| Year |
Citation |
Score |
| 2024 |
Reed ER, Chandler KB, Lopez P, Costello CE, Andersen SL, Perls TT, Li M, Bae H, Soerensen M, Monti S, Sebastiani P. Cross-platform proteomics signatures of extreme old age. Geroscience. PMID 39048883 DOI: 10.1007/s11357-024-01286-x |
0.615 |
|
| 2024 |
Reed ER, Chandler KB, Lopez P, Costello CE, Andersen SL, Perls TT, Li M, Bae H, Soerensen M, Monti S, Sebastiani P. Cross-platform proteomics signatures of extreme old age. Biorxiv : the Preprint Server For Biology. PMID 38645061 DOI: 10.1101/2024.04.10.588876 |
0.611 |
|
| 2023 |
Song Z, Gurinovich A, Nygaard M, Mengel-From J, Andersen S, Cosentino S, Schupf N, Lee J, Zmuda J, Ukraintseva S, Arbeev K, Christensen K, Perls T, Sebastiani P. Rare genetic variants correlate with better processing speed. Neurobiology of Aging. PMID 36813607 DOI: 10.1016/j.neurobiolaging.2022.11.018 |
0.361 |
|
| 2022 |
Bae H, Gurinovich A, Karagiannis TT, Song Z, Leshchyk A, Li M, Andersen SL, Arbeev K, Yashin A, Zmuda J, An P, Feitosa M, Giuliani C, Franceschi C, Garagnani P, ... ... Sebastiani P, et al. A Genome-Wide Association Study of 2304 Extreme Longevity Cases Identifies Novel Longevity Variants. International Journal of Molecular Sciences. 24. PMID 36613555 DOI: 10.3390/ijms24010116 |
0.692 |
|
| 2022 |
Gurinovich A, Li M, Leshchyk A, Bae H, Song Z, Arbeev KG, Nygaard M, Feitosa MF, Perls TT, Sebastiani P. Evaluation of GENESIS, SAIGE, REGENIE and fastGWA-GLMM for genome-wide association studies of binary traits in correlated data. Frontiers in Genetics. 13: 897210. PMID 36212134 DOI: 10.3389/fgene.2022.897210 |
0.662 |
|
| 2022 |
Barral S, Andersen SL, Perls TT, Bae H, Sebastiani P, Christensen K, Thyagarajan B, Lee J, Schupf N. Association between late maternal age and age-related endophenotypes in the Long Life Family Study. Neuroscience Letters. 136737. PMID 35709880 DOI: 10.1016/j.neulet.2022.136737 |
0.642 |
|
| 2021 |
Gurinovich A, Song Z, Zhang W, Federico A, Monti S, Andersen SL, Jennings LL, Glass DJ, Barzilai N, Millman S, Perls TT, Sebastiani P. Effect of longevity genetic variants on the molecular aging rate. Geroscience. PMID 33948810 DOI: 10.1007/s11357-021-00376-4 |
0.345 |
|
| 2020 |
Westerman K, Fernández-Sanlés A, Patil P, Sebastiani P, Jacques P, Starr JM, J Deary I, Liu Q, Liu S, Elosua R, DeMeo DL, Ordovás JM. Epigenomic Assessment of Cardiovascular Disease Risk and Interactions With Traditional Risk Metrics. Journal of the American Heart Association. 9: e015299. PMID 32308120 DOI: 10.1161/Jaha.119.015299 |
0.318 |
|
| 2020 |
Westerman K, Liu Q, Liu S, Parnell LD, Sebastiani P, Jacques P, DeMeo DL, Ordovás JM. A gene-diet interaction-based score predicts response to dietary fat in the Women's Health Initiative. The American Journal of Clinical Nutrition. PMID 32135010 DOI: 10.1093/Ajcn/Nqaa037 |
0.314 |
|
| 2020 |
Kraja AT, Daw EW, Lenzini P, Wang L, Lin SJ, Williams CA, Wells AB, Lunetta KL, Murabito JM, Sebastiani P, Tosto G, Barral S, Minster RL, Yashin A, Perls T, et al. A comparison of genetic imputation methods using Long Life Family Study genotypes and sequence data with the 1000 Genome reference panel International Journal of Bioinformatics Research and Applications. 16: 59. DOI: 10.1504/Ijbra.2020.104855 |
0.357 |
|
| 2019 |
Li A, Chapuy B, Varelas X, Sebastiani P, Monti S. Identification of candidate cancer drivers by integrative Epi-DNA and Gene Expression (iEDGE) data analysis. Scientific Reports. 9: 16904. PMID 31729402 DOI: 10.1038/S41598-019-52886-Z |
0.321 |
|
| 2019 |
Gurinovich A, Andersen SL, Puca A, Atzmon G, Barzilai N, Sebastiani P. Varying Effects of APOE Alleles on Extreme Longevity in European Ethnicities. The Journals of Gerontology. Series a, Biological Sciences and Medical Sciences. 74: S45-S51. PMID 31724059 DOI: 10.1093/Gerona/Glz179 |
0.33 |
|
| 2019 |
Dai Y, Shaikho EM, Perez J, Wilson CA, Liu LY, White MR, Farrell JJ, Chui DHK, Sebastiani P, Steinberg MH. BCL2L1 is associated with γ-globin gene expression. Blood Advances. 3: 2995-3001. PMID 31648320 DOI: 10.1182/Bloodadvances.2019032243 |
0.324 |
|
| 2019 |
Westerman K, Sebastiani P, Jacques P, Liu S, DeMeo D, Ordovás JM. DNA methylation modules associate with incident cardiovascular disease and cumulative risk factor exposure. Clinical Epigenetics. 11: 142. PMID 31615550 DOI: 10.1186/S13148-019-0705-2 |
0.306 |
|
| 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 |
0.438 |
|
| 2019 |
Sebastiani P, Monti S, Morris M, Gurinovich A, Toshiko T, Andersen SL, Sweigart B, Ferrucci L, Jennings LL, Glass DJ, Perls TT. A serum protein signature of APOE genotypes in centenarians. Aging Cell. e13023. PMID 31385390 DOI: 10.1093/Geroni/Igz038.2316 |
0.344 |
|
| 2019 |
Bae H, Lunetta KL, Murabito JM, Andersen SL, Schupf N, Perls T, Sebastiani P. Genetic associations with age of menopause in familial longevity. Menopause (New York, N.Y.). PMID 31188284 DOI: 10.1097/Gme.0000000000001367 |
0.701 |
|
| 2019 |
Kartha VK, Sebastiani P, Kern JG, Zhang L, Varelas X, Monti S. CaDrA: A Computational Framework for Performing Candidate Driver Analyses Using Genomic Features. Frontiers in Genetics. 10: 121. PMID 30838036 DOI: 10.3389/Fgene.2019.00121 |
0.313 |
|
| 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 |
0.692 |
|
| 2019 |
Gurinovich A, Gurinovich A, Song Z, Andersen SL, Perls TT, Sebastiani P. GENOME-WIDE ASSOCIATION STUDY OF EXTREME HUMAN LONGEVITY DISCOVERS UNCOMMON LONGEVITY VARIANTS Innovation in Aging. 3: S209-S209. DOI: 10.1093/Geroni/Igz038.759 |
0.455 |
|
| 2019 |
Bhutkar A, Gurinovich A, Perls TT, Sebastiani P, Monti S. CLONAL HEMATOPOIESIS IN A CENTENARIAN COHORT Innovation in Aging. 3: S105-S106. DOI: 10.1093/Geroni/Igz038.394 |
0.345 |
|
| 2019 |
Sweigart B, Sweigart B, Andersen SL, Cosentino S, Schupf N, Perls TT, Sebastiani P. REDUCED COGNITIVE DECLINE WITH THE APOE ε2/ε2 GENOTYPE IN THE LONG LIFE FAMILY STUDY AND NEW ENGLAND CENTENARIAN STUDY Innovation in Aging. 3: S621-S621. DOI: 10.1093/Geroni/Igz038.2314 |
0.314 |
|
| 2018 |
Nebbia G, Nussbaum L, Helmkamp A, Andersen S, Perls T, Sebastiani P. Manual and Automated Procedures for Compiling a Very Large Sample of Centenarian Pedigrees. North American Actuarial Journal : Naaj. 22: 591-599. PMID 31435182 DOI: 10.1080/10920277.2018.1462716 |
0.323 |
|
| 2018 |
Sebastiani P, Gurinovich A, Nygaard M, Sasaki T, Sweigart B, Bae H, Andersen SL, Villa F, Atzmon G, Christensen K, Arai Y, Barzilai N, Puca A, Christiansen L, Hirose N, et al. APOE Alleles and Extreme Human Longevity. The Journals of Gerontology. Series a, Biological Sciences and Medical Sciences. PMID 30060062 DOI: 10.1093/Gerona/Gly174 |
0.702 |
|
| 2018 |
Du M, Van Ness S, Gordeuk V, Nouraie SM, Nekhai S, Gladwin M, Steinberg MH, Sebastiani P. Biomarker signatures of sickle cell disease severity. Blood Cells, Molecules & Diseases. PMID 29778312 DOI: 10.1016/j.bcmd.2018.05.001 |
0.353 |
|
| 2018 |
Bae H, Gurinovich A, Sweigart B, Lunetta K, Murabito J, Andersen S, Perls T, Sebastiani P. GENETIC INFLUENCE ON AGE OF MENOPAUSE IN THE LONG LIFE FAMILY STUDY AND HEALTH AND RETIREMENT STUDY Innovation in Aging. 2: 100-100. DOI: 10.1093/Geroni/Igy023.375 |
0.668 |
|
| 2018 |
Gurinovich A, Bae H, Andersen S, Puca A, Atzmon G, Barzilai N, Perls T, Sebastiani P. ETHNIC-SPECIFIC EFFECT OF APOE ALLELES ON EXTREME LONGEVITY Innovation in Aging. 2: 99-100. DOI: 10.1093/Geroni/Igy023.373 |
0.651 |
|
| 2018 |
Sebastiani P, Monti S, Morris M, Gurinovich A, Glass D, Jennings L, Perls TT. PROTEIN SIGNATURES OF EXTREME OLD AGE AND LONGEVITY Innovation in Aging. 2: 62-62. DOI: 10.1093/Geroni/Igy023.234 |
0.322 |
|
| 2018 |
Sebastiani P, Andersen SL, Sweigart B, Cosentino S, Thyragajan B, Schupf N, Christiansen K, Perls TT. INTEGRATIVE ANALYSIS OF LONGITUDINAL CHANGES OF NEUROPSYCHOLOGICAL TESTS IN LONG LIFE FAMILY STUDY PARTICIPANTS Innovation in Aging. 2: 404-405. DOI: 10.1093/Geroni/Igy023.1510 |
0.306 |
|
| 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 |
0.704 |
|
| 2017 |
Bae H, Gurinovich A, Malovini A, Atzmon G, Andersen SL, Villa F, Barzilai N, Puca A, Perls TT, Sebastiani P. Effects of FOXO3 Polymorphisms on Survival to Extreme Longevity in Four Centenarian Studies. The Journals of Gerontology. Series a, Biological Sciences and Medical Sciences. PMID 28977569 DOI: 10.1093/Gerona/Glx124 |
0.708 |
|
| 2017 |
Marron MM, Singh J, Boudreau RM, Christensen K, Cosentino S, Feitosa MF, Minster RL, Perls T, Schupf N, Sebastiani P, Ukraintseva S, Wojczynski MK, Newman AB. A novel healthy blood pressure phenotype in the Long Life Family Study. Journal of Hypertension. PMID 28837423 DOI: 10.1097/Hjh.0000000000001514 |
0.308 |
|
| 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 |
0.401 |
|
| 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 |
0.38 |
|
| 2017 |
Sebastiani P, Gurinovich A, Bae H, Andersen S, Malovini A, Atzmon G, Villa F, Kraja AT, Ben-Avraham D, Barzilai N, Puca A, Perls TT. Four Genome-Wide Association Studies Identify New Extreme Longevity Variants. The Journals of Gerontology. Series a, Biological Sciences and Medical Sciences. PMID 28329165 DOI: 10.1093/Gerona/Glx027 |
0.692 |
|
| 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 |
0.708 |
|
| 2017 |
Park S, Gianotti-Sommer A, Molina-Estevez FJ, Vanuytsel K, Skvir N, Leung A, Rozelle SS, Shaikho EM, Weir I, Jiang Z, Luo HY, Chui DH, Figueiredo MS, Alsultan A, Al-Ali A, ... Sebastiani P, et al. A Comprehensive, Ethnically Diverse Library of Sickle Cell Disease-Specific Induced Pluripotent Stem Cells. Stem Cell Reports. PMID 28111279 DOI: 10.1016/J.Stemcr.2016.12.017 |
0.356 |
|
| 2017 |
Sebastiani P, Thyagarajan B, Sun F, Schupf N, Newman AB, Montano M, Perls TT. Biomarker signatures of aging. Aging Cell. PMID 28058805 DOI: 10.1111/Acel.12557 |
0.349 |
|
| 2017 |
Bae H, Sun F, Andersen S, Schupf N, Perls T, Sebastiani P. GENETIC INFLUENCE ON AGE OF MENOPAUSE IN LONG-LIVED INDIVIDUALS Innovation in Aging. 1: 1230-1230. DOI: 10.1093/Geroni/Igx004.4468 |
0.675 |
|
| 2016 |
Fagan E, Sun F, Bae H, Elo I, Andersen SL, Lee J, Christensen K, Thyagarajan B, Sebastiani P, Perls T, Honig LS, Schupf N. Telomere length is longer in women with late maternal age. Menopause (New York, N.Y.). PMID 27922939 DOI: 10.1097/Gme.0000000000000795 |
0.641 |
|
| 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 |
0.424 |
|
| 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 |
0.399 |
|
| 2016 |
Bae H, Monti S, Montano M, Steinberg MH, Perls TT, Sebastiani P. Learning Bayesian Networks from Correlated Data. Scientific Reports. 6: 25156. PMID 27146517 DOI: 10.1038/Srep25156 |
0.656 |
|
| 2016 |
Sebastiani P, Andersen SL, McIntosh AI, Nussbaum L, Stevenson MD, Pierce L, Xia S, Salance K, Perls TT. Familial Risk for Exceptional Longevity. North American Actuarial Journal : Naaj. 20: 57-64. PMID 27041978 DOI: 10.1080/10920277.2015.1061946 |
0.321 |
|
| 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 |
0.465 |
|
| 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 |
0.697 |
|
| 2015 |
Stevenson M, Bae H, Schupf N, Andersen S, Zhang Q, Perls T, Sebastiani P. Erratum: Burden of disease variants in participants of the long life family study. Aging. 7: 450. PMID 26175384 DOI: 10.18632/aging.100761 |
0.618 |
|
| 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 |
0.685 |
|
| 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 |
0.398 |
|
| 2015 |
Sebastiani P, Nussbaum L, Andersen SL, Black MJ, Perls TT. Increasing Sibling Relative Risk of Survival to Older and Older Ages and the Importance of Precise Definitions of "Aging," "Life Span," and "Longevity". The Journals of Gerontology. Series a, Biological Sciences and Medical Sciences. PMID 25814633 DOI: 10.1093/Gerona/Glv020 |
0.33 |
|
| 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 |
0.694 |
|
| 2015 |
Stevenson M, Bae H, Schupf N, Andersen S, Zhang Q, Perls T, Sebastiani P. Burden of disease variants in participants of the Long Life Family Study. Aging. 7: 123-32. PMID 25664523 DOI: 10.18632/AGING.100724 |
0.673 |
|
| 2015 |
Broer L, Buchman AS, Deelen J, Evans DS, Faul JD, Lunetta KL, Sebastiani P, Smith JA, Smith AV, Tanaka T, Yu L, Arnold AM, Aspelund T, Benjamin EJ, De Jager PL, et al. GWAS of longevity in CHARGE consortium confirms APOE and FOXO3 candidacy. The Journals of Gerontology. Series a, Biological Sciences and Medical Sciences. 70: 110-8. PMID 25199915 DOI: 10.1093/Gerona/Glu166 |
0.374 |
|
| 2015 |
Sun F, Sebastiani P, Schupf N, Bae H, Andersen SL, McIntosh A, Abel H, Elo IT, Perls TT. Extended maternal age at birth of last child and women's longevity in the Long Life Family Study. Menopause (New York, N.Y.). 22: 26-31. PMID 24977462 DOI: 10.1097/Gme.0000000000000276 |
0.652 |
|
| 2015 |
Vathipadiekal V, Farrell J, Shuai Z, Edward H, Shappell H, Al-Rubaish AM, Al-Muhanna F, Naserullah Z, Alsuliman A, Simkin I, Farrer L, Jiang Z, Luo HY, Huang S, Mostoslavsky G, ... ... Sebastiani P, et al. A Candidate Trans-Acting Modulator of Fetal Hemoglobin Gene Expression in the Arab-Indian Haplotype of Sickle Cell Anemia Blood. 126: 409-409. DOI: 10.1182/Blood.V126.23.409.409 |
0.408 |
|
| 2015 |
Vathipadiekal V, Alsultan A, Farrell J, Al-Rubaish AM, Al-Muhanna F, Naserullah Z, Alsuliman A, Patra PK, Milton J, Farrer L, Chui DHK, Al-Ali A, Sebastiani P, Steinberg MH. Polymorphisms Associated with the Arab-Indian Haplotype of Sickle Cell Anemia Are Candidate Fetal Hemoglobin Gene Modulators Blood. 126: 3388-3388. DOI: 10.1182/Blood.V126.23.3388.3388 |
0.433 |
|
| 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 |
0.737 |
|
| 2015 |
Stevenson M, Bae H, Schupf N, Andersen S, Zhang Q, Perls T, Sebastiani P. Burden of disease variants in participants of the long life family study Aging. 7: 123-132. |
0.618 |
|
| 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 |
0.385 |
|
| 2014 |
Bae HT, Perls TT, Sebastiani P. An efficient technique for Bayesian modeling of family data using the BUGS software. Frontiers in Genetics. 5: 390. PMID 25477899 DOI: 10.3389/Fgene.2014.00390 |
0.632 |
|
| 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 |
0.424 |
|
| 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 |
0.465 |
|
| 2014 |
Zhang X, Zhang W, Ma SF, Desai AA, Saraf S, Miasniakova G, Sergueeva A, Ammosova T, Xu M, Nekhai S, Abbasi T, Casanova NG, Steinberg MH, Baldwin CT, Sebastiani P, et al. Hypoxic response contributes to altered gene expression and precapillary pulmonary hypertension in patients with sickle cell disease. Circulation. 129: 1650-8. PMID 24515990 DOI: 10.1161/Circulationaha.113.005296 |
0.363 |
|
| 2014 |
Alsultan A, Alabdulaali MK, Griffin PJ, Alsuliman AM, Ghabbour HA, Sebastiani P, Albuali WH, Al-Ali AK, Chui DH, Steinberg MH. Sickle cell disease in Saudi Arabia: the phenotype in adults with the Arab-Indian haplotype is not benign. British Journal of Haematology. 164: 597-604. PMID 24224700 DOI: 10.1111/Bjh.12650 |
0.343 |
|
| 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 |
0.435 |
|
| 2014 |
Sebastiani P, Farrell JJ, Wang S, Edward HL, Shappell HM, Bae HT, Baldwin CT, Al-Rubaish AM, Naserullah Z, Alsuliman A, Patra PK, Farrer LA, Chui DHK, Alsultan A, Ngo DA, et al. BCL11A enhancer Haplotypes Are Associated with the Distribution of HbF in Arab-Indian and African Haplotype Sickle Cell Anemia but Not the Different Population Levels of HbF Blood. 124: 4066-4066. DOI: 10.1182/Blood.V124.21.4066.4066 |
0.7 |
|
| 2013 |
Sebastiani P, Sun FX, Andersen SL, Lee JH, Wojczynski MK, Sanders JL, Yashin A, Newman AB, Perls TT. Families Enriched for Exceptional Longevity also have Increased Health-Span: Findings from the Long Life Family Study. Frontiers in Public Health. 1: 38. PMID 24350207 DOI: 10.3389/Fpubh.2013.00038 |
0.341 |
|
| 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 |
0.7 |
|
| 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 |
0.723 |
|
| 2013 |
Alsultan A, Ngo D, Bae H, Sebastiani P, Baldwin CT, Melista E, Suliman AM, Albuali WH, Nasserullah Z, Luo HY, Chui DH, Steinberg MH, Al-Ali AK. Genetic studies of fetal hemoglobin in the Arab-Indian haplotype sickle cell-β(0) thalassemia. American Journal of Hematology. 88: 531-2. PMID 23483609 DOI: 10.1002/Ajh.23434 |
0.669 |
|
| 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 |
0.804 |
|
| 2013 |
Hartley SW, Sebastiani P. PleioGRiP: genetic risk prediction with pleiotropy. Bioinformatics (Oxford, England). 29: 1086-8. PMID 23419378 DOI: 10.1093/Bioinformatics/Btt081 |
0.43 |
|
| 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 |
0.423 |
|
| 2013 |
Andersen SL, Sun JX, Sebastiani P, Huntly J, Gass JD, Feldman L, Bae H, Christiansen L, Perls TT. Personality factors in the Long Life Family Study. The Journals of Gerontology. Series B, Psychological Sciences and Social Sciences. 68: 739-49. PMID 23275497 DOI: 10.1093/Geronb/Gbs117 |
0.658 |
|
| 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 |
0.445 |
|
| 2013 |
Zhang X, Zhang W, Ma S, Desai AA, Miasnikova GY, Sergueeva A, Ammosova T, Xu M, Nekhai SA, Abbasi T, Casanova NG, Steinberg MH, Baldwin CT, Sebastiani P, Prchal J, et al. Genetic Association Of a MAPK8 Expression Quantitative Trait Locus With Pre-Capillary Pulmonary Hypertension In Sickle Cell Disease Blood. 122: 991-991. DOI: 10.1182/Blood.V122.21.991.991 |
0.381 |
|
| 2012 |
Sebastiani P, Perls TT. The genetics of extreme longevity: lessons from the new England centenarian study. Frontiers in Genetics. 3: 277. PMID 23226160 DOI: 10.3389/Fgene.2012.00277 |
0.391 |
|
| 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 |
0.439 |
|
| 2012 |
Bae HT, Baldwin CT, Sebastiani P, Telen MJ, Ashley-Koch A, Garrett M, Hooper WC, Bean CJ, Debaun MR, Arking DE, Bhatnagar P, Casella JF, Keefer JR, Barron-Casella E, Gordeuk V, et al. Meta-analysis of 2040 sickle cell anemia patients: BCL11A and HBS1L-MYB are the major modifiers of HbF in African Americans. Blood. 120: 1961-2. PMID 22936743 DOI: 10.1182/Blood-2012-06-432849 |
0.659 |
|
| 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 |
0.413 |
|
| 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 |
0.723 |
|
| 2012 |
Sebastiani P, Solovieff N, Sun JX. Naïve Bayesian Classifier and Genetic Risk Score for Genetic Risk Prediction of a Categorical Trait: Not so Different after all! Frontiers in Genetics. 3: 26. PMID 22393331 DOI: 10.3389/Fgene.2012.00026 |
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 |
0.708 |
|
| 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 |
0.742 |
|
| 2012 |
Andersen SL, Sebastiani P, Dworkis DA, Feldman L, Perls TT. Health span approximates life span among many supercentenarians: compression of morbidity at the approximate limit of life span. The Journals of Gerontology. Series a, Biological Sciences and Medical Sciences. 67: 395-405. PMID 22219514 DOI: 10.1093/Gerona/Glr223 |
0.317 |
|
| 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 |
0.714 |
|
| 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 |
0.654 |
|
| 2012 |
Rozelle SS, Smith BW, Melista E, Aneni E, Sebastiani P, Baldwin CT, Alsultan A, Chui DHK, Mostoslavsky G, Steinberg MH, Murphy GJ. Induced Pluripotent Stem Cell Modeling of Sickle Cell Anemia Blood. 120: 3233-3233. DOI: 10.1182/Blood.V120.21.3233.3233 |
0.329 |
|
| 2012 |
Milton JN, Sebastiani P, Baldwin CT, Melista E, Gordeuk VR, Nouraie M, Kato GJ, Minniti C, Taylor JG, Campbell A, Luchtman-Jones L, Rana SR, Castro OL, Zhang Y, Gladwin MT, et al. Prediction of Fetal Hemoglobin in Sickle Cell Anemia Using a Genetic Risk Score Blood. 120: 3216-3216. DOI: 10.1182/Blood.V120.21.3216.3216 |
0.478 |
|
| 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 |
0.391 |
|
| 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 |
0.565 |
|
| 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 |
0.696 |
|
| 2011 |
Akinsheye I, Alsultan A, Solovieff N, Ngo D, Baldwin CT, Sebastiani P, Chui DH, Steinberg MH. Fetal hemoglobin in sickle cell anemia. Blood. 118: 19-27. PMID 21490337 DOI: 10.1182/Blood-2011-03-325258 |
0.71 |
|
| 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 |
0.391 |
|
| 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 |
0.701 |
|
| 2011 |
Bae HT, Baldwin CT, Gladwin MT, Ashley-Koch AE, Garrett M, Soldano K, Taylor JG, Kato GJ, Telen MJ, Sebastiani P, Steinberg MH, Klings ES. An Elevated Tricuspid Regurgitant Jet Velocity in Sickle Cell Disease Is Associated with Polymorphisms in Genes Impacting Innate Immunity Blood. 118: 514-514. DOI: 10.1182/Blood.V118.21.514.514 |
0.716 |
|
| 2011 |
Milton JN, Sebastiani P, Zhang Y, Nouraie M, Lee J, Baldwin CT, Zhao X, Xiong Z, Zeng Q, Kato GJ, Goldsmith JC, Taylor JG, Onyekwere O, Gordeuk VR, Machado RF, et al. Clinical and Genetic Variability of Red Blood Cell Hemolysis in Sickle Cell Anemia Blood. 118: 1077-1077. DOI: 10.1182/Blood.V118.21.1077.1077 |
0.433 |
|
| 2011 |
Alsultan A, Ngo DA, Farrell JJ, Ghabbour H, Akinsheye I, Al-Ali A, Alsuliman A, Al-Baghshi M, Albuali W, Alabdulaali M, Sebastiani P, Baldwin CT, Chui DHK, Steinberg MH. Co-Inheritance of Delta Thalassemia Might Contribute to the High Fetal Hemoglobin in Sickle Cell Anemia Patients with the Saudi-Indian Haplotype Blood. 118: 1056-1056. DOI: 10.1182/Blood.V118.21.1056.1056 |
0.391 |
|
| 2011 |
Solovieff N, Steinberg MH, Sebastiani P. Genetic admixture in sickle cell disease Blood. 118: 4495. DOI: 10.1182/Blood-2011-09-373274 |
0.722 |
|
| 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. |
0.575 |
|
| 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 |
0.706 |
|
| 2010 |
Minniti CP, Eckman J, Sebastiani P, Steinberg MH, Ballas SK. Leg ulcers in sickle cell disease. American Journal of Hematology. 85: 831-3. PMID 20872960 DOI: 10.1002/Ajh.21838 |
0.303 |
|
| 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 |
0.742 |
|
| 2010 |
Sebastiani P, Perls TT. Prediction models that include genetic data. Circulation. Cardiovascular Genetics. 3: 1-2. PMID 20160188 DOI: 10.1161/Circgenetics.110.937862 |
0.368 |
|
| 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 |
0.743 |
|
| 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 |
0.711 |
|
| 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 |
0.704 |
|
| 2010 |
Klings E, Dworkis DA, Safaya S, Li G, Reid L, Sebastiani P, Baldwin CT, Steinberg MH. Alterations In HLA-DR Expression In Peripheral Blood Mononuclear Cells Are Associated with An Elevated Tricuspid Regurgitant Jet Velocity and Pulmonary Hypertension of Sickle Cell Disease Blood. 116: 2640-2640. DOI: 10.1182/Blood.V116.21.2640.2640 |
0.366 |
|
| 2010 |
Farrell JJ, Sherva RM, Chen Z, Hong-yuan L, Chu BF, Ha SY, Li CK, Lee ACW, Li CK, Yuen HL, So JCC, Ma ES, Chan LC, Chan V, Sebastiani P, et al. A 3-Bp Deletion Between Transcription Factor Binding Motifs In the HBS1L-MYB Intergenic Region on Chromosome 6q23 Is Associated with HbF Expression Blood. 116: 1013-1013. DOI: 10.1182/Blood.V116.21.1013.1013 |
0.377 |
|
| 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 |
0.714 |
|
| 2009 |
Sebastiani P, Hadley EC, Province M, Christensen K, Rossi W, Perls TT, Ash AS. A family longevity selection score: ranking sibships by their longevity, size, and availability for study. American Journal of Epidemiology. 170: 1555-62. PMID 19910380 DOI: 10.1093/Aje/Kwp309 |
0.311 |
|
| 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 |
0.417 |
|
| 2009 |
Givens JL, Frederick M, Silverman L, Anderson S, Senville J, Silver M, Sebastiani P, Terry DF, Costa PT, Perls TT. Personality traits of centenarians' offspring. Journal of the American Geriatrics Society. 57: 683-5. PMID 19392961 DOI: 10.1111/J.1532-5415.2009.02189.X |
0.319 |
|
| 2009 |
Sebastiani P, Montano M, Puca A, Solovieff N, Kojima T, Wang MC, Melista E, Meltzer M, Fischer SEJ, Andersen S, Hartley SH, Sedgewick A, Arai Y, Bergman A, Barzilai N, et al. Correction: RNA Editing Genes Associated with Extreme Old Age in Humans and with Lifespan in C. elegans Plos One. 4. DOI: 10.1371/Annotation/387F8074-5F80-4Bdd-Bb0B-B36D49A16Ac0 |
0.657 |
|
| 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 |
0.437 |
|
| 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 |
0.414 |
|
| 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 |
0.474 |
|
| 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 |
0.426 |
|
| 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 |
0.363 |
|
| 2008 |
Nolan VG, Zhang Y, Lash T, Sebastiani P, Steinberg MH. Association between wind speed and the occurrence of sickle cell acute painful episodes: results of a case-crossover study. British Journal of Haematology. 143: 433-8. PMID 18729854 DOI: 10.1111/J.1365-2141.2008.07354.X |
0.575 |
|
| 2008 |
Sedgewick AE, Timofeev N, Sebastiani P, So JC, Ma ES, Chan LC, Fucharoen G, Fucharoen S, Barbosa CG, Vardarajan BN, Farrer LA, Baldwin CT, Steinberg MH, Chui DH. BCL11A is a major HbF quantitative trait locus in three different populations with beta-hemoglobinopathies. Blood Cells, Molecules & Diseases. 41: 255-8. PMID 18691915 DOI: 10.1016/J.Bcmd.2008.06.007 |
0.345 |
|
| 2008 |
Terry DF, Sebastiani P, Andersen SL, Perls TT. Disentangling the roles of disability and morbidity in survival to exceptional old age. Archives of Internal Medicine. 168: 277-83. PMID 18268168 DOI: 10.1001/Archinternmed.2007.75 |
0.302 |
|
| 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 |
0.386 |
|
| 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 |
0.677 |
|
| 2008 |
Dworkis D, Sebastiani P, Melista E, Parente J, Lester G, Quinn JF, Chui DHK, Steinberg MH, Baldwin CT. Fetal Hemoglobin in Sickle Cell Anemia: A Novel Method for High-Resolution Discovery of Associated Genomic Copy Number Variations Blood. 112: 2491-2491. DOI: 10.1182/Blood.V112.11.2491.2491 |
0.422 |
|
| 2008 |
Timofeev N, Sebastiani P, Hartley SH, Baldwin CT, Steinberg MH. Fetal Hemoglobin in Sickle Cell Anemia: A Genome-Wide Association Study of the Response to Hydroxyurea Blood. 112: 2471-2471. DOI: 10.1182/Blood.V112.11.2471.2471 |
0.432 |
|
| 2008 |
Sebastiani P, Timofeev N, Hartley SH, Dworkis D, Farrer L, Baldwin CT, Perls TT, Steinberg MH. Genome-Wide Association Studies Suggest Shared Polymorphisms Are Associated with Severity of Sickle Cell Anemia and Exceptional Longevity. Blood. 112: 1446-1446. DOI: 10.1182/Blood.V112.11.1446.1446 |
0.488 |
|
| 2007 |
Sebastiani P, Nolan VG, Baldwin CT, Abad-Grau MM, Wang L, Adewoye AH, McMahon LC, Farrer LA, Taylor JG, Kato GJ, Gladwin MT, Steinberg MH. A network model to predict the risk of death in sickle cell disease. Blood. 110: 2727-35. PMID 17600133 DOI: 10.1182/Blood-2007-04-084921 |
0.637 |
|
| 2007 |
Nolan VG, Zhang Y, Lash T, Sebastiani P, Steinberg MH. Association of Wind Speed and the Occurrence of Sickle Cell Acute Painful Episodes: Results of a Case-Crossover Study. Blood. 110: 3402-3402. DOI: 10.1182/Blood.V110.11.3402.3402 |
0.582 |
|
| 2007 |
Sebastiani P, Wang L, Perls T, Terry DF, Montano M, Baldwin CT, Steinberg MH. A Repertoire of Genes Modifying the Risk of Death in Sickle Cell Anemia. Blood. 110: 150-150. DOI: 10.1182/Blood.V110.11.150.150 |
0.473 |
|
| 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 |
0.665 |
|
| 2006 |
Sebastiani P, Nolan VG, Baldwin CT, Abad-Grau MM, Wang L, Adewoye AH, McMahon LC, Farrer LA, Taylor JG, Kato GJ, Gladwin MT, Steinberg MH. Severity of Sickle Cell Disease: Modeling Interrelationships among Hemolysis, Pulmonary Hypertension and Risk of Death. Blood. 108: 786-786. DOI: 10.1182/Blood.V108.11.786.786 |
0.633 |
|
| 2006 |
Sebastiani P, Abad-Grau MM, Riva AA, Nolan VG, Melista E, Steinberg MH, Baldwin CT. Fetal Hemoglobin (HbF) in Sickle Cell Anemia: Genome-Wide Association Studies Using Pooled DNA Samples Can Reveal Genetic Associations with HbF Concentration. Blood. 108: 1221-1221. DOI: 10.1182/Blood.V108.11.1221.1221 |
0.683 |
|
| 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 |
0.668 |
|
| 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 |
0.657 |
|
| 2005 |
Sebastiani P, Ramoni MF, Nolan V, Baldwin CT, Steinberg MH. Genetic dissection and prognostic modeling of overt stroke in sickle cell anemia. Nature Genetics. 37: 435-40. PMID 15778708 DOI: 10.1038/Ng1533 |
0.631 |
|
| 2005 |
Klings ES, Safaya S, Adewoye AH, Odhiambo A, Frampton G, Lenburg M, Gerry N, Sebastiani P, Steinberg MH, Farber HW. Differential gene expression in pulmonary artery endothelial cells exposed to sickle cell plasma. Physiological Genomics. 21: 293-8. PMID 15741505 DOI: 10.1152/Physiolgenomics.00246.2004 |
0.306 |
|
| 2005 |
Sebastiani P, Baldwin CT, Nolan V, Wyszynski DF, Ma Q, Farrell J, Bisbee A, Waraska K, Farrer LA, Steinberg MH. Polymorphisms (Snps) in Multiple Genes of the Tgf-ß/Bmp Pathway Are Associated with a Global Measure of Sickle Cell Disease Severity. Blood. 106: 74-74. DOI: 10.1182/Blood.V106.11.74.74 |
0.686 |
|
| 2005 |
Nolan VG, Wilcox MA, Sebastiani P, Baldwin CT, Wyszynski DF, Ma Q, Bisbee A, Farrell JJ, Farrer LA, Steinberg MH. Gene-Gene Interactions and the Pathophysiology of Sickle Cell Disease: Modeling the Effects of SNPs on Sickle Cell-Associated Vasoocclusive Events Using Classification and Regression Trees and Stochastic Gradient Boosting. Blood. 106: 3183-3183. DOI: 10.1182/Blood.V106.11.3183.3183 |
0.673 |
|
| 2005 |
Adewoye AH, Nolan VG, Baldwin CT, Wyszynski DF, Ma Q, Farrell JJ, Bisbee A, Homan E, Sebastiani P, Farrer LA, Steinberg MH. Association of Polymorphisms of the Transforming Growth Factor-β/Bone Morphogenetic Protein (TGF-β/BMP) Pathway with Sickle Cell Bacteremia. Blood. 106: 3170-3170. DOI: 10.1182/Blood.V106.11.3170.3170 |
0.681 |
|
| 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 |
0.682 |
|
| 2004 |
Sebastiani P, Abad MM, Alpargu G, Ramoni MF. Robust transmission/disequilibrium test for incomplete family genotypes. Genetics. 168: 2329-37. PMID 15611196 DOI: 10.1534/Genetics.103.025841 |
0.321 |
|
| 2004 |
Sebastiani P, Nolan V, Baldwin CT, Steinberg MH. Modeling Phenotype Interactions in Sickle Cell Anemia. Blood. 104: 1659-1659. DOI: 10.1182/Blood.V104.11.1659.1659 |
0.652 |
|
| 2004 |
Sebastiani P, Ramoni MF, Nolan V, Baldwin CT, Steinberg MH. Multigenic Dissection and Prognostic Modeling of Overt Stroke in Sickle Cell Anemia. Blood. 104: 1655-1655. DOI: 10.1182/Blood.V104.11.1655.1655 |
0.629 |
|
| 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 |
0.421 |
|
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