Stephen Erickson, Ph.D. - Publications

2006 University of California, Los Angeles, Los Angeles, CA 
Mathematics, Biostatistics Biology

25 high-probability publications. We are testing a new system for linking publications to authors. You can help! If you notice any inaccuracies, please sign in and mark papers as correct or incorrect matches. If you identify any major omissions or other inaccuracies in the publication list, please let us know.

Year Citation  Score
2016 Gilbert KM, Blossom SJ, Erickson SW, Broadfoot B, West K, Bai S, Li J, Cooney CA. Chronic exposure to trichloroethylene increases DNA methylation of the Ifng promoter in CD4(+) T cells. Toxicology Letters. PMID 27553676 DOI: 10.1016/j.toxlet.2016.08.017  0.68
2016 Gilbert KM, Blossom SJ, Erickson SW, Reisfeld B, Zurlinden TJ, Broadfoot B, West K, Bai S, Cooney CA. Chronic exposure to water pollutant trichloroethylene increased epigenetic drift in CD4(+) T cells. Epigenomics. PMID 27092578 DOI: 10.2217/epi-2015-0018  0.68
2015 Li M, Li J, Wei C, Lu Q, Tang X, Erickson SW, MacLeod SL, Hobbs CA. A Three-Way Interaction among Maternal and Fetal Variants Contributing to Congenital Heart Defects. Annals of Human Genetics. PMID 26612412 DOI: 10.1111/ahg.12139  0.68
2015 Webber DM, MacLeod SL, Bamshad MJ, Shaw GM, Finnell RH, Shete SS, Witte JS, Erickson SW, Murphy LD, Hobbs C. Developments in our understanding of the genetic basis of birth defects. Birth Defects Research. Part a, Clinical and Molecular Teratology. PMID 26033863 DOI: 10.1002/bdra.23385  0.68
2015 Tang X, Hobbs CA, Cleves MA, Erickson SW, MacLeod SL, Malik S. Genetic variation affects congenital heart defect susceptibility in offspring exposed to maternal tobacco use. Birth Defects Research. Part a, Clinical and Molecular Teratology. PMID 26033827 DOI: 10.1002/bdra.23370  0.68
2015 Tang X, Cleves MA, Nick TG, Li M, MacLeod SL, Erickson SW, Li J, Shaw GM, Mosley BS, Hobbs CA. Obstructive heart defects associated with candidate genes, maternal obesity, and folic acid supplementation. American Journal of Medical Genetics. Part A. 167: 1231-42. PMID 25846410 DOI: 10.1002/ajmg.a.36867  0.68
2015 Coleman EA, Lee JY, Erickson SW, Goodwin JA, Sanathkumar N, Raj VR, Zhou D, McKelvey KD, Apewokin S, Stephens O, Enderlin CA, Vangsted AJ, Reed PJ, Anaissie EJ. GWAS of 972 autologous stem cell recipients with multiple myeloma identifies 11 genetic variants associated with chemotherapy-induced oral mucositis. Supportive Care in Cancer : Official Journal of the Multinational Association of Supportive Care in Cancer. 23: 841-9. PMID 25218607 DOI: 10.1007/s00520-014-2406-x  0.68
2014 Tang X, Nick TG, Cleves MA, Erickson SW, Li M, Li J, MacLeod SL, Hobbs CA. Maternal obesity and tobacco use modify the impact of genetic variants on the occurrence of conotruncal heart defects. Plos One. 9: e108903. PMID 25275547 DOI: 10.1371/journal.pone.0108903  0.68
2014 Erickson SW, Raj VR, Stephens OW, Dhakal I, Chavan SS, Sanathkumar N, Coleman EA, Lee JY, Goodwin JA, Apewokin S, Zhou D, Epstein J, Heuck CJ, Vangsted AJ. Genome-wide scan identifies variant in 2q12.3 associated with risk for multiple myeloma. Blood. 124: 2001-3. PMID 25237182 DOI: 10.1182/blood-2014-07-586701  0.68
2014 Gilbert KM, Reisfeld B, Zurlinden TJ, Kreps MN, Erickson SW, Blossom SJ. Modeling toxicodynamic effects of trichloroethylene on liver in mouse model of autoimmune hepatitis Toxicology and Applied Pharmacology. 279: 284-293. PMID 25026505 DOI: 10.1016/j.taap.2014.07.003  0.68
2014 Li M, Cleves MA, Mallick H, Erickson SW, Tang X, Nick TG, Macleod SL, Hobbs CA. A genetic association study detects haplotypes associated with obstructive heart defects. Human Genetics. 133: 1127-38. PMID 24894164 DOI: 10.1007/s00439-014-1453-1  0.68
2014 Li M, Erickson SW, Hobbs CA, Li J, Tang X, Nick TG, Macleod SL, Cleves MA. Detecting maternal-fetal genotype interactions associated with conotruncal heart defects: a haplotype-based analysis with penalized logistic regression. Genetic Epidemiology. 38: 198-208. PMID 24585533 DOI: 10.1002/gepi.21793  0.68
2014 Hobbs CA, Cleves MA, Macleod SL, Erickson SW, Tang X, Li J, Li M, Nick T, Malik S. Conotruncal heart defects and common variants in maternal and fetal genes in folate, homocysteine, and transsulfuration pathways. Birth Defects Research. Part a, Clinical and Molecular Teratology. 100: 116-26. PMID 24535845 DOI: 10.1002/bdra.23225  0.68
2014 Hobbs CA, Chowdhury S, Cleves MA, Erickson S, MacLeod SL, Shaw GM, Shete S, Witte JS, Tycko B. Genetic epidemiology and nonsyndromic structural birth defects: from candidate genes to epigenetics. Jama Pediatrics. 168: 371-7. PMID 24515445 DOI: 10.1001/jamapediatrics.2013.4858  0.68
2012 Chowdhury S, Hobbs CA, MacLeod SL, Cleves MA, Melnyk S, James SJ, Hu P, Erickson SW. Associations between maternal genotypes and metabolites implicated in congenital heart defects. Molecular Genetics and Metabolism. 107: 596-604. PMID 23059056 DOI: 10.1016/j.ymgme.2012.09.022  0.68
2012 Erickson SW, MacLeod SL, Hobbs CA. Cheek swabs, SNP chips, and CNVs: assessing the quality of copy number variant calls generated with subject-collected mail-in buccal brush DNA samples on a high-density genotyping microarray. Bmc Medical Genetics. 13: 51. PMID 22734463 DOI: 10.1186/1471-2350-13-51  0.68
2011 Chowdhury S, Erickson SW, MacLeod SL, Cleves MA, Hu P, Karim MA, Hobbs CA. Maternal genome-wide DNA methylation patterns and congenital heart defects. Plos One. 6: e16506. PMID 21297937 DOI: 10.1371/journal.pone.0016506  0.68
2010 PopÅ‚awski AB, Jankowski M, Erickson SW, Díaz de StÃ¥hl T, Partridge EC, Crasto C, Guo J, Gibson J, Menzel U, Bruder CE, Kaczmarczyk A, Benetkiewicz M, Andersson R, Sandgren J, Zegarska B, et al. Frequent genetic differences between matched primary and metastatic breast cancer provide an approach to identification of biomarkers for disease progression. European Journal of Human Genetics : Ejhg. 18: 560-8. PMID 20051991 DOI: 10.1038/ejhg.2009.230  0.68
2009 Beasley TM, Erickson S, Allison DB. Rank-based inverse normal transformations are increasingly used, but are they merited? Behavior Genetics. 39: 580-95. PMID 19526352 DOI: 10.1007/s10519-009-9281-0  0.68
2009 Guimbellot JS, Erickson SW, Mehta T, Wen H, Page GP, Sorscher EJ, Hong JS. Correlation of microRNA levels during hypoxia with predicted target mRNAs through genome-wide microarray analysis. Bmc Medical Genomics. 2: 15. PMID 19320992 DOI: 10.1186/1755-8794-2-15  0.68
2008 Wineinger NE, Kennedy RE, Erickson SW, Wojczynski MK, Bruder CE, Tiwari HK. Statistical issues in the analysis of DNA Copy Number Variations. International Journal of Computational Biology and Drug Design. 1: 368-95. PMID 19774103 DOI: 10.1504/IJCBDD.2008.022208  0.68
2008 Bruder CE, Piotrowski A, Gijsbers AA, Andersson R, Erickson S, Diaz de StÃ¥hl T, Menzel U, Sandgren J, von Tell D, Poplawski A, Crowley M, Crasto C, Partridge EC, Tiwari H, Allison DB, et al. Phenotypically concordant and discordant monozygotic twins display different DNA copy-number-variation profiles. American Journal of Human Genetics. 82: 763-71. PMID 18304490 DOI: 10.1016/j.ajhg.2007.12.011  0.68
2008 Musani SK, Erickson S, Allison DB. Obesity--still highly heritable after all these years. The American Journal of Clinical Nutrition. 87: 275-6. PMID 18258613 DOI: 10.1093/AJCN/87.2.275  0.68
2008 Erickson S. A likelihood-ratio test of twin zygosity using molecular genetic markers. Twin Research and Human Genetics : the Official Journal of the International Society For Twin Studies. 11: 41-3. PMID 18251673 DOI: 10.1375/twin.11.1.41  0.68
2005 Erickson S, Sabatti C. Empirical bayes estimation of a sparse vector of gene expression changes. Statistical Applications in Genetics and Molecular Biology. 4: Article22. PMID 16646840 DOI: 10.2202/1544-6115.1132  0.68
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