| Year |
Citation |
Score |
| 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, ... ... Steinberg MH, 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 |
0.303 |
|
| 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 |
0.357 |
|
| 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 |
0.323 |
|
| 2015 |
Peters ME, Schwartz S, Han D, Rabins PV, Steinberg M, Tschanz JT, Lyketsos CG. Neuropsychiatric symptoms as predictors of progression to severe Alzheimer's dementia and death: the Cache County Dementia Progression Study. The American Journal of Psychiatry. 172: 460-5. PMID 25585033 DOI: 10.1176/Appi.Ajp.2014.14040480 |
0.31 |
|
| 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 |
0.327 |
|
| 2015 |
Park S, Gianotti-Sommer A, Chui DHK, Figueiredo MS, Alsultan A, Al-Ali A, Steinberg MH, Murphy GJ, Mostoslavsky G. A Library of Sickle Cell Anemia Induced Pluripotent Stem Cells of Diverse Haplotypes and Ethnicities Blood. 126: 2354-2354. DOI: 10.1182/Blood.V126.23.2354.2354 |
0.313 |
|
| 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 |
0.38 |
|
| 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 |
0.31 |
|
| 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 |
0.319 |
|
| 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 |
0.7 |
|
| 2014 |
Jiang Z, Huang S, Luo HY, Akar N, Basak A, Al-Allawi N, Unal S, Gumruk F, Davis L, Morrison T, Campbell A, Gallagher PG, Forget BG, Steinberg MH, Chui DH. Assessment of HbF QTLs Affecting Disease Severity and Genetic Analysis in Patients Homozygous for Codon 8 (–AA) β0-Thalassemia Mutation Blood. 124: 2690-2690. DOI: 10.1182/Blood.V124.21.2690.2690 |
0.313 |
|
| 2013 |
Bhatnagar P, Barron-Casella E, Bean CJ, Milton JN, Baldwin CT, Steinberg MH, Debaun M, Casella JF, Arking DE. Genome-wide meta-analysis of systolic blood pressure in children with sickle cell disease. Plos One. 8: e74193. PMID 24058526 DOI: 10.1371/Journal.Pone.0074193 |
0.352 |
|
| 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 |
0.302 |
|
| 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, ... ... Steinberg MH, et al. Genetic determinants of haemolysis in sickle cell anaemia. British Journal of Haematology. 161: 270-8. PMID 23406172 DOI: 10.1111/bjh.12245 |
0.313 |
|
| 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 |
0.316 |
|
| 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, ... ... Steinberg MH, 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 |
0.701 |
|
| 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 |
0.686 |
|
| 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 |
0.615 |
|
| 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, ... Steinberg MH, 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 |
0.358 |
|
| 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 |
0.564 |
|
| 2011 |
Alsultan A, Solovieff N, Aleem A, AlGahtani FH, Al-Shehri A, Osman ME, Kurban K, Bahakim H, Al-Momen AK, Baldwin CT, Chui DH, Steinberg MH. Fetal hemoglobin in sickle cell anemia: Saudi patients from the Southwestern province have similar HBB haplotypes but higher HbF levels than African Americans. American Journal of Hematology. 86: 612-4. PMID 21630302 DOI: 10.1002/Ajh.22032 |
0.312 |
|
| 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 |
0.687 |
|
| 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 |
0.355 |
|
| 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, ... Steinberg MH, 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 |
0.325 |
|
| 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 |
0.69 |
|
| 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 |
0.72 |
|
| 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, ... ... Steinberg MH, 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 |
0.691 |
|
| 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 |
0.686 |
|
| 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 |
0.669 |
|
| 2010 |
Alsultan A, Solovieff N, Aleem A, AlGahtani FH, Al-Shehri A, Osman ME, Kurban K, Bahakim H, Al-Momen AK, Chui DH, Steinberg MH. Fetal Hemoglobin In Sickle Cell Anemia: Molecular Characterization of Saudi Patients From the Southwestern Province. Blood. 116: 1621-1621. DOI: 10.1182/Blood.V116.21.1621.1621 |
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 |
0.672 |
|
| 2009 |
Steinberg MH. Genetic etiologies for phenotypic diversity in sickle cell anemia. Thescientificworldjournal. 9: 46-67. PMID 19151898 DOI: 10.1100/tsw.2009.10 |
0.351 |
|
| 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 |
0.701 |
|
| 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 |
0.694 |
|
| 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 |
0.719 |
|
| 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 |
0.691 |
|
| 2008 |
Treiber KA, Lyketsos CG, Corcoran C, Steinberg M, Norton M, Green RC, Rabins P, Stein DM, Welsh-Bohmer KA, Breitner JC, Tschanz JT. Vascular factors and risk for neuropsychiatric symptoms in Alzheimer's disease: the Cache County Study. International Psychogeriatrics / Ipa. 20: 538-53. PMID 18289451 DOI: 10.1017/S1041610208006704 |
0.306 |
|
| 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 |
0.318 |
|
| 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 |
0.683 |
|
| 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 |
0.341 |
|
| 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 |
0.724 |
|
| 2007 |
Nolan VG, Ma Q, Cohen HT, Adewoye A, Rybicki AC, Baldwin C, Mahabir RN, Homan EP, Wyszynski DF, Fabry ME, Nagel RL, Farrer LA, Steinberg MH. Estimated glomerular filtration rate in sickle cell anemia is associated with polymorphisms of bone morphogenetic protein receptor 1B. American Journal of Hematology. 82: 179-84. PMID 17034027 DOI: 10.1002/Ajh.20800 |
0.312 |
|
| 2007 |
Dworkis DA, Nolan VG, McMahon LC, Klings ES, Steinberg MH. Predicting Acute Chest Syndrome in Sickle Cell Disease Patients Hospitalized for Acute Vasoocclusive Events. Blood. 110: 3390-3390. DOI: 10.1182/Blood.V110.11.3390.3390 |
0.652 |
|
| 2007 |
Martinez-Castaldi C, Nolan VG, Baldwin CT, Farrer LA, Steinberg MH, Klings ES. Association of Genetic Polymorphisms in the TGF-β Pathway with the Acute Chest Syndrome of Sickle Cell Anemia. Blood. 110: 2247-2247. DOI: 10.1182/Blood.V110.11.2247.2247 |
0.316 |
|
| 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 |
0.368 |
|
| 2006 |
Steinberg MH, Adewoye AH. Modifier genes and sickle cell anemia. Current Opinion in Hematology. 13: 131-6. PMID 16567954 DOI: 10.1097/01.moh.0000219656.50291.73 |
0.323 |
|
| 2006 |
Steinberg MH, Ma Q, Kutlar A, Farrer LA, Baldwin CT. Fetal Hemoglobin in Sickle Cell Anemia: Associations with Single Nucleotide Polymorphisms in Quantitative Trait Loci on Chromsomes 8q12 and Xp22. Blood. 108: 1222-1222. DOI: 10.1182/BLOOD.V108.11.1222.1222 |
0.34 |
|
| 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 |
0.322 |
|
| 2006 |
Treiber K, Tschanz J, Corcoran C, Stein D, Steinberg M, Norton M, Welsh-Bohmer K, Breitner J, Lyketsos C. P1-258: Vascular factors are associated with increased risk of neuropsychiatric symptoms in Alzheimer’s disease Alzheimers & Dementia. 2. DOI: 10.1016/J.Jalz.2006.05.635 |
0.312 |
|
| 2005 |
Nolan VG, Baldwin C, Ma Q, Wyszynski DF, Amirault Y, Farrell JJ, Bisbee A, Embury SH, Farrer LA, Steinberg MH. Association of single nucleotide polymorphisms in klotho with priapism in sickle cell anaemia. British Journal of Haematology. 128: 266-72. PMID 15638863 DOI: 10.1111/j.1365-2141.2004.05295.x |
0.336 |
|
| 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 |
0.341 |
|
| 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 |
0.304 |
|
| 2005 |
Nolan VG, Rybicki AC, Baldwin CT, Cohen HT, Adewoye AH, Wyszynski DF, Fabry ME, Nagel RL, Steinberg MH. Creatinine Clearance in Sickle Cell Anemia Is Modulated by Genes in the TGF-β/BMP Pathway. Blood. 106: 3175-3175. DOI: 10.1182/Blood.V106.11.3175.3175 |
0.311 |
|
| 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 |
0.346 |
|
| 2005 |
Nolan VG, Adewoye AH, Baldwin CT, Ma Q, Wyszynski DF, Farrell JJ, Bisbee A, Fourcade M, Farrer LA, Steinberg MH. Leg Ulcers in Sickle Cell Anemia Are Associated with Laboratory Markers of Hemolysis and SNPs in KL and Genes of the TGF-β/BMP Pathway. Blood. 106: 2317-2317. DOI: 10.1182/Blood.V106.11.2317.2317 |
0.343 |
|
| 2005 |
Machado R, Steinberg M, Bonds D, Ballas S, Blackwelder W, Barton B, Waclawiw M, Castro O, Gladwin M. Natriuretic Peptide Levels Correlate with Pulmonary Pressures and Prospective Mortality in SCD: Use of This Biomarker To Identify Prevalence and Mortality of Pulmonary Hypertension in the MSH Cohort. Blood. 106: 1-1. DOI: 10.1182/Blood.V106.11.1.1 |
0.306 |
|
| 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 |
0.317 |
|
| 2004 |
Bassiony MM, Rosenblatt A, Baker A, Steinberg M, Steele CD, Sheppard JM, Lyketsos CG. Falls and age in patients with Alzheimer's disease. The Journal of Nervous and Mental Disease. 192: 570-2. PMID 15387161 DOI: 10.1097/01.Nmd.0000135498.96431.Ef |
0.329 |
|
| 2004 |
Blass DM, Hatanpaa KJ, Brandt J, Rao V, Steinberg M, Troncoso JC, Rabins PV. Dementia in hippocampal sclerosis resembles frontotemporal dementia more than Alzheimer disease. Neurology. 63: 492-7. PMID 15304580 DOI: 10.1212/01.Wnl.0000133008.89613.82 |
0.302 |
|
| 2004 |
Nolan VG, Baldwin C, Ma Q, Wyszynski DF, Farrell JJ, Bisbee A, Farrer LA, Steinberg MH. Association of Single Nucleotide Polymorphisms in Klotho with Priapism in Sickle Cell Anemia. Blood. 104: 1673-1673. DOI: 10.1182/BLOOD.V104.11.1673.1673 |
0.356 |
|
| 2004 |
Wyszynski DF, Baldwin CT, Cleves M, Farrell JJ, Bisbee A, Kutlar A, Farrer LA, Steinberg MH. Genetic Polymorphisms Associated with Fetal Hemoglobin Response to Hydroxyurea in Patients with Sickle Cell Anemia. Blood. 104: 108-108. DOI: 10.1182/BLOOD.V104.11.108.108 |
0.33 |
|
| 2001 |
Lyketsos CG, Sheppard JM, Steinberg M, Tschanz JA, Norton MC, Steffens DC, Breitner JC. Neuropsychiatric disturbance in Alzheimer's disease clusters into three groups: the Cache County study. International Journal of Geriatric Psychiatry. 16: 1043-53. PMID 11746650 DOI: 10.1002/Gps.448 |
0.312 |
|
| 2000 |
Groves WC, Brandt J, Steinberg M, Warren A, Rosenblatt A, Baker A, Lyketsos CG. Vascular dementia and Alzheimer's disease: is there a difference? A comparison of symptoms by disease duration. Journal of Neuropsychiatry and Clinical Neurosciences. 12: 305-315. PMID 10956564 DOI: 10.1176/Jnp.12.3.305 |
0.304 |
|
| 1999 |
Klein DA, Steinberg M, Galik E, Steele C, Sheppard JM, Warren A, Rosenblatt A, Lyketsos CG. Wandering behaviour in community-residing persons with dementia International Journal of Geriatric Psychiatry. 14: 272-279. PMID 10340188 DOI: 10.1002/(Sici)1099-1166(199904)14:4<272::Aid-Gps896>3.0.Co;2-P |
0.308 |
|
| 1996 |
Lu Z, Steinberg M. Fetal hemoglobin in sickle cell anemia: relation to regulatory sequences cis to the beta-globin gene. Multicenter Study of Hydroxyurea Blood. 87: 1604-1611. DOI: 10.1182/Blood.V87.4.1604.Bloodjournal8741604 |
0.336 |
|
| 1992 |
West MS, Wethers D, Smith J, Steinberg M. Laboratory profile of sickle cell disease: A cross-sectional analysis Journal of Clinical Epidemiology. 45: 893-909. PMID 1624972 DOI: 10.1016/0895-4356(92)90073-V |
0.317 |
|
| 1991 |
Coleman M, Steinberg M, Adams Jd. A four-base deletion 5' to the A gamma globin gene is a common polymorphism [letter] Blood. 78: 2473-2474. DOI: 10.1182/Blood.V78.9.2473.Bloodjournal7892473 |
0.342 |
|
| 1988 |
Steinberg M, West, Gallagher D, Mentzer W. Effects of glucose-6-phosphate dehydrogenase deficiency upon sickle cell anemia. Blood. 71: 748-752. DOI: 10.1182/Blood.V71.3.748.Bloodjournal713748 |
0.3 |
|
| 1984 |
Steinberg M, Rosenstock W, Coleman M, Adams J, Platica O, Cedeno M, Rieder R, Wilson J, Milner P, West S. Effects of thalassemia and microcytosis on the hematologic and vasoocclusive severity of sickle cell anemia. Blood. 63: 1353-1360. DOI: 10.1182/Blood.V63.6.1353.Bloodjournal6361353 |
0.31 |
|
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