1016/J.Nbd.2011.03.011 |
0.313 |
|
| 2008 |
Schroeder DI, Myers RM. Multiple transcription start sites for FOXP2 with varying cellular specificities. Gene. 413: 42-8. PMID 18316164 DOI: 10.1016/J.Gene.2008.01.015 |
0.512 |
|
| 2004 |
Feingold EA, Good PJ, Guyer MS, Kamholz S, Liefer L, Wetterstrand K, Collins FS, Gingeras TR, Kampa D, Sekinger EA, Cheng J, Hirsch H, Ghosh S, Zhu Z, Patel S, ... ... Schroeder DI, et al. The ENCODE (ENCyclopedia of DNA Elements) Project Science. 306: 636-640. PMID 15499007 DOI: 10.1126/Science.1105136 |
0.573 |
|
| 2004 |
Trinklein ND, Aldred SF, Hartman SJ, Schroeder DI, Otillar RP, Myers RM. An abundance of bidirectional promoters in the human genome. Genome Research. 14: 62-6. PMID 14707170 DOI: 10.1101/Gr.1982804 |
0.581 |
|
| 2003 |
Wang X, Schroeder D, Dobbs D, Honavar V. Automated data-driven discovery of motif-based protein function classifiers Information Sciences. 155: 1-18. DOI: 10.1016/S0020-0255(03)00067-7 |
0.317 |
|
| 2001 |
Ji Y, Schroeder D, Byrne D, Zipser B, Jellies J, Johansen KM, Johansen J. Molecular identification and sequence analysis of Hillarin, a novel protein localized at the axon hillock. Biochimica Et Biophysica Acta. 1519: 246-9. PMID 11418193 DOI: 10.1016/S0167-4781(01)00234-2 |
0.315 |
|
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