Haemophilia

Aims & Scope

Haemophilia is an international journal dedicated to the exchange of information regarding the comprehensive care of haemophilia.

The Journal contains review articles, original scientific papers and case reports related to haemophilia care, with frequent supplements.

Subjects covered include: clotting factor deficiencies, both inherited and acquired: haemophilia A, B, von Willebrand's disease, deficiencies of factor V, VII, X and XI replacement therapy for clotting factor deficiencies component therapy in the developing world transfusion transmitted disease haemophilia care and paediatrics, orthopaedics, gynaecology and obstetrics nursing laboratory diagnosis carrier detection psycho-social concerns economic issues audit inherited platelet disorders.

View Aims & Scope

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Metrics & Ranking

Impact Factor

Year	Value
2025	3
2024	3.00

SJR (SCImago Journal Rank)

Year	Value
2024	0.926

Quartile

Year	Value
2024	Q1

h-index

Year	Value
2024	107

Journal Rank

Year	Value
2024	5471

Journal Citation Indicator

Year	Value
2024	1579

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Abstracting & Indexing

Journal is indexed in leading academic databases, ensuring global visibility and accessibility of our peer-reviewed research.

• Scopus
• Google Scholar
• Web of Science
• Medline
• Embase

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Subjects & Keywords

Journal’s research areas, covering key disciplines and specialized sub-topics in Medicine, designed to support cutting-edge academic discovery.

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Most Cited Articles

The Most Cited Articles section features the journal's most impactful research, based on citation counts. These articles have been referenced frequently by other researchers, indicating their significant contribution to their respective fields.

• WFH Guidelines for the Management of Hemophilia, 3rd edition

  Citation: 1451

  Authors: Alok, Elena, Alison, Steve, Megan, Steven W., Manuel, Johnny, Margaret V., Jerzy, Adolfo, Nicholas J., Richa, Pradeep M., Brian M., Sandra Zelman, H. Marijke, Glenn F.

• Guidelines for the management of hemophilia

  Citation: 1424

  Authors: A., A. K., E. P., N. S., S., A., C. A., J. N., K., M. C., A.

• von Willebrand disease (VWD): evidence‐based diagnosis and management guidelines, the National Heart, Lung, and Blood Institute (NHLBI) Expert Panel report (USA)¹

  Citation: 738

  Authors: W. L., M. B., A. H., M. J., R. R., T. L., M. E., J. E., M., B. P.

• The epidemiology of inhibitors in haemophilia A: a systematic review

  Citation: 495

  Authors: J., S.

• The rare coagulation disorders – review with guidelines for management from the United Kingdom Haemophilia Centre Doctors' Organisation

  Citation: 418

  Authors: P. H. B., D. J., E. A., L. A., J. T., M. D., P. W., S., G., A. D.

• Range of motion measurements: reference values and a database for comparison studies

  Citation: 344

  Authors: J. M., C., A., S., M., K. E., D.

• Inherited antithrombin deficiency: a review

  Citation: 316

  Authors: M. M., S.

• Hemophilia joint health score reliability study

  Citation: 287

  Authors: P., S., N., B.‐M., C. S., M., M., P., M., B. M.

• Normal range of bleeding scores for the ISTH‐BAT: adult and pediatric data from the merging project

  Citation: 266

  Authors: M., S., J., S., M., A., W., D. S., A. C., M., J., P. A., R. R., M. L., B., P. D.

• The obstetric and gynaecological management of women with inherited bleeding disorders – review with guidelines produced by a taskforce of UK Haemophilia Centre Doctors’ Organization

  Citation: 223

  Authors: C. A., C., S. R., P. H. B., D., A., R. A.

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