| # | Title | Journal | Year | Citations |
|---|
| 1 | Construction of Human Gene Libraries from Small Amounts cf Peripheral Blood: Analysis of β-Like Globin Genes | Hemoglobin | 1982 | 583 |
| 2 | Separation of Human Hemoglobins by Deae-Cellulose Chromatography using Glycine-Kcn-Nacl Developers | Hemoglobin | 1976 | 270 |
| 3 | Hemoglobinopathies in Southeast Asia | Hemoglobin | 1987 | 247 |
| 4 | Location of Amino Acid Residues in Human Deoxy Hemoglobin | Hemoglobin | 1978 | 172 |
| 5 | The Role of Zinc, Copper and Iron in the Pathogenesis of Diabetes and Diabetic Complications: Therapeutic Effects by Chelators | Hemoglobin | 2008 | 149 |
| 6 | Oxidative Stress, Diabetes, and Diabetic Complications | Hemoglobin | 2009 | 141 |
| 7 | Hemoglobinopathies in Southeast Asia: Molecular Biology and Clinical Medicine | Hemoglobin | 1997 | 139 |
| 8 | THE β-THALASSEMIA MUTATION SPECTRUM IN THE IRANIAN POPULATION | Hemoglobin | 2001 | 134 |
| 9 | Magnetic Resonance Imaging Assessment of Excess Iron in Thalassemia, Sickle Cell Disease and Other Iron Overload Diseases | Hemoglobin | 2008 | 124 |
| 10 | Unstable and Thalassemic α Chain Hemoglobin Variants: A Cause of Hb H Disease and Thalassemia Intermedia | Hemoglobin | 2008 | 117 |
| 11 | Newer Aspects of the Pathophysiology of Sickle Cell Disease Vaso-Occlusion | Hemoglobin | 2009 | 116 |
| 12 | Hemoglobins With High Oxygen Affinity Leading to Erythrocytosis. New Variants and New Concepts | Hemoglobin | 2005 | 93 |
| 13 | ABNORMAL HEMOGLOBINS: LABORATORY METHODS | Hemoglobin | 2001 | 87 |
| 14 | Trimodality in Tie Percentages of β Chain Variants in Heterozy-Gotes: The Effect of the Number of Aczive HBαStructural Loci | Hemoglobin | 1977 | 86 |
| 15 | Haplotypes of βSChromosomes Among Patients with Sickle Cell Anemia from Georgia | Hemoglobin | 1986 | 86 |
| 16 | The β- and δ-Thalassemia Repository (Eighth Edition) | Hemoglobin | 1995 | 84 |
| 17 | β-Thalassemia in Turkey | Hemoglobin | 1990 | 83 |
| 18 | Differences in Affinity of Variant β Chains for a Chains: A Possible Explanation for the Variation in the Percentages of β Chain Variants in Heterozygotes | Hemoglobin | 1977 | 79 |
| 19 | β-Cluster Haplotypes, α-Gene Status, and Hematological Data from SS, SC, and S-β-Thalassemia Patients in Southern California | Hemoglobin | 1989 | 77 |
| 20 | A MULTI-CENTER STUDY IN ORDER TO FURTHER DEFINE THE MOLECULAR BASIS OF β-THALASSEMIA IN THAILAND, PAKISTAN, SRI LANKA, MAURITIUS, SYRIA, AND INDIA, AND TO DEVELOP A SIMPLE MOLECULAR DIAGNOSTIC STRATEGY BY AMPLIFICATION REFRACTORY MUTATION SYSTEM-POLYMERASE CHAIN REACTION | Hemoglobin | 2001 | 73 |
| 21 | The Role of Iron and Chelators on Infections in Iron Overload and Non Iron Loaded Conditions: Prospects for the Design of New Antimicrobial Therapies | Hemoglobin | 2010 | 73 |
| 22 | The Sickle Cell Painful Crisis in Adults: Phs and Objective Signs | Hemoglobin | 1995 | 72 |
| 23 | Low Serum Ferritin Levels are Misleading for Detecting Cardiac Iron Overload and Increase the Risk of Cardiomyopathy in Thalassemia Patients. The Importance of Cardiac Iron Overload Monitoring Using Magnetic Resonance Imaging T2 and T2* | Hemoglobin | 2006 | 72 |
| 24 | Results From The North Cyprus Thalassemia Prevention Program | Hemoglobin | 2007 | 71 |
| 25 | α Thalassemia | Hemoglobin | 1989 | 69 |
| 26 | Genetics of Hb F/F Cell Variance in Adults and Heterocellular Hereditary Persistence of Fetal Hemoglobin | Hemoglobin | 1998 | 69 |
| 27 | Patients Welcome the Sickle Cell Disease Mobile Application to Record SymptomsviaTechnology (SMART) | Hemoglobin | 2014 | 68 |
| 28 | Access to a Syllabus of Human Hemoglobin Variants (1996) Via the World Wide Web | Hemoglobin | 1998 | 67 |
| 29 | Measuring Relative Electrophoretic Mobilities of Mutant Hemoglos and Globin Chains | Hemoglobin | 1978 | 66 |
| 30 | Sickle Cell Anemia and Major Organ Failure | Hemoglobin | 1990 | 66 |
| 31 | A Prospective Study of Hepatocellular Carcinoma Incidence in Thalassemia | Hemoglobin | 2006 | 66 |
| 32 | Further Nodification of the Mtcrochromatographic Deternination of Hemoglobin A | Hemoglobin | 1977 | 65 |
| 33 | Hemoglobin Suan-Dok (α2109(G16)LEU-ARGβ2). an Unstable Variant Associated with α-Thalassemia | Hemoglobin | 1979 | 64 |
| 34 | Prevention of Hemoglobinopathies in Egypt | Hemoglobin | 2009 | 64 |
| 35 | Forecasting Hemoglobinopathy Burden Through Neonatal Screening in Omani Neonates | Hemoglobin | 2010 | 64 |
| 36 | Hemoglobin Mizuho or Beta 68 (E 12) Leucine → Proline, a new Ufistarle Variaiit Associated with Severe Hemolytic Anemia | Hemoglobin | 1977 | 63 |
| 37 | Hemoglobin Sunshine Seth - α2(94 (G1) Asp→His)β2 | Hemoglobin | 1979 | 62 |
| 38 | Pathophysiology of Transfusional Iron Overload: Contrasting Patterns in Thalassemia Major and Sickle Cell Disease | Hemoglobin | 2009 | 62 |
| 39 | Usability and Feasibility of an mHealth Intervention for Monitoring and Managing Pain Symptoms in Sickle Cell Disease: The Sickle Cell Disease Mobile Application to Record SymptomsviaTechnology (SMART) | Hemoglobin | 2015 | 62 |
| 40 | Hemoglobins Lepore and Anti-Lepore | Hemoglobin | 1978 | 60 |
| 41 | The β-and -Thalassemia Repository (Ninth Edition; Part I) | Hemoglobin | 1998 | 59 |
| 42 | An Extreme Consequence of Splenectomy in Dehydrated Hereditary Stomatocytosis: Gradual Thrombo‐embolic Pulmonary Hypertension and Lung–Heart Transplantation | Hemoglobin | 2003 | 59 |
| 43 | Iron Overload: Consequences, Assessment, and Monitoring | Hemoglobin | 2009 | 59 |
| 44 | Hb Paksé [(α2) CODON 142 (TAA→TATOR Term→Tyr)] IN THAI PATIENTS WITH EABart's DISEASE AND Hb H DISEASE | Hemoglobin | 2002 | 58 |
| 45 | THE THALASSEMIA SYNDROMES: MOLECULAR CHARACTERIZATION IN THE SPANISH POPULATION | Hemoglobin | 2001 | 57 |
| 46 | Diagnostic Approach to Hemoglobinopathies | Hemoglobin | 2007 | 57 |
| 47 | Hb himeji or β140 (H18) ALA→ASP a slightly unstable hemoglobin with increased βN-terminal glycation | Hemoglobin | 1986 | 55 |
| 48 | β-Thalassemia, HB S-β-Thalassemia and Sickle Cell Anemia Among Tunisians | Hemoglobin | 1991 | 55 |
| 49 | The β- and δ-Thalassemia Repository | Hemoglobin | 1992 | 55 |
| 50 | Leg Ulcers in Sickle Cell Disease: Current Patterns and Practices | Hemoglobin | 2013 | 55 |
