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The International Hemoglobinopathy Research Network (INHERENT): An international initiative to study the role of genetic modifiers in hemoglobinopathies

Kountouris P 1 , Stephanou C 1 , Archer N 2 , Bonifazi F 3 , Giannuzzi V 3 , Kuo KHM 4 Show all authors , Maggio A 5 , Makani J 6 , Mañú-Pereira MDM 7 , Michailidou K 1 , Nkya S 6 , Nnodu OE 8 , Trompeter S 9 , Tshilolo L 10 , Wonkam A 11 , Zilfalil BA 12 , Inusa BPD 13 , Kleanthous M 1 , on behalf of the International Hemoglobinopathy Research Network (INHERENT)

Affiliations 

  • 1 The Cyprus Institute of Neurology and Genetics, Nicosia, Cyprus
  • 2 Pediatric Hematology/Oncology, Dana-Farber/Boston Children's Cancer and Blood Disorders Center, Boston, Massachusetts, USA
  • 3 Fondazione per la Ricerca Farmacologica Gianni Benzi Onlus, Bari, Italy
  • 4 Division of Hematology, Department of Medicine, University of Toronto, Toronto, Ontario, Canada
  • 5 A.O. Villa Sofia-Cervello, Palermo, Italy
  • 6 Muhimbili University of Health and Allied Sciences, Dar es Salaam, Tanzania
  • 7 Translational Research in Child and Adolescent Cancer. Vall d'Hebron Institut de recerca, Barcelona, Spain
  • 8 Department of Haematology and Blood Transfusion, University of Abuja, Abuja, Nigeria
  • 9 University College London Hospitals NHS Trust, London, UK
  • 10 Centre Hospitalier Monkole and CEFA-Institut de Recherche Biomédicale, Kinshasa, Democratic Republic of Congo
  • 11 University of Cape Town, Cape Town, South Africa
  • 12 Universiti Sains Malaysia, Health Campus, Kelantan, Malaysia
  • 13 Paediatric Haematology, Evelina London Children's Hospital, Guy's & St. Thomas' Hospital NHS Foundation Trust, London, UK
Am J Hematol, 2021 Nov 01;96(11):E416-E420.
PMID: 34406671 DOI: 10.1002/ajh.26323

* Title and MeSH Headings from MEDLINE®/PubMed®, a database of the U.S. National Library of Medicine.

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