| Year |
Citation |
Score |
| 2019 |
Deelen J, Evans DS, Arking DE, Tesi N, Nygaard M, Liu X, Wojczynski MK, Biggs ML, van der Spek A, Atzmon G, Ware EB, Sarnowski C, Smith AV, Seppälä I, Cordell HJ, ... ... Sebastiani P, et al. A meta-analysis of genome-wide association studies identifies multiple longevity genes. Nature Communications. 10: 3669. PMID 31413261 DOI: 10.1038/S41467-019-11558-2 |
0.379 |
|
| 2019 |
Gurinovich A, Bae H, Farrell JJ, Andersen SL, Monti S, Puca A, Atzmon G, Barzilai N, Perls TT, Sebastiani P. PopCluster: an algorithm to identify genetic variants with ethnicity-dependent effects. Bioinformatics (Oxford, England). PMID 30624692 DOI: 10.1093/Bioinformatics/Btz017 |
0.365 |
|
| 2017 |
Sebastiani P, Gurinovich A, Bae H, Andersen SL, Perls TT. Assortative Mating by Ethnicity in Longevous Families. Frontiers in Genetics. 8: 186. PMID 29209360 DOI: 10.3389/Fgene.2017.00186 |
0.301 |
|
| 2017 |
Shaikho EM, Farrell JJ, Alsultan A, Qutub H, Al-Ali AK, Figueiredo MS, Chui DHK, Farrer LA, Murphy GJ, Mostoslavsky G, Sebastiani P, Steinberg MH. A phased SNP-based classification of sickle cell anemia HBB haplotypes. Bmc Genomics. 18: 608. PMID 28800727 DOI: 10.1186/S12864-017-4013-Y |
0.366 |
|
| 2017 |
Shaikho EM, Farrell JJ, Alsultan A, Sebastiani P, Steinberg MH. Genetic Determinants of HbF in Saudi Arabian and African Benin Haplotype Sickle Cell Anemia. American Journal of Hematology. PMID 28612458 DOI: 10.1002/Ajh.24822 |
0.313 |
|
| 2017 |
Sebastiani P, Bae H, Gurinovich A, Soerensen M, Puca A, Perls TT. Limitations and risks of meta-analyses of longevity studies. Mechanisms of Ageing and Development. PMID 28143747 DOI: 10.1016/J.Mad.2017.01.008 |
0.371 |
|
| 2016 |
Vathipadiekal V, Farrell JJ, Wang S, Edward HL, Shappell H, Al-Rubaish AM, Al-Muhanna F, Naserullah Z, Alsuliman A, Qutub HO, Simkin I, Farrer LA, Jiang Z, Luo HY, Huang S, ... Sebastiani P, et al. A Candidate Trans-acting Modulator of Fetal Hemoglobin Gene Expression in the Arab-Indian Haplotype of Sickle Cell Anemia: -ANTXR1 Variants and HbF. American Journal of Hematology. PMID 27501013 DOI: 10.1002/Ajh.24527 |
0.346 |
|
| 2016 |
Vathipadiekal V, Alsultan A, Baltrusaitis K, Farrell JJ, Al-Rubaish AM, Al-Muhanna F, Naserullah Z, Suliman A, Patra PK, Milton JN, Farrer LA, Chui DH, Al-Ali AK, Sebastiani P, Steinberg MH. Homozygosity for a haplotype in the HBG2-OR51B4 region is exclusive to Arab-Indian haplotype sickle cell anemia. American Journal of Hematology. 91: E308-11. PMID 27185208 DOI: 10.1002/Ajh.24368 |
0.39 |
|
| 2016 |
Liu L, Pertsemlidis A, Ding LH, Story MD, Steinberg MH, Sebastiani P, Hoppe C, Ballas SK, Pace BS. A case-control genome-wide association study identifies genetic modifiers of fetal hemoglobin in sickle cell disease. Experimental Biology and Medicine (Maywood, N.J.). PMID 27022141 DOI: 10.1177/1535370216642047 |
0.462 |
|
| 2016 |
Zeng Y, Nie C, Min J, Liu X, Li M, Chen H, Xu H, Wang M, Ni T, Li Y, Yan H, Zhang JP, Song C, Chi LQ, Wang HM, ... ... Sebastiani P, et al. Novel loci and pathways significantly associated with longevity. Scientific Reports. 6: 21243. PMID 26912274 DOI: 10.1038/Srep21243 |
0.402 |
|
| 2015 |
Bae H, Perls T, Steinberg M, Sebastiani P. Bayesian Polynomial Regression Models to Fit Multiple Genetic Models for Quantitative Traits. Bayesian Analysis (Online). 10: 53-74. PMID 26029316 DOI: 10.1214/14-Ba880 |
0.353 |
|
| 2015 |
Zhang X, Zhang W, Saraf SL, Nouraie M, Han J, Gowhari M, Hassan J, Miasnikova G, Sergueeva A, Nekhai S, Kittles R, Machado RF, Garcia JG, Gladwin MT, Steinberg MH, Sebastiani P, et al. Genetic polymorphism of APOB is associated with diabetes mellitus in sickle cell disease. Human Genetics. 134: 895-904. PMID 26025476 DOI: 10.1007/S00439-015-1572-3 |
0.34 |
|
| 2015 |
Sebastiani P, Farrell JJ, Alsultan A, Wang S, Edward HL, Shappell H, Bae H, Milton JN, Baldwin CT, Al-Rubaish AM, Naserullah Z, Al-Muhanna F, Alsuliman A, Patra PK, Farrer LA, et al. BCL11A enhancer haplotypes and fetal hemoglobin in sickle cell anemia. Blood Cells, Molecules & Diseases. 54: 224-30. PMID 25703683 DOI: 10.1016/J.Bcmd.2015.01.001 |
0.322 |
|
| 2015 |
Bae HT, Sebastiani P, Gordeuk VR, Zhang Y, Steinberg MH, Kato GJ. Association of FOXO3A Polymorphisms with Hematocrit, LDH and Longevity in Patients with Sickle Cell Anemia from CSSCD, Walk-Phasst, and PUSH Clinical Trials Blood. 126: 2176-2176. DOI: 10.1182/Blood.V126.23.2176.2176 |
0.475 |
|
| 2014 |
Milton JN, Steinberg MH, Sebastiani P. Evaluation of an ensemble of genetic models for prediction of a quantitative trait. Frontiers in Genetics. 5: 474. PMID 25628649 DOI: 10.3389/Fgene.2014.00474 |
0.356 |
|
| 2014 |
Griffin PJ, Sebastiani P, Edward H, Baldwin CT, Gladwin MT, Gordeuk VR, Chui DH, Steinberg MH. The genetics of hemoglobin A2 regulation in sickle cell anemia. American Journal of Hematology. 89: 1019-23. PMID 25042611 DOI: 10.1002/Ajh.23811 |
0.385 |
|
| 2014 |
Milton JN, Gordeuk VR, Taylor JG, Gladwin MT, Steinberg MH, Sebastiani P. Prediction of fetal hemoglobin in sickle cell anemia using an ensemble of genetic risk prediction models. Circulation. Cardiovascular Genetics. 7: 110-5. PMID 24585758 DOI: 10.1161/Circgenetics.113.000387 |
0.483 |
|
| 2014 |
Milton JN, Ashley-Koch AE, Garrett ME, Soldano KL, Orringer EP, Sebastiani P, Dworkis DA, Quillen K, Steinberg MH, Telen MJ. Genes Associated with Alloimmunization to Blood Group Antigens in Sickle Cell Disease Blood. 124: 762-762. DOI: 10.1182/Blood.V124.21.762.762 |
0.413 |
|
| 2013 |
Sebastiani P, Bae H, Sun FX, Andersen SL, Daw EW, Malovini A, Kojima T, Hirose N, Schupf N, Puca A, Perls TT. Meta‐analysis of genetic variants associated with human exceptional longevity. Aging. 5: 653-61. PMID 24244950 |
0.388 |
|
| 2013 |
Bae HT, Sebastiani P, Sun JX, Andersen SL, Daw EW, Terracciano A, Ferrucci L, Perls TT. Genome-wide association study of personality traits in the long life family study. Frontiers in Genetics. 4: 65. PMID 23658558 DOI: 10.3389/Fgene.2013.00065 |
0.439 |
|
| 2013 |
Ngo D, Bae H, Steinberg MH, Sebastiani P, Solovieff N, Baldwin CT, Melista E, Safaya S, Farrer LA, Al-Suliman AM, Albuali WH, Al Bagshi MH, Naserullah Z, Akinsheye I, Gallagher P, et al. Fetal hemoglobin in sickle cell anemia: genetic studies of the Arab-Indian haplotype. Blood Cells, Molecules & Diseases. 51: 22-6. PMID 23465615 DOI: 10.1016/J.Bcmd.2012.12.005 |
0.379 |
|
| 2013 |
Hartley SW, Sebastiani P. PleioGRiP: genetic risk prediction with pleiotropy. Bioinformatics (Oxford, England). 29: 1086-8. PMID 23419378 DOI: 10.1093/Bioinformatics/Btt081 |
0.708 |
|
| 2013 |
Milton JN, Rooks H, Drasar E, McCabe EL, Baldwin CT, Melista E, Gordeuk VR, Nouraie M, Kato GR, Kato GJ, Minniti C, Taylor J, Campbell A, Luchtman-Jones L, Rana S, ... Sebastiani P, et al. Genetic determinants of haemolysis in sickle cell anaemia. British Journal of Haematology. 161: 270-8. PMID 23406172 DOI: 10.1111/bjh.12245 |
0.404 |
|
| 2013 |
Sturiale CL, Puca A, Sebastiani P, Gatto I, Albanese A, Di Rocco C, Maira G, Pola R. Single nucleotide polymorphisms associated with sporadic brain arteriovenous malformations: where do we stand? Brain : a Journal of Neurology. 136: 665-81. PMID 22975391 DOI: 10.1093/Brain/Aws180 |
0.406 |
|
| 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 |
0.712 |
|
| 2012 |
Steinberg MH, Sebastiani P. Genetic modifiers of sickle cell disease. American Journal of Hematology. 87: 795-803. PMID 22641398 DOI: 10.1002/Ajh.23232 |
0.359 |
|
| 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 |
0.69 |
|
| 2012 |
Conneely KN, Capell BC, Erdos MR, Sebastiani P, Solovieff N, Swift AJ, Baldwin CT, Budagov T, Barzilai N, Atzmon G, Puca AA, Perls TT, Geesaman BJ, Boehnke M, Collins FS. Human longevity and common variations in the LMNA gene: a meta-analysis. Aging Cell. 11: 475-81. PMID 22340368 DOI: 10.1111/J.1474-9726.2012.00808.X |
0.328 |
|
| 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 |
0.7 |
|
| 2012 |
Akinsheye I, Solovieff N, Ngo D, Malek A, Sebastiani P, Steinberg MH, Chui DH. Fetal hemoglobin in sickle cell anemia: molecular characterization of the unusually high fetal hemoglobin phenotype in African Americans. American Journal of Hematology. 87: 217-9. PMID 22139998 DOI: 10.1002/Ajh.22221 |
0.36 |
|
| 2011 |
Sebastiani P, Riva A, Montano M, Pham P, Torkamani A, Scherba E, Benson G, Milton JN, Baldwin CT, Andersen S, Schork NJ, Steinberg MH, Perls TT. Whole genome sequences of a male and female supercentenarian, ages greater than 114 years. Frontiers in Genetics. 2: 90. PMID 22303384 DOI: 10.3389/Fgene.2011.00090 |
0.319 |
|
| 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 |
0.509 |
|
| 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 |
0.632 |
|
| 2011 |
Farrell JJ, Sherva RM, Chen ZY, Luo HY, Chu BF, Ha SY, Li CK, Lee AC, Li RC, Li CK, Yuen HL, So JC, Ma ES, Chan LC, Chan V, Sebastiani P, et al. A 3-bp deletion in the HBS1L-MYB intergenic region on chromosome 6q23 is associated with HbF expression. Blood. 117: 4935-45. PMID 21385855 DOI: 10.1182/Blood-2010-11-317081 |
0.371 |
|
| 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 |
0.645 |
|
| 2011 |
Solovieff N, Steinberg MH, Sebastiani P. Genetic admixture in sickle cell disease Blood. 118: 4495. DOI: 10.1182/Blood-2011-09-373274 |
0.369 |
|
| 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 |
0.675 |
|
| 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 |
0.703 |
|
| 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 |
0.722 |
|
| 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 |
0.678 |
|
| 2009 |
Sebastiani P, Montano M, Puca A, Solovieff N, Kojima T, Wang MC, Melista E, Meltzer M, Fischer SE, Andersen S, Hartley SH, Sedgewick A, Arai Y, Bergman A, Barzilai N, et al. RNA editing genes associated with extreme old age in humans and with lifespan in C. elegans. Plos One. 4: e8210. PMID 20011587 DOI: 10.1371/Journal.Pone.0008210 |
0.313 |
|
| 2009 |
Sebastiani P, Timofeev N, Dworkis DA, Perls TT, Steinberg MH. Genome-wide association studies and the genetic dissection of complex traits. American Journal of Hematology. 84: 504-15. PMID 19569043 DOI: 10.1002/Ajh.21440 |
0.428 |
|
| 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 |
0.668 |
|
| 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 |
0.675 |
|
| 2008 |
Sebastiani P, Wang L, Nolan VG, Melista E, Ma Q, Baldwin CT, Steinberg MH. Fetal hemoglobin in sickle cell anemia: Bayesian modeling of genetic associations. American Journal of Hematology. 83: 189-95. PMID 17918249 DOI: 10.1002/Ajh.21048 |
0.403 |
|
| 2006 |
Nolan VG, Adewoye A, Baldwin C, Wang L, Ma Q, Wyszynski DF, Farrell JJ, Sebastiani P, Farrer LA, Steinberg MH. Sickle cell leg ulcers: associations with haemolysis and SNPs in Klotho, TEK and genes of the TGF-beta/BMP pathway. British Journal of Haematology. 133: 570-8. PMID 16681647 DOI: 10.1111/J.1365-2141.2006.06074.X |
0.349 |
|
| 2006 |
Nolan V, Wilcox M, Sebastiani P, Baldwin C, Wyszynski D, Ma Q, Farrer LA, Steinberg MH. Modeling Genetic Polymorphisms and Sickle Cell Associated Vasoocclusive Events Using Classification and Regression Trees (CART) and Stochastic Gradient Boosting (SGB) American Journal of Epidemiology. 163: S130-S130. DOI: 10.1093/Aje/163.Suppl_11.S130-A |
0.384 |
|
| 2005 |
Baldwin C, Nolan VG, Wyszynski DF, Ma QL, Sebastiani P, Embury SH, Bisbee A, Farrell J, Farrer L, Steinberg MH. Association of klotho, bone morphogenic protein 6, and annexin A2 polymorphisms with sickle cell osteonecrosis. Blood. 106: 372-5. PMID 15784727 DOI: 10.1182/Blood-2005-02-0548 |
0.326 |
|
| 2005 |
NOLAN V, SEBASTIANI P, BALDWIN C, WYSZYNSKI D, FARRER L, STEINBERG M. Modeling genetic polymorhphisms and sickle cell associated vasoocclusive events using classification and regression trees (CART) Annals of Epidemiology. 15: 644-644. DOI: 10.1016/J.Annepidem.2005.06.040 |
0.39 |
|
| 2003 |
Sebastiani P, Lazarus R, Weiss ST, Kunkel LM, Kohane IS, Ramoni MF. Minimal haplotype tagging. Proceedings of the National Academy of Sciences of the United States of America. 100: 9900-5. PMID 12900503 DOI: 10.1073/Pnas.1633613100 |
0.482 |
|
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