Stephen W. Hartley, Ph.D. - Publications

Affiliations: 
2012 Boston University, Boston, MA, United States 
Area:
Biostatistics Biology

20 high-probability publications. We are testing a new system for linking publications to authors. You can help! If you notice any innacuracies, 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
2015 Hartley SW, Coon SL, Savastano LE, Mullikin JC, Fu C, Klein DC. Neurotranscriptomics: The Effects of Neonatal Stimulus Deprivation on the Rat Pineal Transcriptome. Plos One. 10: e0137548. PMID 26367423 DOI: 10.1371/journal.pone.0137548  0.92
2015 Hartley SW, Mullikin JC. QoRTs: a comprehensive toolset for quality control and data processing of RNA-Seq experiments. Bmc Bioinformatics. 16: 224. PMID 26187896 DOI: 10.1186/s12859-015-0670-5  0.92
2014 Belfer I, Youngblood V, Darbari DS, Wang Z, Diaw L, Freeman L, Desai K, Dizon M, Allen D, Cunnington C, Channon KM, Milton J, Hartley SW, Nolan V, Kato GJ, et al. A GCH1 haplotype confers sex-specific susceptibility to pain crises and altered endothelial function in adults with sickle cell anemia. American Journal of Hematology. 89: 187-93. PMID 24136375 DOI: 10.1002/ajh.23613  0.92
2013 Hartley SW, Sebastiani P. PleioGRiP: genetic risk prediction with pleiotropy. Bioinformatics (Oxford, England). 29: 1086-8. PMID 23419378 DOI: 10.1093/bioinformatics/btt081  0.92
2012 Hartley SW, Monti S, Liu CT, Steinberg MH, Sebastiani P. Bayesian methods for multivariate modeling of pleiotropic SNP associations and genetic risk prediction. Frontiers in Genetics. 3: 176. PMID 22973300 DOI: 10.3389/fgene.2012.00176  0.92
2012 Milton JN, Sebastiani P, Solovieff N, Hartley SW, Bhatnagar P, Arking DE, Dworkis DA, Casella JF, Barron-Casella E, Bean CJ, Hooper WC, DeBaun MR, Garrett ME, Soldano K, Telen MJ, et al. A genome-wide association study of total bilirubin and cholelithiasis risk in sickle cell anemia. Plos One. 7: e34741. PMID 22558097 DOI: 10.1371/journal.pone.0034741  0.92
2012 Sebastiani P, Solovieff N, Dewan AT, Walsh KM, Puca A, Hartley SW, Melista E, Andersen S, Dworkis DA, Wilk JB, Myers RH, Steinberg MH, Montano M, Baldwin CT, Hoh J, et al. Genetic signatures of exceptional longevity in humans. Plos One. 7: e29848. PMID 22279548 DOI: 10.1371/journal.pone.0029848  0.92
2011 Sebastiani P, Solovieff N, Puca A, Hartley SW, Melista E, Andersen S, Dworkis DA, Wilk JB, Myers RH, Steinberg MH, Montano M, Baldwin CT, Perls TT. Retraction. Science (New York, N.Y.). 333: 404. PMID 21778381 DOI: 10.1126/science.333.6041.404-a  0.92
2011 Solovieff N, Hartley SW, Baldwin CT, Klings ES, Gladwin MT, Taylor JG, Kato GJ, Farrer LA, Steinberg MH, Sebastiani P. Ancestry of African Americans with sickle cell disease. Blood Cells, Molecules & Diseases. 47: 41-5. PMID 21546286 DOI: 10.1016/j.bcmd.2011.04.002  0.92
2011 Dworkis DA, Klings ES, Solovieff N, Li G, Milton JN, Hartley SW, Melista E, Parente J, Sebastiani P, Steinberg MH, Baldwin CT. Severe sickle cell anemia is associated with increased plasma levels of TNF-R1 and VCAM-1. American Journal of Hematology. 86: 220-3. PMID 21264913 DOI: 10.1002/ajh.21928  0.92
2011 Scher AI, Xu Y, Korf ES, Hartley SW, Witter MP, Scheltens P, White LR, Thompson PM, Toga AW, Valentino DJ, Launer LJ. Hippocampal morphometry in population-based incident Alzheimer's disease and vascular dementia: the HAAS. Journal of Neurology, Neurosurgery, and Psychiatry. 82: 373-6. PMID 20826877 DOI: 10.1136/jnnp.2008.165902  0.92
2011 Sebastiani P, Solovieff N, Puca A, Hartley SW, Melista E, Andersen S, Dworkis DA, Wilk JB, Myers RH, Steinberg MH, Montano M, Baldwin CT, Perls TT. Retraction (Science) Science. 333: 404.  0.92
2010 Solovieff N, Hartley SW, Baldwin CT, Perls TT, Steinberg MH, Sebastiani P. Clustering by genetic ancestry using genome-wide SNP data. Bmc Genetics. 11: 108. PMID 21143920 DOI: 10.1186/1471-2156-11-108  0.92
2010 Sebastiani P, Solovieff N, Puca A, Hartley SW, Melista E, Andersen S, Dworkis DA, Wilk JB, Myers RH, Steinberg MH, Montano M, Baldwin CT, Perls TT. Genetic signatures of exceptional longevity in humans. Science (New York, N.Y.). 2010. PMID 20595579 DOI: 10.1126/science.1190532  0.92
2010 Sebastiani P, Solovieff N, Hartley SW, Milton JN, Riva A, Dworkis DA, Melista E, Klings ES, Garrett ME, Telen MJ, Ashley-Koch A, Baldwin CT, Steinberg MH. Genetic modifiers of the severity of sickle cell anemia identified through a genome-wide association study. American Journal of Hematology. 85: 29-35. PMID 20029952 DOI: 10.1002/ajh.21572  0.92
2010 Solovieff N, Milton JN, Hartley SW, Sherva R, Sebastiani P, Dworkis DA, Klings ES, Farrer LA, Garrett ME, Ashley-Koch A, Telen MJ, Fucharoen S, Ha SY, Li CK, Chui DH, et al. Fetal hemoglobin in sickle cell anemia: genome-wide association studies suggest a regulatory region in the 5' olfactory receptor gene cluster. Blood. 115: 1815-22. PMID 20018918 DOI: 10.1182/blood-2009-08-239517  0.92
2008 Zhao Z, Timofeev N, Hartley SW, Chui DH, Fucharoen S, Perls TT, Steinberg MH, Baldwin CT, Sebastiani P. Imputation of missing genotypes: an empirical evaluation of IMPUTE. Bmc Genetics. 9: 85. PMID 19077279 DOI: 10.1186/1471-2156-9-85  0.92
2008 Sebastiani P, Zhao Z, Abad-Grau MM, Riva A, Hartley SW, Sedgewick AE, Doria A, Montano M, Melista E, Terry D, Perls TT, Steinberg MH, Baldwin CT. A hierarchical and modular approach to the discovery of robust associations in genome-wide association studies from pooled DNA samples. Bmc Genetics. 9: 6. PMID 18194558 DOI: 10.1186/1471-2156-9-6  0.92
2007 Scher AI, Xu Y, Korf ES, White LR, Scheltens P, Toga AW, Thompson PM, Hartley SW, Witter MP, Valentino DJ, Launer LJ. Hippocampal shape analysis in Alzheimer's disease: a population-based study. Neuroimage. 36: 8-18. PMID 17434756 DOI: 10.1016/j.neuroimage.2006.12.036  0.92
2006 Hartley SW, Scher AI, Korf ESC, White LR, Launer LJ. Analysis and validation of automated skull stripping tools: A validation study based on 296 MR images from the Honolulu Asia aging study Neuroimage. 30: 1179-1186. PMID 16376107 DOI: 10.1016/j.neuroimage.2005.10.043  0.92
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