Ambroise Wonkam

Ambroise Wonkam is a Cameroonian medical doctor and professor of medical genetics at Johns Hopkins School of Medicine. His research is in sickle cell disease, the genetics of congenital hearing impairment, and ethics in human genetics. He is the current president of the African Society of Human Genetics. Provided by Wikipedia
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  1. 1
    Considerations of Autonomy in Guiding Decisions around the Feedback of Individual Genetic Research Results from Genomics Research: Expectations of and Preferences from Researchers in Botswana

    Considerations of Autonomy in Guiding Decisions around the Feedback of Individual Genetic Research Results from Genomics Research: Expectations of and Preferences from Researchers... by Mary Kasule, Mogomotsi Matshaba, Erisa Mwaka, Ambroise Wonkam, Jantina de Vries

    Published 2022-01-01
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  2. 2
    Competency-based Training Needs Assessment for Research Managers and Administrators in Africa and the United Kingdom to Strengthen Equitable Partnerships [version 1; peer review: 2 approved, 1 approved with reservations]

    Competency-based Training Needs Assessment for Research Managers and Administrators in Africa and the United Kingdom to Strengthen Equitable Partnerships [version 1; peer review: 2... by Paidamoyo Bodzo, Michelle Skelton, Alecia Naidu, Olivia Lelong, Collet Dandara, Alice Mutambiranwa, Colleen Masimirembwa, Annette Hay, Ambroise Wonkam, Simon Glasser, Victoria Nembaware, Ailsa Davies, Anne Priest

    Published 2022-03-01
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  3. 3
    Exome sequencing revealed a novel homozygous variant in TRMT61 A in a multiplex family with atypical Cornelia de Lange Syndrome from Rwanda

    Exome sequencing revealed a novel homozygous variant in TRMT61 A in a multiplex family with atypical Cornelia de Lange Syndrome from Rwanda by Esther Uwibambe, Abdoulaye Yalcouyé, Elvis Twumasi Aboagye, Lettilia Xhakaza, Kalinka Popel, Norbert Dukuze, Thashi Bharadwaj, Carmen de Kock, Isabelle Schrauwen, Suzanne M. Leal, Leon Mutesa, Ambroise Wonkam

    Published 2025-05-01
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  4. 4
    Whole-exome sequencing reveals known and candidate genes for hearing impairment in Mali

    Whole-exome sequencing reveals known and candidate genes for hearing impairment in Mali by Abdoulaye Yalcouyé, Isabelle Schrauwen, Oumou Traoré, Salia Bamba, Elvis Twumasi Aboagye, Anushree Acharya, Thashi Bharadwaj, Rachel Latanich, Kevin Esoh, Cesar A. Fortes-Lima, Carmen de Kock, Mario Jonas, Alassane dit Baneye Maiga, Cheick A.K. Cissé, Moussa A. Sangaré, Cheick O. Guinto, Guida Landouré, Suzanne M. Leal, Ambroise Wonkam

    Published 2025-01-01
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  5. 5
    Sickle Cell Disease in Africa: SickleInAfrica Registry in Ghana, Nigeria and Tanzania

    Sickle Cell Disease in Africa: SickleInAfrica Registry in Ghana, Nigeria and Tanzania by Jack Morrice, Wilson Mupfururirwa, Reuben I. Chianumba, Evans Xorse Amuzu, Daniel Kandonga, Victoria Nembaware, Mario Jonas, Jade Hotchkiss, Upendo Masamu, Arthemon Nguweneza, Bruno P. Mmbando, Irene Minja, Agnes Jonathan, Nicola Mulder, Emmanuel Balandya, Alex Osei‐Akoto, Vivian Paintsil, Julie Makani, Obiageli Nnodu, Members of SPARCO Nigeria, Raphael Z. Sangeda, Andre Pascal Kengne, Gaston Kuzamunu, Ambroise Wonkam

    Published 2025-06-01
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  6. 6
    FLT1 and other candidate fetal haemoglobin modifying loci in sickle cell disease in African ancestries

    FLT1 and other candidate fetal haemoglobin modifying loci in sickle cell disease in African ancestries by Ambroise Wonkam, Kevin Esoh, Rachel M. Levine, Valentina Josiane Ngo Bitoungui, Khuthala Mnika, Nikitha Nimmagadda, Erin A. D. Dempsey, Siana Nkya, Raphael Z. Sangeda, Victoria Nembaware, Jack Morrice, Fujr Osman, Michael A. Beer, Julie Makani, Nicola Mulder, Guillaume Lettre, Martin H. Steinberg, Rachel Latanich, James F. Casella, Daiana Drehmer, Dan E. Arking, Emile R. Chimusa, Jonathan S. Yen, Gregory A. Newby, Stylianos E. Antonarakis

    Published 2025-03-01
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