Year |
Citation |
Score |
2016 |
Hartley SW, Mullikin JC, Klein DC, Park M, Coon SL. Alternative Isoform Analysis of Ttc8 Expression in the Rat Pineal Gland Using a Multi-Platform Sequencing Approach Reveals Neural Regulation. Plos One. 11: e0163590. PMID 27684375 DOI: 10.1371/Journal.Pone.0163590 |
0.306 |
|
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 |
0.378 |
|
2013 |
Hartley SW, Sebastiani P. PleioGRiP: genetic risk prediction with pleiotropy. Bioinformatics (Oxford, England). 29: 1086-8. PMID 23419378 DOI: 10.1093/Bioinformatics/Btt081 |
0.66 |
|
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 |
0.669 |
|
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 |
0.649 |
|
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 |
0.653 |
|
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. Example of 9 clusters of genetic risk profiles in centenarians of the discovery set and 3 similar clusters in replication sets 1 and 2. Plos One. DOI: 10.1371/Journal.Pone.0029848.G008 |
0.315 |
|
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 |
0.383 |
|
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 |
0.573 |
|
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 |
0.602 |
|
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 |
0.629 |
|
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 |
0.655 |
|
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 |
0.685 |
|
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 |
0.64 |
|
2010 |
Dworkis DA, Klings E, Solovieff N, Li G, Milton JN, Hartley SW, Melista E, Parente J, Sebastiani P, Steinberg MH, Baldwin CT. Tumor Necrosis Factor-α Signaling In Sickle Cell Disease: Elevated Biomarker Levels and Genetic Associations with Disease Severity Blood. 116: 2654-2654. DOI: 10.1182/Blood.V116.21.2654.2654 |
0.438 |
|
2009 |
Timofeev N, Milton JN, Hartley SW, Sherva R, Sebastiani P, Dworkis DA, Klings ES, Farrer L, Telen MJ, Ashley-Koch AE, Garrett ME, Chui DH, Baldwin CT, Steinberg MH. Genome-Wide Studies in Sickle Cell Anemia Show Associations Between SNPs in the Olfactory Receptor Gene Cluster and Fetal Hemoglobin Concentration. Blood. 114: 821-821. DOI: 10.1182/Blood.V114.22.821.821 |
0.539 |
|
2009 |
Taylor JG, Belfer I, Desai K, Youngblood V, Freeman LA, Darbari DS, Kato GJ, Milton JN, Hartley SW, Steinberg MH, Goldman D, Max MB. A GCH1 Haplotype Associated with Susceptibility to Vasoocclusive Pain and Impaired Vascular Function in Sickle Cell Anemia. Blood. 114: 575-575. DOI: 10.1182/Blood.V114.22.575.575 |
0.411 |
|
2009 |
Klings ES, Dworkis DA, Sedgewick A, Hartley SW, Allison A, Telen MJ, Kato GJ, Gladwin M, Sebastiani P, Baldwin CT, Steinberg MH. Genetic Polymorphisms in NEDD4L Are Associated with Pulmonary Hypertension of Sickle Cell Anemia. Blood. 114: 2562-2562. DOI: 10.1182/Blood.V114.22.2562.2562 |
0.483 |
|
2009 |
Dworkis DA, Timofeev N, Milton JN, Hartley SW, Gupta M, Sebastiani P, Baldwin CT, Melista E, Parente J, Quillen K, Steinberg MH. A Genome-Wide Association Study of the Alloimmunization Responder Phenotype in Sickle Cell Disease. Blood. 114: 2551-2551. DOI: 10.1182/Blood.V114.22.2551.2551 |
0.545 |
|
2009 |
Sebastiani P, Milton JN, Timofeev N, Hartley SW, Dworkis DA, Melista E, Baldwin CT, Steinberg MH. Genome-Wide Association Study of Stroke in Sickle Cell Anemia. Blood. 114: 1528-1528. DOI: 10.1182/Blood.V114.22.1528.1528 |
0.498 |
|
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 |
0.62 |
|
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 |
0.629 |
|
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