Special Collection: Hereditary Diseases

Journal of Medical Sciences · Special Collection · Volume 22 (2027)

The Journal of Medical Sciences invites submissions to a Special Collection on the epidemiology, diagnosis, challenges and management of hereditary diseases, with particular emphasis on the role of consanguinity and the prevalence of hemoglobinopathies in North Africa and the Middle East.

Key dates

Submissions open 30 September 2026
Submission deadline 30 September 2027
Final decisions by 30 November 2027
Publication Continuous: each article is published online as soon as it is accepted, in Volume 22 (2027) Special Collection

Aim and scope

Consanguineous marriage remains a common cultural practice across North Africa and the Middle East and is a key determinant of the burden of inherited disease in the region. This collection brings together original research and reviews on the genetic, clinical and public health dimensions of these disorders. Topics include, but are not limited to:

  • Epidemiology and burden of hereditary diseases in North Africa and the Middle East
  • Hemoglobinopathies, including sickle cell disease and the thalassemias
  • Hereditary cancers, including BRCA1/2, Lynch syndrome and other cancer predisposition syndromes
  • Molecular and genetic studies, including next-generation sequencing and bioinformatics approaches
  • Premarital and carrier screening programs
  • Genetic counseling, ethical considerations and socio-cultural aspects
  • Newborn screening and early detection strategies
  • Advances in the diagnosis, management and treatment of hereditary conditions
  • Public health policies, prevention and education strategies

Article types

Original research articles, review articles, case reports, short communications and perspectives. Only manuscripts written in English will be considered for this collection.

Editors of the Special Collection

Managing Editors

Prof. Inas Alhudiri ORCID Google Scholar
Editor-in-Chief, Libyan Biotechnology Research Center, Tripoli, Libya

Dr. Ahmed Glewan Google Scholar
Managing Editor, Faculty of Dentistry, Sebha University, Libya

Handling Editors

Dr. Imen Moumni ORCID Google Scholar
Laboratory of Molecular and Cellular Hematology, Pasteur Institute of Tunis, Tunisia

Dr. Salma Shickh Google Scholar
University of British Columbia, Canada

How to submit

  1. Prepare your manuscript according to the Author Guidelines.
  2. Log in or register, and click Make a New Submission.
  3. Select the section Special Collection: Hereditary Diseases, Consanguinity, and Hemoglobinopathies.
  4. State in your cover letter that the manuscript is submitted to this Special Collection.

Peer review and editorial independence

All submissions undergo the journal's standard double-blind peer review by at least two independent reviewers. Manuscripts authored by any editor of this collection are handled by another member of the Editorial Board with no conflict of interest, and the submitting editor has no access to their review. Acceptance depends only on scientific quality; a paper submitted to the collection that is accepted after it closes is published in a regular issue.

Open access and fees

All articles are published open access under the CC BY 4.0 licence. There are no submission or publication fees.

Contact

Editor-in-Chief: Prof. Inas Alhudiri, [email protected]

Submit to this collection