Default: Haematologica

ISSN: 0390-6078

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Haematologica Q1 Unclaimed

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

Haematologica is a journal indexed in SJR in Hematology with an H index of 142. It is an CC BY-NC-ND Journal with a Single blind Peer Review review system, and It has a price of 1600 €. The scope of the journal is focused on hematology, oncology. It has an SJR impact factor of 2,782 and it has a best quartile of Q1. It is published in English. It has an SJR impact factor of 2,782.

Haematologica focuses its scope in these topics and keywords: cell, disease, gene, multiple, myeloid, myeloma, leukemia, lymphoma, allogeneic, graftversushost, ...

Type: Journal

Type of Copyright: CC BY-NC-ND

Languages: English

Open Access Policy: Open Access

Type of publications:

Publication frecuency: -

DOAJ Scopus WOS
Categories: Hematology (Q1)
Price

1600 €

Inmediate OA

NPD

Embargoed OA

- €

Non OA

Metrics

Haematologica

2,782

SJR Impact factor

142

H Index

585

Total Docs (Last Year)

1249

Total Docs (3 years)

17191

Total Refs

5999

Total Cites (3 years)

740

Citable Docs (3 years)

4,70

Cites/Doc (2 years)

29,39

Ref/Doc

Aims and Scope


cell, disease, gene, multiple, myeloid, myeloma, leukemia, lymphoma, allogeneic, graftversushost, transplantation, bone, stem, large, study, marrow, survival, inhibits, cd, minimal, chemotherapeutic, hematology, oncology



Best articles by citations

Alternative donor hematopoietic stem cell transplantation for mature lymphoid malignancies after reduced-intensity conditioning regimen: similar outcomes with umbilical cord blood and unrelated donor peripheral blood

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Characterization of gene mutations and copy number changes in acute myeloid leukemia using a rapid target enrichment protocol

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Analysis of 339 pregnancies in 181 women with 13 different forms of inherited thrombocytopenia

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EVI1 triggers metabolic reprogramming associated with leukemogenesis and increases sensitivity to L-asparaginase

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Primary cold agglutinin-associated lymphoproliferative disease: a B-cell lymphoma of the bone marrow distinct from lymphoplasmacytic lymphoma

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DNA methyltransferase 3a hot-spot locus is not mutated in pediatric patients affected by acute myeloid or T-cell acute lymphoblastic leukemia: an Italian study

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Tumor-infiltrating macrophages correlate with adverse prognosis and Epstein-Barr virus status in classical Hodgkin's lymphoma

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Complement deposition in autoimmune hemolytic anemia is a footprint for difficult-to-detect IgM autoantibodies

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Cytokines in combination to treat radiation-induced myelosuppresssion: evaluation of SCF + glycosylated EPO + pegylated G-CSF as an emergency treatment in highly irradiated monkeys

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Chimeric antigen receptor T-cell therapy for acute myeloid leukemia: how close to reality?

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Mutations in the telomere capping complex in bone marrow failure and related syndromes

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Co-expression of the collagen receptors leukocyte-associated immunoglobulin-like receptor-1 and glycoprotein VI on a subset of megakaryoblasts

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The immune microenvironment in Hodgkin lymphoma: T cells, B cells, and immune checkpoints

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Long-term management of leukocyte adhesion deficiency type III without hematopoietic stem cell transplantation

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Treatment of acute myeloid leukemia

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Current outcome of HLA identical sibling versus unrelated donor transplants in severe aplastic anemia: an EBMT analysis

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Specialized pro-resolving lipid mediators are differentially altered in peripheral blood of patients with multiple sclerosis and attenuate monocyte and blood-brain barrier dysfunction

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Histone deacetylase inhibition in combination with MEK or BCL-2 inhibition in multiple myeloma

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Minimal residual disease in peripheral blood at day 15 identifies a subgroup of childhood B-cell precursor acute lymphoblastic leukemia with superior prognosis

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Conditions associated with polyclonal hypergammaglobulinemia in the IgG4-related disease era: a retrospective study from a hematology tertiary care center

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Cytoskeletal perturbation leads to platelet dysfunction and thrombocytopenia in variant forms of Glanzmann thrombasthenia

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Mutations of PHF6 are associated with mutations of NOTCH1, JAK1 and rearrangement of SET-NUP214 in T-cell acute lymphoblastic leukemia

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Hemophilia A: different phenotypes may be explained by multiple and variable effects of the causative mutation in the

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Identification of minor histocompatibility antigens based on the 1000 Genomes Project

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