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Houssein Mossafa

Affiliation : Université Mohammed VI des Sciences et de la Santé

3Publications (affiliation in Morocco)
4Total publications
3Citations
1h-index

Research profile

Houssein Mossafa has 3 indexed publications (2021–2024). Their work appears mainly in “Egyptian Journal of Medical Human Genetics” and “Clinical Case Reports”. Their most cited article, “Detection of a new deleterious SGCE gene variant in Moroccan family with inherited myoclonus–dystonia” (2022), has been cited 2 times. 2 of these publications date from the last three years of activity. Their work is co-authored with at least 6 researchers.

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Research areas

Genomics and Rare Diseases
Neurological disorders and treatments
Genetic diversity and population structure
Hematopoietic Stem Cell Transplantation
Forensic and Genetic Research

Publications (3)

Conventional and molecular cytogenetic characterization of a Moroccan patient with WAGR syndrome
2024 · Egyptian Journal of Medical Human Genetics · cited 1 times
Detection of a new deleterious SGCE gene variant in Moroccan family with inherited myoclonus–dystonia
2022 · Clinical Case Reports · cited 2 times
Detection of a new deleterious SGCE gene variant in Moroccan family with inherited Myoclonic-dystonia
2021

Publication venues

Egyptian Journal of Medical Human Genetics × 1
Clinical Case Reports × 1

Publications per year

20241
20221
20211

Collaborations

Partner institutions : Institut Pasteur du Maroc · Laboratoire National de Référence · Instituts Supérieurs des Professions Infirmières et Techniques de Santé · École Normale Supérieure Casablanca · University of Hassan II Casablanca

Co-authors

Bibliographic data from OpenAlex (open database).