ISSN: 0363-0269

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Hemoglobin Q3 Unclaimed

Informa Healthcare United States

Unfortunately this journal has not been claimed yet. For this reason, some information may be unavailable.

Hemoglobin is a journal indexed in SJR in Biochemistry (medical) and Hematology with an H index of 44. It has an SJR impact factor of 0,274 and it has a best quartile of Q3. It is published in English. It has an SJR impact factor of 0,274.

Type: Journal

Type of Copyright:

Languages: English

Open Access Policy:

Type of publications:

Publication frecuency: -

Categories: Biochemistry (medical) (Q3) Hematology (Q3) Clinical Biochemistry (Q4) Genetics (clinical) (Q4)

Price

- €

Inmediate OA

NPD

Embargoed OA

- €

Non OA

Metrics

0,274

SJR Impact factor

44

H Index

41

Total Docs (Last Year)

243

Total Docs (3 years)

1543

Total Refs

239

Total Cites (3 years)

242

Citable Docs (3 years)

1.03

Cites/Doc (2 years)

37.63

Ref/Doc

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Biomarkers in Medicine Q3
Journal of International Medical Research Q3
Reports of Biochemistry and Molecular Biology Q3
Molecular Cytogenetics Q3

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Aims and Scope

Best articles by citations

COULD CAPILLARY ZONE ELECTROPHORESIS OF TRYPTIC PEPTIDES BE USED FOR THE CHARACTERIZATION OF HEMOGLOBIN VARIANTS?

Molecular Basis of beta-Thalassemia in the United Arab Emirates

A 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

Evaluation of Iron Overload in beta-Thalassemia Patients Using Magnetic Resonance Imaging

Liver Fibrosis and Iron Levels During Long-Term Deferiprone Treatment of Thalassemia Major Patients

HOMOZYGOSITY FOR Hb E-SASKATOON [beta22(B4)Glu => Lys] IN A TURKISH PATIENT

THE HEMOGLOBINS OF THE "FOSSIL FISH" ACIPENSER NACCARII: FUNCTIONAL PROPERTIES AND THEIR STRUCTURAL BASIS

NOVEL beta-THALASSEMIA MUTATION IN A beta-THALASSEMIA INTERMEDIA PATIENT [POLY A (AATAAA =>GATAAA)]

A 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

Detection of Rare beta-Thalassemia Mutations by Denaturing Gradient Gel Electrophoresis Among Indians

Iron Chelation Therapy for Transfusional Iron Overload: A Swift Evolution

Characterizing a Cohort of a-Thalassemia Couples Collected During Screening for Hemoglobinopathies: 14 Years of an Iranian Experience

SHOW MORE ARTICLES

Microsatellite and Single Nucleotide Polymorphisms in the beta-Globin Locus Control Region-Hypersensitive Site 2: Specificity of Tunisian betaSChromosomes

Two New a Chain Variants: Hb Die [a93(FG5)Val=>Ala (a1)] and Hb Beziers [a99(G6)Lys=>Asn (a1)]

Opioid Management and Dependency Among Adult Patients with Sickle Cell Disease

Three New a-Thalassemia Point Mutations Ascertained Through Newborn Screening

Prevalence of Depression in Patients with beta-Thalassemia as Assessed by the Beck's Depression Inventory

The Mutation of Hb Turriff [a99(G6)Lys=>Glu (AAG=>GAG)] Is Carried by the a1-Globin Gene in a Japanese (Hb Turriff-I)

COMPOUND HETEROZYGOSITY FOR Hb SPANISH TOWN [a27(B8)Glu=>Val], Hb S [beta6(A3)Glu=>Val] AND THE -a(3.7 kb) THALASSEMIA DELETION

Various a-Thalassemia Genotype Combinations of the Saudi-Type Polyadenylation Signal Mutation (aT-Saudia) in the Population of Bahrain: An Update of Genotype-Phenotype Analyses

Preimplantation Genetic Diagnosis for Hemoglobinopathies

Effect of Deferiprone on Liver Iron Overload and Fibrosis in Hepatitis C Virus-Infected Thalassemia

DETECTION OF A SMALL NOVEL DELETION IN THEa-GLOBIN GENE AND TYPE II -a3.7DELETION BY HETERODUPLEX FORMATION

UNSTABLE Hb PERTH IN A TAIWANESE SUBJECT: A T => C SUBSTITUTION AT CODON 32 OF THE beta-GLOBIN GENE CREATES ANMspI SITE