Further confirmation of the association of SLC12A2 with non-syndromic autosomal-dominant hearing impairment von Adadey, Samuel M, Schrauwen, Isabelle, Aboagye, Elvis Twumasi, Bharadwaj, Thashi, Esoh, Kevin K, Basit, Sulman, Acharya, Anushree, Nouel-Saied, Liz M, Liaqat, Khurram, Wonkam-Tingang, Edmond, Mowla, Shaheen, Awandare, Gordon A, Ahmad, Wasim, Leal, Suzanne M, Wonkam, Ambroise

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In Silico Design and Validation of OvMANE1, a Chimeric Antigen for Human Onchocerciasis Diagnosis von Shintouo, Cabirou Mounchili, Shey, Robert Adamu, Nebangwa, Derrick Neba, K. Esoh, Kevin, Nongley, Nkemngo Francis, Nguve, Joel Ebai, Giron, Philippe, Mutesa, Léon, Vanhamme, Luc, Souopgui, Jacob, Ghogomu, Stephen Mbigha, Njemini, Rose

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Fine scale human genetic structure in three regions of Cameroon reveals episodic diversifying selection von Esoh, Kevin K., Apinjoh, Tobias O., Nyanjom, Steven G., Wonkam, Ambroise, Chimusa, Emile R., Amenga-Etego, Lucas, Amambua-Ngwa, Alfred, Achidi, Eric A.

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Five Priorities of African Genomics Research: The Next Frontier von Wonkam, Ambroise, Munung, Nchangwi S, Dandara, Collet, Esoh, Kevin K, Hanchard, Neil A, Landoure, Guida

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Genome-wide association study identifies novel candidate malaria resistance genes in Cameroon von Esoh, Kevin K, Apinjoh, Tobias O, Amambua-Ngwa, Alfred, Nyanjom, Steven G, Chimusa, Emile R, Amenga-Etego, Lucas, Wonkam, Ambroise, Achidi, Eric A

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Whole exome sequencing identifies rare coding variants in novel human-mouse ortholog genes in African individuals diagnosed with non-syndromic hearing impairment von Oluwole, Oluwafemi G, Esoh, Kevin K, Wonkam-Tingang, Edmond, Manyisa, Noluthando, Noubiap, Jean Jacques, Chimusa, Emile R, Wonkam, Ambroise

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A novel variant in DMXL2 gene is associated with autosomal dominant non-syndromic hearing impairment (DFNA71) in a Cameroonian family von Wonkam-Tingang, Edmond, Schrauwen, Isabelle, Esoh, Kevin K, Bharadwaj, Thashi, Nouel-Saied, Liz M, Acharya, Anushree, Nasir, Abdul, Leal, Suzanne M, Wonkam, Ambroise

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GJB4 and GJC3 variants in non-syndromic hearing impairment in Ghana von Adadey, Samuel M, Esoh, Kevin K, Quaye, Osbourne, Amedofu, Geoffrey K, Awandare, Gordon A, Wonkam, Ambroise

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Bi-Allelic Novel Variants in CLIC5 Identified in a Cameroonian Multiplex Family with Non-Syndromic Hearing Impairment von Wonkam-Tingang, Edmond, Schrauwen, Isabelle, Esoh, Kevin K., Bharadwaj, Thashi, Nouel-Saied, Liz M., Acharya, Anushree, Nasir, Abdul, Adadey, Samuel M., Mowla, Shaheen, Leal, Suzanne M., Wonkam, Ambroise

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Genome-wide association study identifies novel candidate malaria resistance genes in Cameroon von Esoh, Kevin K, Apinjoh, Tobias O, Amambua-Ngwa, Alfred, Nyanjom, Steven G, Chimusa, Emile R, Amenga-Etego, Lucas, Wonkam, Ambroise, Achidi, Eric A

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Fine scale human genetic structure in three regions of Cameroon reveals episodic diversifying selection von Esoh, Kevin K, Apinjoh, Tobias O, Nyanjom, Steven G, Wonkam, Ambroise, Chimusa, Emile R, Amenga-Etego, Lucas, Amambua-Ngwa, Alfred, Achidi, Eric A

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A novel variant in DXML2 gene is associated with autosomal dominant non-syndromic hearing impairment (DFNA71) in a Cameroonian family von Wonkam-Tingang, Edmond, Schrauwen, Isabelle, Esoh, Kevin K, Bharadwaj, Thashi, Nouel-Saied, Liz M, Acharya, Anushree, Nasir, Abdul, Leal, Suzanne M, Wonkam, Ambroise

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Exome sequencing of families from Ghana reveals known and candidate hearing impairment genes von Wonkam, Ambroise, Adadey, Samuel Mawuli, Schrauwen, Isabelle, Aboagye, Elvis Twumasi, Wonkam-Tingang, Edmond, Esoh, Kevin, Popel, Kalinka, Manyisa, Noluthando, Jonas, Mario, deKock, Carmen, Nembaware, Victoria, Cornejo Sanchez, Diana M., Bharadwaj, Thashi, Nasir, Abdul, Everard, Jenna L., Kadlubowska, Magda K., Nouel-Saied, Liz M., Acharya, Anushree, Quaye, Osbourne, Amedofu, Geoffrey K., Awandare, Gordon A., Leal, Suzanne M.

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

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Open Science in Kenya: Where Are We? von Mwangi, Kennedy W., Mainye, Nyabuti, Ouso, Daniel O., Esoh, Kevin, Muraya, Angela W., Mwangi, Charles K., Naitore, Careen, Karega, Pauline, Kibet-Rono, Gilbert, Musundi, Sebastian, Mutisya, Jennifer, Mwangi, Elizabeth, Mgawe, Cavin, Miruka, Silviane, Kibet, Caleb K.

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The Sickle Cell Disease Ontology: Enabling Collaborative Research and Co-Designing of New Planetary Health Applications von Nembaware, Victoria, Mazandu, Gaston K, Hotchkiss, Jade, Safari Serufuri, Jean-Michel, Kent, Jill, Kengne, Andre Pascal, Anie, Kofi, Munung, Nchangwi Syntia, Bukini, Daima, Bitoungui, Valentina Josiane Ngo, Munube, Deogratias, Chirwa, Uzima, Chunda-Liyoka, Catherine, Jonathan, Agnes, Flor-Park, Miriam V, Esoh, Kevin Kum, Jonas, Mario, Mnika, Khuthala, Oosterwyk, Chandré, Masamu, Upendo, Morrice, Jack, Uwineza, Annette, Nguweneza, Arthemon, Banda, Kambe, Nyanor, Isaac, Adjei, David Nana, Siebu, Nathan Edward, Nkanyemka, Malula, Kuona, Patience, Tayo, Bamidele O, Campbell, Andrew, Oron, Assaf P, Nnodu, Obiageli E, Painstil, Vivian, Makani, Julie, Mulder, Nicola, Wonkam, Ambroise

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