Year |
Citation |
Score |
2015 |
Vidal AC, Semenova V, Darrah T, Vengosh A, Huang Z, King K, Nye MD, Fry R, Skaar D, Maguire R, Murtha A, Schildkraut J, Murphy S, Hoyo C. Maternal cadmium, iron and zinc levels, DNA methylation and birth weight. Bmc Pharmacology & Toxicology. 16: 20. PMID 26173596 DOI: 10.1186/s40360-015-0020-2 |
1 |
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2015 |
Li Y, Xie C, Murphy SK, Skaar D, Nye M, Vidal AC, Cecil KM, Dietrich KN, Puga A, Jirtle RL, Hoyo C. Lead Exposure during Early Human Development and DNA Methylation of Imprinted Gene Regulatory Elements in Adulthood. Environmental Health Perspectives. PMID 26115033 DOI: 10.1289/ehp.1408577 |
1 |
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2015 |
Vidal AC, Skaar D, Maguire R, Dodor S, Musselwhite LW, Bartlett JA, Oneko O, Obure J, Mlay P, Murphy SK, Hoyo C. IL-10, IL-15, IL-17, and GMCSF levels in cervical cancer tissue of Tanzanian women infected with HPV16/18 vs. non-HPV16/18 genotypes. Infectious Agents and Cancer. 10: 10. PMID 25810759 DOI: 10.1186/s13027-015-0005-1 |
1 |
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2013 |
Bernal AJ, Dolinoy DC, Huang D, Skaar DA, Weinhouse C, Jirtle RL. Adaptive radiation-induced epigenetic alterations mitigated by antioxidants Faseb Journal. 27: 665-671. PMID 23118028 DOI: 10.1096/fj.12-220350 |
1 |
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2012 |
Skaar DA, Li Y, Bernal AJ, Hoyo C, Murphy SK, Jirtle RL. The human imprintome: regulatory mechanisms, methods of ascertainment, and roles in disease susceptibility. Ilar Journal / National Research Council, Institute of Laboratory Animal Resources. 53: 341-358. PMID 23744971 DOI: 10.1093/ilar.53.3-4.341 |
1 |
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2012 |
Hoyo C, Murphy SK, Schildkraut JM, Vidal AC, Skaar D, Millikan RC, Galanko J, Sandler RS, Jirtle R, Keku T. IGF2R genetic variants, circulating IGF2 concentrations and colon cancer risk in African Americans and Whites. Disease Markers. 32: 133-41. PMID 22377707 DOI: 10.3233/DMA-2011-0865 |
1 |
|
2012 |
Stone JL, McMillan RE, Skaar DA, Bradshaw JM, Jirtle RL, Sikes ML. DNA double-strand breaks relieve USF-mediated repression of Dβ2 germline transcription in developing thymocytes. Journal of Immunology (Baltimore, Md. : 1950). 188: 2266-75. PMID 22287717 DOI: 10.4049/jimmunol.1002931 |
1 |
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2011 |
Zhang A, Skaar DA, Li Y, Huang D, Price TM, Murphy SK, Jirtle RL. Novel retrotransposed imprinted locus identified at human 6p25. Nucleic Acids Research. 39: 5388-400. PMID 21421564 DOI: 10.1093/nar/gkr108 |
1 |
|
2009 |
Cukier HN, Skaar DA, Rayner-Evans MY, Konidari I, Whitehead PL, Jaworski JM, Cuccaro ML, Pericak-Vance MA, Gilbert JR. Identification of chromosome 7 inversion breakpoints in an autistic family narrows candidate region for autism susceptibility. Autism Research : Official Journal of the International Society For Autism Research. 2: 258-66. PMID 19877165 DOI: 10.1002/aur.96 |
1 |
|
2009 |
Vasilatos SN, Broadwater G, Barry WT, Baker JC, Lem S, Dietze EC, Bean GR, Bryson AD, Pilie PG, Goldenberg V, Skaar D, Paisie C, Torres-Hernandez A, Grant TL, Wilke LG, et al. CpG island tumor suppressor promoter methylation in non-BRCA-associated early mammary carcinogenesis. Cancer Epidemiology, Biomarkers & Prevention : a Publication of the American Association For Cancer Research, Cosponsored by the American Society of Preventive Oncology. 18: 901-14. PMID 19258476 DOI: 10.1158/1055-9965.EPI-08-0875 |
1 |
|
2007 |
Ashley-Koch AE, Jaworski J, Ma de Q, Mei H, Ritchie MD, Skaar DA, Robert Delong G, Worley G, Abramson RK, Wright HH, Cuccaro ML, Gilbert JR, Martin ER, Pericak-Vance MA. Investigation of potential gene-gene interactions between APOE and RELN contributing to autism risk. Psychiatric Genetics. 17: 221-6. PMID 17621165 DOI: 10.1097/YPG.0b013e32809c2f75 |
1 |
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2005 |
Skaar DA, Shao Y, Haines JL, Stenger JE, Jaworski J, Martin ER, DeLong GR, Moore JH, McCauley JL, Sutcliffe JS, Ashley-Koch AE, Cuccaro ML, Folstein SE, Gilbert JR, Pericak-Vance MA. Analysis of the RELN gene as a genetic risk factor for autism. Molecular Psychiatry. 10: 563-71. PMID 15558079 DOI: 10.1038/sj.mp.4001614 |
1 |
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2002 |
Skaar DA, Greenleaf AL. The RNA polymerase II CTD kinase CTDK-I affects pre-mRNA 3' cleavage/polyadenylation through the processing component Pti1p. Molecular Cell. 10: 1429-39. PMID 12504017 DOI: 10.1016/S1097-2765(02)00731-1 |
1 |
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