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Study of the Role of Genetic Modifiers in Hemoglobinopathies
Sponsor: Cyprus Institute of Neurology and Genetics
Summary
This study will investigate the role of genetic modifiers in hemoglobinopathies through a large-scale, multi-ethnic genome-wide association study (GWAS).
Key Details
Gender
All
Age Range
2 Years - Any
Study Type
OBSERVATIONAL
Enrollment
30000
Start Date
2022-10-01
Completion Date
2027-09-30
Last Updated
2024-03-20
Healthy Volunteers
No
Interventions
GWAS
The study will perform a GWAS experiments for all recruited subjects. The blood sample will be collected during routine clinical visits, only if DNA is not already available in existing biobanks. All individuals will provide consent for participation in the study.
Locations (26)
Boston Children's Hospital
Boston, Massachusetts, United States
Lucrecia Paím Maternity
Luanda, Angola
University of Buenos Aires
Buenos Aires, Argentina
University Hospitals Leuven
Leuven, Belgium
Universiti Brunei Darussalam
Brunei, Brunei
Larnaca General Hospital
Larnaca, Cyprus
Limassol General Hospital
Limassol, Cyprus
Archbishop Makarios III Hospital
Nicosia, Cyprus
Paphos General Hospital
Paphos, Cyprus
Centre Hospitalier Monkole
Kinshasa, Democratic Republic of the Congo
Rigshospitalet
Copenhagen, Denmark
Hippokrateio Hospital of Athens
Athens, Greece
Laiko General Hospital
Athens, Greece
National and Kapodistrian University of Athens
Athens, Greece
General Hospital of Larissa
Larissa, Greece
Emek Medical Centre
Afula, Israel
University of Turin
Turin, Italy
Ampang Hospital
Ampang, Malaysia
Universiti Kebangsaan Malaysia
Bangi, Malaysia
Universiti Sains Malaysia
Kota Bharu, Malaysia
University of Abuja
Abuja, Nigeria
Kaduna State University
Kaduna, Nigeria
Ahmadu Bello University
Zaria, Nigeria
University of Lahore
Lahore, Pakistan
Centro Hospitalar e Universitário de Coimbra
Coimbra, Portugal
Hospital Clínico San Carlos
Madrid, Spain