Hemoglobin
Hemoglobin is a journal indexed in SJR in Biochemistry (medical) and Hematology with an H index of 45. It has an SJR impact factor of 0,329 and it has a best quartile of Q3. It is published in English. It has an SJR impact factor of 0,329.
Metrics
Scimago and CountryOfPapers database fields
SJR Impact
0,329
H-index
45
Docs (year)
69
Docs 3y
194
Total refs
1813
Cites 3y
189
Citable 3y
191
Cites/Doc 2y
0.98
Ref/Doc
26.28
Immediate OA
—
Embargoed OA
NPD
Non OA / Submission
—
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Best articles by citations
Characterizing a Cohort of a-Thalassemia Couples Collected During Screening for Hemoglobinopathies: 14 Years of an Iranian Experience
View moreVarious a-Thalassemia Genotype Combinations of the Saudi-Type Polyadenylation Signal Mutation (aT-Saudia) in the Population of Bahrain: An Update of Genotype-Phenotype Analyses
View moreExpression of CD55 on Red Blood Cells of beta-Thalassemia Patients
View moreEvaluation of Iron Overload in beta-Thalassemia Patients Using Magnetic Resonance Imaging
View moreEffect of Deferiprone on Liver Iron Overload and Fibrosis in Hepatitis C Virus-Infected Thalassemia
View moreDiagnosis and Characterization of Hb C/Hb Iowa: A Rare but Easily Misidentified Compound Heterozygous Condition
View moreDetection of Three Common, Deletional a-Thalassemia Determinants in Southern China by a Single-Tube Multiplex Polymerase Chain Reaction Method
View moreDetection of Rare beta-Thalassemia Mutations by Denaturing Gradient Gel Electrophoresis Among Indians
View moreDETECTION OF A SMALL NOVEL DELETION IN THEa-GLOBIN GENE AND TYPE II -a3.7DELETION BY HETERODUPLEX FORMATION
View moreDefining the Phenotypes of Sickle Cell Disease
View moreCOULD CAPILLARY ZONE ELECTROPHORESIS OF TRYPTIC PEPTIDES BE USED FOR THE CHARACTERIZATION OF HEMOGLOBIN VARIANTS?
View moreCOMPOUND HETEROZYGOSITY FOR Hb SPANISH TOWN [a27(B8)Glu=>Val], Hb S [beta6(A3)Glu=>Val] AND THE -a(3.7 kb) THALASSEMIA DELETION
View moreCompensation of CD55 Underexpression on Red Blood Cells ofbeta-Thalassemia Major Patients
View moreA Confidential Inquiry Estimating the Number of Patients Affected with Sickle Cell Disease and Thalassemia Major Confirms the Need for a Prevention Strategy in The Netherlands
View moreBIOLOGICAL AND CLINICAL PRESENTATION OF PATIENTS WITH HEMOGLOBINOPATHIES ATTENDING AN URBAN HOSPITAL IN OUAGADOUGOU: CONFIRMATION OF THE MODIFICATION OF THE BALANCE BETWEEN Hb S AND Hb C IN BURKINA FASO
View morebeta-Thalassemia Major Resulting from Compound Heterozygosity forHBB: c.92+2T>C [formerly known as IVS-I-2 (T>C)] and a Novel beta0-Thalassemia Frameshift Mutation:HBB: c.209delG; p.Gly70Valfs*20
View moreA RARE CASE OF OSTEOMYELITIS OF THE STERNUM IN AN ADULT WITH SICKLE CELL DISEASE
View moreA NOVELbeta-GLOBIN VARIANT: Hb PO?aOS DE CALDAS [beta61(E5)Lys=>Gln]
View moreA NOVEL SPLICE ACCEPTOR SITE MUTATION OF THE a2-GLOBIN GENE CAUSING a-THALASSEMIA
View moreA NEWG gamma CHAIN VARIANT: Hb F-COIGNIERES [ gamma75(E19)Ile => Val]
View moreA NEW UNSTABLE HEMOGLOBIN VARIANT WITH LOW OXYGEN AFFINITY: Hb ILMENAU [beta41(C7)Phe=>Cys]
View moreA new Unstable a2-Globin Gene Variant: Hb Chartres [a33(B14)Phe=>Ser]
View moreA New High A2-beta-Thalassemia Due to a 468 bp Deletion (- 475 to - 8) in the beta-Globin Gene Promoter of the Intact beta-Globin Structural Gene
View moreA New Hemoglobin Variant, Hb Fukui [a139(HC1)Lys=>Asn (AAA=>AAC) (a2)]
View more