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Year Number of Results
2019 1
2020 4
2021 10
2022 8
2023 2
2024 0

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Page 1
Five Priorities of African Genomics Research: The Next Frontier.
Wonkam A, Munung NS, Dandara C, Esoh KK, Hanchard NA, Landoure G. Wonkam A, et al. Among authors: esoh kk. Annu Rev Genomics Hum Genet. 2022 Aug 31;23:499-521. doi: 10.1146/annurev-genom-111521-102452. Epub 2022 May 16. Annu Rev Genomics Hum Genet. 2022. PMID: 35576571 Free article. Review.
Novel variant in CADM3 causes Charcot-Marie-Tooth disease.
Yalcouyé A, Rebelo AP, Cissé L, Rives L, Bamba S, Cogan J, Esoh K, Diarra S, Ezell KM, Taméga A, Guinto CO, Dohrn MF, Hamid R, Fischbeck KH, Zuchner S, Landouré G. Yalcouyé A, et al. Among authors: esoh k. Brain Commun. 2023 Sep 5;5(5):fcad227. doi: 10.1093/braincomms/fcad227. eCollection 2023. Brain Commun. 2023. PMID: 38074074 Free PMC article.
Open Science in Kenya: Where Are We?
Mwangi KW, Mainye N, Ouso DO, Esoh K, Muraya AW, Mwangi CK, Naitore C, Karega P, Kibet-Rono G, Musundi S, Mutisya J, Mwangi E, Mgawe C, Miruka S, Kibet CK; OpenScienceKE Collaborators. Mwangi KW, et al. Among authors: esoh k. Front Res Metr Anal. 2021 May 13;6:669675. doi: 10.3389/frma.2021.669675. eCollection 2021. Front Res Metr Anal. 2021. PMID: 34056516 Free PMC article.
A monoallelic variant in EYA1 is associated with Branchio-Otic syndrome in a Malian family.
Yalcouyé A, Traoré O, Diarra S, Schrauwen I, Esoh K, Kadlubowska MK, Bharadwaj T, Adadey SM, Kéita M, Guinto CO, Leal SM, Landouré G, Wonkam A. Yalcouyé A, et al. Among authors: esoh k. Mol Genet Genomic Med. 2022 Jul;10(7):e1995. doi: 10.1002/mgg3.1995. Epub 2022 Jun 14. Mol Genet Genomic Med. 2022. PMID: 35698919 Free PMC article.
GJB4 and GJC3 variants in non-syndromic hearing impairment in Ghana.
Adadey SM, Esoh KK, Quaye O, Amedofu GK, Awandare GA, Wonkam A. Adadey SM, et al. Among authors: esoh kk. Exp Biol Med (Maywood). 2020 Sep;245(15):1355-1367. doi: 10.1177/1535370220931035. Epub 2020 Jun 11. Exp Biol Med (Maywood). 2020. PMID: 32524838 Free PMC article.
23 results