Wiley

Haemophilia Template

Write in a clean editor, then format for Haemophilia in one click — DocuGuru applies the official Wiley template with author–year references and exports a submission-ready PDF plus the editable LaTeX source. Free to start.

About the Haemophilia format

Haemophilia is a peer-reviewed journal published by Wiley, covering Hemophilia Treatment and Research, Platelet Disorders and Treatments, Blood Coagulation and Thrombosis Mechanisms.

PublisherWiley
Reference styleAuthor–year (Chicago)
Author–year — (Smith, 2023) in the text
Smith, Ada, Ben Jones, and Cara Lee. 2023. "A Representative Article Title." Haemophilia 12 (3): 45–58.

Formats any DOI in Haemophilia style. No sign-up.

Publishes research inHemophilia Treatment and Research Platelet Disorders and Treatments Blood Coagulation and Thrombosis Mechanisms Coagulation, Bradykinin, Polyphosphates, and Angioedema Hemostasis and retained surgical items
ISSN1351-8216
Citation impact (2-yr)2.06
h-index123
i10-index3,458
Total citations145,640
Article processing charge$4,530
Top institutions publishing hereUniversity College London
Journal websiteonlinelibrary.wiley.com
You getA submission-ready PDF and the editable LaTeX source — ready to submit.

Papers published in Haemophilia per year

266
2014
254
2015
308
2016
260
2017
286
2018
260
2019
330
2020
269
2021
263
2022
203
2023
221
2024
226
2025

Citation impact of Haemophilia by publication year

5.2K
2014
4.9K
2015
5.1K
2016
3.9K
2017
4K
2018
3.6K
2019
6.3K
2020
2.8K
2021
2.2K
2022
1.1K
2023
923
2024
258
2025

Citations each year’s papers have accumulated so far — the most recent years are still building up.

Most-cited papers in Haemophilia

Guidelines for the management of hemophilia

Alok Srivastava, A. Brewer, Evelien P. Mauser‐Bunschoten et al. · 6 Jul 2012

Hemophilia is a rare disorder that is complex to diagnose and to manage. These evidence-based guidelines offer practical recommendations on the diagnosis and general management of hemophilia, as well as the management of complications including musculoskeletal issues, inhibitors, and transfusion-transmitted infections. By compiling these guidelines, the World Federation of Hemophilia aims to assist healthcare providers…

1,928 citations Cite SaveGo to paper →
von Willebrand disease (VWD): evidence‐based diagnosis and management guidelines, the National Heart, Lung, and Blood Institute (NHLBI) Expert Panel report (USA) <sup>1</sup>

William L. Nichols, MB Hultin, Allison James et al. · 28 Feb 2008

von Willebrand disease (VWD) is a commonly encountered inherited bleeding disorder affecting both males and females, causing mucous membrane and skin bleeding symptoms, and bleeding with surgical or other haemostatic challenges. VWD may be disproportionately symptomatic in women of child-bearing age. It may also occur less frequently as an acquired disorder (acquired von Willebrand syndrome).…

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

Paula Bolton‐Maggs, David J. Perry, Elizabeth Chalmers et al. · 1 Sep 2004

The rare coagulation disorders are heritable abnormalities of haemostasis that may present significant difficulties in diagnosis and management. This review summarizes the current literature for disorders of fibrinogen, and deficiencies of prothrombin, factor V, FV + VIII, FVII, FX, the combined vitamin K-dependent factors, FXI and FXIII. Based on both collective clinical experience and the…

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

J. Michael Soucie, Chang-Wen Wang, Angela Forsyth et al. · 11 Nov 2010

Many diseases and injuries can impair joint mobility. Normal reference values are needed to determine extent of impairment to assess and monitor joint motion. There is very little published data describing normal joint range of motion (ROM) for healthy men and women across a wide span of ages. We enrolled male and female subjects aged…

Haemophilia template — frequently asked questions

How do I write a paper in the Haemophilia format?
In DocuGuru you write your manuscript in a normal editor — no LaTeX setup required — and select the Haemophilia template. When you export, DocuGuru compiles the paper into the official Wiley format and hands you a submission-ready PDF along with the editable LaTeX source.
What reference style does Haemophilia use?
Haemophilia uses Author–year (Chicago) references, shown as author–year markers such as (Smith, 2023) in the text. DocuGuru formats every in-text citation and the reference list in this exact style automatically. A reference appears like this: Smith, Ada, Ben Jones, and Cara Lee. 2023. "A Representative Article Title." Haemophilia 12 (3): 45–58.
Do I need to know LaTeX to submit to Haemophilia?
No. DocuGuru generates the USG LaTeX class and compiles the PDF for you in the background, so you get a Wiley-ready Haemophilia document without writing any LaTeX. If you do want it, the LaTeX source is included in the export.
Can I import an existing draft into the Haemophilia template?
Yes. Paste or upload your current manuscript — Word, LaTeX, Markdown, or plain text — and DocuGuru reflows it into the Haemophilia format with correct headings, figures, tables, and author–year citations.
Who publishes Haemophilia?
Haemophilia is a multidisciplinary journal published by Wiley. DocuGuru's Haemophilia template matches Wiley's official submission format.
Can I export a submission-ready Haemophilia PDF?
Yes — DocuGuru produces a PDF built with the official Haemophilia template (the USG class) that is ready to submit to Wiley, together with the matching LaTeX source files.
How much does the Haemophilia template cost?
You can start writing in the Haemophilia template for free. Exporting the final submission-ready Haemophilia PDF and LaTeX source is part of DocuGuru's paid plans — see the app for current pricing.
Use the Haemophilia template